| 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 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and 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 | copy fasta | chr11 | 3670019 | 3802554 |
| a0002 | 0/0 | 1800 | 10 | 0 | 7 | 0 | 1 | 2 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0003 | 0/0 | 1800 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0004 | 0/0 | 1800 | 4 | 0 | 0 | 4 | 0 | 0 | 2 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0005 | 0/0 | 1800 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0006 | 0/0 | 1800 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0007 | 0/0 | 1800 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0008 | 0/0 | 1800 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0009 | 0/0 | 1800 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0010 | 0/0 | 1800 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0011 | 0/0 | 1800 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0012 | 0/0 | 1800 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0013 | 0/0 | 1800 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0014 | 0/0 | 1800 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0015 | 0/0 | 1800 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0016 | 0/0 | 1800 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0017 | 0/0 | 1800 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0018 | 0/0 | 1800 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0019 | 0/0 | 1800 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0020 | 0/0 | 1800 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0021 | 0/0 | 1800 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 5403 | 181 | 43 | 30 | 82 | 3 | 22 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| c0002 | 0/0 | 5403 | 96 | 18 | 6 | 62 | 2 | 8 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| c0003 | 0/0 | 5403 | 7 | 6 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| c0004 | 0/0 | 5403 | 6 | 6 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| c0005 | 0/0 | 5403 | 6 | 0 | 4 | 0 | 1 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| c0006 | 0/1 | 5403 | 5 | 2 | 2 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| c0007 | 0/0 | 5403 | 4 | 0 | 0 | 4 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| c0008 | 0/0 | 5403 | 4 | 0 | 3 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| c0009 | 0/0 | 5403 | 3 | 3 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| c0010 | 0/0 | 5403 | 2 | 2 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| c0011 | 0/0 | 5403 | 2 | 0 | 0 | 0 | 0 | 2 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| c0012 | 0/0 | 5403 | 2 | 2 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| c0013 | 0/0 | 5403 | 2 | 0 | 2 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| c0014 | 0/0 | 5403 | 2 | 0 | 0 | 2 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| c0015 | 0/0 | 5403 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| c0016 | 0/0 | 5403 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| c0017 | 0/0 | 5403 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| c0018 | 0/0 | 5403 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| c0019 | 0/0 | 5403 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| c0020 | 0/0 | 5403 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| c0021 | 0/0 | 5403 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| c0022 | 0/0 | 5403 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| c0023 | 0/0 | 5403 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| c0024 | 0/0 | 5403 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| c0025 | 0/0 | 5403 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| c0026 | 0/0 | 5403 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| c0027 | 0/0 | 5403 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| c0028 | 0/0 | 5403 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| c0029 | 0/0 | 5403 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| c0030 | 0/0 | 5403 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| c0031 | 0/0 | 5403 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| c0032 | 0/0 | 5403 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| c0033 | 0/0 | 5403 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| c0034 | 0/0 | 5403 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 1324 | 318 | 78 | 43 | 153 | 6 | 36 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| t0002 | 0/0 | 1320 | 12 | 9 | 3 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| t0003 | 0/0 | 1324 | 3 | 0 | 3 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| t0004 | 0/0 | 1324 | 2 | 2 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| t0005 | 0/0 | 1324 | 2 | 0 | 2 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| t0006 | 0/0 | 1324 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| t0007 | 0/0 | 1324 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| t0008 | 0/0 | 1324 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| t0009 | 0/0 | 1324 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| t0010 | 0/0 | 1324 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0190 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0238 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 5403 | 181 | 43 | 30 | 82 | 3 | 22 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0001c0002 | 0/0 | 5403 | 96 | 18 | 6 | 62 | 2 | 8 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0001c0003 | 0/0 | 5403 | 7 | 6 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0001c0006 | 0/1 | 5403 | 5 | 2 | 2 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0001c0012 | 0/0 | 5403 | 2 | 2 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0001c0016 | 0/0 | 5403 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0001c0017 | 0/0 | 5403 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0001c0020 | 0/0 | 5403 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0001c0024 | 0/0 | 5403 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0001c0026 | 0/0 | 5403 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0001c0032 | 0/0 | 5403 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0002c0005 | 0/0 | 5403 | 6 | 0 | 4 | 0 | 1 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0002c0008 | 0/0 | 5403 | 4 | 0 | 3 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0003c0004 | 0/0 | 5403 | 6 | 6 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0004c0007 | 0/0 | 5403 | 4 | 0 | 0 | 4 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0005c0010 | 0/0 | 5403 | 2 | 2 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0005c0021 | 0/0 | 5403 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0006c0009 | 0/0 | 5403 | 3 | 3 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0007c0027 | 0/0 | 5403 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0007c0028 | 0/0 | 5403 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0008c0011 | 0/0 | 5403 | 2 | 0 | 0 | 0 | 0 | 2 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0009c0013 | 0/0 | 5403 | 2 | 0 | 2 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0010c0014 | 0/0 | 5403 | 2 | 0 | 0 | 2 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0011c0034 | 0/0 | 5403 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0012c0033 | 0/0 | 5403 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0013c0015 | 0/0 | 5403 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0014c0031 | 0/0 | 5403 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0015c0030 | 0/0 | 5403 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0016c0029 | 0/0 | 5403 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0017c0023 | 0/0 | 5403 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0018c0019 | 0/0 | 5403 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0019c0022 | 0/0 | 5403 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0020c0025 | 0/0 | 5403 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0021c0018 | 0/0 | 5403 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | 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 | copy fasta | chr11 | 3670019 | 3802554 |
| a0001c0001t0002 | 0/0 | 6722 | 4 | 2 | 2 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0001c0001t0004 | 0/0 | 6726 | 2 | 2 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0001c0001t0006 | 0/0 | 6726 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0001c0001t0008 | 0/0 | 6726 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0001c0002t0001 | 0/0 | 6726 | 94 | 18 | 6 | 60 | 2 | 8 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0001c0002t0007 | 0/0 | 6726 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0001c0002t0010 | 0/0 | 6726 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0001c0003t0002 | 0/0 | 6722 | 7 | 6 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0001c0006t0001 | 0/1 | 6726 | 5 | 2 | 2 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0001c0012t0001 | 0/0 | 6726 | 2 | 2 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0001c0016t0001 | 0/0 | 6726 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0001c0017t0002 | 0/0 | 6722 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0001c0020t0001 | 0/0 | 6726 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0001c0024t0001 | 0/0 | 6726 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0001c0026t0001 | 0/0 | 6726 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0001c0032t0001 | 0/0 | 6726 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0002c0005t0001 | 0/0 | 6726 | 6 | 0 | 4 | 0 | 1 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0002c0008t0001 | 0/0 | 6726 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0002c0008t0003 | 0/0 | 6726 | 3 | 0 | 3 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0003c0004t0001 | 0/0 | 6726 | 6 | 6 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0004c0007t0001 | 0/0 | 6726 | 4 | 0 | 0 | 4 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0005c0010t0001 | 0/0 | 6726 | 2 | 2 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0005c0021t0001 | 0/0 | 6726 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0006c0009t0001 | 0/0 | 6726 | 3 | 3 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0007c0027t0001 | 0/0 | 6726 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0007c0028t0001 | 0/0 | 6726 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0008c0011t0001 | 0/0 | 6726 | 2 | 0 | 0 | 0 | 0 | 2 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0009c0013t0005 | 0/0 | 6726 | 2 | 0 | 2 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0010c0014t0001 | 0/0 | 6726 | 2 | 0 | 0 | 2 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0011c0034t0001 | 0/0 | 6726 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0012c0033t0001 | 0/0 | 6726 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0013c0015t0001 | 0/0 | 6726 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0014c0031t0001 | 0/0 | 6726 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0015c0030t0009 | 0/0 | 6726 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0016c0029t0001 | 0/0 | 6726 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0017c0023t0001 | 0/0 | 6726 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0018c0019t0001 | 0/0 | 6726 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0019c0022t0001 | 0/0 | 6726 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0020c0025t0001 | 0/0 | 6726 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| a0021c0018t0001 | 0/0 | 6726 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | copy fasta | chr11 | 3670019 | 3802554 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and 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 | 1 | 0 | 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 | 1 | 0 | 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 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0084 | 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 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| a0001c0001t0001g0147 | 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 |
| a0001c0001t0001g0153 | 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 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0188 | 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 |
| 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 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| a0001c0001t0001g0205 | 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 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| a0001c0001t0001g0294 | 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 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| a0001c0002t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| 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 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0002t0001g0085 | 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 | 1 | 0 | 0 | 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 |
| a0001c0002t0001g0206 | 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 |
| a0001c0002t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| a0001c0002t0001g0293 | 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 |
| a0001c0006t0001g0190 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| a0001c0006t0001g0203 | 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 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| a0002c0005t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| a0002c0005t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| a0002c0005t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 |
| a0007c0027t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| a0007c0028t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| a0008c0011t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| a0008c0011t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| a0009c0013t0005g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| a0009c0013t0005g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 |
| a0011c0034t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| a0012c0033t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| a0013c0015t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0015c0030t0009g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| a0016c0029t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| a0017c0023t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| a0018c0019t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| a0019c0022t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| a0020c0025t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| a0021c0018t0001g0099 | 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 | g0270 | 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 | g0151 | 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 | g0161 | EAS | CHS | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0051 | 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 | g0142 | EAS | CHS | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0248 | 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 | g0249 | 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 | g0042 | 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 | g0300 | AMR | PUR | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| HG01081 | hp2 | a0020 | 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 | g0247 | 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 | g0302 | 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 | g0041 | 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 | a0019 | 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 | a0009 | c0013 | t0005 | g0220 | 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 | g0229 | 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 | g0203 | AMR | CLM | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0228 | 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 | g0301 | 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 | a0016 | 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 | a0009 | 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 | g0188 | EAS | KHV | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0165 | 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 | g0143 | 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 | a0007 | c0028 | t0001 | g0148 | EAS | KHV | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | KHV | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| HG02129 | hp2 | a0001 | c0002 | t0001 | g0086 | EAS | KHV | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| HG02132 | hp1 | a0007 | c0027 | t0001 | g0154 | 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 | g0034 | AFR | GWD | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0044 | 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 | a0012 | 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 | g0219 | 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 | g0224 | SAS | PJL | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0225 | 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 | g0292 | 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 | g0294 | 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 | g0087 | 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 | a0017 | 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 | g0221 | SAS | PJL | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0146 | 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 | g0222 | 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 | g0073 | 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 | g0074 | 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 | a0008 | 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 | g0226 | SAS | PJL | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0015 | SAS | PJL | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| HG03492 | hp1 | a0008 | c0011 | t0001 | g0071 | SAS | PJL | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0227 | SAS | PJL | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0204 | 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 | g0293 | 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 | g0033 | 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 | g0299 | SAS | PJL | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| HG03654 | hp2 | a0018 | c0019 | t0001 | g0218 | 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 | g0206 | 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 | g0097 | 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 | g0156 | 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 | g0269 | 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 | g0189 | 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 | g0271 | 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 | g0276 | 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 | g0157 | 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 | g0019 | 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 | g0045 | 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 | g0083 | 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 | g0098 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| NA18974 | hp1 | a0001 | c0002 | t0001 | g0017 | 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 | g0153 | 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 | g0145 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0144 | 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 | g0016 | 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 | g0277 | 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 | g0230 | 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 | g0075 | 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 | g0223 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| NA19009 | hp1 | a0001 | c0002 | t0001 | g0268 | 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 | g0160 | 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 | a0011 | 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 | a0013 | c0015 | t0001 | g0283 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0152 | 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 | g0205 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| NA19060 | hp1 | a0001 | c0002 | t0001 | g0082 | 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 | g0084 | 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 | g0162 | 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 | g0147 | 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 | g0085 | 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 | g0018 | 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 | a0021 | c0018 | t0001 | g0099 | EAS | JPT | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0150 | 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 | g0166 | 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 | a0015 | 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 | g0020 | 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 | g0155 | 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 | g0291 | 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 | g0043 | 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 | hp1 | a0001 | c0006 | t0001 | g0190 | REF | REF | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0238 | REF | REF | NUP98_chr11_3670019_3802554 | NUP98 | chr11 | 3670019 | 3802554 |
| 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 | a0019 | 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 | a0018 | 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 | a0009 | 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 | a0017 | 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 | a0020 | 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 | a0008 | 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 | a0011 | 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 | a0007 | 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 | a0021 | 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 | a0016 | 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 | a0015 | 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 | a0013 | 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 | a0013 | 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 | a0011a0012 | 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 |
| 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 | a0001c0002a0003c0004a0007c0027others(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 | a0001c0012a0001c0026 | 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 | a0001c0006a0018c0019 | 6 | HG00741.hp2 HG01361.hp2 HG02896.hp1 others(3): 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 |
| 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 | a0009c0013t0005 | 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 | a0001c0001t0002a0001c0003t0002a0001c0017t0002 | 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 | a0015c0030t0009 | 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 | a0001c0001t0004a0001c0001t0006 | 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 |
| 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 | a0001c0001t0001g0275a0001c0001t0001g0307a0001c0002t0001g0211 | 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 | a0001c0001t0002g0002a0001c0001t0002g0314a0001c0001t0002g0317others(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 | a0001c0001t0001g0219 | 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 | a0004c0007t0001g0216a0004c0007t0001g0246 | 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 | a0001c0001t0001g0026a0001c0001t0001g0038a0001c0001t0001g0042others(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 | 102 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0028others(99): Show | 102 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(99): 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 | a0001c0001t0001g0065a0001c0001t0001g0172a0001c0001t0001g0184others(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 | a0001c0001t0001g0137a0001c0016t0001g0114a0001c0032t0001g0032others(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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | 174 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0028others(171): Show | 174 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(171): 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 | a0001c0002t0001g0262a0001c0002t0001g0264 | 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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0001c0001t0001g0121a0001c0001t0001g0129a0006c0009t0001g0033others(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 | 196 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(193): Show | 196 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(193): 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 | a0001c0001t0001g0144 | 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 | a0001c0001t0001g0028a0001c0001t0001g0051a0001c0001t0001g0053others(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 | a0001c0002t0001g0262a0001c0002t0001g0264a0001c0002t0001g0265others(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 | a0001c0001t0004g0330a0001c0001t0004g0331 | 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 | a0001c0001t0001g0275a0001c0001t0001g0307a0001c0012t0001g0319others(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 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(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 | 3 | a0001c0006t0001g0190a0001c0006t0001g0203a0001c0006t0001g0242 | 3 | HG00741.hp2 HG01361.hp2 homoSapiens_chm13v2.hp1 |
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 | a0001c0012t0001g0319a0001c0012t0001g0320 | 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 | a0001c0001t0001g0135a0001c0001t0001g0171a0001c0001t0001g0172others(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 | a0001c0001t0001g0029a0001c0001t0001g0039a0001c0001t0001g0049others(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 | a0001c0001t0001g0026a0001c0001t0001g0038a0001c0001t0001g0039others(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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0001c0001t0001g0006a0001c0001t0001g0075a0001c0001t0001g0081others(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 | a0001c0012t0001g0319a0001c0012t0001g0320a0001c0026t0001g0298 | 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 | a0001c0012t0001g0319a0001c0012t0001g0320 | 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 | a0001c0001t0002g0309a0001c0017t0002g0116 | 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 | a0001c0001t0001g0275a0001c0001t0001g0307a0001c0012t0001g0319others(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 | a0001c0001t0001g0026a0001c0001t0001g0038a0001c0001t0001g0039others(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 | a0001c0001t0001g0006a0001c0001t0001g0028a0001c0001t0001g0029others(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 | a0001c0001t0002g0309a0001c0002t0001g0092a0001c0002t0001g0103others(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 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0250others(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 | a0001c0001t0001g0026a0001c0001t0001g0042a0001c0001t0001g0043others(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 | a0001c0001t0001g0275a0001c0001t0001g0307 | 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 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0231 | 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 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0340 | 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 | a0001c0001t0001g0225 | 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 | a0001c0001t0004g0330a0001c0001t0004g0331 | 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 | 172 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(169): Show | 172 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(169): Show |
intron_variant | MODIFIER | c.4919-192T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 30/32 | chr11 | 3679900 | ||||||
| chr11:3679947
|
T | C | 171 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(168): Show | 171 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(168): 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 | a0001c0001t0001g0029a0001c0001t0001g0278a0001c0001t0001g0328 | 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 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0336others(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 | a0001c0001t0001g0026a0001c0001t0001g0038a0001c0001t0001g0039others(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 | a0001c0001t0001g0026a0001c0001t0001g0038a0001c0001t0001g0039others(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 | a0001c0001t0001g0068a0001c0001t0001g0275a0001c0001t0001g0307others(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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0001c0001t0001g0029a0001c0001t0001g0278a0001c0001t0001g0328 | 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 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0048others(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 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0336others(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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0001c0001t0001g0144 | 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 | 269 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(266): Show | 269 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(266): 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 | a0001c0001t0002g0309a0001c0017t0002g0116 | 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 | a0001c0001t0001g0026a0001c0001t0001g0038a0001c0001t0001g0039others(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 | a0001c0002t0001g0091a0001c0032t0001g0032 | 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 | a0001c0001t0001g0329a0001c0006t0001g0126a0001c0006t0001g0127 | 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 | a0001c0001t0001g0275a0001c0001t0001g0307a0001c0012t0001g0319others(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 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0340 | 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 | a0001c0001t0002g0309a0001c0017t0002g0116 | 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 | a0005c0010t0001g0338a0005c0010t0001g0339a0005c0021t0001g0259 | 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 | a0001c0001t0001g0026a0001c0001t0001g0038a0001c0001t0001g0039others(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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | 307 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(304): Show | 307 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(304): 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 | 223 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(220): Show | 223 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(220): Show |
intron_variant | MODIFIER | c.4677-273delA | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 29/32 | chr11 | 3683713 | ||||||
| chr11:3683805
|
C | T | 269 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(266): Show | 269 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(266): 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 | a0001c0001t0001g0275a0001c0001t0001g0307a0001c0001t0001g0337others(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 | 174 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(171): Show | 174 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(171): 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 | 167 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(164): Show | 167 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(164): 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 | 269 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(266): Show | 269 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(266): 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 | a0001c0002t0001g0015 | 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 | a0001c0001t0001g0029a0001c0001t0001g0278a0001c0001t0001g0328others(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 | a0001c0016t0001g0114a0005c0010t0001g0338a0005c0010t0001g0339others(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 | a0009c0013t0005g0037 | 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 | a0001c0002t0001g0070a0001c0002t0001g0077a0001c0002t0001g0080others(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 | a0001c0002t0001g0069a0001c0002t0001g0079a0001c0002t0001g0085others(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 | a0001c0002t0001g0088a0001c0002t0001g0093a0001c0002t0001g0094others(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 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044others(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 | a0001c0001t0001g0113a0001c0001t0001g0221a0001c0001t0001g0250others(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 | a0001c0001t0001g0275a0001c0001t0001g0307a0001c0001t0001g0337others(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 | a0001c0001t0001g0029a0001c0001t0001g0328 | 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 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0052others(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 | 150 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(147): Show | 150 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(147): 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 | a0001c0001t0001g0129a0001c0001t0001g0183a0001c0001t0001g0197others(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 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0336others(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 | a0013c0015t0001g0283 | 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 | 269 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(266): Show | 269 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(266): 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 | a0001c0006t0001g0126a0001c0006t0001g0127 | 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 | a0013c0015t0001g0283 | 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 | a0013c0015t0001g0283 | 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 | a0001c0001t0001g0029a0001c0001t0001g0278a0001c0001t0001g0328 | 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 | 176 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(173): Show | 176 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(173): 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 | a0001c0001t0001g0026a0001c0001t0001g0038a0001c0001t0001g0039others(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 | 230 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(227): Show | 230 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(227): Show |
intron_variant | MODIFIER | c.4676+757C>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 29/32 | chr11 | 3685216 | ||||||
| chr11:3685383
|
G | T | 105 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0028others(102): Show | 105 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(102): 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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0013c0015t0001g0283 | 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 | a0001c0001t0002g0309a0001c0017t0002g0116 | 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 | a0005c0010t0001g0338a0005c0010t0001g0339a0005c0021t0001g0259 | 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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | 158 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(155): Show | 158 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(155): 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 | a0001c0001t0001g0183a0001c0002t0001g0007a0001c0002t0001g0008others(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 | a0001c0001t0001g0026a0001c0001t0001g0038a0001c0001t0001g0039others(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 | a0001c0001t0001g0029a0001c0001t0001g0328 | 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 | a0001c0001t0001g0026a0001c0001t0001g0038a0001c0001t0001g0039others(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 | a0001c0001t0001g0275a0001c0001t0001g0307 | 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 | a0001c0002t0001g0085 | 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 | a0001c0012t0001g0319a0001c0012t0001g0320a0001c0026t0001g0298 | 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 | 168 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(165): Show | 168 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(165): 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 | a0001c0001t0001g0191a0001c0001t0001g0195a0001c0001t0001g0196others(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 | a0001c0001t0001g0026a0001c0001t0001g0038a0001c0001t0001g0039others(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 | a0001c0001t0001g0036a0001c0001t0001g0121a0001c0001t0001g0129others(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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0001c0012t0001g0319a0001c0012t0001g0320 | 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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0336others(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 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0336others(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 | a0001c0001t0001g0183a0001c0002t0001g0007a0001c0002t0001g0008others(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 | 270 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(267): Show | 270 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(267): 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 | a0001c0002t0001g0262a0001c0002t0001g0264a0001c0002t0001g0265others(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 | a0011c0034t0001g0122 | 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 | a0001c0001t0001g0029a0001c0001t0001g0278a0001c0001t0001g0328 | 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 | a0001c0001t0001g0183a0001c0002t0001g0007a0001c0002t0001g0008others(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 | a0017c0023t0001g0001 | 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 | a0001c0001t0001g0026a0001c0001t0001g0038a0001c0001t0001g0039others(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 | a0001c0001t0001g0026a0001c0001t0001g0038a0001c0001t0001g0039others(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 | a0001c0001t0001g0137a0001c0001t0001g0179a0001c0001t0001g0223others(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 | a0001c0001t0001g0232a0001c0016t0001g0114a0002c0005t0001g0302others(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 | a0001c0001t0001g0068a0001c0001t0001g0337 | 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 | a0001c0001t0001g0324a0001c0001t0008g0325 | 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 | a0001c0002t0001g0090a0002c0005t0001g0299a0002c0005t0001g0300others(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 | a0001c0001t0001g0038a0001c0001t0001g0287a0001c0001t0001g0310others(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 | a0001c0001t0001g0026a0001c0001t0001g0039a0001c0001t0001g0042others(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 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0076others(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 | a0001c0001t0001g0048a0001c0001t0001g0248a0004c0007t0001g0246 | 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 | 119 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0028others(116): Show | 119 | HG00323.hp1 HG00408.hp2 HG00609.hp2 others(116): 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 | a0001c0001t0001g0030a0001c0001t0001g0247a0001c0001t0001g0252others(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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0011c0034t0001g0122 | 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 | a0001c0002t0001g0262a0001c0002t0001g0264a0001c0002t0001g0265others(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 | a0001c0001t0001g0029a0001c0001t0001g0278a0001c0001t0001g0328 | 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 | a0001c0001t0002g0309a0001c0017t0002g0116 | 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 | 338 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(335): Show | 338 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(335): 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 | a0001c0001t0002g0309a0001c0017t0002g0116 | 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 | a0001c0001t0001g0004a0001c0001t0001g0053a0001c0001t0001g0055others(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 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0031others(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 | a0001c0001t0001g0026a0001c0001t0001g0038a0001c0001t0001g0039others(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 | a0001c0001t0001g0006a0001c0001t0001g0075a0001c0001t0001g0081others(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 | 3 | a0001c0006t0001g0190a0001c0006t0001g0203a0001c0006t0001g0242 | 3 | HG00741.hp2 HG01361.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.4454+895C>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 28/32 | chr11 | 3690452 | ||||||
| chr11:3690453
|
G | T | 2 | a0001c0001t0001g0029a0001c0001t0001g0328 | 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 | a0007c0028t0001g0148 | 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 | a0005c0010t0001g0338a0005c0010t0001g0339a0005c0021t0001g0259 | 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 | a0001c0001t0001g0026a0001c0001t0001g0038a0001c0001t0001g0039others(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 | a0001c0001t0001g0026a0001c0001t0001g0038a0001c0001t0001g0039others(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 | a0001c0001t0004g0330a0001c0001t0004g0331a0001c0001t0006g0297 | 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 | a0001c0001t0001g0226a0001c0001t0001g0227 | 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 | a0001c0002t0001g0260a0001c0002t0001g0269a0001c0002t0001g0270others(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 | a0001c0001t0001g0026a0001c0001t0001g0038a0001c0001t0001g0039others(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 | a0001c0001t0001g0042 | 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 | a0001c0012t0001g0319a0001c0012t0001g0320 | 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 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0048others(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 | a0001c0001t0001g0029a0001c0001t0001g0278a0001c0001t0001g0328 | 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 | a0001c0001t0001g0004a0001c0001t0001g0041a0001c0001t0001g0146others(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 | a0001c0001t0001g0029a0001c0001t0001g0278a0001c0001t0001g0328 | 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 | a0001c0002t0001g0079a0001c0002t0001g0080a0001c0002t0001g0092others(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 | a0001c0016t0001g0114a0005c0010t0001g0338a0005c0010t0001g0339others(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 | a0001c0016t0001g0114a0005c0010t0001g0338a0005c0010t0001g0339others(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 | a0001c0001t0001g0068a0001c0001t0001g0180a0001c0001t0001g0209others(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 | a0001c0001t0001g0026a0001c0001t0001g0038a0001c0001t0001g0039others(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 | a0001c0002t0001g0080a0003c0004t0001g0115a0003c0004t0001g0117others(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 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0336others(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 | a0001c0001t0001g0029a0001c0001t0001g0278a0001c0001t0001g0328 | 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 | a0001c0001t0001g0006a0001c0001t0001g0075a0001c0001t0001g0081others(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 | a0001c0002t0001g0007a0001c0002t0001g0008a0001c0002t0001g0009others(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 | a0001c0001t0001g0113a0001c0001t0001g0275a0001c0001t0001g0307others(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 | a0001c0001t0001g0026a0001c0001t0001g0038a0001c0001t0001g0039others(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 | a0001c0001t0001g0036a0001c0001t0001g0121a0001c0001t0001g0129others(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 | a0001c0001t0001g0006a0001c0001t0001g0026a0001c0001t0001g0029others(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 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0157others(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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0001c0001t0001g0036a0001c0001t0001g0121a0001c0001t0001g0129others(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 | a0001c0002t0001g0007a0001c0002t0001g0008a0001c0002t0001g0009others(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 | a0001c0001t0001g0138a0001c0001t0001g0159a0001c0001t0001g0160 | 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 | a0001c0001t0001g0113a0001c0001t0001g0173a0001c0001t0001g0275others(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 | a0001c0002t0001g0077a0001c0002t0001g0082a0001c0002t0001g0083others(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 | a0001c0002t0001g0069a0001c0002t0001g0070a0001c0002t0001g0073others(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 | a0001c0002t0001g0069a0001c0002t0001g0070a0001c0002t0001g0073others(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 | a0001c0001t0001g0136a0001c0001t0001g0147 | 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 | a0001c0001t0002g0309a0001c0017t0002g0116 | 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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0001c0001t0001g0183a0001c0002t0001g0007a0001c0002t0001g0008others(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 | a0001c0001t0001g0026a0001c0001t0001g0038a0001c0001t0001g0039others(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 | a0001c0001t0002g0309a0001c0017t0002g0116a0002c0005t0001g0299others(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 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0164others(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 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0336others(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 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0038others(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 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0038others(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 | a0001c0001t0001g0146 | 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 | a0001c0001t0001g0241a0001c0001t0002g0002a0001c0001t0002g0314others(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 | a0001c0001t0001g0068a0001c0001t0001g0275a0001c0001t0001g0307others(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 | a0001c0001t0001g0180a0001c0001t0001g0182 | 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 | a0001c0001t0002g0002a0001c0001t0002g0314a0001c0001t0002g0317others(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 | a0005c0010t0001g0338a0005c0010t0001g0339a0005c0021t0001g0259 | 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 | 3 | a0001c0006t0001g0190a0001c0006t0001g0203a0001c0006t0001g0242 | 3 | HG00741.hp2 HG01361.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.4167+332G>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 26/32 | chr11 | 3695117 | ||||||
| chr11:3695154
|
C | T | 4 | a0001c0016t0001g0114a0005c0010t0001g0338a0005c0010t0001g0339others(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 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0038others(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 | a0005c0010t0001g0338a0005c0010t0001g0339a0005c0021t0001g0259 | 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 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0336others(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 | a0001c0001t0001g0029a0001c0001t0001g0278a0001c0001t0001g0328 | 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 | a0001c0002t0001g0007a0001c0002t0001g0008a0001c0002t0001g0009others(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 | a0001c0002t0001g0286a0001c0002t0001g0288 | 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 | a0001c0001t0001g0188 | 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 | a0001c0001t0001g0247a0001c0001t0001g0249a0001c0001t0001g0252 | 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 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0340 | 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 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0336others(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 | a0007c0027t0001g0154 | 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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0001c0002t0001g0206 | 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 | a0001c0001t0001g0029a0001c0001t0001g0068a0001c0001t0001g0275others(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 | a0004c0007t0001g0213a0004c0007t0001g0245 | 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 | a0001c0001t0001g0006a0001c0001t0001g0075a0001c0001t0001g0081others(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 | a0001c0001t0001g0026a0001c0001t0001g0038a0001c0001t0001g0039others(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 | a0001c0001t0001g0026a0001c0001t0001g0038a0001c0001t0001g0039others(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 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0183others(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 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0038others(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 | a0001c0002t0001g0069a0001c0002t0001g0073a0001c0002t0001g0079others(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 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0081others(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 | a0001c0002t0001g0082a0001c0002t0001g0091a0001c0002t0001g0101others(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 | 89 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0051others(86): Show | 89 | HG00323.hp1 HG00408.hp2 HG00609.hp1 others(86): Show |
intron_variant | MODIFIER | c.4009+1261delT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 25/32 | chr11 | 3697820 | ||||||
| chr11:3697820
|
TAA | T | 61 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0030others(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 | a0001c0001t0001g0151a0001c0001t0001g0164a0001c0001t0001g0170others(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 | a0001c0001t0001g0029a0001c0001t0001g0328a0002c0005t0001g0299others(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 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0048others(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 | a0001c0001t0001g0026a0001c0001t0001g0038a0001c0001t0001g0039others(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 | a0001c0001t0001g0029a0001c0001t0001g0328 | 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 | a0001c0001t0001g0183a0001c0001t0001g0292a0001c0001t0001g0294others(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 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0336others(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 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0081others(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 | a0011c0034t0001g0122 | 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 | a0001c0001t0001g0006a0001c0001t0001g0026a0001c0001t0001g0030others(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 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0049others(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 | a0001c0001t0001g0113a0001c0001t0001g0159a0001c0001t0001g0275others(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 | a0001c0001t0001g0036a0001c0001t0001g0053a0001c0001t0001g0068others(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 | a0001c0001t0001g0336a0001c0001t0002g0309a0001c0012t0001g0319others(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 | a0005c0010t0001g0338a0005c0010t0001g0339a0005c0021t0001g0259 | 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 | a0001c0001t0001g0029a0001c0001t0001g0068a0001c0001t0001g0324others(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 | a0001c0001t0001g0006a0001c0001t0001g0075a0001c0001t0001g0078others(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 | a0003c0004t0001g0115a0003c0004t0001g0117a0003c0004t0001g0118others(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 | a0002c0008t0001g0003a0002c0008t0003g0040a0002c0008t0003g0062others(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 | a0001c0001t0001g0183a0001c0001t0001g0292a0001c0001t0001g0294others(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 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0038others(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 | a0001c0001t0001g0183a0001c0001t0001g0292a0001c0001t0001g0294others(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 | a0001c0002t0001g0087a0001c0002t0001g0088a0001c0002t0001g0104 | 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 | ||||||
| chr11:3700239
|
A | G | 341 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(338): Show | 341 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(338): Show |
intron_variant | MODIFIER | c.3742+371T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 24/32 | chr11 | 3700239 | ||||||
| chr11:3700249
|
A | G | 1 | a0001c0001t0001g0219 | 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 | a0001c0001t0001g0026a0001c0001t0001g0038a0001c0001t0001g0039others(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 | a0001c0001t0001g0029a0001c0001t0001g0202a0001c0001t0001g0324others(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 | a0001c0001t0001g0181a0001c0001t0001g0183a0001c0001t0001g0191others(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 | a0001c0001t0001g0006a0001c0001t0001g0084a0001c0001t0001g0112others(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 | a0001c0001t0001g0055a0001c0001t0001g0066 | 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 | a0001c0002t0001g0286a0001c0002t0001g0288 | 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 | a0001c0001t0002g0309a0001c0017t0002g0116 | 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 | a0001c0001t0001g0081a0001c0001t0001g0278a0001c0001t0001g0287others(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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0001c0001t0001g0149 | 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 | a0005c0010t0001g0338a0005c0010t0001g0339a0005c0021t0001g0259 | 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 | a0001c0001t0001g0036a0001c0001t0001g0055a0001c0001t0001g0200others(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 | a0001c0001t0001g0050a0001c0001t0001g0068a0001c0001t0001g0113others(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 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0038others(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 | a0001c0002t0001g0289a0001c0012t0001g0319a0001c0012t0001g0320others(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 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0038others(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 | a0001c0001t0002g0309a0001c0012t0001g0319a0001c0012t0001g0320others(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 | a0011c0034t0001g0122 | 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 | a0001c0001t0001g0006a0001c0001t0001g0135a0001c0001t0001g0137others(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 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0038others(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 | a0001c0001t0001g0225 | 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 | a0001c0001t0002g0002a0001c0001t0002g0314a0001c0001t0002g0317others(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 | a0001c0001t0001g0223 | 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 | a0001c0001t0001g0006a0001c0001t0001g0026a0001c0001t0001g0029others(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 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0333 | 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 | a0001c0001t0001g0156 | 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 | a0001c0001t0001g0113a0001c0001t0001g0329 | 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 | a0001c0001t0001g0068a0001c0001t0001g0310 | 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 | a0001c0001t0001g0324a0001c0001t0008g0325 | 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 | a0001c0002t0001g0315a0011c0034t0001g0122a0016c0029t0001g0134 | 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 | a0002c0005t0001g0300 | 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 | a0001c0032t0001g0032a0002c0008t0001g0003a0002c0008t0003g0040others(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 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0231others(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 | a0001c0001t0001g0166a0001c0001t0001g0173a0001c0001t0001g0228others(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 | a0001c0001t0001g0084a0001c0001t0001g0121a0001c0001t0001g0129others(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 | a0001c0001t0001g0004a0001c0001t0001g0075a0001c0001t0001g0112others(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 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0150others(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 | a0001c0001t0001g0006a0001c0001t0001g0042a0001c0001t0001g0142others(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 | a0001c0001t0001g0030a0001c0001t0001g0038a0001c0001t0001g0045others(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 | a0001c0001t0001g0031a0001c0001t0001g0048a0001c0001t0001g0063others(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 | a0001c0001t0001g0050a0001c0001t0001g0135a0001c0001t0001g0144others(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 | a0001c0001t0001g0026a0001c0001t0001g0036a0001c0001t0001g0039others(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 | a0001c0001t0001g0029a0001c0001t0001g0067a0001c0001t0001g0328others(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 | a0001c0006t0001g0126a0001c0006t0001g0127a0002c0005t0001g0299others(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 | a0001c0001t0001g0292a0001c0001t0001g0294a0001c0001t0001g0296others(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 | a0001c0002t0001g0073a0001c0002t0001g0074 | 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 | 69 | a0001c0001t0001g0028a0001c0001t0001g0051a0001c0001t0001g0052others(66): Show | 69 | HG00323.hp1 HG00408.hp2 HG00609.hp2 others(66): 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 | a0001c0001t0001g0133a0001c0001t0001g0179a0001c0001t0001g0180others(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 | a0001c0001t0001g0133a0001c0001t0001g0179a0001c0001t0002g0314others(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 | a0001c0001t0001g0112a0001c0001t0001g0139a0001c0001t0002g0002others(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 | a0004c0007t0001g0213a0004c0007t0001g0245 | 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 | a0001c0001t0001g0158a0001c0001t0001g0237a0001c0001t0001g0258others(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 | a0004c0007t0001g0216a0004c0007t0001g0246 | 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 | a0001c0001t0001g0005a0001c0001t0001g0306a0001c0002t0001g0206others(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 | a0001c0001t0001g0042a0001c0001t0001g0275a0001c0001t0001g0307others(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 | 41 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(38): Show | 41 | HG00408.hp2 HG00639.hp1 HG00733.hp1 others(38): 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 | a0001c0001t0001g0051a0001c0001t0001g0059a0001c0001t0001g0186 | 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 | a0001c0001t0001g0028a0001c0001t0001g0189a0001c0001t0001g0198others(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 | a0001c0001t0001g0204a0001c0001t0001g0222a0001c0001t0001g0240 | 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 | a0001c0001t0001g0030a0001c0001t0001g0038a0001c0001t0001g0042others(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 | a0001c0001t0001g0180a0001c0001t0001g0191a0001c0001t0001g0194others(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 | a0001c0001t0001g0031a0001c0001t0001g0038a0001c0001t0001g0042others(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 | a0001c0001t0001g0038a0001c0001t0001g0042a0001c0001t0001g0045others(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 | a0001c0001t0001g0026a0001c0001t0001g0036a0001c0001t0001g0038others(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 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0038others(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 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0038others(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 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0038others(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 | a0001c0001t0001g0026a0001c0001t0001g0050a0001c0002t0001g0322 | 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 | a0001c0002t0001g0073a0001c0002t0001g0074 | 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 | a0001c0001t0001g0275a0001c0001t0001g0307 | 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 | a0001c0001t0002g0314a0001c0001t0002g0317 | 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 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0133others(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 | a0001c0001t0001g0228 | 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 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0038others(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 | a0001c0001t0001g0194a0001c0001t0001g0205a0001c0001t0001g0250 | 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 | a0001c0001t0001g0006a0001c0001t0001g0075a0001c0001t0001g0078others(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 | a0005c0010t0001g0339a0005c0021t0001g0259 | 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 | a0001c0001t0001g0237a0020c0025t0001g0236 | 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 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0081others(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 | a0001c0001t0001g0275a0001c0001t0001g0307 | 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 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0081others(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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0011c0034t0001g0122 | 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 | a0001c0001t0001g0029a0001c0001t0001g0068a0001c0001t0001g0324others(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 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0336others(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 | a0001c0001t0001g0308a0001c0003t0002g0311a0017c0023t0001g0001 | 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 | a0001c0002t0001g0077a0001c0002t0001g0082a0001c0002t0001g0083others(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 | a0001c0001t0001g0029a0001c0001t0001g0328 | 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 | a0001c0012t0001g0319a0001c0012t0001g0320 | 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 | a0001c0001t0001g0026a0001c0001t0001g0038a0001c0001t0001g0039others(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 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0031others(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 | a0001c0001t0001g0029a0001c0001t0001g0038a0001c0001t0001g0039others(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 | a0001c0001t0001g0324a0001c0001t0008g0325a0005c0010t0001g0338others(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 | a0001c0001t0001g0324a0001c0001t0008g0325a0005c0010t0001g0338others(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 | a0001c0001t0001g0068a0001c0001t0001g0336 | 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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0001c0001t0001g0329a0001c0001t0001g0337a0001c0001t0004g0330others(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 | a0001c0001t0001g0026a0001c0002t0001g0015 | 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 | a0001c0001t0001g0029a0001c0001t0001g0060a0001c0001t0001g0063others(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 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0045others(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 | a0001c0001t0001g0042a0001c0001t0001g0057a0001c0001t0001g0061others(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 | a0001c0001t0001g0113a0001c0026t0001g0298 | 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 |
58 | a0001c0001t0001g0005a0001c0001t0001g0028a0001c0001t0001g0108others(55): Show | 58 | HG00323.hp1 HG00544.hp2 HG00621.hp1 others(55): 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 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0036others(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 | a0001c0001t0001g0026a0001c0001t0001g0199a0001c0001t0001g0202others(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 | a0001c0001t0001g0205a0001c0002t0001g0019a0001c0002t0001g0027others(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 | a0001c0001t0001g0041a0001c0001t0001g0043a0001c0001t0001g0075others(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 | a0001c0001t0001g0044a0001c0001t0001g0078a0001c0001t0001g0081others(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 | a0001c0001t0001g0006a0001c0001t0001g0145a0001c0001t0001g0150others(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 | a0001c0001t0001g0112a0001c0001t0001g0136a0001c0001t0001g0138others(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 | a0001c0001t0001g0141a0001c0001t0001g0144a0001c0001t0001g0161others(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 | a0001c0001t0001g0188a0001c0002t0001g0260 | 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 | a0001c0001t0001g0159a0001c0001t0001g0169a0001c0001t0001g0170others(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 | a0015c0030t0009g0168 | 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 | a0001c0001t0001g0140a0001c0001t0001g0174a0001c0001t0001g0176 | 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 | a0011c0034t0001g0122 | 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 | a0001c0001t0001g0136a0001c0001t0001g0147 | 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 | a0001c0001t0002g0314a0001c0001t0002g0317a0001c0002t0001g0123 | 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 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0030others(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 | a0005c0010t0001g0338a0005c0010t0001g0339 | 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 | a0001c0001t0001g0005a0001c0001t0001g0068a0001c0001t0001g0169others(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 | a0001c0012t0001g0319a0001c0012t0001g0320 | 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 | a0001c0001t0001g0029a0001c0001t0001g0328 | 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 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0041others(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 | a0003c0004t0001g0115a0003c0004t0001g0118a0003c0004t0001g0120 | 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 | 321 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0026others(318): Show | 321 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(318): 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 | a0001c0012t0001g0319a0001c0012t0001g0320 | 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 | a0001c0001t0001g0036a0001c0001t0001g0050a0001c0001t0001g0059others(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 | a0001c0001t0001g0006a0001c0001t0001g0075a0001c0001t0001g0076others(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 | 227 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0026others(224): Show | 227 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(224): 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 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0039others(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 | a0001c0001t0001g0228a0001c0016t0001g0114 | 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 | a0001c0001t0001g0113a0001c0001t0001g0333a0001c0001t0001g0334 | 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 | a0001c0001t0001g0043a0001c0001t0001g0063a0001c0001t0001g0075others(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 | a0001c0001t0001g0030a0001c0001t0001g0068a0001c0001t0001g0147others(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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0041others(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 | a0001c0002t0001g0086 | 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 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(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 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0336others(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 | a0001c0002t0001g0086a0001c0002t0001g0101a0001c0002t0001g0106 | 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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0001c0001t0001g0029a0001c0001t0001g0328 | 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 | a0001c0002t0001g0073a0001c0002t0001g0074a0001c0002t0001g0322 | 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 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0336others(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 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0336others(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 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0030others(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 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0078others(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 | a0001c0012t0001g0319a0001c0012t0001g0320 | 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 | a0001c0001t0001g0333a0001c0001t0001g0334a0001c0017t0002g0116 | 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 | a0001c0001t0001g0036a0001c0001t0001g0179 | 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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0336others(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 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0030others(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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0001c0002t0001g0192a0001c0002t0001g0193a0001c0002t0001g0211 | 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 | a0001c0001t0001g0138a0001c0001t0001g0159a0001c0001t0001g0160 | 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 | a0001c0001t0001g0329a0001c0001t0001g0337a0001c0001t0004g0330others(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 | a0001c0002t0001g0193a0001c0002t0001g0211 | 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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0001c0001t0001g0324a0001c0001t0008g0325a0005c0010t0001g0338others(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 | a0001c0001t0001g0028a0001c0001t0001g0038a0001c0001t0001g0186others(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 | a0001c0012t0001g0319a0001c0012t0001g0320 | 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 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0030others(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 | a0001c0001t0001g0324a0001c0001t0008g0325a0005c0010t0001g0338others(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 | a0005c0010t0001g0338a0005c0010t0001g0339 | 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 | a0001c0002t0001g0267a0001c0002t0001g0271 | 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 | a0017c0023t0001g0001 | 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 | a0001c0001t0001g0006a0001c0001t0001g0026a0001c0001t0001g0029others(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 | a0009c0013t0005g0220 | 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 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0078others(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 | a0001c0001t0001g0191a0001c0001t0001g0195a0001c0001t0001g0196others(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 | a0001c0001t0001g0026a0001c0001t0001g0030a0001c0001t0001g0031others(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 | a0001c0001t0001g0108a0001c0001t0001g0324a0001c0001t0008g0325others(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 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053others(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 | a0001c0001t0001g0165 | 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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0001c0001t0001g0041a0001c0001t0001g0043a0001c0001t0001g0044others(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 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0336others(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 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0030others(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 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0078others(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 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0336others(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 | a0001c0002t0001g0262a0001c0002t0001g0264a0010c0014t0001g0263 | 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 | a0001c0001t0002g0002a0001c0001t0002g0309a0001c0002t0001g0123others(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 | a0001c0001t0001g0329a0001c0001t0001g0337a0001c0001t0004g0330others(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 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0336others(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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0001c0001t0001g0180a0001c0001t0001g0182 | 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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0001c0001t0001g0333a0001c0001t0001g0334 | 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 | a0001c0001t0001g0026a0001c0001t0001g0030a0001c0001t0001g0031others(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 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0333others(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 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0041others(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 | a0001c0001t0001g0026a0001c0001t0001g0030a0001c0001t0001g0031others(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 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0336others(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 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0030others(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 | a0001c0001t0001g0135a0001c0001t0001g0171a0001c0001t0001g0172others(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 | a0005c0010t0001g0338a0005c0010t0001g0339 | 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 | a0001c0002t0001g0069a0001c0002t0001g0093a0001c0002t0001g0095others(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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0011c0034t0001g0122 | 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 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0068others(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 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0038others(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 | a0001c0001t0001g0184a0001c0001t0001g0324a0001c0001t0008g0325others(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 | a0001c0001t0001g0068a0001c0001t0001g0230a0001c0001t0001g0335others(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 | a0001c0001t0001g0026a0001c0001t0001g0051a0001c0001t0001g0183others(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 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0038others(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 | a0001c0001t0001g0044a0001c0001t0001g0053a0001c0001t0001g0054others(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 | a0001c0001t0001g0055a0001c0001t0001g0060a0001c0001t0001g0066others(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 | a0001c0001t0001g0052a0001c0001t0001g0329a0002c0005t0001g0304 | 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 | a0001c0001t0001g0113a0001c0001t0001g0337 | 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 | 91 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0108others(88): Show | 91 | HG00323.hp1 HG00423.hp2 HG00544.hp2 others(88): 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 | a0001c0001t0001g0006a0001c0001t0001g0112a0001c0001t0001g0136others(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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0001c0012t0001g0319a0001c0012t0001g0320 | 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 | a0001c0001t0001g0224 | 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 | a0001c0001t0001g0026a0001c0001t0001g0030a0001c0001t0001g0031others(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 | a0001c0001t0001g0051 | 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 | a0001c0001t0001g0029a0001c0001t0001g0038a0001c0001t0001g0039others(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 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0030others(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 | a0001c0001t0002g0002a0001c0002t0001g0124a0001c0002t0001g0131others(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 | a0001c0003t0002g0290a0001c0003t0002g0311a0001c0003t0002g0312others(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 | a0001c0001t0001g0031a0001c0001t0001g0047a0001c0001t0001g0113others(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 | a0001c0001t0001g0068a0001c0001t0001g0226a0001c0001t0001g0231others(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 | a0001c0001t0001g0026a0001c0001t0001g0030a0001c0001t0001g0031others(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 | a0001c0002t0001g0192a0001c0002t0001g0193a0001c0002t0001g0211 | 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 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227 | 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 | a0001c0001t0001g0026a0001c0001t0001g0030a0001c0001t0001g0031others(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 | a0001c0001t0001g0029a0001c0001t0001g0068a0001c0001t0001g0324others(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 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0042others(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 | a0001c0001t0001g0026a0001c0001t0001g0030a0001c0001t0001g0031others(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 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0042others(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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0001c0001t0002g0002a0001c0001t0002g0309a0001c0002t0001g0124others(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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0030others(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 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0042others(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 | a0001c0001t0001g0109a0001c0001t0001g0329 | 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 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0030others(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 | a0001c0001t0001g0068a0001c0001t0001g0129a0001c0001t0001g0324others(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 | a0001c0001t0001g0324a0001c0001t0008g0325a0005c0010t0001g0338others(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 | a0001c0003t0002g0290a0001c0003t0002g0311a0001c0003t0002g0312others(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 | a0001c0001t0001g0068a0001c0001t0001g0336 | 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 | a0001c0001t0001g0292a0001c0001t0001g0294a0001c0001t0001g0296others(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 | a0001c0001t0001g0324a0001c0001t0008g0325a0005c0010t0001g0338others(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 | a0001c0002t0001g0073a0001c0002t0001g0074a0001c0002t0001g0192others(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 | a0001c0001t0001g0026a0001c0001t0001g0030a0001c0001t0001g0031others(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 | a0001c0002t0001g0012a0001c0002t0001g0020a0001c0002t0001g0021others(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 | a0005c0010t0001g0338a0005c0010t0001g0339 | 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 | a0001c0001t0001g0324a0001c0001t0008g0325 | 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 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0047others(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 | a0001c0001t0001g0029a0001c0001t0001g0038a0001c0001t0001g0039others(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 | a0001c0001t0001g0054a0001c0001t0001g0113a0001c0001t0001g0254others(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 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0287others(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 | a0001c0001t0001g0078a0001c0001t0001g0081a0001c0002t0001g0079others(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 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0084others(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 | a0001c0002t0001g0281a0001c0002t0001g0326 | 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 | a0001c0001t0001g0041a0001c0001t0001g0278a0001c0002t0001g0261 | 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 | a0001c0001t0001g0068a0001c0001t0001g0336 | 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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0012c0033t0001g0130 | 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 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0030others(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 | a0001c0001t0001g0335a0001c0001t0002g0314a0001c0001t0002g0317others(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 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0336others(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 | a0001c0012t0001g0319a0001c0012t0001g0320 | 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 | a0005c0010t0001g0338a0005c0010t0001g0339 | 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 | a0001c0001t0001g0199a0001c0001t0001g0201a0001c0001t0001g0202 | 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 | a0001c0001t0002g0314a0001c0001t0002g0317a0003c0004t0001g0316 | 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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0001c0001t0001g0329a0001c0001t0001g0337a0001c0001t0004g0330others(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 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0042others(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 | a0001c0001t0001g0042a0001c0001t0001g0061a0001c0001t0001g0253others(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 | a0001c0001t0001g0042a0001c0001t0001g0061a0001c0001t0001g0253others(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 | a0001c0001t0001g0231a0001c0001t0001g0292a0001c0001t0001g0294others(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 | a0001c0001t0001g0068a0001c0001t0001g0336a0001c0002t0001g0098others(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 | a0003c0004t0001g0115a0003c0004t0001g0117a0003c0004t0001g0118others(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 | a0001c0001t0001g0068a0001c0001t0001g0336 | 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 | a0001c0012t0001g0319a0001c0012t0001g0320 | 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 | a0001c0001t0001g0324a0001c0001t0008g0325a0005c0010t0001g0338others(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 | a0001c0001t0002g0314a0001c0001t0002g0317a0003c0004t0001g0316 | 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 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0336others(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 | a0001c0001t0001g0041a0001c0001t0001g0043a0001c0001t0001g0044others(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 | a0005c0010t0001g0338a0005c0010t0001g0339 | 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 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0336others(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 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0336others(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 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0336others(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 | a0001c0001t0001g0026a0001c0001t0001g0030a0001c0001t0001g0031others(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 | a0001c0003t0002g0290a0001c0003t0002g0311a0001c0003t0002g0312others(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 | a0001c0002t0001g0012a0001c0032t0001g0032 | 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 | a0003c0004t0001g0115a0003c0004t0001g0117a0003c0004t0001g0118others(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 | a0001c0001t0002g0314a0001c0001t0002g0317a0003c0004t0001g0316 | 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 | a0015c0030t0009g0168 | 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 | a0001c0001t0001g0159a0001c0001t0001g0160 | 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 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0041others(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 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0041others(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 | a0001c0001t0001g0324a0001c0001t0008g0325 | 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 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0336others(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 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0336others(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 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0030others(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 | a0005c0010t0001g0338a0005c0010t0001g0339 | 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 | a0020c0025t0001g0236 | 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 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0030others(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 | a0005c0010t0001g0338a0005c0010t0001g0339 | 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 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0030others(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 | a0001c0002t0001g0268 | 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 | a0001c0001t0001g0029a0001c0001t0001g0038a0001c0001t0001g0039others(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 | a0001c0001t0001g0052a0001c0001t0001g0060 | 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 | a0002c0005t0001g0299 | 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 | a0001c0001t0001g0109a0001c0001t0001g0112a0001c0001t0001g0135others(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 | a0001c0001t0001g0006a0001c0001t0001g0036a0001c0001t0001g0068others(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 | a0001c0001t0001g0324a0001c0012t0001g0319a0001c0012t0001g0320others(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 | a0001c0001t0001g0038a0001c0001t0001g0041a0001c0001t0001g0042others(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 | 42 | a0001c0001t0001g0006a0001c0001t0001g0036a0001c0001t0001g0112others(39): Show | 42 | HG00544.hp2 HG00639.hp1 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.1730+1675dupT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 14/32 | chr11 | 3729715 | ||||||
| chr11:3729715
|
C | CAA | 7 | a0001c0001t0001g0214a0001c0001t0001g0335a0001c0003t0002g0290others(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 | a0001c0001t0001g0038a0001c0001t0001g0055 | 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 | a0001c0001t0001g0255a0001c0001t0008g0325a0002c0005t0001g0302 | 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 | a0001c0001t0001g0324a0002c0005t0001g0300a0002c0005t0001g0303 | 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 | a0001c0001t0001g0054a0001c0001t0001g0334a0002c0005t0001g0301others(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 | a0001c0001t0001g0253a0012c0033t0001g0130 | 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 | a0001c0001t0001g0050a0002c0005t0001g0299 | 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 | a0001c0001t0001g0041a0001c0001t0001g0047 | 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 | a0001c0001t0001g0043a0001c0001t0001g0049a0001c0001t0001g0254others(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 | a0011c0034t0001g0122 | 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 | a0001c0001t0001g0059a0002c0008t0003g0040a0002c0008t0003g0062 | 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 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0048others(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 | a0001c0001t0001g0061a0001c0001t0002g0317 | 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 | a0001c0001t0001g0051a0001c0001t0001g0052a0002c0008t0003g0064 | 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 | a0001c0001t0001g0004a0001c0001t0001g0044a0001c0001t0001g0133others(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 | a0001c0001t0001g0039a0001c0001t0001g0075a0001c0001t0001g0076others(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 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0121others(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 | a0001c0001t0001g0026a0001c0001t0001g0068a0001c0001t0001g0336others(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 | a0001c0001t0001g0228 | 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 | a0001c0001t0001g0307a0001c0002t0001g0073a0001c0002t0001g0074others(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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0001c0001t0001g0068a0001c0001t0001g0336 | 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 | a0001c0001t0001g0237a0020c0025t0001g0236 | 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 | a0001c0012t0001g0319a0001c0012t0001g0320 | 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 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0042others(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 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0336others(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 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0336others(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 | a0001c0001t0001g0026a0001c0001t0001g0030a0001c0001t0001g0031others(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 | a0002c0008t0003g0040a0002c0008t0003g0062a0002c0008t0003g0064 | 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 | a0001c0001t0001g0329a0001c0001t0001g0337a0001c0001t0004g0330others(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 | a0001c0001t0001g0068a0001c0001t0001g0336 | 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 | a0001c0001t0001g0324a0001c0001t0008g0325 | 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 | a0001c0001t0001g0333a0001c0001t0001g0334 | 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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0001c0012t0001g0319a0001c0012t0001g0320 | 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 | a0001c0001t0001g0143a0001c0001t0001g0150a0001c0001t0001g0151others(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 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0336others(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 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0329others(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 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(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 | a0001c0006t0001g0126a0001c0006t0001g0127 | 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 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0336others(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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0001c0012t0001g0319a0001c0012t0001g0320a0002c0005t0001g0299others(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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0001c0001t0001g0029a0001c0001t0001g0038a0001c0001t0001g0039others(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 | a0001c0001t0001g0068a0001c0001t0001g0336 | 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 | a0001c0001t0001g0029a0001c0001t0001g0328 | 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 | a0001c0001t0001g0026a0001c0001t0001g0030a0001c0001t0001g0031others(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 | a0001c0001t0001g0324a0001c0001t0008g0325a0005c0010t0001g0338others(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 | a0001c0001t0001g0324a0001c0001t0008g0325 | 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 | a0001c0012t0001g0319a0001c0012t0001g0320 | 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 | a0001c0001t0001g0308a0017c0023t0001g0001 | 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 | a0001c0001t0001g0292a0001c0001t0001g0294a0001c0001t0001g0296others(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 | a0001c0001t0001g0199a0001c0001t0001g0201a0001c0001t0001g0202others(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 | a0001c0003t0002g0290a0001c0003t0002g0311a0001c0003t0002g0312others(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 | a0001c0001t0001g0142a0001c0001t0001g0145a0001c0001t0001g0156 | 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 | a0001c0012t0001g0319a0001c0012t0001g0320 | 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 | a0001c0001t0001g0163a0001c0001t0001g0200a0001c0001t0001g0228others(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 | a0001c0001t0001g0113a0001c0001t0001g0305a0001c0001t0001g0306others(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 | a0001c0001t0002g0314a0001c0001t0002g0317 | 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 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0041others(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 | a0001c0003t0002g0290a0001c0003t0002g0311a0001c0003t0002g0312others(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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0001c0001t0001g0135a0001c0001t0001g0171a0001c0001t0001g0172others(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 | a0001c0001t0001g0191a0001c0001t0001g0195a0001c0001t0001g0196others(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 | a0001c0001t0001g0185a0001c0001t0001g0199a0001c0001t0001g0207others(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 | a0001c0001t0001g0006a0001c0001t0001g0036a0001c0001t0001g0038others(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 | a0001c0001t0001g0039a0001c0001t0001g0041a0001c0001t0001g0042others(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 | a0001c0001t0001g0029a0001c0001t0001g0247a0001c0001t0001g0252others(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 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0044others(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 | a0001c0001t0001g0026a0001c0001t0001g0121a0001c0001t0001g0129others(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 | a0001c0001t0001g0324a0001c0001t0008g0325a0001c0002t0001g0192others(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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0001c0001t0001g0191a0001c0001t0001g0196a0001c0001t0001g0241 | 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 | a0001c0001t0001g0287a0001c0001t0001g0324a0001c0001t0008g0325others(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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | 313 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(310): Show | 313 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(310): 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 | a0001c0001t0001g0006a0001c0001t0001g0026a0001c0001t0001g0038others(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 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0078others(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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0001c0001t0001g0324a0001c0001t0008g0325a0005c0010t0001g0338others(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 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0030others(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 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0336others(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 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0336others(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 | a0001c0001t0001g0258a0005c0021t0001g0259 | 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 | a0001c0001t0001g0258a0005c0021t0001g0259 | 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 | a0001c0001t0001g0305a0001c0001t0001g0306 | 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 | a0001c0001t0001g0006a0001c0001t0001g0112a0001c0001t0001g0135others(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 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0030others(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 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0030others(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 | a0001c0001t0001g0026a0001c0001t0001g0030a0001c0001t0001g0031others(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 | a0001c0001t0001g0041a0001c0001t0001g0043a0001c0001t0001g0044others(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 | 126 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0030others(123): Show | 126 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(123): Show |
intron_variant | MODIFIER | c.1409-1998delT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3737321 | ||||||
| chr11:3737321
|
CAA | C | 8 | a0001c0001t0001g0068a0001c0001t0001g0250a0001c0001t0001g0336others(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 | a0001c0002t0001g0270 | 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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0336others(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 | a0001c0003t0002g0290a0001c0003t0002g0311a0001c0003t0002g0312others(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 | a0001c0001t0001g0324a0001c0001t0008g0325 | 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 | a0001c0012t0001g0319a0001c0012t0001g0320 | 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 | a0009c0013t0005g0037 | 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 | a0001c0001t0001g0329a0001c0001t0001g0337a0001c0001t0004g0330others(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 | a0001c0001t0001g0042 | 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 | a0002c0005t0001g0302a0002c0005t0001g0303 | 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 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0142others(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 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0042others(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 | a0001c0001t0001g0177a0001c0001t0001g0228a0001c0001t0001g0234others(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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0302others(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 | a0002c0005t0001g0301 | 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 | a0005c0010t0001g0338a0005c0010t0001g0339 | 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 | a0001c0001t0001g0036a0001c0001t0001g0179 | 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 | a0001c0001t0001g0113a0001c0016t0001g0114 | 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 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0336others(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 | 303 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(300): Show | 303 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(300): Show |
intron_variant | MODIFIER | c.1409-3453dupT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3738776 | ||||||
| chr11:3738776
|
C | CAA | 33 | a0001c0001t0001g0026a0001c0001t0001g0039a0001c0001t0001g0042others(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 | a0001c0001t0001g0006a0001c0001t0001g0026a0001c0001t0001g0029others(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 | a0001c0001t0001g0333a0001c0001t0001g0334 | 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 | a0001c0001t0001g0045 | 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 | a0001c0001t0001g0068a0001c0001t0001g0336 | 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 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0030others(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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0001c0001t0001g0329a0001c0001t0001g0337a0001c0001t0004g0330others(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 | a0001c0012t0001g0319a0001c0012t0001g0320 | 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 | a0001c0001t0001g0026a0001c0001t0001g0030a0001c0001t0001g0031others(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 | a0001c0001t0001g0324a0001c0001t0008g0325a0005c0010t0001g0338others(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 | a0001c0001t0001g0006a0001c0001t0001g0137a0001c0001t0001g0149others(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 | ||||||
| chr11:3740466
|
A | G | 341 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(338): Show | 341 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(338): Show |
intron_variant | MODIFIER | c.1408+4043T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3740466 | ||||||
| chr11:3740516
|
C | CA | 11 | a0001c0001t0001g0329a0001c0001t0001g0337a0001c0001t0004g0330others(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 | a0001c0001t0001g0185a0001c0001t0001g0191a0001c0001t0001g0195others(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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0001c0001t0001g0075 | 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 | a0001c0001t0001g0075 | 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 | a0001c0001t0001g0075 | 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 | a0001c0001t0001g0075 | 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 | a0001c0001t0001g0075 | 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 | a0001c0001t0001g0075 | 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 | a0001c0001t0001g0075 | 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 | a0001c0001t0001g0026a0001c0001t0001g0030a0001c0001t0001g0031others(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 | a0002c0005t0001g0299 | 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 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0030others(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 | a0001c0001t0001g0109a0001c0001t0001g0219a0001c0017t0002g0116 | 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 | a0001c0026t0001g0298a0005c0021t0001g0259 | 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 | a0001c0001t0001g0029a0001c0001t0001g0328 | 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 | a0004c0007t0001g0213a0004c0007t0001g0245 | 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 | a0001c0001t0001g0068a0001c0001t0001g0336 | 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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | ||||||
| chr11:3741342
|
G | GC | 341 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(338): Show | 341 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(338): Show |
intron_variant | MODIFIER | c.1408+3166dupG | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3741342 | ||||||
| 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 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0078others(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 | 323 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(320): Show | 323 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(320): 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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0001c0001t0001g0053a0001c0001t0001g0054 | 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 | a0001c0001t0001g0333a0001c0001t0001g0334a0001c0017t0002g0116 | 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 | a0001c0001t0001g0026a0001c0001t0001g0239a0001c0001t0001g0307others(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 | 241 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(238): Show | 241 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(238): Show |
intron_variant | MODIFIER | c.1408+1809delT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3742699 | ||||||
| chr11:3742699
|
CAA | C | 7 | a0001c0002t0001g0082a0001c0003t0002g0311a0001c0003t0002g0312others(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 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0336others(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 | a0001c0001t0001g0324a0001c0001t0008g0325a0005c0010t0001g0338others(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 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0336others(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 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0164others(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 | a0001c0001t0001g0030a0001c0001t0001g0031 | 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 | a0001c0001t0001g0038a0001c0001t0001g0173a0001c0001t0001g0204others(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 | a0001c0001t0001g0005a0001c0001t0001g0030a0001c0001t0001g0031others(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 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0030others(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 | a0001c0001t0001g0042a0001c0001t0001g0061a0001c0001t0001g0253others(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 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0336others(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 | a0001c0003t0002g0290a0001c0003t0002g0311a0001c0003t0002g0312others(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 | a0001c0001t0001g0042 | 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 | ||||||
| chr11:3744114
|
C | T | 341 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(338): Show | 341 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(338): Show |
intron_variant | MODIFIER | c.1408+395G>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 12/32 | chr11 | 3744114 | ||||||
| chr11:3744353
|
GGATCTAT others(6): Show |
G | 8 | a0001c0002t0001g0069a0001c0002t0001g0093a0001c0002t0001g0095others(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 | a0001c0001t0001g0029a0001c0001t0001g0328 | 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 | a0001c0012t0001g0319a0001c0012t0001g0320 | 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 | a0001c0001t0001g0234a0001c0001t0001g0235 | 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 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0030others(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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0001c0001t0001g0026a0001c0001t0001g0030a0001c0001t0001g0031others(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 | 340 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(337): Show | 340 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(337): 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 | a0001c0001t0001g0028a0001c0001t0001g0172a0001c0001t0001g0175others(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 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0155others(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 | a0001c0001t0001g0030a0001c0001t0001g0052a0001c0001t0001g0057others(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 | a0001c0001t0001g0031a0001c0001t0001g0039a0001c0001t0001g0041others(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 | a0001c0001t0001g0026a0001c0001t0001g0038a0001c0001t0001g0042others(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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0001c0001t0001g0029a0001c0001t0001g0050a0001c0001t0001g0068others(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 | a0001c0012t0001g0319a0001c0012t0001g0320 | 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 | a0001c0002t0001g0073a0001c0002t0001g0074a0001c0002t0001g0087others(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 | a0009c0013t0005g0220 | 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 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0121others(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 | a0001c0012t0001g0319a0001c0012t0001g0320 | 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 | a0001c0001t0001g0068a0001c0001t0001g0336 | 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 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0336others(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 | a0001c0001t0001g0026a0001c0001t0001g0030a0001c0001t0001g0031others(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 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0336others(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 | a0001c0012t0001g0319a0001c0012t0001g0320 | 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 | a0001c0012t0001g0319a0001c0012t0001g0320 | 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 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0030others(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 | a0001c0012t0001g0319a0001c0012t0001g0320 | 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 | a0001c0012t0001g0319a0001c0012t0001g0320 | 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 | a0001c0001t0001g0041a0001c0001t0001g0043a0001c0001t0001g0044others(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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0001c0001t0001g0324a0001c0001t0008g0325a0005c0010t0001g0338others(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 | a0011c0034t0001g0122 | 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 | a0001c0001t0001g0333a0001c0001t0001g0334 | 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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0001c0001t0001g0068a0001c0001t0001g0336 | 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 | a0002c0005t0001g0299 | 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 | a0001c0002t0001g0073a0001c0002t0001g0074a0001c0002t0001g0322 | 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 | a0011c0034t0001g0122a0012c0033t0001g0130 | 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 | a0001c0001t0001g0041a0001c0001t0001g0043a0001c0001t0001g0044others(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 | a0001c0001t0001g0162 | 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 | a0001c0001t0001g0162 | 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 | a0001c0001t0001g0292a0001c0001t0001g0294a0001c0001t0001g0296others(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 | 4 | a0001c0006t0001g0190a0001c0006t0001g0203a0001c0006t0001g0242others(1): Show | 4 | HG00741.hp2 HG01361.hp2 HG03654.hp2 others(1): Show |
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 | a0001c0001t0001g0328a0001c0002t0001g0015 | 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 | a0017c0023t0001g0001 | 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 | a0001c0001t0001g0113a0001c0001t0001g0324a0001c0001t0008g0325others(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 | a0001c0001t0001g0305a0001c0001t0001g0306 | 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 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0340 | 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 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0336others(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 | a0001c0001t0001g0113a0001c0016t0001g0114a0001c0032t0001g0032 | 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 | a0001c0001t0001g0006a0001c0001t0001g0026a0001c0001t0001g0029others(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 | a0001c0001t0001g0324a0001c0001t0008g0325a0001c0012t0001g0319others(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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0002c0008t0003g0040a0002c0008t0003g0062a0002c0008t0003g0064 | 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 | a0001c0001t0001g0194a0001c0001t0001g0205a0001c0001t0001g0250 | 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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0001c0002t0001g0291 | 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 | a0001c0001t0001g0324a0001c0001t0008g0325a0005c0010t0001g0338others(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 | a0001c0001t0001g0143 | 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 | a0001c0001t0001g0219 | 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 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0030others(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 | a0001c0001t0001g0029a0001c0001t0001g0038a0001c0001t0001g0039others(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 | a0001c0001t0001g0146 | 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 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0336others(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 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0336others(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 | a0001c0001t0001g0068a0001c0001t0001g0336 | 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 | a0001c0001t0001g0055a0001c0001t0001g0066 | 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 | a0001c0001t0002g0314a0001c0001t0002g0317a0001c0017t0002g0116others(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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0001c0001t0001g0029a0001c0001t0001g0038a0001c0001t0001g0039others(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 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0336others(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 | a0001c0002t0001g0262a0001c0002t0001g0264a0001c0002t0001g0265others(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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0011c0034t0001g0122 | 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 | a0001c0001t0001g0075a0001c0001t0001g0084 | 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 | a0001c0001t0001g0029a0001c0001t0001g0038a0001c0001t0001g0039others(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 | a0001c0001t0001g0225 | 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 | a0001c0001t0001g0225 | 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 | a0001c0001t0001g0225 | 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 | a0001c0001t0001g0225 | 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 | a0001c0001t0001g0225 | 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 | a0001c0001t0001g0225 | 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 | a0001c0001t0001g0225 | 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 | a0001c0001t0001g0225 | 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 | a0001c0001t0001g0225 | 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 | a0001c0001t0001g0225 | 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 | a0001c0001t0001g0225 | 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 | a0001c0001t0001g0225 | 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 | a0001c0001t0001g0225 | 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 | a0001c0001t0001g0225 | 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 | a0001c0001t0001g0225 | 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 | a0001c0001t0001g0225 | 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 | a0001c0001t0001g0225 | 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 | a0001c0001t0001g0225 | 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 | a0001c0001t0001g0225 | 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 | a0001c0001t0001g0225 | 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 | a0001c0001t0001g0225 | 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 | a0001c0001t0001g0225 | 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 | a0001c0001t0001g0225 | 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 | a0001c0001t0001g0225 | 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 | a0001c0001t0001g0225 | 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 | a0001c0001t0001g0225 | 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 | a0001c0001t0001g0225 | 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 | a0001c0001t0001g0225 | 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 | a0001c0001t0001g0225 | 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 | a0001c0001t0001g0225 | 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 | a0001c0001t0001g0225 | 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 | a0001c0001t0001g0225 | 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 | a0001c0001t0001g0225 | 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 | a0001c0001t0001g0225 | 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 | a0001c0001t0001g0225 | 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 | a0001c0001t0001g0225 | 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 | a0001c0001t0001g0225 | 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 | a0001c0001t0001g0225 | 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 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0078others(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 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0336others(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 | a0001c0002t0001g0268 | 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 | a0001c0001t0001g0028a0001c0001t0001g0041a0001c0001t0001g0043others(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 | a0001c0001t0001g0076a0001c0002t0001g0091a0008c0011t0001g0071others(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 | a0001c0012t0001g0319a0001c0012t0001g0320 | 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 | a0001c0001t0001g0043a0001c0001t0001g0044 | 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 | a0001c0002t0001g0015 | 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 | a0001c0016t0001g0114a0001c0032t0001g0032 | 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 | a0001c0001t0001g0149a0001c0001t0001g0165 | 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 | a0001c0001t0001g0249 | 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 | 54 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0109others(51): Show | 54 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.1175-348dupT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3753755 | ||||||
| chr11:3753755
|
C | CAA | 31 | a0001c0001t0001g0006a0001c0001t0001g0110a0001c0001t0001g0135others(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 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0138others(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 | a0001c0001t0001g0049a0001c0001t0001g0068a0001c0001t0001g0075others(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 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0038others(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 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0042others(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 | a0001c0012t0001g0319a0001c0012t0001g0320 | 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 | a0001c0001t0001g0153 | 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 | a0018c0019t0001g0218 | 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 | a0001c0001t0001g0152 | 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 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0336others(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 | a0001c0001t0001g0191a0001c0001t0001g0195a0001c0001t0001g0196others(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 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0038others(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 | a0001c0001t0001g0026a0001c0001t0001g0067a0001c0001t0001g0183others(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 | a0001c0001t0001g0113a0001c0001t0001g0151a0001c0001t0001g0181others(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 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0030others(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 | a0001c0016t0001g0114a0002c0005t0001g0299a0002c0005t0001g0300others(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 | a0001c0001t0001g0029a0001c0001t0001g0328 | 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 | a0001c0012t0001g0319a0001c0012t0001g0320 | 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 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0030others(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 | a0001c0001t0001g0041a0001c0001t0001g0043a0001c0001t0001g0044others(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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0001c0002t0001g0193a0001c0002t0001g0211 | 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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0001c0001t0001g0029a0001c0001t0001g0038a0001c0001t0001g0039others(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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0001c0001t0001g0029a0001c0001t0001g0038a0001c0001t0001g0039others(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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0001c0002t0001g0010a0001c0002t0001g0011a0001c0002t0001g0012others(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 | a0001c0001t0001g0026a0001c0002t0001g0007a0001c0002t0001g0008others(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 | a0001c0001t0001g0138a0001c0001t0001g0159a0001c0001t0001g0160 | 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 | a0001c0001t0001g0078a0001c0002t0001g0094 | 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 | a0001c0001t0001g0029a0001c0001t0001g0038a0001c0001t0001g0039others(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 | ||||||
| chr11:3756637
|
A | AG | 341 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(338): Show | 341 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(338): Show |
intron_variant | MODIFIER | c.1175-3230_1175-322 others(5): Show |
NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 10/32 | chr11 | 3756637 | ||||||
| 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 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0336others(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 | a0001c0012t0001g0319a0001c0012t0001g0320 | 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 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0078others(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 | a0001c0001t0001g0038a0001c0001t0001g0042a0001c0001t0001g0061others(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 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0030others(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 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053others(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 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0030others(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 | a0001c0001t0001g0068a0001c0001t0001g0307a0001c0001t0001g0335 | 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 | a0001c0012t0001g0319a0001c0012t0001g0320 | 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 | a0001c0001t0001g0029a0001c0001t0001g0038a0001c0001t0001g0039others(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 | a0001c0001t0002g0314a0001c0001t0002g0317a0003c0004t0001g0316others(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 | a0001c0001t0001g0029a0001c0001t0001g0038a0001c0001t0001g0039others(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 | a0001c0001t0001g0068a0001c0001t0001g0336 | 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 | a0001c0012t0001g0319a0001c0012t0001g0320 | 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 | a0001c0002t0001g0087a0001c0002t0001g0088a0001c0002t0001g0104 | 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 | a0001c0001t0001g0324a0001c0001t0008g0325a0005c0010t0001g0338others(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 | a0001c0001t0001g0143 | 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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0336others(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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0030others(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 | a0001c0001t0001g0075a0001c0001t0001g0084a0001c0002t0001g0077others(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 | a0001c0012t0001g0319a0001c0012t0001g0320a0001c0032t0001g0032 | 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 | a0001c0001t0001g0292a0001c0001t0001g0294a0001c0001t0001g0296others(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 | a0001c0001t0001g0146 | 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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0001c0001t0001g0112a0001c0001t0001g0136a0001c0001t0001g0138others(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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0001c0001t0001g0026a0001c0002t0001g0015 | 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 | a0001c0001t0001g0029a0001c0001t0001g0038a0001c0001t0001g0039others(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 | a0001c0001t0001g0006a0001c0001t0001g0026a0001c0001t0001g0030others(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 | a0001c0001t0001g0029a0001c0001t0001g0038a0001c0001t0001g0039others(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 | a0001c0001t0001g0068a0001c0001t0001g0336a0001c0012t0001g0319others(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 | a0001c0002t0001g0069a0001c0002t0001g0095a0021c0018t0001g0099 | 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 | a0001c0001t0001g0067a0001c0001t0001g0335 | 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 | a0001c0001t0002g0314a0001c0001t0002g0317a0003c0004t0001g0316others(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 | a0001c0001t0001g0247a0001c0001t0001g0248a0001c0001t0001g0249others(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 | a0001c0001t0001g0307a0001c0003t0002g0290a0001c0003t0002g0311others(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 | a0001c0001t0001g0333a0001c0001t0001g0334 | 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 | a0001c0001t0001g0026a0001c0001t0001g0030a0001c0001t0001g0031others(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 | a0001c0001t0001g0029a0001c0001t0001g0184a0001c0001t0001g0328 | 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 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0336others(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 | a0001c0001t0001g0068a0001c0001t0001g0336 | 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 | a0011c0034t0001g0122a0012c0033t0001g0130 | 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 | a0001c0001t0001g0230 | 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 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0336others(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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0019c0022t0001g0128 | 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 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0336others(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 | a0001c0001t0001g0067a0001c0001t0001g0139a0001c0001t0001g0144others(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 | a0001c0001t0001g0250a0001c0001t0001g0333a0001c0001t0001g0334others(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 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0078others(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 | a0001c0001t0001g0333a0001c0001t0001g0334a0001c0001t0006g0297 | 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 | a0001c0002t0001g0016 | 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 | 3 | a0001c0006t0001g0190a0001c0006t0001g0203a0001c0006t0001g0242 | 3 | HG00741.hp2 HG01361.hp2 homoSapiens_chm13v2.hp1 |
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 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0336others(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 | a0001c0012t0001g0319a0001c0012t0001g0320 | 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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0001c0001t0001g0324a0001c0001t0008g0325a0005c0010t0001g0338others(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 | a0001c0001t0001g0029a0001c0001t0001g0038a0001c0001t0001g0039others(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 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0336others(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 | a0001c0006t0001g0126a0001c0006t0001g0127 | 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 | a0001c0001t0001g0308a0017c0023t0001g0001 | 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 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0041others(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 | a0001c0002t0001g0015 | 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 | a0001c0001t0001g0335a0002c0005t0001g0299a0002c0005t0001g0300others(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 | a0001c0001t0001g0194a0001c0001t0001g0205a0001c0001t0001g0250 | 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 | a0001c0001t0001g0333a0001c0001t0001g0334 | 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 | a0001c0001t0001g0068a0001c0001t0001g0336 | 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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0001c0001t0001g0333a0001c0001t0001g0334 | 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 | a0001c0001t0001g0234a0001c0001t0001g0235 | 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 | a0001c0001t0001g0324a0001c0001t0008g0325 | 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 | a0001c0002t0001g0269 | 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 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0031others(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 | a0001c0001t0001g0047a0001c0001t0001g0067a0001c0001t0001g0140others(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 | a0001c0001t0001g0068a0001c0012t0001g0319a0001c0012t0001g0320others(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 | a0001c0001t0001g0159a0001c0001t0001g0162a0001c0001t0001g0191others(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 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0078others(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 | a0001c0002t0001g0192a0001c0002t0001g0193a0001c0002t0001g0211 | 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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0001c0001t0001g0121a0001c0001t0001g0129a0006c0009t0001g0033others(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 | a0001c0001t0001g0226a0001c0001t0001g0227 | 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 | a0001c0003t0002g0290a0001c0003t0002g0311a0001c0003t0002g0312others(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 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0067others(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 | a0001c0001t0001g0205a0001c0001t0001g0209a0001c0001t0001g0235others(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 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0305others(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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0001c0001t0001g0147 | 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 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0030others(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 | a0001c0001t0002g0314a0001c0001t0002g0317a0003c0004t0001g0316others(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 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0336others(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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0001c0003t0002g0290a0001c0003t0002g0311a0001c0003t0002g0312others(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 | 324 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(321): Show | 324 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(321): 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 | a0001c0001t0001g0026a0001c0001t0001g0030a0001c0001t0001g0031others(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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0001c0001t0001g0026a0001c0001t0001g0030a0001c0001t0001g0031others(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 | a0001c0001t0001g0026a0001c0001t0001g0039a0001c0001t0001g0068others(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 | a0001c0001t0001g0026a0001c0001t0001g0030a0001c0001t0001g0031others(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 | a0013c0015t0001g0283 | 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 | a0001c0001t0001g0113a0001c0001t0001g0138a0001c0001t0001g0198others(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 | a0001c0001t0001g0029a0001c0001t0001g0038a0001c0001t0001g0039others(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 | a0001c0001t0001g0239a0001c0001t0001g0307 | 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 | a0011c0034t0001g0122a0012c0033t0001g0130 | 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 | a0001c0001t0001g0247a0001c0001t0001g0248a0001c0001t0001g0249others(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 | a0001c0001t0001g0026a0001c0001t0001g0030a0001c0001t0001g0031others(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 | a0001c0001t0001g0324a0001c0001t0008g0325 | 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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0001c0001t0001g0006a0001c0001t0001g0026a0001c0001t0001g0029others(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 | a0001c0001t0001g0333a0001c0001t0001g0334a0001c0002t0001g0093others(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 | a0001c0001t0001g0337a0001c0001t0004g0330a0001c0001t0004g0331 | 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 | a0001c0002t0001g0276a0001c0002t0001g0277a0001c0002t0001g0282others(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 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0078others(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 | a0001c0001t0001g0005a0001c0001t0001g0081a0001c0001t0001g0113others(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 | a0001c0001t0001g0004a0001c0001t0001g0140a0001c0003t0002g0290others(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 | a0001c0002t0001g0279a0001c0002t0001g0280a0001c0002t0001g0326others(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 | a0001c0001t0001g0029a0001c0001t0001g0038a0001c0001t0001g0039others(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 | a0001c0001t0001g0112a0001c0001t0001g0135a0001c0001t0001g0136others(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 | a0001c0002t0001g0279a0001c0002t0001g0280a0001c0002t0001g0326others(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 | a0002c0005t0001g0299 | 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 | a0001c0001t0001g0237a0020c0025t0001g0236 | 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 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110others(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 | a0001c0001t0001g0324a0001c0001t0008g0325 | 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 | a0001c0012t0001g0319a0001c0012t0001g0320 | 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 | a0001c0001t0001g0026a0001c0001t0001g0030a0001c0001t0001g0031others(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 | a0001c0002t0001g0007a0001c0002t0001g0018a0001c0002t0001g0019others(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 | a0001c0001t0001g0026a0001c0001t0001g0030a0001c0001t0001g0031others(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 | a0001c0001t0001g0180a0001c0001t0001g0182a0001c0001t0001g0214 | 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 | a0001c0001t0001g0337a0001c0001t0004g0330a0001c0001t0004g0331 | 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 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0078others(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 | a0001c0001t0001g0237a0020c0025t0001g0236 | 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 | a0001c0001t0001g0026a0001c0001t0001g0030a0001c0001t0001g0031others(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 | a0001c0001t0001g0029a0001c0001t0001g0038a0001c0001t0001g0039others(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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0001c0001t0001g0068a0001c0001t0001g0336 | 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 | a0001c0001t0001g0068a0001c0001t0001g0336 | 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 | a0001c0001t0001g0221 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.603+284A>G | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 6/32 | chr11 | 3773348 | ||||||
| chr11:3773465
|
A | T | 1 | a0001c0006t0001g0190 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.603+167T>A | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 6/32 | chr11 | 3773465 | ||||||
| chr11:3773504
|
A | G | 1 | a0001c0002t0001g0097 | 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 | a0001c0001t0001g0026a0001c0002t0001g0015 | 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 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0078others(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 | a0001c0001t0001g0026a0001c0001t0001g0030a0001c0001t0001g0031others(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 | a0001c0001t0001g0308a0017c0023t0001g0001 | 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 | a0001c0001t0002g0314a0001c0001t0002g0317a0003c0004t0001g0316others(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 | a0001c0002t0001g0178a0001c0002t0001g0212 | 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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0001c0003t0002g0290a0001c0003t0002g0311a0001c0003t0002g0312others(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 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0030others(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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0007c0028t0001g0148 | 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 | a0001c0001t0001g0324a0001c0001t0008g0325a0005c0010t0001g0338others(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 | a0001c0001t0001g0324a0001c0001t0008g0325a0005c0010t0001g0338others(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 | a0001c0001t0001g0075a0001c0001t0001g0084a0001c0001t0001g0137others(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 | a0001c0003t0002g0290a0001c0003t0002g0311a0001c0003t0002g0312others(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 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0336others(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 | a0001c0001t0001g0026a0001c0001t0001g0030a0001c0001t0001g0031others(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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0001c0001t0001g0036a0001c0001t0001g0067a0001c0001t0001g0068others(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 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0075others(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 | a0001c0001t0001g0026a0001c0001t0001g0076a0001c0002t0001g0011others(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 | a0001c0001t0001g0026a0001c0001t0001g0030a0001c0001t0001g0031others(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 | 323 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(320): Show | 323 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(320): 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 | a0001c0001t0001g0112a0001c0001t0001g0166a0001c0001t0001g0183others(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 | a0001c0001t0001g0026a0001c0001t0001g0030a0001c0001t0001g0031others(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 | a0001c0001t0001g0026a0001c0001t0001g0030a0001c0001t0001g0031others(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 | a0001c0012t0001g0319a0001c0012t0001g0320 | 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 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0030others(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 | a0001c0001t0001g0026a0001c0001t0001g0030a0001c0001t0001g0031others(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 | ||||||
| chr11:3776801
|
A | AT | 341 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(338): Show | 341 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(338): Show |
intron_variant | MODIFIER | c.356-781dupA | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 4/32 | chr11 | 3776801 | ||||||
| chr11:3776816
|
T | C | 5 | a0001c0001t0001g0028a0001c0001t0001g0186a0001c0001t0001g0189others(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 | a0001c0001t0001g0333a0001c0001t0001g0334a0001c0001t0006g0297 | 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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0001c0001t0002g0314a0001c0001t0002g0317a0001c0002t0001g0073others(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 | a0005c0010t0001g0338a0005c0010t0001g0339 | 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 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0336others(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 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0038others(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 | a0001c0001t0001g0068a0001c0001t0001g0111a0001c0001t0001g0121others(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 | a0001c0001t0001g0222 | 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 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0336others(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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0078others(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 | a0001c0001t0001g0337a0001c0001t0004g0330a0001c0001t0004g0331others(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 | a0001c0001t0001g0029a0001c0001t0001g0051a0001c0001t0001g0052others(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 | a0001c0002t0001g0262a0001c0002t0001g0264a0001c0002t0001g0265others(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 | a0001c0001t0001g0068a0001c0001t0001g0336 | 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 | a0001c0012t0001g0319a0001c0012t0001g0320a0017c0023t0001g0001 | 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 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0336others(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 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0336others(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 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0030others(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 | a0016c0029t0001g0134 | 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 | a0001c0012t0001g0319a0001c0012t0001g0320a0017c0023t0001g0001 | 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 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0336others(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 | a0001c0002t0001g0007a0001c0002t0001g0018a0001c0002t0001g0019others(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 | a0001c0012t0001g0319a0001c0012t0001g0320a0017c0023t0001g0001 | 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 | a0013c0015t0001g0283 | 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 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0121others(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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0001c0001t0001g0146 | 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 | 323 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(320): Show | 323 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(320): Show |
intron_variant | MODIFIER | c.77-385delT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 2/32 | chr11 | 3779641 | ||||||
| chr11:3779641
|
CAA | C | 17 | a0001c0001t0001g0068a0001c0001t0001g0166a0001c0001t0001g0294others(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 | a0013c0015t0001g0283 | 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 | a0013c0015t0001g0283 | 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 | a0001c0001t0001g0068a0001c0001t0001g0336 | 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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0336others(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 | a0001c0001t0001g0029a0001c0001t0001g0038a0001c0001t0001g0039others(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 | a0001c0012t0001g0319a0001c0012t0001g0320a0017c0023t0001g0001 | 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 | a0001c0012t0001g0319a0001c0012t0001g0320a0017c0023t0001g0001 | 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 | a0001c0001t0001g0109a0001c0002t0001g0018a0001c0002t0001g0086others(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 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0030others(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 | a0001c0001t0001g0146 | 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 | a0001c0001t0001g0043a0001c0001t0001g0044 | 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 | a0001c0012t0001g0319a0001c0012t0001g0320a0017c0023t0001g0001 | 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 | ||||||
| chr11:3780461
|
A | G | 341 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(338): Show | 341 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(338): Show |
intron_variant | MODIFIER | c.77-1204T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 2/32 | chr11 | 3780461 | ||||||
| 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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0001c0001t0001g0026a0001c0001t0001g0030a0001c0001t0001g0031others(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 | a0001c0001t0001g0029a0001c0001t0001g0038a0001c0001t0001g0039others(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 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0078others(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 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0335others(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 | a0001c0001t0001g0333a0001c0001t0001g0334a0001c0001t0006g0297others(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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0002c0008t0003g0040a0002c0008t0003g0062a0002c0008t0003g0064 | 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 | a0013c0015t0001g0283 | 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 | a0013c0015t0001g0283 | 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 | a0013c0015t0001g0283 | 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 | a0001c0001t0001g0144 | 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 | a0001c0001t0001g0029a0001c0001t0001g0038a0001c0001t0001g0039others(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 | a0001c0012t0001g0319a0001c0012t0001g0320a0017c0023t0001g0001 | 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 | a0001c0001t0001g0060a0001c0001t0001g0068a0001c0001t0001g0075others(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 | a0001c0001t0001g0026a0001c0001t0001g0030a0001c0001t0001g0031others(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 | a0001c0001t0001g0005a0001c0001t0001g0163a0001c0001t0001g0179others(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 | a0013c0015t0001g0283 | 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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0001c0012t0001g0319a0001c0012t0001g0320a0017c0023t0001g0001 | 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 | a0001c0001t0001g0029a0001c0001t0001g0038a0001c0001t0001g0055others(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 | a0001c0001t0001g0039a0001c0001t0001g0041a0001c0001t0001g0042others(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 | a0001c0001t0001g0063a0001c0001t0001g0076a0001c0001t0001g0078others(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 | a0001c0001t0001g0075a0001c0002t0001g0073a0001c0002t0001g0074others(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 | a0001c0001t0001g0026a0001c0001t0001g0030a0001c0001t0001g0031others(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 | a0001c0001t0001g0113a0001c0001t0001g0163a0001c0012t0001g0319others(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 | a0001c0001t0001g0036a0001c0001t0001g0141a0001c0001t0001g0160others(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 | a0001c0001t0001g0005a0001c0001t0001g0188a0001c0001t0001g0294others(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 | ||||||
| chr11:3781519
|
C | A | 341 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(338): Show | 341 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(338): Show |
intron_variant | MODIFIER | c.76+523G>T | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 2/32 | chr11 | 3781519 | ||||||
| chr11:3781578
|
T | C | 6 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0001c0001t0001g0026a0001c0001t0001g0030a0001c0001t0001g0031others(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 | a0001c0001t0001g0029a0001c0001t0001g0038a0001c0001t0001g0039others(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 | a0001c0012t0001g0319a0001c0012t0001g0320a0017c0023t0001g0001 | 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 | a0001c0001t0001g0205a0001c0002t0001g0016a0001c0002t0001g0069others(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 | a0001c0012t0001g0319a0001c0012t0001g0320a0017c0023t0001g0001 | 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 | a0001c0001t0001g0143 | 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 | a0001c0001t0001g0029a0001c0001t0001g0142a0001c0001t0001g0165others(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 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0041others(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 | a0001c0001t0001g0292a0001c0001t0001g0296a0001c0002t0001g0178others(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 | a0001c0001t0001g0026a0001c0001t0001g0031a0001c0001t0001g0036others(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 | a0001c0001t0001g0179a0001c0001t0001g0324a0001c0001t0008g0325others(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 | ||||||
| chr11:3782668
|
A | G | 341 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(338): Show | 341 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(338): Show |
intron_variant | MODIFIER | c.-28-523T>C | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3782668 | ||||||
| chr11:3782701
|
CCTGT | C | 52 | a0001c0001t0001g0026a0001c0001t0001g0030a0001c0001t0001g0031others(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 | a0011c0034t0001g0122a0012c0033t0001g0130 | 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 | 340 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(337): Show | 340 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(337): 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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0001c0001t0001g0068a0001c0001t0001g0336 | 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 | a0001c0012t0001g0319a0001c0012t0001g0320a0017c0023t0001g0001 | 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 | a0001c0012t0001g0319a0001c0012t0001g0320a0017c0023t0001g0001 | 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 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0335others(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 | a0001c0001t0001g0141a0001c0016t0001g0114 | 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 | a0001c0001t0001g0068a0001c0001t0001g0113a0001c0001t0001g0324others(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 | a0001c0001t0001g0029a0001c0001t0001g0328 | 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 | a0001c0001t0001g0324a0001c0001t0008g0325a0005c0010t0001g0338others(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 | a0001c0001t0001g0324a0001c0001t0008g0325a0005c0010t0001g0338others(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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0335others(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 | a0001c0001t0001g0333a0001c0001t0001g0334a0001c0001t0006g0297 | 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 | a0001c0001t0001g0026a0001c0001t0001g0030a0001c0001t0001g0031others(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 | a0001c0001t0001g0068a0001c0001t0001g0113a0001c0001t0001g0324others(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 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0030others(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 | a0001c0001t0001g0026a0001c0001t0001g0030a0001c0001t0001g0031others(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 | a0001c0001t0001g0029a0001c0001t0001g0038a0001c0001t0001g0039others(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 | a0001c0001t0001g0324a0001c0001t0001g0335a0001c0001t0008g0325others(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 | a0001c0001t0001g0068a0001c0001t0001g0336a0002c0005t0001g0299others(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 | a0008c0011t0001g0071a0008c0011t0001g0072 | 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 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0047others(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 | a0001c0001t0001g0029a0001c0001t0001g0041a0001c0001t0001g0042others(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 | a0001c0001t0001g0026a0001c0001t0001g0030a0001c0001t0001g0031others(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 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0335others(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 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0335others(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 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0078others(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 | a0001c0012t0001g0319a0001c0012t0001g0320a0017c0023t0001g0001 | 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 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0335others(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 | a0001c0012t0001g0319a0001c0012t0001g0320a0002c0005t0001g0299others(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 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0335others(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 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0335others(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 | a0011c0034t0001g0122a0012c0033t0001g0130 | 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 | a0001c0002t0001g0022a0001c0002t0001g0023 | 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 | a0011c0034t0001g0122a0012c0033t0001g0130 | 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 | a0001c0017t0002g0116a0003c0004t0001g0115a0003c0004t0001g0117others(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 | a0001c0001t0001g0029a0001c0001t0001g0038a0001c0001t0001g0039others(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 | a0001c0001t0001g0029a0001c0001t0001g0038a0001c0001t0001g0039others(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 | a0001c0001t0001g0329a0001c0001t0001g0337a0001c0001t0004g0330others(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 | a0001c0001t0001g0185a0001c0001t0001g0207a0001c0001t0001g0208others(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 | a0011c0034t0001g0122a0012c0033t0001g0130 | 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 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0078others(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 | 337 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(334): Show | 337 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(334): 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 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0063 | 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 | a0001c0002t0001g0070a0001c0002t0001g0090a0001c0002t0001g0100 | 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 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0335others(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 | a0001c0001t0001g0335a0001c0012t0001g0319a0001c0012t0001g0320 | 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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0336others(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 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0078others(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 | a0001c0002t0001g0261a0001c0002t0001g0281 | 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 | a0001c0012t0001g0319a0001c0012t0001g0320 | 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 | a0001c0001t0001g0039a0001c0001t0001g0067a0001c0001t0001g0139others(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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0001c0001t0001g0060a0001c0001t0001g0129a0001c0001t0001g0183others(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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0335others(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 | a0001c0006t0001g0126a0001c0006t0001g0127 | 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 | a0001c0001t0001g0324a0001c0001t0008g0325a0005c0010t0001g0338others(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 | a0001c0001t0001g0026a0001c0001t0001g0030a0001c0001t0001g0031others(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 | a0001c0002t0001g0262a0001c0002t0001g0264a0001c0002t0001g0265others(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 | a0009c0013t0005g0037 | 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 | a0001c0001t0001g0273a0001c0002t0001g0260a0001c0002t0001g0261others(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 | a0001c0001t0001g0209a0001c0001t0001g0257 | 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 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0041others(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 | a0001c0002t0001g0276a0001c0002t0001g0277 | 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 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0030others(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 | a0001c0001t0002g0314a0001c0001t0002g0317a0003c0004t0001g0316others(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 | a0001c0012t0001g0319a0001c0012t0001g0320a0002c0005t0001g0299others(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 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0335others(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 | a0001c0001t0001g0029a0001c0001t0001g0328a0001c0001t0001g0335others(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 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0078others(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 | a0001c0001t0001g0026a0001c0001t0001g0030a0001c0001t0001g0031others(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 | a0001c0001t0001g0324a0001c0001t0008g0325a0001c0003t0002g0290others(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 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0041others(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 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0041others(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 | a0001c0001t0001g0183a0001c0001t0001g0209a0001c0001t0001g0257 | 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 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0078others(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 | a0001c0003t0002g0290a0001c0003t0002g0311a0001c0003t0002g0312others(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 | a0001c0001t0001g0329a0001c0016t0001g0114 | 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 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0030others(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 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053others(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 | a0001c0001t0001g0113a0002c0008t0003g0040a0002c0008t0003g0062others(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 | a0001c0001t0001g0113a0002c0008t0003g0040a0002c0008t0003g0062others(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 | a0001c0001t0001g0324a0001c0001t0008g0325a0005c0010t0001g0338others(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 | a0002c0008t0003g0040a0002c0008t0003g0062a0002c0008t0003g0064 | 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 | a0002c0008t0003g0040a0002c0008t0003g0062a0002c0008t0003g0064 | 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 | a0002c0008t0003g0040a0002c0008t0003g0062a0002c0008t0003g0064 | 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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0335others(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 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0335others(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 | a0001c0001t0001g0036a0001c0001t0001g0135a0001c0001t0001g0173others(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 | a0001c0001t0001g0324a0001c0001t0008g0325a0001c0003t0002g0290others(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 | a0001c0001t0001g0335a0001c0003t0002g0313a0001c0003t0002g0323others(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 | a0001c0001t0001g0063a0001c0001t0001g0067a0001c0001t0001g0112others(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 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0041others(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 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0030others(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 | a0001c0001t0001g0324a0001c0001t0008g0325 | 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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0001c0001t0001g0006a0001c0001t0001g0068a0001c0001t0001g0243others(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 | a0001c0003t0002g0290a0001c0003t0002g0312a0001c0003t0002g0313others(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 | a0001c0001t0001g0112a0001c0001t0001g0179a0001c0001t0001g0183others(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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0335others(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 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0041others(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 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0335others(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 | a0001c0003t0002g0290a0001c0003t0002g0311a0001c0003t0002g0312others(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 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(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 | a0001c0012t0001g0319a0001c0012t0001g0320 | 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 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0335others(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 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0041others(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 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0335others(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 | a0001c0001t0001g0247a0001c0001t0001g0248a0001c0001t0001g0249others(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 | 92 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0028others(89): Show | 92 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.-29+5221delT | NUP98 | ENSG00000110713.18 | transcript | ENST00000324932.12 | protein_coding | 1/32 | chr11 | 3792178 | ||||||
| chr11:3792178
|
CAA | C | 6 | a0001c0001t0001g0036a0001c0001t0001g0136a0001c0001t0001g0179others(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 | a0001c0002t0001g0103a0001c0002t0001g0104a0001c0002t0001g0105others(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 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0078others(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 | a0001c0001t0001g0026a0001c0001t0001g0065a0001c0001t0001g0066others(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 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0041others(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 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0121others(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 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0336others(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 | a0001c0001t0001g0029a0001c0001t0001g0328 | 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 | a0001c0003t0002g0290a0001c0003t0002g0311a0001c0003t0002g0312others(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 | a0001c0001t0001g0112a0001c0001t0001g0135a0001c0001t0001g0136others(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 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0335others(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 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0335others(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 | a0001c0012t0001g0319a0001c0012t0001g0320a0002c0005t0001g0299others(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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0001c0012t0001g0319a0001c0012t0001g0320a0002c0005t0001g0299others(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 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0335others(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 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0335others(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 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0336others(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 | a0001c0001t0001g0287a0001c0002t0001g0285a0001c0002t0001g0286others(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 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0030others(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 | a0001c0001t0001g0333a0001c0001t0001g0334 | 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 | a0016c0029t0001g0134 | 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 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0335others(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 | a0001c0003t0002g0290a0001c0003t0002g0311a0001c0003t0002g0312others(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 | a0001c0001t0001g0068a0001c0001t0001g0336 | 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 | a0001c0001t0001g0324a0001c0001t0001g0335a0001c0001t0008g0325others(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 | a0001c0003t0002g0290a0001c0003t0002g0311a0001c0003t0002g0312others(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 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0030others(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 | a0001c0012t0001g0319a0001c0012t0001g0320 | 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 | a0001c0003t0002g0290a0001c0003t0002g0311a0001c0003t0002g0312others(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 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0336others(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 | a0001c0012t0001g0319a0001c0012t0001g0320 | 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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0030others(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 | a0001c0001t0001g0068a0001c0001t0001g0336 | 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 | a0001c0001t0001g0068a0001c0001t0001g0336 | 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 | a0006c0009t0001g0033a0006c0009t0001g0034a0006c0009t0001g0035 | 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 | a0001c0001t0001g0324a0001c0001t0001g0335a0001c0001t0008g0325others(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 | a0001c0001t0001g0068a0001c0001t0001g0336 | 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 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0335others(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 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0030others(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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0041others(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 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0078others(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 | a0002c0005t0001g0299a0002c0005t0001g0300a0002c0005t0001g0301others(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 | a0001c0003t0002g0290a0001c0003t0002g0311a0001c0003t0002g0312others(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 | a0001c0001t0001g0292a0001c0001t0001g0294a0001c0001t0001g0296others(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 | a0001c0001t0001g0333a0001c0001t0001g0334a0001c0001t0001g0335others(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 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(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 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(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 | a0001c0001t0001g0307a0001c0001t0001g0308 | 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 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0002t0001g0007others(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 | a0001c0001t0001g0305a0001c0001t0001g0306a0002c0005t0001g0299others(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 | a0001c0001t0001g0333a0001c0001t0001g0334a0001c0001t0001g0340others(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 | a0001c0001t0001g0333a0001c0001t0001g0334 | 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 | a0001c0001t0001g0004a0001c0001t0001g0005a0002c0008t0001g0003 | 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 | a0001c0001t0001g0305a0001c0001t0001g0306a0001c0001t0001g0307others(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 | a0017c0023t0001g0001 | 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 | a0001c0001t0001g0324a0001c0001t0008g0325 | 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 | a0001c0002t0001g0326a0001c0002t0001g0327 | 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 | a0001c0001t0001g0328a0001c0001t0001g0329a0001c0001t0004g0330others(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 | a0001c0001t0001g0333a0001c0001t0001g0334a0001c0001t0001g0335others(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 |