Item | Value |
---|---|
geneid | 4928 |
ensemblid | ENSG00000110713.18 |
hgncid | 8068 |
symbol | NUP98 |
name | nucleoporin 98 and 96 precursor |
refseq_nuc | NM_016320.5 |
refseq_prot | NP_057404.2 |
ensembl_nuc | ENST00000324932.12 |
ensembl_prot | ENSP00000316032.7 |
mane_status | MANE Select |
chr | chr11 |
start | 3675019 |
end | 3797554 |
strand | - |
ver | v1.2 |
region | chr11:3675019-3797554 |
region5000 | chr11:3670019-3802554 |
regionname0 | NUP98_chr11_3675019_3797554 |
regionname5000 | NUP98_chr11_3670019_3802554 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1800 | 297 | 75 | 39 | 145 | 5 | 31 | 109 | NUP98_chr11_3670019_3802554 | NUP98 | MFNKS others(1795): Show |
chr11 | 3670019 | 3802554 |
a0002 | 0/0 | 1800 | 10 | 0 | 7 | 0 | 1 | 2 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | MFNKS others(1795): Show |
chr11 | 3670019 | 3802554 |
a0003 | 0/0 | 1800 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | MFNKS others(1795): Show |
chr11 | 3670019 | 3802554 |
a0004 | 0/0 | 1800 | 4 | 0 | 0 | 4 | 0 | 0 | 2 | NUP98_chr11_3670019_3802554 | NUP98 | MFNKS others(1795): Show |
chr11 | 3670019 | 3802554 |
a0005 | 0/0 | 1800 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | MFNKS others(1795): Show |
chr11 | 3670019 | 3802554 |
a0006 | 0/0 | 1800 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | MFNKS others(1795): Show |
chr11 | 3670019 | 3802554 |
a0007 | 0/0 | 1800 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | MFNKS others(1795): Show |
chr11 | 3670019 | 3802554 |
a0008 | 0/0 | 1800 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | MFNKS others(1795): Show |
chr11 | 3670019 | 3802554 |
a0009 | 0/0 | 1800 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | MFNKS others(1795): Show |
chr11 | 3670019 | 3802554 |
a0010 | 0/0 | 1800 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | NUP98_chr11_3670019_3802554 | NUP98 | MFNKS others(1795): Show |
chr11 | 3670019 | 3802554 |
a0011 | 0/0 | 1800 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | MFNKS others(1795): Show |
chr11 | 3670019 | 3802554 |
a0012 | 0/0 | 1800 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | MFNKS others(1795): Show |
chr11 | 3670019 | 3802554 |
a0013 | 0/0 | 1800 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | MFNKS others(1795): Show |
chr11 | 3670019 | 3802554 |
a0014 | 0/0 | 1800 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | MFNKS others(1795): Show |
chr11 | 3670019 | 3802554 |
a0015 | 0/0 | 1800 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | MFNKS others(1795): Show |
chr11 | 3670019 | 3802554 |
a0016 | 0/0 | 1800 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | MFNKS others(1795): Show |
chr11 | 3670019 | 3802554 |
a0017 | 0/0 | 1800 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | MFNKS others(1795): Show |
chr11 | 3670019 | 3802554 |
a0018 | 0/0 | 1800 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | MFNKS others(1795): Show |
chr11 | 3670019 | 3802554 |
a0019 | 0/0 | 1800 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | MFNKS others(1795): Show |
chr11 | 3670019 | 3802554 |
a0020 | 0/0 | 1800 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | MFNKS others(1795): Show |
chr11 | 3670019 | 3802554 |
a0021 | 0/0 | 1800 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | MFNKS others(1795): Show |
chr11 | 3670019 | 3802554 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 5400 | 181 | 43 | 30 | 82 | 3 | 22 | NUP98_chr11_3670019_3802554 | NUP98 | ATGTT others(5395): Show |
chr11 | 3670019 | 3802554 | ||
a0001c0002 | 0/0 | 5400 | 96 | 18 | 6 | 62 | 2 | 8 | NUP98_chr11_3670019_3802554 | NUP98 | ATGTT others(5395): Show |
chr11 | 3670019 | 3802554 | ||
a0001c0003 | 0/0 | 5400 | 7 | 6 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | ATGTT others(5395): Show |
chr11 | 3670019 | 3802554 | ||
a0001c0006 | 0/1 | 5400 | 5 | 2 | 2 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | ATGTT others(5395): Show |
chr11 | 3670019 | 3802554 | ||
a0001c0012 | 0/0 | 5400 | 2 | 2 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | ATGTT others(5395): Show |
chr11 | 3670019 | 3802554 | ||
a0001c0016 | 0/0 | 5400 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | ATGTT others(5395): Show |
chr11 | 3670019 | 3802554 | ||
a0001c0017 | 0/0 | 5400 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | ATGTT others(5395): Show |
chr11 | 3670019 | 3802554 | ||
a0001c0020 | 0/0 | 5400 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | ATGTT others(5395): Show |
chr11 | 3670019 | 3802554 | ||
a0001c0024 | 0/0 | 5400 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | ATGTT others(5395): Show |
chr11 | 3670019 | 3802554 | ||
a0001c0026 | 0/0 | 5400 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | ATGTT others(5395): Show |
chr11 | 3670019 | 3802554 | ||
a0001c0032 | 0/0 | 5400 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | ATGTT others(5395): Show |
chr11 | 3670019 | 3802554 | ||
a0002c0005 | 0/0 | 5400 | 6 | 0 | 4 | 0 | 1 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | ATGTT others(5395): Show |
chr11 | 3670019 | 3802554 | ||
a0002c0008 | 0/0 | 5400 | 4 | 0 | 3 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | ATGTT others(5395): Show |
chr11 | 3670019 | 3802554 | ||
a0003c0004 | 0/0 | 5400 | 6 | 6 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | ATGTT others(5395): Show |
chr11 | 3670019 | 3802554 | ||
a0004c0007 | 0/0 | 5400 | 4 | 0 | 0 | 4 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | ATGTT others(5395): Show |
chr11 | 3670019 | 3802554 | ||
a0005c0010 | 0/0 | 5400 | 2 | 2 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | ATGTT others(5395): Show |
chr11 | 3670019 | 3802554 | ||
a0005c0021 | 0/0 | 5400 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | ATGTT others(5395): Show |
chr11 | 3670019 | 3802554 | ||
a0006c0009 | 0/0 | 5400 | 3 | 3 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | ATGTT others(5395): Show |
chr11 | 3670019 | 3802554 | ||
a0007c0013 | 0/0 | 5400 | 2 | 0 | 2 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | ATGTT others(5395): Show |
chr11 | 3670019 | 3802554 | ||
a0008c0027 | 0/0 | 5400 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | ATGTT others(5395): Show |
chr11 | 3670019 | 3802554 | ||
a0008c0028 | 0/0 | 5400 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | ATGTT others(5395): Show |
chr11 | 3670019 | 3802554 | ||
a0009c0011 | 0/0 | 5400 | 2 | 0 | 0 | 0 | 0 | 2 | NUP98_chr11_3670019_3802554 | NUP98 | ATGTT others(5395): Show |
chr11 | 3670019 | 3802554 | ||
a0010c0014 | 0/0 | 5400 | 2 | 0 | 0 | 2 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | ATGTT others(5395): Show |
chr11 | 3670019 | 3802554 | ||
a0011c0025 | 0/0 | 5400 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | ATGTT others(5395): Show |
chr11 | 3670019 | 3802554 | ||
a0012c0022 | 0/0 | 5400 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | ATGTT others(5395): Show |
chr11 | 3670019 | 3802554 | ||
a0013c0029 | 0/0 | 5400 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | ATGTT others(5395): Show |
chr11 | 3670019 | 3802554 | ||
a0014c0031 | 0/0 | 5400 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | ATGTT others(5395): Show |
chr11 | 3670019 | 3802554 | ||
a0015c0033 | 0/0 | 5400 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | ATGTT others(5395): Show |
chr11 | 3670019 | 3802554 | ||
a0016c0023 | 0/0 | 5400 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | ATGTT others(5395): Show |
chr11 | 3670019 | 3802554 | ||
a0017c0019 | 0/0 | 5400 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | ATGTT others(5395): Show |
chr11 | 3670019 | 3802554 | ||
a0018c0034 | 0/0 | 5400 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | ATGTT others(5395): Show |
chr11 | 3670019 | 3802554 | ||
a0019c0015 | 0/0 | 5400 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | ATGTT others(5395): Show |
chr11 | 3670019 | 3802554 | ||
a0020c0018 | 0/0 | 5400 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | ATGTT others(5395): Show |
chr11 | 3670019 | 3802554 | ||
a0021c0030 | 0/0 | 5400 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | ATGTT others(5395): Show |
chr11 | 3670019 | 3802554 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 6726 | 173 | 38 | 27 | 82 | 3 | 22 | NUP98_chr11_3670019_3802554 | NUP98 | GCAGT others(6721): Show |
chr11 | 3670019 | 3802554 |
a0001c0001t0002 | 0/0 | 6722 | 4 | 2 | 2 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | GCAGT others(6717): Show |
chr11 | 3670019 | 3802554 |
a0001c0001t0004 | 0/0 | 6726 | 2 | 2 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | GCAGT others(6721): Show |
chr11 | 3670019 | 3802554 |
a0001c0001t0006 | 0/0 | 6726 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | GCAGT others(6721): Show |
chr11 | 3670019 | 3802554 |
a0001c0001t0008 | 0/0 | 6726 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | GCAGT others(6721): Show |
chr11 | 3670019 | 3802554 |
a0001c0002t0001 | 0/0 | 6726 | 94 | 18 | 6 | 60 | 2 | 8 | NUP98_chr11_3670019_3802554 | NUP98 | GCAGT others(6721): Show |
chr11 | 3670019 | 3802554 |
a0001c0002t0007 | 0/0 | 6726 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | GCAGT others(6721): Show |
chr11 | 3670019 | 3802554 |
a0001c0002t0010 | 0/0 | 6726 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | GCAGT others(6721): Show |
chr11 | 3670019 | 3802554 |
a0001c0003t0002 | 0/0 | 6722 | 7 | 6 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | GCAGT others(6717): Show |
chr11 | 3670019 | 3802554 |
a0001c0006t0001 | 0/1 | 6726 | 5 | 2 | 2 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | GCAGT others(6721): Show |
chr11 | 3670019 | 3802554 |
a0001c0012t0001 | 0/0 | 6726 | 2 | 2 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | GCAGT others(6721): Show |
chr11 | 3670019 | 3802554 |
a0001c0016t0001 | 0/0 | 6726 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | GCAGT others(6721): Show |
chr11 | 3670019 | 3802554 |
a0001c0017t0002 | 0/0 | 6722 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | GCAGT others(6717): Show |
chr11 | 3670019 | 3802554 |
a0001c0020t0001 | 0/0 | 6726 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | GCAGT others(6721): Show |
chr11 | 3670019 | 3802554 |
a0001c0024t0001 | 0/0 | 6726 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | GCAGT others(6721): Show |
chr11 | 3670019 | 3802554 |
a0001c0026t0001 | 0/0 | 6726 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | GCAGT others(6721): Show |
chr11 | 3670019 | 3802554 |
a0001c0032t0001 | 0/0 | 6726 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | GCAGT others(6721): Show |
chr11 | 3670019 | 3802554 |
a0002c0005t0001 | 0/0 | 6726 | 6 | 0 | 4 | 0 | 1 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | GCAGT others(6721): Show |
chr11 | 3670019 | 3802554 |
a0002c0008t0001 | 0/0 | 6726 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | GCAGT others(6721): Show |
chr11 | 3670019 | 3802554 |
a0002c0008t0003 | 0/0 | 6726 | 3 | 0 | 3 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | GCAGT others(6721): Show |
chr11 | 3670019 | 3802554 |
a0003c0004t0001 | 0/0 | 6726 | 6 | 6 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | GCAGT others(6721): Show |
chr11 | 3670019 | 3802554 |
a0004c0007t0001 | 0/0 | 6726 | 4 | 0 | 0 | 4 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | GCAGT others(6721): Show |
chr11 | 3670019 | 3802554 |
a0005c0010t0001 | 0/0 | 6726 | 2 | 2 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | GCAGT others(6721): Show |
chr11 | 3670019 | 3802554 |
a0005c0021t0001 | 0/0 | 6726 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | GCAGT others(6721): Show |
chr11 | 3670019 | 3802554 |
a0006c0009t0001 | 0/0 | 6726 | 3 | 3 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | GCAGT others(6721): Show |
chr11 | 3670019 | 3802554 |
a0007c0013t0005 | 0/0 | 6726 | 2 | 0 | 2 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | GCAGT others(6721): Show |
chr11 | 3670019 | 3802554 |
a0008c0027t0001 | 0/0 | 6726 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | GCAGT others(6721): Show |
chr11 | 3670019 | 3802554 |
a0008c0028t0001 | 0/0 | 6726 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | GCAGT others(6721): Show |
chr11 | 3670019 | 3802554 |
a0009c0011t0001 | 0/0 | 6726 | 2 | 0 | 0 | 0 | 0 | 2 | NUP98_chr11_3670019_3802554 | NUP98 | GCAGT others(6721): Show |
chr11 | 3670019 | 3802554 |
a0010c0014t0001 | 0/0 | 6726 | 2 | 0 | 0 | 2 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | GCAGT others(6721): Show |
chr11 | 3670019 | 3802554 |
a0011c0025t0001 | 0/0 | 6726 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | GCAGT others(6721): Show |
chr11 | 3670019 | 3802554 |
a0012c0022t0001 | 0/0 | 6726 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | GCAGT others(6721): Show |
chr11 | 3670019 | 3802554 |
a0013c0029t0001 | 0/0 | 6726 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | GCAGT others(6721): Show |
chr11 | 3670019 | 3802554 |
a0014c0031t0001 | 0/0 | 6726 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | GCAGT others(6721): Show |
chr11 | 3670019 | 3802554 |
a0015c0033t0001 | 0/0 | 6726 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | GCAGT others(6721): Show |
chr11 | 3670019 | 3802554 |
a0016c0023t0001 | 0/0 | 6726 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | GCAGT others(6721): Show |
chr11 | 3670019 | 3802554 |
a0017c0019t0001 | 0/0 | 6726 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | GCAGT others(6721): Show |
chr11 | 3670019 | 3802554 |
a0018c0034t0001 | 0/0 | 6726 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | GCAGT others(6721): Show |
chr11 | 3670019 | 3802554 |
a0019c0015t0001 | 0/0 | 6726 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | GCAGT others(6721): Show |
chr11 | 3670019 | 3802554 |
a0020c0018t0001 | 0/0 | 6726 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | GCAGT others(6721): Show |
chr11 | 3670019 | 3802554 |
a0021c0030t0009 | 0/0 | 6726 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | GCAGT others(6721): Show |
chr11 | 3670019 | 3802554 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0238 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0002g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0002g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0002g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0002g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0004g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0004g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0006g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0001t0008g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0007g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0002t0010g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0003t0002g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0003t0002g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0003t0002g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0003t0002g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0003t0002g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0003t0002g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0003t0002g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0006t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0006t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0006t0001g0188 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0006t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0006t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0012t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0012t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0016t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0017t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0020t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0024t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0026t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0001c0032t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0002c0005t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0002c0005t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0002c0005t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0002c0005t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0002c0005t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0002c0005t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0002c0008t0001g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0002c0008t0003g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0002c0008t0003g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0002c0008t0003g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0003c0004t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0003c0004t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0003c0004t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0003c0004t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0003c0004t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0003c0004t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0004c0007t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0004c0007t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0004c0007t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0004c0007t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0005c0010t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0005c0010t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0005c0021t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0006c0009t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0006c0009t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0006c0009t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0007c0013t0005g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0007c0013t0005g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0008c0027t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0008c0028t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0009c0011t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0009c0011t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0010c0014t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0010c0014t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0011c0025t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0012c0022t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0013c0029t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0014c0031t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0015c0033t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0016c0023t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0017c0019t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0018c0034t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0019c0015t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0020c0018t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
a0021c0030t0009g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00323 | hp1 | a0001 | c0001 | t0001 | g0208 | EUR | FIN | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG00323 | hp2 | a0001 | c0002 | t0001 | g0285 | EUR | FIN | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | CHS | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | CHS | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG00423 | hp1 | a0001 | c0002 | t0001 | g0271 | EAS | CHS | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG00423 | hp2 | a0004 | c0007 | t0001 | g0245 | EAS | CHS | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | CHS | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG00438 | hp2 | a0001 | c0002 | t0001 | g0102 | EAS | CHS | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG00544 | hp1 | a0001 | c0002 | t0010 | g0342 | EAS | CHS | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG00544 | hp2 | a0004 | c0007 | t0001 | g0213 | EAS | CHS | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | CHS | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG00558 | hp2 | a0001 | c0002 | t0001 | g0070 | EAS | CHS | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG00597 | hp1 | a0001 | c0002 | t0001 | g0021 | EAS | CHS | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG00597 | hp2 | a0001 | c0002 | t0001 | g0281 | EAS | CHS | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | CHS | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | CHS | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG00621 | hp1 | a0001 | c0002 | t0001 | g0187 | EAS | CHS | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | CHS | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | PUR | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0317 | AMR | PUR | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG00642 | hp1 | a0001 | c0001 | t0008 | g0325 | AMR | PUR | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0248 | AMR | PUR | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG00733 | hp2 | a0001 | c0002 | t0001 | g0089 | AMR | PUR | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG00735 | hp1 | a0002 | c0008 | t0003 | g0040 | AMR | PUR | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG00738 | hp1 | a0001 | c0002 | t0001 | g0092 | AMR | PUR | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG00741 | hp1 | a0002 | c0008 | t0003 | g0064 | AMR | PUR | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG00741 | hp2 | a0001 | c0006 | t0001 | g0242 | AMR | PUR | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG01081 | hp1 | a0002 | c0005 | t0001 | g0299 | AMR | PUR | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG01081 | hp2 | a0011 | c0025 | t0001 | g0236 | AMR | PUR | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG01099 | hp1 | a0001 | c0002 | t0001 | g0080 | AMR | PUR | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0305 | AMR | PUR | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG01106 | hp1 | a0002 | c0008 | t0003 | g0062 | AMR | PUR | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | PUR | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0249 | AMR | PUR | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG01109 | hp2 | a0001 | c0003 | t0002 | g0323 | AMR | PUR | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG01167 | hp1 | a0002 | c0005 | t0001 | g0303 | AMR | PUR | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG01167 | hp2 | a0001 | c0002 | t0001 | g0094 | AMR | PUR | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG01168 | hp1 | a0002 | c0005 | t0001 | g0304 | AMR | PUR | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG01169 | hp2 | a0002 | c0005 | t0001 | g0301 | AMR | PUR | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG01243 | hp1 | a0001 | c0002 | t0001 | g0295 | AMR | PUR | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG01243 | hp2 | a0012 | c0022 | t0001 | g0128 | AMR | PUR | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0253 | AMR | CLM | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG01255 | hp2 | a0007 | c0013 | t0005 | g0218 | AMR | CLM | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | CLM | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | CLM | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0308 | AMR | CLM | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | CLM | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG01361 | hp2 | a0001 | c0006 | t0001 | g0204 | AMR | CLM | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | CLM | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0335 | AMR | CLM | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG01515 | hp1 | a0002 | c0005 | t0001 | g0300 | EUR | IBS | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0215 | EUR | IBS | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0306 | AFR | ACB | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0340 | AFR | ACB | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | ACB | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | PEL | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG01934 | hp2 | a0013 | c0029 | t0001 | g0134 | AMR | PEL | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0314 | AMR | PEL | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG01943 | hp2 | a0014 | c0031 | t0001 | g0107 | AMR | PEL | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PEL | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG01952 | hp2 | a0007 | c0013 | t0005 | g0037 | AMR | PEL | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG01993 | hp1 | a0001 | c0002 | t0001 | g0024 | AMR | PEL | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PEL | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | PEL | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PEL | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | KHV | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG02015 | hp2 | a0001 | c0002 | t0007 | g0132 | EAS | KHV | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG02027 | hp1 | a0001 | c0002 | t0001 | g0167 | EAS | KHV | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | KHV | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | ACB | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG02055 | hp2 | a0001 | c0003 | t0002 | g0290 | AFR | ACB | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG02056 | hp2 | a0001 | c0002 | t0001 | g0101 | EAS | KHV | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | KHV | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG02080 | hp1 | a0001 | c0002 | t0001 | g0103 | EAS | KHV | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | KHV | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG02083 | hp1 | a0008 | c0028 | t0001 | g0147 | EAS | KHV | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | KHV | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | KHV | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG02129 | hp2 | a0001 | c0002 | t0001 | g0087 | EAS | KHV | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG02132 | hp1 | a0008 | c0027 | t0001 | g0153 | EAS | KHV | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG02135 | hp1 | a0001 | c0002 | t0001 | g0106 | EAS | KHV | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG02135 | hp2 | a0001 | c0024 | t0001 | g0251 | EAS | KHV | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0334 | AFR | ACB | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PEL | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PEL | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | CDX | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | CDX | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG02165 | hp1 | a0001 | c0002 | t0001 | g0096 | EAS | CDX | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | CDX | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG02257 | hp1 | a0001 | c0002 | t0001 | g0212 | AFR | ACB | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG02257 | hp2 | a0001 | c0001 | t0006 | g0297 | AFR | ACB | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG02258 | hp1 | a0001 | c0002 | t0001 | g0318 | AFR | ACB | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | ACB | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG02280 | hp1 | a0005 | c0021 | t0001 | g0259 | AFR | ACB | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG02451 | hp1 | a0001 | c0032 | t0001 | g0032 | AFR | ACB | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | ACB | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG02572 | hp1 | a0003 | c0004 | t0001 | g0117 | AFR | GWD | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | GWD | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG02615 | hp1 | a0006 | c0009 | t0001 | g0033 | AFR | GWD | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0324 | AFR | GWD | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0296 | AFR | GWD | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG02630 | hp1 | a0015 | c0033 | t0001 | g0130 | AFR | GWD | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | GWD | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG02647 | hp2 | a0001 | c0001 | t0004 | g0331 | AFR | GWD | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0230 | SAS | PJL | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG02717 | hp1 | a0003 | c0004 | t0001 | g0118 | AFR | GWD | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG02717 | hp2 | a0001 | c0001 | t0004 | g0330 | AFR | GWD | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0223 | SAS | PJL | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0224 | SAS | PJL | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG02809 | hp1 | a0001 | c0012 | t0001 | g0319 | AFR | GWD | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG02818 | hp1 | a0006 | c0009 | t0001 | g0035 | AFR | GWD | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG02818 | hp2 | a0001 | c0003 | t0002 | g0312 | AFR | GWD | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG02886 | hp1 | a0003 | c0004 | t0001 | g0119 | AFR | GWD | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG02886 | hp2 | a0005 | c0010 | t0001 | g0338 | AFR | GWD | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0293 | AFR | GWD | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG02895 | hp2 | a0001 | c0003 | t0002 | g0311 | AFR | GWD | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG02896 | hp1 | a0001 | c0006 | t0001 | g0127 | AFR | GWD | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0291 | AFR | GWD | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0329 | AFR | ESN | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG02922 | hp2 | a0001 | c0002 | t0001 | g0073 | AFR | ESN | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG02965 | hp1 | a0001 | c0002 | t0001 | g0178 | AFR | ESN | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | ESN | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG02970 | hp1 | a0016 | c0023 | t0001 | g0001 | AFR | ESN | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | ESN | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0336 | AFR | ESN | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0275 | AFR | ESN | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG03041 | hp1 | a0001 | c0002 | t0001 | g0322 | AFR | GWD | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG03041 | hp2 | a0001 | c0003 | t0002 | g0341 | AFR | GWD | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | MSL | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | MSL | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG03130 | hp1 | a0001 | c0002 | t0001 | g0074 | AFR | ESN | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG03130 | hp2 | a0001 | c0001 | t0002 | g0309 | AFR | ESN | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG03139 | hp1 | a0003 | c0004 | t0001 | g0115 | AFR | ESN | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0337 | AFR | ESN | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG03195 | hp1 | a0001 | c0002 | t0001 | g0075 | AFR | ESN | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG03195 | hp2 | a0001 | c0002 | t0001 | g0193 | AFR | ESN | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG03209 | hp1 | a0001 | c0002 | t0001 | g0088 | AFR | MSL | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG03209 | hp2 | a0001 | c0002 | t0001 | g0123 | AFR | MSL | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG03239 | hp1 | a0001 | c0002 | t0001 | g0008 | SAS | PJL | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0287 | SAS | PJL | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0307 | AFR | MSL | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG03453 | hp2 | a0001 | c0003 | t0002 | g0313 | AFR | MSL | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0310 | AFR | MSL | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0328 | AFR | MSL | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG03490 | hp1 | a0009 | c0011 | t0001 | g0072 | SAS | PJL | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0225 | SAS | PJL | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG03491 | hp2 | a0001 | c0002 | t0001 | g0016 | SAS | PJL | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG03492 | hp1 | a0009 | c0011 | t0001 | g0071 | SAS | PJL | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | ESN | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG03516 | hp2 | a0001 | c0006 | t0001 | g0126 | AFR | ESN | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG03540 | hp1 | a0001 | c0002 | t0001 | g0294 | AFR | GWD | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0333 | AFR | GWD | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG03579 | hp1 | a0006 | c0009 | t0001 | g0034 | AFR | MSL | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG03579 | hp2 | a0001 | c0002 | t0001 | g0315 | AFR | MSL | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG03654 | hp1 | a0002 | c0005 | t0001 | g0302 | SAS | PJL | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG03654 | hp2 | a0017 | c0019 | t0001 | g0222 | SAS | PJL | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG03688 | hp1 | a0001 | c0002 | t0001 | g0288 | SAS | STU | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG03688 | hp2 | a0002 | c0008 | t0001 | g0003 | SAS | STU | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG03710 | hp1 | a0001 | c0002 | t0001 | g0124 | SAS | PJL | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | BEB | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG03831 | hp2 | a0001 | c0002 | t0001 | g0282 | SAS | BEB | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | STU | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG04115 | hp2 | a0001 | c0020 | t0001 | g0210 | SAS | STU | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | BEB | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG04184 | hp2 | a0001 | c0002 | t0001 | g0091 | SAS | BEB | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG04199 | hp1 | a0001 | c0002 | t0001 | g0203 | SAS | STU | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG04199 | hp2 | a0001 | c0002 | t0001 | g0286 | SAS | STU | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0173 | SAS | STU | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0332 | SAS | STU | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | STU | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | STU | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA18522 | hp1 | a0001 | c0002 | t0001 | g0192 | AFR | YRI | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA18522 | hp2 | a0001 | c0002 | t0001 | g0131 | AFR | YRI | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA18612 | hp1 | a0001 | c0002 | t0001 | g0098 | EAS | CHB | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA18612 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | CHB | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA18942 | hp1 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA18942 | hp2 | a0001 | c0002 | t0001 | g0260 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA18944 | hp1 | a0004 | c0007 | t0001 | g0246 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA18944 | hp2 | a0001 | c0002 | t0001 | g0077 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA18947 | hp1 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA18947 | hp2 | a0001 | c0002 | t0001 | g0270 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA18950 | hp1 | a0001 | c0002 | t0001 | g0023 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA18954 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA18957 | hp1 | a0001 | c0002 | t0001 | g0264 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA18959 | hp2 | a0001 | c0002 | t0001 | g0268 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA18960 | hp2 | a0001 | c0002 | t0001 | g0277 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA18961 | hp2 | a0001 | c0002 | t0001 | g0100 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA18962 | hp2 | a0001 | c0002 | t0001 | g0289 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA18964 | hp2 | a0001 | c0002 | t0001 | g0125 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA18965 | hp1 | a0001 | c0002 | t0001 | g0020 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA18965 | hp2 | a0001 | c0002 | t0001 | g0105 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA18966 | hp2 | a0001 | c0002 | t0001 | g0093 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA18970 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA18971 | hp1 | a0001 | c0002 | t0001 | g0084 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA18973 | hp2 | a0001 | c0002 | t0001 | g0097 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA18974 | hp1 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA18980 | hp1 | a0001 | c0002 | t0001 | g0279 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA18981 | hp2 | a0001 | c0002 | t0001 | g0274 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA18983 | hp2 | a0001 | c0002 | t0001 | g0095 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA18984 | hp1 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA18984 | hp2 | a0001 | c0002 | t0001 | g0069 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA18986 | hp1 | a0001 | c0002 | t0001 | g0090 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA18990 | hp1 | a0001 | c0002 | t0001 | g0280 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA18995 | hp1 | a0001 | c0002 | t0001 | g0276 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA19000 | hp1 | a0010 | c0014 | t0001 | g0284 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA19002 | hp2 | a0001 | c0002 | t0001 | g0265 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA19003 | hp1 | a0001 | c0002 | t0001 | g0027 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA19007 | hp1 | a0001 | c0002 | t0001 | g0022 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA19009 | hp1 | a0001 | c0002 | t0001 | g0269 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA19012 | hp1 | a0001 | c0002 | t0001 | g0272 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA19030 | hp1 | a0001 | c0002 | t0001 | g0104 | AFR | LWK | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA19030 | hp2 | a0001 | c0016 | t0001 | g0114 | AFR | LWK | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA19043 | hp1 | a0018 | c0034 | t0001 | g0122 | AFR | LWK | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA19043 | hp2 | a0001 | c0026 | t0001 | g0298 | AFR | LWK | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA19055 | hp2 | a0019 | c0015 | t0001 | g0283 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA19057 | hp1 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA19057 | hp2 | a0001 | c0002 | t0001 | g0327 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA19058 | hp1 | a0001 | c0002 | t0001 | g0267 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA19060 | hp1 | a0001 | c0002 | t0001 | g0083 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA19063 | hp2 | a0001 | c0002 | t0001 | g0261 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA19064 | hp1 | a0001 | c0002 | t0001 | g0266 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA19066 | hp1 | a0001 | c0002 | t0001 | g0326 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA19068 | hp1 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA19079 | hp1 | a0001 | c0002 | t0001 | g0086 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA19081 | hp1 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA19082 | hp1 | a0020 | c0018 | t0001 | g0099 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA19083 | hp1 | a0010 | c0014 | t0001 | g0263 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA19084 | hp1 | a0001 | c0002 | t0001 | g0025 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA19084 | hp2 | a0004 | c0007 | t0001 | g0216 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA19086 | hp1 | a0021 | c0030 | t0009 | g0168 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA19087 | hp1 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA20805 | hp1 | a0001 | c0002 | t0001 | g0079 | EUR | TSI | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0255 | EUR | TSI | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG02109 | hp1 | a0001 | c0012 | t0001 | g0320 | AFR | ACB | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG02109 | hp2 | a0001 | c0002 | t0001 | g0292 | AFR | ACB | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG02486 | hp1 | a0001 | c0017 | t0002 | g0116 | AFR | ACB | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | ACB | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG02559 | hp1 | a0005 | c0010 | t0001 | g0339 | AFR | ACB | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG02559 | hp2 | a0001 | c0002 | t0001 | g0211 | AFR | ACB | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | MSL | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG03471 | hp2 | a0001 | c0003 | t0002 | g0321 | AFR | MSL | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG06807 | hp1 | a0003 | c0004 | t0001 | g0316 | AFR | USA | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | USA | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA18955 | hp1 | a0001 | c0002 | t0001 | g0262 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA20300 | hp1 | a0003 | c0004 | t0001 | g0120 | AFR | USA | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | USA | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA21309 | hp1 | a0001 | c0002 | t0001 | g0046 | AFR | LWK | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | LWK | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
homoSapiens | chm13v2 | a0001 | c0006 | t0001 | g0188 | REF | REF | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0238 | REF | REF | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:3676364 | C | T | 1 | a0004 | 4 | HG00423.hp2 HG00544.hp2 NA18944.hp1 others(1): Show |
missense_variant | MODERATE | c.5198G>A | p.Arg1733His | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 33/33 | 5381/6726 | 5198/5403 | 1733/1800 | chr11 | 3676364 | |||
chr11:3676367 | T | A | 1 | a0012 | 1 | HG01243.hp2 | missense_variant | MODERATE | c.5195A>T | p.Lys1732Ile | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 33/33 | 5378/6726 | 5195/5403 | 1732/1800 | chr11 | 3676367 | |||
chr11:3676607 | C | T | 1 | a0017 | 1 | HG03654.hp2 | missense_variant | MODERATE | c.5087G>A | p.Gly1696Asp | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 32/33 | 5270/6726 | 5087/5403 | 1696/1800 | chr11 | 3676607 | |||
chr11:3679646 | C | T | 1 | a0007 | 2 | HG01255.hp2 HG01952.hp2 |
missense_variant | MODERATE | c.4981G>A | p.Glu1661Lys | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 31/33 | 5164/6726 | 4981/5403 | 1661/1800 | chr11 | 3679646 | |||
chr11:3683214 | C | T | 1 | a0005 | 3 | HG02280.hp1 HG02559.hp1 HG02886.hp2 |
missense_variant | MODERATE | c.4904G>A | p.Arg1635Gln | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 30/33 | 5087/6726 | 4904/5403 | 1635/1800 | chr11 | 3683214 | |||
chr11:3683224 | G | A | 1 | a0016 | 1 | HG02970.hp1 | missense_variant | MODERATE | c.4894C>T | p.Leu1632Phe | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 30/33 | 5077/6726 | 4894/5403 | 1632/1800 | chr11 | 3683224 | |||
chr11:3686156 | A | G | 1 | a0003 | 6 | HG02572.hp1 HG02717.hp1 HG02886.hp1 others(3): Show |
missense_variant | MODERATE | c.4493T>C | p.Ile1498Thr | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 29/33 | 4676/6726 | 4493/5403 | 1498/1800 | chr11 | 3686156 | |||
chr11:3695553 | G | A | 1 | a0011 | 1 | HG01081.hp2 | missense_variant | MODERATE | c.4063C>T | p.Arg1355Trp | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 26/33 | 4246/6726 | 4063/5403 | 1355/1800 | chr11 | 3695553 | |||
chr11:3700646 | C | T | 1 | a0009 | 2 | HG03490.hp1 HG03492.hp1 |
missense_variant | MODERATE | c.3706G>A | p.Val1236Ile | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 24/33 | 3889/6726 | 3706/5403 | 1236/1800 | chr11 | 3700646 | |||
chr11:3702544 | T | C | 1 | a0010 | 2 | NA19000.hp1 NA19083.hp1 |
missense_variant | MODERATE | c.3431A>G | p.Asn1144Ser | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 23/33 | 3614/6726 | 3431/5403 | 1144/1800 | chr11 | 3702544 | |||
chr11:3702551 | G | C | 1 | a0002 | 10 | HG00735.hp1 HG00741.hp1 HG01081.hp1 others(7): Show |
missense_variant | MODERATE | c.3424C>G | p.Gln1142Glu | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 23/33 | 3607/6726 | 3424/5403 | 1142/1800 | chr11 | 3702551 | |||
chr11:3705217 | G | A | 1 | a0018 | 1 | NA19043.hp1 | missense_variant | MODERATE | c.3065C>T | p.Ser1022Leu | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 22/33 | 3248/6726 | 3065/5403 | 1022/1800 | chr11 | 3705217 | |||
chr11:3712610 | G | A | 1 | a0008 | 2 | HG02083.hp1 HG02132.hp1 |
missense_variant | MODERATE | c.2696C>T | p.Thr899Met | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 20/33 | 2879/6726 | 2696/5403 | 899/1800 | chr11 | 3712610 | |||
chr11:3723196 | C | T | 1 | a0020 | 1 | NA19082.hp1 | missense_variant | MODERATE | c.2107G>A | p.Glu703Lys | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 16/33 | 2290/6726 | 2107/5403 | 703/1800 | chr11 | 3723196 | |||
chr11:3723274 | G | A | 1 | a0013 | 1 | HG01934.hp2 | missense_variant | MODERATE | c.2029C>T | p.Arg677Cys | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 16/33 | 2212/6726 | 2029/5403 | 677/1800 | chr11 | 3723274 | |||
chr11:3731457 | T | C | 1 | a0006 | 3 | HG02615.hp1 HG02818.hp1 HG03579.hp1 |
missense_variant | MODERATE | c.1664A>G | p.Lys555Arg | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/33 | 1847/6726 | 1664/5403 | 555/1800 | chr11 | 3731457 | |||
chr11:3753391 | T | C | 1 | a0021 | 1 | NA19086.hp1 | missense_variant | MODERATE | c.1192A>G | p.Ser398Gly | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/33 | 1375/6726 | 1192/5403 | 398/1800 | chr11 | 3753391 | |||
chr11:3762984 | G | A | 1 | a0014 | 1 | HG01943.hp2 | missense_variant | MODERATE | c.1004C>T | p.Thr335Ile | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 9/33 | 1187/6726 | 1004/5403 | 335/1800 | chr11 | 3762984 | |||
chr11:3778912 | T | G | 1 | a0019 | 1 | NA19055.hp2 | missense_variant | MODERATE | c.316A>C | p.Asn106His | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 4/33 | 499/6726 | 316/5403 | 106/1800 | chr11 | 3778912 | |||
chr11:3778915 | G | T | 1 | a0019 | 1 | NA19055.hp2 | missense_variant | MODERATE | c.313C>A | p.Gln105Lys | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 4/33 | 496/6726 | 313/5403 | 105/1800 | chr11 | 3778915 | |||
chr11:3778975 | T | C | 2 | a0015 a0018 |
2 | HG02630.hp1 NA19043.hp1 |
missense_variant | MODERATE | c.253A>G | p.Thr85Ala | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 4/33 | 436/6726 | 253/5403 | 85/1800 | chr11 | 3778975 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:3676333 | A | G | 1 | a0001c0032 | 1 | HG02451.hp1 | synonymous_variant | LOW | c.5229T>C | p.Ser1743Ser | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 33/33 | 5412/6726 | 5229/5403 | 1743/1800 | chr11 | 3676333 | |||
chr11:3686017 | G | A | 1 | a0001c0024 | 1 | HG02135.hp2 | synonymous_variant | LOW | c.4632C>T | p.Leu1544Leu | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 29/33 | 4815/6726 | 4632/5403 | 1544/1800 | chr11 | 3686017 | |||
chr11:3691466 | A | G | 1 | a0001c0020 | 1 | HG04115.hp2 | synonymous_variant | LOW | c.4335T>C | p.Tyr1445Tyr | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/33 | 4518/6726 | 4335/5403 | 1445/1800 | chr11 | 3691466 | |||
chr11:3693259 | C | T | 8 | a0001c0002 a0003c0004 a0008c0027 others(5): Show |
110 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(107): Show |
synonymous_variant | LOW | c.4284G>A | p.Ala1428Ala | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 27/33 | 4467/6726 | 4284/5403 | 1428/1800 | chr11 | 3693259 | |||
chr11:3695605 | C | T | 2 | a0001c0012 a0001c0026 |
3 | HG02109.hp1 HG02809.hp1 NA19043.hp2 |
splice_region_variant&synonymous_variant | LOW | c.4011G>A | p.Gly1337Gly | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 26/33 | 4194/6726 | 4011/5403 | 1337/1800 | chr11 | 3695605 | |||
chr11:3699167 | G | C | 1 | a0001c0026 | 1 | NA19043.hp2 | synonymous_variant | LOW | c.3924C>G | p.Thr1308Thr | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 25/33 | 4107/6726 | 3924/5403 | 1308/1800 | chr11 | 3699167 | |||
chr11:3702711 | C | T | 2 | a0001c0006 a0017c0019 |
5 | HG00741.hp2 HG01361.hp2 HG02896.hp1 others(2): Show |
synonymous_variant | LOW | c.3264G>A | p.Pro1088Pro | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 23/33 | 3447/6726 | 3264/5403 | 1088/1800 | chr11 | 3702711 | |||
chr11:3702717 | C | T | 1 | a0001c0016 | 1 | NA19030.hp2 | synonymous_variant | LOW | c.3258G>A | p.Glu1086Glu | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 23/33 | 3441/6726 | 3258/5403 | 1086/1800 | chr11 | 3702717 | |||
chr11:3712669 | C | T | 1 | a0002c0005 | 6 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(3): Show |
synonymous_variant | LOW | c.2637G>A | p.Pro879Pro | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 20/33 | 2820/6726 | 2637/5403 | 879/1800 | chr11 | 3712669 | |||
chr11:3731497 | T | G | 1 | a0002c0005 | 6 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(3): Show |
synonymous_variant | LOW | c.1624A>C | p.Arg542Arg | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/33 | 1807/6726 | 1624/5403 | 542/1800 | chr11 | 3731497 | |||
chr11:3744549 | C | T | 1 | a0005c0010 | 2 | HG02559.hp1 HG02886.hp2 |
synonymous_variant | LOW | c.1368G>A | p.Thr456Thr | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/33 | 1551/6726 | 1368/5403 | 456/1800 | chr11 | 3744549 | |||
chr11:3744558 | A | G | 1 | a0001c0017 | 1 | HG02486.hp1 | synonymous_variant | LOW | c.1359T>C | p.Phe453Phe | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/33 | 1542/6726 | 1359/5403 | 453/1800 | chr11 | 3744558 | |||
chr11:3768677 | G | C | 1 | a0001c0032 | 1 | HG02451.hp1 | synonymous_variant | LOW | c.852C>G | p.Leu284Leu | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 8/33 | 1035/6726 | 852/5403 | 284/1800 | chr11 | 3768677 | |||
chr11:3771851 | C | T | 1 | a0001c0016 | 1 | NA19030.hp2 | synonymous_variant | LOW | c.681G>A | p.Leu227Leu | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 7/33 | 864/6726 | 681/5403 | 227/1800 | chr11 | 3771851 | |||
chr11:3775882 | G | A | 1 | a0001c0003 | 7 | HG01109.hp2 HG02055.hp2 HG02818.hp2 others(4): Show |
splice_region_variant&synonymous_variant | LOW | c.495C>T | p.Asn165Asn | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 5/33 | 678/6726 | 495/5403 | 165/1800 | chr11 | 3775882 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:3675228 | A | C | 1 | a0007c0013t0005 | 2 | HG01255.hp2 HG01952.hp2 |
3_prime_UTR_variant | MODIFIER | c.*931T>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 33/33 | 931 | chr11 | 3675228 | ||||||
chr11:3675252 | C | T | 1 | a0001c0001t0004 | 2 | HG02647.hp2 HG02717.hp2 |
3_prime_UTR_variant | MODIFIER | c.*907G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 33/33 | 907 | chr11 | 3675252 | ||||||
chr11:3675406 | CCAGA | C | 3 | a0001c0001t0002 a0001c0003t0002 a0001c0017t0002 |
12 | HG00639.hp2 HG01109.hp2 HG01943.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*749_*752delTCTG | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 33/33 | 749 | chr11 | 3675406 | ||||||
chr11:3675421 | G | A | 1 | a0001c0002t0007 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*738C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 33/33 | 738 | chr11 | 3675421 | ||||||
chr11:3675577 | G | A | 1 | a0001c0001t0008 | 1 | HG00642.hp1 | 3_prime_UTR_variant | MODIFIER | c.*582C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 33/33 | 582 | chr11 | 3675577 | ||||||
chr11:3676046 | G | A | 1 | a0021c0030t0009 | 1 | NA19086.hp1 | 3_prime_UTR_variant | MODIFIER | c.*113C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 33/33 | 113 | chr11 | 3676046 | ||||||
chr11:3676081 | C | G | 2 | a0001c0001t0004 a0001c0001t0006 |
3 | HG02257.hp2 HG02647.hp2 HG02717.hp2 |
3_prime_UTR_variant | MODIFIER | c.*78G>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 33/33 | 78 | chr11 | 3676081 | ||||||
chr11:3782127 | G | T | 1 | a0002c0008t0003 | 3 | HG00735.hp1 HG00741.hp1 HG01106.hp1 |
5_prime_UTR_variant | MODIFIER | c.-10C>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 2/33 | 10 | chr11 | 3782127 | ||||||
chr11:3797479 | G | A | 1 | a0001c0002t0010 | 1 | HG00544.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-108C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/33 | chr11 | 3797479 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:3676788 | A | C | 3 | a0001c0001t0001g0275 a0001c0001t0001g0307 a0001c0002t0001g0211 |
3 | HG02559.hp2 HG02976.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.5074-168T>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 31/32 | chr11 | 3676788 | |||||||
chr11:3676814 | G | C | 1 | a0001c0001t0001g0057 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.5074-194C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 31/32 | chr11 | 3676814 | |||||||
chr11:3676858 | C | T | 10 | a0001c0001t0002g0002 a0001c0001t0002g0314 a0001c0001t0002g0317 others(7): Show |
10 | HG00639.hp2 HG01109.hp2 HG01943.hp1 others(7): Show |
intron_variant | MODIFIER | c.5074-238G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 31/32 | chr11 | 3676858 | |||||||
chr11:3676930 | G | C | 1 | a0001c0001t0001g0230 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.5074-310C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 31/32 | chr11 | 3676930 | |||||||
chr11:3677223 | G | A | 2 | a0004c0007t0001g0216 a0004c0007t0001g0246 |
2 | NA18944.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.5074-603C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 31/32 | chr11 | 3677223 | |||||||
chr11:3677410 | G | GT | 42 | a0001c0001t0001g0026 a0001c0001t0001g0038 a0001c0001t0001g0041 others(39): Show |
42 | HG00438.hp2 HG00639.hp1 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.5074-791dupA | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 31/32 | chr11 | 3677410 | |||||||
chr11:3677410 | G | GTT | 101 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0028 others(98): Show |
101 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.5074-792_5074-791d others(4): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 31/32 | chr11 | 3677410 | |||||||
chr11:3677410 | G | GTTT | 9 | a0001c0001t0001g0065 a0001c0001t0001g0172 a0001c0001t0001g0184 others(6): Show |
9 | HG00423.hp2 HG01169.hp1 HG02148.hp1 others(6): Show |
intron_variant | MODIFIER | c.5074-793_5074-791d others(5): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 31/32 | chr11 | 3677410 | |||||||
chr11:3677410 | GT | G | 6 | a0001c0001t0001g0137 a0001c0016t0001g0114 a0001c0032t0001g0032 others(3): Show |
6 | HG02280.hp1 HG02451.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.5074-791delA | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 31/32 | chr11 | 3677410 | |||||||
chr11:3677410 | GTTTT | G | 10 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(7): Show |
10 | HG00735.hp1 HG00741.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.5074-794_5074-791d others(6): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 31/32 | chr11 | 3677410 | |||||||
chr11:3677418 | T | G | 1 | a0001c0002t0001g0014 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.5074-798A>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 31/32 | chr11 | 3677418 | |||||||
chr11:3677447 | T | C | 173 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0028 others(170): Show |
173 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(170): Show |
intron_variant | MODIFIER | c.5074-827A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 31/32 | chr11 | 3677447 | |||||||
chr11:3677457 | C | T | 2 | a0001c0002t0001g0262 a0001c0002t0001g0264 |
2 | NA18955.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.5074-837G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 31/32 | chr11 | 3677457 | |||||||
chr11:3677504 | G | C | 7 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(4): Show |
7 | HG00741.hp1 HG01081.hp1 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.5074-884C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 31/32 | chr11 | 3677504 | |||||||
chr11:3677511 | A | C | 5 | a0001c0001t0001g0121 a0001c0001t0001g0129 a0006c0009t0001g0033 others(2): Show |
5 | HG02615.hp1 HG02818.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.5074-891T>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 31/32 | chr11 | 3677511 | |||||||
chr11:3677613 | G | A | 195 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(192): Show |
195 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(192): Show |
intron_variant | MODIFIER | c.5074-993C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 31/32 | chr11 | 3677613 | |||||||
chr11:3677646 | G | A | 1 | a0001c0001t0001g0143 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.5074-1026C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 31/32 | chr11 | 3677646 | |||||||
chr11:3677718 | T | A | 28 | a0001c0001t0001g0028 a0001c0001t0001g0052 a0001c0001t0001g0053 others(25): Show |
28 | HG00408.hp2 HG00609.hp2 HG01192.hp1 others(25): Show |
intron_variant | MODIFIER | c.5074-1098A>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 31/32 | chr11 | 3677718 | |||||||
chr11:3677725 | T | C | 4 | a0001c0002t0001g0262 a0001c0002t0001g0264 a0001c0002t0001g0265 others(1): Show |
4 | NA18955.hp1 NA18957.hp1 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.5074-1105A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 31/32 | chr11 | 3677725 | |||||||
chr11:3677844 | G | A | 2 | a0001c0001t0004g0330 a0001c0001t0004g0331 |
2 | HG02647.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.5074-1224C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 31/32 | chr11 | 3677844 | |||||||
chr11:3677879 | G | A | 5 | a0001c0001t0001g0275 a0001c0001t0001g0307 a0001c0012t0001g0319 others(2): Show |
5 | HG02109.hp1 HG02809.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.5074-1259C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 31/32 | chr11 | 3677879 | |||||||
chr11:3677888 | T | G | 1 | a0001c0001t0001g0135 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.5074-1268A>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 31/32 | chr11 | 3677888 | |||||||
chr11:3677979 | T | TAC | 173 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(170): Show |
173 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(170): Show |
intron_variant | MODIFIER | c.5074-1361_5074-136 others(6): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 31/32 | chr11 | 3677979 | |||||||
chr11:3677979 | TACACACA others(3): Show |
T | 2 | a0001c0006t0001g0204 a0001c0006t0001g0242 |
2 | HG00741.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.5074-1369_5074-136 others(14): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 31/32 | chr11 | 3677979 | |||||||
chr11:3678010 | T | C | 2 | a0001c0012t0001g0319 a0001c0012t0001g0320 |
2 | HG02109.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.5074-1390A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 31/32 | chr11 | 3678010 | |||||||
chr11:3678022 | G | C | 4 | a0001c0001t0001g0135 a0001c0001t0001g0171 a0001c0001t0001g0172 others(1): Show |
4 | HG00642.hp2 HG01952.hp1 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.5074-1402C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 31/32 | chr11 | 3678022 | |||||||
chr11:3678136 | T | TA | 28 | a0001c0001t0001g0029 a0001c0001t0001g0039 a0001c0001t0001g0049 others(25): Show |
28 | HG00597.hp1 HG00639.hp1 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.5073+1417dupT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 31/32 | chr11 | 3678136 | |||||||
chr11:3678192 | A | G | 1 | a0001c0001t0001g0137 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.5073+1362T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 31/32 | chr11 | 3678192 | |||||||
chr11:3678234 | A | G | 53 | a0001c0001t0001g0026 a0001c0001t0001g0038 a0001c0001t0001g0039 others(50): Show |
53 | HG00639.hp1 HG00642.hp1 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.5073+1320T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 31/32 | chr11 | 3678234 | |||||||
chr11:3678281 | CGA | C | 10 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(7): Show |
10 | HG00735.hp1 HG00741.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.5073+1271_5073+127 others(6): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 31/32 | chr11 | 3678281 | |||||||
chr11:3678305 | A | G | 10 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(7): Show |
10 | HG00735.hp1 HG00741.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.5073+1249T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 31/32 | chr11 | 3678305 | |||||||
chr11:3678335 | C | A | 53 | a0001c0001t0001g0006 a0001c0001t0001g0081 a0001c0001t0001g0082 others(50): Show |
53 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.5073+1219G>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 31/32 | chr11 | 3678335 | |||||||
chr11:3678592 | G | A | 3 | a0001c0012t0001g0319 a0001c0012t0001g0320 a0001c0026t0001g0298 |
3 | HG02109.hp1 HG02809.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.5073+962C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 31/32 | chr11 | 3678592 | |||||||
chr11:3678806 | T | C | 1 | a0002c0005t0001g0304 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.5073+748A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 31/32 | chr11 | 3678806 | |||||||
chr11:3678897 | C | T | 1 | a0001c0001t0001g0026 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.5073+657G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 31/32 | chr11 | 3678897 | |||||||
chr11:3678900 | T | C | 2 | a0001c0012t0001g0319 a0001c0012t0001g0320 |
2 | HG02109.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.5073+654A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 31/32 | chr11 | 3678900 | |||||||
chr11:3678982 | T | C | 2 | a0001c0001t0002g0309 a0001c0017t0002g0116 |
2 | HG02486.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.5073+572A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 31/32 | chr11 | 3678982 | |||||||
chr11:3679106 | G | C | 5 | a0001c0001t0001g0275 a0001c0001t0001g0307 a0001c0012t0001g0319 others(2): Show |
5 | HG02109.hp1 HG02809.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.5073+448C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 31/32 | chr11 | 3679106 | |||||||
chr11:3679121 | C | T | 53 | a0001c0001t0001g0026 a0001c0001t0001g0038 a0001c0001t0001g0039 others(50): Show |
53 | HG00639.hp1 HG00642.hp1 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.5073+433G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 31/32 | chr11 | 3679121 | |||||||
chr11:3679122 | C | CA | 79 | a0001c0001t0001g0006 a0001c0001t0001g0028 a0001c0001t0001g0029 others(76): Show |
79 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.5073+431dupT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 31/32 | chr11 | 3679122 | |||||||
chr11:3679122 | C | CAA | 8 | a0001c0001t0002g0309 a0001c0002t0001g0092 a0001c0002t0001g0103 others(5): Show |
8 | HG00738.hp1 HG01081.hp2 HG02080.hp1 others(5): Show |
intron_variant | MODIFIER | c.5073+430_5073+431d others(4): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 31/32 | chr11 | 3679122 | |||||||
chr11:3679122 | CAA | C | 8 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0250 others(5): Show |
8 | HG01361.hp1 HG02074.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.5073+430_5073+431d others(4): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 31/32 | chr11 | 3679122 | |||||||
chr11:3679122 | CAAA | C | 45 | a0001c0001t0001g0026 a0001c0001t0001g0041 a0001c0001t0001g0043 others(42): Show |
45 | HG00639.hp1 HG00642.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.5073+429_5073+431d others(5): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 31/32 | chr11 | 3679122 | |||||||
chr11:3679219 | C | A | 2 | a0001c0001t0001g0275 a0001c0001t0001g0307 |
2 | HG02976.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.5073+335G>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 31/32 | chr11 | 3679219 | |||||||
chr11:3679319 | C | T | 3 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0231 |
3 | HG03491.hp1 HG03492.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.5073+235G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 31/32 | chr11 | 3679319 | |||||||
chr11:3679334 | T | C | 3 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0340 |
3 | HG01884.hp1 HG01891.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.5073+220A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 31/32 | chr11 | 3679334 | |||||||
chr11:3679337 | C | T | 1 | a0001c0001t0001g0224 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.5073+217G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 31/32 | chr11 | 3679337 | |||||||
chr11:3679461 | TTCTCAAG others(4): Show |
T | 2 | a0001c0001t0004g0330 a0001c0001t0004g0331 |
2 | HG02647.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.5073+82_5073+92del others(11): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 31/32 | chr11 | 3679461 | |||||||
chr11:3679764 | T | C | 1 | a0001c0001t0002g0314 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.4919-56A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 30/32 | chr11 | 3679764 | |||||||
chr11:3679859 | G | C | 1 | a0001c0001t0001g0337 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.4919-151C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 30/32 | chr11 | 3679859 | |||||||
chr11:3679900 | A | G | 171 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(168): Show |
171 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(168): Show |
intron_variant | MODIFIER | c.4919-192T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 30/32 | chr11 | 3679900 | |||||||
chr11:3679947 | T | C | 170 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(167): Show |
170 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.4919-239A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 30/32 | chr11 | 3679947 | |||||||
chr11:3680014 | C | T | 3 | a0001c0001t0001g0029 a0001c0001t0001g0278 a0001c0001t0001g0328 |
3 | HG02280.hp2 HG02572.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.4919-306G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 30/32 | chr11 | 3680014 | |||||||
chr11:3680146 | T | C | 4 | a0001c0001t0001g0068 a0001c0001t0001g0324 a0001c0001t0001g0336 others(1): Show |
4 | HG00642.hp1 HG02622.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.4919-438A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 30/32 | chr11 | 3680146 | |||||||
chr11:3680221 | A | G | 29 | a0001c0001t0001g0026 a0001c0001t0001g0038 a0001c0001t0001g0039 others(26): Show |
29 | HG00639.hp1 HG00738.hp2 HG01346.hp1 others(26): Show |
intron_variant | MODIFIER | c.4919-513T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 30/32 | chr11 | 3680221 | |||||||
chr11:3680501 | A | G | 1 | a0001c0001t0001g0310 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.4919-793T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 30/32 | chr11 | 3680501 | |||||||
chr11:3680562 | G | A | 29 | a0001c0001t0001g0026 a0001c0001t0001g0038 a0001c0001t0001g0039 others(26): Show |
29 | HG00639.hp1 HG00738.hp2 HG01346.hp1 others(26): Show |
intron_variant | MODIFIER | c.4919-854C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 30/32 | chr11 | 3680562 | |||||||
chr11:3680885 | G | A | 13 | a0001c0001t0001g0068 a0001c0001t0001g0275 a0001c0001t0001g0307 others(10): Show |
13 | HG00642.hp1 HG02109.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.4919-1177C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 30/32 | chr11 | 3680885 | |||||||
chr11:3681107 | G | T | 10 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(7): Show |
10 | HG00735.hp1 HG00741.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.4919-1399C>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 30/32 | chr11 | 3681107 | |||||||
chr11:3681213 | G | T | 1 | a0001c0001t0008g0325 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.4919-1505C>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 30/32 | chr11 | 3681213 | |||||||
chr11:3681287 | C | T | 3 | a0001c0001t0001g0029 a0001c0001t0001g0278 a0001c0001t0001g0328 |
3 | HG02280.hp2 HG02572.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.4919-1579G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 30/32 | chr11 | 3681287 | |||||||
chr11:3681322 | C | T | 5 | a0001c0001t0001g0041 a0001c0001t0001g0047 a0001c0001t0001g0048 others(2): Show |
5 | NA18961.hp1 NA18969.hp2 NA18973.hp1 others(2): Show |
intron_variant | MODIFIER | c.4919-1614G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 30/32 | chr11 | 3681322 | |||||||
chr11:3681548 | G | A | 4 | a0001c0001t0001g0068 a0001c0001t0001g0324 a0001c0001t0001g0336 others(1): Show |
4 | HG00642.hp1 HG02622.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.4918+1652C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 30/32 | chr11 | 3681548 | |||||||
chr11:3681554 | A | C | 1 | a0001c0002t0001g0096 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.4918+1646T>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 30/32 | chr11 | 3681554 | |||||||
chr11:3681611 | AT | A | 10 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(7): Show |
10 | HG00735.hp1 HG00741.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.4918+1588delA | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 30/32 | chr11 | 3681611 | |||||||
chr11:3681708 | G | A | 1 | a0001c0001t0001g0143 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.4918+1492C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 30/32 | chr11 | 3681708 | |||||||
chr11:3681713 | C | T | 268 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(265): Show |
268 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(265): Show |
intron_variant | MODIFIER | c.4918+1487G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 30/32 | chr11 | 3681713 | |||||||
chr11:3681935 | T | C | 1 | a0001c0001t0001g0214 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.4918+1265A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 30/32 | chr11 | 3681935 | |||||||
chr11:3682092 | G | A | 2 | a0001c0001t0002g0309 a0001c0017t0002g0116 |
2 | HG02486.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.4918+1108C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 30/32 | chr11 | 3682092 | |||||||
chr11:3682141 | A | G | 29 | a0001c0001t0001g0026 a0001c0001t0001g0038 a0001c0001t0001g0039 others(26): Show |
29 | HG00639.hp1 HG00738.hp2 HG01346.hp1 others(26): Show |
intron_variant | MODIFIER | c.4918+1059T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 30/32 | chr11 | 3682141 | |||||||
chr11:3682218 | C | T | 2 | a0001c0002t0001g0091 a0001c0032t0001g0032 |
2 | HG02451.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.4918+982G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 30/32 | chr11 | 3682218 | |||||||
chr11:3682283 | T | C | 3 | a0001c0001t0001g0329 a0001c0006t0001g0126 a0001c0006t0001g0127 |
3 | HG02896.hp1 HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.4918+917A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 30/32 | chr11 | 3682283 | |||||||
chr11:3682317 | C | G | 5 | a0001c0001t0001g0275 a0001c0001t0001g0307 a0001c0012t0001g0319 others(2): Show |
5 | HG02109.hp1 HG02809.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.4918+883G>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 30/32 | chr11 | 3682317 | |||||||
chr11:3682440 | C | T | 3 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0340 |
3 | HG01884.hp1 HG01891.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.4918+760G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 30/32 | chr11 | 3682440 | |||||||
chr11:3682525 | G | A | 1 | a0001c0001t0001g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.4918+675C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 30/32 | chr11 | 3682525 | |||||||
chr11:3682566 | T | C | 2 | a0001c0001t0002g0309 a0001c0017t0002g0116 |
2 | HG02486.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.4918+634A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 30/32 | chr11 | 3682566 | |||||||
chr11:3682632 | A | G | 1 | a0001c0026t0001g0298 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.4918+568T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 30/32 | chr11 | 3682632 | |||||||
chr11:3682826 | A | G | 1 | a0001c0001t0001g0038 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.4918+374T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 30/32 | chr11 | 3682826 | |||||||
chr11:3682963 | T | C | 1 | a0001c0001t0001g0337 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.4918+237A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 30/32 | chr11 | 3682963 | |||||||
chr11:3683107 | G | A | 3 | a0005c0010t0001g0338 a0005c0010t0001g0339 a0005c0021t0001g0259 |
3 | HG02280.hp1 HG02559.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.4918+93C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 30/32 | chr11 | 3683107 | |||||||
chr11:3683474 | T | C | 47 | a0001c0001t0001g0026 a0001c0001t0001g0038 a0001c0001t0001g0039 others(44): Show |
47 | HG00639.hp1 HG00642.hp1 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.4677-33A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 29/32 | chr11 | 3683474 | |||||||
chr11:3683540 | C | T | 10 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(7): Show |
10 | HG00735.hp1 HG00741.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.4677-99G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 29/32 | chr11 | 3683540 | |||||||
chr11:3683545 | CT | C | 306 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(303): Show |
306 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(303): Show |
intron_variant | MODIFIER | c.4677-105delA | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 29/32 | chr11 | 3683545 | |||||||
chr11:3683612 | C | A | 1 | a0002c0008t0001g0003 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.4677-171G>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 29/32 | chr11 | 3683612 | |||||||
chr11:3683713 | AT | A | 222 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(219): Show |
222 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(219): Show |
intron_variant | MODIFIER | c.4677-273delA | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 29/32 | chr11 | 3683713 | |||||||
chr11:3683805 | C | T | 268 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(265): Show |
268 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(265): Show |
intron_variant | MODIFIER | c.4677-364G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 29/32 | chr11 | 3683805 | |||||||
chr11:3683806 | A | G | 1 | a0001c0002t0001g0193 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.4677-365T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 29/32 | chr11 | 3683806 | |||||||
chr11:3683832 | C | T | 6 | a0001c0001t0001g0275 a0001c0001t0001g0307 a0001c0001t0001g0337 others(3): Show |
6 | HG02109.hp1 HG02809.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.4677-391G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 29/32 | chr11 | 3683832 | |||||||
chr11:3683943 | C | A | 1 | a0001c0032t0001g0032 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.4677-502G>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 29/32 | chr11 | 3683943 | |||||||
chr11:3684004 | TCAAGAC | T | 173 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(170): Show |
173 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(170): Show |
intron_variant | MODIFIER | c.4677-569_4677-564d others(8): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 29/32 | chr11 | 3684004 | |||||||
chr11:3684056 | A | T | 166 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(163): Show |
166 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.4677-615T>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 29/32 | chr11 | 3684056 | |||||||
chr11:3684068 | T | C | 1 | a0001c0001t0001g0068 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.4677-627A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 29/32 | chr11 | 3684068 | |||||||
chr11:3684168 | C | T | 1 | a0001c0001t0001g0036 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.4677-727G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 29/32 | chr11 | 3684168 | |||||||
chr11:3684172 | A | G | 1 | a0001c0002t0001g0046 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.4677-731T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 29/32 | chr11 | 3684172 | |||||||
chr11:3684198 | C | G | 268 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(265): Show |
268 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(265): Show |
intron_variant | MODIFIER | c.4677-757G>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 29/32 | chr11 | 3684198 | |||||||
chr11:3684316 | A | C | 1 | a0001c0001t0001g0175 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.4677-875T>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 29/32 | chr11 | 3684316 | |||||||
chr11:3684435 | A | G | 1 | a0001c0002t0001g0016 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.4677-994T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 29/32 | chr11 | 3684435 | |||||||
chr11:3684437 | G | T | 5 | a0001c0001t0001g0029 a0001c0001t0001g0278 a0001c0001t0001g0328 others(2): Show |
5 | HG02280.hp2 HG02486.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.4677-996C>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 29/32 | chr11 | 3684437 | |||||||
chr11:3684446 | T | G | 4 | a0001c0016t0001g0114 a0005c0010t0001g0338 a0005c0010t0001g0339 others(1): Show |
4 | HG02280.hp1 HG02559.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.4677-1005A>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 29/32 | chr11 | 3684446 | |||||||
chr11:3684656 | A | C | 1 | a0007c0013t0005g0037 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.4677-1215T>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 29/32 | chr11 | 3684656 | |||||||
chr11:3684766 | C | CA | 18 | a0001c0002t0001g0070 a0001c0002t0001g0077 a0001c0002t0001g0080 others(15): Show |
18 | HG00558.hp2 HG00738.hp1 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.4676+1206dupT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 29/32 | chr11 | 3684766 | |||||||
chr11:3684766 | C | CAA | 17 | a0001c0002t0001g0069 a0001c0002t0001g0079 a0001c0002t0001g0086 others(14): Show |
17 | HG00423.hp1 HG00544.hp1 HG00621.hp1 others(14): Show |
intron_variant | MODIFIER | c.4676+1205_4676+120 others(6): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 29/32 | chr11 | 3684766 | |||||||
chr11:3684766 | C | CAAA | 17 | a0001c0002t0001g0088 a0001c0002t0001g0093 a0001c0002t0001g0094 others(14): Show |
17 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(14): Show |
intron_variant | MODIFIER | c.4676+1204_4676+120 others(7): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 29/32 | chr11 | 3684766 | |||||||
chr11:3684766 | C | CAAAAAAA others(5): Show |
1 | a0001c0032t0001g0032 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.4676+1195_4676+120 others(16): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 29/32 | chr11 | 3684766 | |||||||
chr11:3684766 | CAAAAAA | C | 26 | a0001c0001t0001g0041 a0001c0001t0001g0043 a0001c0001t0001g0044 others(23): Show |
26 | HG00639.hp1 HG00735.hp1 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.4676+1201_4676+120 others(10): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 29/32 | chr11 | 3684766 | |||||||
chr11:3684766 | CAAAAAAA | C | 15 | a0001c0001t0001g0113 a0001c0001t0001g0219 a0001c0001t0001g0250 others(12): Show |
15 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.4676+1200_4676+120 others(11): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 29/32 | chr11 | 3684766 | |||||||
chr11:3684766 | CAAAAAAA others(1): Show |
C | 16 | a0001c0001t0001g0275 a0001c0001t0001g0307 a0001c0001t0001g0337 others(13): Show |
16 | HG00639.hp2 HG01109.hp2 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.4676+1199_4676+120 others(12): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 29/32 | chr11 | 3684766 | |||||||
chr11:3684766 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0278 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.4676+1197_4676+120 others(14): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 29/32 | chr11 | 3684766 | |||||||
chr11:3684766 | CAAAAAAA others(4): Show |
C | 2 | a0001c0001t0001g0029 a0001c0001t0001g0328 |
2 | HG02280.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.4676+1196_4676+120 others(15): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 29/32 | chr11 | 3684766 | |||||||
chr11:3684766 | CAAAAAAA others(6): Show |
C | 6 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0051 others(3): Show |
6 | HG01884.hp1 HG02083.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.4676+1194_4676+120 others(17): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 29/32 | chr11 | 3684766 | |||||||
chr11:3684766 | CAAAAAAA others(7): Show |
C | 149 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(146): Show |
149 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.4676+1193_4676+120 others(18): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 29/32 | chr11 | 3684766 | |||||||
chr11:3684766 | CAAAAAAA others(8): Show |
C | 42 | a0001c0001t0001g0129 a0001c0001t0001g0183 a0001c0001t0001g0197 others(39): Show |
42 | HG00597.hp1 HG01243.hp1 HG01993.hp1 others(39): Show |
intron_variant | MODIFIER | c.4676+1192_4676+120 others(19): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 29/32 | chr11 | 3684766 | |||||||
chr11:3684766 | CAAAAAAA others(13): Show |
C | 4 | a0001c0001t0001g0068 a0001c0001t0001g0324 a0001c0001t0001g0336 others(1): Show |
4 | HG00642.hp1 HG02622.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.4676+1187_4676+120 others(24): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 29/32 | chr11 | 3684766 | |||||||
chr11:3684799 | G | A | 1 | a0019c0015t0001g0283 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.4676+1174C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 29/32 | chr11 | 3684799 | |||||||
chr11:3684807 | C | T | 268 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(265): Show |
268 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(265): Show |
intron_variant | MODIFIER | c.4676+1166G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 29/32 | chr11 | 3684807 | |||||||
chr11:3684852 | T | C | 2 | a0001c0006t0001g0126 a0001c0006t0001g0127 |
2 | HG02896.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.4676+1121A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 29/32 | chr11 | 3684852 | |||||||
chr11:3684907 | T | C | 1 | a0019c0015t0001g0283 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.4676+1066A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 29/32 | chr11 | 3684907 | |||||||
chr11:3684909 | C | T | 1 | a0019c0015t0001g0283 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.4676+1064G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 29/32 | chr11 | 3684909 | |||||||
chr11:3685007 | T | C | 3 | a0001c0001t0001g0029 a0001c0001t0001g0278 a0001c0001t0001g0328 |
3 | HG02280.hp2 HG02572.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.4676+966A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 29/32 | chr11 | 3685007 | |||||||
chr11:3685046 | G | A | 175 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(172): Show |
175 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(172): Show |
intron_variant | MODIFIER | c.4676+927C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 29/32 | chr11 | 3685046 | |||||||
chr11:3685095 | A | G | 1 | a0001c0001t0001g0113 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4676+878T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 29/32 | chr11 | 3685095 | |||||||
chr11:3685100 | A | C | 53 | a0001c0001t0001g0026 a0001c0001t0001g0038 a0001c0001t0001g0039 others(50): Show |
53 | HG00639.hp1 HG00642.hp1 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.4676+873T>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 29/32 | chr11 | 3685100 | |||||||
chr11:3685112 | T | C | 1 | a0001c0002t0001g0211 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.4676+861A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 29/32 | chr11 | 3685112 | |||||||
chr11:3685216 | G | A | 229 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(226): Show |
229 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(226): Show |
intron_variant | MODIFIER | c.4676+757C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 29/32 | chr11 | 3685216 | |||||||
chr11:3685383 | G | T | 104 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0028 others(101): Show |
104 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.4676+590C>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 29/32 | chr11 | 3685383 | |||||||
chr11:3685566 | GT | G | 10 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(7): Show |
10 | HG00735.hp1 HG00741.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.4676+406delA | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 29/32 | chr11 | 3685566 | |||||||
chr11:3685836 | T | A | 1 | a0019c0015t0001g0283 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.4676+137A>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 29/32 | chr11 | 3685836 | |||||||
chr11:3686206 | G | A | 2 | a0001c0001t0002g0309 a0001c0017t0002g0116 |
2 | HG02486.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.4455-12C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/32 | chr11 | 3686206 | |||||||
chr11:3686212 | A | G | 1 | a0001c0001t0001g0215 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.4455-18T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/32 | chr11 | 3686212 | |||||||
chr11:3686372 | G | A | 3 | a0005c0010t0001g0338 a0005c0010t0001g0339 a0005c0021t0001g0259 |
3 | HG02280.hp1 HG02559.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.4455-178C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/32 | chr11 | 3686372 | |||||||
chr11:3686431 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4455-237A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/32 | chr11 | 3686431 | |||||||
chr11:3686679 | A | G | 10 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(7): Show |
10 | HG00735.hp1 HG00741.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.4455-485T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/32 | chr11 | 3686679 | |||||||
chr11:3686758 | C | T | 157 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(154): Show |
157 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.4455-564G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/32 | chr11 | 3686758 | |||||||
chr11:3686759 | G | A | 22 | a0001c0001t0001g0183 a0001c0002t0001g0007 a0001c0002t0001g0008 others(19): Show |
22 | HG00597.hp1 HG01993.hp1 HG03239.hp1 others(19): Show |
intron_variant | MODIFIER | c.4455-565C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/32 | chr11 | 3686759 | |||||||
chr11:3686872 | G | A | 30 | a0001c0001t0001g0026 a0001c0001t0001g0038 a0001c0001t0001g0039 others(27): Show |
30 | HG00639.hp1 HG00738.hp2 HG01346.hp1 others(27): Show |
intron_variant | MODIFIER | c.4455-678C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/32 | chr11 | 3686872 | |||||||
chr11:3686930 | T | C | 1 | a0001c0002t0001g0080 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.4455-736A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/32 | chr11 | 3686930 | |||||||
chr11:3686942 | A | T | 2 | a0001c0001t0001g0029 a0001c0001t0001g0328 |
2 | HG02280.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.4455-748T>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/32 | chr11 | 3686942 | |||||||
chr11:3686979 | A | AAAT | 34 | a0001c0001t0001g0026 a0001c0001t0001g0038 a0001c0001t0001g0039 others(31): Show |
34 | HG00423.hp2 HG00544.hp2 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.4455-788_4455-786d others(5): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/32 | chr11 | 3686979 | |||||||
chr11:3687005 | T | C | 2 | a0001c0001t0001g0275 a0001c0001t0001g0307 |
2 | HG02976.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.4455-811A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/32 | chr11 | 3687005 | |||||||
chr11:3687035 | T | G | 1 | a0001c0002t0001g0086 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.4455-841A>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/32 | chr11 | 3687035 | |||||||
chr11:3687098 | T | A | 3 | a0001c0012t0001g0319 a0001c0012t0001g0320 a0001c0026t0001g0298 |
3 | HG02109.hp1 HG02809.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.4455-904A>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/32 | chr11 | 3687098 | |||||||
chr11:3687161 | T | G | 1 | a0001c0001t0001g0250 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.4455-967A>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/32 | chr11 | 3687161 | |||||||
chr11:3687202 | G | A | 1 | a0001c0026t0001g0298 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.4455-1008C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/32 | chr11 | 3687202 | |||||||
chr11:3687303 | G | A | 167 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(164): Show |
167 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.4455-1109C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/32 | chr11 | 3687303 | |||||||
chr11:3687327 | C | T | 1 | a0001c0001t0001g0164 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.4455-1133G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/32 | chr11 | 3687327 | |||||||
chr11:3687473 | G | C | 5 | a0001c0001t0001g0191 a0001c0001t0001g0195 a0001c0001t0001g0196 others(2): Show |
5 | NA18950.hp2 NA18952.hp1 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.4455-1279C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/32 | chr11 | 3687473 | |||||||
chr11:3687495 | T | G | 36 | a0001c0001t0001g0026 a0001c0001t0001g0038 a0001c0001t0001g0039 others(33): Show |
36 | HG00423.hp2 HG00544.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.4455-1301A>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/32 | chr11 | 3687495 | |||||||
chr11:3687656 | A | G | 1 | a0001c0002t0001g0315 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.4455-1462T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/32 | chr11 | 3687656 | |||||||
chr11:3687674 | C | A | 7 | a0001c0001t0001g0036 a0001c0001t0001g0121 a0001c0001t0001g0129 others(4): Show |
7 | HG02145.hp2 HG02451.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.4455-1480G>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/32 | chr11 | 3687674 | |||||||
chr11:3687818 | T | G | 10 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(7): Show |
10 | HG00735.hp1 HG00741.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.4455-1624A>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/32 | chr11 | 3687818 | |||||||
chr11:3687853 | A | T | 2 | a0001c0012t0001g0319 a0001c0012t0001g0320 |
2 | HG02109.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.4455-1659T>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/32 | chr11 | 3687853 | |||||||
chr11:3687869 | G | A | 10 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(7): Show |
10 | HG00735.hp1 HG00741.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.4455-1675C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/32 | chr11 | 3687869 | |||||||
chr11:3687898 | C | T | 10 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(7): Show |
10 | HG00735.hp1 HG00741.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.4455-1704G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/32 | chr11 | 3687898 | |||||||
chr11:3688090 | C | A | 4 | a0001c0001t0001g0068 a0001c0001t0001g0324 a0001c0001t0001g0336 others(1): Show |
4 | HG00642.hp1 HG02622.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.4455-1896G>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/32 | chr11 | 3688090 | |||||||
chr11:3688091 | A | T | 4 | a0001c0001t0001g0068 a0001c0001t0001g0324 a0001c0001t0001g0336 others(1): Show |
4 | HG00642.hp1 HG02622.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.4455-1897T>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/32 | chr11 | 3688091 | |||||||
chr11:3688121 | T | C | 38 | a0001c0001t0001g0183 a0001c0002t0001g0007 a0001c0002t0001g0008 others(35): Show |
38 | HG00597.hp1 HG01243.hp1 HG01993.hp1 others(35): Show |
intron_variant | MODIFIER | c.4455-1927A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/32 | chr11 | 3688121 | |||||||
chr11:3688131 | A | G | 269 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(266): Show |
269 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(266): Show |
intron_variant | MODIFIER | c.4455-1937T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/32 | chr11 | 3688131 | |||||||
chr11:3688137 | G | A | 1 | a0001c0001t0001g0029 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.4455-1943C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/32 | chr11 | 3688137 | |||||||
chr11:3688241 | C | T | 4 | a0001c0002t0001g0262 a0001c0002t0001g0264 a0001c0002t0001g0265 others(1): Show |
4 | NA18955.hp1 NA18957.hp1 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.4455-2047G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/32 | chr11 | 3688241 | |||||||
chr11:3688407 | A | G | 1 | a0018c0034t0001g0122 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4455-2213T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/32 | chr11 | 3688407 | |||||||
chr11:3688595 | G | C | 3 | a0001c0001t0001g0029 a0001c0001t0001g0278 a0001c0001t0001g0328 |
3 | HG02280.hp2 HG02572.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.4455-2401C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/32 | chr11 | 3688595 | |||||||
chr11:3688616 | A | G | 1 | a0001c0002t0001g0315 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.4455-2422T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/32 | chr11 | 3688616 | |||||||
chr11:3688663 | C | A | 37 | a0001c0001t0001g0183 a0001c0002t0001g0007 a0001c0002t0001g0008 others(34): Show |
37 | HG00597.hp1 HG01243.hp1 HG01993.hp1 others(34): Show |
intron_variant | MODIFIER | c.4455-2469G>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/32 | chr11 | 3688663 | |||||||
chr11:3688664 | G | A | 1 | a0016c0023t0001g0001 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.4455-2470C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/32 | chr11 | 3688664 | |||||||
chr11:3688711 | C | T | 34 | a0001c0001t0001g0026 a0001c0001t0001g0038 a0001c0001t0001g0039 others(31): Show |
34 | HG00423.hp2 HG00544.hp2 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.4455-2517G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/32 | chr11 | 3688711 | |||||||
chr11:3688785 | A | ACT | 59 | a0001c0001t0001g0026 a0001c0001t0001g0038 a0001c0001t0001g0039 others(56): Show |
59 | HG00423.hp2 HG00544.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.4454+2560_4454+256 others(6): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/32 | chr11 | 3688785 | |||||||
chr11:3688820 | C | CAT | 9 | a0001c0001t0001g0137 a0001c0001t0001g0179 a0001c0001t0001g0221 others(6): Show |
9 | HG02129.hp2 HG02451.hp2 HG03491.hp2 others(6): Show |
intron_variant | MODIFIER | c.4454+2525_4454+252 others(6): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/32 | chr11 | 3688820 | |||||||
chr11:3688820 | C | CATAT | 4 | a0001c0001t0001g0232 a0001c0016t0001g0114 a0002c0005t0001g0301 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.4454+2523_4454+252 others(8): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/32 | chr11 | 3688820 | |||||||
chr11:3688820 | C | CATATACA others(3): Show |
2 | a0001c0001t0001g0068 a0001c0001t0001g0337 |
2 | HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.4454+2526_4454+252 others(14): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/32 | chr11 | 3688820 | |||||||
chr11:3688820 | C | CATATACA others(5): Show |
1 | a0001c0001t0001g0336 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.4454+2526_4454+252 others(16): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/32 | chr11 | 3688820 | |||||||
chr11:3688820 | C | CATATACA others(7): Show |
2 | a0001c0001t0001g0324 a0001c0001t0008g0325 |
2 | HG00642.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.4454+2526_4454+252 others(18): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/32 | chr11 | 3688820 | |||||||
chr11:3688820 | C | CATATACA others(11): Show |
1 | a0001c0001t0001g0275 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4454+2526_4454+252 others(22): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/32 | chr11 | 3688820 | |||||||
chr11:3688820 | C | CATATACA others(13): Show |
1 | a0001c0001t0001g0307 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4454+2526_4454+252 others(24): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/32 | chr11 | 3688820 | |||||||
chr11:3688820 | C | CATATACA others(39): Show |
1 | a0001c0012t0001g0320 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.4454+2526_4454+252 others(50): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/32 | chr11 | 3688820 | |||||||
chr11:3688820 | C | CATATACA others(41): Show |
1 | a0001c0012t0001g0319 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.4454+2526_4454+252 others(52): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/32 | chr11 | 3688820 | |||||||
chr11:3688820 | C | CATATACA others(33): Show |
1 | a0001c0026t0001g0298 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.4454+2526_4454+252 others(44): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/32 | chr11 | 3688820 | |||||||
chr11:3688820 | C | CATATAT | 9 | a0001c0002t0001g0090 a0002c0005t0001g0299 a0002c0005t0001g0300 others(6): Show |
9 | HG00735.hp1 HG00741.hp1 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.4454+2521_4454+252 others(10): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/32 | chr11 | 3688820 | |||||||
chr11:3688820 | C | CATATATA others(3): Show |
9 | a0001c0001t0001g0038 a0001c0001t0001g0287 a0001c0001t0001g0310 others(6): Show |
9 | HG01361.hp1 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.4454+2517_4454+252 others(14): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/32 | chr11 | 3688820 | |||||||
chr11:3688820 | C | CATATATA others(5): Show |
16 | a0001c0001t0001g0026 a0001c0001t0001g0039 a0001c0001t0001g0041 others(13): Show |
16 | HG00423.hp2 HG00544.hp2 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.4454+2515_4454+252 others(16): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/32 | chr11 | 3688820 | |||||||
chr11:3688820 | C | CATATATA others(7): Show |
8 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0076 others(5): Show |
8 | HG01346.hp1 HG02280.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.4454+2513_4454+252 others(18): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/32 | chr11 | 3688820 | |||||||
chr11:3688820 | C | CATATATA others(9): Show |
3 | a0001c0001t0001g0048 a0001c0001t0001g0247 a0004c0007t0001g0246 |
3 | HG00639.hp1 NA18944.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.4454+2511_4454+252 others(20): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/32 | chr11 | 3688820 | |||||||
chr11:3688820 | CAT | C | 118 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0028 others(115): Show |
118 | HG00323.hp1 HG00408.hp2 HG00609.hp2 others(115): Show |
intron_variant | MODIFIER | c.4454+2525_4454+252 others(6): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/32 | chr11 | 3688820 | |||||||
chr11:3688820 | CATAT | C | 5 | a0001c0001t0001g0030 a0001c0001t0001g0249 a0001c0001t0001g0252 others(2): Show |
5 | HG00735.hp2 HG01109.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.4454+2523_4454+252 others(8): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/32 | chr11 | 3688820 | |||||||
chr11:3688824 | T | TATATATA others(17): Show |
1 | a0001c0001t0001g0113 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4454+2522_4454+252 others(28): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/32 | chr11 | 3688824 | |||||||
chr11:3688975 | T | C | 10 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(7): Show |
10 | HG00735.hp1 HG00741.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.4454+2372A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/32 | chr11 | 3688975 | |||||||
chr11:3689063 | G | A | 1 | a0018c0034t0001g0122 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4454+2284C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/32 | chr11 | 3689063 | |||||||
chr11:3689119 | G | C | 1 | a0001c0001t0001g0036 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.4454+2228C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/32 | chr11 | 3689119 | |||||||
chr11:3689252 | T | C | 4 | a0001c0002t0001g0262 a0001c0002t0001g0264 a0001c0002t0001g0265 others(1): Show |
4 | NA18955.hp1 NA18957.hp1 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.4454+2095A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/32 | chr11 | 3689252 | |||||||
chr11:3689258 | G | C | 1 | a0001c0001t0001g0335 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.4454+2089C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/32 | chr11 | 3689258 | |||||||
chr11:3689309 | G | A | 3 | a0001c0001t0001g0029 a0001c0001t0001g0278 a0001c0001t0001g0328 |
3 | HG02280.hp2 HG02572.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.4454+2038C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/32 | chr11 | 3689309 | |||||||
chr11:3689342 | C | T | 2 | a0001c0001t0002g0309 a0001c0017t0002g0116 |
2 | HG02486.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.4454+2005G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/32 | chr11 | 3689342 | |||||||
chr11:3689514 | A | G | 337 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(334): Show |
337 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(334): Show |
intron_variant | MODIFIER | c.4454+1833T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/32 | chr11 | 3689514 | |||||||
chr11:3689625 | T | A | 1 | a0001c0001t0001g0208 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.4454+1722A>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/32 | chr11 | 3689625 | |||||||
chr11:3689874 | T | A | 1 | a0001c0001t0001g0181 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.4454+1473A>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/32 | chr11 | 3689874 | |||||||
chr11:3689876 | A | G | 2 | a0001c0001t0002g0309 a0001c0017t0002g0116 |
2 | HG02486.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.4454+1471T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/32 | chr11 | 3689876 | |||||||
chr11:3689940 | A | AT | 48 | a0001c0001t0001g0004 a0001c0001t0001g0053 a0001c0001t0001g0055 others(45): Show |
48 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.4454+1406dupA | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/32 | chr11 | 3689940 | |||||||
chr11:3689940 | AT | A | 84 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0031 others(81): Show |
84 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.4454+1406delA | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/32 | chr11 | 3689940 | |||||||
chr11:3689940 | ATTTTTTT others(6): Show |
A | 1 | a0001c0001t0001g0173 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.4454+1394_4454+140 others(17): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/32 | chr11 | 3689940 | |||||||
chr11:3690077 | A | G | 1 | a0001c0001t0001g0113 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4454+1270T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/32 | chr11 | 3690077 | |||||||
chr11:3690101 | A | T | 1 | a0001c0002t0001g0123 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.4454+1246T>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/32 | chr11 | 3690101 | |||||||
chr11:3690124 | G | A | 52 | a0001c0001t0001g0026 a0001c0001t0001g0038 a0001c0001t0001g0039 others(49): Show |
52 | HG00639.hp1 HG00642.hp1 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.4454+1223C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/32 | chr11 | 3690124 | |||||||
chr11:3690259 | A | AT | 53 | a0001c0001t0001g0006 a0001c0001t0001g0081 a0001c0001t0001g0082 others(50): Show |
53 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.4454+1087dupA | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/32 | chr11 | 3690259 | |||||||
chr11:3690452 | G | C | 2 | a0001c0006t0001g0204 a0001c0006t0001g0242 |
2 | HG00741.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.4454+895C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/32 | chr11 | 3690452 | |||||||
chr11:3690453 | G | T | 2 | a0001c0001t0001g0029 a0001c0001t0001g0328 |
2 | HG02280.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.4454+894C>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/32 | chr11 | 3690453 | |||||||
chr11:3690496 | G | A | 1 | a0008c0028t0001g0147 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.4454+851C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/32 | chr11 | 3690496 | |||||||
chr11:3690526 | C | T | 3 | a0005c0010t0001g0338 a0005c0010t0001g0339 a0005c0021t0001g0259 |
3 | HG02280.hp1 HG02559.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.4454+821G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/32 | chr11 | 3690526 | |||||||
chr11:3690721 | A | G | 54 | a0001c0001t0001g0026 a0001c0001t0001g0038 a0001c0001t0001g0039 others(51): Show |
54 | HG00639.hp1 HG00642.hp1 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.4454+626T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/32 | chr11 | 3690721 | |||||||
chr11:3690755 | T | C | 1 | a0002c0008t0001g0003 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.4454+592A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/32 | chr11 | 3690755 | |||||||
chr11:3690827 | C | T | 54 | a0001c0001t0001g0026 a0001c0001t0001g0038 a0001c0001t0001g0039 others(51): Show |
54 | HG00639.hp1 HG00642.hp1 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.4454+520G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/32 | chr11 | 3690827 | |||||||
chr11:3691077 | T | C | 1 | a0001c0001t0001g0307 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4454+270A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/32 | chr11 | 3691077 | |||||||
chr11:3691174 | G | A | 3 | a0001c0001t0004g0330 a0001c0001t0004g0331 a0001c0001t0006g0297 |
3 | HG02257.hp2 HG02647.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.4454+173C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/32 | chr11 | 3691174 | |||||||
chr11:3691254 | T | A | 2 | a0001c0001t0001g0225 a0001c0001t0001g0226 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.4454+93A>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/32 | chr11 | 3691254 | |||||||
chr11:3691285 | C | T | 1 | a0001c0001t0001g0275 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4454+62G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/32 | chr11 | 3691285 | |||||||
chr11:3691307 | T | C | 11 | a0001c0002t0001g0260 a0001c0002t0001g0270 a0001c0002t0001g0271 others(8): Show |
11 | HG00423.hp1 HG00544.hp1 HG02132.hp1 others(8): Show |
intron_variant | MODIFIER | c.4454+40A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/32 | chr11 | 3691307 | |||||||
chr11:3691605 | G | A | 33 | a0001c0001t0001g0026 a0001c0001t0001g0038 a0001c0001t0001g0039 others(30): Show |
33 | HG00423.hp2 HG00544.hp2 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.4312-116C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 27/32 | chr11 | 3691605 | |||||||
chr11:3691607 | G | A | 1 | a0001c0001t0001g0043 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.4312-118C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 27/32 | chr11 | 3691607 | |||||||
chr11:3691744 | G | A | 2 | a0001c0012t0001g0319 a0001c0012t0001g0320 |
2 | HG02109.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.4312-255C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 27/32 | chr11 | 3691744 | |||||||
chr11:3691843 | C | T | 5 | a0001c0001t0001g0041 a0001c0001t0001g0047 a0001c0001t0001g0048 others(2): Show |
5 | NA18961.hp1 NA18969.hp2 NA18973.hp1 others(2): Show |
intron_variant | MODIFIER | c.4312-354G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 27/32 | chr11 | 3691843 | |||||||
chr11:3691850 | G | A | 3 | a0001c0001t0001g0029 a0001c0001t0001g0278 a0001c0001t0001g0328 |
3 | HG02280.hp2 HG02572.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.4312-361C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 27/32 | chr11 | 3691850 | |||||||
chr11:3692103 | C | T | 20 | a0001c0001t0001g0004 a0001c0001t0001g0042 a0001c0001t0001g0145 others(17): Show |
20 | HG01081.hp2 HG01168.hp2 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.4312-614G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 27/32 | chr11 | 3692103 | |||||||
chr11:3692142 | G | C | 3 | a0001c0001t0001g0029 a0001c0001t0001g0278 a0001c0001t0001g0328 |
3 | HG02280.hp2 HG02572.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.4312-653C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 27/32 | chr11 | 3692142 | |||||||
chr11:3692166 | A | T | 9 | a0001c0002t0001g0079 a0001c0002t0001g0080 a0001c0002t0001g0092 others(6): Show |
9 | HG00738.hp1 HG01099.hp1 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.4312-677T>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 27/32 | chr11 | 3692166 | |||||||
chr11:3692167 | T | A | 1 | a0001c0001t0001g0257 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.4312-678A>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 27/32 | chr11 | 3692167 | |||||||
chr11:3692193 | G | A | 4 | a0001c0016t0001g0114 a0005c0010t0001g0338 a0005c0010t0001g0339 others(1): Show |
4 | HG02280.hp1 HG02559.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.4312-704C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 27/32 | chr11 | 3692193 | |||||||
chr11:3692251 | G | A | 4 | a0001c0016t0001g0114 a0005c0010t0001g0338 a0005c0010t0001g0339 others(1): Show |
4 | HG02280.hp1 HG02559.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.4312-762C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 27/32 | chr11 | 3692251 | |||||||
chr11:3692322 | G | GA | 63 | a0001c0001t0001g0068 a0001c0001t0001g0180 a0001c0001t0001g0209 others(60): Show |
63 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.4312-834dupT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 27/32 | chr11 | 3692322 | |||||||
chr11:3692368 | C | T | 1 | a0001c0026t0001g0298 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.4311+864G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 27/32 | chr11 | 3692368 | |||||||
chr11:3692455 | G | A | 1 | a0001c0001t0001g0217 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.4311+777C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 27/32 | chr11 | 3692455 | |||||||
chr11:3692544 | G | A | 1 | a0001c0002t0001g0261 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.4311+688C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 27/32 | chr11 | 3692544 | |||||||
chr11:3692594 | C | CA | 38 | a0001c0001t0001g0026 a0001c0001t0001g0038 a0001c0001t0001g0039 others(35): Show |
38 | HG00423.hp2 HG00544.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.4311+637dupT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 27/32 | chr11 | 3692594 | |||||||
chr11:3692594 | CA | C | 7 | a0001c0002t0001g0080 a0003c0004t0001g0115 a0003c0004t0001g0117 others(4): Show |
7 | HG01099.hp1 HG02572.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.4311+637delT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 27/32 | chr11 | 3692594 | |||||||
chr11:3692684 | T | C | 4 | a0001c0001t0001g0068 a0001c0001t0001g0324 a0001c0001t0001g0336 others(1): Show |
4 | HG00642.hp1 HG02622.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.4311+548A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 27/32 | chr11 | 3692684 | |||||||
chr11:3692780 | T | A | 3 | a0001c0001t0001g0029 a0001c0001t0001g0278 a0001c0001t0001g0328 |
3 | HG02280.hp2 HG02572.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.4311+452A>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 27/32 | chr11 | 3692780 | |||||||
chr11:3692806 | T | C | 1 | a0001c0002t0001g0281 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.4311+426A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 27/32 | chr11 | 3692806 | |||||||
chr11:3692816 | G | A | 52 | a0001c0001t0001g0006 a0001c0001t0001g0081 a0001c0001t0001g0082 others(49): Show |
52 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.4311+416C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 27/32 | chr11 | 3692816 | |||||||
chr11:3692859 | A | G | 37 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0009 others(34): Show |
37 | HG00597.hp1 HG01243.hp1 HG01993.hp1 others(34): Show |
intron_variant | MODIFIER | c.4311+373T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 27/32 | chr11 | 3692859 | |||||||
chr11:3693081 | T | A | 115 | a0001c0001t0001g0113 a0001c0001t0001g0275 a0001c0001t0001g0307 others(112): Show |
115 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.4311+151A>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 27/32 | chr11 | 3693081 | |||||||
chr11:3693166 | C | T | 35 | a0001c0001t0001g0026 a0001c0001t0001g0038 a0001c0001t0001g0039 others(32): Show |
35 | HG00423.hp2 HG00544.hp2 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.4311+66G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 27/32 | chr11 | 3693166 | |||||||
chr11:3693175 | T | C | 7 | a0001c0001t0001g0036 a0001c0001t0001g0121 a0001c0001t0001g0129 others(4): Show |
7 | HG02145.hp2 HG02451.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.4311+57A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 27/32 | chr11 | 3693175 | |||||||
chr11:3693581 | C | T | 1 | a0001c0002t0001g0094 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.4168-206G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 26/32 | chr11 | 3693581 | |||||||
chr11:3693806 | G | T | 230 | a0001c0001t0001g0006 a0001c0001t0001g0026 a0001c0001t0001g0029 others(227): Show |
230 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(227): Show |
intron_variant | MODIFIER | c.4168-431C>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 26/32 | chr11 | 3693806 | |||||||
chr11:3693845 | A | G | 5 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0156 others(2): Show |
5 | NA18964.hp1 NA18977.hp2 NA19056.hp1 others(2): Show |
intron_variant | MODIFIER | c.4168-470T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 26/32 | chr11 | 3693845 | |||||||
chr11:3693921 | A | G | 1 | a0001c0002t0001g0327 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.4168-546T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 26/32 | chr11 | 3693921 | |||||||
chr11:3693970 | C | A | 10 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(7): Show |
10 | HG00735.hp1 HG00741.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.4168-595G>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 26/32 | chr11 | 3693970 | |||||||
chr11:3693997 | G | A | 7 | a0001c0001t0001g0036 a0001c0001t0001g0121 a0001c0001t0001g0129 others(4): Show |
7 | HG02145.hp2 HG02451.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.4168-622C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 26/32 | chr11 | 3693997 | |||||||
chr11:3694041 | G | C | 109 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0009 others(106): Show |
109 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.4168-666C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 26/32 | chr11 | 3694041 | |||||||
chr11:3694056 | C | A | 3 | a0001c0001t0001g0138 a0001c0001t0001g0159 a0001c0001t0001g0161 |
3 | NA18983.hp1 NA18998.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.4168-681G>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 26/32 | chr11 | 3694056 | |||||||
chr11:3694076 | C | CA | 112 | a0001c0001t0001g0113 a0001c0001t0001g0173 a0001c0001t0001g0275 others(109): Show |
112 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.4168-702dupT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 26/32 | chr11 | 3694076 | |||||||
chr11:3694076 | C | CAA | 8 | a0001c0002t0001g0077 a0001c0002t0001g0083 a0001c0002t0001g0084 others(5): Show |
8 | HG02056.hp2 HG02080.hp1 HG02129.hp2 others(5): Show |
intron_variant | MODIFIER | c.4168-703_4168-702d others(4): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 26/32 | chr11 | 3694076 | |||||||
chr11:3694124 | C | T | 72 | a0001c0002t0001g0069 a0001c0002t0001g0070 a0001c0002t0001g0073 others(69): Show |
72 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.4168-749G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 26/32 | chr11 | 3694124 | |||||||
chr11:3694142 | T | C | 72 | a0001c0002t0001g0069 a0001c0002t0001g0070 a0001c0002t0001g0073 others(69): Show |
72 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.4168-767A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 26/32 | chr11 | 3694142 | |||||||
chr11:3694161 | C | T | 2 | a0001c0001t0001g0136 a0001c0001t0001g0146 |
2 | NA18962.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.4168-786G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 26/32 | chr11 | 3694161 | |||||||
chr11:3694224 | A | C | 2 | a0001c0001t0002g0309 a0001c0017t0002g0116 |
2 | HG02486.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.4168-849T>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 26/32 | chr11 | 3694224 | |||||||
chr11:3694231 | C | T | 10 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(7): Show |
10 | HG00735.hp1 HG00741.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.4168-856G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 26/32 | chr11 | 3694231 | |||||||
chr11:3694249 | T | C | 1 | a0001c0002t0001g0318 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.4168-874A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 26/32 | chr11 | 3694249 | |||||||
chr11:3694357 | C | T | 1 | a0001c0001t0001g0329 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.4168-982G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 26/32 | chr11 | 3694357 | |||||||
chr11:3694374 | A | C | 109 | a0001c0001t0001g0183 a0001c0002t0001g0007 a0001c0002t0001g0008 others(106): Show |
109 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.4168-999T>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 26/32 | chr11 | 3694374 | |||||||
chr11:3694437 | T | TA | 36 | a0001c0001t0001g0026 a0001c0001t0001g0038 a0001c0001t0001g0039 others(33): Show |
36 | HG00423.hp2 HG00544.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.4167+1011dupT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 26/32 | chr11 | 3694437 | |||||||
chr11:3694437 | TA | T | 10 | a0001c0001t0002g0309 a0001c0017t0002g0116 a0002c0005t0001g0299 others(7): Show |
10 | HG00735.hp1 HG00741.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.4167+1011delT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 26/32 | chr11 | 3694437 | |||||||
chr11:3694461 | C | T | 5 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0164 others(2): Show |
5 | HG00408.hp1 NA18995.hp2 NA19060.hp2 others(2): Show |
intron_variant | MODIFIER | c.4167+988G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 26/32 | chr11 | 3694461 | |||||||
chr11:3694468 | C | T | 8 | a0001c0001t0001g0068 a0001c0001t0001g0324 a0001c0001t0001g0336 others(5): Show |
8 | HG00642.hp1 HG02280.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.4167+981G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 26/32 | chr11 | 3694468 | |||||||
chr11:3694506 | T | C | 174 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0038 others(171): Show |
174 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(171): Show |
intron_variant | MODIFIER | c.4167+943A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 26/32 | chr11 | 3694506 | |||||||
chr11:3694559 | T | A | 1 | a0001c0002t0001g0167 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.4167+890A>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 26/32 | chr11 | 3694559 | |||||||
chr11:3694567 | T | C | 184 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0038 others(181): Show |
184 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(181): Show |
intron_variant | MODIFIER | c.4167+882A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 26/32 | chr11 | 3694567 | |||||||
chr11:3694578 | A | C | 1 | a0001c0002t0001g0080 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.4167+871T>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 26/32 | chr11 | 3694578 | |||||||
chr11:3694584 | C | G | 1 | a0001c0001t0001g0145 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.4167+865G>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 26/32 | chr11 | 3694584 | |||||||
chr11:3694744 | G | GA | 13 | a0001c0001t0001g0241 a0001c0001t0002g0002 a0001c0001t0002g0314 others(10): Show |
13 | HG00639.hp2 HG01109.hp2 HG01255.hp2 others(10): Show |
intron_variant | MODIFIER | c.4167+704dupT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 26/32 | chr11 | 3694744 | |||||||
chr11:3694745 | A | G | 10 | a0001c0001t0001g0068 a0001c0001t0001g0275 a0001c0001t0001g0307 others(7): Show |
10 | HG00642.hp1 HG02109.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.4167+704T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 26/32 | chr11 | 3694745 | |||||||
chr11:3694796 | C | T | 2 | a0001c0001t0001g0180 a0001c0001t0001g0182 |
2 | NA18990.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.4167+653G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 26/32 | chr11 | 3694796 | |||||||
chr11:3694846 | T | C | 1 | a0001c0002t0001g0280 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.4167+603A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 26/32 | chr11 | 3694846 | |||||||
chr11:3694918 | TA | T | 10 | a0001c0001t0002g0002 a0001c0001t0002g0314 a0001c0001t0002g0317 others(7): Show |
10 | HG00639.hp2 HG01109.hp2 HG01943.hp1 others(7): Show |
intron_variant | MODIFIER | c.4167+530delT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 26/32 | chr11 | 3694918 | |||||||
chr11:3694960 | G | T | 1 | a0001c0001t0001g0305 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.4167+489C>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 26/32 | chr11 | 3694960 | |||||||
chr11:3695116 | T | G | 3 | a0005c0010t0001g0338 a0005c0010t0001g0339 a0005c0021t0001g0259 |
3 | HG02280.hp1 HG02559.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.4167+333A>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 26/32 | chr11 | 3695116 | |||||||
chr11:3695117 | C | A | 2 | a0001c0006t0001g0204 a0001c0006t0001g0242 |
2 | HG00741.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.4167+332G>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 26/32 | chr11 | 3695117 | |||||||
chr11:3695154 | C | T | 4 | a0001c0016t0001g0114 a0005c0010t0001g0338 a0005c0010t0001g0339 others(1): Show |
4 | HG02280.hp1 HG02559.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.4167+295G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 26/32 | chr11 | 3695154 | |||||||
chr11:3695208 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4167+241A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 26/32 | chr11 | 3695208 | |||||||
chr11:3695320 | T | C | 39 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0038 others(36): Show |
39 | HG00423.hp2 HG00544.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.4167+129A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 26/32 | chr11 | 3695320 | |||||||
chr11:3695335 | A | G | 3 | a0005c0010t0001g0338 a0005c0010t0001g0339 a0005c0021t0001g0259 |
3 | HG02280.hp1 HG02559.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.4167+114T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 26/32 | chr11 | 3695335 | |||||||
chr11:3695407 | G | A | 1 | a0001c0002t0001g0295 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.4167+42C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 26/32 | chr11 | 3695407 | |||||||
chr11:3695720 | G | A | 1 | a0001c0026t0001g0298 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.4010-114C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 25/32 | chr11 | 3695720 | |||||||
chr11:3695751 | T | C | 4 | a0001c0001t0001g0068 a0001c0001t0001g0324 a0001c0001t0001g0336 others(1): Show |
4 | HG00642.hp1 HG02622.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.4010-145A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 25/32 | chr11 | 3695751 | |||||||
chr11:3695806 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.4010-200G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 25/32 | chr11 | 3695806 | |||||||
chr11:3695885 | C | T | 3 | a0001c0001t0001g0029 a0001c0001t0001g0278 a0001c0001t0001g0328 |
3 | HG02280.hp2 HG02572.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.4010-279G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 25/32 | chr11 | 3695885 | |||||||
chr11:3695890 | G | A | 112 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0009 others(109): Show |
112 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.4010-284C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 25/32 | chr11 | 3695890 | |||||||
chr11:3695915 | G | A | 2 | a0001c0002t0001g0286 a0001c0002t0001g0288 |
2 | HG03688.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.4010-309C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 25/32 | chr11 | 3695915 | |||||||
chr11:3696048 | G | A | 1 | a0001c0001t0001g0189 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.4010-442C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 25/32 | chr11 | 3696048 | |||||||
chr11:3696051 | C | T | 1 | a0001c0002t0001g0260 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.4010-445G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 25/32 | chr11 | 3696051 | |||||||
chr11:3696091 | T | C | 1 | a0001c0016t0001g0114 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.4010-485A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 25/32 | chr11 | 3696091 | |||||||
chr11:3696210 | T | C | 1 | a0001c0001t0001g0328 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.4010-604A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 25/32 | chr11 | 3696210 | |||||||
chr11:3696230 | G | A | 3 | a0001c0001t0001g0248 a0001c0001t0001g0249 a0001c0001t0001g0252 |
3 | HG00733.hp1 HG00735.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.4010-624C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 25/32 | chr11 | 3696230 | |||||||
chr11:3696311 | C | T | 3 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0340 |
3 | HG01884.hp1 HG01891.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.4010-705G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 25/32 | chr11 | 3696311 | |||||||
chr11:3696394 | CAA | C | 4 | a0001c0001t0001g0068 a0001c0001t0001g0324 a0001c0001t0001g0336 others(1): Show |
4 | HG00642.hp1 HG02622.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.4010-790_4010-789d others(4): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 25/32 | chr11 | 3696394 | |||||||
chr11:3696398 | A | C | 1 | a0008c0027t0001g0153 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.4010-792T>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 25/32 | chr11 | 3696398 | |||||||
chr11:3696426 | C | T | 10 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(7): Show |
10 | HG00735.hp1 HG00741.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.4010-820G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 25/32 | chr11 | 3696426 | |||||||
chr11:3696428 | G | C | 1 | a0001c0002t0001g0203 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.4010-822C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 25/32 | chr11 | 3696428 | |||||||
chr11:3696507 | A | G | 27 | a0001c0001t0001g0029 a0001c0001t0001g0068 a0001c0001t0001g0275 others(24): Show |
27 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.4010-901T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 25/32 | chr11 | 3696507 | |||||||
chr11:3696531 | G | A | 2 | a0004c0007t0001g0213 a0004c0007t0001g0245 |
2 | HG00423.hp2 HG00544.hp2 |
intron_variant | MODIFIER | c.4010-925C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 25/32 | chr11 | 3696531 | |||||||
chr11:3696546 | C | T | 46 | a0001c0001t0001g0006 a0001c0001t0001g0081 a0001c0001t0001g0082 others(43): Show |
46 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.4010-940G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 25/32 | chr11 | 3696546 | |||||||
chr11:3696585 | G | C | 36 | a0001c0001t0001g0026 a0001c0001t0001g0038 a0001c0001t0001g0039 others(33): Show |
36 | HG00423.hp2 HG00544.hp2 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.4010-979C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 25/32 | chr11 | 3696585 | |||||||
chr11:3696607 | G | C | 37 | a0001c0001t0001g0026 a0001c0001t0001g0038 a0001c0001t0001g0039 others(34): Show |
37 | HG00423.hp2 HG00544.hp2 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.4010-1001C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 25/32 | chr11 | 3696607 | |||||||
chr11:3696635 | G | A | 1 | a0001c0001t0001g0278 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.4010-1029C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 25/32 | chr11 | 3696635 | |||||||
chr11:3696830 | C | CA | 124 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0183 others(121): Show |
124 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.4010-1225dupT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 25/32 | chr11 | 3696830 | |||||||
chr11:3696899 | A | C | 32 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0038 others(29): Show |
32 | HG00423.hp2 HG00544.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.4010-1293T>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 25/32 | chr11 | 3696899 | |||||||
chr11:3697033 | T | C | 1 | a0001c0002t0001g0046 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.4010-1427A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 25/32 | chr11 | 3697033 | |||||||
chr11:3697481 | T | G | 1 | a0001c0001t0001g0050 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.4009+1601A>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 25/32 | chr11 | 3697481 | |||||||
chr11:3697561 | G | A | 1 | a0001c0001t0001g0329 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.4009+1521C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 25/32 | chr11 | 3697561 | |||||||
chr11:3697600 | C | T | 1 | a0001c0001t0001g0029 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.4009+1482G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 25/32 | chr11 | 3697600 | |||||||
chr11:3697820 | T | TAA | 7 | a0001c0002t0001g0069 a0001c0002t0001g0074 a0001c0002t0001g0079 others(4): Show |
7 | HG00733.hp2 HG01167.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.4009+1260_4009+126 others(6): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 25/32 | chr11 | 3697820 | |||||||
chr11:3697820 | T | TAAA | 59 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0081 others(56): Show |
59 | HG00323.hp2 HG00438.hp2 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.4009+1259_4009+126 others(7): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 25/32 | chr11 | 3697820 | |||||||
chr11:3697820 | T | TAAAA | 8 | a0001c0002t0001g0083 a0001c0002t0001g0091 a0001c0002t0001g0101 others(5): Show |
8 | HG00423.hp1 HG02056.hp2 HG04184.hp2 others(5): Show |
intron_variant | MODIFIER | c.4009+1258_4009+126 others(8): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 25/32 | chr11 | 3697820 | |||||||
chr11:3697820 | TA | T | 88 | a0001c0001t0001g0028 a0001c0001t0001g0036 a0001c0001t0001g0051 others(85): Show |
88 | HG00323.hp1 HG00408.hp2 HG00609.hp1 others(85): Show |
intron_variant | MODIFIER | c.4009+1261delT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 25/32 | chr11 | 3697820 | |||||||
chr11:3697820 | TAA | T | 61 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0030 others(58): Show |
61 | HG00408.hp1 HG00438.hp1 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.4009+1260_4009+126 others(6): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 25/32 | chr11 | 3697820 | |||||||
chr11:3697820 | TAAA | T | 6 | a0001c0001t0001g0150 a0001c0001t0001g0164 a0001c0001t0001g0170 others(3): Show |
6 | HG00558.hp1 HG02647.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.4009+1259_4009+126 others(7): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 25/32 | chr11 | 3697820 | |||||||
chr11:3697820 | TAAAA | T | 12 | a0001c0001t0001g0029 a0001c0001t0001g0328 a0002c0005t0001g0299 others(9): Show |
12 | HG00735.hp1 HG00741.hp1 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.4009+1258_4009+126 others(8): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 25/32 | chr11 | 3697820 | |||||||
chr11:3697820 | TAAAAAAA others(4): Show |
T | 6 | a0001c0001t0001g0041 a0001c0001t0001g0047 a0001c0001t0001g0048 others(3): Show |
6 | NA18961.hp1 NA18969.hp2 NA18973.hp1 others(3): Show |
intron_variant | MODIFIER | c.4009+1251_4009+126 others(15): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 25/32 | chr11 | 3697820 | |||||||
chr11:3697820 | TAAAAAAA others(5): Show |
T | 26 | a0001c0001t0001g0026 a0001c0001t0001g0038 a0001c0001t0001g0039 others(23): Show |
26 | HG00423.hp2 HG00544.hp2 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.4009+1250_4009+126 others(16): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 25/32 | chr11 | 3697820 | |||||||
chr11:3697827 | A | G | 2 | a0001c0001t0001g0029 a0001c0001t0001g0328 |
2 | HG02280.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.4009+1255T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 25/32 | chr11 | 3697827 | |||||||
chr11:3698175 | G | A | 42 | a0001c0001t0001g0183 a0001c0001t0001g0291 a0001c0001t0001g0293 others(39): Show |
42 | HG00597.hp1 HG01243.hp1 HG01993.hp1 others(39): Show |
intron_variant | MODIFIER | c.4009+907C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 25/32 | chr11 | 3698175 | |||||||
chr11:3698200 | C | T | 1 | a0001c0002t0001g0094 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.4009+882G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 25/32 | chr11 | 3698200 | |||||||
chr11:3698220 | A | G | 1 | a0001c0016t0001g0114 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.4009+862T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 25/32 | chr11 | 3698220 | |||||||
chr11:3698478 | A | C | 1 | a0001c0001t0001g0113 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4009+604T>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 25/32 | chr11 | 3698478 | |||||||
chr11:3698534 | C | A | 4 | a0001c0001t0001g0068 a0001c0001t0001g0324 a0001c0001t0001g0336 others(1): Show |
4 | HG00642.hp1 HG02622.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.4009+548G>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 25/32 | chr11 | 3698534 | |||||||
chr11:3698613 | G | A | 1 | a0001c0001t0001g0278 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.4009+469C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 25/32 | chr11 | 3698613 | |||||||
chr11:3698688 | T | C | 120 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0081 others(117): Show |
120 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.4009+394A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 25/32 | chr11 | 3698688 | |||||||
chr11:3698708 | C | A | 1 | a0018c0034t0001g0122 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4009+374G>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 25/32 | chr11 | 3698708 | |||||||
chr11:3698725 | C | CA | 58 | a0001c0001t0001g0006 a0001c0001t0001g0026 a0001c0001t0001g0030 others(55): Show |
58 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.4009+356dupT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 25/32 | chr11 | 3698725 | |||||||
chr11:3698725 | C | CAA | 56 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0049 others(53): Show |
56 | HG00639.hp2 HG01109.hp2 HG01243.hp1 others(53): Show |
intron_variant | MODIFIER | c.4009+355_4009+356d others(4): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 25/32 | chr11 | 3698725 | |||||||
chr11:3698725 | C | CAAA | 9 | a0001c0001t0001g0113 a0001c0001t0001g0159 a0001c0001t0001g0275 others(6): Show |
9 | HG00597.hp1 HG02572.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.4009+354_4009+356d others(5): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 25/32 | chr11 | 3698725 | |||||||
chr11:3698725 | CA | C | 13 | a0001c0001t0001g0036 a0001c0001t0001g0053 a0001c0001t0001g0068 others(10): Show |
13 | HG00642.hp1 HG01168.hp2 HG01943.hp2 others(10): Show |
intron_variant | MODIFIER | c.4009+356delT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 25/32 | chr11 | 3698725 | |||||||
chr11:3698725 | CAA | C | 14 | a0001c0001t0001g0336 a0001c0001t0002g0309 a0001c0012t0001g0319 others(11): Show |
14 | HG00735.hp1 HG00741.hp1 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.4009+355_4009+356d others(4): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 25/32 | chr11 | 3698725 | |||||||
chr11:3698772 | G | C | 1 | a0001c0001t0001g0113 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4009+310C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 25/32 | chr11 | 3698772 | |||||||
chr11:3698886 | C | T | 3 | a0005c0010t0001g0338 a0005c0010t0001g0339 a0005c0021t0001g0259 |
3 | HG02280.hp1 HG02559.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.4009+196G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 25/32 | chr11 | 3698886 | |||||||
chr11:3698928 | A | G | 1 | a0001c0001t0001g0336 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.4009+154T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 25/32 | chr11 | 3698928 | |||||||
chr11:3698997 | G | C | 1 | a0001c0001t0001g0113 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4009+85C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 25/32 | chr11 | 3698997 | |||||||
chr11:3699423 | G | T | 6 | a0001c0001t0001g0029 a0001c0001t0001g0068 a0001c0001t0001g0324 others(3): Show |
6 | HG00642.hp1 HG02280.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.3743-75C>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 24/32 | chr11 | 3699423 | |||||||
chr11:3699552 | G | C | 68 | a0001c0001t0001g0006 a0001c0001t0001g0078 a0001c0001t0001g0082 others(65): Show |
68 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.3743-204C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 24/32 | chr11 | 3699552 | |||||||
chr11:3699589 | G | C | 6 | a0003c0004t0001g0115 a0003c0004t0001g0117 a0003c0004t0001g0118 others(3): Show |
6 | HG02572.hp1 HG02717.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.3743-241C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 24/32 | chr11 | 3699589 | |||||||
chr11:3699646 | T | C | 1 | a0001c0001t0001g0029 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3743-298A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 24/32 | chr11 | 3699646 | |||||||
chr11:3699763 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.3743-415G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 24/32 | chr11 | 3699763 | |||||||
chr11:3699766 | T | C | 4 | a0002c0008t0001g0003 a0002c0008t0003g0040 a0002c0008t0003g0062 others(1): Show |
4 | HG00735.hp1 HG00741.hp1 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.3743-418A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 24/32 | chr11 | 3699766 | |||||||
chr11:3699803 | T | A | 1 | a0001c0001t0001g0258 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3743-455A>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 24/32 | chr11 | 3699803 | |||||||
chr11:3699823 | G | C | 41 | a0001c0001t0001g0183 a0001c0001t0001g0291 a0001c0001t0001g0293 others(38): Show |
41 | HG00597.hp1 HG01243.hp1 HG01993.hp1 others(38): Show |
intron_variant | MODIFIER | c.3743-475C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 24/32 | chr11 | 3699823 | |||||||
chr11:3699882 | T | C | 47 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0038 others(44): Show |
47 | HG00642.hp1 HG00738.hp2 HG01081.hp1 others(44): Show |
intron_variant | MODIFIER | c.3743-534A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 24/32 | chr11 | 3699882 | |||||||
chr11:3699896 | T | C | 44 | a0001c0001t0001g0183 a0001c0001t0001g0291 a0001c0001t0001g0293 others(41): Show |
44 | HG00597.hp1 HG01243.hp1 HG01993.hp1 others(41): Show |
intron_variant | MODIFIER | c.3743-548A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 24/32 | chr11 | 3699896 | |||||||
chr11:3700180 | C | T | 3 | a0001c0002t0001g0073 a0001c0002t0001g0088 a0001c0002t0001g0104 |
3 | HG02922.hp2 HG03209.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.3742+430G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 24/32 | chr11 | 3700180 | |||||||
chr11:3700249 | A | G | 1 | a0001c0001t0001g0230 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.3742+361T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 24/32 | chr11 | 3700249 | |||||||
chr11:3700268 | C | CA | 110 | a0001c0001t0001g0026 a0001c0001t0001g0038 a0001c0001t0001g0039 others(107): Show |
110 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.3742+341dupT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 24/32 | chr11 | 3700268 | |||||||
chr11:3700268 | C | CAA | 15 | a0001c0001t0001g0029 a0001c0001t0001g0202 a0001c0001t0001g0324 others(12): Show |
15 | HG00642.hp1 HG01891.hp2 HG02056.hp2 others(12): Show |
intron_variant | MODIFIER | c.3742+340_3742+341d others(4): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 24/32 | chr11 | 3700268 | |||||||
chr11:3700268 | CA | C | 42 | a0001c0001t0001g0181 a0001c0001t0001g0183 a0001c0001t0001g0191 others(39): Show |
42 | HG00597.hp1 HG01243.hp1 HG01433.hp2 others(39): Show |
intron_variant | MODIFIER | c.3742+341delT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 24/32 | chr11 | 3700268 | |||||||
chr11:3700268 | CAAAAA | C | 47 | a0001c0001t0001g0006 a0001c0001t0001g0085 a0001c0001t0001g0112 others(44): Show |
47 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.3742+337_3742+341d others(7): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 24/32 | chr11 | 3700268 | |||||||
chr11:3700441 | G | A | 2 | a0001c0001t0001g0055 a0001c0001t0001g0066 |
2 | HG02080.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.3742+169C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 24/32 | chr11 | 3700441 | |||||||
chr11:3700493 | T | A | 2 | a0001c0002t0001g0286 a0001c0002t0001g0288 |
2 | HG03688.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.3742+117A>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 24/32 | chr11 | 3700493 | |||||||
chr11:3700572 | T | C | 1 | a0001c0002t0001g0123 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3742+38A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 24/32 | chr11 | 3700572 | |||||||
chr11:3700892 | G | A | 2 | a0001c0001t0002g0309 a0001c0017t0002g0116 |
2 | HG02486.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.3513-53C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 23/32 | chr11 | 3700892 | |||||||
chr11:3701074 | T | C | 71 | a0001c0001t0001g0081 a0001c0001t0001g0278 a0001c0001t0001g0287 others(68): Show |
71 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.3513-235A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 23/32 | chr11 | 3701074 | |||||||
chr11:3701112 | A | T | 1 | a0001c0001t0001g0179 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3513-273T>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 23/32 | chr11 | 3701112 | |||||||
chr11:3701113 | A | T | 1 | a0001c0001t0001g0179 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3513-274T>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 23/32 | chr11 | 3701113 | |||||||
chr11:3701142 | T | C | 10 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(7): Show |
10 | HG00735.hp1 HG00741.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.3513-303A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 23/32 | chr11 | 3701142 | |||||||
chr11:3701202 | A | G | 1 | a0001c0001t0001g0148 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.3513-363T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 23/32 | chr11 | 3701202 | |||||||
chr11:3701231 | T | C | 3 | a0005c0010t0001g0338 a0005c0010t0001g0339 a0005c0021t0001g0259 |
3 | HG02280.hp1 HG02559.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.3513-392A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 23/32 | chr11 | 3701231 | |||||||
chr11:3701244 | G | T | 1 | a0001c0001t0001g0239 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.3513-405C>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 23/32 | chr11 | 3701244 | |||||||
chr11:3701255 | A | AT | 9 | a0001c0001t0001g0036 a0001c0001t0001g0055 a0001c0001t0001g0200 others(6): Show |
9 | HG01081.hp2 HG01433.hp1 HG01934.hp1 others(6): Show |
intron_variant | MODIFIER | c.3513-417dupA | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 23/32 | chr11 | 3701255 | |||||||
chr11:3701255 | AT | A | 70 | a0001c0001t0001g0050 a0001c0001t0001g0068 a0001c0001t0001g0113 others(67): Show |
70 | HG00423.hp1 HG00597.hp1 HG00639.hp2 others(67): Show |
intron_variant | MODIFIER | c.3513-417delA | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 23/32 | chr11 | 3701255 | |||||||
chr11:3701255 | ATT | A | 93 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0038 others(90): Show |
93 | HG00323.hp2 HG00438.hp2 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.3513-418_3513-417d others(4): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 23/32 | chr11 | 3701255 | |||||||
chr11:3701255 | ATTT | A | 13 | a0001c0002t0001g0289 a0001c0012t0001g0319 a0001c0012t0001g0320 others(10): Show |
13 | HG00735.hp1 HG00741.hp1 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.3513-419_3513-417d others(5): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 23/32 | chr11 | 3701255 | |||||||
chr11:3701419 | C | G | 45 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0038 others(42): Show |
45 | HG00642.hp1 HG00735.hp1 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.3513-580G>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 23/32 | chr11 | 3701419 | |||||||
chr11:3701685 | TTCTC | T | 4 | a0001c0001t0002g0309 a0001c0012t0001g0319 a0001c0012t0001g0320 others(1): Show |
4 | HG02109.hp1 HG02486.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.3512+774_3512+777d others(6): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 23/32 | chr11 | 3701685 | |||||||
chr11:3701723 | T | C | 1 | a0018c0034t0001g0122 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3512+740A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 23/32 | chr11 | 3701723 | |||||||
chr11:3701747 | G | A | 1 | a0005c0010t0001g0338 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3512+716C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 23/32 | chr11 | 3701747 | |||||||
chr11:3701793 | C | T | 1 | a0001c0002t0001g0285 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.3512+670G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 23/32 | chr11 | 3701793 | |||||||
chr11:3701874 | A | C | 14 | a0001c0001t0001g0006 a0001c0001t0001g0135 a0001c0001t0001g0137 others(11): Show |
14 | HG00642.hp2 HG01952.hp1 HG01993.hp2 others(11): Show |
intron_variant | MODIFIER | c.3512+589T>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 23/32 | chr11 | 3701874 | |||||||
chr11:3701935 | T | C | 34 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0038 others(31): Show |
34 | HG00642.hp1 HG00738.hp2 HG01346.hp1 others(31): Show |
intron_variant | MODIFIER | c.3512+528A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 23/32 | chr11 | 3701935 | |||||||
chr11:3701955 | G | A | 1 | a0001c0001t0001g0224 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.3512+508C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 23/32 | chr11 | 3701955 | |||||||
chr11:3701956 | G | C | 1 | a0001c0001t0001g0137 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.3512+507C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 23/32 | chr11 | 3701956 | |||||||
chr11:3702031 | C | G | 10 | a0001c0001t0002g0002 a0001c0001t0002g0314 a0001c0001t0002g0317 others(7): Show |
10 | HG00639.hp2 HG01109.hp2 HG01943.hp1 others(7): Show |
intron_variant | MODIFIER | c.3512+432G>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 23/32 | chr11 | 3702031 | |||||||
chr11:3702241 | A | C | 1 | a0001c0001t0001g0221 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.3512+222T>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 23/32 | chr11 | 3702241 | |||||||
chr11:3702259 | G | A | 1 | a0001c0001t0001g0036 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3512+204C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 23/32 | chr11 | 3702259 | |||||||
chr11:3702259 | G | T | 236 | a0001c0001t0001g0006 a0001c0001t0001g0026 a0001c0001t0001g0029 others(233): Show |
236 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(233): Show |
intron_variant | MODIFIER | c.3512+204C>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 23/32 | chr11 | 3702259 | |||||||
chr11:3702301 | ACACACAC others(17): Show |
A | 1 | a0001c0001t0001g0197 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.3512+138_3512+161d others(26): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 23/32 | chr11 | 3702301 | |||||||
chr11:3702307 | ACACACAC others(3): Show |
A | 3 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0333 |
3 | HG01168.hp2 HG01169.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.3512+146_3512+155d others(12): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 23/32 | chr11 | 3702307 | |||||||
chr11:3702309 | ACACACTC others(3): Show |
A | 1 | a0001c0001t0002g0309 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3512+144_3512+153d others(12): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 23/32 | chr11 | 3702309 | |||||||
chr11:3702309 | ACACACTC others(5): Show |
A | 1 | a0001c0017t0002g0116 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3512+142_3512+153d others(14): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 23/32 | chr11 | 3702309 | |||||||
chr11:3702309 | ACACACTC others(7): Show |
A | 1 | a0001c0001t0001g0155 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.3512+140_3512+153d others(16): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 23/32 | chr11 | 3702309 | |||||||
chr11:3702309 | ACACACTC others(9): Show |
A | 2 | a0001c0001t0001g0113 a0001c0001t0001g0329 |
2 | HG02809.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.3512+138_3512+153d others(18): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 23/32 | chr11 | 3702309 | |||||||
chr11:3702309 | ACACACTC others(15): Show |
A | 1 | a0001c0001t0001g0278 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3512+132_3512+153d others(24): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 23/32 | chr11 | 3702309 | |||||||
chr11:3702309 | ACACACTC others(23): Show |
A | 1 | a0001c0001t0001g0336 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3512+124_3512+153d others(32): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 23/32 | chr11 | 3702309 | |||||||
chr11:3702309 | ACACACTC others(25): Show |
A | 2 | a0001c0001t0001g0068 a0001c0001t0001g0310 |
2 | HG02965.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.3512+122_3512+153d others(34): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 23/32 | chr11 | 3702309 | |||||||
chr11:3702309 | ACACACTC others(29): Show |
A | 2 | a0001c0001t0001g0324 a0001c0001t0008g0325 |
2 | HG00642.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.3512+118_3512+153d others(38): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 23/32 | chr11 | 3702309 | |||||||
chr11:3702311 | ACACTCTC others(5): Show |
A | 1 | a0001c0012t0001g0319 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3512+140_3512+151d others(14): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 23/32 | chr11 | 3702311 | |||||||
chr11:3702311 | ACACTCTC others(9): Show |
A | 3 | a0001c0002t0001g0315 a0013c0029t0001g0134 a0018c0034t0001g0122 |
3 | HG01934.hp2 HG03579.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.3512+136_3512+151d others(18): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 23/32 | chr11 | 3702311 | |||||||
chr11:3702311 | ACACTCTC others(11): Show |
A | 1 | a0001c0002t0001g0024 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.3512+134_3512+151d others(20): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 23/32 | chr11 | 3702311 | |||||||
chr11:3702311 | ACACTCTC others(15): Show |
A | 1 | a0002c0005t0001g0299 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3512+130_3512+151d others(24): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 23/32 | chr11 | 3702311 | |||||||
chr11:3702311 | ACACTCTC others(17): Show |
A | 5 | a0001c0032t0001g0032 a0002c0008t0001g0003 a0002c0008t0003g0040 others(2): Show |
5 | HG00735.hp1 HG00741.hp1 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.3512+128_3512+151d others(26): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 23/32 | chr11 | 3702311 | |||||||
chr11:3702313 | A | T | 5 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0231 others(2): Show |
5 | HG00423.hp2 HG00544.hp2 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.3512+150T>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 23/32 | chr11 | 3702313 | |||||||
chr11:3702313 | ACT | A | 7 | a0001c0001t0001g0165 a0001c0001t0001g0173 a0001c0001t0001g0227 others(4): Show |
7 | HG01081.hp2 HG01109.hp2 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.3512+148_3512+149d others(4): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 23/32 | chr11 | 3702313 | |||||||
chr11:3702313 | ACTCT | A | 14 | a0001c0001t0001g0085 a0001c0001t0001g0121 a0001c0001t0001g0129 others(11): Show |
14 | HG00558.hp1 HG01243.hp2 HG01952.hp2 others(11): Show |
intron_variant | MODIFIER | c.3512+146_3512+149d others(6): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 23/32 | chr11 | 3702313 | |||||||
chr11:3702313 | ACTCTCT | A | 14 | a0001c0001t0001g0004 a0001c0001t0001g0082 a0001c0001t0001g0112 others(11): Show |
14 | HG00408.hp1 HG01255.hp2 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.3512+144_3512+149d others(8): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 23/32 | chr11 | 3702313 | |||||||
chr11:3702313 | ACTCTCTC others(1): Show |
A | 20 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0149 others(17): Show |
20 | HG00738.hp1 HG01258.hp1 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.3512+142_3512+149d others(10): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 23/32 | chr11 | 3702313 | |||||||
chr11:3702313 | ACTCTCTC others(3): Show |
A | 16 | a0001c0001t0001g0006 a0001c0001t0001g0043 a0001c0001t0001g0144 others(13): Show |
16 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.3512+140_3512+149d others(12): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 23/32 | chr11 | 3702313 | |||||||
chr11:3702313 | ACTCTCTC others(5): Show |
A | 22 | a0001c0001t0001g0030 a0001c0001t0001g0038 a0001c0001t0001g0041 others(19): Show |
22 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(19): Show |
intron_variant | MODIFIER | c.3512+138_3512+149d others(14): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 23/32 | chr11 | 3702313 | |||||||
chr11:3702313 | ACTCTCTC others(7): Show |
A | 39 | a0001c0001t0001g0031 a0001c0001t0001g0048 a0001c0001t0001g0063 others(36): Show |
39 | HG00438.hp2 HG00642.hp2 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.3512+136_3512+149d others(16): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 23/32 | chr11 | 3702313 | |||||||
chr11:3702313 | ACTCTCTC others(9): Show |
A | 47 | a0001c0001t0001g0050 a0001c0001t0001g0135 a0001c0001t0001g0143 others(44): Show |
47 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.3512+134_3512+149d others(18): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 23/32 | chr11 | 3702313 | |||||||
chr11:3702313 | ACTCTCTC others(11): Show |
A | 17 | a0001c0001t0001g0026 a0001c0001t0001g0036 a0001c0001t0001g0039 others(14): Show |
17 | HG02074.hp1 HG02145.hp2 HG02165.hp1 others(14): Show |
intron_variant | MODIFIER | c.3512+132_3512+149d others(20): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 23/32 | chr11 | 3702313 | |||||||
chr11:3702313 | ACTCTCTC others(13): Show |
A | 13 | a0001c0001t0001g0029 a0001c0001t0001g0067 a0001c0001t0001g0328 others(10): Show |
13 | HG00323.hp2 HG00621.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.3512+130_3512+149d others(22): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 23/32 | chr11 | 3702313 | |||||||
chr11:3702313 | ACTCTCTC others(15): Show |
A | 7 | a0001c0006t0001g0126 a0001c0006t0001g0127 a0002c0005t0001g0300 others(4): Show |
7 | HG01167.hp1 HG01168.hp1 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.3512+128_3512+149d others(24): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 23/32 | chr11 | 3702313 | |||||||
chr11:3702313 | ACTCTCTC others(17): Show |
A | 6 | a0001c0001t0001g0291 a0001c0001t0001g0293 a0001c0001t0001g0296 others(3): Show |
6 | HG02109.hp2 HG02622.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.3512+126_3512+149d others(26): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 23/32 | chr11 | 3702313 | |||||||
chr11:3702313 | ACTCTCTC others(19): Show |
A | 1 | a0001c0002t0001g0322 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3512+124_3512+149d others(28): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 23/32 | chr11 | 3702313 | |||||||
chr11:3702313 | ACTCTCTC others(21): Show |
A | 1 | a0001c0026t0001g0298 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3512+122_3512+149d others(30): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 23/32 | chr11 | 3702313 | |||||||
chr11:3702313 | ACTCTCTC others(23): Show |
A | 2 | a0001c0002t0001g0074 a0001c0002t0001g0075 |
2 | HG03130.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.3512+120_3512+149d others(32): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 23/32 | chr11 | 3702313 | |||||||
chr11:3702315 | T | A | 68 | a0001c0001t0001g0028 a0001c0001t0001g0051 a0001c0001t0001g0052 others(65): Show |
68 | HG00323.hp1 HG00408.hp2 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.3512+148A>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 23/32 | chr11 | 3702315 | |||||||
chr11:3702317 | T | A | 16 | a0001c0001t0001g0133 a0001c0001t0001g0179 a0001c0001t0001g0180 others(13): Show |
16 | HG00639.hp2 HG01081.hp2 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.3512+146A>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 23/32 | chr11 | 3702317 | |||||||
chr11:3702319 | T | A | 12 | a0001c0001t0001g0133 a0001c0001t0001g0179 a0001c0001t0002g0314 others(9): Show |
12 | HG00639.hp2 HG01081.hp2 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.3512+144A>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 23/32 | chr11 | 3702319 | |||||||
chr11:3702321 | T | A | 11 | a0001c0001t0001g0112 a0001c0001t0001g0139 a0001c0001t0002g0002 others(8): Show |
11 | HG00639.hp2 HG01109.hp2 HG01943.hp1 others(8): Show |
intron_variant | MODIFIER | c.3512+142A>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 23/32 | chr11 | 3702321 | |||||||
chr11:3702322 | CTCTCTCT others(6): Show |
C | 2 | a0004c0007t0001g0213 a0004c0007t0001g0245 |
2 | HG00423.hp2 HG00544.hp2 |
intron_variant | MODIFIER | c.3512+128_3512+140d others(15): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 23/32 | chr11 | 3702322 | |||||||
chr11:3702323 | T | A | 14 | a0001c0001t0001g0158 a0001c0001t0001g0237 a0001c0001t0001g0258 others(11): Show |
14 | HG00738.hp1 HG01109.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.3512+140A>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 23/32 | chr11 | 3702323 | |||||||
chr11:3702324 | CTCTCTCT others(4): Show |
C | 2 | a0004c0007t0001g0216 a0004c0007t0001g0246 |
2 | NA18944.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.3512+128_3512+138d others(13): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 23/32 | chr11 | 3702324 | |||||||
chr11:3702324 | CTCTCTCT others(6): Show |
C | 4 | a0001c0001t0001g0005 a0001c0001t0001g0306 a0001c0002t0001g0203 others(1): Show |
4 | HG01361.hp2 HG01884.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.3512+126_3512+138d others(15): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 23/32 | chr11 | 3702324 | |||||||
chr11:3702324 | CTCTCTCT others(10): Show |
C | 1 | a0001c0001t0001g0305 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.3512+122_3512+138d others(19): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 23/32 | chr11 | 3702324 | |||||||
chr11:3702325 | T | A | 12 | a0001c0001t0001g0043 a0001c0001t0001g0275 a0001c0001t0001g0307 others(9): Show |
12 | HG00738.hp1 HG00738.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.3512+138A>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 23/32 | chr11 | 3702325 | |||||||
chr11:3702326 | CTCTCTCT others(4): Show |
C | 40 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(37): Show |
40 | HG00408.hp2 HG00639.hp1 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.3512+126_3512+136d others(13): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 23/32 | chr11 | 3702326 | |||||||
chr11:3702326 | CTCTCTCT others(6): Show |
C | 3 | a0001c0001t0001g0052 a0001c0001t0001g0059 a0001c0001t0001g0186 |
3 | HG00609.hp2 NA19077.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.3512+124_3512+136d others(15): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 23/32 | chr11 | 3702326 | |||||||
chr11:3702326 | CTCTCTCT others(8): Show |
C | 5 | a0001c0001t0001g0028 a0001c0001t0001g0190 a0001c0001t0001g0198 others(2): Show |
5 | HG00323.hp1 HG01258.hp2 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.3512+122_3512+136d others(17): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 23/32 | chr11 | 3702326 | |||||||
chr11:3702326 | CTCTCTCT others(10): Show |
C | 3 | a0001c0001t0001g0205 a0001c0001t0001g0220 a0001c0001t0001g0240 |
3 | HG02970.hp2 HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3512+120_3512+136d others(19): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 23/32 | chr11 | 3702326 | |||||||
chr11:3702326 | CTCTCTCT others(16): Show |
C | 1 | a0001c0001t0001g0256 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.3512+114_3512+136d others(25): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 23/32 | chr11 | 3702326 | |||||||
chr11:3702327 | T | A | 22 | a0001c0001t0001g0030 a0001c0001t0001g0038 a0001c0001t0001g0041 others(19): Show |
22 | HG00597.hp1 HG00597.hp2 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.3512+136A>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 23/32 | chr11 | 3702327 | |||||||
chr11:3702328 | CTCTCTCT others(2): Show |
C | 5 | a0001c0001t0001g0180 a0001c0001t0001g0191 a0001c0001t0001g0194 others(2): Show |
5 | HG02683.hp2 HG04115.hp2 NA18960.hp1 others(2): Show |
intron_variant | MODIFIER | c.3512+126_3512+134d others(11): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 23/32 | chr11 | 3702328 | |||||||
chr11:3702328 | CTCTCTCT others(6): Show |
C | 1 | a0001c0001t0001g0250 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.3512+122_3512+134d others(15): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 23/32 | chr11 | 3702328 | |||||||
chr11:3702328 | CTCTCTCT others(8): Show |
C | 1 | a0001c0001t0001g0201 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3512+120_3512+134d others(17): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 23/32 | chr11 | 3702328 | |||||||
chr11:3702329 | T | A | 53 | a0001c0001t0001g0031 a0001c0001t0001g0038 a0001c0001t0001g0041 others(50): Show |
53 | HG00438.hp2 HG00597.hp1 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.3512+134A>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 23/32 | chr11 | 3702329 | |||||||
chr11:3702331 | T | A | 73 | a0001c0001t0001g0038 a0001c0001t0001g0041 a0001c0001t0001g0043 others(70): Show |
73 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.3512+132A>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 23/32 | chr11 | 3702331 | |||||||
chr11:3702333 | T | A | 48 | a0001c0001t0001g0026 a0001c0001t0001g0036 a0001c0001t0001g0038 others(45): Show |
48 | HG01346.hp1 HG01361.hp1 HG01891.hp2 others(45): Show |
intron_variant | MODIFIER | c.3512+130A>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 23/32 | chr11 | 3702333 | |||||||
chr11:3702335 | T | A | 41 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0038 others(38): Show |
41 | HG00323.hp2 HG00621.hp1 HG01346.hp1 others(38): Show |
intron_variant | MODIFIER | c.3512+128A>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 23/32 | chr11 | 3702335 | |||||||
chr11:3702337 | T | A | 25 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0038 others(22): Show |
25 | HG01346.hp1 HG01361.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.3512+126A>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 23/32 | chr11 | 3702337 | |||||||
chr11:3702339 | T | A | 29 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0038 others(26): Show |
29 | HG01346.hp1 HG01361.hp1 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.3512+124A>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 23/32 | chr11 | 3702339 | |||||||
chr11:3702341 | T | A | 3 | a0001c0001t0001g0026 a0001c0001t0001g0050 a0001c0002t0001g0322 |
3 | HG02647.hp1 HG03041.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.3512+122A>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 23/32 | chr11 | 3702341 | |||||||
chr11:3702345 | T | A | 2 | a0001c0002t0001g0074 a0001c0002t0001g0075 |
2 | HG03130.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.3512+118A>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 23/32 | chr11 | 3702345 | |||||||
chr11:3702356 | C | G | 1 | a0001c0001t0001g0036 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3512+107G>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 23/32 | chr11 | 3702356 | |||||||
chr11:3702919 | G | C | 2 | a0001c0001t0001g0275 a0001c0001t0001g0307 |
2 | HG02976.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.3083-27C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 22/32 | chr11 | 3702919 | |||||||
chr11:3703043 | T | C | 2 | a0001c0001t0002g0314 a0001c0001t0002g0317 |
2 | HG00639.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.3083-151A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 22/32 | chr11 | 3703043 | |||||||
chr11:3703216 | C | CT | 15 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0133 others(12): Show |
15 | HG00544.hp1 HG00597.hp2 HG00642.hp1 others(12): Show |
intron_variant | MODIFIER | c.3083-325dupA | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 22/32 | chr11 | 3703216 | |||||||
chr11:3703312 | G | A | 1 | a0001c0001t0001g0253 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.3083-420C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 22/32 | chr11 | 3703312 | |||||||
chr11:3703390 | G | T | 1 | a0001c0001t0001g0227 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.3083-498C>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 22/32 | chr11 | 3703390 | |||||||
chr11:3703489 | T | C | 53 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0038 others(50): Show |
53 | HG00423.hp2 HG00544.hp2 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.3083-597A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 22/32 | chr11 | 3703489 | |||||||
chr11:3703557 | G | A | 3 | a0001c0001t0001g0194 a0001c0001t0001g0206 a0001c0001t0001g0250 |
3 | NA18960.hp1 NA19055.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.3083-665C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 22/32 | chr11 | 3703557 | |||||||
chr11:3703721 | A | G | 52 | a0001c0001t0001g0006 a0001c0001t0001g0078 a0001c0001t0001g0082 others(49): Show |
52 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.3083-829T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 22/32 | chr11 | 3703721 | |||||||
chr11:3703827 | A | T | 2 | a0005c0010t0001g0339 a0005c0021t0001g0259 |
2 | HG02280.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.3083-935T>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 22/32 | chr11 | 3703827 | |||||||
chr11:3704097 | C | T | 2 | a0001c0001t0001g0237 a0011c0025t0001g0236 |
2 | HG01081.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.3082+1103G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 22/32 | chr11 | 3704097 | |||||||
chr11:3704317 | T | G | 1 | a0001c0001t0001g0335 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.3082+883A>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 22/32 | chr11 | 3704317 | |||||||
chr11:3704405 | T | A | 74 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0081 others(71): Show |
74 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.3082+795A>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 22/32 | chr11 | 3704405 | |||||||
chr11:3704521 | C | T | 2 | a0001c0001t0001g0275 a0001c0001t0001g0307 |
2 | HG02976.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.3082+679G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 22/32 | chr11 | 3704521 | |||||||
chr11:3704783 | A | C | 74 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0081 others(71): Show |
74 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.3082+417T>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 22/32 | chr11 | 3704783 | |||||||
chr11:3704794 | C | A | 10 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(7): Show |
10 | HG00735.hp1 HG00741.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.3082+406G>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 22/32 | chr11 | 3704794 | |||||||
chr11:3704794 | C | T | 1 | a0018c0034t0001g0122 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3082+406G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 22/32 | chr11 | 3704794 | |||||||
chr11:3704832 | T | G | 1 | a0001c0002t0001g0094 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.3082+368A>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 22/32 | chr11 | 3704832 | |||||||
chr11:3705130 | G | C | 6 | a0001c0001t0001g0029 a0001c0001t0001g0068 a0001c0001t0001g0324 others(3): Show |
6 | HG00642.hp1 HG02280.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.3082+70C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 22/32 | chr11 | 3705130 | |||||||
chr11:3705495 | T | C | 4 | a0001c0001t0001g0068 a0001c0001t0001g0324 a0001c0001t0001g0336 others(1): Show |
4 | HG00642.hp1 HG02622.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.2926-139A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 21/32 | chr11 | 3705495 | |||||||
chr11:3705642 | G | T | 3 | a0001c0001t0001g0308 a0001c0003t0002g0311 a0016c0023t0001g0001 |
3 | HG01346.hp1 HG02895.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.2926-286C>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 21/32 | chr11 | 3705642 | |||||||
chr11:3705734 | A | C | 1 | a0001c0001t0001g0307 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2926-378T>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 21/32 | chr11 | 3705734 | |||||||
chr11:3705825 | A | G | 9 | a0001c0002t0001g0077 a0001c0002t0001g0083 a0001c0002t0001g0084 others(6): Show |
9 | HG02056.hp2 HG02080.hp1 HG02129.hp2 others(6): Show |
intron_variant | MODIFIER | c.2926-469T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 21/32 | chr11 | 3705825 | |||||||
chr11:3705920 | C | T | 2 | a0001c0001t0001g0029 a0001c0001t0001g0328 |
2 | HG02280.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2925+525G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 21/32 | chr11 | 3705920 | |||||||
chr11:3705942 | G | C | 2 | a0001c0012t0001g0319 a0001c0012t0001g0320 |
2 | HG02109.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2925+503C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 21/32 | chr11 | 3705942 | |||||||
chr11:3705996 | C | CA | 41 | a0001c0001t0001g0026 a0001c0001t0001g0038 a0001c0001t0001g0039 others(38): Show |
41 | HG00642.hp1 HG00642.hp2 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.2925+448dupT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 21/32 | chr11 | 3705996 | |||||||
chr11:3705996 | CA | C | 181 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0031 others(178): Show |
181 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.2925+448delT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 21/32 | chr11 | 3705996 | |||||||
chr11:3706029 | G | A | 1 | a0001c0001t0001g0307 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2925+416C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 21/32 | chr11 | 3706029 | |||||||
chr11:3706113 | G | T | 1 | a0001c0001t0001g0078 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2925+332C>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 21/32 | chr11 | 3706113 | |||||||
chr11:3706431 | G | T | 27 | a0001c0001t0001g0029 a0001c0001t0001g0038 a0001c0001t0001g0039 others(24): Show |
27 | HG00642.hp1 HG00738.hp2 HG01361.hp1 others(24): Show |
intron_variant | MODIFIER | c.2925+14C>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 21/32 | chr11 | 3706431 | |||||||
chr11:3706681 | T | C | 4 | a0001c0001t0001g0324 a0001c0001t0008g0325 a0005c0010t0001g0338 others(1): Show |
4 | HG00642.hp1 HG02559.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.2743-54A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 20/32 | chr11 | 3706681 | |||||||
chr11:3707037 | CAA | C | 4 | a0001c0001t0001g0324 a0001c0001t0008g0325 a0005c0010t0001g0338 others(1): Show |
4 | HG00642.hp1 HG02559.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.2743-412_2743-411d others(4): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 20/32 | chr11 | 3707037 | |||||||
chr11:3707328 | A | G | 2 | a0001c0001t0001g0068 a0001c0001t0001g0336 |
2 | HG02965.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.2743-701T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 20/32 | chr11 | 3707328 | |||||||
chr11:3707621 | G | A | 6 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.2743-994C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 20/32 | chr11 | 3707621 | |||||||
chr11:3707636 | C | T | 5 | a0001c0001t0001g0329 a0001c0001t0001g0337 a0001c0001t0004g0330 others(2): Show |
5 | HG02486.hp1 HG02647.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.2743-1009G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 20/32 | chr11 | 3707636 | |||||||
chr11:3707643 | C | T | 2 | a0001c0001t0001g0026 a0001c0002t0001g0016 |
2 | HG03491.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.2743-1016G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 20/32 | chr11 | 3707643 | |||||||
chr11:3707660 | C | T | 1 | a0001c0002t0001g0260 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2743-1033G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 20/32 | chr11 | 3707660 | |||||||
chr11:3707738 | C | CAAAAAAA others(3): Show |
11 | a0001c0001t0001g0029 a0001c0001t0001g0060 a0001c0001t0001g0063 others(8): Show |
11 | HG00558.hp2 HG00642.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.2743-1121_2743-111 others(14): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 20/32 | chr11 | 3707738 | |||||||
chr11:3707738 | C | CAAAAAAA others(4): Show |
30 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0041 others(27): Show |
30 | HG00609.hp2 HG00735.hp1 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.2743-1122_2743-111 others(15): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 20/32 | chr11 | 3707738 | |||||||
chr11:3707738 | C | CAAAAAAA others(5): Show |
16 | a0001c0001t0001g0043 a0001c0001t0001g0057 a0001c0001t0001g0061 others(13): Show |
16 | HG00408.hp2 HG00738.hp2 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.2743-1123_2743-111 others(16): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 20/32 | chr11 | 3707738 | |||||||
chr11:3707738 | C | CAAAAAAA others(6): Show |
2 | a0001c0001t0001g0113 a0001c0026t0001g0298 |
2 | HG02809.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2743-1124_2743-111 others(17): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 20/32 | chr11 | 3707738 | |||||||
chr11:3707738 | C | CAAAAAAA others(7): Show |
57 | a0001c0001t0001g0005 a0001c0001t0001g0028 a0001c0001t0001g0108 others(54): Show |
57 | HG00323.hp1 HG00544.hp2 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.2743-1125_2743-111 others(18): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 20/32 | chr11 | 3707738 | |||||||
chr11:3707738 | C | CAAAAAAA others(8): Show |
46 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0036 others(43): Show |
46 | HG00423.hp2 HG00733.hp1 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.2743-1126_2743-111 others(19): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 20/32 | chr11 | 3707738 | |||||||
chr11:3707738 | C | CAAAAAAA others(9): Show |
20 | a0001c0001t0001g0026 a0001c0001t0001g0199 a0001c0001t0001g0202 others(17): Show |
20 | HG00597.hp1 HG01433.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.2743-1127_2743-111 others(20): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 20/32 | chr11 | 3707738 | |||||||
chr11:3707738 | C | CAAAAAAA others(10): Show |
6 | a0001c0001t0001g0206 a0001c0002t0001g0020 a0001c0002t0001g0027 others(3): Show |
6 | HG02486.hp1 HG02615.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.2743-1112_2743-111 others(21): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 20/32 | chr11 | 3707738 | |||||||
chr11:3707738 | C | CAAAAAAA others(12): Show |
1 | a0001c0001t0001g0241 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.2743-1112_2743-111 others(23): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 20/32 | chr11 | 3707738 | |||||||
chr11:3707738 | C | CAAAAAAA others(13): Show |
40 | a0001c0001t0001g0042 a0001c0001t0001g0044 a0001c0001t0001g0082 others(37): Show |
40 | HG00423.hp1 HG00544.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.2743-1112_2743-111 others(24): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 20/32 | chr11 | 3707738 | |||||||
chr11:3707738 | C | CAAAAAAA others(14): Show |
42 | a0001c0001t0001g0045 a0001c0001t0001g0078 a0001c0001t0001g0081 others(39): Show |
42 | HG00438.hp2 HG00597.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.2743-1112_2743-111 others(25): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 20/32 | chr11 | 3707738 | |||||||
chr11:3707738 | C | CAAAAAAA others(15): Show |
16 | a0001c0001t0001g0006 a0001c0001t0001g0144 a0001c0001t0001g0149 others(13): Show |
16 | HG00323.hp2 HG00558.hp1 HG01934.hp2 others(13): Show |
intron_variant | MODIFIER | c.2743-1112_2743-111 others(26): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 20/32 | chr11 | 3707738 | |||||||
chr11:3707738 | C | CAAAAAAA others(16): Show |
9 | a0001c0001t0001g0112 a0001c0001t0001g0136 a0001c0001t0001g0138 others(6): Show |
9 | HG01109.hp2 HG03453.hp2 HG04184.hp2 others(6): Show |
intron_variant | MODIFIER | c.2743-1112_2743-111 others(27): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 20/32 | chr11 | 3707738 | |||||||
chr11:3707738 | C | CAAAAAAA others(17): Show |
5 | a0001c0001t0001g0141 a0001c0001t0001g0143 a0001c0001t0001g0162 others(2): Show |
5 | HG00438.hp1 HG00609.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.2743-1112_2743-111 others(28): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 20/32 | chr11 | 3707738 | |||||||
chr11:3707738 | C | CAAAAAAA others(18): Show |
1 | a0001c0003t0002g0290 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2743-1112_2743-111 others(29): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 20/32 | chr11 | 3707738 | |||||||
chr11:3707738 | C | CAAAAAAA others(19): Show |
2 | a0001c0001t0001g0189 a0001c0002t0001g0260 |
2 | HG02027.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.2743-1112_2743-111 others(30): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 20/32 | chr11 | 3707738 | |||||||
chr11:3707738 | C | CAAAAAAA others(20): Show |
1 | a0001c0001t0001g0076 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2743-1112_2743-111 others(31): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 20/32 | chr11 | 3707738 | |||||||
chr11:3707738 | C | CAAAAAAA others(21): Show |
4 | a0001c0001t0001g0159 a0001c0001t0001g0169 a0001c0001t0001g0170 others(1): Show |
4 | HG02976.hp2 NA18959.hp1 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.2743-1112_2743-111 others(32): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 20/32 | chr11 | 3707738 | |||||||
chr11:3707738 | C | CAAAAAAA others(22): Show |
1 | a0021c0030t0009g0168 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2743-1112_2743-111 others(33): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 20/32 | chr11 | 3707738 | |||||||
chr11:3707738 | C | CAAAAAAA others(27): Show |
1 | a0001c0001t0001g0164 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.2743-1112_2743-111 others(38): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 20/32 | chr11 | 3707738 | |||||||
chr11:3707738 | C | CAAAAAAA others(33): Show |
3 | a0001c0001t0001g0140 a0001c0001t0001g0174 a0001c0001t0001g0176 |
3 | HG00408.hp1 NA18995.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.2743-1112_2743-111 others(44): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 20/32 | chr11 | 3707738 | |||||||
chr11:3707738 | C | CAAAAAAA others(34): Show |
1 | a0001c0001t0001g0139 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.2743-1112_2743-111 others(45): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 20/32 | chr11 | 3707738 | |||||||
chr11:3707738 | C | CACAAAAA others(11): Show |
1 | a0018c0034t0001g0122 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2743-1112_2743-111 others(22): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 20/32 | chr11 | 3707738 | |||||||
chr11:3707970 | G | A | 1 | a0001c0001t0001g0197 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2743-1343C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 20/32 | chr11 | 3707970 | |||||||
chr11:3708168 | T | C | 2 | a0001c0001t0001g0136 a0001c0001t0001g0146 |
2 | NA18962.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.2743-1541A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 20/32 | chr11 | 3708168 | |||||||
chr11:3708198 | T | C | 3 | a0001c0001t0002g0314 a0001c0001t0002g0317 a0001c0002t0001g0123 |
3 | HG00639.hp2 HG01943.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2743-1571A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 20/32 | chr11 | 3708198 | |||||||
chr11:3708446 | G | A | 130 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0030 others(127): Show |
130 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.2743-1819C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 20/32 | chr11 | 3708446 | |||||||
chr11:3708508 | C | T | 2 | a0005c0010t0001g0338 a0005c0010t0001g0339 |
2 | HG02559.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2743-1881G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 20/32 | chr11 | 3708508 | |||||||
chr11:3708550 | G | A | 1 | a0001c0003t0002g0313 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2743-1923C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 20/32 | chr11 | 3708550 | |||||||
chr11:3708586 | G | A | 1 | a0001c0002t0001g0092 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2743-1959C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 20/32 | chr11 | 3708586 | |||||||
chr11:3708723 | T | C | 1 | a0001c0002t0001g0025 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2743-2096A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 20/32 | chr11 | 3708723 | |||||||
chr11:3708724 | TA | T | 12 | a0001c0001t0001g0005 a0001c0001t0001g0068 a0001c0001t0001g0169 others(9): Show |
12 | HG00323.hp1 HG00642.hp1 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.2743-2098delT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 20/32 | chr11 | 3708724 | |||||||
chr11:3708783 | C | A | 2 | a0001c0012t0001g0319 a0001c0012t0001g0320 |
2 | HG02109.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2743-2156G>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 20/32 | chr11 | 3708783 | |||||||
chr11:3708879 | G | A | 2 | a0001c0001t0001g0029 a0001c0001t0001g0328 |
2 | HG02280.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2743-2252C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 20/32 | chr11 | 3708879 | |||||||
chr11:3708888 | A | C | 40 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0041 others(37): Show |
40 | HG00408.hp2 HG00609.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.2743-2261T>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 20/32 | chr11 | 3708888 | |||||||
chr11:3708914 | C | A | 1 | a0003c0004t0001g0316 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2743-2287G>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 20/32 | chr11 | 3708914 | |||||||
chr11:3709111 | C | T | 3 | a0003c0004t0001g0115 a0003c0004t0001g0118 a0003c0004t0001g0120 |
3 | HG02717.hp1 HG03139.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2743-2484G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 20/32 | chr11 | 3709111 | |||||||
chr11:3709366 | C | T | 1 | a0001c0001t0001g0063 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2743-2739G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 20/32 | chr11 | 3709366 | |||||||
chr11:3709488 | C | T | 320 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0026 others(317): Show |
320 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(317): Show |
intron_variant | MODIFIER | c.2743-2861G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 20/32 | chr11 | 3709488 | |||||||
chr11:3709654 | C | T | 2 | a0001c0012t0001g0319 a0001c0012t0001g0320 |
2 | HG02109.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2742+2910G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 20/32 | chr11 | 3709654 | |||||||
chr11:3709677 | A | T | 1 | a0001c0032t0001g0032 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2742+2887T>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 20/32 | chr11 | 3709677 | |||||||
chr11:3709827 | A | AG | 22 | a0001c0001t0001g0036 a0001c0001t0001g0050 a0001c0001t0001g0059 others(19): Show |
22 | HG00544.hp2 HG00642.hp1 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.2742+2736dupC | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 20/32 | chr11 | 3709827 | |||||||
chr11:3709837 | GGGGAGGG others(1): Show |
G | 113 | a0001c0001t0001g0006 a0001c0001t0001g0076 a0001c0001t0001g0078 others(110): Show |
113 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.2742+2719_2742+272 others(12): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 20/32 | chr11 | 3709837 | |||||||
chr11:3709841 | A | G | 1 | a0001c0002t0001g0295 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2742+2723T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 20/32 | chr11 | 3709841 | |||||||
chr11:3709842 | G | A | 1 | a0001c0002t0001g0295 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2742+2722C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 20/32 | chr11 | 3709842 | |||||||
chr11:3709844 | GT | G | 226 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0026 others(223): Show |
226 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(223): Show |
intron_variant | MODIFIER | c.2742+2719delA | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 20/32 | chr11 | 3709844 | |||||||
chr11:3709845 | T | G | 1 | a0001c0002t0001g0295 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2742+2719A>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 20/32 | chr11 | 3709845 | |||||||
chr11:3709981 | T | TA | 173 | a0001c0001t0001g0006 a0001c0001t0001g0038 a0001c0001t0001g0039 others(170): Show |
173 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(170): Show |
intron_variant | MODIFIER | c.2742+2582dupT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 20/32 | chr11 | 3709981 | |||||||
chr11:3709982 | A | T | 2 | a0001c0001t0001g0227 a0001c0016t0001g0114 |
2 | HG01433.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2742+2582T>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 20/32 | chr11 | 3709982 | |||||||
chr11:3709988 | A | C | 3 | a0001c0001t0001g0113 a0001c0001t0001g0333 a0001c0001t0001g0334 |
3 | HG02145.hp1 HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2742+2576T>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 20/32 | chr11 | 3709988 | |||||||
chr11:3709998 | C | CA | 67 | a0001c0001t0001g0044 a0001c0001t0001g0063 a0001c0001t0001g0076 others(64): Show |
67 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.2742+2565dupT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 20/32 | chr11 | 3709998 | |||||||
chr11:3709998 | CA | C | 6 | a0001c0001t0001g0030 a0001c0001t0001g0068 a0001c0001t0001g0146 others(3): Show |
6 | HG01884.hp1 HG02559.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.2742+2565delT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 20/32 | chr11 | 3709998 | |||||||
chr11:3709998 | CAAAAAA | C | 6 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.2742+2560_2742+256 others(10): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 20/32 | chr11 | 3709998 | |||||||
chr11:3710078 | G | C | 40 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0041 others(37): Show |
40 | HG00408.hp2 HG00609.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.2742+2486C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 20/32 | chr11 | 3710078 | |||||||
chr11:3710127 | A | C | 1 | a0001c0002t0001g0087 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2742+2437T>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 20/32 | chr11 | 3710127 | |||||||
chr11:3710452 | G | A | 1 | a0001c0002t0001g0089 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2742+2112C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 20/32 | chr11 | 3710452 | |||||||
chr11:3710654 | A | T | 4 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0182 others(1): Show |
4 | NA18990.hp2 NA18999.hp1 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.2742+1910T>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 20/32 | chr11 | 3710654 | |||||||
chr11:3710866 | T | C | 8 | a0001c0001t0001g0068 a0001c0001t0001g0324 a0001c0001t0001g0336 others(5): Show |
8 | HG00642.hp1 HG02109.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.2742+1698A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 20/32 | chr11 | 3710866 | |||||||
chr11:3710928 | T | C | 3 | a0001c0002t0001g0087 a0001c0002t0001g0101 a0001c0002t0001g0106 |
3 | HG02056.hp2 HG02129.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.2742+1636A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 20/32 | chr11 | 3710928 | |||||||
chr11:3711240 | G | T | 6 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.2742+1324C>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 20/32 | chr11 | 3711240 | |||||||
chr11:3711259 | C | A | 2 | a0001c0001t0001g0029 a0001c0001t0001g0328 |
2 | HG02280.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2742+1305G>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 20/32 | chr11 | 3711259 | |||||||
chr11:3711317 | G | C | 3 | a0001c0002t0001g0074 a0001c0002t0001g0075 a0001c0002t0001g0322 |
3 | HG03041.hp1 HG03130.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2742+1247C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 20/32 | chr11 | 3711317 | |||||||
chr11:3711412 | A | G | 14 | a0001c0001t0001g0068 a0001c0001t0001g0324 a0001c0001t0001g0336 others(11): Show |
14 | HG00642.hp1 HG01081.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.2742+1152T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 20/32 | chr11 | 3711412 | |||||||
chr11:3711526 | G | C | 1 | a0001c0001t0001g0278 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2742+1038C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 20/32 | chr11 | 3711526 | |||||||
chr11:3711568 | C | T | 14 | a0001c0001t0001g0068 a0001c0001t0001g0324 a0001c0001t0001g0336 others(11): Show |
14 | HG00642.hp1 HG01081.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.2742+996G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 20/32 | chr11 | 3711568 | |||||||
chr11:3711688 | C | A | 1 | a0001c0001t0001g0310 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2742+876G>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 20/32 | chr11 | 3711688 | |||||||
chr11:3711730 | C | A | 182 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0030 others(179): Show |
182 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(179): Show |
intron_variant | MODIFIER | c.2742+834G>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 20/32 | chr11 | 3711730 | |||||||
chr11:3712007 | C | T | 1 | a0001c0002t0001g0014 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2742+557G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 20/32 | chr11 | 3712007 | |||||||
chr11:3712203 | CTG | C | 70 | a0001c0001t0001g0076 a0001c0001t0001g0078 a0001c0001t0001g0081 others(67): Show |
70 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.2742+359_2742+360d others(4): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 20/32 | chr11 | 3712203 | |||||||
chr11:3712452 | T | G | 2 | a0001c0012t0001g0319 a0001c0012t0001g0320 |
2 | HG02109.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2742+112A>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 20/32 | chr11 | 3712452 | |||||||
chr11:3712478 | T | C | 3 | a0001c0001t0001g0333 a0001c0001t0001g0334 a0001c0017t0002g0116 |
3 | HG02145.hp1 HG02486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2742+86A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 20/32 | chr11 | 3712478 | |||||||
chr11:3712904 | G | C | 2 | a0001c0001t0001g0036 a0001c0001t0001g0179 |
2 | HG02145.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.2578-176C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 19/32 | chr11 | 3712904 | |||||||
chr11:3712912 | C | T | 1 | a0001c0001t0001g0199 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2578-184G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 19/32 | chr11 | 3712912 | |||||||
chr11:3713048 | C | G | 6 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.2578-320G>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 19/32 | chr11 | 3713048 | |||||||
chr11:3713195 | T | G | 6 | a0001c0001t0001g0068 a0001c0001t0001g0324 a0001c0001t0001g0336 others(3): Show |
6 | HG00642.hp1 HG02559.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.2578-467A>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 19/32 | chr11 | 3713195 | |||||||
chr11:3713666 | C | T | 1 | a0001c0016t0001g0114 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2577+152G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 19/32 | chr11 | 3713666 | |||||||
chr11:3713710 | A | C | 206 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0030 others(203): Show |
206 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(203): Show |
intron_variant | MODIFIER | c.2577+108T>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 19/32 | chr11 | 3713710 | |||||||
chr11:3713782 | G | A | 1 | a0001c0001t0001g0215 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.2577+36C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 19/32 | chr11 | 3713782 | |||||||
chr11:3714009 | C | T | 6 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.2400-14G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 18/32 | chr11 | 3714009 | |||||||
chr11:3714038 | C | T | 1 | a0001c0002t0001g0131 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2400-43G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 18/32 | chr11 | 3714038 | |||||||
chr11:3714048 | A | G | 3 | a0001c0002t0001g0192 a0001c0002t0001g0193 a0001c0002t0001g0211 |
3 | HG02559.hp2 HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2400-53T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 18/32 | chr11 | 3714048 | |||||||
chr11:3714086 | A | C | 3 | a0001c0001t0001g0138 a0001c0001t0001g0159 a0001c0001t0001g0161 |
3 | NA18983.hp1 NA18998.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.2400-91T>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 18/32 | chr11 | 3714086 | |||||||
chr11:3714170 | T | C | 6 | a0001c0001t0001g0329 a0001c0001t0001g0337 a0001c0001t0004g0330 others(3): Show |
6 | HG02257.hp2 HG02486.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.2400-175A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 18/32 | chr11 | 3714170 | |||||||
chr11:3714170 | T | G | 2 | a0001c0002t0001g0193 a0001c0002t0001g0211 |
2 | HG02559.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2400-175A>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 18/32 | chr11 | 3714170 | |||||||
chr11:3714297 | C | T | 1 | a0001c0003t0002g0312 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2400-302G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 18/32 | chr11 | 3714297 | |||||||
chr11:3714343 | C | A | 6 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.2400-348G>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 18/32 | chr11 | 3714343 | |||||||
chr11:3714362 | A | T | 1 | a0001c0001t0001g0209 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.2400-367T>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 18/32 | chr11 | 3714362 | |||||||
chr11:3714394 | T | C | 6 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.2400-399A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 18/32 | chr11 | 3714394 | |||||||
chr11:3714513 | TACATCTA others(3): Show |
T | 1 | a0001c0026t0001g0298 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2400-528_2400-519d others(12): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 18/32 | chr11 | 3714513 | |||||||
chr11:3714546 | A | C | 4 | a0001c0001t0001g0324 a0001c0001t0008g0325 a0005c0010t0001g0338 others(1): Show |
4 | HG00642.hp1 HG02559.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.2400-551T>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 18/32 | chr11 | 3714546 | |||||||
chr11:3714846 | T | G | 6 | a0001c0001t0001g0028 a0001c0001t0001g0038 a0001c0001t0001g0186 others(3): Show |
6 | HG01258.hp2 HG01361.hp1 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.2400-851A>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 18/32 | chr11 | 3714846 | |||||||
chr11:3714918 | T | C | 2 | a0001c0012t0001g0319 a0001c0012t0001g0320 |
2 | HG02109.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2400-923A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 18/32 | chr11 | 3714918 | |||||||
chr11:3715291 | T | C | 193 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0030 others(190): Show |
193 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(190): Show |
intron_variant | MODIFIER | c.2400-1296A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 18/32 | chr11 | 3715291 | |||||||
chr11:3715440 | T | C | 4 | a0001c0001t0001g0324 a0001c0001t0008g0325 a0005c0010t0001g0338 others(1): Show |
4 | HG00642.hp1 HG02559.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.2400-1445A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 18/32 | chr11 | 3715440 | |||||||
chr11:3715566 | T | C | 2 | a0005c0010t0001g0338 a0005c0010t0001g0339 |
2 | HG02559.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2400-1571A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 18/32 | chr11 | 3715566 | |||||||
chr11:3715607 | G | T | 1 | a0001c0001t0001g0059 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2400-1612C>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 18/32 | chr11 | 3715607 | |||||||
chr11:3715615 | G | A | 2 | a0001c0002t0001g0267 a0001c0002t0001g0268 |
2 | NA18959.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.2400-1620C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 18/32 | chr11 | 3715615 | |||||||
chr11:3715678 | C | G | 1 | a0016c0023t0001g0001 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2400-1683G>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 18/32 | chr11 | 3715678 | |||||||
chr11:3715709 | C | G | 1 | a0001c0001t0001g0081 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2400-1714G>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 18/32 | chr11 | 3715709 | |||||||
chr11:3715790 | A | AT | 263 | a0001c0001t0001g0006 a0001c0001t0001g0026 a0001c0001t0001g0029 others(260): Show |
263 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(260): Show |
intron_variant | MODIFIER | c.2400-1796dupA | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 18/32 | chr11 | 3715790 | |||||||
chr11:3715834 | T | G | 1 | a0004c0007t0001g0213 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2400-1839A>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 18/32 | chr11 | 3715834 | |||||||
chr11:3716093 | T | C | 1 | a0007c0013t0005g0218 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2400-2098A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 18/32 | chr11 | 3716093 | |||||||
chr11:3716168 | C | T | 72 | a0001c0001t0001g0076 a0001c0001t0001g0078 a0001c0001t0001g0081 others(69): Show |
72 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.2400-2173G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 18/32 | chr11 | 3716168 | |||||||
chr11:3716242 | T | A | 1 | a0001c0001t0001g0049 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2400-2247A>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 18/32 | chr11 | 3716242 | |||||||
chr11:3716271 | T | A | 5 | a0001c0001t0001g0191 a0001c0001t0001g0195 a0001c0001t0001g0196 others(2): Show |
5 | NA18950.hp2 NA18952.hp1 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.2400-2276A>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 18/32 | chr11 | 3716271 | |||||||
chr11:3716273 | T | C | 58 | a0001c0001t0001g0026 a0001c0001t0001g0030 a0001c0001t0001g0031 others(55): Show |
58 | HG00597.hp1 HG00639.hp2 HG01243.hp2 others(55): Show |
intron_variant | MODIFIER | c.2400-2278A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 18/32 | chr11 | 3716273 | |||||||
chr11:3716297 | A | G | 1 | a0001c0026t0001g0298 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2400-2302T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 18/32 | chr11 | 3716297 | |||||||
chr11:3716338 | AT | A | 12 | a0001c0001t0001g0108 a0001c0001t0001g0324 a0001c0001t0008g0325 others(9): Show |
12 | HG00642.hp1 HG01081.hp1 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.2400-2344delA | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 18/32 | chr11 | 3716338 | |||||||
chr11:3716362 | T | A | 1 | a0001c0016t0001g0114 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2400-2367A>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 18/32 | chr11 | 3716362 | |||||||
chr11:3716375 | C | T | 12 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(9): Show |
12 | HG00408.hp2 HG00609.hp2 HG02015.hp1 others(9): Show |
intron_variant | MODIFIER | c.2400-2380G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 18/32 | chr11 | 3716375 | |||||||
chr11:3716398 | T | G | 1 | a0001c0001t0001g0166 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2400-2403A>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 18/32 | chr11 | 3716398 | |||||||
chr11:3716409 | C | T | 6 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.2400-2414G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 18/32 | chr11 | 3716409 | |||||||
chr11:3716436 | T | G | 74 | a0001c0001t0001g0042 a0001c0001t0001g0044 a0001c0001t0001g0045 others(71): Show |
74 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.2400-2441A>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 18/32 | chr11 | 3716436 | |||||||
chr11:3716641 | G | T | 1 | a0001c0001t0001g0058 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2400-2646C>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 18/32 | chr11 | 3716641 | |||||||
chr11:3716716 | T | G | 1 | a0005c0010t0001g0339 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2399+2696A>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 18/32 | chr11 | 3716716 | |||||||
chr11:3716889 | AG | A | 8 | a0001c0001t0001g0068 a0001c0001t0001g0324 a0001c0001t0001g0336 others(5): Show |
8 | HG00642.hp1 HG02109.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.2399+2522delC | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 18/32 | chr11 | 3716889 | |||||||
chr11:3716937 | G | A | 202 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0030 others(199): Show |
202 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.2399+2475C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 18/32 | chr11 | 3716937 | |||||||
chr11:3717026 | C | A | 1 | a0001c0001t0001g0184 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2399+2386G>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 18/32 | chr11 | 3717026 | |||||||
chr11:3717065 | G | A | 1 | a0001c0026t0001g0298 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2399+2347C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 18/32 | chr11 | 3717065 | |||||||
chr11:3717141 | T | C | 1 | a0001c0001t0001g0078 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2399+2271A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 18/32 | chr11 | 3717141 | |||||||
chr11:3717324 | G | A | 72 | a0001c0001t0001g0076 a0001c0001t0001g0078 a0001c0001t0001g0081 others(69): Show |
72 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.2399+2088C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 18/32 | chr11 | 3717324 | |||||||
chr11:3717433 | A | G | 1 | a0001c0001t0001g0078 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2399+1979T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 18/32 | chr11 | 3717433 | |||||||
chr11:3717435 | A | G | 8 | a0001c0001t0001g0068 a0001c0001t0001g0324 a0001c0001t0001g0336 others(5): Show |
8 | HG00642.hp1 HG02109.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.2399+1977T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 18/32 | chr11 | 3717435 | |||||||
chr11:3717704 | A | G | 3 | a0001c0002t0001g0262 a0001c0002t0001g0264 a0010c0014t0001g0263 |
3 | NA18955.hp1 NA18957.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.2399+1708T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 18/32 | chr11 | 3717704 | |||||||
chr11:3718021 | T | C | 1 | a0001c0001t0001g0332 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2399+1391A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 18/32 | chr11 | 3718021 | |||||||
chr11:3718032 | T | C | 15 | a0001c0001t0002g0002 a0001c0001t0002g0309 a0001c0002t0001g0123 others(12): Show |
15 | HG01243.hp2 HG02258.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.2399+1380A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 18/32 | chr11 | 3718032 | |||||||
chr11:3718072 | C | T | 5 | a0001c0001t0001g0329 a0001c0001t0001g0337 a0001c0001t0004g0330 others(2): Show |
5 | HG02486.hp1 HG02647.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.2399+1340G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 18/32 | chr11 | 3718072 | |||||||
chr11:3718073 | G | A | 1 | a0001c0032t0001g0032 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2399+1339C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 18/32 | chr11 | 3718073 | |||||||
chr11:3718160 | C | T | 15 | a0001c0001t0001g0068 a0001c0001t0001g0324 a0001c0001t0001g0336 others(12): Show |
15 | HG00642.hp1 HG01109.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.2399+1252G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 18/32 | chr11 | 3718160 | |||||||
chr11:3718365 | G | A | 1 | a0001c0002t0001g0089 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2399+1047C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 18/32 | chr11 | 3718365 | |||||||
chr11:3718740 | TAG | T | 6 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.2399+670_2399+671d others(4): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 18/32 | chr11 | 3718740 | |||||||
chr11:3718742 | G | C | 1 | a0001c0001t0001g0232 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2399+670C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 18/32 | chr11 | 3718742 | |||||||
chr11:3718818 | GGACCCAA others(265): Show |
G | 2 | a0001c0001t0001g0180 a0001c0001t0001g0182 |
2 | NA18990.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.2399+322_2399+593d others(2): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 18/32 | chr11 | 3718818 | |||||||
chr11:3718991 | G | A | 6 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.2399+421C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 18/32 | chr11 | 3718991 | |||||||
chr11:3718993 | G | A | 2 | a0001c0001t0001g0333 a0001c0001t0001g0334 |
2 | HG02145.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2399+419C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 18/32 | chr11 | 3718993 | |||||||
chr11:3719021 | G | A | 50 | a0001c0001t0001g0026 a0001c0001t0001g0030 a0001c0001t0001g0031 others(47): Show |
50 | HG00597.hp1 HG01243.hp2 HG01884.hp1 others(47): Show |
intron_variant | MODIFIER | c.2399+391C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 18/32 | chr11 | 3719021 | |||||||
chr11:3719120 | CA | C | 16 | a0001c0001t0001g0068 a0001c0001t0001g0324 a0001c0001t0001g0333 others(13): Show |
16 | HG00642.hp1 HG01081.hp1 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.2399+291delT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 18/32 | chr11 | 3719120 | |||||||
chr11:3719344 | C | T | 39 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0041 others(36): Show |
39 | HG00408.hp2 HG00609.hp2 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.2399+68G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 18/32 | chr11 | 3719344 | |||||||
chr11:3719358 | G | T | 123 | a0001c0001t0001g0026 a0001c0001t0001g0030 a0001c0001t0001g0031 others(120): Show |
123 | HG00323.hp2 HG00438.hp2 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.2399+54C>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 18/32 | chr11 | 3719358 | |||||||
chr11:3719579 | T | C | 8 | a0001c0001t0001g0068 a0001c0001t0001g0324 a0001c0001t0001g0336 others(5): Show |
8 | HG00642.hp1 HG02109.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.2261-29A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 17/32 | chr11 | 3719579 | |||||||
chr11:3719610 | C | T | 1 | a0001c0001t0001g0275 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2261-60G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 17/32 | chr11 | 3719610 | |||||||
chr11:3719709 | GGA | G | 202 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0030 others(199): Show |
202 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.2261-161_2261-160d others(4): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 17/32 | chr11 | 3719709 | |||||||
chr11:3720150 | A | G | 4 | a0001c0001t0001g0135 a0001c0001t0001g0171 a0001c0001t0001g0172 others(1): Show |
4 | HG00642.hp2 HG01952.hp1 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.2260+562T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 17/32 | chr11 | 3720150 | |||||||
chr11:3720422 | C | T | 2 | a0005c0010t0001g0338 a0005c0010t0001g0339 |
2 | HG02559.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2260+290G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 17/32 | chr11 | 3720422 | |||||||
chr11:3720436 | G | C | 8 | a0001c0002t0001g0069 a0001c0002t0001g0093 a0001c0002t0001g0095 others(5): Show |
8 | HG02015.hp2 HG02165.hp1 NA18965.hp2 others(5): Show |
intron_variant | MODIFIER | c.2260+276C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 17/32 | chr11 | 3720436 | |||||||
chr11:3720552 | C | T | 6 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.2260+160G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 17/32 | chr11 | 3720552 | |||||||
chr11:3720617 | G | A | 1 | a0001c0001t0001g0215 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.2260+95C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 17/32 | chr11 | 3720617 | |||||||
chr11:3720629 | T | C | 1 | a0001c0032t0001g0032 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2260+83A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 17/32 | chr11 | 3720629 | |||||||
chr11:3720696 | C | G | 1 | a0018c0034t0001g0122 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2260+16G>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 17/32 | chr11 | 3720696 | |||||||
chr11:3720832 | C | CA | 126 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0068 others(123): Show |
126 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(123): Show |
splice_region_variant&intron_variant | LOW | c.2147-8dupT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 16/32 | chr11 | 3720832 | |||||||
chr11:3720832 | C | CAA | 50 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0038 others(47): Show |
50 | HG00408.hp2 HG00735.hp1 HG00741.hp1 others(47): Show |
splice_region_variant&intron_variant | LOW | c.2147-9_2147-8dupTT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 16/32 | chr11 | 3720832 | |||||||
chr11:3720832 | CA | C | 10 | a0001c0001t0001g0184 a0001c0001t0001g0324 a0001c0001t0008g0325 others(7): Show |
10 | HG00642.hp1 HG01081.hp1 HG01167.hp1 others(7): Show |
splice_region_variant&intron_variant | LOW | c.2147-8delT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 16/32 | chr11 | 3720832 | |||||||
chr11:3720975 | A | AGAGTGTG others(7): Show |
1 | a0001c0026t0001g0298 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2147-151_2147-150i others(16): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 16/32 | chr11 | 3720975 | |||||||
chr11:3720975 | A | AGT | 12 | a0001c0001t0001g0068 a0001c0001t0001g0229 a0001c0001t0001g0335 others(9): Show |
12 | HG01433.hp2 HG02559.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.2147-152_2147-151d others(4): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 16/32 | chr11 | 3720975 | |||||||
chr11:3720975 | A | AGTGT | 40 | a0001c0001t0001g0026 a0001c0001t0001g0052 a0001c0001t0001g0183 others(37): Show |
40 | HG00597.hp1 HG00597.hp2 HG00609.hp2 others(37): Show |
intron_variant | MODIFIER | c.2147-154_2147-151d others(6): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 16/32 | chr11 | 3720975 | |||||||
chr11:3720975 | A | AGTGTGT | 87 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0038 others(84): Show |
87 | HG00423.hp1 HG00544.hp1 HG00733.hp2 others(84): Show |
intron_variant | MODIFIER | c.2147-156_2147-151d others(8): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 16/32 | chr11 | 3720975 | |||||||
chr11:3720975 | A | AGTGTGTG others(1): Show |
32 | a0001c0001t0001g0045 a0001c0001t0001g0053 a0001c0001t0001g0054 others(29): Show |
32 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.2147-158_2147-151d others(10): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 16/32 | chr11 | 3720975 | |||||||
chr11:3720975 | A | AGTGTGTG others(3): Show |
20 | a0001c0001t0001g0055 a0001c0001t0001g0060 a0001c0001t0001g0066 others(17): Show |
20 | HG01081.hp1 HG01099.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.2147-160_2147-151d others(12): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 16/32 | chr11 | 3720975 | |||||||
chr11:3720975 | A | AGTGTGTG others(5): Show |
3 | a0001c0001t0001g0051 a0001c0001t0001g0329 a0002c0005t0001g0304 |
3 | HG01168.hp1 HG02083.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2147-162_2147-151d others(14): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 16/32 | chr11 | 3720975 | |||||||
chr11:3720975 | A | AGTGTGTG others(7): Show |
2 | a0001c0001t0001g0113 a0001c0001t0001g0337 |
2 | HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2147-164_2147-151d others(16): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 16/32 | chr11 | 3720975 | |||||||
chr11:3720975 | AGT | A | 90 | a0001c0001t0001g0028 a0001c0001t0001g0036 a0001c0001t0001g0108 others(87): Show |
90 | HG00323.hp1 HG00423.hp2 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.2147-152_2147-151d others(4): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 16/32 | chr11 | 3720975 | |||||||
chr11:3720975 | AGTGT | A | 35 | a0001c0001t0001g0006 a0001c0001t0001g0112 a0001c0001t0001g0136 others(32): Show |
35 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.2147-154_2147-151d others(6): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 16/32 | chr11 | 3720975 | |||||||
chr11:3721242 | C | T | 6 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.2147-417G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 16/32 | chr11 | 3721242 | |||||||
chr11:3721294 | T | C | 2 | a0001c0012t0001g0319 a0001c0012t0001g0320 |
2 | HG02109.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2147-469A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 16/32 | chr11 | 3721294 | |||||||
chr11:3721373 | T | C | 1 | a0001c0001t0001g0223 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2147-548A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 16/32 | chr11 | 3721373 | |||||||
chr11:3721404 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2147-579C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 16/32 | chr11 | 3721404 | |||||||
chr11:3721528 | T | C | 50 | a0001c0001t0001g0026 a0001c0001t0001g0030 a0001c0001t0001g0031 others(47): Show |
50 | HG00597.hp1 HG01243.hp2 HG01884.hp1 others(47): Show |
intron_variant | MODIFIER | c.2147-703A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 16/32 | chr11 | 3721528 | |||||||
chr11:3721546 | A | C | 1 | a0001c0001t0001g0057 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2147-721T>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 16/32 | chr11 | 3721546 | |||||||
chr11:3721563 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2147-738C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 16/32 | chr11 | 3721563 | |||||||
chr11:3721640 | A | C | 43 | a0001c0001t0001g0029 a0001c0001t0001g0038 a0001c0001t0001g0039 others(40): Show |
43 | HG00408.hp2 HG00609.hp2 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.2147-815T>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 16/32 | chr11 | 3721640 | |||||||
chr11:3721816 | G | A | 178 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0030 others(175): Show |
178 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(175): Show |
intron_variant | MODIFIER | c.2147-991C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 16/32 | chr11 | 3721816 | |||||||
chr11:3721881 | C | G | 12 | a0001c0001t0002g0002 a0001c0002t0001g0124 a0001c0002t0001g0131 others(9): Show |
12 | HG01243.hp2 HG02258.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.2147-1056G>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 16/32 | chr11 | 3721881 | |||||||
chr11:3722042 | T | C | 7 | a0001c0003t0002g0290 a0001c0003t0002g0311 a0001c0003t0002g0312 others(4): Show |
7 | HG01109.hp2 HG02055.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2146+1115A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 16/32 | chr11 | 3722042 | |||||||
chr11:3722073 | C | T | 1 | a0001c0002t0001g0046 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2146+1084G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 16/32 | chr11 | 3722073 | |||||||
chr11:3722105 | C | CT | 35 | a0001c0001t0001g0031 a0001c0001t0001g0047 a0001c0001t0001g0113 others(32): Show |
35 | HG00597.hp1 HG01993.hp1 HG02056.hp2 others(32): Show |
intron_variant | MODIFIER | c.2146+1051dupA | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 16/32 | chr11 | 3722105 | |||||||
chr11:3722105 | CT | C | 18 | a0001c0001t0001g0068 a0001c0001t0001g0225 a0001c0001t0001g0231 others(15): Show |
18 | HG00323.hp2 HG00558.hp2 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.2146+1051delA | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 16/32 | chr11 | 3722105 | |||||||
chr11:3722172 | G | T | 1 | a0001c0026t0001g0298 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2146+985C>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 16/32 | chr11 | 3722172 | |||||||
chr11:3722276 | C | T | 1 | a0001c0002t0001g0106 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2146+881G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 16/32 | chr11 | 3722276 | |||||||
chr11:3722460 | A | AAT | 55 | a0001c0001t0001g0026 a0001c0001t0001g0030 a0001c0001t0001g0031 others(52): Show |
55 | HG00597.hp1 HG00639.hp2 HG01243.hp2 others(52): Show |
intron_variant | MODIFIER | c.2146+695_2146+696d others(4): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 16/32 | chr11 | 3722460 | |||||||
chr11:3722460 | A | AATAT | 3 | a0001c0002t0001g0192 a0001c0002t0001g0193 a0001c0002t0001g0211 |
3 | HG02559.hp2 HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2146+693_2146+696d others(6): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 16/32 | chr11 | 3722460 | |||||||
chr11:3722476 | T | A | 3 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 |
3 | HG02735.hp2 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.2146+681A>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 16/32 | chr11 | 3722476 | |||||||
chr11:3722672 | G | A | 1 | a0001c0001t0001g0181 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2146+485C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 16/32 | chr11 | 3722672 | |||||||
chr11:3722711 | G | T | 1 | a0001c0001t0001g0307 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2146+446C>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 16/32 | chr11 | 3722711 | |||||||
chr11:3722787 | T | G | 1 | a0001c0001t0001g0078 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2146+370A>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 16/32 | chr11 | 3722787 | |||||||
chr11:3722849 | T | C | 58 | a0001c0001t0001g0026 a0001c0001t0001g0030 a0001c0001t0001g0031 others(55): Show |
58 | HG00597.hp1 HG00639.hp2 HG01243.hp2 others(55): Show |
intron_variant | MODIFIER | c.2146+308A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 16/32 | chr11 | 3722849 | |||||||
chr11:3722997 | A | G | 1 | a0001c0001t0001g0253 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2146+160T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 16/32 | chr11 | 3722997 | |||||||
chr11:3723023 | C | T | 1 | a0001c0001t0001g0184 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2146+134G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 16/32 | chr11 | 3723023 | |||||||
chr11:3723548 | C | T | 1 | a0001c0002t0001g0046 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1848-93G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 15/32 | chr11 | 3723548 | |||||||
chr11:3723635 | T | C | 1 | a0001c0001t0001g0175 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1848-180A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 15/32 | chr11 | 3723635 | |||||||
chr11:3723744 | AAAT | A | 8 | a0001c0001t0001g0029 a0001c0001t0001g0068 a0001c0001t0001g0324 others(5): Show |
8 | HG00642.hp1 HG02280.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1848-292_1848-290d others(5): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 15/32 | chr11 | 3723744 | |||||||
chr11:3723829 | C | CT | 37 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0041 others(34): Show |
37 | HG00408.hp2 HG00609.hp2 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.1848-375dupA | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 15/32 | chr11 | 3723829 | |||||||
chr11:3723829 | CTTTT | C | 49 | a0001c0001t0001g0026 a0001c0001t0001g0030 a0001c0001t0001g0031 others(46): Show |
49 | HG00597.hp1 HG01243.hp2 HG01884.hp1 others(46): Show |
intron_variant | MODIFIER | c.1848-378_1848-375d others(6): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 15/32 | chr11 | 3723829 | |||||||
chr11:3723935 | G | A | 37 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0041 others(34): Show |
37 | HG00408.hp2 HG00609.hp2 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.1848-480C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 15/32 | chr11 | 3723935 | |||||||
chr11:3723947 | T | G | 6 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.1848-492A>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 15/32 | chr11 | 3723947 | |||||||
chr11:3724156 | G | C | 1 | a0001c0002t0001g0021 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1848-701C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 15/32 | chr11 | 3724156 | |||||||
chr11:3724283 | A | G | 14 | a0001c0001t0002g0002 a0001c0001t0002g0309 a0001c0002t0001g0124 others(11): Show |
14 | HG01243.hp2 HG02258.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.1847+820T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 15/32 | chr11 | 3724283 | |||||||
chr11:3724374 | T | C | 6 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.1847+729A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 15/32 | chr11 | 3724374 | |||||||
chr11:3724375 | A | G | 187 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0030 others(184): Show |
187 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.1847+728T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 15/32 | chr11 | 3724375 | |||||||
chr11:3724436 | CA | C | 47 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0041 others(44): Show |
47 | HG00408.hp2 HG00609.hp2 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.1847+666delT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 15/32 | chr11 | 3724436 | |||||||
chr11:3724445 | A | T | 2 | a0001c0001t0001g0109 a0001c0001t0001g0329 |
2 | HG02148.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1847+658T>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 15/32 | chr11 | 3724445 | |||||||
chr11:3724446 | A | T | 1 | a0005c0010t0001g0339 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1847+657T>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 15/32 | chr11 | 3724446 | |||||||
chr11:3724448 | AT | A | 132 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0030 others(129): Show |
132 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.1847+654delA | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 15/32 | chr11 | 3724448 | |||||||
chr11:3724449 | T | A | 8 | a0001c0001t0001g0068 a0001c0001t0001g0129 a0001c0001t0001g0324 others(5): Show |
8 | HG00642.hp1 HG02559.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1847+654A>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 15/32 | chr11 | 3724449 | |||||||
chr11:3724450 | A | T | 4 | a0001c0001t0001g0324 a0001c0001t0008g0325 a0005c0010t0001g0338 others(1): Show |
4 | HG00642.hp1 HG02559.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1847+653T>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 15/32 | chr11 | 3724450 | |||||||
chr11:3724519 | C | T | 7 | a0001c0003t0002g0290 a0001c0003t0002g0311 a0001c0003t0002g0312 others(4): Show |
7 | HG01109.hp2 HG02055.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1847+584G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 15/32 | chr11 | 3724519 | |||||||
chr11:3724589 | C | T | 1 | a0001c0002t0001g0280 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1847+514G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 15/32 | chr11 | 3724589 | |||||||
chr11:3724618 | C | A | 2 | a0001c0001t0001g0068 a0001c0001t0001g0336 |
2 | HG02965.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1847+485G>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 15/32 | chr11 | 3724618 | |||||||
chr11:3724661 | C | T | 8 | a0001c0001t0001g0291 a0001c0001t0001g0293 a0001c0001t0001g0296 others(5): Show |
8 | HG01243.hp1 HG02109.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1847+442G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 15/32 | chr11 | 3724661 | |||||||
chr11:3724744 | G | A | 4 | a0001c0001t0001g0324 a0001c0001t0008g0325 a0005c0010t0001g0338 others(1): Show |
4 | HG00642.hp1 HG02559.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1847+359C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 15/32 | chr11 | 3724744 | |||||||
chr11:3724780 | C | CAAAAAAA others(4): Show |
6 | a0001c0002t0001g0074 a0001c0002t0001g0075 a0001c0002t0001g0192 others(3): Show |
6 | HG02559.hp2 HG03041.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.1847+312_1847+322d others(13): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 15/32 | chr11 | 3724780 | |||||||
chr11:3724780 | C | CAAAAAAA others(5): Show |
39 | a0001c0001t0001g0026 a0001c0001t0001g0030 a0001c0001t0001g0031 others(36): Show |
39 | HG01884.hp1 HG01891.hp1 HG01993.hp1 others(36): Show |
intron_variant | MODIFIER | c.1847+311_1847+322d others(14): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 15/32 | chr11 | 3724780 | |||||||
chr11:3724780 | C | CAAAAAAA others(6): Show |
8 | a0001c0002t0001g0012 a0001c0002t0001g0018 a0001c0002t0001g0021 others(5): Show |
8 | HG00597.hp1 HG01243.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1847+322_1847+323i others(15): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 15/32 | chr11 | 3724780 | |||||||
chr11:3724780 | C | CAAAAAAA others(8): Show |
2 | a0005c0010t0001g0338 a0005c0010t0001g0339 |
2 | HG02559.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1847+322_1847+323i others(17): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 15/32 | chr11 | 3724780 | |||||||
chr11:3724780 | C | CAAAAAAA others(9): Show |
2 | a0001c0001t0001g0324 a0001c0001t0008g0325 |
2 | HG00642.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1847+322_1847+323i others(18): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 15/32 | chr11 | 3724780 | |||||||
chr11:3724780 | C | CAAAAAAA others(10): Show |
24 | a0001c0001t0001g0041 a0001c0001t0001g0043 a0001c0001t0001g0047 others(21): Show |
24 | HG00408.hp2 HG00609.hp2 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.1847+322_1847+323i others(19): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 15/32 | chr11 | 3724780 | |||||||
chr11:3724780 | C | CAAAAAAA others(11): Show |
12 | a0001c0001t0001g0029 a0001c0001t0001g0038 a0001c0001t0001g0039 others(9): Show |
12 | HG01106.hp1 HG01361.hp1 HG02074.hp1 others(9): Show |
intron_variant | MODIFIER | c.1847+322_1847+323i others(20): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 15/32 | chr11 | 3724780 | |||||||
chr11:3724780 | C | CAAAAAAA others(12): Show |
8 | a0001c0001t0001g0054 a0001c0001t0001g0113 a0001c0001t0001g0254 others(5): Show |
8 | HG00735.hp1 HG02004.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.1847+322_1847+323i others(21): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 15/32 | chr11 | 3724780 | |||||||
chr11:3724780 | C | CAAAAAAA others(13): Show |
27 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0287 others(24): Show |
27 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(24): Show |
intron_variant | MODIFIER | c.1847+322_1847+323i others(22): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 15/32 | chr11 | 3724780 | |||||||
chr11:3724780 | C | CAAAAAAA others(14): Show |
21 | a0001c0001t0001g0078 a0001c0001t0001g0081 a0001c0002t0001g0079 others(18): Show |
21 | HG00423.hp1 HG01167.hp2 HG02056.hp2 others(18): Show |
intron_variant | MODIFIER | c.1847+322_1847+323i others(23): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 15/32 | chr11 | 3724780 | |||||||
chr11:3724780 | C | CAAAAAAA others(15): Show |
18 | a0001c0001t0001g0076 a0001c0001t0001g0082 a0001c0001t0001g0085 others(15): Show |
18 | HG00438.hp2 HG00738.hp1 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.1847+322_1847+323i others(24): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 15/32 | chr11 | 3724780 | |||||||
chr11:3724780 | C | CAAAAAAA others(16): Show |
2 | a0001c0002t0001g0281 a0001c0002t0001g0326 |
2 | HG00597.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.1847+322_1847+323i others(25): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 15/32 | chr11 | 3724780 | |||||||
chr11:3724780 | C | CAAAAAAA others(17): Show |
3 | a0001c0001t0001g0042 a0001c0001t0001g0278 a0001c0002t0001g0261 |
3 | HG01192.hp2 HG02572.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.1847+322_1847+323i others(26): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 15/32 | chr11 | 3724780 | |||||||
chr11:3724780 | C | CAAAAAAA others(18): Show |
1 | a0001c0001t0001g0335 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1847+322_1847+323i others(27): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 15/32 | chr11 | 3724780 | |||||||
chr11:3724780 | C | CAAAAAAA others(20): Show |
1 | a0001c0001t0001g0307 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1847+322_1847+323i others(29): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 15/32 | chr11 | 3724780 | |||||||
chr11:3724780 | C | CAAAAAAA others(25): Show |
1 | a0001c0001t0002g0314 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1847+322_1847+323i others(34): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 15/32 | chr11 | 3724780 | |||||||
chr11:3724780 | C | CAAAAAAA others(52): Show |
1 | a0001c0001t0002g0317 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1847+322_1847+323i others(61): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 15/32 | chr11 | 3724780 | |||||||
chr11:3724789 | A | AAAAAAAA others(12): Show |
2 | a0001c0001t0001g0068 a0001c0001t0001g0336 |
2 | HG02965.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1847+313_1847+314i others(21): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 15/32 | chr11 | 3724789 | |||||||
chr11:3724793 | G | A | 6 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.1847+310C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 15/32 | chr11 | 3724793 | |||||||
chr11:3724857 | C | T | 1 | a0005c0010t0001g0339 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1847+246G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 15/32 | chr11 | 3724857 | |||||||
chr11:3724873 | T | A | 1 | a0001c0001t0001g0113 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1847+230A>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 15/32 | chr11 | 3724873 | |||||||
chr11:3725048 | A | T | 1 | a0015c0033t0001g0130 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1847+55T>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 15/32 | chr11 | 3725048 | |||||||
chr11:3725234 | C | T | 1 | a0001c0002t0001g0267 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1731-15G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3725234 | |||||||
chr11:3725235 | C | G | 137 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0030 others(134): Show |
137 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.1731-16G>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3725235 | |||||||
chr11:3725260 | A | G | 1 | a0001c0001t0001g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1731-41T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3725260 | |||||||
chr11:3725454 | G | A | 5 | a0001c0001t0001g0335 a0001c0001t0002g0314 a0001c0001t0002g0317 others(2): Show |
5 | HG00639.hp2 HG01433.hp2 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.1731-235C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3725454 | |||||||
chr11:3725655 | C | T | 14 | a0001c0001t0001g0068 a0001c0001t0001g0324 a0001c0001t0001g0336 others(11): Show |
14 | HG00642.hp1 HG01081.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.1731-436G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3725655 | |||||||
chr11:3725656 | A | G | 1 | a0001c0001t0001g0081 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1731-437T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3725656 | |||||||
chr11:3725854 | C | T | 2 | a0001c0012t0001g0319 a0001c0012t0001g0320 |
2 | HG02109.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1731-635G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3725854 | |||||||
chr11:3725877 | G | A | 2 | a0005c0010t0001g0338 a0005c0010t0001g0339 |
2 | HG02559.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1731-658C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3725877 | |||||||
chr11:3725997 | G | C | 3 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0202 |
3 | HG01891.hp2 HG03471.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1731-778C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3725997 | |||||||
chr11:3726101 | A | C | 3 | a0001c0001t0002g0314 a0001c0001t0002g0317 a0003c0004t0001g0316 |
3 | HG00639.hp2 HG01943.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1731-882T>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3726101 | |||||||
chr11:3726287 | C | T | 6 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.1731-1068G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3726287 | |||||||
chr11:3726312 | G | T | 1 | a0001c0002t0001g0023 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1731-1093C>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3726312 | |||||||
chr11:3726338 | T | C | 5 | a0001c0001t0001g0329 a0001c0001t0001g0337 a0001c0001t0004g0330 others(2): Show |
5 | HG02486.hp1 HG02647.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1731-1119A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3726338 | |||||||
chr11:3726408 | T | A | 36 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0041 others(33): Show |
36 | HG00408.hp2 HG00609.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.1731-1189A>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3726408 | |||||||
chr11:3726410 | CTTTGAAG others(1): Show |
C | 7 | a0001c0001t0001g0043 a0001c0001t0001g0061 a0001c0001t0001g0253 others(4): Show |
7 | HG00738.hp2 HG01106.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.1731-1199_1731-119 others(12): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3726410 | |||||||
chr11:3726420 | A | C | 7 | a0001c0001t0001g0043 a0001c0001t0001g0061 a0001c0001t0001g0253 others(4): Show |
7 | HG00738.hp2 HG01106.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.1731-1201T>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3726420 | |||||||
chr11:3726524 | T | A | 1 | a0001c0001t0001g0076 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1731-1305A>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3726524 | |||||||
chr11:3726525 | T | TA | 10 | a0001c0001t0001g0231 a0001c0001t0001g0291 a0001c0001t0001g0293 others(7): Show |
10 | HG01243.hp1 HG02109.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1731-1307dupT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3726525 | |||||||
chr11:3726525 | TA | T | 7 | a0001c0001t0001g0068 a0001c0001t0001g0336 a0001c0002t0001g0097 others(4): Show |
7 | HG02109.hp1 HG02809.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1731-1307delT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3726525 | |||||||
chr11:3726697 | A | G | 1 | a0001c0001t0001g0335 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1731-1478T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3726697 | |||||||
chr11:3726832 | G | A | 5 | a0003c0004t0001g0115 a0003c0004t0001g0117 a0003c0004t0001g0118 others(2): Show |
5 | HG02572.hp1 HG02717.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1731-1613C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3726832 | |||||||
chr11:3726916 | C | T | 1 | a0001c0002t0001g0187 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1731-1697G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3726916 | |||||||
chr11:3726918 | T | C | 1 | a0001c0001t0001g0068 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1731-1699A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3726918 | |||||||
chr11:3726988 | T | C | 1 | a0001c0001t0001g0310 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1731-1769A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3726988 | |||||||
chr11:3727210 | A | G | 2 | a0001c0001t0001g0068 a0001c0001t0001g0336 |
2 | HG02965.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1731-1991T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3727210 | |||||||
chr11:3727247 | A | G | 2 | a0001c0012t0001g0319 a0001c0012t0001g0320 |
2 | HG02109.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1731-2028T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3727247 | |||||||
chr11:3727329 | G | A | 4 | a0001c0001t0001g0324 a0001c0001t0008g0325 a0005c0010t0001g0338 others(1): Show |
4 | HG00642.hp1 HG02559.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1731-2110C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3727329 | |||||||
chr11:3727530 | T | C | 3 | a0001c0001t0002g0314 a0001c0001t0002g0317 a0003c0004t0001g0316 |
3 | HG00639.hp2 HG01943.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1731-2311A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3727530 | |||||||
chr11:3727543 | T | C | 1 | a0001c0001t0001g0240 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1731-2324A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3727543 | |||||||
chr11:3727590 | T | C | 1 | a0001c0001t0001g0275 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1731-2371A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3727590 | |||||||
chr11:3727599 | T | G | 14 | a0001c0001t0001g0068 a0001c0001t0001g0324 a0001c0001t0001g0336 others(11): Show |
14 | HG00642.hp1 HG01081.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.1731-2380A>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3727599 | |||||||
chr11:3727601 | G | A | 75 | a0001c0001t0001g0042 a0001c0001t0001g0044 a0001c0001t0001g0045 others(72): Show |
75 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.1731-2382C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3727601 | |||||||
chr11:3727722 | C | T | 2 | a0005c0010t0001g0338 a0005c0010t0001g0339 |
2 | HG02559.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1731-2503G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3727722 | |||||||
chr11:3727723 | A | G | 14 | a0001c0001t0001g0068 a0001c0001t0001g0324 a0001c0001t0001g0336 others(11): Show |
14 | HG00642.hp1 HG01081.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.1731-2504T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3727723 | |||||||
chr11:3727724 | G | A | 14 | a0001c0001t0001g0068 a0001c0001t0001g0324 a0001c0001t0001g0336 others(11): Show |
14 | HG00642.hp1 HG01081.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.1731-2505C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3727724 | |||||||
chr11:3727738 | T | A | 14 | a0001c0001t0001g0068 a0001c0001t0001g0324 a0001c0001t0001g0336 others(11): Show |
14 | HG00642.hp1 HG01081.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.1731-2519A>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3727738 | |||||||
chr11:3727793 | G | A | 56 | a0001c0001t0001g0026 a0001c0001t0001g0030 a0001c0001t0001g0031 others(53): Show |
56 | HG00597.hp1 HG00639.hp2 HG01243.hp2 others(53): Show |
intron_variant | MODIFIER | c.1731-2574C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3727793 | |||||||
chr11:3727829 | G | C | 7 | a0001c0003t0002g0290 a0001c0003t0002g0311 a0001c0003t0002g0312 others(4): Show |
7 | HG01109.hp2 HG02055.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1731-2610C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3727829 | |||||||
chr11:3727940 | G | A | 1 | a0001c0001t0001g0337 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1731-2721C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3727940 | |||||||
chr11:3727984 | G | A | 2 | a0001c0002t0001g0012 a0001c0032t0001g0032 |
2 | HG02451.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.1731-2765C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3727984 | |||||||
chr11:3728015 | C | T | 5 | a0003c0004t0001g0115 a0003c0004t0001g0117 a0003c0004t0001g0118 others(2): Show |
5 | HG02572.hp1 HG02717.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1731-2796G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3728015 | |||||||
chr11:3728093 | G | A | 3 | a0001c0001t0002g0314 a0001c0001t0002g0317 a0003c0004t0001g0316 |
3 | HG00639.hp2 HG01943.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1731-2874C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3728093 | |||||||
chr11:3728134 | A | G | 1 | a0001c0017t0002g0116 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1731-2915T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3728134 | |||||||
chr11:3728144 | T | C | 1 | a0021c0030t0009g0168 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1731-2925A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3728144 | |||||||
chr11:3728147 | G | C | 1 | a0001c0001t0001g0113 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1731-2928C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3728147 | |||||||
chr11:3728184 | C | G | 2 | a0001c0001t0001g0159 a0001c0001t0001g0161 |
2 | NA18998.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.1731-2965G>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3728184 | |||||||
chr11:3728355 | A | C | 40 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0041 others(37): Show |
40 | HG00408.hp2 HG00609.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.1730+3036T>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3728355 | |||||||
chr11:3728466 | C | T | 39 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0041 others(36): Show |
39 | HG00408.hp2 HG00609.hp2 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.1730+2925G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3728466 | |||||||
chr11:3728518 | G | A | 2 | a0001c0001t0001g0324 a0001c0001t0008g0325 |
2 | HG00642.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1730+2873C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3728518 | |||||||
chr11:3728610 | G | A | 1 | a0001c0001t0001g0060 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1730+2781C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3728610 | |||||||
chr11:3728611 | C | A | 6 | a0001c0001t0001g0068 a0001c0001t0001g0324 a0001c0001t0001g0336 others(3): Show |
6 | HG00642.hp1 HG02559.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1730+2780G>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3728611 | |||||||
chr11:3728638 | C | G | 6 | a0001c0001t0001g0068 a0001c0001t0001g0324 a0001c0001t0001g0336 others(3): Show |
6 | HG00642.hp1 HG02559.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1730+2753G>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3728638 | |||||||
chr11:3728693 | G | C | 200 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0030 others(197): Show |
200 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(197): Show |
intron_variant | MODIFIER | c.1730+2698C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3728693 | |||||||
chr11:3728824 | A | G | 2 | a0005c0010t0001g0338 a0005c0010t0001g0339 |
2 | HG02559.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1730+2567T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3728824 | |||||||
chr11:3729144 | A | C | 1 | a0011c0025t0001g0236 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1730+2247T>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3729144 | |||||||
chr11:3729164 | C | T | 185 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0030 others(182): Show |
185 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.1730+2227G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3729164 | |||||||
chr11:3729178 | A | G | 1 | a0001c0002t0001g0093 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1730+2213T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3729178 | |||||||
chr11:3729216 | T | C | 1 | a0001c0016t0001g0114 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1730+2175A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3729216 | |||||||
chr11:3729354 | G | T | 2 | a0005c0010t0001g0338 a0005c0010t0001g0339 |
2 | HG02559.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1730+2037C>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3729354 | |||||||
chr11:3729398 | C | T | 185 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0030 others(182): Show |
185 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.1730+1993G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3729398 | |||||||
chr11:3729404 | A | G | 1 | a0001c0002t0001g0269 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1730+1987T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3729404 | |||||||
chr11:3729443 | C | T | 42 | a0001c0001t0001g0029 a0001c0001t0001g0038 a0001c0001t0001g0039 others(39): Show |
42 | HG00408.hp2 HG00609.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.1730+1948G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3729443 | |||||||
chr11:3729454 | A | G | 2 | a0001c0001t0001g0051 a0001c0001t0001g0060 |
2 | HG02083.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.1730+1937T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3729454 | |||||||
chr11:3729518 | G | C | 1 | a0002c0005t0001g0302 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1730+1873C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3729518 | |||||||
chr11:3729543 | C | CA | 66 | a0001c0001t0001g0109 a0001c0001t0001g0112 a0001c0001t0001g0135 others(63): Show |
66 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.1730+1847dupT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3729543 | |||||||
chr11:3729543 | C | CAA | 8 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0068 others(5): Show |
8 | HG00642.hp1 HG01169.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1730+1846_1730+184 others(6): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3729543 | |||||||
chr11:3729543 | C | CAAA | 9 | a0001c0001t0001g0324 a0001c0012t0001g0319 a0001c0012t0001g0320 others(6): Show |
9 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.1730+1845_1730+184 others(7): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3729543 | |||||||
chr11:3729543 | CA | C | 102 | a0001c0001t0001g0038 a0001c0001t0001g0041 a0001c0001t0001g0042 others(99): Show |
102 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.1730+1847delT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3729543 | |||||||
chr11:3729543 | CAAAAAAA others(9): Show |
C | 1 | a0001c0002t0001g0102 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1730+1832_1730+184 others(20): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3729543 | |||||||
chr11:3729543 | CAAAAAAA others(10): Show |
C | 1 | a0001c0001t0001g0305 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1730+1831_1730+184 others(21): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3729543 | |||||||
chr11:3729715 | C | CA | 41 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0112 others(38): Show |
41 | HG00544.hp2 HG00639.hp1 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.1730+1675dupT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3729715 | |||||||
chr11:3729715 | C | CAA | 7 | a0001c0001t0001g0214 a0001c0001t0001g0335 a0001c0003t0002g0290 others(4): Show |
7 | HG01433.hp2 HG02055.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1730+1674_1730+167 others(6): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3729715 | |||||||
chr11:3729715 | C | CAAAAAAA others(3): Show |
1 | a0001c0001t0001g0056 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1730+1666_1730+167 others(14): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3729715 | |||||||
chr11:3729715 | C | CAAAAAAA others(4): Show |
2 | a0001c0001t0001g0038 a0001c0001t0001g0055 |
2 | HG01361.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.1730+1665_1730+167 others(15): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3729715 | |||||||
chr11:3729715 | C | CAAAAAAA others(5): Show |
1 | a0001c0001t0001g0066 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1730+1664_1730+167 others(16): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3729715 | |||||||
chr11:3729715 | C | CAAAAAAA others(6): Show |
3 | a0001c0001t0001g0255 a0001c0001t0008g0325 a0002c0005t0001g0301 |
3 | HG00642.hp1 HG01169.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1730+1663_1730+167 others(17): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3729715 | |||||||
chr11:3729715 | C | CAAAAAAA others(7): Show |
3 | a0001c0001t0001g0324 a0002c0005t0001g0299 a0002c0005t0001g0303 |
3 | HG01081.hp1 HG01167.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1730+1662_1730+167 others(18): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3729715 | |||||||
chr11:3729715 | C | CAAAAAAA others(8): Show |
5 | a0001c0001t0001g0054 a0001c0001t0001g0334 a0002c0005t0001g0300 others(2): Show |
5 | HG01168.hp1 HG01515.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.1730+1661_1730+167 others(19): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3729715 | |||||||
chr11:3729715 | C | CAAAAAAA others(9): Show |
1 | a0001c0001t0001g0256 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1730+1660_1730+167 others(20): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3729715 | |||||||
chr11:3729715 | C | CAAAAAAA others(10): Show |
2 | a0001c0001t0001g0253 a0015c0033t0001g0130 |
2 | HG01255.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1730+1659_1730+167 others(21): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3729715 | |||||||
chr11:3729715 | C | CAAAAAAA others(13): Show |
2 | a0001c0001t0001g0050 a0002c0005t0001g0302 |
2 | HG02647.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.1730+1656_1730+167 others(24): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3729715 | |||||||
chr11:3729715 | C | CAAAAAAA others(14): Show |
2 | a0001c0001t0001g0042 a0001c0001t0001g0047 |
2 | HG01192.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.1730+1655_1730+167 others(25): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3729715 | |||||||
chr11:3729715 | C | CAAAAAAA others(15): Show |
4 | a0001c0001t0001g0044 a0001c0001t0001g0049 a0001c0001t0001g0254 others(1): Show |
4 | HG02004.hp1 HG02886.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1730+1654_1730+167 others(26): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3729715 | |||||||
chr11:3729715 | C | CAAAAAAA others(17): Show |
1 | a0018c0034t0001g0122 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1730+1652_1730+167 others(28): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3729715 | |||||||
chr11:3729715 | C | CAAAAAAA others(18): Show |
1 | a0001c0001t0001g0063 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1730+1651_1730+167 others(29): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3729715 | |||||||
chr11:3729715 | C | CAAAAAAA others(19): Show |
3 | a0001c0001t0001g0059 a0002c0008t0003g0040 a0002c0008t0003g0062 |
3 | HG00735.hp1 HG01106.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.1730+1650_1730+167 others(30): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3729715 | |||||||
chr11:3729715 | C | CAAAAAAA others(20): Show |
4 | a0001c0001t0001g0041 a0001c0001t0001g0043 a0001c0001t0001g0048 others(1): Show |
4 | HG00738.hp2 NA18954.hp2 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.1730+1675_1730+167 others(31): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3729715 | |||||||
chr11:3729715 | C | CAAAAAAA others(21): Show |
1 | a0001c0001t0001g0332 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1730+1675_1730+167 others(32): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3729715 | |||||||
chr11:3729715 | C | CAAAAAAA others(22): Show |
2 | a0001c0001t0001g0061 a0001c0001t0002g0317 |
2 | HG00639.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.1730+1675_1730+167 others(33): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3729715 | |||||||
chr11:3729715 | C | CAAAAAAA others(23): Show |
3 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0002c0008t0003g0064 |
3 | HG00609.hp2 HG00741.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.1730+1675_1730+167 others(34): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3729715 | |||||||
chr11:3729715 | C | CAAAAAAA others(24): Show |
1 | a0001c0001t0001g0333 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1730+1675_1730+167 others(35): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3729715 | |||||||
chr11:3729715 | C | CAAAAAAA others(25): Show |
1 | a0001c0001t0001g0058 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1730+1675_1730+167 others(36): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3729715 | |||||||
chr11:3729715 | C | CAAAAAAA others(27): Show |
1 | a0001c0001t0001g0057 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1730+1675_1730+167 others(38): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3729715 | |||||||
chr11:3729715 | C | CAAAAAAA others(29): Show |
1 | a0001c0001t0001g0053 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1730+1675_1730+167 others(40): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3729715 | |||||||
chr11:3729715 | C | CAAAAAAA others(31): Show |
1 | a0001c0001t0001g0065 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1730+1675_1730+167 others(42): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3729715 | |||||||
chr11:3729715 | C | CAAAAAAA others(35): Show |
1 | a0001c0001t0001g0310 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1730+1675_1730+167 others(46): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3729715 | |||||||
chr11:3729715 | CA | C | 10 | a0001c0001t0001g0004 a0001c0001t0001g0045 a0001c0001t0001g0133 others(7): Show |
10 | HG00423.hp1 HG02615.hp2 HG03831.hp2 others(7): Show |
intron_variant | MODIFIER | c.1730+1675delT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3729715 | |||||||
chr11:3729715 | CAA | C | 66 | a0001c0001t0001g0039 a0001c0001t0001g0076 a0001c0001t0001g0078 others(63): Show |
66 | HG00323.hp2 HG00438.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.1730+1674_1730+167 others(6): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3729715 | |||||||
chr11:3729715 | CAAAAA | C | 15 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0121 others(12): Show |
15 | HG01243.hp2 HG01346.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.1730+1671_1730+167 others(9): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3729715 | |||||||
chr11:3729715 | CAAAAAA | C | 36 | a0001c0001t0001g0026 a0001c0001t0001g0068 a0001c0001t0001g0336 others(33): Show |
36 | HG00597.hp1 HG01993.hp1 HG02258.hp1 others(33): Show |
intron_variant | MODIFIER | c.1730+1670_1730+167 others(10): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3729715 | |||||||
chr11:3729715 | CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0001g0227 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1730+1664_1730+167 others(16): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3729715 | |||||||
chr11:3729846 | T | C | 1 | a0001c0001t0001g0307 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1730+1545A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3729846 | |||||||
chr11:3729930 | G | A | 4 | a0001c0001t0001g0307 a0001c0002t0001g0074 a0001c0002t0001g0075 others(1): Show |
4 | HG03041.hp1 HG03130.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1730+1461C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3729930 | |||||||
chr11:3729964 | G | A | 6 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.1730+1427C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3729964 | |||||||
chr11:3730097 | TGGTGGCA others(11): Show |
T | 1 | a0001c0024t0001g0251 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1730+1276_1730+129 others(22): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3730097 | |||||||
chr11:3730177 | G | C | 1 | a0001c0001t0001g0113 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1730+1214C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3730177 | |||||||
chr11:3730216 | C | T | 6 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.1730+1175G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3730216 | |||||||
chr11:3730222 | G | A | 1 | a0001c0002t0001g0322 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1730+1169C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3730222 | |||||||
chr11:3730509 | C | T | 1 | a0001c0001t0001g0307 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1730+882G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3730509 | |||||||
chr11:3730513 | C | T | 2 | a0001c0001t0001g0068 a0001c0001t0001g0336 |
2 | HG02965.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1730+878G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3730513 | |||||||
chr11:3730600 | G | C | 2 | a0001c0001t0001g0237 a0011c0025t0001g0236 |
2 | HG01081.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.1730+791C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3730600 | |||||||
chr11:3730614 | T | A | 1 | a0001c0001t0001g0207 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1730+777A>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3730614 | |||||||
chr11:3730665 | G | C | 1 | a0001c0001t0001g0307 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1730+726C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3730665 | |||||||
chr11:3730692 | T | C | 2 | a0001c0012t0001g0319 a0001c0012t0001g0320 |
2 | HG02109.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1730+699A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3730692 | |||||||
chr11:3731014 | C | A | 36 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0041 others(33): Show |
36 | HG00408.hp2 HG00609.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.1730+377G>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3731014 | |||||||
chr11:3731051 | A | G | 9 | a0001c0001t0001g0068 a0001c0001t0001g0324 a0001c0001t0001g0336 others(6): Show |
9 | HG00642.hp1 HG02109.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1730+340T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3731051 | |||||||
chr11:3731083 | T | G | 8 | a0001c0001t0001g0068 a0001c0001t0001g0324 a0001c0001t0001g0336 others(5): Show |
8 | HG00642.hp1 HG02109.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1730+308A>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3731083 | |||||||
chr11:3731125 | G | C | 48 | a0001c0001t0001g0026 a0001c0001t0001g0030 a0001c0001t0001g0031 others(45): Show |
48 | HG00597.hp1 HG01243.hp2 HG01884.hp1 others(45): Show |
intron_variant | MODIFIER | c.1730+266C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3731125 | |||||||
chr11:3731146 | C | G | 3 | a0002c0008t0003g0040 a0002c0008t0003g0062 a0002c0008t0003g0064 |
3 | HG00735.hp1 HG00741.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.1730+245G>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3731146 | |||||||
chr11:3731225 | T | C | 5 | a0001c0001t0001g0329 a0001c0001t0001g0337 a0001c0001t0004g0330 others(2): Show |
5 | HG02486.hp1 HG02647.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1730+166A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3731225 | |||||||
chr11:3731269 | C | T | 2 | a0001c0001t0001g0068 a0001c0001t0001g0336 |
2 | HG02965.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1730+122G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3731269 | |||||||
chr11:3731291 | T | C | 1 | a0001c0001t0001g0201 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1730+100A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3731291 | |||||||
chr11:3731675 | T | A | 2 | a0001c0001t0001g0324 a0001c0001t0008g0325 |
2 | HG00642.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1543-97A>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 13/32 | chr11 | 3731675 | |||||||
chr11:3731691 | T | C | 1 | a0001c0001t0001g0055 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1543-113A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 13/32 | chr11 | 3731691 | |||||||
chr11:3731857 | T | C | 1 | a0001c0002t0001g0090 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1543-279A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 13/32 | chr11 | 3731857 | |||||||
chr11:3731858 | C | A | 1 | a0001c0002t0001g0090 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1543-280G>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 13/32 | chr11 | 3731858 | |||||||
chr11:3731878 | A | G | 2 | a0001c0001t0001g0333 a0001c0001t0001g0334 |
2 | HG02145.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1543-300T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 13/32 | chr11 | 3731878 | |||||||
chr11:3731980 | G | T | 6 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.1543-402C>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 13/32 | chr11 | 3731980 | |||||||
chr11:3731993 | G | A | 1 | a0001c0001t0001g0039 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1543-415C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 13/32 | chr11 | 3731993 | |||||||
chr11:3732026 | C | T | 2 | a0001c0012t0001g0319 a0001c0012t0001g0320 |
2 | HG02109.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1543-448G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 13/32 | chr11 | 3732026 | |||||||
chr11:3732196 | C | T | 9 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0150 others(6): Show |
9 | HG00558.hp1 HG02056.hp1 NA18964.hp1 others(6): Show |
intron_variant | MODIFIER | c.1543-618G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 13/32 | chr11 | 3732196 | |||||||
chr11:3732264 | T | C | 8 | a0001c0001t0001g0068 a0001c0001t0001g0324 a0001c0001t0001g0336 others(5): Show |
8 | HG00642.hp1 HG02109.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1543-686A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 13/32 | chr11 | 3732264 | |||||||
chr11:3732433 | T | C | 5 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0001g0329 others(2): Show |
5 | HG02027.hp1 HG02922.hp1 NA18959.hp1 others(2): Show |
intron_variant | MODIFIER | c.1543-855A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 13/32 | chr11 | 3732433 | |||||||
chr11:3732558 | C | CTTGTA | 4 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0182 others(1): Show |
4 | NA18990.hp2 NA18999.hp1 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.1543-985_1543-981d others(7): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 13/32 | chr11 | 3732558 | |||||||
chr11:3732627 | A | G | 2 | a0001c0006t0001g0126 a0001c0006t0001g0127 |
2 | HG02896.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1543-1049T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 13/32 | chr11 | 3732627 | |||||||
chr11:3732734 | A | T | 1 | a0001c0001t0001g0310 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1543-1156T>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 13/32 | chr11 | 3732734 | |||||||
chr11:3732874 | A | G | 6 | a0001c0001t0001g0068 a0001c0001t0001g0324 a0001c0001t0001g0336 others(3): Show |
6 | HG00642.hp1 HG02559.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1543-1296T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 13/32 | chr11 | 3732874 | |||||||
chr11:3733063 | T | C | 6 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.1543-1485A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 13/32 | chr11 | 3733063 | |||||||
chr11:3733209 | G | C | 1 | a0001c0001t0006g0297 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1543-1631C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 13/32 | chr11 | 3733209 | |||||||
chr11:3733236 | T | TG | 8 | a0001c0012t0001g0319 a0001c0012t0001g0320 a0002c0005t0001g0299 others(5): Show |
8 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.1543-1659dupC | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 13/32 | chr11 | 3733236 | |||||||
chr11:3733338 | T | C | 6 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.1543-1760A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 13/32 | chr11 | 3733338 | |||||||
chr11:3733566 | C | T | 43 | a0001c0001t0001g0029 a0001c0001t0001g0038 a0001c0001t0001g0039 others(40): Show |
43 | HG00408.hp2 HG00609.hp2 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.1542+1625G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 13/32 | chr11 | 3733566 | |||||||
chr11:3733927 | A | G | 2 | a0001c0001t0001g0068 a0001c0001t0001g0336 |
2 | HG02965.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1542+1264T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 13/32 | chr11 | 3733927 | |||||||
chr11:3733946 | C | T | 2 | a0001c0001t0001g0029 a0001c0001t0001g0328 |
2 | HG02280.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1542+1245G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 13/32 | chr11 | 3733946 | |||||||
chr11:3734040 | C | CT | 51 | a0001c0001t0001g0026 a0001c0001t0001g0030 a0001c0001t0001g0031 others(48): Show |
51 | HG00597.hp1 HG01243.hp2 HG01884.hp1 others(48): Show |
intron_variant | MODIFIER | c.1542+1150dupA | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 13/32 | chr11 | 3734040 | |||||||
chr11:3734066 | G | A | 4 | a0001c0001t0001g0324 a0001c0001t0008g0325 a0005c0010t0001g0338 others(1): Show |
4 | HG00642.hp1 HG02559.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1542+1125C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 13/32 | chr11 | 3734066 | |||||||
chr11:3734110 | A | G | 2 | a0001c0001t0001g0324 a0001c0001t0008g0325 |
2 | HG00642.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1542+1081T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 13/32 | chr11 | 3734110 | |||||||
chr11:3734219 | A | G | 2 | a0001c0012t0001g0319 a0001c0012t0001g0320 |
2 | HG02109.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1542+972T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 13/32 | chr11 | 3734219 | |||||||
chr11:3734283 | T | C | 2 | a0001c0001t0001g0308 a0016c0023t0001g0001 |
2 | HG01346.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1542+908A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 13/32 | chr11 | 3734283 | |||||||
chr11:3734285 | G | A | 7 | a0001c0001t0001g0291 a0001c0001t0001g0293 a0001c0001t0001g0296 others(4): Show |
7 | HG02109.hp2 HG02257.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1542+906C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 13/32 | chr11 | 3734285 | |||||||
chr11:3734298 | G | C | 1 | a0001c0001t0001g0068 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1542+893C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 13/32 | chr11 | 3734298 | |||||||
chr11:3734327 | C | T | 1 | a0001c0002t0001g0192 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1542+864G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 13/32 | chr11 | 3734327 | |||||||
chr11:3734328 | G | A | 6 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0202 others(3): Show |
6 | HG01891.hp2 HG02970.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1542+863C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 13/32 | chr11 | 3734328 | |||||||
chr11:3734330 | G | A | 1 | a0001c0032t0001g0032 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1542+861C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 13/32 | chr11 | 3734330 | |||||||
chr11:3734630 | G | C | 7 | a0001c0003t0002g0290 a0001c0003t0002g0311 a0001c0003t0002g0312 others(4): Show |
7 | HG01109.hp2 HG02055.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1542+561C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 13/32 | chr11 | 3734630 | |||||||
chr11:3735047 | C | T | 3 | a0001c0001t0001g0144 a0001c0001t0001g0155 a0001c0001t0001g0157 |
3 | HG00621.hp2 NA18943.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.1542+144G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 13/32 | chr11 | 3735047 | |||||||
chr11:3735075 | T | C | 1 | a0001c0001t0002g0309 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1542+116A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 13/32 | chr11 | 3735075 | |||||||
chr11:3735171 | A | C | 2 | a0001c0012t0001g0319 a0001c0012t0001g0320 |
2 | HG02109.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1542+20T>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 13/32 | chr11 | 3735171 | |||||||
chr11:3735329 | TA | T | 6 | a0001c0001t0001g0163 a0001c0001t0001g0200 a0001c0001t0001g0227 others(3): Show |
6 | HG01433.hp1 HG02004.hp1 HG02155.hp2 others(3): Show |
splice_region_variant&intron_variant | LOW | c.1409-6delT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3735329 | |||||||
chr11:3735351 | A | AAT | 11 | a0001c0001t0001g0113 a0001c0001t0001g0305 a0001c0001t0001g0306 others(8): Show |
11 | HG01099.hp1 HG01099.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.1409-29_1409-28dup others(2): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3735351 | |||||||
chr11:3735353 | T | A | 2 | a0001c0001t0002g0314 a0001c0001t0002g0317 |
2 | HG00639.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.1409-29A>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3735353 | |||||||
chr11:3735379 | T | C | 1 | a0001c0002t0001g0091 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1409-55A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3735379 | |||||||
chr11:3735391 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1409-67C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3735391 | |||||||
chr11:3735448 | T | C | 1 | a0001c0001t0001g0030 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1409-124A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3735448 | |||||||
chr11:3735456 | T | C | 44 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0041 others(41): Show |
44 | HG00408.hp2 HG00609.hp2 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.1409-132A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3735456 | |||||||
chr11:3735707 | GT | G | 7 | a0001c0003t0002g0290 a0001c0003t0002g0311 a0001c0003t0002g0312 others(4): Show |
7 | HG01109.hp2 HG02055.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1409-384delA | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3735707 | |||||||
chr11:3735735 | A | G | 6 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.1409-411T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3735735 | |||||||
chr11:3735748 | A | AGT | 15 | a0001c0001t0001g0135 a0001c0001t0001g0171 a0001c0001t0001g0172 others(12): Show |
15 | HG00423.hp2 HG00544.hp2 HG00642.hp2 others(12): Show |
intron_variant | MODIFIER | c.1409-426_1409-425d others(4): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3735748 | |||||||
chr11:3735748 | A | AGTGT | 14 | a0001c0001t0001g0191 a0001c0001t0001g0195 a0001c0001t0001g0196 others(11): Show |
14 | HG00323.hp1 HG00621.hp1 HG01952.hp2 others(11): Show |
intron_variant | MODIFIER | c.1409-428_1409-425d others(6): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3735748 | |||||||
chr11:3735748 | A | AGTGTGT | 6 | a0001c0001t0001g0185 a0001c0001t0001g0199 a0001c0001t0001g0207 others(3): Show |
6 | HG03453.hp1 HG03471.hp1 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.1409-430_1409-425d others(8): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3735748 | |||||||
chr11:3735748 | A | AGTGTGTG others(3): Show |
1 | a0001c0001t0001g0335 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1409-434_1409-425d others(12): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3735748 | |||||||
chr11:3735748 | AGT | A | 57 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0038 others(54): Show |
57 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.1409-426_1409-425d others(4): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3735748 | |||||||
chr11:3735748 | AGTGT | A | 42 | a0001c0001t0001g0039 a0001c0001t0001g0042 a0001c0001t0001g0043 others(39): Show |
42 | HG00408.hp2 HG00609.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.1409-428_1409-425d others(6): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3735748 | |||||||
chr11:3735748 | AGTGTGT | A | 19 | a0001c0001t0001g0029 a0001c0001t0001g0249 a0001c0001t0001g0252 others(16): Show |
19 | HG00323.hp2 HG00597.hp2 HG00639.hp2 others(16): Show |
intron_variant | MODIFIER | c.1409-430_1409-425d others(8): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3735748 | |||||||
chr11:3735748 | AGTGTGTG others(1): Show |
A | 81 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0045 others(78): Show |
81 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.1409-432_1409-425d others(10): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3735748 | |||||||
chr11:3735748 | AGTGTGTG others(3): Show |
A | 36 | a0001c0001t0001g0026 a0001c0001t0001g0121 a0001c0001t0001g0129 others(33): Show |
36 | HG00597.hp1 HG01243.hp2 HG01993.hp1 others(33): Show |
intron_variant | MODIFIER | c.1409-434_1409-425d others(12): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3735748 | |||||||
chr11:3735748 | AGTGTGTG others(5): Show |
A | 7 | a0001c0001t0001g0324 a0001c0001t0008g0325 a0001c0002t0001g0192 others(4): Show |
7 | HG00642.hp1 HG02559.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1409-436_1409-425d others(14): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3735748 | |||||||
chr11:3735748 | AGTGTGTG others(9): Show |
A | 6 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.1409-440_1409-425d others(18): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3735748 | |||||||
chr11:3735788 | T | C | 6 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.1409-464A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3735788 | |||||||
chr11:3735795 | G | A | 3 | a0001c0001t0001g0191 a0001c0001t0001g0196 a0001c0001t0001g0241 |
3 | NA18950.hp2 NA18969.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.1409-471C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3735795 | |||||||
chr11:3735833 | C | CTG | 7 | a0001c0001t0001g0287 a0001c0001t0001g0324 a0001c0001t0008g0325 others(4): Show |
7 | HG00323.hp2 HG00642.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1409-511_1409-510d others(4): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3735833 | |||||||
chr11:3735833 | CTGTG | C | 6 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.1409-513_1409-510d others(6): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3735833 | |||||||
chr11:3735925 | TAC | T | 312 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(309): Show |
312 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(309): Show |
intron_variant | MODIFIER | c.1409-603_1409-602d others(4): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3735925 | |||||||
chr11:3735966 | G | C | 1 | a0001c0012t0001g0320 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1409-642C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3735966 | |||||||
chr11:3736076 | T | TTG | 132 | a0001c0001t0001g0006 a0001c0001t0001g0026 a0001c0001t0001g0038 others(129): Show |
132 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.1409-754_1409-753d others(4): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3736076 | |||||||
chr11:3736098 | GTT | G | 66 | a0001c0001t0001g0076 a0001c0001t0001g0078 a0001c0001t0001g0081 others(63): Show |
66 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.1409-776_1409-775d others(4): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3736098 | |||||||
chr11:3736099 | T | TG | 6 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.1409-776_1409-775i others(3): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3736099 | |||||||
chr11:3736099 | T | TGTG | 4 | a0001c0001t0001g0324 a0001c0001t0008g0325 a0005c0010t0001g0338 others(1): Show |
4 | HG00642.hp1 HG02559.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1409-776_1409-775i others(5): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3736099 | |||||||
chr11:3736100 | T | G | 66 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0030 others(63): Show |
66 | HG00597.hp1 HG00639.hp2 HG01243.hp2 others(63): Show |
intron_variant | MODIFIER | c.1409-776A>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3736100 | |||||||
chr11:3736103 | G | T | 14 | a0001c0001t0001g0068 a0001c0001t0001g0324 a0001c0001t0001g0336 others(11): Show |
14 | HG00642.hp1 HG01081.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.1409-779C>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3736103 | |||||||
chr11:3736104 | T | G | 14 | a0001c0001t0001g0068 a0001c0001t0001g0324 a0001c0001t0001g0336 others(11): Show |
14 | HG00642.hp1 HG01081.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.1409-780A>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3736104 | |||||||
chr11:3736182 | T | G | 2 | a0001c0001t0001g0258 a0005c0021t0001g0259 |
2 | HG02280.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1409-858A>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3736182 | |||||||
chr11:3736197 | G | A | 2 | a0001c0001t0001g0258 a0005c0021t0001g0259 |
2 | HG02280.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1409-873C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3736197 | |||||||
chr11:3736348 | C | A | 2 | a0001c0001t0001g0305 a0001c0001t0001g0306 |
2 | HG01099.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.1409-1024G>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3736348 | |||||||
chr11:3736363 | G | A | 51 | a0001c0001t0001g0006 a0001c0001t0001g0112 a0001c0001t0001g0135 others(48): Show |
51 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.1409-1039C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3736363 | |||||||
chr11:3736899 | C | A | 187 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0030 others(184): Show |
187 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.1409-1575G>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3736899 | |||||||
chr11:3736923 | G | A | 1 | a0001c0032t0001g0032 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1409-1599C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3736923 | |||||||
chr11:3736998 | A | G | 202 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0030 others(199): Show |
202 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.1409-1674T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3736998 | |||||||
chr11:3737143 | C | T | 55 | a0001c0001t0001g0026 a0001c0001t0001g0030 a0001c0001t0001g0031 others(52): Show |
55 | HG00597.hp1 HG00639.hp2 HG01243.hp2 others(52): Show |
intron_variant | MODIFIER | c.1409-1819G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3737143 | |||||||
chr11:3737242 | C | G | 1 | a0001c0001t0001g0335 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1409-1918G>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3737242 | |||||||
chr11:3737321 | C | CA | 70 | a0001c0001t0001g0042 a0001c0001t0001g0044 a0001c0001t0001g0045 others(67): Show |
70 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.1409-1998dupT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3737321 | |||||||
chr11:3737321 | CA | C | 125 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0030 others(122): Show |
125 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(122): Show |
intron_variant | MODIFIER | c.1409-1998delT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3737321 | |||||||
chr11:3737321 | CAA | C | 8 | a0001c0001t0001g0068 a0001c0001t0001g0250 a0001c0001t0001g0336 others(5): Show |
8 | HG02109.hp1 HG02451.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1409-1999_1409-199 others(6): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3737321 | |||||||
chr11:3737377 | G | A | 1 | a0001c0002t0001g0271 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1409-2053C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3737377 | |||||||
chr11:3737422 | G | A | 1 | a0001c0001t0001g0275 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1409-2098C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3737422 | |||||||
chr11:3737624 | C | T | 6 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.1409-2300G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3737624 | |||||||
chr11:3737736 | G | A | 6 | a0001c0001t0001g0068 a0001c0001t0001g0324 a0001c0001t0001g0336 others(3): Show |
6 | HG00642.hp1 HG02559.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1409-2412C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3737736 | |||||||
chr11:3737780 | G | T | 7 | a0001c0003t0002g0290 a0001c0003t0002g0311 a0001c0003t0002g0312 others(4): Show |
7 | HG01109.hp2 HG02055.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1409-2456C>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3737780 | |||||||
chr11:3737825 | C | T | 1 | a0004c0007t0001g0216 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1409-2501G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3737825 | |||||||
chr11:3737827 | T | C | 2 | a0001c0001t0001g0324 a0001c0001t0008g0325 |
2 | HG00642.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1409-2503A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3737827 | |||||||
chr11:3737922 | C | T | 2 | a0001c0012t0001g0319 a0001c0012t0001g0320 |
2 | HG02109.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1409-2598G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3737922 | |||||||
chr11:3737935 | G | T | 1 | a0007c0013t0005g0037 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1409-2611C>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3737935 | |||||||
chr11:3737965 | A | G | 5 | a0001c0001t0001g0329 a0001c0001t0001g0337 a0001c0001t0004g0330 others(2): Show |
5 | HG02257.hp2 HG02647.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1409-2641T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3737965 | |||||||
chr11:3738070 | T | C | 1 | a0001c0001t0001g0043 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1409-2746A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3738070 | |||||||
chr11:3738082 | G | A | 2 | a0002c0005t0001g0301 a0002c0005t0001g0303 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1409-2758C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3738082 | |||||||
chr11:3738087 | C | CA | 20 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0144 others(17): Show |
20 | HG00621.hp2 HG01891.hp2 HG02027.hp2 others(17): Show |
intron_variant | MODIFIER | c.1409-2764dupT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3738087 | |||||||
chr11:3738087 | C | CAAA | 45 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0041 others(42): Show |
45 | HG00408.hp2 HG00609.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.1409-2766_1409-276 others(7): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3738087 | |||||||
chr11:3738087 | C | CAAAAAAA others(3): Show |
1 | a0001c0001t0001g0068 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1409-2773_1409-276 others(14): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3738087 | |||||||
chr11:3738087 | CA | C | 9 | a0001c0001t0001g0177 a0001c0001t0001g0227 a0001c0001t0001g0234 others(6): Show |
9 | HG00544.hp1 HG01168.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.1409-2764delT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3738087 | |||||||
chr11:3738107 | A | AAAACAAA others(8): Show |
5 | a0002c0005t0001g0299 a0002c0005t0001g0301 a0002c0005t0001g0302 others(2): Show |
5 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(2): Show |
intron_variant | MODIFIER | c.1409-2784_1409-278 others(19): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3738107 | |||||||
chr11:3738107 | A | AAACAAAA others(7): Show |
1 | a0002c0005t0001g0300 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1409-2784_1409-278 others(18): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3738107 | |||||||
chr11:3738429 | G | C | 2 | a0005c0010t0001g0338 a0005c0010t0001g0339 |
2 | HG02559.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1409-3105C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3738429 | |||||||
chr11:3738474 | G | T | 2 | a0001c0001t0001g0036 a0001c0001t0001g0179 |
2 | HG02145.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.1409-3150C>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3738474 | |||||||
chr11:3738481 | A | G | 2 | a0001c0001t0001g0113 a0001c0016t0001g0114 |
2 | HG02809.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1409-3157T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3738481 | |||||||
chr11:3738506 | T | C | 6 | a0001c0001t0001g0068 a0001c0001t0001g0324 a0001c0001t0001g0336 others(3): Show |
6 | HG00642.hp1 HG02559.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1409-3182A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3738506 | |||||||
chr11:3738545 | G | A | 1 | a0001c0001t0001g0335 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1409-3221C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3738545 | |||||||
chr11:3738554 | G | C | 1 | a0001c0032t0001g0032 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1409-3230C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3738554 | |||||||
chr11:3738756 | T | C | 1 | a0001c0001t0001g0335 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1409-3432A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3738756 | |||||||
chr11:3738776 | C | CA | 302 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(299): Show |
302 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(299): Show |
intron_variant | MODIFIER | c.1409-3453dupT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3738776 | |||||||
chr11:3738776 | C | CAA | 33 | a0001c0001t0001g0026 a0001c0001t0001g0039 a0001c0001t0001g0043 others(30): Show |
33 | HG00597.hp2 HG00642.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.1409-3454_1409-345 others(6): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3738776 | |||||||
chr11:3738914 | A | G | 1 | a0001c0001t0001g0307 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1409-3590T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3738914 | |||||||
chr11:3739038 | A | T | 1 | a0001c0002t0001g0105 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1409-3714T>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3739038 | |||||||
chr11:3739182 | G | C | 1 | a0001c0001t0001g0171 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1409-3858C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3739182 | |||||||
chr11:3739256 | A | C | 1 | a0001c0026t0001g0298 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1409-3932T>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3739256 | |||||||
chr11:3739302 | C | T | 241 | a0001c0001t0001g0006 a0001c0001t0001g0026 a0001c0001t0001g0029 others(238): Show |
241 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(238): Show |
intron_variant | MODIFIER | c.1409-3978G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3739302 | |||||||
chr11:3739303 | G | A | 1 | a0001c0001t0001g0307 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1409-3979C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3739303 | |||||||
chr11:3739311 | G | A | 1 | a0001c0001t0001g0232 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1409-3987C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3739311 | |||||||
chr11:3739318 | C | T | 1 | a0001c0002t0001g0105 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1409-3994G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3739318 | |||||||
chr11:3739346 | C | T | 2 | a0001c0001t0001g0333 a0001c0001t0001g0334 |
2 | HG02145.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1409-4022G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3739346 | |||||||
chr11:3739402 | C | T | 1 | a0001c0001t0001g0041 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1409-4078G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3739402 | |||||||
chr11:3739407 | C | A | 1 | a0001c0001t0001g0332 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1409-4083G>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3739407 | |||||||
chr11:3739451 | G | T | 1 | a0001c0001t0001g0278 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1409-4127C>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3739451 | |||||||
chr11:3739745 | T | C | 2 | a0001c0001t0001g0068 a0001c0001t0001g0336 |
2 | HG02965.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1409-4421A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3739745 | |||||||
chr11:3739996 | G | A | 184 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0030 others(181): Show |
184 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(181): Show |
intron_variant | MODIFIER | c.1408+4513C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3739996 | |||||||
chr11:3740091 | G | T | 6 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.1408+4418C>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3740091 | |||||||
chr11:3740177 | T | C | 1 | a0001c0001t0006g0297 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1408+4332A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3740177 | |||||||
chr11:3740179 | G | T | 1 | a0001c0001t0001g0039 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1408+4330C>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3740179 | |||||||
chr11:3740239 | G | A | 4 | a0001c0001t0001g0329 a0001c0001t0001g0337 a0001c0001t0004g0330 others(1): Show |
4 | HG02647.hp2 HG02717.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1408+4270C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3740239 | |||||||
chr11:3740282 | G | C | 2 | a0001c0012t0001g0319 a0001c0012t0001g0320 |
2 | HG02109.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1408+4227C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3740282 | |||||||
chr11:3740314 | C | T | 54 | a0001c0001t0001g0026 a0001c0001t0001g0030 a0001c0001t0001g0031 others(51): Show |
54 | HG00597.hp1 HG00639.hp2 HG01243.hp2 others(51): Show |
intron_variant | MODIFIER | c.1408+4195G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3740314 | |||||||
chr11:3740326 | T | C | 4 | a0001c0001t0001g0324 a0001c0001t0008g0325 a0005c0010t0001g0338 others(1): Show |
4 | HG00642.hp1 HG02559.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1408+4183A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3740326 | |||||||
chr11:3740336 | C | T | 1 | a0001c0002t0001g0102 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1408+4173G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3740336 | |||||||
chr11:3740436 | G | A | 5 | a0001c0001t0001g0006 a0001c0001t0001g0137 a0001c0001t0001g0148 others(2): Show |
5 | HG02055.hp1 HG02129.hp1 HG02165.hp2 others(2): Show |
intron_variant | MODIFIER | c.1408+4073C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3740436 | |||||||
chr11:3740516 | C | CA | 11 | a0001c0001t0001g0329 a0001c0001t0001g0337 a0001c0001t0004g0330 others(8): Show |
11 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.1408+3992dupT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3740516 | |||||||
chr11:3740524 | A | G | 1 | a0001c0001t0001g0307 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1408+3985T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3740524 | |||||||
chr11:3740607 | C | T | 9 | a0001c0001t0001g0185 a0001c0001t0001g0191 a0001c0001t0001g0195 others(6): Show |
9 | HG00323.hp1 NA18950.hp2 NA18952.hp1 others(6): Show |
intron_variant | MODIFIER | c.1408+3902G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3740607 | |||||||
chr11:3740643 | A | C | 6 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.1408+3866T>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3740643 | |||||||
chr11:3740672 | G | A | 1 | a0001c0001t0001g0082 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1408+3837C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3740672 | |||||||
chr11:3740684 | A | G | 1 | a0001c0001t0001g0082 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1408+3825T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3740684 | |||||||
chr11:3740686 | A | T | 1 | a0001c0001t0001g0082 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1408+3823T>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3740686 | |||||||
chr11:3740688 | T | A | 1 | a0001c0001t0001g0082 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1408+3821A>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3740688 | |||||||
chr11:3740689 | C | A | 1 | a0001c0001t0001g0082 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1408+3820G>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3740689 | |||||||
chr11:3740690 | T | G | 1 | a0001c0001t0001g0082 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1408+3819A>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3740690 | |||||||
chr11:3740697 | T | A | 1 | a0001c0001t0001g0082 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1408+3812A>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3740697 | |||||||
chr11:3740803 | A | G | 58 | a0001c0001t0001g0026 a0001c0001t0001g0030 a0001c0001t0001g0031 others(55): Show |
58 | HG00597.hp1 HG00639.hp2 HG01243.hp2 others(55): Show |
intron_variant | MODIFIER | c.1408+3706T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3740803 | |||||||
chr11:3740822 | A | T | 1 | a0002c0005t0001g0302 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1408+3687T>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3740822 | |||||||
chr11:3740824 | A | T | 182 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0030 others(179): Show |
182 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(179): Show |
intron_variant | MODIFIER | c.1408+3685T>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3740824 | |||||||
chr11:3740825 | T | TA | 3 | a0001c0001t0001g0109 a0001c0001t0001g0230 a0001c0017t0002g0116 |
3 | HG02148.hp2 HG02486.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.1408+3683_1408+368 others(5): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3740825 | |||||||
chr11:3740826 | T | A | 2 | a0001c0026t0001g0298 a0005c0021t0001g0259 |
2 | HG02280.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1408+3683A>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3740826 | |||||||
chr11:3740858 | G | C | 2 | a0001c0001t0001g0029 a0001c0001t0001g0328 |
2 | HG02280.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1408+3651C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3740858 | |||||||
chr11:3740947 | T | C | 1 | a0001c0026t0001g0298 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1408+3562A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3740947 | |||||||
chr11:3740966 | G | A | 1 | a0001c0002t0001g0212 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1408+3543C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3740966 | |||||||
chr11:3740992 | T | C | 1 | a0001c0026t0001g0298 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1408+3517A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3740992 | |||||||
chr11:3741033 | G | C | 2 | a0004c0007t0001g0213 a0004c0007t0001g0245 |
2 | HG00423.hp2 HG00544.hp2 |
intron_variant | MODIFIER | c.1408+3476C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3741033 | |||||||
chr11:3741076 | C | T | 1 | a0001c0001t0001g0039 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1408+3433G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3741076 | |||||||
chr11:3741294 | C | A | 2 | a0001c0001t0001g0068 a0001c0001t0001g0336 |
2 | HG02965.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1408+3215G>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3741294 | |||||||
chr11:3741339 | C | T | 6 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.1408+3170G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3741339 | |||||||
chr11:3741356 | T | A | 1 | a0001c0001t0001g0133 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1408+3153A>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3741356 | |||||||
chr11:3741564 | T | A | 69 | a0001c0001t0001g0076 a0001c0001t0001g0078 a0001c0001t0001g0081 others(66): Show |
69 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.1408+2945A>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3741564 | |||||||
chr11:3741753 | G | C | 1 | a0001c0001t0001g0336 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1408+2756C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3741753 | |||||||
chr11:3741938 | G | T | 322 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(319): Show |
322 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(319): Show |
intron_variant | MODIFIER | c.1408+2571C>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3741938 | |||||||
chr11:3742560 | G | A | 6 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.1408+1949C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3742560 | |||||||
chr11:3742647 | C | T | 1 | a0001c0001t0001g0036 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1408+1862G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3742647 | |||||||
chr11:3742666 | T | C | 2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | NA18966.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1408+1843A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3742666 | |||||||
chr11:3742692 | C | CT | 3 | a0001c0001t0001g0333 a0001c0001t0001g0334 a0001c0017t0002g0116 |
3 | HG02145.hp1 HG02486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1408+1816dupA | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3742692 | |||||||
chr11:3742699 | C | CA | 8 | a0001c0001t0001g0026 a0001c0001t0001g0239 a0001c0001t0001g0307 others(5): Show |
8 | HG00597.hp1 HG00642.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1408+1809dupT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3742699 | |||||||
chr11:3742699 | CA | C | 240 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(237): Show |
240 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.1408+1809delT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3742699 | |||||||
chr11:3742699 | CAA | C | 7 | a0001c0002t0001g0083 a0001c0003t0002g0311 a0001c0003t0002g0312 others(4): Show |
7 | HG01109.hp2 HG02818.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1408+1808_1408+180 others(6): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3742699 | |||||||
chr11:3742720 | G | A | 6 | a0001c0001t0001g0068 a0001c0001t0001g0324 a0001c0001t0001g0336 others(3): Show |
6 | HG00642.hp1 HG02559.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1408+1789C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3742720 | |||||||
chr11:3742722 | T | A | 4 | a0001c0001t0001g0324 a0001c0001t0008g0325 a0005c0010t0001g0338 others(1): Show |
4 | HG00642.hp1 HG02559.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1408+1787A>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3742722 | |||||||
chr11:3742847 | A | C | 1 | a0001c0001t0001g0335 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1408+1662T>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3742847 | |||||||
chr11:3742872 | T | C | 8 | a0001c0001t0001g0068 a0001c0001t0001g0324 a0001c0001t0001g0336 others(5): Show |
8 | HG00642.hp1 HG02109.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1408+1637A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3742872 | |||||||
chr11:3742913 | TACAGAA | T | 5 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0164 others(2): Show |
5 | HG00408.hp1 NA18995.hp2 NA19060.hp2 others(2): Show |
intron_variant | MODIFIER | c.1408+1590_1408+159 others(10): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3742913 | |||||||
chr11:3743296 | C | T | 1 | a0001c0001t0001g0335 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1408+1213G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3743296 | |||||||
chr11:3743396 | C | T | 1 | a0001c0002t0001g0187 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1408+1113G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3743396 | |||||||
chr11:3743461 | A | G | 1 | a0001c0001t0002g0309 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1408+1048T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3743461 | |||||||
chr11:3743503 | T | C | 2 | a0001c0001t0001g0030 a0001c0001t0001g0031 |
2 | HG01884.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1408+1006A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3743503 | |||||||
chr11:3743646 | C | CA | 10 | a0001c0001t0001g0038 a0001c0001t0001g0173 a0001c0001t0001g0205 others(7): Show |
10 | HG01361.hp1 HG02135.hp1 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.1408+862dupT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3743646 | |||||||
chr11:3743646 | CA | C | 55 | a0001c0001t0001g0005 a0001c0001t0001g0030 a0001c0001t0001g0031 others(52): Show |
55 | HG00597.hp1 HG01243.hp2 HG01884.hp1 others(52): Show |
intron_variant | MODIFIER | c.1408+862delT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3743646 | |||||||
chr11:3743728 | C | G | 173 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0030 others(170): Show |
173 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.1408+781G>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3743728 | |||||||
chr11:3743737 | G | A | 1 | a0001c0001t0001g0006 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1408+772C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3743737 | |||||||
chr11:3743836 | G | A | 6 | a0001c0001t0001g0043 a0001c0001t0001g0061 a0001c0001t0001g0253 others(3): Show |
6 | HG00738.hp2 HG01106.hp2 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.1408+673C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3743836 | |||||||
chr11:3743863 | C | T | 1 | a0001c0001t0001g0335 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1408+646G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3743863 | |||||||
chr11:3743864 | G | C | 14 | a0001c0001t0001g0068 a0001c0001t0001g0324 a0001c0001t0001g0336 others(11): Show |
14 | HG00642.hp1 HG01081.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.1408+645C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3743864 | |||||||
chr11:3743898 | CA | C | 10 | a0001c0003t0002g0290 a0001c0003t0002g0311 a0001c0003t0002g0312 others(7): Show |
10 | HG01109.hp2 HG02055.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1408+610delT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3743898 | |||||||
chr11:3743962 | G | A | 1 | a0001c0002t0001g0315 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1408+547C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3743962 | |||||||
chr11:3743976 | T | C | 1 | a0001c0001t0001g0029 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1408+533A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3743976 | |||||||
chr11:3743995 | G | A | 1 | a0001c0001t0001g0176 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1408+514C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3743995 | |||||||
chr11:3744045 | C | T | 1 | a0001c0001t0001g0043 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1408+464G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3744045 | |||||||
chr11:3744089 | T | C | 1 | a0001c0001t0001g0060 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1408+420A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3744089 | |||||||
chr11:3744353 | GGATCTAT others(6): Show |
G | 8 | a0001c0002t0001g0069 a0001c0002t0001g0093 a0001c0002t0001g0095 others(5): Show |
8 | HG02015.hp2 HG02165.hp1 NA18965.hp2 others(5): Show |
intron_variant | MODIFIER | c.1408+143_1408+155d others(15): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3744353 | |||||||
chr11:3744478 | A | C | 2 | a0001c0001t0001g0029 a0001c0001t0001g0328 |
2 | HG02280.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1408+31T>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3744478 | |||||||
chr11:3744719 | C | T | 1 | a0001c0001t0001g0335 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1268-70G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3744719 | |||||||
chr11:3744746 | T | A | 1 | a0001c0001t0001g0335 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1268-97A>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3744746 | |||||||
chr11:3744839 | A | G | 2 | a0001c0012t0001g0319 a0001c0012t0001g0320 |
2 | HG02109.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1268-190T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3744839 | |||||||
chr11:3744852 | C | T | 2 | a0001c0001t0001g0234 a0001c0001t0001g0235 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1268-203G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3744852 | |||||||
chr11:3744912 | C | A | 1 | a0001c0001t0001g0337 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1268-263G>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3744912 | |||||||
chr11:3744962 | A | T | 190 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0030 others(187): Show |
190 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(187): Show |
intron_variant | MODIFIER | c.1268-313T>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3744962 | |||||||
chr11:3745064 | T | C | 1 | a0001c0001t0001g0332 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1268-415A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3745064 | |||||||
chr11:3745209 | CAACT | C | 6 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.1268-564_1268-561d others(6): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3745209 | |||||||
chr11:3745404 | G | A | 1 | a0001c0026t0001g0298 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1268-755C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3745404 | |||||||
chr11:3745843 | A | G | 1 | a0001c0001t0001g0113 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1268-1194T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3745843 | |||||||
chr11:3746050 | A | C | 1 | a0001c0001t0001g0335 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1268-1401T>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3746050 | |||||||
chr11:3746141 | A | G | 139 | a0001c0001t0001g0026 a0001c0001t0001g0030 a0001c0001t0001g0031 others(136): Show |
139 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.1268-1492T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3746141 | |||||||
chr11:3746250 | CAAGAGCA others(637): Show |
C | 1 | a0001c0001t0001g0113 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1268-2245_1268-160 others(4): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3746250 | |||||||
chr11:3746263 | T | C | 339 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(336): Show |
339 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(336): Show |
intron_variant | MODIFIER | c.1268-1614A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3746263 | |||||||
chr11:3746269 | C | CA | 10 | a0001c0001t0001g0028 a0001c0001t0001g0172 a0001c0001t0001g0175 others(7): Show |
10 | HG01258.hp2 HG02148.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1268-1621dupT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3746269 | |||||||
chr11:3746269 | CA | C | 8 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0154 others(5): Show |
8 | HG00408.hp1 HG01099.hp2 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.1268-1621delT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3746269 | |||||||
chr11:3746294 | A | AAAAAAAA others(11): Show |
1 | a0001c0032t0001g0032 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1268-1646_1268-164 others(22): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3746294 | |||||||
chr11:3746294 | A | AAAAAAAG | 15 | a0001c0001t0001g0030 a0001c0001t0001g0051 a0001c0001t0001g0057 others(12): Show |
15 | HG00408.hp2 HG01346.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.1268-1646_1268-164 others(11): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3746294 | |||||||
chr11:3746294 | A | AAAAAAG | 46 | a0001c0001t0001g0031 a0001c0001t0001g0039 a0001c0001t0001g0042 others(43): Show |
46 | HG00597.hp2 HG00639.hp2 HG01192.hp1 others(43): Show |
intron_variant | MODIFIER | c.1268-1646_1268-164 others(10): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3746294 | |||||||
chr11:3746294 | A | AAAAAG | 106 | a0001c0001t0001g0026 a0001c0001t0001g0038 a0001c0001t0001g0041 others(103): Show |
106 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.1268-1646_1268-164 others(9): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3746294 | |||||||
chr11:3746294 | A | AAAACG | 6 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.1268-1646_1268-164 others(9): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3746294 | |||||||
chr11:3746294 | A | AAAAG | 11 | a0001c0001t0001g0029 a0001c0001t0001g0050 a0001c0001t0001g0068 others(8): Show |
11 | HG00323.hp2 HG02280.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.1268-1646_1268-164 others(8): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3746294 | |||||||
chr11:3746294 | A | G | 1 | a0001c0001t0001g0335 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1268-1645T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3746294 | |||||||
chr11:3746353 | C | T | 1 | a0001c0002t0001g0315 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1268-1704G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3746353 | |||||||
chr11:3746402 | G | C | 1 | a0001c0002t0001g0193 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1268-1753C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3746402 | |||||||
chr11:3746478 | G | A | 2 | a0001c0012t0001g0319 a0001c0012t0001g0320 |
2 | HG02109.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1268-1829C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3746478 | |||||||
chr11:3746520 | T | C | 6 | a0001c0002t0001g0073 a0001c0002t0001g0074 a0001c0002t0001g0075 others(3): Show |
6 | HG02922.hp2 HG03041.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.1268-1871A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3746520 | |||||||
chr11:3746592 | T | G | 1 | a0001c0001t0001g0335 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1268-1943A>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3746592 | |||||||
chr11:3746597 | G | C | 1 | a0007c0013t0005g0218 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1268-1948C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3746597 | |||||||
chr11:3746651 | G | T | 1 | a0001c0002t0001g0105 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1268-2002C>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3746651 | |||||||
chr11:3746664 | G | A | 8 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0121 others(5): Show |
8 | HG01884.hp1 HG01891.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1268-2015C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3746664 | |||||||
chr11:3746666 | A | C | 1 | a0001c0001t0001g0307 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1268-2017T>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3746666 | |||||||
chr11:3746798 | G | T | 2 | a0001c0012t0001g0319 a0001c0012t0001g0320 |
2 | HG02109.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1268-2149C>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3746798 | |||||||
chr11:3746837 | C | T | 2 | a0001c0001t0001g0068 a0001c0001t0001g0336 |
2 | HG02965.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1268-2188G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3746837 | |||||||
chr11:3746906 | G | T | 14 | a0001c0001t0001g0068 a0001c0001t0001g0324 a0001c0001t0001g0336 others(11): Show |
14 | HG00642.hp1 HG01081.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.1268-2257C>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3746906 | |||||||
chr11:3746913 | C | CA | 68 | a0001c0001t0001g0026 a0001c0001t0001g0030 a0001c0001t0001g0031 others(65): Show |
68 | HG00597.hp1 HG00621.hp2 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.1268-2265dupT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3746913 | |||||||
chr11:3746919 | A | C | 8 | a0001c0001t0001g0068 a0001c0001t0001g0324 a0001c0001t0001g0336 others(5): Show |
8 | HG00642.hp1 HG02109.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1268-2270T>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3746919 | |||||||
chr11:3746930 | A | G | 2 | a0001c0012t0001g0319 a0001c0012t0001g0320 |
2 | HG02109.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1268-2281T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3746930 | |||||||
chr11:3746961 | G | C | 2 | a0001c0012t0001g0319 a0001c0012t0001g0320 |
2 | HG02109.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1268-2312C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3746961 | |||||||
chr11:3746976 | A | C | 1 | a0001c0001t0001g0307 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1268-2327T>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3746976 | |||||||
chr11:3747042 | C | T | 1 | a0001c0001t0001g0179 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1268-2393G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3747042 | |||||||
chr11:3747071 | G | C | 202 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0030 others(199): Show |
202 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.1268-2422C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3747071 | |||||||
chr11:3747137 | T | A | 2 | a0001c0012t0001g0319 a0001c0012t0001g0320 |
2 | HG02109.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1268-2488A>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3747137 | |||||||
chr11:3747159 | G | A | 1 | a0001c0001t0001g0307 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1268-2510C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3747159 | |||||||
chr11:3747436 | A | G | 2 | a0001c0012t0001g0319 a0001c0012t0001g0320 |
2 | HG02109.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1268-2787T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3747436 | |||||||
chr11:3747489 | T | C | 78 | a0001c0001t0001g0042 a0001c0001t0001g0044 a0001c0001t0001g0045 others(75): Show |
78 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.1268-2840A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3747489 | |||||||
chr11:3747604 | G | C | 1 | a0001c0001t0001g0170 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1268-2955C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3747604 | |||||||
chr11:3747764 | C | G | 6 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.1268-3115G>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3747764 | |||||||
chr11:3747827 | G | T | 4 | a0001c0001t0001g0324 a0001c0001t0008g0325 a0005c0010t0001g0338 others(1): Show |
4 | HG00642.hp1 HG02559.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1268-3178C>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3747827 | |||||||
chr11:3747899 | C | G | 1 | a0001c0001t0001g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1268-3250G>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3747899 | |||||||
chr11:3747922 | T | C | 1 | a0018c0034t0001g0122 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1268-3273A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3747922 | |||||||
chr11:3747953 | A | G | 2 | a0001c0001t0001g0333 a0001c0001t0001g0334 |
2 | HG02145.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1268-3304T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3747953 | |||||||
chr11:3748048 | T | C | 6 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.1268-3399A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3748048 | |||||||
chr11:3748138 | T | G | 1 | a0001c0001t0001g0214 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1268-3489A>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3748138 | |||||||
chr11:3748206 | T | C | 2 | a0001c0001t0001g0068 a0001c0001t0001g0336 |
2 | HG02965.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1268-3557A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3748206 | |||||||
chr11:3748209 | G | A | 1 | a0002c0005t0001g0302 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1268-3560C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3748209 | |||||||
chr11:3748363 | A | C | 3 | a0001c0002t0001g0074 a0001c0002t0001g0075 a0001c0002t0001g0322 |
3 | HG03041.hp1 HG03130.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1268-3714T>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3748363 | |||||||
chr11:3748426 | C | T | 2 | a0015c0033t0001g0130 a0018c0034t0001g0122 |
2 | HG02630.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1268-3777G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3748426 | |||||||
chr11:3748550 | A | C | 79 | a0001c0001t0001g0042 a0001c0001t0001g0044 a0001c0001t0001g0045 others(76): Show |
79 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.1268-3901T>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3748550 | |||||||
chr11:3748716 | G | A | 1 | a0001c0001t0001g0160 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1268-4067C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3748716 | |||||||
chr11:3748717 | A | G | 1 | a0001c0001t0001g0160 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1268-4068T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3748717 | |||||||
chr11:3748741 | C | T | 1 | a0001c0001t0002g0002 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1268-4092G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3748741 | |||||||
chr11:3748865 | T | A | 1 | a0001c0002t0001g0077 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1268-4216A>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3748865 | |||||||
chr11:3748947 | TA | T | 8 | a0001c0001t0001g0291 a0001c0001t0001g0293 a0001c0001t0001g0296 others(5): Show |
8 | HG02109.hp2 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1268-4299delT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3748947 | |||||||
chr11:3748960 | AC | A | 3 | a0001c0006t0001g0204 a0001c0006t0001g0242 a0017c0019t0001g0222 |
3 | HG00741.hp2 HG01361.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.1268-4312delG | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3748960 | |||||||
chr11:3748977 | A | T | 1 | a0001c0001t0001g0307 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1268-4328T>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3748977 | |||||||
chr11:3749046 | C | T | 2 | a0001c0001t0001g0328 a0001c0002t0001g0016 |
2 | HG03486.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.1267+4270G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3749046 | |||||||
chr11:3749047 | G | A | 1 | a0001c0032t0001g0032 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1267+4269C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3749047 | |||||||
chr11:3749151 | A | G | 1 | a0016c0023t0001g0001 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1267+4165T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3749151 | |||||||
chr11:3749170 | C | T | 5 | a0001c0001t0001g0113 a0001c0001t0001g0324 a0001c0001t0008g0325 others(2): Show |
5 | HG00642.hp1 HG02451.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1267+4146G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3749170 | |||||||
chr11:3749232 | C | T | 2 | a0001c0001t0001g0305 a0001c0001t0001g0306 |
2 | HG01099.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.1267+4084G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3749232 | |||||||
chr11:3749239 | C | T | 3 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0340 |
3 | HG01884.hp1 HG01891.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1267+4077G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3749239 | |||||||
chr11:3749265 | A | G | 14 | a0001c0001t0001g0068 a0001c0001t0001g0324 a0001c0001t0001g0336 others(11): Show |
14 | HG00642.hp1 HG01081.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.1267+4051T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3749265 | |||||||
chr11:3749270 | T | C | 3 | a0001c0001t0001g0113 a0001c0016t0001g0114 a0001c0032t0001g0032 |
3 | HG02451.hp1 HG02809.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1267+4046A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3749270 | |||||||
chr11:3749301 | C | G | 1 | a0001c0017t0002g0116 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1267+4015G>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3749301 | |||||||
chr11:3749321 | A | T | 1 | a0001c0001t0001g0241 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1267+3995T>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3749321 | |||||||
chr11:3749325 | T | A | 158 | a0001c0001t0001g0006 a0001c0001t0001g0026 a0001c0001t0001g0029 others(155): Show |
158 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(155): Show |
intron_variant | MODIFIER | c.1267+3991A>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3749325 | |||||||
chr11:3749328 | A | G | 6 | a0001c0001t0001g0324 a0001c0001t0008g0325 a0001c0012t0001g0319 others(3): Show |
6 | HG00642.hp1 HG02109.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1267+3988T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3749328 | |||||||
chr11:3749378 | A | G | 1 | a0001c0003t0002g0290 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1267+3938T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3749378 | |||||||
chr11:3749422 | C | T | 6 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.1267+3894G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3749422 | |||||||
chr11:3749557 | G | A | 3 | a0002c0008t0003g0040 a0002c0008t0003g0062 a0002c0008t0003g0064 |
3 | HG00735.hp1 HG00741.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.1267+3759C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3749557 | |||||||
chr11:3749667 | T | A | 3 | a0001c0001t0001g0194 a0001c0001t0001g0206 a0001c0001t0001g0250 |
3 | NA18960.hp1 NA19055.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.1267+3649A>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3749667 | |||||||
chr11:3749667 | TTAGTGGT others(5): Show |
T | 1 | a0001c0002t0001g0193 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1267+3637_1267+364 others(16): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3749667 | |||||||
chr11:3749682 | G | GA | 6 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.1267+3633dupT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3749682 | |||||||
chr11:3749721 | C | A | 1 | a0001c0002t0001g0292 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1267+3595G>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3749721 | |||||||
chr11:3749739 | A | T | 4 | a0001c0001t0001g0324 a0001c0001t0008g0325 a0005c0010t0001g0338 others(1): Show |
4 | HG00642.hp1 HG02559.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1267+3577T>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3749739 | |||||||
chr11:3749765 | T | A | 1 | a0001c0002t0001g0094 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1267+3551A>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3749765 | |||||||
chr11:3749793 | G | C | 1 | a0001c0001t0001g0142 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1267+3523C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3749793 | |||||||
chr11:3749816 | T | C | 1 | a0001c0001t0001g0230 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1267+3500A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3749816 | |||||||
chr11:3749958 | G | A | 171 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0030 others(168): Show |
171 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(168): Show |
intron_variant | MODIFIER | c.1267+3358C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3749958 | |||||||
chr11:3749970 | T | C | 43 | a0001c0001t0001g0029 a0001c0001t0001g0038 a0001c0001t0001g0039 others(40): Show |
43 | HG00408.hp2 HG00609.hp2 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.1267+3346A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3749970 | |||||||
chr11:3750046 | A | G | 1 | a0001c0001t0001g0145 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1267+3270T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3750046 | |||||||
chr11:3750253 | T | C | 14 | a0001c0001t0001g0068 a0001c0001t0001g0324 a0001c0001t0001g0336 others(11): Show |
14 | HG00642.hp1 HG01081.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.1267+3063A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3750253 | |||||||
chr11:3750309 | G | A | 1 | a0001c0001t0001g0335 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1267+3007C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3750309 | |||||||
chr11:3750404 | C | G | 14 | a0001c0001t0001g0068 a0001c0001t0001g0324 a0001c0001t0001g0336 others(11): Show |
14 | HG00642.hp1 HG01081.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.1267+2912G>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3750404 | |||||||
chr11:3750460 | T | C | 2 | a0001c0001t0001g0068 a0001c0001t0001g0336 |
2 | HG02965.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1267+2856A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3750460 | |||||||
chr11:3750611 | A | C | 2 | a0001c0001t0001g0055 a0001c0001t0001g0066 |
2 | HG02080.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.1267+2705T>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3750611 | |||||||
chr11:3750623 | G | GT | 11 | a0001c0001t0002g0314 a0001c0001t0002g0317 a0001c0017t0002g0116 others(8): Show |
11 | HG00639.hp2 HG01081.hp1 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.1267+2692dupA | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3750623 | |||||||
chr11:3750624 | T | G | 1 | a0001c0001t0001g0307 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1267+2692A>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3750624 | |||||||
chr11:3750637 | T | TG | 6 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.1267+2678_1267+267 others(5): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3750637 | |||||||
chr11:3750694 | C | T | 40 | a0001c0001t0001g0029 a0001c0001t0001g0038 a0001c0001t0001g0039 others(37): Show |
40 | HG00408.hp2 HG00609.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.1267+2622G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3750694 | |||||||
chr11:3750744 | C | A | 8 | a0001c0001t0001g0068 a0001c0001t0001g0324 a0001c0001t0001g0336 others(5): Show |
8 | HG00642.hp1 HG02109.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1267+2572G>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3750744 | |||||||
chr11:3751080 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1267+2236G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3751080 | |||||||
chr11:3751117 | G | C | 5 | a0001c0002t0001g0262 a0001c0002t0001g0264 a0001c0002t0001g0265 others(2): Show |
5 | NA18955.hp1 NA18957.hp1 NA19002.hp2 others(2): Show |
intron_variant | MODIFIER | c.1267+2199C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3751117 | |||||||
chr11:3751124 | C | T | 6 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.1267+2192G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3751124 | |||||||
chr11:3751155 | T | C | 6 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.1267+2161A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3751155 | |||||||
chr11:3751290 | G | A | 1 | a0018c0034t0001g0122 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1267+2026C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3751290 | |||||||
chr11:3751307 | G | A | 2 | a0001c0001t0001g0082 a0001c0001t0001g0085 |
2 | NA19003.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.1267+2009C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3751307 | |||||||
chr11:3751319 | T | C | 1 | a0001c0001t0001g0254 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1267+1997A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3751319 | |||||||
chr11:3751506 | A | G | 51 | a0001c0001t0001g0029 a0001c0001t0001g0038 a0001c0001t0001g0039 others(48): Show |
51 | HG00408.hp2 HG00609.hp2 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.1267+1810T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3751506 | |||||||
chr11:3751682 | G | A | 1 | a0001c0001t0001g0028 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1267+1634C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3751682 | |||||||
chr11:3751706 | A | T | 1 | a0001c0001t0001g0224 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1267+1610T>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3751706 | |||||||
chr11:3751707 | A | T | 1 | a0001c0001t0001g0224 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1267+1609T>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3751707 | |||||||
chr11:3751718 | G | T | 1 | a0001c0001t0001g0224 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1267+1598C>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3751718 | |||||||
chr11:3751723 | G | C | 1 | a0001c0001t0001g0224 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1267+1593C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3751723 | |||||||
chr11:3751725 | G | GCTATAAA others(3): Show |
1 | a0001c0001t0001g0224 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1267+1590_1267+159 others(14): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3751725 | |||||||
chr11:3751726 | G | A | 1 | a0001c0001t0001g0224 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1267+1590C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3751726 | |||||||
chr11:3751728 | T | A | 1 | a0001c0001t0001g0224 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1267+1588A>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3751728 | |||||||
chr11:3751734 | C | T | 1 | a0001c0001t0001g0224 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1267+1582G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3751734 | |||||||
chr11:3751741 | C | G | 1 | a0001c0001t0001g0224 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1267+1575G>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3751741 | |||||||
chr11:3751742 | C | G | 1 | a0001c0001t0001g0224 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1267+1574G>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3751742 | |||||||
chr11:3751745 | G | C | 1 | a0001c0001t0001g0224 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1267+1571C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3751745 | |||||||
chr11:3751756 | G | T | 1 | a0001c0001t0001g0224 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1267+1560C>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3751756 | |||||||
chr11:3751757 | G | T | 1 | a0001c0001t0001g0224 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1267+1559C>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3751757 | |||||||
chr11:3751759 | T | A | 1 | a0001c0001t0001g0224 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1267+1557A>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3751759 | |||||||
chr11:3751760 | G | C | 1 | a0001c0001t0001g0224 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1267+1556C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3751760 | |||||||
chr11:3751762 | G | A | 1 | a0001c0001t0001g0224 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1267+1554C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3751762 | |||||||
chr11:3751763 | G | T | 1 | a0001c0001t0001g0224 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1267+1553C>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3751763 | |||||||
chr11:3751764 | T | A | 1 | a0001c0001t0001g0224 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1267+1552A>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3751764 | |||||||
chr11:3751766 | G | C | 1 | a0001c0001t0001g0224 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1267+1550C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3751766 | |||||||
chr11:3751767 | G | A | 1 | a0001c0001t0001g0224 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1267+1549C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3751767 | |||||||
chr11:3751769 | G | A | 1 | a0001c0001t0001g0224 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1267+1547C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3751769 | |||||||
chr11:3751774 | G | C | 1 | a0001c0001t0001g0224 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1267+1542C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3751774 | |||||||
chr11:3751777 | T | G | 1 | a0001c0001t0001g0224 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1267+1539A>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3751777 | |||||||
chr11:3751780 | G | A | 1 | a0001c0001t0001g0224 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1267+1536C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3751780 | |||||||
chr11:3751786 | G | A | 1 | a0001c0001t0001g0224 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1267+1530C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3751786 | |||||||
chr11:3751788 | G | C | 1 | a0001c0001t0001g0224 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1267+1528C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3751788 | |||||||
chr11:3751789 | G | C | 1 | a0001c0001t0001g0224 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1267+1527C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3751789 | |||||||
chr11:3751790 | T | C | 1 | a0001c0001t0001g0224 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1267+1526A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3751790 | |||||||
chr11:3751792 | G | A | 1 | a0001c0001t0001g0224 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1267+1524C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3751792 | |||||||
chr11:3751794 | G | T | 1 | a0001c0001t0001g0224 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1267+1522C>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3751794 | |||||||
chr11:3751797 | T | A | 1 | a0001c0001t0001g0224 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1267+1519A>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3751797 | |||||||
chr11:3751798 | G | T | 1 | a0001c0001t0001g0224 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1267+1518C>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3751798 | |||||||
chr11:3751801 | G | A | 1 | a0001c0001t0001g0224 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1267+1515C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3751801 | |||||||
chr11:3751805 | G | A | 1 | a0001c0001t0001g0224 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1267+1511C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3751805 | |||||||
chr11:3751813 | C | T | 1 | a0001c0001t0001g0224 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1267+1503G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3751813 | |||||||
chr11:3751815 | T | A | 1 | a0001c0001t0001g0224 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1267+1501A>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3751815 | |||||||
chr11:3751817 | C | A | 1 | a0001c0001t0001g0224 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1267+1499G>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3751817 | |||||||
chr11:3751818 | C | A | 1 | a0001c0001t0001g0224 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1267+1498G>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3751818 | |||||||
chr11:3751896 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1267+1420C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3751896 | |||||||
chr11:3751974 | G | A | 71 | a0001c0001t0001g0076 a0001c0001t0001g0078 a0001c0001t0001g0081 others(68): Show |
71 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.1267+1342C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3751974 | |||||||
chr11:3751996 | G | T | 14 | a0001c0001t0001g0068 a0001c0001t0001g0324 a0001c0001t0001g0336 others(11): Show |
14 | HG00642.hp1 HG01081.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.1267+1320C>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3751996 | |||||||
chr11:3752044 | C | T | 1 | a0001c0002t0001g0269 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1267+1272G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3752044 | |||||||
chr11:3752245 | C | T | 1 | a0001c0002t0001g0123 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1267+1071G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3752245 | |||||||
chr11:3752345 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1267+971G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3752345 | |||||||
chr11:3752518 | A | AAAAT | 90 | a0001c0001t0001g0028 a0001c0001t0001g0042 a0001c0001t0001g0044 others(87): Show |
90 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.1267+794_1267+797d others(6): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3752518 | |||||||
chr11:3752518 | A | AAAATAAA others(1): Show |
4 | a0001c0001t0001g0076 a0001c0002t0001g0091 a0009c0011t0001g0071 others(1): Show |
4 | HG02683.hp1 HG03490.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.1267+790_1267+797d others(10): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3752518 | |||||||
chr11:3752518 | A | T | 2 | a0001c0012t0001g0319 a0001c0012t0001g0320 |
2 | HG02109.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1267+798T>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3752518 | |||||||
chr11:3752568 | T | C | 2 | a0001c0001t0001g0044 a0001c0001t0001g0045 |
2 | HG02615.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1267+748A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3752568 | |||||||
chr11:3752746 | A | G | 1 | a0004c0007t0001g0246 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1267+570T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3752746 | |||||||
chr11:3752748 | A | G | 1 | a0001c0002t0001g0016 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1267+568T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3752748 | |||||||
chr11:3752907 | T | C | 2 | a0001c0016t0001g0114 a0001c0032t0001g0032 |
2 | HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1267+409A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3752907 | |||||||
chr11:3753179 | G | A | 2 | a0001c0001t0001g0148 a0001c0001t0001g0166 |
2 | HG02055.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.1267+137C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3753179 | |||||||
chr11:3753269 | A | C | 1 | a0001c0001t0001g0081 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1267+47T>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 11/32 | chr11 | 3753269 | |||||||
chr11:3753701 | A | G | 1 | a0001c0001t0002g0309 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1175-293T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3753701 | |||||||
chr11:3753740 | G | A | 1 | a0001c0001t0001g0248 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1175-332C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3753740 | |||||||
chr11:3753755 | C | CA | 53 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0109 others(50): Show |
53 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.1175-348dupT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3753755 | |||||||
chr11:3753755 | C | CAA | 31 | a0001c0001t0001g0006 a0001c0001t0001g0110 a0001c0001t0001g0135 others(28): Show |
31 | HG00423.hp2 HG01109.hp2 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.1175-349_1175-348d others(4): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3753755 | |||||||
chr11:3753755 | C | CAAA | 16 | a0001c0001t0001g0028 a0001c0001t0001g0036 a0001c0001t0001g0138 others(13): Show |
16 | HG01934.hp2 HG01952.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.1175-350_1175-348d others(5): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3753755 | |||||||
chr11:3753755 | CAAAAA | C | 37 | a0001c0001t0001g0049 a0001c0001t0001g0068 a0001c0001t0001g0081 others(34): Show |
37 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(34): Show |
intron_variant | MODIFIER | c.1175-352_1175-348d others(7): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3753755 | |||||||
chr11:3753755 | CAAAAAA | C | 80 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0038 others(77): Show |
80 | HG00558.hp2 HG00741.hp1 HG01081.hp1 others(77): Show |
intron_variant | MODIFIER | c.1175-353_1175-348d others(8): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3753755 | |||||||
chr11:3753755 | CAAAAAAA | C | 58 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0041 others(55): Show |
58 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.1175-354_1175-348d others(9): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3753755 | |||||||
chr11:3753755 | CAAAAAAA others(4): Show |
C | 2 | a0001c0012t0001g0319 a0001c0012t0001g0320 |
2 | HG02109.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1175-358_1175-348d others(13): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3753755 | |||||||
chr11:3753755 | CAAAAAAA others(7): Show |
C | 1 | a0001c0001t0001g0152 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1175-361_1175-348d others(16): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3753755 | |||||||
chr11:3753755 | CAAAAAAA others(13): Show |
C | 1 | a0017c0019t0001g0222 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1175-367_1175-348d others(22): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3753755 | |||||||
chr11:3753821 | C | T | 1 | a0001c0001t0001g0306 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1175-413G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3753821 | |||||||
chr11:3753885 | G | T | 1 | a0001c0001t0001g0151 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1175-477C>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3753885 | |||||||
chr11:3753980 | G | A | 1 | a0005c0010t0001g0339 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1175-572C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3753980 | |||||||
chr11:3754167 | G | T | 1 | a0001c0002t0001g0315 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1175-759C>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3754167 | |||||||
chr11:3754399 | A | G | 1 | a0002c0008t0001g0003 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1175-991T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3754399 | |||||||
chr11:3754559 | A | G | 8 | a0001c0001t0001g0068 a0001c0001t0001g0324 a0001c0001t0001g0336 others(5): Show |
8 | HG00642.hp1 HG02109.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1175-1151T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3754559 | |||||||
chr11:3754757 | C | A | 5 | a0001c0001t0001g0191 a0001c0001t0001g0195 a0001c0001t0001g0196 others(2): Show |
5 | NA18950.hp2 NA18952.hp1 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.1175-1349G>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3754757 | |||||||
chr11:3754941 | C | CA | 175 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0038 others(172): Show |
175 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(172): Show |
intron_variant | MODIFIER | c.1175-1534dupT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3754941 | |||||||
chr11:3754941 | C | CAA | 13 | a0001c0001t0001g0026 a0001c0001t0001g0067 a0001c0001t0001g0183 others(10): Show |
13 | HG02135.hp1 HG02257.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.1175-1535_1175-153 others(6): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3754941 | |||||||
chr11:3754941 | CA | C | 8 | a0001c0001t0001g0113 a0001c0001t0001g0150 a0001c0001t0001g0181 others(5): Show |
8 | HG00558.hp1 HG01168.hp2 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.1175-1534delT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3754941 | |||||||
chr11:3754968 | A | G | 203 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0030 others(200): Show |
203 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(200): Show |
intron_variant | MODIFIER | c.1175-1560T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3754968 | |||||||
chr11:3754975 | TCAAA | T | 7 | a0001c0016t0001g0114 a0002c0005t0001g0299 a0002c0005t0001g0300 others(4): Show |
7 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.1175-1571_1175-156 others(8): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3754975 | |||||||
chr11:3754996 | T | C | 2 | a0001c0001t0001g0029 a0001c0001t0001g0328 |
2 | HG02280.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1175-1588A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3754996 | |||||||
chr11:3755101 | C | A | 2 | a0001c0012t0001g0319 a0001c0012t0001g0320 |
2 | HG02109.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1175-1693G>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3755101 | |||||||
chr11:3755141 | C | T | 193 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0030 others(190): Show |
193 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(190): Show |
intron_variant | MODIFIER | c.1175-1733G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3755141 | |||||||
chr11:3755234 | T | C | 1 | a0001c0002t0001g0008 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1175-1826A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3755234 | |||||||
chr11:3755261 | G | C | 1 | a0005c0010t0001g0339 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1175-1853C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3755261 | |||||||
chr11:3755298 | G | GA | 90 | a0001c0001t0001g0042 a0001c0001t0001g0044 a0001c0001t0001g0045 others(87): Show |
90 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.1175-1891dupT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3755298 | |||||||
chr11:3755313 | A | T | 1 | a0001c0001t0001g0232 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1175-1905T>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3755313 | |||||||
chr11:3755337 | G | A | 6 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.1175-1929C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3755337 | |||||||
chr11:3755440 | G | A | 1 | a0001c0001t0001g0039 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1175-2032C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3755440 | |||||||
chr11:3755570 | G | A | 2 | a0001c0002t0001g0193 a0001c0002t0001g0211 |
2 | HG02559.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1175-2162C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3755570 | |||||||
chr11:3755788 | C | G | 6 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.1175-2380G>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3755788 | |||||||
chr11:3755820 | C | T | 41 | a0001c0001t0001g0029 a0001c0001t0001g0038 a0001c0001t0001g0039 others(38): Show |
41 | HG00408.hp2 HG00609.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.1175-2412G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3755820 | |||||||
chr11:3755838 | CCTATAAT others(5): Show |
C | 6 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.1175-2442_1175-243 others(16): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3755838 | |||||||
chr11:3755876 | C | G | 40 | a0001c0001t0001g0029 a0001c0001t0001g0038 a0001c0001t0001g0039 others(37): Show |
40 | HG00408.hp2 HG00609.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.1175-2468G>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3755876 | |||||||
chr11:3755919 | C | T | 6 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.1175-2511G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3755919 | |||||||
chr11:3755978 | A | G | 7 | a0001c0002t0001g0010 a0001c0002t0001g0011 a0001c0002t0001g0012 others(4): Show |
7 | NA18942.hp1 NA18947.hp1 NA18964.hp2 others(4): Show |
intron_variant | MODIFIER | c.1175-2570T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3755978 | |||||||
chr11:3756039 | T | C | 22 | a0001c0001t0001g0026 a0001c0002t0001g0007 a0001c0002t0001g0008 others(19): Show |
22 | HG00597.hp1 HG01993.hp1 HG03239.hp1 others(19): Show |
intron_variant | MODIFIER | c.1175-2631A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3756039 | |||||||
chr11:3756091 | G | A | 1 | a0001c0001t0001g0335 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1175-2683C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3756091 | |||||||
chr11:3756274 | T | C | 1 | a0001c0001t0001g0337 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1175-2866A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3756274 | |||||||
chr11:3756288 | T | C | 3 | a0001c0001t0001g0138 a0001c0001t0001g0159 a0001c0001t0001g0161 |
3 | NA18983.hp1 NA18998.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.1175-2880A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3756288 | |||||||
chr11:3756498 | C | T | 2 | a0001c0001t0001g0078 a0001c0002t0001g0094 |
2 | HG01167.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.1175-3090G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3756498 | |||||||
chr11:3756577 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1175-3169G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3756577 | |||||||
chr11:3756605 | T | C | 48 | a0001c0001t0001g0029 a0001c0001t0001g0038 a0001c0001t0001g0039 others(45): Show |
48 | HG00408.hp2 HG00609.hp2 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.1175-3197A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3756605 | |||||||
chr11:3756798 | A | T | 1 | a0001c0001t0001g0163 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1175-3390T>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3756798 | |||||||
chr11:3756803 | G | A | 14 | a0001c0001t0001g0068 a0001c0001t0001g0324 a0001c0001t0001g0336 others(11): Show |
14 | HG00642.hp1 HG01081.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.1175-3395C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3756803 | |||||||
chr11:3756846 | G | A | 1 | a0001c0001t0001g0335 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1175-3438C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3756846 | |||||||
chr11:3756880 | G | A | 2 | a0001c0012t0001g0319 a0001c0012t0001g0320 |
2 | HG02109.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1175-3472C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3756880 | |||||||
chr11:3756915 | G | A | 1 | a0001c0003t0002g0311 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1175-3507C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3756915 | |||||||
chr11:3757020 | G | A | 1 | a0001c0001t0001g0036 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1174+3519C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3757020 | |||||||
chr11:3757081 | C | A | 77 | a0001c0001t0001g0076 a0001c0001t0001g0078 a0001c0001t0001g0081 others(74): Show |
77 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.1174+3458G>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3757081 | |||||||
chr11:3757094 | A | T | 8 | a0001c0001t0001g0038 a0001c0001t0001g0043 a0001c0001t0001g0061 others(5): Show |
8 | HG00738.hp2 HG01106.hp2 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.1174+3445T>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3757094 | |||||||
chr11:3757096 | A | T | 178 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0030 others(175): Show |
178 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(175): Show |
intron_variant | MODIFIER | c.1174+3443T>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3757096 | |||||||
chr11:3757103 | A | C | 17 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(14): Show |
17 | HG00408.hp2 HG00609.hp2 HG00642.hp1 others(14): Show |
intron_variant | MODIFIER | c.1174+3436T>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3757103 | |||||||
chr11:3757105 | A | C | 1 | a0001c0001t0001g0307 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1174+3434T>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3757105 | |||||||
chr11:3757139 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1174+3400C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3757139 | |||||||
chr11:3757139 | G | GTA | 203 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0030 others(200): Show |
203 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(200): Show |
intron_variant | MODIFIER | c.1174+3398_1174+339 others(6): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3757139 | |||||||
chr11:3757139 | G | GTATA | 3 | a0001c0001t0001g0068 a0001c0001t0001g0307 a0001c0001t0001g0335 |
3 | HG01433.hp2 HG02965.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1174+3396_1174+339 others(8): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3757139 | |||||||
chr11:3757171 | T | C | 2 | a0001c0012t0001g0319 a0001c0012t0001g0320 |
2 | HG02109.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1174+3368A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3757171 | |||||||
chr11:3757202 | T | C | 49 | a0001c0001t0001g0029 a0001c0001t0001g0038 a0001c0001t0001g0039 others(46): Show |
49 | HG00408.hp2 HG00609.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.1174+3337A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3757202 | |||||||
chr11:3757205 | C | T | 1 | a0001c0002t0001g0315 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1174+3334G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3757205 | |||||||
chr11:3757549 | A | C | 5 | a0001c0001t0002g0314 a0001c0001t0002g0317 a0003c0004t0001g0316 others(2): Show |
5 | HG00639.hp2 HG01943.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1174+2990T>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3757549 | |||||||
chr11:3757615 | A | G | 49 | a0001c0001t0001g0029 a0001c0001t0001g0038 a0001c0001t0001g0039 others(46): Show |
49 | HG00408.hp2 HG00609.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.1174+2924T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3757615 | |||||||
chr11:3757653 | G | A | 1 | a0001c0001t0001g0307 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1174+2886C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3757653 | |||||||
chr11:3757732 | G | T | 2 | a0001c0001t0001g0068 a0001c0001t0001g0336 |
2 | HG02965.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1174+2807C>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3757732 | |||||||
chr11:3757756 | G | A | 1 | a0001c0002t0001g0315 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1174+2783C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3757756 | |||||||
chr11:3757815 | AAATAATA others(13): Show |
A | 2 | a0001c0012t0001g0319 a0001c0012t0001g0320 |
2 | HG02109.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1174+2704_1174+272 others(24): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3757815 | |||||||
chr11:3757837 | T | C | 3 | a0001c0002t0001g0073 a0001c0002t0001g0088 a0001c0002t0001g0104 |
3 | HG02922.hp2 HG03209.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1174+2702A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3757837 | |||||||
chr11:3757838 | G | A | 4 | a0001c0001t0001g0324 a0001c0001t0008g0325 a0005c0010t0001g0338 others(1): Show |
4 | HG00642.hp1 HG02559.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1174+2701C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3757838 | |||||||
chr11:3758099 | T | C | 1 | a0001c0001t0001g0067 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1174+2440A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3758099 | |||||||
chr11:3758292 | G | A | 1 | a0001c0002t0001g0024 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1174+2247C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3758292 | |||||||
chr11:3758308 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1174+2231C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3758308 | |||||||
chr11:3758315 | C | T | 6 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.1174+2224G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3758315 | |||||||
chr11:3758320 | CA | C | 14 | a0001c0001t0001g0068 a0001c0001t0001g0324 a0001c0001t0001g0336 others(11): Show |
14 | HG00642.hp1 HG01081.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.1174+2218delT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3758320 | |||||||
chr11:3758385 | A | T | 6 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.1174+2154T>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3758385 | |||||||
chr11:3758452 | C | T | 187 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0030 others(184): Show |
187 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.1174+2087G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3758452 | |||||||
chr11:3758551 | G | A | 11 | a0001c0001t0001g0082 a0001c0001t0001g0085 a0001c0002t0001g0077 others(8): Show |
11 | HG02056.hp2 HG02080.hp1 HG02129.hp2 others(8): Show |
intron_variant | MODIFIER | c.1174+1988C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3758551 | |||||||
chr11:3758720 | G | A | 1 | a0001c0001t0001g0336 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1174+1819C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3758720 | |||||||
chr11:3758791 | GAGAGAC | G | 3 | a0001c0012t0001g0319 a0001c0012t0001g0320 a0001c0032t0001g0032 |
3 | HG02109.hp1 HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1174+1742_1174+174 others(10): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3758791 | |||||||
chr11:3758864 | A | G | 8 | a0001c0001t0001g0291 a0001c0001t0001g0293 a0001c0001t0001g0296 others(5): Show |
8 | HG01243.hp1 HG02109.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1174+1675T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3758864 | |||||||
chr11:3759113 | T | C | 1 | a0001c0001t0001g0145 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1174+1426A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3759113 | |||||||
chr11:3759153 | G | A | 1 | a0001c0001t0001g0335 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1174+1386C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3759153 | |||||||
chr11:3759163 | G | C | 6 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.1174+1376C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3759163 | |||||||
chr11:3759216 | A | G | 1 | a0001c0002t0001g0131 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1174+1323T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3759216 | |||||||
chr11:3759332 | C | T | 1 | a0001c0002t0001g0267 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1174+1207G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3759332 | |||||||
chr11:3759457 | C | A | 1 | a0001c0016t0001g0114 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1174+1082G>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3759457 | |||||||
chr11:3759511 | C | T | 15 | a0001c0001t0001g0112 a0001c0001t0001g0136 a0001c0001t0001g0138 others(12): Show |
15 | HG00438.hp1 HG00609.hp1 HG02027.hp1 others(12): Show |
intron_variant | MODIFIER | c.1174+1028G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3759511 | |||||||
chr11:3759680 | T | A | 1 | a0001c0001t0001g0217 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1174+859A>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3759680 | |||||||
chr11:3759782 | AC | A | 6 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.1174+756delG | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3759782 | |||||||
chr11:3759799 | C | T | 1 | a0001c0001t0001g0307 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1174+740G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3759799 | |||||||
chr11:3759896 | T | G | 2 | a0001c0001t0001g0026 a0001c0002t0001g0016 |
2 | HG03491.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1174+643A>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3759896 | |||||||
chr11:3760107 | T | G | 42 | a0001c0001t0001g0029 a0001c0001t0001g0038 a0001c0001t0001g0039 others(39): Show |
42 | HG00408.hp2 HG00609.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.1174+432A>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3760107 | |||||||
chr11:3760112 | C | CA | 72 | a0001c0001t0001g0006 a0001c0001t0001g0026 a0001c0001t0001g0030 others(69): Show |
72 | HG00438.hp2 HG00597.hp1 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.1174+426dupT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3760112 | |||||||
chr11:3760112 | CA | C | 41 | a0001c0001t0001g0029 a0001c0001t0001g0038 a0001c0001t0001g0039 others(38): Show |
41 | HG00408.hp2 HG00609.hp2 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.1174+426delT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3760112 | |||||||
chr11:3760112 | CAAA | C | 10 | a0001c0001t0001g0068 a0001c0001t0001g0336 a0001c0012t0001g0319 others(7): Show |
10 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.1174+424_1174+426d others(5): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3760112 | |||||||
chr11:3760124 | A | C | 3 | a0001c0002t0001g0069 a0001c0002t0001g0095 a0020c0018t0001g0099 |
3 | NA18983.hp2 NA18984.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.1174+415T>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3760124 | |||||||
chr11:3760125 | A | C | 1 | a0001c0002t0001g0100 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1174+414T>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3760125 | |||||||
chr11:3760129 | A | C | 1 | a0001c0001t0001g0067 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1174+410T>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3760129 | |||||||
chr11:3760130 | C | A | 1 | a0001c0001t0001g0067 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1174+409G>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3760130 | |||||||
chr11:3760131 | A | C | 2 | a0001c0001t0001g0067 a0001c0001t0001g0335 |
2 | HG01433.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1174+408T>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3760131 | |||||||
chr11:3760230 | T | C | 1 | a0001c0002t0001g0315 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1174+309A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3760230 | |||||||
chr11:3760681 | C | T | 5 | a0001c0001t0002g0314 a0001c0001t0002g0317 a0003c0004t0001g0316 others(2): Show |
5 | HG00639.hp2 HG01943.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1087-55G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 9/32 | chr11 | 3760681 | |||||||
chr11:3760886 | A | G | 4 | a0001c0001t0001g0247 a0001c0001t0001g0248 a0001c0001t0001g0249 others(1): Show |
4 | HG00639.hp1 HG00733.hp1 HG00735.hp2 others(1): Show |
intron_variant | MODIFIER | c.1087-260T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 9/32 | chr11 | 3760886 | |||||||
chr11:3761074 | C | T | 8 | a0001c0001t0001g0307 a0001c0003t0002g0290 a0001c0003t0002g0311 others(5): Show |
8 | HG01109.hp2 HG02055.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.1087-448G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 9/32 | chr11 | 3761074 | |||||||
chr11:3761203 | T | C | 1 | a0001c0002t0001g0124 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1087-577A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 9/32 | chr11 | 3761203 | |||||||
chr11:3761229 | T | C | 1 | a0001c0001t0001g0004 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1087-603A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 9/32 | chr11 | 3761229 | |||||||
chr11:3761254 | A | C | 2 | a0001c0001t0001g0333 a0001c0001t0001g0334 |
2 | HG02145.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1087-628T>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 9/32 | chr11 | 3761254 | |||||||
chr11:3761452 | C | A | 1 | a0001c0001t0001g0197 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1087-826G>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 9/32 | chr11 | 3761452 | |||||||
chr11:3761518 | C | T | 54 | a0001c0001t0001g0026 a0001c0001t0001g0030 a0001c0001t0001g0031 others(51): Show |
54 | HG00597.hp1 HG00639.hp2 HG01243.hp2 others(51): Show |
intron_variant | MODIFIER | c.1087-892G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 9/32 | chr11 | 3761518 | |||||||
chr11:3761542 | G | A | 1 | a0001c0002t0001g0009 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1087-916C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 9/32 | chr11 | 3761542 | |||||||
chr11:3761566 | T | C | 3 | a0001c0001t0001g0029 a0001c0001t0001g0184 a0001c0001t0001g0328 |
3 | HG02280.hp2 HG02630.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1087-940A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 9/32 | chr11 | 3761566 | |||||||
chr11:3761619 | C | T | 6 | a0001c0001t0001g0068 a0001c0001t0001g0324 a0001c0001t0001g0336 others(3): Show |
6 | HG00642.hp1 HG02559.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1087-993G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 9/32 | chr11 | 3761619 | |||||||
chr11:3761652 | G | A | 2 | a0001c0001t0001g0068 a0001c0001t0001g0336 |
2 | HG02965.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1087-1026C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 9/32 | chr11 | 3761652 | |||||||
chr11:3761706 | C | T | 2 | a0015c0033t0001g0130 a0018c0034t0001g0122 |
2 | HG02630.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1087-1080G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 9/32 | chr11 | 3761706 | |||||||
chr11:3761726 | C | T | 1 | a0001c0001t0001g0229 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1087-1100G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 9/32 | chr11 | 3761726 | |||||||
chr11:3761745 | C | A | 1 | a0001c0001t0002g0309 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1087-1119G>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 9/32 | chr11 | 3761745 | |||||||
chr11:3761771 | CAAAACAA others(5): Show |
C | 8 | a0001c0001t0001g0068 a0001c0001t0001g0324 a0001c0001t0001g0336 others(5): Show |
8 | HG00642.hp1 HG02109.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1086+1119_1086+113 others(16): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 9/32 | chr11 | 3761771 | |||||||
chr11:3761879 | G | A | 6 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.1086+1023C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 9/32 | chr11 | 3761879 | |||||||
chr11:3761949 | C | A | 1 | a0012c0022t0001g0128 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1086+953G>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 9/32 | chr11 | 3761949 | |||||||
chr11:3761975 | G | A | 6 | a0001c0001t0001g0068 a0001c0001t0001g0324 a0001c0001t0001g0336 others(3): Show |
6 | HG00642.hp1 HG02559.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1086+927C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 9/32 | chr11 | 3761975 | |||||||
chr11:3762279 | G | GT | 16 | a0001c0001t0001g0067 a0001c0001t0001g0139 a0001c0001t0001g0143 others(13): Show |
16 | HG00597.hp1 HG00735.hp2 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.1086+622dupA | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 9/32 | chr11 | 3762279 | |||||||
chr11:3762279 | GT | G | 6 | a0001c0001t0001g0250 a0001c0001t0001g0333 a0001c0001t0001g0334 others(3): Show |
6 | HG02145.hp1 HG02647.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1086+622delA | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 9/32 | chr11 | 3762279 | |||||||
chr11:3762282 | T | G | 77 | a0001c0001t0001g0076 a0001c0001t0001g0078 a0001c0001t0001g0081 others(74): Show |
77 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.1086+620A>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 9/32 | chr11 | 3762282 | |||||||
chr11:3762526 | C | T | 1 | a0001c0001t0001g0337 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1086+376G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 9/32 | chr11 | 3762526 | |||||||
chr11:3762611 | T | C | 1 | a0001c0001t0001g0159 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1086+291A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 9/32 | chr11 | 3762611 | |||||||
chr11:3762751 | A | G | 3 | a0001c0001t0001g0333 a0001c0001t0001g0334 a0001c0001t0006g0297 |
3 | HG02145.hp1 HG02257.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1086+151T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 9/32 | chr11 | 3762751 | |||||||
chr11:3762821 | A | G | 1 | a0001c0001t0001g0241 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1086+81T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 9/32 | chr11 | 3762821 | |||||||
chr11:3762869 | A | G | 1 | a0001c0002t0001g0017 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1086+33T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 9/32 | chr11 | 3762869 | |||||||
chr11:3763114 | A | T | 2 | a0001c0006t0001g0204 a0001c0006t0001g0242 |
2 | HG00741.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.949-75T>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 8/32 | chr11 | 3763114 | |||||||
chr11:3763181 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.949-142G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 8/32 | chr11 | 3763181 | |||||||
chr11:3763217 | A | G | 1 | a0001c0001t0001g0307 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.949-178T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 8/32 | chr11 | 3763217 | |||||||
chr11:3763264 | A | C | 1 | a0001c0001t0001g0006 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.949-225T>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 8/32 | chr11 | 3763264 | |||||||
chr11:3763265 | A | G | 14 | a0001c0001t0001g0068 a0001c0001t0001g0324 a0001c0001t0001g0336 others(11): Show |
14 | HG00642.hp1 HG01081.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.949-226T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 8/32 | chr11 | 3763265 | |||||||
chr11:3763326 | C | G | 2 | a0001c0012t0001g0319 a0001c0012t0001g0320 |
2 | HG02109.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.949-287G>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 8/32 | chr11 | 3763326 | |||||||
chr11:3763402 | G | A | 6 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.949-363C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 8/32 | chr11 | 3763402 | |||||||
chr11:3763419 | C | A | 4 | a0001c0001t0001g0324 a0001c0001t0008g0325 a0005c0010t0001g0338 others(1): Show |
4 | HG00642.hp1 HG02559.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.949-380G>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 8/32 | chr11 | 3763419 | |||||||
chr11:3763661 | G | A | 41 | a0001c0001t0001g0029 a0001c0001t0001g0038 a0001c0001t0001g0039 others(38): Show |
41 | HG00408.hp2 HG00609.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.949-622C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 8/32 | chr11 | 3763661 | |||||||
chr11:3763794 | T | C | 14 | a0001c0001t0001g0068 a0001c0001t0001g0324 a0001c0001t0001g0336 others(11): Show |
14 | HG00642.hp1 HG01081.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.949-755A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 8/32 | chr11 | 3763794 | |||||||
chr11:3764021 | T | C | 2 | a0001c0006t0001g0126 a0001c0006t0001g0127 |
2 | HG02896.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.949-982A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 8/32 | chr11 | 3764021 | |||||||
chr11:3764088 | C | G | 1 | a0001c0016t0001g0114 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.949-1049G>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 8/32 | chr11 | 3764088 | |||||||
chr11:3764090 | C | G | 2 | a0001c0001t0001g0308 a0016c0023t0001g0001 |
2 | HG01346.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.949-1051G>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 8/32 | chr11 | 3764090 | |||||||
chr11:3764158 | A | AT | 29 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0041 others(26): Show |
29 | HG00408.hp2 HG00544.hp2 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.949-1120dupA | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 8/32 | chr11 | 3764158 | |||||||
chr11:3764191 | G | A | 1 | a0001c0002t0001g0016 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.949-1152C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 8/32 | chr11 | 3764191 | |||||||
chr11:3764368 | T | C | 1 | a0001c0001t0001g0307 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.949-1329A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 8/32 | chr11 | 3764368 | |||||||
chr11:3764672 | G | A | 7 | a0001c0001t0001g0335 a0002c0005t0001g0299 a0002c0005t0001g0300 others(4): Show |
7 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.949-1633C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 8/32 | chr11 | 3764672 | |||||||
chr11:3764699 | C | G | 3 | a0001c0001t0001g0194 a0001c0001t0001g0206 a0001c0001t0001g0250 |
3 | NA18960.hp1 NA19055.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.949-1660G>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 8/32 | chr11 | 3764699 | |||||||
chr11:3764769 | G | A | 2 | a0001c0001t0001g0333 a0001c0001t0001g0334 |
2 | HG02145.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.949-1730C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 8/32 | chr11 | 3764769 | |||||||
chr11:3764830 | G | A | 1 | a0001c0002t0001g0212 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.949-1791C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 8/32 | chr11 | 3764830 | |||||||
chr11:3764862 | G | A | 2 | a0001c0001t0001g0068 a0001c0001t0001g0336 |
2 | HG02965.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.949-1823C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 8/32 | chr11 | 3764862 | |||||||
chr11:3764876 | C | T | 6 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.949-1837G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 8/32 | chr11 | 3764876 | |||||||
chr11:3764919 | T | C | 2 | a0001c0001t0001g0333 a0001c0001t0001g0334 |
2 | HG02145.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.949-1880A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 8/32 | chr11 | 3764919 | |||||||
chr11:3764988 | A | C | 1 | a0001c0001t0001g0059 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.949-1949T>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 8/32 | chr11 | 3764988 | |||||||
chr11:3765157 | G | C | 1 | a0001c0001t0001g0337 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.949-2118C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 8/32 | chr11 | 3765157 | |||||||
chr11:3765267 | T | C | 1 | a0001c0032t0001g0032 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.949-2228A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 8/32 | chr11 | 3765267 | |||||||
chr11:3765317 | C | T | 2 | a0001c0001t0001g0234 a0001c0001t0001g0235 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.949-2278G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 8/32 | chr11 | 3765317 | |||||||
chr11:3765399 | C | G | 1 | a0001c0002t0001g0092 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.949-2360G>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 8/32 | chr11 | 3765399 | |||||||
chr11:3765405 | T | C | 1 | a0001c0001t0001g0307 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.949-2366A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 8/32 | chr11 | 3765405 | |||||||
chr11:3765459 | G | C | 1 | a0001c0016t0001g0114 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.949-2420C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 8/32 | chr11 | 3765459 | |||||||
chr11:3765575 | G | A | 2 | a0001c0001t0001g0324 a0001c0001t0008g0325 |
2 | HG00642.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.949-2536C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 8/32 | chr11 | 3765575 | |||||||
chr11:3765575 | G | C | 1 | a0001c0002t0001g0124 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.949-2536C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 8/32 | chr11 | 3765575 | |||||||
chr11:3765616 | A | G | 1 | a0001c0001t0001g0335 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.949-2577T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 8/32 | chr11 | 3765616 | |||||||
chr11:3765763 | T | C | 1 | a0001c0002t0001g0270 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.949-2724A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 8/32 | chr11 | 3765763 | |||||||
chr11:3765801 | C | CA | 108 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0031 others(105): Show |
108 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(105): Show |
intron_variant | MODIFIER | c.949-2763dupT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 8/32 | chr11 | 3765801 | |||||||
chr11:3765801 | C | CAA | 12 | a0001c0001t0001g0047 a0001c0001t0001g0067 a0001c0001t0001g0140 others(9): Show |
12 | HG00408.hp1 HG00642.hp1 HG01515.hp1 others(9): Show |
intron_variant | MODIFIER | c.949-2764_949-2763d others(4): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 8/32 | chr11 | 3765801 | |||||||
chr11:3765801 | C | CAAA | 10 | a0001c0001t0001g0068 a0001c0012t0001g0319 a0001c0012t0001g0320 others(7): Show |
10 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.949-2765_949-2763d others(5): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 8/32 | chr11 | 3765801 | |||||||
chr11:3765801 | CA | C | 8 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0191 others(5): Show |
8 | HG01515.hp2 HG02735.hp1 HG02735.hp2 others(5): Show |
intron_variant | MODIFIER | c.949-2763delT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 8/32 | chr11 | 3765801 | |||||||
chr11:3765805 | A | G | 76 | a0001c0001t0001g0076 a0001c0001t0001g0078 a0001c0001t0001g0081 others(73): Show |
76 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.949-2766T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 8/32 | chr11 | 3765805 | |||||||
chr11:3766004 | C | CTCACTT | 3 | a0001c0002t0001g0192 a0001c0002t0001g0193 a0001c0002t0001g0211 |
3 | HG02559.hp2 HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.948+2571_948+2576d others(8): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 8/32 | chr11 | 3766004 | |||||||
chr11:3766099 | G | C | 6 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.948+2482C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 8/32 | chr11 | 3766099 | |||||||
chr11:3766114 | C | T | 1 | a0001c0001t0001g0179 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.948+2467G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 8/32 | chr11 | 3766114 | |||||||
chr11:3766153 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.948+2428A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 8/32 | chr11 | 3766153 | |||||||
chr11:3766230 | C | G | 1 | a0001c0003t0002g0312 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.948+2351G>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 8/32 | chr11 | 3766230 | |||||||
chr11:3766380 | T | A | 5 | a0001c0001t0001g0121 a0001c0001t0001g0129 a0006c0009t0001g0033 others(2): Show |
5 | HG02615.hp1 HG02818.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.948+2201A>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 8/32 | chr11 | 3766380 | |||||||
chr11:3766485 | T | C | 2 | a0001c0001t0001g0225 a0001c0001t0001g0226 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.948+2096A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 8/32 | chr11 | 3766485 | |||||||
chr11:3766596 | G | A | 7 | a0001c0003t0002g0290 a0001c0003t0002g0311 a0001c0003t0002g0312 others(4): Show |
7 | HG01109.hp2 HG02055.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.948+1985C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 8/32 | chr11 | 3766596 | |||||||
chr11:3766685 | G | A | 1 | a0001c0016t0001g0114 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.948+1896C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 8/32 | chr11 | 3766685 | |||||||
chr11:3766689 | C | CA | 31 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0067 others(28): Show |
31 | HG00733.hp2 HG01109.hp2 HG01258.hp2 others(28): Show |
intron_variant | MODIFIER | c.948+1891dupT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 8/32 | chr11 | 3766689 | |||||||
chr11:3766689 | CA | C | 9 | a0001c0001t0001g0206 a0001c0001t0001g0209 a0001c0001t0001g0235 others(6): Show |
9 | HG01099.hp2 HG01169.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.948+1891delT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 8/32 | chr11 | 3766689 | |||||||
chr11:3766689 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0163 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.948+1882_948+1891d others(12): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 8/32 | chr11 | 3766689 | |||||||
chr11:3766786 | T | C | 6 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0305 others(3): Show |
6 | HG01099.hp2 HG01884.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.948+1795A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 8/32 | chr11 | 3766786 | |||||||
chr11:3766800 | A | C | 1 | a0001c0001t0001g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.948+1781T>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 8/32 | chr11 | 3766800 | |||||||
chr11:3767019 | C | T | 1 | a0001c0002t0001g0212 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.948+1562G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 8/32 | chr11 | 3767019 | |||||||
chr11:3767092 | G | A | 1 | a0001c0001t0001g0255 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.948+1489C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 8/32 | chr11 | 3767092 | |||||||
chr11:3767097 | T | C | 6 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.948+1484A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 8/32 | chr11 | 3767097 | |||||||
chr11:3767203 | C | T | 1 | a0001c0001t0001g0307 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.948+1378G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 8/32 | chr11 | 3767203 | |||||||
chr11:3767334 | T | A | 1 | a0001c0001t0001g0146 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.948+1247A>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 8/32 | chr11 | 3767334 | |||||||
chr11:3767415 | C | T | 172 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0030 others(169): Show |
172 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(169): Show |
intron_variant | MODIFIER | c.948+1166G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 8/32 | chr11 | 3767415 | |||||||
chr11:3767445 | C | T | 1 | a0001c0001t0001g0217 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.948+1136G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 8/32 | chr11 | 3767445 | |||||||
chr11:3767499 | G | A | 1 | a0001c0002t0001g0092 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.948+1082C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 8/32 | chr11 | 3767499 | |||||||
chr11:3767828 | A | C | 5 | a0001c0001t0002g0314 a0001c0001t0002g0317 a0003c0004t0001g0316 others(2): Show |
5 | HG00639.hp2 HG01943.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.948+753T>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 8/32 | chr11 | 3767828 | |||||||
chr11:3767830 | C | A | 1 | a0001c0001t0001g0250 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.948+751G>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 8/32 | chr11 | 3767830 | |||||||
chr11:3767867 | G | C | 14 | a0001c0001t0001g0068 a0001c0001t0001g0324 a0001c0001t0001g0336 others(11): Show |
14 | HG00642.hp1 HG01081.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.948+714C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 8/32 | chr11 | 3767867 | |||||||
chr11:3767976 | T | C | 6 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.948+605A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 8/32 | chr11 | 3767976 | |||||||
chr11:3768094 | G | A | 1 | a0001c0002t0001g0103 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.948+487C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 8/32 | chr11 | 3768094 | |||||||
chr11:3768095 | C | A | 7 | a0001c0003t0002g0290 a0001c0003t0002g0311 a0001c0003t0002g0312 others(4): Show |
7 | HG01109.hp2 HG02055.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.948+486G>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 8/32 | chr11 | 3768095 | |||||||
chr11:3768139 | T | C | 323 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(320): Show |
323 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(320): Show |
intron_variant | MODIFIER | c.948+442A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 8/32 | chr11 | 3768139 | |||||||
chr11:3768149 | C | T | 1 | a0001c0001t0001g0307 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.948+432G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 8/32 | chr11 | 3768149 | |||||||
chr11:3768204 | G | A | 131 | a0001c0001t0001g0026 a0001c0001t0001g0030 a0001c0001t0001g0031 others(128): Show |
131 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.948+377C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 8/32 | chr11 | 3768204 | |||||||
chr11:3768314 | G | A | 6 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.948+267C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 8/32 | chr11 | 3768314 | |||||||
chr11:3768334 | T | C | 1 | a0001c0001t0001g0170 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.948+247A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 8/32 | chr11 | 3768334 | |||||||
chr11:3768351 | G | A | 1 | a0001c0002t0001g0080 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.948+230C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 8/32 | chr11 | 3768351 | |||||||
chr11:3768382 | C | A | 131 | a0001c0001t0001g0026 a0001c0001t0001g0030 a0001c0001t0001g0031 others(128): Show |
131 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.948+199G>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 8/32 | chr11 | 3768382 | |||||||
chr11:3768420 | C | CA | 12 | a0001c0001t0001g0026 a0001c0001t0001g0039 a0001c0001t0001g0068 others(9): Show |
12 | HG02074.hp1 HG02615.hp1 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.948+160dupT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 8/32 | chr11 | 3768420 | |||||||
chr11:3768752 | GAAAAAGA others(4): Show |
G | 131 | a0001c0001t0001g0026 a0001c0001t0001g0030 a0001c0001t0001g0031 others(128): Show |
131 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.785-19_785-9delTTT others(8): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 7/32 | chr11 | 3768752 | |||||||
chr11:3768926 | A | C | 1 | a0019c0015t0001g0283 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.785-182T>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 7/32 | chr11 | 3768926 | |||||||
chr11:3769365 | G | GCGGGGAG others(14): Show |
1 | a0001c0002t0001g0105 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.785-642_785-622dup others(21): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 7/32 | chr11 | 3769365 | |||||||
chr11:3769515 | G | T | 1 | a0001c0001t0001g0250 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.785-771C>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 7/32 | chr11 | 3769515 | |||||||
chr11:3769575 | C | CA | 28 | a0001c0001t0001g0113 a0001c0001t0001g0138 a0001c0001t0001g0198 others(25): Show |
28 | HG02132.hp2 HG02486.hp1 HG02486.hp2 others(25): Show |
intron_variant | MODIFIER | c.785-832dupT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 7/32 | chr11 | 3769575 | |||||||
chr11:3769575 | CA | C | 63 | a0001c0001t0001g0029 a0001c0001t0001g0038 a0001c0001t0001g0039 others(60): Show |
63 | HG00408.hp2 HG00609.hp2 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.785-832delT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 7/32 | chr11 | 3769575 | |||||||
chr11:3769577 | A | C | 1 | a0001c0001t0001g0307 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.785-833T>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 7/32 | chr11 | 3769577 | |||||||
chr11:3769597 | A | G | 2 | a0001c0001t0001g0239 a0001c0001t0001g0307 |
2 | HG03453.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.785-853T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 7/32 | chr11 | 3769597 | |||||||
chr11:3769675 | G | A | 1 | a0001c0001t0001g0307 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.785-931C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 7/32 | chr11 | 3769675 | |||||||
chr11:3769675 | G | T | 2 | a0015c0033t0001g0130 a0018c0034t0001g0122 |
2 | HG02630.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.785-931C>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 7/32 | chr11 | 3769675 | |||||||
chr11:3769744 | CTAAAAAT | C | 4 | a0001c0001t0001g0247 a0001c0001t0001g0248 a0001c0001t0001g0249 others(1): Show |
4 | HG00639.hp1 HG00733.hp1 HG00735.hp2 others(1): Show |
intron_variant | MODIFIER | c.785-1007_785-1001d others(9): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 7/32 | chr11 | 3769744 | |||||||
chr11:3769752 | T | C | 131 | a0001c0001t0001g0026 a0001c0001t0001g0030 a0001c0001t0001g0031 others(128): Show |
131 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.785-1008A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 7/32 | chr11 | 3769752 | |||||||
chr11:3769800 | T | C | 1 | a0001c0001t0001g0038 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.785-1056A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 7/32 | chr11 | 3769800 | |||||||
chr11:3769843 | A | G | 1 | a0001c0032t0001g0032 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.785-1099T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 7/32 | chr11 | 3769843 | |||||||
chr11:3769903 | G | T | 2 | a0001c0001t0001g0324 a0001c0001t0008g0325 |
2 | HG00642.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.785-1159C>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 7/32 | chr11 | 3769903 | |||||||
chr11:3770026 | G | A | 1 | a0001c0001t0001g0275 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.785-1282C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 7/32 | chr11 | 3770026 | |||||||
chr11:3770030 | G | A | 6 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.785-1286C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 7/32 | chr11 | 3770030 | |||||||
chr11:3770042 | C | CA | 177 | a0001c0001t0001g0006 a0001c0001t0001g0026 a0001c0001t0001g0029 others(174): Show |
177 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(174): Show |
intron_variant | MODIFIER | c.785-1299dupT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 7/32 | chr11 | 3770042 | |||||||
chr11:3770042 | C | CAA | 8 | a0001c0001t0001g0333 a0001c0001t0001g0334 a0001c0002t0001g0093 others(5): Show |
8 | HG00597.hp2 HG02109.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.785-1300_785-1299d others(4): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 7/32 | chr11 | 3770042 | |||||||
chr11:3770107 | G | A | 3 | a0001c0001t0001g0337 a0001c0001t0004g0330 a0001c0001t0004g0331 |
3 | HG02647.hp2 HG02717.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.785-1363C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 7/32 | chr11 | 3770107 | |||||||
chr11:3770144 | AGACCAGC others(3): Show |
A | 1 | a0001c0026t0001g0298 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.785-1410_785-1401d others(12): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 7/32 | chr11 | 3770144 | |||||||
chr11:3770156 | C | G | 1 | a0001c0026t0001g0298 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.785-1412G>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 7/32 | chr11 | 3770156 | |||||||
chr11:3770331 | AT | A | 4 | a0001c0002t0001g0276 a0001c0002t0001g0277 a0001c0002t0001g0282 others(1): Show |
4 | HG00544.hp1 HG03831.hp2 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.784+1416delA | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 7/32 | chr11 | 3770331 | |||||||
chr11:3770363 | T | C | 1 | a0001c0001t0001g0060 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.784+1385A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 7/32 | chr11 | 3770363 | |||||||
chr11:3770367 | T | C | 1 | a0001c0001t0001g0179 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.784+1381A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 7/32 | chr11 | 3770367 | |||||||
chr11:3770486 | CAAGAA | C | 81 | a0001c0001t0001g0076 a0001c0001t0001g0078 a0001c0001t0001g0081 others(78): Show |
81 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.784+1257_784+1261d others(7): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 7/32 | chr11 | 3770486 | |||||||
chr11:3770547 | T | TTG | 40 | a0001c0001t0001g0005 a0001c0001t0001g0081 a0001c0001t0001g0113 others(37): Show |
40 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(37): Show |
intron_variant | MODIFIER | c.784+1199_784+1200d others(4): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 7/32 | chr11 | 3770547 | |||||||
chr11:3770547 | T | TTGTG | 11 | a0001c0001t0001g0004 a0001c0001t0001g0140 a0001c0003t0002g0290 others(8): Show |
11 | HG00408.hp1 HG01109.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.784+1197_784+1200d others(6): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 7/32 | chr11 | 3770547 | |||||||
chr11:3770547 | TTG | T | 5 | a0001c0002t0001g0279 a0001c0002t0001g0280 a0001c0002t0001g0326 others(2): Show |
5 | NA18980.hp1 NA18990.hp1 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.784+1199_784+1200d others(4): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 7/32 | chr11 | 3770547 | |||||||
chr11:3770547 | TTGTG | T | 39 | a0001c0001t0001g0029 a0001c0001t0001g0038 a0001c0001t0001g0039 others(36): Show |
39 | HG00408.hp2 HG00609.hp2 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.784+1197_784+1200d others(6): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 7/32 | chr11 | 3770547 | |||||||
chr11:3770547 | TTGTGTGT others(3): Show |
T | 1 | a0001c0002t0001g0315 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.784+1191_784+1200d others(12): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 7/32 | chr11 | 3770547 | |||||||
chr11:3770575 | A | G | 50 | a0001c0001t0001g0112 a0001c0001t0001g0135 a0001c0001t0001g0136 others(47): Show |
50 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.784+1173T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 7/32 | chr11 | 3770575 | |||||||
chr11:3770607 | A | C | 1 | a0001c0002t0001g0093 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.784+1141T>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 7/32 | chr11 | 3770607 | |||||||
chr11:3770704 | G | A | 5 | a0001c0002t0001g0279 a0001c0002t0001g0280 a0001c0002t0001g0326 others(2): Show |
5 | NA18980.hp1 NA18990.hp1 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.784+1044C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 7/32 | chr11 | 3770704 | |||||||
chr11:3770809 | G | A | 1 | a0002c0005t0001g0302 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.784+939C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 7/32 | chr11 | 3770809 | |||||||
chr11:3770972 | C | G | 2 | a0001c0001t0001g0237 a0011c0025t0001g0236 |
2 | HG01081.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.784+776G>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 7/32 | chr11 | 3770972 | |||||||
chr11:3771016 | C | T | 8 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0110 others(5): Show |
8 | HG00558.hp2 HG01192.hp1 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.784+732G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 7/32 | chr11 | 3771016 | |||||||
chr11:3771049 | G | T | 1 | a0001c0002t0001g0102 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.784+699C>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 7/32 | chr11 | 3771049 | |||||||
chr11:3771142 | C | T | 2 | a0001c0001t0001g0324 a0001c0001t0008g0325 |
2 | HG00642.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.784+606G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 7/32 | chr11 | 3771142 | |||||||
chr11:3771198 | T | A | 2 | a0001c0012t0001g0319 a0001c0012t0001g0320 |
2 | HG02109.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.784+550A>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 7/32 | chr11 | 3771198 | |||||||
chr11:3771209 | T | C | 1 | a0001c0001t0001g0335 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.784+539A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 7/32 | chr11 | 3771209 | |||||||
chr11:3771217 | T | C | 1 | a0001c0001t0001g0179 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.784+531A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 7/32 | chr11 | 3771217 | |||||||
chr11:3771261 | G | C | 1 | a0001c0032t0001g0032 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.784+487C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 7/32 | chr11 | 3771261 | |||||||
chr11:3771427 | G | T | 56 | a0001c0001t0001g0026 a0001c0001t0001g0030 a0001c0001t0001g0031 others(53): Show |
56 | HG00597.hp1 HG00639.hp2 HG01243.hp2 others(53): Show |
intron_variant | MODIFIER | c.784+321C>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 7/32 | chr11 | 3771427 | |||||||
chr11:3771436 | C | CA | 4 | a0001c0002t0001g0007 a0001c0002t0001g0018 a0001c0002t0001g0019 others(1): Show |
4 | NA18612.hp2 NA18965.hp1 NA19081.hp1 others(1): Show |
intron_variant | MODIFIER | c.784+311dupT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 7/32 | chr11 | 3771436 | |||||||
chr11:3771461 | T | C | 144 | a0001c0001t0001g0026 a0001c0001t0001g0030 a0001c0001t0001g0031 others(141): Show |
144 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(141): Show |
intron_variant | MODIFIER | c.784+287A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 7/32 | chr11 | 3771461 | |||||||
chr11:3771641 | T | C | 1 | a0001c0001t0001g0183 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.784+107A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 7/32 | chr11 | 3771641 | |||||||
chr11:3771661 | T | G | 3 | a0001c0001t0001g0180 a0001c0001t0001g0182 a0001c0001t0001g0214 |
3 | NA18990.hp2 NA18999.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.784+87A>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 7/32 | chr11 | 3771661 | |||||||
chr11:3771932 | A | T | 1 | a0001c0002t0001g0187 | 1 | HG00621.hp1 | splice_region_variant&intron_variant | LOW | c.604-4T>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 6/32 | chr11 | 3771932 | |||||||
chr11:3771979 | TTATTTAG others(15): Show |
T | 1 | a0001c0001t0001g0234 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.604-73_604-52delCA others(20): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 6/32 | chr11 | 3771979 | |||||||
chr11:3772170 | C | A | 3 | a0001c0001t0001g0337 a0001c0001t0004g0330 a0001c0001t0004g0331 |
3 | HG02647.hp2 HG02717.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.604-242G>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 6/32 | chr11 | 3772170 | |||||||
chr11:3772365 | A | T | 1 | a0005c0010t0001g0338 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.604-437T>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 6/32 | chr11 | 3772365 | |||||||
chr11:3772545 | C | T | 1 | a0001c0001t0001g0307 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.604-617G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 6/32 | chr11 | 3772545 | |||||||
chr11:3772593 | G | A | 72 | a0001c0001t0001g0076 a0001c0001t0001g0078 a0001c0001t0001g0081 others(69): Show |
72 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.604-665C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 6/32 | chr11 | 3772593 | |||||||
chr11:3772684 | G | A | 2 | a0001c0001t0001g0237 a0011c0025t0001g0236 |
2 | HG01081.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.604-756C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 6/32 | chr11 | 3772684 | |||||||
chr11:3772812 | C | CA | 142 | a0001c0001t0001g0026 a0001c0001t0001g0030 a0001c0001t0001g0031 others(139): Show |
142 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(139): Show |
intron_variant | MODIFIER | c.603+819dupT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 6/32 | chr11 | 3772812 | |||||||
chr11:3772812 | C | CAA | 52 | a0001c0001t0001g0029 a0001c0001t0001g0038 a0001c0001t0001g0039 others(49): Show |
52 | HG00408.hp2 HG00609.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.603+818_603+819dup others(2): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 6/32 | chr11 | 3772812 | |||||||
chr11:3772829 | T | A | 1 | a0001c0001t0001g0234 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.603+803A>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 6/32 | chr11 | 3772829 | |||||||
chr11:3772843 | T | C | 1 | a0001c0002t0001g0102 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.603+789A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 6/32 | chr11 | 3772843 | |||||||
chr11:3772882 | G | A | 6 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.603+750C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 6/32 | chr11 | 3772882 | |||||||
chr11:3773009 | C | A | 2 | a0001c0001t0001g0068 a0001c0001t0001g0336 |
2 | HG02965.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.603+623G>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 6/32 | chr11 | 3773009 | |||||||
chr11:3773205 | C | A | 2 | a0001c0001t0001g0068 a0001c0001t0001g0336 |
2 | HG02965.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.603+427G>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 6/32 | chr11 | 3773205 | |||||||
chr11:3773348 | T | C | 1 | a0001c0001t0001g0219 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.603+284A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 6/32 | chr11 | 3773348 | |||||||
chr11:3773504 | A | G | 1 | a0001c0002t0001g0098 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.603+128T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 6/32 | chr11 | 3773504 | |||||||
chr11:3773541 | C | G | 1 | a0001c0002t0001g0167 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.603+91G>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 6/32 | chr11 | 3773541 | |||||||
chr11:3773954 | C | A | 1 | a0001c0002t0001g0318 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.496-215G>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 5/32 | chr11 | 3773954 | |||||||
chr11:3774005 | T | C | 2 | a0001c0001t0001g0026 a0001c0002t0001g0016 |
2 | HG03491.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.496-266A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 5/32 | chr11 | 3774005 | |||||||
chr11:3774085 | C | T | 1 | a0001c0001t0001g0214 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.496-346G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 5/32 | chr11 | 3774085 | |||||||
chr11:3774086 | G | A | 1 | a0001c0001t0001g0337 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.496-347C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 5/32 | chr11 | 3774086 | |||||||
chr11:3774224 | C | G | 72 | a0001c0001t0001g0076 a0001c0001t0001g0078 a0001c0001t0001g0081 others(69): Show |
72 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.496-485G>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 5/32 | chr11 | 3774224 | |||||||
chr11:3774227 | G | A | 128 | a0001c0001t0001g0026 a0001c0001t0001g0030 a0001c0001t0001g0031 others(125): Show |
128 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.496-488C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 5/32 | chr11 | 3774227 | |||||||
chr11:3774234 | CTAAAAAA others(8): Show |
C | 1 | a0001c0001t0001g0038 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.496-510_496-496del others(15): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 5/32 | chr11 | 3774234 | |||||||
chr11:3774326 | C | T | 1 | a0001c0032t0001g0032 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.496-587G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 5/32 | chr11 | 3774326 | |||||||
chr11:3774327 | G | A | 2 | a0001c0001t0001g0308 a0016c0023t0001g0001 |
2 | HG01346.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.496-588C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 5/32 | chr11 | 3774327 | |||||||
chr11:3774335 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.496-596G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 5/32 | chr11 | 3774335 | |||||||
chr11:3774491 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.496-752C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 5/32 | chr11 | 3774491 | |||||||
chr11:3774654 | T | G | 5 | a0001c0001t0002g0314 a0001c0001t0002g0317 a0003c0004t0001g0316 others(2): Show |
5 | HG00639.hp2 HG01943.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.496-915A>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 5/32 | chr11 | 3774654 | |||||||
chr11:3774681 | C | T | 2 | a0001c0002t0001g0178 a0001c0002t0001g0212 |
2 | HG02257.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.496-942G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 5/32 | chr11 | 3774681 | |||||||
chr11:3774928 | A | C | 6 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.495+954T>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 5/32 | chr11 | 3774928 | |||||||
chr11:3774928 | A | T | 1 | a0001c0001t0001g0113 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.495+954T>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 5/32 | chr11 | 3774928 | |||||||
chr11:3775025 | A | G | 1 | a0001c0002t0001g0123 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.495+857T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 5/32 | chr11 | 3775025 | |||||||
chr11:3775176 | G | A | 7 | a0001c0003t0002g0290 a0001c0003t0002g0311 a0001c0003t0002g0312 others(4): Show |
7 | HG01109.hp2 HG02055.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.495+706C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 5/32 | chr11 | 3775176 | |||||||
chr11:3775176 | G | T | 183 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0030 others(180): Show |
183 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.495+706C>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 5/32 | chr11 | 3775176 | |||||||
chr11:3775253 | G | C | 1 | a0001c0026t0001g0298 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.495+629C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 5/32 | chr11 | 3775253 | |||||||
chr11:3775360 | T | A | 1 | a0001c0001t0001g0307 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.495+522A>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 5/32 | chr11 | 3775360 | |||||||
chr11:3775406 | G | A | 1 | a0001c0001t0001g0181 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.495+476C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 5/32 | chr11 | 3775406 | |||||||
chr11:3775436 | G | A | 6 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.495+446C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 5/32 | chr11 | 3775436 | |||||||
chr11:3775477 | A | G | 1 | a0008c0028t0001g0147 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.495+405T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 5/32 | chr11 | 3775477 | |||||||
chr11:3775550 | A | ACC | 4 | a0001c0001t0001g0324 a0001c0001t0008g0325 a0005c0010t0001g0338 others(1): Show |
4 | HG00642.hp1 HG02559.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.495+331_495+332ins others(2): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 5/32 | chr11 | 3775550 | |||||||
chr11:3775552 | C | A | 4 | a0001c0001t0001g0324 a0001c0001t0008g0325 a0005c0010t0001g0338 others(1): Show |
4 | HG00642.hp1 HG02559.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.495+330G>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 5/32 | chr11 | 3775552 | |||||||
chr11:3775552 | C | CA | 18 | a0001c0001t0001g0082 a0001c0001t0001g0085 a0001c0001t0001g0137 others(15): Show |
18 | HG01168.hp2 HG02056.hp2 HG02080.hp1 others(15): Show |
intron_variant | MODIFIER | c.495+329dupT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 5/32 | chr11 | 3775552 | |||||||
chr11:3775552 | CA | C | 9 | a0001c0003t0002g0290 a0001c0003t0002g0311 a0001c0003t0002g0312 others(6): Show |
9 | HG01109.hp2 HG02055.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.495+329delT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 5/32 | chr11 | 3775552 | |||||||
chr11:3775555 | A | C | 1 | a0001c0016t0001g0114 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.495+327T>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 5/32 | chr11 | 3775555 | |||||||
chr11:3775606 | C | A | 1 | a0001c0001t0001g0332 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.495+276G>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 5/32 | chr11 | 3775606 | |||||||
chr11:3775629 | C | T | 1 | a0001c0002t0001g0261 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.495+253G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 5/32 | chr11 | 3775629 | |||||||
chr11:3775666 | A | T | 1 | a0001c0001t0001g0234 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.495+216T>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 5/32 | chr11 | 3775666 | |||||||
chr11:3775687 | A | AT | 6 | a0001c0001t0001g0068 a0001c0001t0001g0324 a0001c0001t0001g0336 others(3): Show |
6 | HG00642.hp1 HG02559.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.495+194dupA | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 5/32 | chr11 | 3775687 | |||||||
chr11:3775696 | G | A | 141 | a0001c0001t0001g0026 a0001c0001t0001g0030 a0001c0001t0001g0031 others(138): Show |
141 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(138): Show |
intron_variant | MODIFIER | c.495+186C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 5/32 | chr11 | 3775696 | |||||||
chr11:3775702 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.495+180A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 5/32 | chr11 | 3775702 | |||||||
chr11:3775835 | T | C | 6 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.495+47A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 5/32 | chr11 | 3775835 | |||||||
chr11:3775876 | A | G | 1 | a0001c0001t0001g0163 | 1 | HG02165.hp2 | splice_region_variant&intron_variant | LOW | c.495+6T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 5/32 | chr11 | 3775876 | |||||||
chr11:3776100 | G | A | 1 | a0001c0001t0001g0335 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.356-79C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 4/32 | chr11 | 3776100 | |||||||
chr11:3776121 | A | AT | 20 | a0001c0001t0001g0036 a0001c0001t0001g0067 a0001c0001t0001g0068 others(17): Show |
20 | HG00642.hp1 HG00741.hp1 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.356-101dupA | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 4/32 | chr11 | 3776121 | |||||||
chr11:3776121 | A | ATT | 114 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0078 others(111): Show |
114 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.356-102_356-101dup others(2): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 4/32 | chr11 | 3776121 | |||||||
chr11:3776121 | A | ATTT | 11 | a0001c0001t0001g0026 a0001c0001t0001g0076 a0001c0002t0001g0011 others(8): Show |
11 | HG02572.hp1 HG02683.hp1 HG03209.hp2 others(8): Show |
intron_variant | MODIFIER | c.356-103_356-101dup others(3): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 4/32 | chr11 | 3776121 | |||||||
chr11:3776334 | G | A | 141 | a0001c0001t0001g0026 a0001c0001t0001g0030 a0001c0001t0001g0031 others(138): Show |
141 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(138): Show |
intron_variant | MODIFIER | c.356-313C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 4/32 | chr11 | 3776334 | |||||||
chr11:3776443 | C | T | 322 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(319): Show |
322 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(319): Show |
intron_variant | MODIFIER | c.356-422G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 4/32 | chr11 | 3776443 | |||||||
chr11:3776486 | C | CT | 6 | a0001c0001t0001g0112 a0001c0001t0001g0165 a0001c0001t0001g0183 others(3): Show |
6 | HG03098.hp1 HG03704.hp2 NA18974.hp2 others(3): Show |
intron_variant | MODIFIER | c.356-466dupA | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 4/32 | chr11 | 3776486 | |||||||
chr11:3776486 | CT | C | 128 | a0001c0001t0001g0026 a0001c0001t0001g0030 a0001c0001t0001g0031 others(125): Show |
128 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.356-466delA | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 4/32 | chr11 | 3776486 | |||||||
chr11:3776508 | G | T | 1 | a0001c0001t0001g0307 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.356-487C>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 4/32 | chr11 | 3776508 | |||||||
chr11:3776566 | C | T | 51 | a0001c0001t0001g0026 a0001c0001t0001g0030 a0001c0001t0001g0031 others(48): Show |
51 | HG00597.hp1 HG00639.hp2 HG01243.hp2 others(48): Show |
intron_variant | MODIFIER | c.356-545G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 4/32 | chr11 | 3776566 | |||||||
chr11:3776633 | C | T | 2 | a0001c0012t0001g0319 a0001c0012t0001g0320 |
2 | HG02109.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.356-612G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 4/32 | chr11 | 3776633 | |||||||
chr11:3776728 | A | G | 187 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0030 others(184): Show |
187 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.356-707T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 4/32 | chr11 | 3776728 | |||||||
chr11:3776788 | G | A | 127 | a0001c0001t0001g0026 a0001c0001t0001g0030 a0001c0001t0001g0031 others(124): Show |
127 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.356-767C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 4/32 | chr11 | 3776788 | |||||||
chr11:3776816 | T | C | 5 | a0001c0001t0001g0028 a0001c0001t0001g0186 a0001c0001t0001g0190 others(2): Show |
5 | HG01258.hp2 HG02132.hp2 NA18952.hp2 others(2): Show |
intron_variant | MODIFIER | c.356-795A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 4/32 | chr11 | 3776816 | |||||||
chr11:3776818 | C | T | 3 | a0001c0001t0001g0333 a0001c0001t0001g0334 a0001c0001t0006g0297 |
3 | HG02145.hp1 HG02257.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.356-797G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 4/32 | chr11 | 3776818 | |||||||
chr11:3776837 | C | G | 6 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.356-816G>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 4/32 | chr11 | 3776837 | |||||||
chr11:3776871 | A | C | 1 | a0001c0001t0001g0335 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.356-850T>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 4/32 | chr11 | 3776871 | |||||||
chr11:3777065 | T | C | 1 | a0001c0001t0001g0335 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.356-1044A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 4/32 | chr11 | 3777065 | |||||||
chr11:3777130 | G | C | 8 | a0001c0001t0002g0314 a0001c0001t0002g0317 a0001c0002t0001g0074 others(5): Show |
8 | HG00639.hp2 HG01943.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.356-1109C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 4/32 | chr11 | 3777130 | |||||||
chr11:3777152 | C | G | 1 | a0001c0001t0001g0335 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.356-1131G>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 4/32 | chr11 | 3777152 | |||||||
chr11:3777152 | C | T | 2 | a0005c0010t0001g0338 a0005c0010t0001g0339 |
2 | HG02559.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.356-1131G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 4/32 | chr11 | 3777152 | |||||||
chr11:3777433 | C | T | 6 | a0001c0001t0001g0068 a0001c0001t0001g0324 a0001c0001t0001g0336 others(3): Show |
6 | HG00642.hp1 HG02559.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.356-1412G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 4/32 | chr11 | 3777433 | |||||||
chr11:3777546 | G | A | 1 | a0001c0002t0001g0103 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.355+1327C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 4/32 | chr11 | 3777546 | |||||||
chr11:3777620 | C | CA | 69 | a0001c0001t0001g0006 a0001c0001t0001g0029 a0001c0001t0001g0038 others(66): Show |
69 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.355+1252dupT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 4/32 | chr11 | 3777620 | |||||||
chr11:3777620 | CA | C | 10 | a0001c0001t0001g0068 a0001c0001t0001g0111 a0001c0001t0001g0121 others(7): Show |
10 | HG01081.hp1 HG01192.hp1 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.355+1252delT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 4/32 | chr11 | 3777620 | |||||||
chr11:3777803 | A | G | 1 | a0001c0001t0001g0220 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.355+1070T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 4/32 | chr11 | 3777803 | |||||||
chr11:3777810 | C | T | 15 | a0001c0001t0001g0068 a0001c0001t0001g0324 a0001c0001t0001g0336 others(12): Show |
15 | HG00642.hp1 HG01081.hp1 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.355+1063G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 4/32 | chr11 | 3777810 | |||||||
chr11:3777908 | C | A | 1 | a0001c0001t0001g0217 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.355+965G>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 4/32 | chr11 | 3777908 | |||||||
chr11:3777926 | C | T | 6 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.355+947G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 4/32 | chr11 | 3777926 | |||||||
chr11:3777981 | G | A | 1 | a0001c0002t0001g0023 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.355+892C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 4/32 | chr11 | 3777981 | |||||||
chr11:3777994 | C | T | 1 | a0001c0016t0001g0114 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.355+879G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 4/32 | chr11 | 3777994 | |||||||
chr11:3778014 | T | C | 1 | a0001c0032t0001g0032 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.355+859A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 4/32 | chr11 | 3778014 | |||||||
chr11:3778057 | G | A | 1 | a0001c0001t0001g0336 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.355+816C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 4/32 | chr11 | 3778057 | |||||||
chr11:3778198 | C | CA | 75 | a0001c0001t0001g0076 a0001c0001t0001g0078 a0001c0001t0001g0081 others(72): Show |
75 | HG00323.hp2 HG00438.hp2 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.355+674dupT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 4/32 | chr11 | 3778198 | |||||||
chr11:3778198 | C | CAA | 15 | a0001c0001t0001g0337 a0001c0001t0004g0330 a0001c0001t0004g0331 others(12): Show |
15 | HG00423.hp1 HG00738.hp1 HG02056.hp2 others(12): Show |
intron_variant | MODIFIER | c.355+673_355+674dup others(2): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 4/32 | chr11 | 3778198 | |||||||
chr11:3778198 | CA | C | 29 | a0001c0001t0001g0029 a0001c0001t0001g0051 a0001c0001t0001g0052 others(26): Show |
29 | HG00609.hp2 HG01081.hp1 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.355+674delT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 4/32 | chr11 | 3778198 | |||||||
chr11:3778198 | CAAAAAAA others(5): Show |
C | 5 | a0001c0002t0001g0262 a0001c0002t0001g0264 a0001c0002t0001g0265 others(2): Show |
5 | NA18955.hp1 NA18957.hp1 NA19002.hp2 others(2): Show |
intron_variant | MODIFIER | c.355+663_355+674del others(12): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 4/32 | chr11 | 3778198 | |||||||
chr11:3778217 | A | G | 2 | a0001c0001t0001g0068 a0001c0001t0001g0336 |
2 | HG02965.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.355+656T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 4/32 | chr11 | 3778217 | |||||||
chr11:3778276 | G | A | 1 | a0001c0001t0001g0181 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.355+597C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 4/32 | chr11 | 3778276 | |||||||
chr11:3778287 | C | A | 1 | a0001c0001t0001g0140 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.355+586G>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 4/32 | chr11 | 3778287 | |||||||
chr11:3778297 | C | T | 1 | a0001c0001t0001g0307 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.355+576G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 4/32 | chr11 | 3778297 | |||||||
chr11:3778342 | G | A | 3 | a0001c0012t0001g0319 a0001c0012t0001g0320 a0016c0023t0001g0001 |
3 | HG02109.hp1 HG02809.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.355+531C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 4/32 | chr11 | 3778342 | |||||||
chr11:3778432 | A | G | 6 | a0001c0001t0001g0068 a0001c0001t0001g0324 a0001c0001t0001g0336 others(3): Show |
6 | HG00642.hp1 HG02559.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.355+441T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 4/32 | chr11 | 3778432 | |||||||
chr11:3778522 | T | C | 1 | a0001c0001t0006g0297 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.355+351A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 4/32 | chr11 | 3778522 | |||||||
chr11:3778533 | G | A | 15 | a0001c0001t0001g0068 a0001c0001t0001g0324 a0001c0001t0001g0336 others(12): Show |
15 | HG00642.hp1 HG01081.hp1 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.355+340C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 4/32 | chr11 | 3778533 | |||||||
chr11:3778691 | C | T | 1 | a0001c0001t0001g0278 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.355+182G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 4/32 | chr11 | 3778691 | |||||||
chr11:3778709 | A | G | 1 | a0004c0007t0001g0216 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.355+164T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 4/32 | chr11 | 3778709 | |||||||
chr11:3778755 | G | A | 196 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0030 others(193): Show |
196 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(193): Show |
intron_variant | MODIFIER | c.355+118C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 4/32 | chr11 | 3778755 | |||||||
chr11:3778799 | AACGGAGA others(9): Show |
A | 1 | a0013c0029t0001g0134 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.355+58_355+73delGT others(14): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 4/32 | chr11 | 3778799 | |||||||
chr11:3778822 | A | G | 3 | a0001c0012t0001g0319 a0001c0012t0001g0320 a0016c0023t0001g0001 |
3 | HG02109.hp1 HG02809.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.355+51T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 4/32 | chr11 | 3778822 | |||||||
chr11:3778866 | C | T | 15 | a0001c0001t0001g0068 a0001c0001t0001g0324 a0001c0001t0001g0336 others(12): Show |
15 | HG00642.hp1 HG01081.hp1 HG01167.hp1 others(12): Show |
splice_region_variant&intron_variant | LOW | c.355+7G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 4/32 | chr11 | 3778866 | |||||||
chr11:3779056 | A | C | 7 | a0001c0002t0001g0007 a0001c0002t0001g0018 a0001c0002t0001g0019 others(4): Show |
7 | HG00597.hp1 NA18612.hp2 NA18950.hp1 others(4): Show |
splice_region_variant&intron_variant | LOW | c.179-7T>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 3/32 | chr11 | 3779056 | |||||||
chr11:3779379 | C | T | 1 | a0001c0001t0001g0335 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.77-122G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 2/32 | chr11 | 3779379 | |||||||
chr11:3779380 | G | A | 1 | a0001c0001t0001g0029 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.77-123C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 2/32 | chr11 | 3779380 | |||||||
chr11:3779411 | G | A | 3 | a0001c0012t0001g0319 a0001c0012t0001g0320 a0016c0023t0001g0001 |
3 | HG02109.hp1 HG02809.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.77-154C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 2/32 | chr11 | 3779411 | |||||||
chr11:3779432 | G | A | 1 | a0001c0002t0001g0288 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.77-175C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 2/32 | chr11 | 3779432 | |||||||
chr11:3779531 | C | G | 1 | a0001c0001t0001g0308 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.77-274G>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 2/32 | chr11 | 3779531 | |||||||
chr11:3779578 | T | G | 1 | a0019c0015t0001g0283 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.77-321A>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 2/32 | chr11 | 3779578 | |||||||
chr11:3779589 | C | T | 10 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0121 others(7): Show |
10 | HG01884.hp1 HG01891.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.77-332G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 2/32 | chr11 | 3779589 | |||||||
chr11:3779607 | C | T | 6 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.77-350G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 2/32 | chr11 | 3779607 | |||||||
chr11:3779635 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.77-378G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 2/32 | chr11 | 3779635 | |||||||
chr11:3779641 | CA | C | 322 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(319): Show |
322 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(319): Show |
intron_variant | MODIFIER | c.77-385delT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 2/32 | chr11 | 3779641 | |||||||
chr11:3779641 | CAA | C | 17 | a0001c0001t0001g0068 a0001c0001t0001g0165 a0001c0001t0001g0291 others(14): Show |
17 | HG00642.hp1 HG01081.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.77-386_77-385delTT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 2/32 | chr11 | 3779641 | |||||||
chr11:3779647 | A | G | 1 | a0019c0015t0001g0283 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.77-390T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 2/32 | chr11 | 3779647 | |||||||
chr11:3779789 | A | T | 1 | a0019c0015t0001g0283 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.77-532T>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 2/32 | chr11 | 3779789 | |||||||
chr11:3779794 | G | A | 2 | a0001c0001t0001g0068 a0001c0001t0001g0336 |
2 | HG02965.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.77-537C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 2/32 | chr11 | 3779794 | |||||||
chr11:3779901 | G | A | 6 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.77-644C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 2/32 | chr11 | 3779901 | |||||||
chr11:3779997 | G | C | 1 | a0001c0001t0001g0307 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.77-740C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 2/32 | chr11 | 3779997 | |||||||
chr11:3780028 | A | T | 1 | a0005c0010t0001g0338 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.77-771T>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 2/32 | chr11 | 3780028 | |||||||
chr11:3780122 | C | T | 15 | a0001c0001t0001g0068 a0001c0001t0001g0324 a0001c0001t0001g0336 others(12): Show |
15 | HG00642.hp1 HG01081.hp1 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.77-865G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 2/32 | chr11 | 3780122 | |||||||
chr11:3780189 | G | T | 38 | a0001c0001t0001g0029 a0001c0001t0001g0038 a0001c0001t0001g0039 others(35): Show |
38 | HG00408.hp2 HG00609.hp2 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.77-932C>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 2/32 | chr11 | 3780189 | |||||||
chr11:3780235 | T | A | 3 | a0001c0012t0001g0319 a0001c0012t0001g0320 a0016c0023t0001g0001 |
3 | HG02109.hp1 HG02809.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.77-978A>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 2/32 | chr11 | 3780235 | |||||||
chr11:3780246 | G | A | 3 | a0001c0012t0001g0319 a0001c0012t0001g0320 a0016c0023t0001g0001 |
3 | HG02109.hp1 HG02809.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.77-989C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 2/32 | chr11 | 3780246 | |||||||
chr11:3780373 | A | AC | 8 | a0001c0001t0001g0109 a0001c0002t0001g0019 a0001c0002t0001g0087 others(5): Show |
8 | HG02109.hp1 HG02129.hp2 HG02148.hp2 others(5): Show |
intron_variant | MODIFIER | c.77-1117_77-1116ins others(1): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 2/32 | chr11 | 3780373 | |||||||
chr11:3780374 | A | C | 185 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0030 others(182): Show |
185 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.77-1117T>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 2/32 | chr11 | 3780374 | |||||||
chr11:3780377 | A | T | 1 | a0001c0001t0001g0145 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.77-1120T>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 2/32 | chr11 | 3780377 | |||||||
chr11:3780413 | G | A | 2 | a0001c0001t0001g0044 a0001c0001t0001g0045 |
2 | HG02615.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.77-1156C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 2/32 | chr11 | 3780413 | |||||||
chr11:3780437 | G | T | 3 | a0001c0012t0001g0319 a0001c0012t0001g0320 a0016c0023t0001g0001 |
3 | HG02109.hp1 HG02809.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.77-1180C>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 2/32 | chr11 | 3780437 | |||||||
chr11:3780473 | C | T | 1 | a0001c0016t0001g0114 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.77-1216G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 2/32 | chr11 | 3780473 | |||||||
chr11:3780503 | C | T | 6 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.77-1246G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 2/32 | chr11 | 3780503 | |||||||
chr11:3780528 | C | T | 1 | a0001c0032t0001g0032 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.77-1271G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 2/32 | chr11 | 3780528 | |||||||
chr11:3780541 | CA | C | 124 | a0001c0001t0001g0026 a0001c0001t0001g0030 a0001c0001t0001g0031 others(121): Show |
124 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(121): Show |
intron_variant | MODIFIER | c.77-1285delT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 2/32 | chr11 | 3780541 | |||||||
chr11:3780541 | CAA | C | 40 | a0001c0001t0001g0029 a0001c0001t0001g0038 a0001c0001t0001g0039 others(37): Show |
40 | HG00408.hp2 HG00609.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.77-1286_77-1285del others(2): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 2/32 | chr11 | 3780541 | |||||||
chr11:3780541 | CAAA | C | 69 | a0001c0001t0001g0076 a0001c0001t0001g0078 a0001c0001t0001g0081 others(66): Show |
69 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.77-1287_77-1285del others(3): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 2/32 | chr11 | 3780541 | |||||||
chr11:3780546 | AAAAAAAA others(10): Show |
A | 7 | a0001c0001t0001g0068 a0001c0001t0001g0324 a0001c0001t0001g0335 others(4): Show |
7 | HG00642.hp1 HG01433.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.77-1306_77-1290del others(17): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 2/32 | chr11 | 3780546 | |||||||
chr11:3780557 | A | G | 10 | a0001c0001t0001g0333 a0001c0001t0001g0334 a0001c0001t0006g0297 others(7): Show |
10 | HG01109.hp2 HG02055.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.77-1300T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 2/32 | chr11 | 3780557 | |||||||
chr11:3780558 | AAAAAG | A | 6 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.77-1306_77-1302del others(5): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 2/32 | chr11 | 3780558 | |||||||
chr11:3780559 | A | C | 3 | a0002c0008t0003g0040 a0002c0008t0003g0062 a0002c0008t0003g0064 |
3 | HG00735.hp1 HG00741.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.77-1302T>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 2/32 | chr11 | 3780559 | |||||||
chr11:3780564 | A | G | 1 | a0019c0015t0001g0283 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.77-1307T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 2/32 | chr11 | 3780564 | |||||||
chr11:3780575 | G | A | 1 | a0019c0015t0001g0283 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.77-1318C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 2/32 | chr11 | 3780575 | |||||||
chr11:3780576 | A | G | 1 | a0019c0015t0001g0283 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.77-1319T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 2/32 | chr11 | 3780576 | |||||||
chr11:3780688 | C | T | 1 | a0001c0001t0001g0143 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.76+1354G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 2/32 | chr11 | 3780688 | |||||||
chr11:3780925 | T | C | 1 | a0001c0002t0001g0318 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.76+1117A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 2/32 | chr11 | 3780925 | |||||||
chr11:3780936 | C | T | 1 | a0001c0002t0001g0167 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.76+1106G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 2/32 | chr11 | 3780936 | |||||||
chr11:3780988 | G | A | 1 | a0001c0001t0001g0215 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.76+1054C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 2/32 | chr11 | 3780988 | |||||||
chr11:3781139 | T | C | 48 | a0001c0001t0001g0029 a0001c0001t0001g0038 a0001c0001t0001g0039 others(45): Show |
48 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.76+903A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 2/32 | chr11 | 3781139 | |||||||
chr11:3781146 | A | G | 3 | a0001c0012t0001g0319 a0001c0012t0001g0320 a0016c0023t0001g0001 |
3 | HG02109.hp1 HG02809.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.76+896T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 2/32 | chr11 | 3781146 | |||||||
chr11:3781185 | C | CA | 93 | a0001c0001t0001g0060 a0001c0001t0001g0068 a0001c0001t0001g0076 others(90): Show |
93 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.76+856dupT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 2/32 | chr11 | 3781185 | |||||||
chr11:3781185 | C | CAA | 53 | a0001c0001t0001g0026 a0001c0001t0001g0030 a0001c0001t0001g0031 others(50): Show |
53 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.76+855_76+856dupTT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 2/32 | chr11 | 3781185 | |||||||
chr11:3781185 | CA | C | 6 | a0001c0001t0001g0005 a0001c0001t0001g0163 a0001c0001t0001g0179 others(3): Show |
6 | HG01099.hp2 HG02165.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.76+856delT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 2/32 | chr11 | 3781185 | |||||||
chr11:3781332 | A | AGAATCCG others(31): Show |
1 | a0019c0015t0001g0283 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.76+709_76+710insGT others(36): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 2/32 | chr11 | 3781332 | |||||||
chr11:3781353 | A | G | 6 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.76+689T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 2/32 | chr11 | 3781353 | |||||||
chr11:3781429 | G | C | 1 | a0001c0001t0001g0186 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.76+613C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 2/32 | chr11 | 3781429 | |||||||
chr11:3781488 | GT | G | 3 | a0001c0012t0001g0319 a0001c0012t0001g0320 a0016c0023t0001g0001 |
3 | HG02109.hp1 HG02809.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.76+553delA | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 2/32 | chr11 | 3781488 | |||||||
chr11:3781488 | GTT | G | 10 | a0001c0001t0001g0029 a0001c0001t0001g0038 a0001c0001t0001g0055 others(7): Show |
10 | HG01106.hp2 HG01361.hp1 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.76+552_76+553delAA | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 2/32 | chr11 | 3781488 | |||||||
chr11:3781490 | TTTA | T | 49 | a0001c0001t0001g0039 a0001c0001t0001g0041 a0001c0001t0001g0042 others(46): Show |
49 | HG00408.hp2 HG00438.hp2 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.76+549_76+551delTA others(1): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 2/32 | chr11 | 3781490 | |||||||
chr11:3781490 | TTTAA | T | 78 | a0001c0001t0001g0063 a0001c0001t0001g0076 a0001c0001t0001g0078 others(75): Show |
78 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.76+548_76+551delTT others(2): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 2/32 | chr11 | 3781490 | |||||||
chr11:3781490 | TTTAAA | T | 8 | a0001c0001t0001g0082 a0001c0002t0001g0074 a0001c0002t0001g0075 others(5): Show |
8 | HG00597.hp2 HG03041.hp1 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.76+547_76+551delTT others(3): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 2/32 | chr11 | 3781490 | |||||||
chr11:3781490 | TTTAAAAA | T | 45 | a0001c0001t0001g0026 a0001c0001t0001g0030 a0001c0001t0001g0031 others(42): Show |
45 | HG00597.hp1 HG01243.hp2 HG01884.hp1 others(42): Show |
intron_variant | MODIFIER | c.76+545_76+551delTT others(5): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 2/32 | chr11 | 3781490 | |||||||
chr11:3781492 | T | A | 5 | a0001c0001t0001g0113 a0001c0001t0001g0163 a0001c0012t0001g0319 others(2): Show |
5 | HG02109.hp1 HG02165.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.76+550A>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 2/32 | chr11 | 3781492 | |||||||
chr11:3781492 | T | TA | 19 | a0001c0001t0001g0036 a0001c0001t0001g0141 a0001c0001t0001g0161 others(16): Show |
19 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(16): Show |
intron_variant | MODIFIER | c.76+549dupT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 2/32 | chr11 | 3781492 | |||||||
chr11:3781492 | TA | T | 6 | a0001c0001t0001g0005 a0001c0001t0001g0189 a0001c0001t0001g0291 others(3): Show |
6 | HG01255.hp2 HG02027.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.76+549delT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 2/32 | chr11 | 3781492 | |||||||
chr11:3781492 | TAAAAAAA others(4): Show |
T | 1 | a0001c0001t0001g0006 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.76+539_76+549delTT others(9): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 2/32 | chr11 | 3781492 | |||||||
chr11:3781503 | A | C | 1 | a0001c0001t0001g0335 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.76+539T>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 2/32 | chr11 | 3781503 | |||||||
chr11:3781511 | A | C | 1 | a0001c0002t0001g0101 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.76+531T>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 2/32 | chr11 | 3781511 | |||||||
chr11:3781578 | T | C | 6 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.76+464A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 2/32 | chr11 | 3781578 | |||||||
chr11:3781589 | G | A | 1 | a0001c0001t0001g0232 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.76+453C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 2/32 | chr11 | 3781589 | |||||||
chr11:3781589 | G | T | 1 | a0001c0001t0001g0275 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.76+453C>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 2/32 | chr11 | 3781589 | |||||||
chr11:3781841 | A | G | 128 | a0001c0001t0001g0026 a0001c0001t0001g0030 a0001c0001t0001g0031 others(125): Show |
128 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.76+201T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 2/32 | chr11 | 3781841 | |||||||
chr11:3781842 | G | T | 43 | a0001c0001t0001g0029 a0001c0001t0001g0038 a0001c0001t0001g0039 others(40): Show |
43 | HG00408.hp2 HG00609.hp2 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.76+200C>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 2/32 | chr11 | 3781842 | |||||||
chr11:3781888 | T | C | 1 | a0001c0002t0001g0327 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.76+154A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 2/32 | chr11 | 3781888 | |||||||
chr11:3781975 | A | G | 1 | a0001c0002t0001g0046 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.76+67T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 2/32 | chr11 | 3781975 | |||||||
chr11:3782015 | C | A | 1 | a0001c0001t0001g0278 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.76+27G>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 2/32 | chr11 | 3782015 | |||||||
chr11:3782022 | T | C | 3 | a0001c0012t0001g0319 a0001c0012t0001g0320 a0016c0023t0001g0001 |
3 | HG02109.hp1 HG02809.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.76+20A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 2/32 | chr11 | 3782022 | |||||||
chr11:3782417 | CT | C | 14 | a0001c0001t0001g0206 a0001c0002t0001g0017 a0001c0002t0001g0069 others(11): Show |
14 | HG01109.hp2 HG01168.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.-28-273delA | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3782417 | |||||||
chr11:3782451 | T | G | 3 | a0001c0012t0001g0319 a0001c0012t0001g0320 a0016c0023t0001g0001 |
3 | HG02109.hp1 HG02809.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-28-306A>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3782451 | |||||||
chr11:3782458 | A | G | 1 | a0001c0001t0001g0142 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-28-313T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3782458 | |||||||
chr11:3782570 | A | AT | 18 | a0001c0001t0001g0029 a0001c0001t0001g0157 a0001c0001t0001g0166 others(15): Show |
18 | HG00621.hp2 HG01081.hp1 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.-28-426dupA | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3782570 | |||||||
chr11:3782570 | A | ATT | 34 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0042 others(31): Show |
34 | HG00408.hp2 HG00609.hp2 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.-28-427_-28-426dup others(2): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3782570 | |||||||
chr11:3782570 | A | T | 7 | a0001c0001t0001g0293 a0001c0001t0001g0296 a0001c0002t0001g0178 others(4): Show |
7 | HG01243.hp1 HG02109.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.-28-425T>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3782570 | |||||||
chr11:3782570 | AT | A | 128 | a0001c0001t0001g0026 a0001c0001t0001g0031 a0001c0001t0001g0036 others(125): Show |
128 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.-28-426delA | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3782570 | |||||||
chr11:3782570 | ATT | A | 8 | a0001c0001t0001g0179 a0001c0001t0001g0324 a0001c0001t0008g0325 others(5): Show |
8 | HG00642.hp1 HG02451.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.-28-427_-28-426del others(2): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3782570 | |||||||
chr11:3782605 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-28-460G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3782605 | |||||||
chr11:3782701 | CCTGT | C | 52 | a0001c0001t0001g0026 a0001c0001t0001g0030 a0001c0001t0001g0031 others(49): Show |
52 | HG00597.hp1 HG00639.hp2 HG01243.hp2 others(49): Show |
intron_variant | MODIFIER | c.-28-560_-28-557del others(4): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3782701 | |||||||
chr11:3782718 | A | C | 2 | a0015c0033t0001g0130 a0018c0034t0001g0122 |
2 | HG02630.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-28-573T>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3782718 | |||||||
chr11:3782726 | G | T | 339 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(336): Show |
339 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(336): Show |
intron_variant | MODIFIER | c.-28-581C>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3782726 | |||||||
chr11:3782846 | C | G | 6 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.-28-701G>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3782846 | |||||||
chr11:3782917 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-28-772A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3782917 | |||||||
chr11:3782963 | G | A | 1 | a0001c0001t0001g0324 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-28-818C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3782963 | |||||||
chr11:3783020 | G | A | 1 | a0001c0001t0001g0335 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-28-875C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3783020 | |||||||
chr11:3783349 | C | T | 6 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.-28-1204G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3783349 | |||||||
chr11:3783398 | A | T | 2 | a0001c0001t0001g0068 a0001c0001t0001g0336 |
2 | HG02965.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-28-1253T>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3783398 | |||||||
chr11:3783427 | G | A | 1 | a0001c0001t0001g0171 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-28-1282C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3783427 | |||||||
chr11:3783433 | T | A | 3 | a0001c0012t0001g0319 a0001c0012t0001g0320 a0016c0023t0001g0001 |
3 | HG02109.hp1 HG02809.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-28-1288A>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3783433 | |||||||
chr11:3783434 | C | T | 3 | a0001c0012t0001g0319 a0001c0012t0001g0320 a0016c0023t0001g0001 |
3 | HG02109.hp1 HG02809.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-28-1289G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3783434 | |||||||
chr11:3783568 | G | A | 1 | a0001c0001t0001g0308 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-28-1423C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3783568 | |||||||
chr11:3783614 | G | A | 1 | a0001c0026t0001g0298 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-28-1469C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3783614 | |||||||
chr11:3783816 | C | A | 16 | a0001c0001t0001g0068 a0001c0001t0001g0324 a0001c0001t0001g0335 others(13): Show |
16 | HG00642.hp1 HG01081.hp1 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.-28-1671G>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3783816 | |||||||
chr11:3783890 | A | T | 2 | a0001c0001t0001g0141 a0001c0016t0001g0114 |
2 | HG00438.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-28-1745T>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3783890 | |||||||
chr11:3783987 | T | A | 21 | a0001c0001t0001g0068 a0001c0001t0001g0113 a0001c0001t0001g0324 others(18): Show |
21 | HG00642.hp1 HG01081.hp1 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.-28-1842A>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3783987 | |||||||
chr11:3784052 | A | T | 2 | a0001c0001t0001g0029 a0001c0001t0001g0328 |
2 | HG02280.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-28-1907T>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3784052 | |||||||
chr11:3784080 | G | A | 4 | a0001c0001t0001g0324 a0001c0001t0008g0325 a0005c0010t0001g0338 others(1): Show |
4 | HG00642.hp1 HG02559.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.-28-1935C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3784080 | |||||||
chr11:3784090 | T | C | 4 | a0001c0001t0001g0324 a0001c0001t0008g0325 a0005c0010t0001g0338 others(1): Show |
4 | HG00642.hp1 HG02559.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.-28-1945A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3784090 | |||||||
chr11:3784323 | A | AG | 6 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.-28-2179dupC | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3784323 | |||||||
chr11:3784325 | G | GA | 10 | a0001c0001t0001g0068 a0001c0001t0001g0324 a0001c0001t0001g0335 others(7): Show |
10 | HG00642.hp1 HG01433.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.-28-2181dupT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3784325 | |||||||
chr11:3784326 | A | G | 3 | a0001c0001t0001g0333 a0001c0001t0001g0334 a0001c0001t0006g0297 |
3 | HG02145.hp1 HG02257.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-28-2181T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3784326 | |||||||
chr11:3784444 | A | C | 1 | a0001c0001t0001g0307 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-28-2299T>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3784444 | |||||||
chr11:3784457 | T | C | 133 | a0001c0001t0001g0026 a0001c0001t0001g0030 a0001c0001t0001g0031 others(130): Show |
133 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(130): Show |
intron_variant | MODIFIER | c.-28-2312A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3784457 | |||||||
chr11:3784579 | T | TA | 21 | a0001c0001t0001g0068 a0001c0001t0001g0113 a0001c0001t0001g0324 others(18): Show |
21 | HG00642.hp1 HG01081.hp1 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.-28-2435dupT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3784579 | |||||||
chr11:3784585 | C | A | 188 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0030 others(185): Show |
188 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(185): Show |
intron_variant | MODIFIER | c.-28-2440G>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3784585 | |||||||
chr11:3784587 | A | AC | 131 | a0001c0001t0001g0026 a0001c0001t0001g0030 a0001c0001t0001g0031 others(128): Show |
131 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.-28-2443_-28-2442i others(3): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3784587 | |||||||
chr11:3784596 | C | A | 47 | a0001c0001t0001g0029 a0001c0001t0001g0038 a0001c0001t0001g0039 others(44): Show |
47 | HG00408.hp2 HG00609.hp2 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.-28-2451G>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3784596 | |||||||
chr11:3784596 | C | CAA | 8 | a0001c0001t0001g0324 a0001c0001t0001g0335 a0001c0001t0008g0325 others(5): Show |
8 | HG00642.hp1 HG01433.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.-28-2453_-28-2452d others(4): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3784596 | |||||||
chr11:3784596 | C | CAAA | 8 | a0001c0001t0001g0068 a0001c0001t0001g0336 a0002c0005t0001g0299 others(5): Show |
8 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.-28-2454_-28-2452d others(5): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3784596 | |||||||
chr11:3784601 | A | C | 1 | a0001c0001t0001g0180 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-28-2456T>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3784601 | |||||||
chr11:3784604 | A | C | 2 | a0009c0011t0001g0071 a0009c0011t0001g0072 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-28-2459T>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3784604 | |||||||
chr11:3784605 | A | AAC | 18 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0047 others(15): Show |
18 | HG00408.hp2 HG00741.hp1 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.-28-2461_-28-2460i others(4): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3784605 | |||||||
chr11:3784605 | A | AC | 26 | a0001c0001t0001g0029 a0001c0001t0001g0041 a0001c0001t0001g0042 others(23): Show |
26 | HG00609.hp2 HG00735.hp1 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.-28-2461dupG | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3784605 | |||||||
chr11:3784605 | A | C | 140 | a0001c0001t0001g0026 a0001c0001t0001g0030 a0001c0001t0001g0031 others(137): Show |
140 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(137): Show |
intron_variant | MODIFIER | c.-28-2460T>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3784605 | |||||||
chr11:3784606 | C | A | 1 | a0001c0002t0001g0021 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-28-2461G>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3784606 | |||||||
chr11:3784630 | C | T | 16 | a0001c0001t0001g0068 a0001c0001t0001g0324 a0001c0001t0001g0335 others(13): Show |
16 | HG00642.hp1 HG01081.hp1 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.-28-2485G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3784630 | |||||||
chr11:3784748 | T | C | 1 | a0001c0001t0002g0317 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-28-2603A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3784748 | |||||||
chr11:3784755 | C | T | 1 | a0001c0001t0001g0307 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-28-2610G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3784755 | |||||||
chr11:3784806 | C | T | 16 | a0001c0001t0001g0068 a0001c0001t0001g0324 a0001c0001t0001g0335 others(13): Show |
16 | HG00642.hp1 HG01081.hp1 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.-28-2661G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3784806 | |||||||
chr11:3784838 | C | T | 1 | a0001c0001t0001g0232 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-28-2693G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3784838 | |||||||
chr11:3784859 | G | A | 1 | a0001c0001t0001g0232 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-28-2714C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3784859 | |||||||
chr11:3784864 | C | T | 1 | a0001c0024t0001g0251 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-28-2719G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3784864 | |||||||
chr11:3784918 | C | T | 76 | a0001c0001t0001g0076 a0001c0001t0001g0078 a0001c0001t0001g0081 others(73): Show |
76 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.-28-2773G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3784918 | |||||||
chr11:3784992 | G | A | 3 | a0001c0012t0001g0319 a0001c0012t0001g0320 a0016c0023t0001g0001 |
3 | HG02109.hp1 HG02809.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-28-2847C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3784992 | |||||||
chr11:3785016 | C | T | 16 | a0001c0001t0001g0068 a0001c0001t0001g0324 a0001c0001t0001g0335 others(13): Show |
16 | HG00642.hp1 HG01081.hp1 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.-28-2871G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3785016 | |||||||
chr11:3785125 | G | A | 1 | a0001c0001t0001g0215 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-28-2980C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3785125 | |||||||
chr11:3785154 | TA | T | 9 | a0001c0012t0001g0319 a0001c0012t0001g0320 a0002c0005t0001g0299 others(6): Show |
9 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.-28-3010delT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3785154 | |||||||
chr11:3785318 | T | C | 16 | a0001c0001t0001g0068 a0001c0001t0001g0324 a0001c0001t0001g0335 others(13): Show |
16 | HG00642.hp1 HG01081.hp1 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.-28-3173A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3785318 | |||||||
chr11:3785366 | C | CCACT | 16 | a0001c0001t0001g0068 a0001c0001t0001g0324 a0001c0001t0001g0335 others(13): Show |
16 | HG00642.hp1 HG01081.hp1 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.-28-3222_-28-3221i others(6): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3785366 | |||||||
chr11:3785386 | T | C | 2 | a0015c0033t0001g0130 a0018c0034t0001g0122 |
2 | HG02630.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-28-3241A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3785386 | |||||||
chr11:3785412 | T | C | 1 | a0001c0032t0001g0032 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-28-3267A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3785412 | |||||||
chr11:3785417 | C | A | 1 | a0001c0001t0001g0307 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-28-3272G>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3785417 | |||||||
chr11:3785418 | T | A | 1 | a0001c0001t0001g0307 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-28-3273A>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3785418 | |||||||
chr11:3785532 | G | A | 1 | a0001c0002t0001g0187 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-28-3387C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3785532 | |||||||
chr11:3785971 | C | A | 1 | a0001c0001t0001g0172 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-28-3826G>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3785971 | |||||||
chr11:3786096 | C | T | 1 | a0001c0001t0001g0163 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-28-3951G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3786096 | |||||||
chr11:3786197 | G | C | 2 | a0001c0002t0001g0022 a0001c0002t0001g0023 |
2 | NA18950.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.-28-4052C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3786197 | |||||||
chr11:3786300 | G | C | 1 | a0001c0001t0001g0163 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-28-4155C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3786300 | |||||||
chr11:3786692 | C | A | 1 | a0001c0001t0001g0215 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-28-4547G>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3786692 | |||||||
chr11:3786739 | A | G | 2 | a0015c0033t0001g0130 a0018c0034t0001g0122 |
2 | HG02630.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-28-4594T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3786739 | |||||||
chr11:3786784 | G | C | 6 | a0001c0017t0002g0116 a0003c0004t0001g0115 a0003c0004t0001g0117 others(3): Show |
6 | HG02486.hp1 HG02572.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-28-4639C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3786784 | |||||||
chr11:3786820 | G | A | 1 | a0001c0002t0001g0327 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-28-4675C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3786820 | |||||||
chr11:3786908 | T | G | 47 | a0001c0001t0001g0029 a0001c0001t0001g0038 a0001c0001t0001g0039 others(44): Show |
47 | HG00408.hp2 HG00609.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.-28-4763A>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3786908 | |||||||
chr11:3786995 | T | G | 41 | a0001c0001t0001g0029 a0001c0001t0001g0038 a0001c0001t0001g0039 others(38): Show |
41 | HG00408.hp2 HG00609.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.-28-4850A>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3786995 | |||||||
chr11:3787110 | C | G | 4 | a0001c0001t0001g0329 a0001c0001t0001g0337 a0001c0001t0004g0330 others(1): Show |
4 | HG02647.hp2 HG02717.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-28-4965G>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3787110 | |||||||
chr11:3787114 | G | C | 4 | a0001c0001t0001g0185 a0001c0001t0001g0207 a0001c0001t0001g0208 others(1): Show |
4 | HG00323.hp1 NA18971.hp2 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.-28-4969C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3787114 | |||||||
chr11:3787131 | G | A | 2 | a0015c0033t0001g0130 a0018c0034t0001g0122 |
2 | HG02630.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-28-4986C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3787131 | |||||||
chr11:3787137 | C | G | 77 | a0001c0001t0001g0076 a0001c0001t0001g0078 a0001c0001t0001g0081 others(74): Show |
77 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.-28-4992G>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3787137 | |||||||
chr11:3787253 | C | T | 1 | a0001c0001t0001g0217 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.-28-5108G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3787253 | |||||||
chr11:3787404 | A | G | 1 | a0001c0003t0002g0311 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-28-5259T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3787404 | |||||||
chr11:3787476 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-28-5331C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3787476 | |||||||
chr11:3787515 | A | G | 336 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(333): Show |
336 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(333): Show |
intron_variant | MODIFIER | c.-28-5370T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3787515 | |||||||
chr11:3787612 | T | C | 1 | a0001c0016t0001g0114 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-28-5467A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3787612 | |||||||
chr11:3787658 | T | C | 3 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0063 |
3 | NA18961.hp1 NA19009.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.-28-5513A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3787658 | |||||||
chr11:3787775 | C | T | 1 | a0001c0001t0001g0335 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-28-5630G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3787775 | |||||||
chr11:3788000 | A | G | 3 | a0001c0002t0001g0070 a0001c0002t0001g0090 a0001c0002t0001g0100 |
3 | HG00558.hp2 NA18961.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.-28-5855T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3788000 | |||||||
chr11:3788119 | C | T | 15 | a0001c0001t0001g0068 a0001c0001t0001g0324 a0001c0001t0001g0335 others(12): Show |
15 | HG00642.hp1 HG01081.hp1 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.-28-5974G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3788119 | |||||||
chr11:3788401 | G | A | 1 | a0001c0001t0001g0278 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-28-6256C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3788401 | |||||||
chr11:3788554 | G | T | 1 | a0001c0032t0001g0032 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-28-6409C>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3788554 | |||||||
chr11:3788601 | A | G | 3 | a0001c0001t0001g0335 a0001c0012t0001g0319 a0001c0012t0001g0320 |
3 | HG01433.hp2 HG02109.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.-28-6456T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3788601 | |||||||
chr11:3788778 | C | G | 6 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.-28-6633G>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3788778 | |||||||
chr11:3788815 | C | T | 6 | a0001c0001t0001g0068 a0001c0001t0001g0324 a0001c0001t0001g0336 others(3): Show |
6 | HG00642.hp1 HG02559.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-28-6670G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3788815 | |||||||
chr11:3788861 | C | T | 72 | a0001c0001t0001g0076 a0001c0001t0001g0078 a0001c0001t0001g0081 others(69): Show |
72 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.-28-6716G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3788861 | |||||||
chr11:3788884 | T | C | 2 | a0001c0002t0001g0261 a0001c0002t0001g0281 |
2 | HG00597.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.-28-6739A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3788884 | |||||||
chr11:3788895 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-28-6750G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3788895 | |||||||
chr11:3789015 | A | G | 2 | a0001c0012t0001g0319 a0001c0012t0001g0320 |
2 | HG02109.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.-28-6870T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3789015 | |||||||
chr11:3789147 | G | C | 1 | a0001c0001t0001g0307 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-28-7002C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3789147 | |||||||
chr11:3789149 | A | G | 1 | a0001c0001t0001g0336 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-28-7004T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3789149 | |||||||
chr11:3789271 | C | A | 1 | a0001c0016t0001g0114 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-28-7126G>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3789271 | |||||||
chr11:3789337 | A | T | 1 | a0001c0001t0001g0067 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-28-7192T>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3789337 | |||||||
chr11:3789459 | C | A | 1 | a0001c0002t0001g0089 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-28-7314G>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3789459 | |||||||
chr11:3789501 | C | CT | 14 | a0001c0001t0001g0039 a0001c0001t0001g0067 a0001c0001t0001g0139 others(11): Show |
14 | HG00323.hp2 HG00408.hp1 HG01952.hp2 others(11): Show |
intron_variant | MODIFIER | c.-28-7357dupA | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3789501 | |||||||
chr11:3789501 | C | CTTT | 6 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.-28-7359_-28-7357d others(5): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3789501 | |||||||
chr11:3789501 | CT | C | 9 | a0001c0001t0001g0060 a0001c0001t0001g0129 a0001c0001t0001g0183 others(6): Show |
9 | HG01433.hp2 HG02896.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.-28-7357delA | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3789501 | |||||||
chr11:3789658 | G | A | 6 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.-28-7513C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3789658 | |||||||
chr11:3789908 | T | C | 22 | a0001c0001t0001g0068 a0001c0001t0001g0324 a0001c0001t0001g0335 others(19): Show |
22 | HG00642.hp1 HG01081.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.-29+7492A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3789908 | |||||||
chr11:3789909 | C | T | 2 | a0001c0006t0001g0126 a0001c0006t0001g0127 |
2 | HG02896.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-29+7491G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3789909 | |||||||
chr11:3789922 | C | T | 4 | a0001c0001t0001g0324 a0001c0001t0008g0325 a0005c0010t0001g0338 others(1): Show |
4 | HG00642.hp1 HG02559.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29+7478G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3789922 | |||||||
chr11:3790018 | C | T | 52 | a0001c0001t0001g0026 a0001c0001t0001g0030 a0001c0001t0001g0031 others(49): Show |
52 | HG00597.hp1 HG00639.hp2 HG01884.hp1 others(49): Show |
intron_variant | MODIFIER | c.-29+7382G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3790018 | |||||||
chr11:3790071 | C | T | 5 | a0001c0002t0001g0262 a0001c0002t0001g0264 a0001c0002t0001g0265 others(2): Show |
5 | NA18955.hp1 NA18957.hp1 NA19002.hp2 others(2): Show |
intron_variant | MODIFIER | c.-29+7329G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3790071 | |||||||
chr11:3790132 | G | A | 1 | a0007c0013t0005g0037 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-29+7268C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3790132 | |||||||
chr11:3790139 | G | A | 1 | a0001c0001t0001g0275 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-29+7261C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3790139 | |||||||
chr11:3790221 | C | G | 27 | a0001c0001t0001g0273 a0001c0002t0001g0260 a0001c0002t0001g0261 others(24): Show |
27 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(24): Show |
intron_variant | MODIFIER | c.-29+7179G>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3790221 | |||||||
chr11:3790270 | T | C | 2 | a0001c0001t0001g0209 a0001c0001t0001g0257 |
2 | NA18943.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.-29+7130A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3790270 | |||||||
chr11:3790295 | T | C | 39 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0041 others(36): Show |
39 | HG00408.hp2 HG00609.hp2 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.-29+7105A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3790295 | |||||||
chr11:3790399 | C | T | 1 | a0001c0001t0001g0255 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-29+7001G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3790399 | |||||||
chr11:3790520 | G | A | 2 | a0001c0002t0001g0276 a0001c0002t0001g0277 |
2 | NA18960.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.-29+6880C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3790520 | |||||||
chr11:3790563 | T | C | 260 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0030 others(257): Show |
260 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(257): Show |
intron_variant | MODIFIER | c.-29+6837A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3790563 | |||||||
chr11:3790564 | G | A | 1 | a0001c0001t0001g0050 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-29+6836C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3790564 | |||||||
chr11:3790644 | C | T | 5 | a0001c0001t0002g0314 a0001c0001t0002g0317 a0003c0004t0001g0316 others(2): Show |
5 | HG00639.hp2 HG01943.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-29+6756G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3790644 | |||||||
chr11:3790751 | C | T | 1 | a0001c0001t0001g0335 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-29+6649G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3790751 | |||||||
chr11:3790823 | A | G | 1 | a0001c0001t0001g0307 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-29+6577T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3790823 | |||||||
chr11:3790849 | T | A | 8 | a0001c0012t0001g0319 a0001c0012t0001g0320 a0002c0005t0001g0299 others(5): Show |
8 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.-29+6551A>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3790849 | |||||||
chr11:3790860 | G | A | 22 | a0001c0001t0001g0068 a0001c0001t0001g0324 a0001c0001t0001g0335 others(19): Show |
22 | HG00642.hp1 HG01081.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.-29+6540C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3790860 | |||||||
chr11:3790898 | A | AT | 7 | a0001c0001t0001g0029 a0001c0001t0001g0328 a0001c0001t0001g0335 others(4): Show |
7 | HG01433.hp2 HG02280.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-29+6501dupA | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3790898 | |||||||
chr11:3790898 | A | ATT | 74 | a0001c0001t0001g0076 a0001c0001t0001g0078 a0001c0001t0001g0081 others(71): Show |
74 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.-29+6500_-29+6501d others(4): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3790898 | |||||||
chr11:3790898 | A | ATTT | 40 | a0001c0001t0001g0026 a0001c0001t0001g0030 a0001c0001t0001g0031 others(37): Show |
40 | HG00639.hp2 HG01243.hp2 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.-29+6499_-29+6501d others(5): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3790898 | |||||||
chr11:3790898 | AT | A | 12 | a0001c0001t0001g0324 a0001c0001t0008g0325 a0001c0003t0002g0290 others(9): Show |
12 | HG00642.hp1 HG01109.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.-29+6501delA | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3790898 | |||||||
chr11:3790934 | T | C | 43 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0041 others(40): Show |
43 | HG00408.hp2 HG00609.hp2 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.-29+6466A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3790934 | |||||||
chr11:3790935 | G | A | 42 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0041 others(39): Show |
42 | HG00408.hp2 HG00609.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.-29+6465C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3790935 | |||||||
chr11:3790960 | A | G | 1 | a0004c0007t0001g0216 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-29+6440T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3790960 | |||||||
chr11:3791010 | G | A | 1 | a0001c0001t0001g0329 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-29+6390C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3791010 | |||||||
chr11:3791010 | G | C | 3 | a0001c0001t0001g0183 a0001c0001t0001g0209 a0001c0001t0001g0257 |
3 | HG03704.hp2 NA18943.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.-29+6390C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3791010 | |||||||
chr11:3791057 | A | G | 1 | a0001c0032t0001g0032 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-29+6343T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3791057 | |||||||
chr11:3791085 | C | T | 56 | a0001c0001t0001g0076 a0001c0001t0001g0078 a0001c0001t0001g0081 others(53): Show |
56 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.-29+6315G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3791085 | |||||||
chr11:3791089 | T | G | 7 | a0001c0003t0002g0290 a0001c0003t0002g0311 a0001c0003t0002g0312 others(4): Show |
7 | HG01109.hp2 HG02055.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-29+6311A>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3791089 | |||||||
chr11:3791097 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-29+6303C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3791097 | |||||||
chr11:3791102 | A | G | 2 | a0001c0001t0001g0329 a0001c0016t0001g0114 |
2 | HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-29+6298T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3791102 | |||||||
chr11:3791102 | A | T | 1 | a0001c0002t0001g0187 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-29+6298T>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3791102 | |||||||
chr11:3791110 | T | C | 1 | a0001c0001t0001g0255 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-29+6290A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3791110 | |||||||
chr11:3791116 | C | T | 146 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0030 others(143): Show |
146 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(143): Show |
intron_variant | MODIFIER | c.-29+6284G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3791116 | |||||||
chr11:3791117 | G | A | 11 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(8): Show |
11 | HG00408.hp2 HG00609.hp2 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.-29+6283C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3791117 | |||||||
chr11:3791117 | G | C | 1 | a0001c0020t0001g0210 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-29+6283C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3791117 | |||||||
chr11:3791130 | T | C | 4 | a0001c0001t0001g0113 a0002c0008t0003g0040 a0002c0008t0003g0062 others(1): Show |
4 | HG00735.hp1 HG00741.hp1 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29+6270A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3791130 | |||||||
chr11:3791142 | C | G | 4 | a0001c0001t0001g0113 a0002c0008t0003g0040 a0002c0008t0003g0062 others(1): Show |
4 | HG00735.hp1 HG00741.hp1 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29+6258G>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3791142 | |||||||
chr11:3791143 | C | G | 4 | a0001c0001t0001g0324 a0001c0001t0008g0325 a0005c0010t0001g0338 others(1): Show |
4 | HG00642.hp1 HG02559.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29+6257G>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3791143 | |||||||
chr11:3791146 | C | T | 3 | a0002c0008t0003g0040 a0002c0008t0003g0062 a0002c0008t0003g0064 |
3 | HG00735.hp1 HG00741.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.-29+6254G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3791146 | |||||||
chr11:3791147 | A | G | 3 | a0002c0008t0003g0040 a0002c0008t0003g0062 a0002c0008t0003g0064 |
3 | HG00735.hp1 HG00741.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.-29+6253T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3791147 | |||||||
chr11:3791154 | C | T | 3 | a0002c0008t0003g0040 a0002c0008t0003g0062 a0002c0008t0003g0064 |
3 | HG00735.hp1 HG00741.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.-29+6246G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3791154 | |||||||
chr11:3791167 | T | A | 1 | a0001c0002t0001g0106 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-29+6233A>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3791167 | |||||||
chr11:3791184 | T | C | 1 | a0001c0001t0001g0335 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-29+6216A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3791184 | |||||||
chr11:3791219 | T | C | 1 | a0001c0001t0001g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-29+6181A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3791219 | |||||||
chr11:3791338 | G | A | 1 | a0001c0001t0001g0335 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-29+6062C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3791338 | |||||||
chr11:3791366 | CTACTAAA others(2): Show |
C | 6 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.-29+6025_-29+6033d others(11): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3791366 | |||||||
chr11:3791482 | T | C | 22 | a0001c0001t0001g0068 a0001c0001t0001g0324 a0001c0001t0001g0335 others(19): Show |
22 | HG00642.hp1 HG01081.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.-29+5918A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3791482 | |||||||
chr11:3791494 | A | G | 23 | a0001c0001t0001g0068 a0001c0001t0001g0324 a0001c0001t0001g0335 others(20): Show |
23 | HG00642.hp1 HG01081.hp1 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.-29+5906T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3791494 | |||||||
chr11:3791533 | C | CA | 13 | a0001c0001t0001g0036 a0001c0001t0001g0135 a0001c0001t0001g0173 others(10): Show |
13 | HG00735.hp2 HG00741.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.-29+5866dupT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3791533 | |||||||
chr11:3791533 | C | CAA | 9 | a0001c0001t0001g0324 a0001c0001t0008g0325 a0001c0003t0002g0290 others(6): Show |
9 | HG00642.hp1 HG02055.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.-29+5865_-29+5866d others(4): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3791533 | |||||||
chr11:3791533 | C | CAAA | 9 | a0001c0001t0001g0335 a0001c0003t0002g0313 a0001c0003t0002g0323 others(6): Show |
9 | HG01081.hp1 HG01109.hp2 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.-29+5864_-29+5866d others(5): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3791533 | |||||||
chr11:3791533 | CA | C | 44 | a0001c0001t0001g0063 a0001c0001t0001g0067 a0001c0001t0001g0112 others(41): Show |
44 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.-29+5866delT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3791533 | |||||||
chr11:3791533 | CAA | C | 37 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0041 others(34): Show |
37 | HG00408.hp2 HG00609.hp2 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.-29+5865_-29+5866d others(4): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3791533 | |||||||
chr11:3791533 | CAAAA | C | 120 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0030 others(117): Show |
120 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.-29+5863_-29+5866d others(6): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3791533 | |||||||
chr11:3791568 | G | GGCATGGT others(7): Show |
2 | a0001c0001t0001g0324 a0001c0001t0008g0325 |
2 | HG00642.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.-29+5818_-29+5831d others(16): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3791568 | |||||||
chr11:3791756 | T | C | 1 | a0001c0001t0001g0335 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-29+5644A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3791756 | |||||||
chr11:3791791 | G | A | 6 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.-29+5609C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3791791 | |||||||
chr11:3791799 | G | A | 6 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.-29+5601C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3791799 | |||||||
chr11:3791840 | T | TA | 18 | a0001c0001t0001g0006 a0001c0001t0001g0068 a0001c0001t0001g0243 others(15): Show |
18 | HG00423.hp2 HG00544.hp2 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.-29+5559dupT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3791840 | |||||||
chr11:3791840 | T | TAA | 6 | a0001c0003t0002g0290 a0001c0003t0002g0312 a0001c0003t0002g0313 others(3): Show |
6 | HG01109.hp2 HG02055.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.-29+5558_-29+5559d others(4): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3791840 | |||||||
chr11:3791840 | TA | T | 7 | a0001c0001t0001g0112 a0001c0001t0001g0179 a0001c0001t0001g0183 others(4): Show |
7 | HG01943.hp1 HG02451.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.-29+5559delT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3791840 | |||||||
chr11:3791858 | AAT | A | 6 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.-29+5540_-29+5541d others(4): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3791858 | |||||||
chr11:3791860 | T | A | 16 | a0001c0001t0001g0068 a0001c0001t0001g0324 a0001c0001t0001g0335 others(13): Show |
16 | HG00642.hp1 HG01109.hp2 HG01433.hp2 others(13): Show |
intron_variant | MODIFIER | c.-29+5540A>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3791860 | |||||||
chr11:3791877 | C | T | 38 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0041 others(35): Show |
38 | HG00408.hp2 HG00609.hp2 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.-29+5523G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3791877 | |||||||
chr11:3791952 | A | G | 1 | a0001c0001t0001g0183 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-29+5448T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3791952 | |||||||
chr11:3791975 | C | A | 7 | a0001c0001t0001g0068 a0001c0001t0001g0324 a0001c0001t0001g0335 others(4): Show |
7 | HG00642.hp1 HG01433.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.-29+5425G>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3791975 | |||||||
chr11:3791985 | C | T | 1 | a0001c0001t0001g0039 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-29+5415G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3791985 | |||||||
chr11:3792032 | A | G | 7 | a0001c0003t0002g0290 a0001c0003t0002g0311 a0001c0003t0002g0312 others(4): Show |
7 | HG01109.hp2 HG02055.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-29+5368T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3792032 | |||||||
chr11:3792042 | GGTGGCAC others(114): Show |
G | 4 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0182 others(1): Show |
4 | NA18990.hp2 NA18999.hp1 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.-29+5237_-29+5357d others(2): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3792042 | |||||||
chr11:3792049 | C | T | 2 | a0001c0012t0001g0319 a0001c0012t0001g0320 |
2 | HG02109.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.-29+5351G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3792049 | |||||||
chr11:3792123 | A | G | 22 | a0001c0001t0001g0068 a0001c0001t0001g0324 a0001c0001t0001g0335 others(19): Show |
22 | HG00642.hp1 HG01081.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.-29+5277T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3792123 | |||||||
chr11:3792133 | C | T | 39 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0041 others(36): Show |
39 | HG00408.hp2 HG00609.hp2 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.-29+5267G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3792133 | |||||||
chr11:3792165 | T | C | 22 | a0001c0001t0001g0068 a0001c0001t0001g0324 a0001c0001t0001g0335 others(19): Show |
22 | HG00642.hp1 HG01081.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.-29+5235A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3792165 | |||||||
chr11:3792178 | C | CA | 8 | a0001c0001t0001g0247 a0001c0001t0001g0248 a0001c0001t0001g0249 others(5): Show |
8 | HG00639.hp1 HG00733.hp1 HG00735.hp2 others(5): Show |
intron_variant | MODIFIER | c.-29+5221dupT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3792178 | |||||||
chr11:3792178 | CA | C | 91 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0028 others(88): Show |
91 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.-29+5221delT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3792178 | |||||||
chr11:3792178 | CAA | C | 6 | a0001c0001t0001g0036 a0001c0001t0001g0136 a0001c0001t0001g0179 others(3): Show |
6 | HG01943.hp2 HG02145.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-29+5220_-29+5221d others(4): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3792178 | |||||||
chr11:3792178 | CAAA | C | 9 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(6): Show |
9 | HG02080.hp1 HG02135.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.-29+5219_-29+5221d others(5): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3792178 | |||||||
chr11:3792178 | CAAAA | C | 63 | a0001c0001t0001g0076 a0001c0001t0001g0078 a0001c0001t0001g0081 others(60): Show |
63 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.-29+5218_-29+5221d others(6): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3792178 | |||||||
chr11:3792178 | CAAAAA | C | 11 | a0001c0001t0001g0026 a0001c0001t0001g0065 a0001c0001t0001g0066 others(8): Show |
11 | HG00741.hp1 HG01106.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.-29+5217_-29+5221d others(7): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3792178 | |||||||
chr11:3792178 | CAAAAAA | C | 75 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0041 others(72): Show |
75 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(72): Show |
intron_variant | MODIFIER | c.-29+5216_-29+5221d others(8): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3792178 | |||||||
chr11:3792178 | CAAAAAAA | C | 9 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0121 others(6): Show |
9 | HG00639.hp2 HG01884.hp1 HG01943.hp1 others(6): Show |
intron_variant | MODIFIER | c.-29+5215_-29+5221d others(9): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3792178 | |||||||
chr11:3792178 | CAAAAAAA others(2): Show |
C | 12 | a0001c0001t0001g0068 a0001c0001t0001g0324 a0001c0001t0001g0336 others(9): Show |
12 | HG00642.hp1 HG01081.hp1 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.-29+5213_-29+5221d others(11): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3792178 | |||||||
chr11:3792178 | CAAAAAAA others(3): Show |
C | 2 | a0001c0001t0001g0029 a0001c0001t0001g0328 |
2 | HG02280.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-29+5212_-29+5221d others(12): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3792178 | |||||||
chr11:3792178 | CAAAAAAA others(4): Show |
C | 7 | a0001c0003t0002g0290 a0001c0003t0002g0311 a0001c0003t0002g0312 others(4): Show |
7 | HG01109.hp2 HG02055.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-29+5211_-29+5221d others(13): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3792178 | |||||||
chr11:3792178 | CAAAAAAA others(7): Show |
C | 1 | a0001c0002t0001g0178 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-29+5208_-29+5221d others(16): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3792178 | |||||||
chr11:3792198 | A | C | 53 | a0001c0001t0001g0112 a0001c0001t0001g0135 a0001c0001t0001g0136 others(50): Show |
53 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.-29+5202T>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3792198 | |||||||
chr11:3792336 | T | G | 22 | a0001c0001t0001g0068 a0001c0001t0001g0324 a0001c0001t0001g0335 others(19): Show |
22 | HG00642.hp1 HG01081.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.-29+5064A>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3792336 | |||||||
chr11:3792396 | T | G | 22 | a0001c0001t0001g0068 a0001c0001t0001g0324 a0001c0001t0001g0335 others(19): Show |
22 | HG00642.hp1 HG01081.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.-29+5004A>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3792396 | |||||||
chr11:3792620 | G | C | 8 | a0001c0012t0001g0319 a0001c0012t0001g0320 a0002c0005t0001g0299 others(5): Show |
8 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.-29+4780C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3792620 | |||||||
chr11:3792637 | AAAC | A | 6 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.-29+4760_-29+4762d others(5): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3792637 | |||||||
chr11:3792707 | T | TA | 8 | a0001c0012t0001g0319 a0001c0012t0001g0320 a0002c0005t0001g0299 others(5): Show |
8 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.-29+4692dupT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3792707 | |||||||
chr11:3792717 | G | T | 1 | a0001c0026t0001g0298 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-29+4683C>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3792717 | |||||||
chr11:3792731 | T | C | 22 | a0001c0001t0001g0068 a0001c0001t0001g0324 a0001c0001t0001g0335 others(19): Show |
22 | HG00642.hp1 HG01081.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.-29+4669A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3792731 | |||||||
chr11:3792774 | A | G | 22 | a0001c0001t0001g0068 a0001c0001t0001g0324 a0001c0001t0001g0335 others(19): Show |
22 | HG00642.hp1 HG01081.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.-29+4626T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3792774 | |||||||
chr11:3792890 | A | G | 15 | a0001c0001t0001g0068 a0001c0001t0001g0324 a0001c0001t0001g0336 others(12): Show |
15 | HG00642.hp1 HG01109.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.-29+4510T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3792890 | |||||||
chr11:3793040 | G | A | 4 | a0001c0001t0001g0287 a0001c0002t0001g0285 a0001c0002t0001g0286 others(1): Show |
4 | HG00323.hp2 HG03239.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29+4360C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3793040 | |||||||
chr11:3793056 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-29+4344G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3793056 | |||||||
chr11:3793247 | C | G | 134 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0030 others(131): Show |
134 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(131): Show |
intron_variant | MODIFIER | c.-29+4153G>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3793247 | |||||||
chr11:3793382 | T | C | 1 | a0001c0002t0001g0131 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-29+4018A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3793382 | |||||||
chr11:3793385 | G | A | 2 | a0001c0001t0001g0333 a0001c0001t0001g0334 |
2 | HG02145.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-29+4015C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3793385 | |||||||
chr11:3793434 | C | T | 1 | a0013c0029t0001g0134 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-29+3966G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3793434 | |||||||
chr11:3793460 | C | G | 22 | a0001c0001t0001g0068 a0001c0001t0001g0324 a0001c0001t0001g0335 others(19): Show |
22 | HG00642.hp1 HG01081.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.-29+3940G>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3793460 | |||||||
chr11:3793502 | G | A | 7 | a0001c0003t0002g0290 a0001c0003t0002g0311 a0001c0003t0002g0312 others(4): Show |
7 | HG01109.hp2 HG02055.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-29+3898C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3793502 | |||||||
chr11:3793527 | C | T | 1 | a0001c0001t0001g0038 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-29+3873G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3793527 | |||||||
chr11:3793584 | C | T | 1 | a0001c0001t0001g0335 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-29+3816G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3793584 | |||||||
chr11:3793595 | A | G | 1 | a0001c0001t0001g0133 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-29+3805T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3793595 | |||||||
chr11:3793632 | C | T | 2 | a0001c0001t0001g0068 a0001c0001t0001g0336 |
2 | HG02965.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-29+3768G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3793632 | |||||||
chr11:3793840 | C | T | 1 | a0001c0001t0001g0328 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-29+3560G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3793840 | |||||||
chr11:3793858 | A | G | 5 | a0001c0001t0001g0324 a0001c0001t0001g0335 a0001c0001t0008g0325 others(2): Show |
5 | HG00642.hp1 HG01433.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-29+3542T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3793858 | |||||||
chr11:3793895 | C | T | 7 | a0001c0003t0002g0290 a0001c0003t0002g0311 a0001c0003t0002g0312 others(4): Show |
7 | HG01109.hp2 HG02055.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-29+3505G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3793895 | |||||||
chr11:3793926 | A | G | 192 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0030 others(189): Show |
192 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(189): Show |
intron_variant | MODIFIER | c.-29+3474T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3793926 | |||||||
chr11:3793939 | A | C | 2 | a0001c0012t0001g0319 a0001c0012t0001g0320 |
2 | HG02109.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.-29+3461T>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3793939 | |||||||
chr11:3793954 | A | G | 7 | a0001c0003t0002g0290 a0001c0003t0002g0311 a0001c0003t0002g0312 others(4): Show |
7 | HG01109.hp2 HG02055.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-29+3446T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3793954 | |||||||
chr11:3793955 | G | C | 1 | a0001c0016t0001g0114 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-29+3445C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3793955 | |||||||
chr11:3793972 | A | AAAAT | 19 | a0001c0001t0001g0068 a0001c0001t0001g0324 a0001c0001t0001g0336 others(16): Show |
19 | HG00642.hp1 HG01081.hp1 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.-29+3424_-29+3427d others(6): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3793972 | |||||||
chr11:3794085 | G | A | 2 | a0001c0012t0001g0319 a0001c0012t0001g0320 |
2 | HG02109.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.-29+3315C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3794085 | |||||||
chr11:3794136 | T | A | 1 | a0001c0026t0001g0298 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-29+3264A>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3794136 | |||||||
chr11:3794141 | T | A | 6 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.-29+3259A>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3794141 | |||||||
chr11:3794306 | A | G | 198 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0030 others(195): Show |
198 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(195): Show |
intron_variant | MODIFIER | c.-29+3094T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3794306 | |||||||
chr11:3794378 | T | C | 2 | a0001c0001t0001g0068 a0001c0001t0001g0336 |
2 | HG02965.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-29+3022A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3794378 | |||||||
chr11:3794385 | A | C | 2 | a0001c0001t0001g0068 a0001c0001t0001g0336 |
2 | HG02965.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-29+3015T>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3794385 | |||||||
chr11:3794446 | G | A | 3 | a0006c0009t0001g0033 a0006c0009t0001g0034 a0006c0009t0001g0035 |
3 | HG02615.hp1 HG02818.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-29+2954C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3794446 | |||||||
chr11:3794496 | A | T | 1 | a0001c0016t0001g0114 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-29+2904T>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3794496 | |||||||
chr11:3794632 | T | C | 1 | a0001c0002t0001g0289 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-29+2768A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3794632 | |||||||
chr11:3794669 | A | C | 20 | a0001c0001t0001g0324 a0001c0001t0001g0335 a0001c0001t0008g0325 others(17): Show |
20 | HG00642.hp1 HG01081.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.-29+2731T>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3794669 | |||||||
chr11:3794669 | A | T | 2 | a0001c0001t0001g0068 a0001c0001t0001g0336 |
2 | HG02965.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-29+2731T>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3794669 | |||||||
chr11:3794872 | T | C | 24 | a0001c0001t0001g0068 a0001c0001t0001g0324 a0001c0001t0001g0335 others(21): Show |
24 | HG00642.hp1 HG01081.hp1 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.-29+2528A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3794872 | |||||||
chr11:3794967 | A | C | 194 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0030 others(191): Show |
194 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(191): Show |
intron_variant | MODIFIER | c.-29+2433T>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3794967 | |||||||
chr11:3795193 | C | T | 6 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.-29+2207G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3795193 | |||||||
chr11:3795240 | T | C | 57 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0041 others(54): Show |
57 | HG00408.hp2 HG00609.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.-29+2160A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3795240 | |||||||
chr11:3795359 | T | C | 77 | a0001c0001t0001g0076 a0001c0001t0001g0078 a0001c0001t0001g0081 others(74): Show |
77 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.-29+2041A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3795359 | |||||||
chr11:3795478 | A | G | 6 | a0002c0005t0001g0299 a0002c0005t0001g0300 a0002c0005t0001g0301 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.-29+1922T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3795478 | |||||||
chr11:3795547 | T | C | 6 | a0001c0003t0002g0290 a0001c0003t0002g0311 a0001c0003t0002g0312 others(3): Show |
6 | HG01109.hp2 HG02055.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.-29+1853A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3795547 | |||||||
chr11:3795580 | G | A | 6 | a0001c0001t0001g0291 a0001c0001t0001g0293 a0001c0001t0001g0296 others(3): Show |
6 | HG01243.hp1 HG02109.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-29+1820C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3795580 | |||||||
chr11:3795612 | G | A | 5 | a0001c0001t0001g0333 a0001c0001t0001g0334 a0001c0001t0001g0335 others(2): Show |
5 | HG01433.hp2 HG02145.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.-29+1788C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3795612 | |||||||
chr11:3795631 | A | T | 4 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(1): Show |
4 | HG01884.hp1 HG02280.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.-29+1769T>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3795631 | |||||||
chr11:3795850 | G | T | 1 | a0001c0001t0001g0112 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-29+1550C>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3795850 | |||||||
chr11:3795981 | G | T | 109 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(106): Show |
109 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.-29+1419C>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3795981 | |||||||
chr11:3796064 | C | T | 2 | a0001c0001t0001g0307 a0001c0001t0001g0308 |
2 | HG01346.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-29+1336G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3796064 | |||||||
chr11:3796120 | C | T | 22 | a0001c0001t0001g0026 a0001c0001t0001g0028 a0001c0002t0001g0007 others(19): Show |
22 | HG00597.hp1 HG01993.hp1 HG03239.hp1 others(19): Show |
intron_variant | MODIFIER | c.-29+1280G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3796120 | |||||||
chr11:3796212 | C | T | 8 | a0001c0001t0001g0305 a0001c0001t0001g0306 a0002c0005t0001g0299 others(5): Show |
8 | HG01081.hp1 HG01099.hp2 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.-29+1188G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3796212 | |||||||
chr11:3796410 | A | G | 1 | a0001c0001t0001g0335 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-29+990T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3796410 | |||||||
chr11:3796575 | T | C | 6 | a0001c0001t0001g0333 a0001c0001t0001g0334 a0001c0001t0001g0340 others(3): Show |
6 | HG01891.hp1 HG02145.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-29+825A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3796575 | |||||||
chr11:3796585 | A | C | 2 | a0001c0001t0001g0333 a0001c0001t0001g0334 |
2 | HG02145.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-29+815T>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3796585 | |||||||
chr11:3796626 | C | T | 1 | a0001c0001t0001g0006 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-29+774G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3796626 | |||||||
chr11:3796793 | A | C | 3 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0002c0008t0001g0003 |
3 | HG03490.hp2 HG03688.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.-29+607T>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3796793 | |||||||
chr11:3796813 | C | T | 1 | a0001c0001t0002g0002 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-29+587G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3796813 | |||||||
chr11:3796905 | G | C | 40 | a0001c0001t0001g0305 a0001c0001t0001g0306 a0001c0001t0001g0307 others(37): Show |
40 | HG00639.hp2 HG00642.hp1 HG01081.hp1 others(37): Show |
intron_variant | MODIFIER | c.-29+495C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3796905 | |||||||
chr11:3797010 | C | T | 1 | a0016c0023t0001g0001 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-29+390G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3797010 | |||||||
chr11:3797135 | G | A | 2 | a0001c0001t0001g0324 a0001c0001t0008g0325 |
2 | HG00642.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.-29+265C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3797135 | |||||||
chr11:3797195 | T | G | 2 | a0001c0002t0001g0326 a0001c0002t0001g0327 |
2 | NA19057.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.-29+205A>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3797195 | |||||||
chr11:3797294 | T | C | 1 | a0001c0001t0001g0332 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-29+106A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3797294 | |||||||
chr11:3797308 | G | A | 4 | a0001c0001t0001g0328 a0001c0001t0001g0329 a0001c0001t0004g0330 others(1): Show |
4 | HG02647.hp2 HG02717.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29+92C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3797308 | |||||||
chr11:3797324 | C | A | 1 | a0001c0001t0001g0332 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-29+76G>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3797324 | |||||||
chr11:3797385 | G | A | 9 | a0001c0001t0001g0333 a0001c0001t0001g0334 a0001c0001t0001g0335 others(6): Show |
9 | HG01433.hp2 HG01891.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.-29+15C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3797385 |