Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 8021 |
|---|---|
| ensemblid | ENSG00000126883.19 |
| hgncid | 8064 |
| symbol | NUP214 |
| name | nucleoporin 214 |
| refseq_nuc | NM_005085.4 |
| refseq_prot | NP_005076.3 |
| ensembl_nuc | ENST00000359428.10 |
| ensembl_prot | ENSP00000352400.5 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 131125586 |
| end | 131234663 |
| strand | + |
| ver | v1.2 |
| region | chr9:131125586-131234663 |
| region5000 | chr9:131120586-131239663 |
| regionname0 | NUP214_chr9_131125586_131234663 |
| regionname5000 | NUP214_chr9_131120586_131239663 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 2090 | 112 | 31 | 22 | 39 | 5 | 14 | 23 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| a0002 | 1/0 | 2090 | 98 | 21 | 17 | 40 | 3 | 16 | 30 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| a0003 | 0/0 | 2090 | 5 | 2 | 0 | 0 | 0 | 3 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| a0004 | 0/0 | 2090 | 3 | 0 | 0 | 3 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| a0005 | 0/0 | 2090 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| a0006 | 0/0 | 2090 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| a0007 | 0/0 | 2090 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| a0008 | 0/0 | 2090 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| a0009 | 0/0 | 2090 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| a0010 | 0/0 | 2090 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| a0011 | 0/0 | 2090 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| a0012 | 0/0 | 2090 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| a0013 | 0/0 | 2090 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| a0014 | 0/0 | 2090 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| a0015 | 0/0 | 2090 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| a0016 | 0/0 | 2090 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 6273 | 80 | 19 | 19 | 25 | 4 | 12 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| c0002 | 0/0 | 6273 | 74 | 6 | 15 | 35 | 3 | 15 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| c0003 | 1/0 | 6273 | 21 | 13 | 2 | 5 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| c0004 | 0/0 | 6273 | 13 | 3 | 1 | 6 | 1 | 2 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| c0005 | 0/0 | 6273 | 5 | 4 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| c0006 | 0/0 | 6273 | 4 | 0 | 0 | 4 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| c0007 | 0/0 | 6273 | 3 | 3 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| c0008 | 0/0 | 6273 | 3 | 3 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| c0009 | 0/0 | 6273 | 3 | 0 | 0 | 3 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| c0010 | 0/0 | 6273 | 3 | 2 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| c0011 | 0/0 | 6273 | 3 | 1 | 0 | 0 | 0 | 2 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| c0012 | 0/0 | 6273 | 3 | 2 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| c0013 | 0/0 | 6273 | 2 | 1 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| c0014 | 0/0 | 6273 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| c0015 | 0/0 | 6273 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| c0016 | 0/0 | 6273 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| c0017 | 0/0 | 6273 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| c0018 | 0/0 | 6273 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| c0019 | 0/0 | 6273 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| c0020 | 0/0 | 6273 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| c0021 | 0/0 | 6273 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| c0022 | 0/0 | 6273 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| c0023 | 0/0 | 6273 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| c0024 | 0/0 | 6273 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| c0025 | 0/0 | 6273 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| c0026 | 0/0 | 6273 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| c0027 | 0/0 | 6273 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| c0028 | 0/0 | 6273 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| c0029 | 0/0 | 6273 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| c0030 | 0/0 | 6273 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 1296 | 216 | 55 | 37 | 82 | 8 | 32 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| t0002 | 0/0 | 1295 | 5 | 3 | 1 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| t0003 | 0/0 | 1296 | 4 | 3 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| t0004 | 0/0 | 1295 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| t0005 | 0/0 | 1296 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| t0006 | 0/0 | 1296 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| t0007 | 0/0 | 1296 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| t0008 | 0/0 | 1295 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| t0009 | 0/0 | 1296 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| t0010 | 0/0 | 1296 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| t0011 | 0/0 | 1296 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| t0012 | 0/0 | 1296 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0078 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0127 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 6273 | 80 | 19 | 19 | 25 | 4 | 12 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| a0001c0004 | 0/0 | 6273 | 13 | 3 | 1 | 6 | 1 | 2 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| a0001c0005 | 0/0 | 6273 | 5 | 4 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| a0001c0006 | 0/0 | 6273 | 4 | 0 | 0 | 4 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| a0001c0007 | 0/0 | 6273 | 3 | 3 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| a0001c0010 | 0/0 | 6273 | 3 | 2 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| a0001c0015 | 0/0 | 6273 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| a0001c0024 | 0/0 | 6273 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| a0001c0026 | 0/0 | 6273 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| a0001c0027 | 0/0 | 6273 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| a0002c0002 | 0/0 | 6273 | 74 | 6 | 15 | 35 | 3 | 15 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| a0002c0003 | 1/0 | 6273 | 21 | 13 | 2 | 5 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| a0002c0016 | 0/0 | 6273 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| a0002c0018 | 0/0 | 6273 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| a0002c0020 | 0/0 | 6273 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| a0003c0011 | 0/0 | 6273 | 3 | 1 | 0 | 0 | 0 | 2 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| a0003c0013 | 0/0 | 6273 | 2 | 1 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| a0004c0009 | 0/0 | 6273 | 3 | 0 | 0 | 3 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| a0005c0008 | 0/0 | 6273 | 3 | 3 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| a0006c0012 | 0/0 | 6273 | 3 | 2 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| a0007c0030 | 0/0 | 6273 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| a0008c0014 | 0/0 | 6273 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| a0009c0019 | 0/0 | 6273 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| a0010c0017 | 0/0 | 6273 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| a0011c0021 | 0/0 | 6273 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| a0012c0022 | 0/0 | 6273 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| a0013c0023 | 0/0 | 6273 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| a0014c0025 | 0/0 | 6273 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| a0015c0028 | 0/0 | 6273 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| a0016c0029 | 0/0 | 6273 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 7568 | 76 | 19 | 18 | 23 | 4 | 11 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| a0001c0001t0006 | 0/0 | 7568 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| a0001c0001t0007 | 0/0 | 7568 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| a0001c0001t0009 | 0/0 | 7568 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| a0001c0001t0010 | 0/0 | 7568 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| a0001c0004t0001 | 0/0 | 7568 | 13 | 3 | 1 | 6 | 1 | 2 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| a0001c0005t0002 | 0/0 | 7567 | 4 | 3 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| a0001c0005t0003 | 0/0 | 7568 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| a0001c0006t0001 | 0/0 | 7568 | 4 | 0 | 0 | 4 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| a0001c0007t0001 | 0/0 | 7568 | 3 | 3 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| a0001c0010t0003 | 0/0 | 7568 | 3 | 2 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| a0001c0015t0001 | 0/0 | 7568 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| a0001c0024t0001 | 0/0 | 7568 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| a0001c0026t0001 | 0/0 | 7568 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| a0001c0027t0001 | 0/0 | 7568 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| a0002c0002t0001 | 0/0 | 7568 | 72 | 6 | 15 | 33 | 3 | 15 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| a0002c0002t0008 | 0/0 | 7567 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| a0002c0002t0011 | 0/0 | 7568 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| a0002c0003t0001 | 1/0 | 7568 | 21 | 13 | 2 | 5 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| a0002c0016t0001 | 0/0 | 7568 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| a0002c0018t0002 | 0/0 | 7567 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| a0002c0020t0012 | 0/0 | 7568 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| a0003c0011t0001 | 0/0 | 7568 | 3 | 1 | 0 | 0 | 0 | 2 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| a0003c0013t0001 | 0/0 | 7568 | 2 | 1 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| a0004c0009t0001 | 0/0 | 7568 | 3 | 0 | 0 | 3 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| a0005c0008t0001 | 0/0 | 7568 | 3 | 3 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| a0006c0012t0001 | 0/0 | 7568 | 3 | 2 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| a0007c0030t0001 | 0/0 | 7568 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| a0008c0014t0001 | 0/0 | 7568 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| a0009c0019t0001 | 0/0 | 7568 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| a0010c0017t0001 | 0/0 | 7568 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| a0011c0021t0001 | 0/0 | 7568 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| a0012c0022t0001 | 0/0 | 7568 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| a0013c0023t0005 | 0/0 | 7568 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| a0014c0025t0001 | 0/0 | 7568 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| a0015c0028t0004 | 0/0 | 7567 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| a0016c0029t0001 | 0/0 | 7568 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | copy fasta | chr9 | 131120586 | 131239663 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0078 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0006g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0007g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0009g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0010g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0004t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0004t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0004t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0004t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0004t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0004t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0004t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0004t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0004t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0004t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0004t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0004t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0004t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0005t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0005t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0005t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0005t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0005t0003g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0006t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0006t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0006t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0006t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0007t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0007t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0007t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0010t0003g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0010t0003g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0010t0003g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0015t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0024t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0026t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0027t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0008g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0011g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0003t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0003t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0003t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0003t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0003t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0003t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0003t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0003t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0003t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0003t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0003t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0003t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0003t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0003t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0003t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0003t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0003t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0003t0001g0127 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0003t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0003t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0003t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0016t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0018t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0020t0012g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0003c0011t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0003c0011t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0003c0011t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0003c0013t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0003c0013t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0004c0009t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0004c0009t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0004c0009t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0005c0008t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0005c0008t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0005c0008t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0006c0012t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0006c0012t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0006c0012t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0007c0030t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0008c0014t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0009c0019t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0010c0017t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0011c0021t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0012c0022t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0013c0023t0005g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0014c0025t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0015c0028t0004g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0016c0029t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0059 | EUR | GBR | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG00099 | hp2 | a0002 | c0002 | t0001 | g0201 | EUR | GBR | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | CHS | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG00408 | hp2 | a0001 | c0006 | t0001 | g0168 | EAS | CHS | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | CHS | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG00423 | hp2 | a0002 | c0002 | t0001 | g0193 | EAS | CHS | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG00438 | hp1 | a0001 | c0001 | t0010 | g0234 | EAS | CHS | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG00438 | hp2 | a0001 | c0001 | t0006 | g0076 | EAS | CHS | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG00544 | hp1 | a0001 | c0006 | t0001 | g0169 | EAS | CHS | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG00544 | hp2 | a0014 | c0025 | t0001 | g0086 | EAS | CHS | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG00558 | hp2 | a0002 | c0002 | t0001 | g0142 | EAS | CHS | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG00597 | hp1 | a0002 | c0002 | t0001 | g0150 | EAS | CHS | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG00597 | hp2 | a0004 | c0009 | t0001 | g0009 | EAS | CHS | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG00609 | hp1 | a0004 | c0009 | t0001 | g0045 | EAS | CHS | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG00609 | hp2 | a0001 | c0004 | t0001 | g0140 | EAS | CHS | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG00639 | hp2 | a0002 | c0002 | t0001 | g0011 | AMR | PUR | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG00642 | hp1 | a0002 | c0002 | t0001 | g0080 | AMR | PUR | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG00733 | hp1 | a0002 | c0002 | t0001 | g0136 | AMR | PUR | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG00741 | hp2 | a0002 | c0002 | t0001 | g0158 | AMR | PUR | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG01074 | hp2 | a0002 | c0003 | t0001 | g0042 | AMR | PUR | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG01106 | hp2 | a0006 | c0012 | t0001 | g0007 | AMR | PUR | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG01109 | hp1 | a0001 | c0010 | t0003 | g0214 | AMR | PUR | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG01168 | hp2 | a0002 | c0002 | t0001 | g0199 | AMR | PUR | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG01169 | hp1 | a0002 | c0002 | t0001 | g0195 | AMR | PUR | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG01175 | hp1 | a0002 | c0002 | t0001 | g0184 | AMR | PUR | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG01243 | hp1 | a0002 | c0002 | t0001 | g0208 | AMR | PUR | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG01243 | hp2 | a0002 | c0003 | t0001 | g0043 | AMR | PUR | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG01361 | hp1 | a0001 | c0004 | t0001 | g0131 | AMR | CLM | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG01361 | hp2 | a0002 | c0002 | t0001 | g0223 | AMR | CLM | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | CLM | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG01433 | hp2 | a0002 | c0002 | t0001 | g0200 | AMR | CLM | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | CLM | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG01496 | hp2 | a0001 | c0005 | t0002 | g0213 | AMR | CLM | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0077 | EUR | IBS | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG01515 | hp2 | a0002 | c0002 | t0001 | g0161 | EUR | IBS | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0230 | EUR | IBS | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG01516 | hp2 | a0001 | c0004 | t0001 | g0202 | EUR | IBS | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG01884 | hp1 | a0002 | c0003 | t0001 | g0125 | AFR | ACB | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG01884 | hp2 | a0002 | c0002 | t0001 | g0226 | AFR | ACB | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | ACB | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG01891 | hp2 | a0001 | c0005 | t0003 | g0211 | AFR | ACB | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG01928 | hp1 | a0001 | c0001 | t0007 | g0046 | AMR | PEL | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG01928 | hp2 | a0002 | c0002 | t0001 | g0194 | AMR | PEL | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG01943 | hp2 | a0002 | c0002 | t0001 | g0224 | AMR | PEL | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG01981 | hp1 | a0002 | c0002 | t0001 | g0162 | AMR | PEL | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG01993 | hp1 | a0002 | c0002 | t0001 | g0178 | AMR | PEL | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02015 | hp1 | a0002 | c0002 | t0001 | g0167 | EAS | KHV | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | KHV | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02027 | hp2 | a0002 | c0002 | t0001 | g0188 | EAS | KHV | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02055 | hp1 | a0002 | c0002 | t0001 | g0166 | AFR | ACB | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | ACB | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02056 | hp1 | a0002 | c0002 | t0001 | g0133 | EAS | KHV | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02056 | hp2 | a0001 | c0027 | t0001 | g0087 | EAS | KHV | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02083 | hp1 | a0002 | c0002 | t0001 | g0183 | EAS | KHV | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02083 | hp2 | a0001 | c0015 | t0001 | g0047 | EAS | KHV | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02132 | hp1 | a0002 | c0002 | t0001 | g0179 | EAS | KHV | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | KHV | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02135 | hp2 | a0002 | c0002 | t0001 | g0210 | EAS | KHV | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02145 | hp1 | a0015 | c0028 | t0004 | g0207 | AFR | ACB | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02145 | hp2 | a0001 | c0007 | t0001 | g0088 | AFR | ACB | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | CDX | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02165 | hp2 | a0001 | c0004 | t0001 | g0198 | EAS | CDX | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02258 | hp1 | a0002 | c0003 | t0001 | g0126 | AFR | ACB | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02293 | hp1 | a0002 | c0002 | t0001 | g0191 | AMR | PEL | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | ACB | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02451 | hp2 | a0001 | c0005 | t0002 | g0206 | AFR | ACB | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02523 | hp1 | a0016 | c0029 | t0001 | g0063 | EAS | KHV | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02523 | hp2 | a0002 | c0002 | t0001 | g0187 | EAS | KHV | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02615 | hp1 | a0003 | c0013 | t0001 | g0071 | AFR | GWD | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02615 | hp2 | a0001 | c0004 | t0001 | g0227 | AFR | GWD | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02630 | hp1 | a0002 | c0003 | t0001 | g0123 | AFR | GWD | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02630 | hp2 | a0001 | c0005 | t0002 | g0212 | AFR | GWD | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0175 | SAS | PJL | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02723 | hp1 | a0002 | c0003 | t0001 | g0075 | AFR | GWD | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02723 | hp2 | a0006 | c0012 | t0001 | g0006 | AFR | GWD | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02735 | hp2 | a0002 | c0002 | t0001 | g0130 | SAS | PJL | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02738 | hp1 | a0002 | c0002 | t0001 | g0147 | SAS | PJL | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02738 | hp2 | a0002 | c0002 | t0001 | g0146 | SAS | PJL | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02809 | hp1 | a0002 | c0002 | t0001 | g0221 | AFR | GWD | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02809 | hp2 | a0002 | c0003 | t0001 | g0124 | AFR | GWD | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02818 | hp1 | a0001 | c0010 | t0003 | g0229 | AFR | GWD | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02818 | hp2 | a0002 | c0002 | t0001 | g0225 | AFR | GWD | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02886 | hp1 | a0010 | c0017 | t0001 | g0108 | AFR | GWD | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02886 | hp2 | a0001 | c0010 | t0003 | g0228 | AFR | GWD | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02897 | hp1 | a0006 | c0012 | t0001 | g0005 | AFR | GWD | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02897 | hp2 | a0001 | c0007 | t0001 | g0089 | AFR | GWD | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02922 | hp1 | a0002 | c0002 | t0001 | g0222 | AFR | ESN | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | ESN | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | ESN | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | ESN | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | ESN | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02970 | hp2 | a0001 | c0005 | t0002 | g0205 | AFR | ESN | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | ESN | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02976 | hp2 | a0002 | c0003 | t0001 | g0121 | AFR | ESN | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG03041 | hp1 | a0002 | c0003 | t0001 | g0064 | AFR | GWD | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG03041 | hp2 | a0001 | c0007 | t0001 | g0065 | AFR | GWD | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG03130 | hp1 | a0002 | c0003 | t0001 | g0128 | AFR | ESN | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | ESN | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG03195 | hp1 | a0002 | c0003 | t0001 | g0072 | AFR | ESN | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | ESN | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG03209 | hp1 | a0007 | c0030 | t0001 | g0091 | AFR | MSL | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG03209 | hp2 | a0002 | c0003 | t0001 | g0122 | AFR | MSL | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG03239 | hp1 | a0003 | c0013 | t0001 | g0040 | SAS | PJL | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG03239 | hp2 | a0002 | c0002 | t0001 | g0028 | SAS | PJL | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG03486 | hp1 | a0002 | c0020 | t0012 | g0132 | AFR | MSL | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG03486 | hp2 | a0002 | c0003 | t0001 | g0215 | AFR | MSL | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG03490 | hp2 | a0002 | c0002 | t0001 | g0134 | SAS | PJL | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG03491 | hp2 | a0002 | c0002 | t0001 | g0154 | SAS | PJL | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG03492 | hp1 | a0002 | c0002 | t0001 | g0155 | SAS | PJL | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG03540 | hp1 | a0001 | c0004 | t0001 | g0220 | AFR | GWD | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG03579 | hp1 | a0013 | c0023 | t0005 | g0003 | AFR | MSL | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG03579 | hp2 | a0002 | c0016 | t0001 | g0101 | AFR | MSL | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG03688 | hp1 | a0003 | c0011 | t0001 | g0177 | SAS | STU | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | STU | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG03704 | hp1 | a0002 | c0002 | t0001 | g0068 | SAS | PJL | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG03831 | hp1 | a0011 | c0021 | t0001 | g0181 | SAS | BEB | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0233 | SAS | BEB | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG03927 | hp1 | a0002 | c0002 | t0001 | g0139 | SAS | BEB | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG03927 | hp2 | a0001 | c0004 | t0001 | g0165 | SAS | BEB | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG03942 | hp1 | a0002 | c0002 | t0001 | g0173 | SAS | BEB | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG03942 | hp2 | a0002 | c0002 | t0001 | g0104 | SAS | BEB | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG04184 | hp1 | a0001 | c0001 | t0009 | g0073 | SAS | BEB | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG04184 | hp2 | a0001 | c0004 | t0001 | g0209 | SAS | BEB | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | STU | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG04199 | hp2 | a0002 | c0002 | t0001 | g0113 | SAS | STU | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG04204 | hp1 | a0002 | c0002 | t0001 | g0185 | SAS | STU | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG04204 | hp2 | a0003 | c0011 | t0001 | g0192 | SAS | STU | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG04228 | hp1 | a0002 | c0002 | t0001 | g0079 | SAS | STU | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG04228 | hp2 | a0002 | c0018 | t0002 | g0107 | SAS | STU | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA18522 | hp1 | a0005 | c0008 | t0001 | g0109 | AFR | YRI | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | YRI | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA18944 | hp2 | a0002 | c0002 | t0001 | g0143 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA18945 | hp1 | a0002 | c0002 | t0001 | g0159 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA18945 | hp2 | a0001 | c0024 | t0001 | g0056 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA18948 | hp2 | a0002 | c0002 | t0001 | g0151 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA18949 | hp1 | a0002 | c0003 | t0001 | g0098 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA18949 | hp2 | a0002 | c0002 | t0001 | g0156 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA18952 | hp1 | a0002 | c0002 | t0001 | g0118 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA18952 | hp2 | a0001 | c0004 | t0001 | g0204 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA18953 | hp1 | a0002 | c0002 | t0001 | g0135 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA18953 | hp2 | a0002 | c0002 | t0001 | g0152 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA18960 | hp2 | a0002 | c0002 | t0001 | g0149 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA18961 | hp1 | a0001 | c0004 | t0001 | g0138 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA18962 | hp1 | a0002 | c0003 | t0001 | g0094 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA18968 | hp1 | a0002 | c0002 | t0001 | g0157 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA18968 | hp2 | a0002 | c0002 | t0001 | g0145 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA18969 | hp2 | a0002 | c0002 | t0001 | g0164 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA18971 | hp1 | a0002 | c0002 | t0001 | g0117 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA18983 | hp2 | a0001 | c0004 | t0001 | g0197 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA18991 | hp1 | a0001 | c0006 | t0001 | g0182 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA19000 | hp1 | a0002 | c0002 | t0001 | g0163 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA19000 | hp2 | a0002 | c0002 | t0001 | g0115 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA19001 | hp1 | a0002 | c0002 | t0001 | g0190 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA19001 | hp2 | a0002 | c0003 | t0001 | g0070 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA19002 | hp2 | a0002 | c0002 | t0011 | g0105 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA19009 | hp1 | a0002 | c0002 | t0001 | g0172 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA19009 | hp2 | a0008 | c0014 | t0001 | g0100 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA19010 | hp1 | a0002 | c0002 | t0001 | g0160 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA19010 | hp2 | a0002 | c0003 | t0001 | g0085 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA19011 | hp1 | a0002 | c0002 | t0001 | g0116 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | LWK | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA19030 | hp2 | a0001 | c0004 | t0001 | g0137 | AFR | LWK | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | LWK | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA19054 | hp1 | a0002 | c0002 | t0001 | g0153 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA19055 | hp1 | a0004 | c0009 | t0001 | g0008 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA19055 | hp2 | a0002 | c0002 | t0008 | g0148 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA19060 | hp1 | a0001 | c0004 | t0001 | g0196 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA19060 | hp2 | a0001 | c0006 | t0001 | g0176 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA19074 | hp1 | a0002 | c0002 | t0001 | g0119 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA19074 | hp2 | a0001 | c0026 | t0001 | g0055 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA19080 | hp1 | a0002 | c0002 | t0001 | g0144 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA19081 | hp1 | a0002 | c0003 | t0001 | g0019 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA19081 | hp2 | a0002 | c0002 | t0001 | g0180 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA19084 | hp1 | a0002 | c0002 | t0001 | g0106 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA19091 | hp1 | a0009 | c0019 | t0001 | g0141 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA19240 | hp1 | a0002 | c0003 | t0001 | g0120 | AFR | YRI | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA19240 | hp2 | a0012 | c0022 | t0001 | g0112 | AFR | YRI | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0057 | EUR | TSI | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA20805 | hp2 | a0002 | c0002 | t0001 | g0203 | EUR | TSI | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | ACB | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02109 | hp2 | a0005 | c0008 | t0001 | g0022 | AFR | ACB | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02559 | hp1 | a0005 | c0008 | t0001 | g0021 | AFR | ACB | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02559 | hp2 | a0002 | c0002 | t0001 | g0219 | AFR | ACB | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | USA | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG06807 | hp2 | a0002 | c0003 | t0001 | g0129 | AFR | USA | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA20300 | hp1 | a0003 | c0011 | t0001 | g0186 | AFR | USA | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | USA | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0078 | REF | REF | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| homoSapiens_grch38 | hp1 | a0002 | c0003 | t0001 | g0127 | REF | REF | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:131127647
|
A | C | 1 | a0007 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.169A>C | p.Ser57Arg | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 2/36 | 288/7568 | 169/6273 | 57/2090 | chr9 | 131127647 | ||
| chr9:131128416
|
C | T | 1 | a0006 | 3 | HG01106.hp2 HG02723.hp2 HG02897.hp1 |
missense_variant | MODERATE | c.326C>T | p.Ala109Val | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 3/36 | 445/7568 | 326/6273 | 109/2090 | chr9 | 131128416 | ||
| chr9:131140677
|
T | G | 1 | a0008 | 1 | NA19009.hp2 | missense_variant | MODERATE | c.1261T>G | p.Ser421Ala | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 11/36 | 1380/7568 | 1261/6273 | 421/2090 | chr9 | 131140677 | ||
| chr9:131144699
|
A | G | 2 | a0003a0016 | 6 | HG02523.hp1 HG02615.hp1 HG03239.hp1 others(3): Show |
missense_variant | MODERATE | c.1714A>G | p.Met572Val | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 12/36 | 1833/7568 | 1714/6273 | 572/2090 | chr9 | 131144699 | ||
| chr9:131144705
|
C | T | 11 | a0001a0004a0005others(8): Show | 128 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(125): Show |
missense_variant | MODERATE | c.1720C>T | p.Pro574Ser | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 12/36 | 1839/7568 | 1720/6273 | 574/2090 | chr9 | 131144705 | ||
| chr9:131150710
|
G | T | 1 | a0004 | 3 | HG00597.hp2 HG00609.hp1 NA19055.hp1 |
missense_variant | MODERATE | c.2222G>T | p.Arg741Leu | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 16/36 | 2341/7568 | 2222/6273 | 741/2090 | chr9 | 131150710 | ||
| chr9:131151751
|
A | G | 1 | a0011 | 1 | HG03831.hp1 | missense_variant | MODERATE | c.2293A>G | p.Ile765Val | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/36 | 2412/7568 | 2293/6273 | 765/2090 | chr9 | 131151751 | ||
| chr9:131163116
|
A | G | 1 | a0015 | 1 | HG02145.hp1 | missense_variant | MODERATE | c.2666A>G | p.Lys889Arg | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 19/36 | 2785/7568 | 2666/6273 | 889/2090 | chr9 | 131163116 | ||
| chr9:131175568
|
C | T | 1 | a0009 | 1 | NA19091.hp1 | missense_variant | MODERATE | c.3266C>T | p.Pro1089Leu | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 23/36 | 3385/7568 | 3266/6273 | 1089/2090 | chr9 | 131175568 | ||
| chr9:131198269
|
G | C | 3 | a0010a0012a0013 | 3 | HG02886.hp1 HG03579.hp1 NA19240.hp2 |
missense_variant | MODERATE | c.4775G>C | p.Gly1592Ala | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 29/36 | 4894/7568 | 4775/6273 | 1592/2090 | chr9 | 131198269 | ||
| chr9:131198511
|
G | C | 1 | a0005 | 3 | HG02109.hp2 HG02559.hp1 NA18522.hp1 |
missense_variant | MODERATE | c.5017G>C | p.Val1673Leu | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 29/36 | 5136/7568 | 5017/6273 | 1673/2090 | chr9 | 131198511 | ||
| chr9:131198701
|
C | T | 1 | a0013 | 1 | HG03579.hp1 | missense_variant | MODERATE | c.5207C>T | p.Ala1736Val | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 29/36 | 5326/7568 | 5207/6273 | 1736/2090 | chr9 | 131198701 | ||
| chr9:131198745
|
A | G | 1 | a0014 | 1 | HG00544.hp2 | missense_variant | MODERATE | c.5251A>G | p.Ser1751Gly | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 29/36 | 5370/7568 | 5251/6273 | 1751/2090 | chr9 | 131198745 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:131144593
|
G | A | 1 | a0001c0015 | 1 | HG02083.hp2 | synonymous_variant | LOW | c.1608G>A | p.Ala536Ala | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 12/36 | 1727/7568 | 1608/6273 | 536/2090 | chr9 | 131144593 | ||
| chr9:131146243
|
A | G | 12 | a0001c0004a0001c0005a0001c0006others(9): Show | 108 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(105): Show |
synonymous_variant | LOW | c.1884A>G | p.Thr628Thr | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 13/36 | 2003/7568 | 1884/6273 | 628/2090 | chr9 | 131146243 | ||
| chr9:131150637
|
T | C | 1 | a0001c0006 | 4 | HG00408.hp2 HG00544.hp1 NA18991.hp1 others(1): Show |
synonymous_variant | LOW | c.2149T>C | p.Leu717Leu | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 16/36 | 2268/7568 | 2149/6273 | 717/2090 | chr9 | 131150637 | ||
| chr9:131163096
|
T | G | 2 | a0001c0007a0002c0016 | 4 | HG02145.hp2 HG02897.hp2 HG03041.hp2 others(1): Show |
synonymous_variant | LOW | c.2646T>G | p.Leu882Leu | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 19/36 | 2765/7568 | 2646/6273 | 882/2090 | chr9 | 131163096 | ||
| chr9:131174212
|
C | T | 1 | a0002c0020 | 1 | HG03486.hp1 | synonymous_variant | LOW | c.3051C>T | p.Pro1017Pro | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 22/36 | 3170/7568 | 3051/6273 | 1017/2090 | chr9 | 131174212 | ||
| chr9:131178336
|
G | T | 1 | a0001c0026 | 1 | NA19074.hp2 | synonymous_variant | LOW | c.3345G>T | p.Thr1115Thr | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/36 | 3464/7568 | 3345/6273 | 1115/2090 | chr9 | 131178336 | ||
| chr9:131187346
|
T | C | 5 | a0001c0005a0001c0010a0002c0018others(2): Show | 11 | HG01109.hp1 HG01496.hp2 HG01891.hp2 others(8): Show |
synonymous_variant | LOW | c.3477T>C | p.Ala1159Ala | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 25/36 | 3596/7568 | 3477/6273 | 1159/2090 | chr9 | 131187346 | ||
| chr9:131198420
|
A | G | 3 | a0001c0005a0002c0018a0015c0028 | 7 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(4): Show |
synonymous_variant | LOW | c.4926A>G | p.Ser1642Ser | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 29/36 | 5045/7568 | 4926/6273 | 1642/2090 | chr9 | 131198420 | ||
| chr9:131233457
|
T | C | 3 | a0001c0024a0001c0026a0001c0027 | 3 | HG02056.hp2 NA18945.hp2 NA19074.hp2 |
synonymous_variant | LOW | c.6243T>C | p.Ser2081Ser | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 36/36 | 6362/7568 | 6243/6273 | 2081/2090 | chr9 | 131233457 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:131125667
|
G | T | 1 | a0002c0020t0012 | 1 | HG03486.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-38G>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 1/36 | chr9 | 131125667 | ||||||
| chr9:131125677
|
G | A | 2 | a0013c0023t0005a0015c0028t0004 | 2 | HG02145.hp1 HG03579.hp1 |
5_prime_UTR_variant | MODIFIER | c.-28G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 1/36 | 28 | chr9 | 131125677 | |||||
| chr9:131233491
|
C | T | 1 | a0002c0002t0011 | 1 | NA19002.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 36/36 | 4 | chr9 | 131233491 | |||||
| chr9:131233509
|
G | A | 1 | a0002c0020t0012 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*22G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 36/36 | 22 | chr9 | 131233509 | |||||
| chr9:131233538
|
T | G | 1 | a0001c0001t0006 | 1 | HG00438.hp2 | 3_prime_UTR_variant | MODIFIER | c.*51T>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 36/36 | 51 | chr9 | 131233538 | |||||
| chr9:131233612
|
A | C | 1 | a0001c0001t0010 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*125A>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 36/36 | 125 | chr9 | 131233612 | |||||
| chr9:131233671
|
T | C | 1 | a0002c0020t0012 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*184T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 36/36 | 184 | chr9 | 131233671 | |||||
| chr9:131233894
|
A | G | 1 | a0001c0001t0009 | 1 | HG04184.hp1 | 3_prime_UTR_variant | MODIFIER | c.*407A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 36/36 | 407 | chr9 | 131233894 | |||||
| chr9:131233936
|
T | C | 6 | a0001c0005t0002a0001c0005t0003a0001c0010t0003others(3): Show | 11 | HG01109.hp1 HG01496.hp2 HG01891.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*449T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 36/36 | 449 | chr9 | 131233936 | |||||
| chr9:131233981
|
T | G | 1 | a0001c0001t0007 | 1 | HG01928.hp1 | 3_prime_UTR_variant | MODIFIER | c.*494T>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 36/36 | 494 | chr9 | 131233981 | |||||
| chr9:131234587
|
AT | A | 4 | a0001c0005t0002a0002c0002t0008a0002c0018t0002others(1): Show | 7 | HG01496.hp2 HG02145.hp1 HG02451.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1111delT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 36/36 | 1111 | INFO_REALIGN_3_PRIME | chr9 | 131234587 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:131125771
|
C | G | 5 | a0001c0001t0001g0230a0001c0001t0001g0231a0001c0001t0001g0232others(2): Show | 5 | HG00438.hp1 HG00642.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.45+22C>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 1/35 | chr9 | 131125771 | ||||||
| chr9:131125777
|
C | T | 2 | a0001c0010t0003g0228a0001c0010t0003g0229 | 2 | HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.45+28C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 1/35 | chr9 | 131125777 | ||||||
| chr9:131125865
|
C | T | 13 | a0001c0001t0001g0216a0001c0001t0001g0217a0001c0001t0001g0218others(10): Show | 13 | HG01361.hp2 HG01884.hp2 HG01943.hp2 others(10): Show |
intron_variant | MODIFIER | c.45+116C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 1/35 | chr9 | 131125865 | ||||||
| chr9:131125900
|
C | T | 3 | a0001c0010t0003g0214a0001c0010t0003g0228a0001c0010t0003g0229 | 3 | HG01109.hp1 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.45+151C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 1/35 | chr9 | 131125900 | ||||||
| chr9:131125988
|
C | T | 1 | a0001c0005t0002g0213 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.45+239C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 1/35 | chr9 | 131125988 | ||||||
| chr9:131126419
|
G | C | 124 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(121): Show | 124 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.45+670G>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 1/35 | chr9 | 131126419 | ||||||
| chr9:131126550
|
A | AT | 13 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0114others(10): Show | 13 | HG01106.hp1 HG01361.hp1 HG02735.hp2 others(10): Show |
intron_variant | MODIFIER | c.45+816dupT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 1/35 | INFO_REALIGN_3_PRIME | chr9 | 131126550 | |||||
| chr9:131126550
|
A | ATT | 86 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0174others(83): Show | 86 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.45+815_45+816dupTT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 1/35 | INFO_REALIGN_3_PRIME | chr9 | 131126550 | |||||
| chr9:131126550
|
A | ATTT | 5 | a0001c0004t0001g0209a0001c0005t0002g0212a0001c0005t0002g0213others(2): Show | 5 | HG01496.hp2 HG01891.hp2 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.45+814_45+816dupTT others(1): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 1/35 | INFO_REALIGN_3_PRIME | chr9 | 131126550 | |||||
| chr9:131126692
|
C | T | 1 | a0002c0002t0001g0208 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.46-832C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 1/35 | chr9 | 131126692 | ||||||
| chr9:131126713
|
A | G | 1 | a0010c0017t0001g0108 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.46-811A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 1/35 | chr9 | 131126713 | ||||||
| chr9:131126732
|
T | C | 1 | a0001c0001t0001g0001 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.46-792T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 1/35 | chr9 | 131126732 | ||||||
| chr9:131126995
|
C | A | 3 | a0001c0010t0003g0214a0001c0010t0003g0228a0001c0010t0003g0229 | 3 | HG01109.hp1 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.46-529C>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 1/35 | chr9 | 131126995 | ||||||
| chr9:131127109
|
T | C | 90 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0174others(87): Show | 90 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.46-415T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 1/35 | chr9 | 131127109 | ||||||
| chr9:131127240
|
G | A | 1 | a0001c0001t0001g0002 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.46-284G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 1/35 | chr9 | 131127240 | ||||||
| chr9:131127519
|
A | G | 1 | a0015c0028t0004g0207 | 1 | HG02145.hp1 | splice_region_variant&intron_variant | LOW | c.46-5A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 1/35 | chr9 | 131127519 | ||||||
| chr9:131127817
|
A | G | 1 | a0002c0018t0002g0107 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.241+98A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 2/35 | chr9 | 131127817 | ||||||
| chr9:131127876
|
C | T | 119 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(116): Show | 119 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.241+157C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 2/35 | chr9 | 131127876 | ||||||
| chr9:131128214
|
T | C | 6 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0212others(3): Show | 6 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.242-118T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 2/35 | chr9 | 131128214 | ||||||
| chr9:131128513
|
A | G | 85 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0174others(82): Show | 85 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.393+30A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 3/35 | chr9 | 131128513 | ||||||
| chr9:131128607
|
T | TA | 6 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0212others(3): Show | 6 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.393+133dupA | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 3/35 | INFO_REALIGN_3_PRIME | chr9 | 131128607 | |||||
| chr9:131129525
|
A | C | 97 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0174others(94): Show | 97 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.592+48A>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 4/35 | chr9 | 131129525 | ||||||
| chr9:131129575
|
G | GT | 6 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0010t0003g0214others(3): Show | 6 | HG01109.hp1 HG02818.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.592+108dupT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr9 | 131129575 | |||||
| chr9:131129575
|
G | T | 6 | a0001c0004t0001g0131a0001c0004t0001g0202a0002c0002t0001g0199others(3): Show | 6 | HG00099.hp2 HG01168.hp2 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.592+98G>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 4/35 | chr9 | 131129575 | ||||||
| chr9:131129713
|
C | T | 1 | a0001c0004t0001g0227 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.592+236C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 4/35 | chr9 | 131129713 | ||||||
| chr9:131129753
|
G | A | 1 | a0002c0002t0001g0133 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.592+276G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 4/35 | chr9 | 131129753 | ||||||
| chr9:131130132
|
G | GTTTTGTT others(6): Show |
2 | a0001c0004t0001g0138a0002c0002t0001g0139 | 2 | HG03927.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.593-629_593-617dup others(13): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr9 | 131130132 | |||||
| chr9:131130132
|
G | GTTTTTTT others(3): Show |
1 | a0015c0028t0004g0207 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.593-630_593-629ins others(10): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr9 | 131130132 | |||||
| chr9:131130137
|
G | GT | 92 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0013others(89): Show | 92 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.593-616dupT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr9 | 131130137 | |||||
| chr9:131130137
|
G | GTT | 24 | a0001c0001t0001g0001a0001c0001t0001g0090a0001c0001t0001g0092others(21): Show | 24 | HG00438.hp1 HG00741.hp1 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.593-617_593-616dup others(2): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr9 | 131130137 | |||||
| chr9:131130137
|
G | GTTTTGTT others(8): Show |
1 | a0002c0002t0001g0134 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.593-625_593-624ins others(15): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr9 | 131130137 | |||||
| chr9:131130137
|
G | GTTTTGTT others(9): Show |
1 | a0002c0002t0001g0130 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.593-625_593-624ins others(16): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr9 | 131130137 | |||||
| chr9:131130137
|
G | GTTTTTGT others(5): Show |
1 | a0002c0002t0001g0135 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.593-624_593-623ins others(12): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr9 | 131130137 | |||||
| chr9:131130137
|
G | GTTTTTTT others(6): Show |
1 | a0002c0002t0001g0136 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.593-618_593-617ins others(13): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr9 | 131130137 | |||||
| chr9:131130137
|
G | GTTTTTTT others(7): Show |
2 | a0001c0004t0001g0137a0002c0002t0001g0208 | 2 | HG01243.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.593-618_593-617ins others(14): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr9 | 131130137 | |||||
| chr9:131130137
|
G | GTTTTTTT others(5): Show |
1 | a0002c0002t0001g0157 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.593-627_593-616dup others(12): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr9 | 131130137 | |||||
| chr9:131130137
|
G | GTTTTTTT others(7): Show |
1 | a0001c0004t0001g0140 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.593-617_593-616ins others(14): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr9 | 131130137 | |||||
| chr9:131130137
|
G | GTTTTTTT others(10): Show |
1 | a0009c0019t0001g0141 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.593-617_593-616ins others(17): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr9 | 131130137 | |||||
| chr9:131130137
|
G | GTTTTTTT others(6): Show |
2 | a0002c0002t0001g0158a0002c0002t0001g0159 | 2 | HG00741.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.593-628_593-616dup others(13): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr9 | 131130137 | |||||
| chr9:131130137
|
G | GTTTTTTT others(7): Show |
7 | a0001c0004t0001g0202a0001c0004t0001g0204a0002c0002t0001g0160others(4): Show | 7 | HG00099.hp2 HG01433.hp2 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.593-616_593-615ins others(14): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr9 | 131130137 | |||||
| chr9:131130137
|
G | GTTTTTTT others(8): Show |
16 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0004t0001g0131others(13): Show | 16 | HG00408.hp2 HG00544.hp1 HG01361.hp1 others(13): Show |
intron_variant | MODIFIER | c.593-616_593-615ins others(15): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr9 | 131130137 | |||||
| chr9:131130137
|
G | GTTTTTTT others(9): Show |
13 | a0001c0001t0001g0174a0001c0006t0001g0176a0001c0006t0001g0182others(10): Show | 13 | HG01943.hp2 HG01993.hp1 HG02132.hp1 others(10): Show |
intron_variant | MODIFIER | c.593-616_593-615ins others(16): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr9 | 131130137 | |||||
| chr9:131130137
|
G | GTTTTTTT others(10): Show |
9 | a0001c0001t0001g0189a0002c0002t0001g0106a0002c0002t0001g0116others(6): Show | 9 | HG01175.hp1 HG02027.hp2 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.593-616_593-615ins others(17): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr9 | 131130137 | |||||
| chr9:131130137
|
G | GTTTTTTT others(11): Show |
9 | a0001c0005t0002g0212a0002c0002t0001g0117a0002c0002t0001g0118others(6): Show | 9 | HG01884.hp2 HG02293.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.593-616_593-615ins others(18): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr9 | 131130137 | |||||
| chr9:131130137
|
G | GTTTTTTT others(13): Show |
1 | a0001c0004t0001g0209 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.593-616_593-615ins others(20): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr9 | 131130137 | |||||
| chr9:131130137
|
G | GTTTTTTT others(15): Show |
1 | a0001c0005t0002g0205 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.593-616_593-615ins others(22): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr9 | 131130137 | |||||
| chr9:131130137
|
G | GTTTTTTT others(17): Show |
3 | a0002c0002t0001g0193a0002c0002t0001g0194a0002c0002t0001g0210 | 3 | HG00423.hp2 HG01928.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.593-616_593-615ins others(24): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr9 | 131130137 | |||||
| chr9:131130137
|
G | GTTTTTTT others(18): Show |
1 | a0002c0002t0001g0195 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.593-616_593-615ins others(25): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr9 | 131130137 | |||||
| chr9:131130137
|
G | GTTTTTTT others(21): Show |
1 | a0001c0004t0001g0196 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.593-616_593-615ins others(28): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr9 | 131130137 | |||||
| chr9:131130137
|
G | GTTTTTTT others(22): Show |
2 | a0001c0004t0001g0197a0001c0005t0002g0206 | 2 | HG02451.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.593-616_593-615ins others(29): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr9 | 131130137 | |||||
| chr9:131130137
|
G | GTTTTTTT others(23): Show |
1 | a0001c0004t0001g0198 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.593-616_593-615ins others(30): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr9 | 131130137 | |||||
| chr9:131130137
|
G | T | 2 | a0001c0005t0002g0213a0015c0028t0004g0207 | 2 | HG01496.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.593-629G>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 4/35 | chr9 | 131130137 | ||||||
| chr9:131130138
|
T | G | 1 | a0001c0004t0001g0227 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.593-628T>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 4/35 | chr9 | 131130138 | ||||||
| chr9:131130141
|
TTTTTTTT others(3): Show |
T | 1 | a0001c0001t0001g0102 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.593-615_593-606del others(10): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr9 | 131130141 | |||||
| chr9:131130151
|
G | T | 213 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(210): Show | 213 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(210): Show |
intron_variant | MODIFIER | c.593-615G>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 4/35 | chr9 | 131130151 | ||||||
| chr9:131130239
|
G | A | 3 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015 | 3 | HG00733.hp2 HG01074.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.593-527G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 4/35 | chr9 | 131130239 | ||||||
| chr9:131130271
|
G | A | 1 | a0002c0002t0001g0183 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.593-495G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 4/35 | chr9 | 131130271 | ||||||
| chr9:131130289
|
G | A | 1 | a0002c0002t0001g0184 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.593-477G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 4/35 | chr9 | 131130289 | ||||||
| chr9:131130437
|
G | A | 7 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0212others(4): Show | 7 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.593-329G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 4/35 | chr9 | 131130437 | ||||||
| chr9:131130575
|
G | T | 2 | a0002c0002t0001g0115a0002c0002t0001g0119 | 2 | NA19000.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.593-191G>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 4/35 | chr9 | 131130575 | ||||||
| chr9:131130671
|
C | T | 1 | a0002c0018t0002g0107 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.593-95C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 4/35 | chr9 | 131130671 | ||||||
| chr9:131130903
|
G | A | 1 | a0009c0019t0001g0141 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.663+67G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 5/35 | chr9 | 131130903 | ||||||
| chr9:131131094
|
T | G | 106 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0174others(103): Show | 106 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.663+258T>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 5/35 | chr9 | 131131094 | ||||||
| chr9:131131133
|
G | A | 7 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0212others(4): Show | 7 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.663+297G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 5/35 | chr9 | 131131133 | ||||||
| chr9:131131241
|
T | C | 3 | a0001c0010t0003g0214a0001c0010t0003g0228a0001c0010t0003g0229 | 3 | HG01109.hp1 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.663+405T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 5/35 | chr9 | 131131241 | ||||||
| chr9:131131271
|
A | G | 1 | a0001c0001t0010g0234 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.663+435A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 5/35 | chr9 | 131131271 | ||||||
| chr9:131131374
|
A | T | 7 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0212others(4): Show | 7 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.663+538A>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 5/35 | chr9 | 131131374 | ||||||
| chr9:131131597
|
A | G | 1 | a0002c0002t0001g0172 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.663+761A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 5/35 | chr9 | 131131597 | ||||||
| chr9:131131632
|
T | C | 1 | a0002c0020t0012g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.663+796T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 5/35 | chr9 | 131131632 | ||||||
| chr9:131131674
|
T | A | 1 | a0002c0002t0001g0133 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.663+838T>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 5/35 | chr9 | 131131674 | ||||||
| chr9:131131695
|
T | A | 94 | a0001c0001t0001g0016a0001c0001t0001g0170a0001c0001t0001g0171others(91): Show | 94 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.663+859T>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 5/35 | chr9 | 131131695 | ||||||
| chr9:131131777
|
C | T | 1 | a0001c0004t0001g0196 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.664-819C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 5/35 | chr9 | 131131777 | ||||||
| chr9:131131816
|
G | C | 1 | a0001c0001t0001g0017 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.664-780G>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 5/35 | chr9 | 131131816 | ||||||
| chr9:131131933
|
C | T | 1 | a0002c0018t0002g0107 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.664-663C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 5/35 | chr9 | 131131933 | ||||||
| chr9:131132025
|
G | A | 1 | a0002c0018t0002g0107 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.664-571G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 5/35 | chr9 | 131132025 | ||||||
| chr9:131132030
|
G | A | 3 | a0001c0001t0001g0216a0001c0001t0001g0217a0001c0001t0001g0218 | 3 | HG02109.hp1 HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.664-566G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 5/35 | chr9 | 131132030 | ||||||
| chr9:131132054
|
T | C | 1 | a0002c0020t0012g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.664-542T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 5/35 | chr9 | 131132054 | ||||||
| chr9:131132115
|
C | CT | 111 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(108): Show | 111 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.664-478dupT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 5/35 | INFO_REALIGN_3_PRIME | chr9 | 131132115 | |||||
| chr9:131132115
|
C | CTT | 6 | a0001c0001t0001g0001a0001c0007t0001g0088a0001c0027t0001g0087others(3): Show | 6 | HG02056.hp2 HG02145.hp2 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.664-479_664-478dup others(2): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 5/35 | INFO_REALIGN_3_PRIME | chr9 | 131132115 | |||||
| chr9:131132115
|
CTTTCTTT others(5): Show |
C | 1 | a0001c0001t0001g0018 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.664-477_664-466del others(12): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 5/35 | INFO_REALIGN_3_PRIME | chr9 | 131132115 | |||||
| chr9:131132118
|
TC | T | 92 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0174others(89): Show | 92 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.664-477delC | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 5/35 | chr9 | 131132118 | ||||||
| chr9:131132119
|
C | T | 125 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(122): Show | 125 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.664-477C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 5/35 | chr9 | 131132119 | ||||||
| chr9:131132126
|
T | C | 5 | a0001c0004t0001g0209a0001c0005t0002g0205a0001c0005t0002g0206others(2): Show | 5 | HG01496.hp2 HG02451.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.664-470T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 5/35 | chr9 | 131132126 | ||||||
| chr9:131132261
|
G | A | 1 | a0013c0023t0005g0003 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.664-335G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 5/35 | chr9 | 131132261 | ||||||
| chr9:131132274
|
A | G | 104 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0174others(101): Show | 104 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.664-322A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 5/35 | chr9 | 131132274 | ||||||
| chr9:131132495
|
T | C | 1 | a0012c0022t0001g0112 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.664-101T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 5/35 | chr9 | 131132495 | ||||||
| chr9:131132740
|
C | T | 1 | a0014c0025t0001g0086 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.727+81C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 6/35 | chr9 | 131132740 | ||||||
| chr9:131133004
|
A | AT | 8 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0212others(5): Show | 8 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.728-92dupT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 6/35 | INFO_REALIGN_3_PRIME | chr9 | 131133004 | |||||
| chr9:131133304
|
G | GT | 9 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(6): Show | 9 | HG00423.hp1 HG01106.hp1 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.831+113dupT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 7/35 | INFO_REALIGN_3_PRIME | chr9 | 131133304 | |||||
| chr9:131133304
|
G | GTTT | 88 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0174others(85): Show | 88 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.831+111_831+113dup others(3): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 7/35 | INFO_REALIGN_3_PRIME | chr9 | 131133304 | |||||
| chr9:131133304
|
GT | G | 6 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0212others(3): Show | 6 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.831+113delT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 7/35 | INFO_REALIGN_3_PRIME | chr9 | 131133304 | |||||
| chr9:131133333
|
C | G | 97 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0174others(94): Show | 97 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.831+124C>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 7/35 | chr9 | 131133333 | ||||||
| chr9:131133343
|
C | T | 3 | a0006c0012t0001g0005a0006c0012t0001g0006a0006c0012t0001g0007 | 3 | HG01106.hp2 HG02723.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.831+134C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 7/35 | chr9 | 131133343 | ||||||
| chr9:131133374
|
A | G | 220 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(217): Show | 220 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(217): Show |
intron_variant | MODIFIER | c.831+165A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 7/35 | chr9 | 131133374 | ||||||
| chr9:131133390
|
G | C | 6 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0212others(3): Show | 6 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.831+181G>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 7/35 | chr9 | 131133390 | ||||||
| chr9:131133559
|
T | C | 104 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0174others(101): Show | 104 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.831+350T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 7/35 | chr9 | 131133559 | ||||||
| chr9:131133762
|
A | G | 104 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0174others(101): Show | 104 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.831+553A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 7/35 | chr9 | 131133762 | ||||||
| chr9:131133839
|
G | A | 97 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0174others(94): Show | 97 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.831+630G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 7/35 | chr9 | 131133839 | ||||||
| chr9:131133876
|
A | G | 1 | a0001c0005t0003g0211 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.831+667A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 7/35 | chr9 | 131133876 | ||||||
| chr9:131134071
|
C | T | 2 | a0001c0001t0001g0170a0001c0001t0001g0171 | 2 | HG03017.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.832-827C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 7/35 | chr9 | 131134071 | ||||||
| chr9:131134192
|
C | T | 7 | a0002c0002t0001g0149a0002c0002t0001g0150a0002c0002t0001g0151others(4): Show | 7 | HG00597.hp1 NA18948.hp2 NA18949.hp2 others(4): Show |
intron_variant | MODIFIER | c.832-706C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 7/35 | chr9 | 131134192 | ||||||
| chr9:131134654
|
A | G | 1 | a0001c0001t0001g0081 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.832-244A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 7/35 | chr9 | 131134654 | ||||||
| chr9:131134771
|
C | T | 2 | a0002c0002t0001g0172a0002c0002t0001g0180 | 2 | NA19009.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.832-127C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 7/35 | chr9 | 131134771 | ||||||
| chr9:131134849
|
T | C | 101 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0174others(98): Show | 101 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.832-49T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 7/35 | chr9 | 131134849 | ||||||
| chr9:131135344
|
A | G | 1 | a0001c0001t0001g0189 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.938+340A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 8/35 | chr9 | 131135344 | ||||||
| chr9:131135470
|
A | G | 1 | a0001c0005t0002g0213 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.938+466A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 8/35 | chr9 | 131135470 | ||||||
| chr9:131136033
|
G | A | 1 | a0013c0023t0005g0003 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1005+27G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 9/35 | chr9 | 131136033 | ||||||
| chr9:131136162
|
C | G | 6 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0212others(3): Show | 6 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.1005+156C>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 9/35 | chr9 | 131136162 | ||||||
| chr9:131136185
|
G | A | 3 | a0001c0001t0001g0170a0001c0001t0001g0171a0002c0002t0001g0173 | 3 | HG03017.hp2 HG03491.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1005+179G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 9/35 | chr9 | 131136185 | ||||||
| chr9:131136197
|
A | G | 104 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0174others(101): Show | 104 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.1005+191A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 9/35 | chr9 | 131136197 | ||||||
| chr9:131136237
|
G | A | 94 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0174others(91): Show | 94 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.1005+231G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 9/35 | chr9 | 131136237 | ||||||
| chr9:131136535
|
C | A | 97 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0174others(94): Show | 97 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.1005+529C>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 9/35 | chr9 | 131136535 | ||||||
| chr9:131136565
|
T | C | 1 | a0002c0018t0002g0107 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1005+559T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 9/35 | chr9 | 131136565 | ||||||
| chr9:131136593
|
A | T | 94 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0174others(91): Show | 94 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.1005+587A>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 9/35 | chr9 | 131136593 | ||||||
| chr9:131136772
|
T | A | 1 | a0011c0021t0001g0181 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1005+766T>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 9/35 | chr9 | 131136772 | ||||||
| chr9:131136793
|
C | T | 2 | a0002c0002t0001g0079a0002c0002t0001g0080 | 2 | HG00642.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1005+787C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 9/35 | chr9 | 131136793 | ||||||
| chr9:131136907
|
A | G | 6 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0212others(3): Show | 6 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.1005+901A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 9/35 | chr9 | 131136907 | ||||||
| chr9:131137148
|
T | C | 104 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0174others(101): Show | 104 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.1005+1142T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 9/35 | chr9 | 131137148 | ||||||
| chr9:131137368
|
T | A | 1 | a0015c0028t0004g0207 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1005+1362T>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 9/35 | chr9 | 131137368 | ||||||
| chr9:131137414
|
C | T | 2 | a0002c0003t0001g0085a0002c0020t0012g0132 | 2 | HG03486.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.1005+1408C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 9/35 | chr9 | 131137414 | ||||||
| chr9:131137535
|
C | T | 94 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0174others(91): Show | 94 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.1005+1529C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 9/35 | chr9 | 131137535 | ||||||
| chr9:131137552
|
C | CT | 7 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0099others(4): Show | 7 | HG00642.hp1 HG01175.hp2 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.1005+1569dupT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 9/35 | INFO_REALIGN_3_PRIME | chr9 | 131137552 | |||||
| chr9:131137552
|
CT | C | 139 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0023others(136): Show | 139 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.1005+1569delT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 9/35 | INFO_REALIGN_3_PRIME | chr9 | 131137552 | |||||
| chr9:131137552
|
CTT | C | 8 | a0001c0001t0001g0020a0001c0005t0002g0205a0001c0005t0002g0206others(5): Show | 8 | HG00558.hp1 HG01496.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.1005+1568_1005+156 others(6): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 9/35 | INFO_REALIGN_3_PRIME | chr9 | 131137552 | |||||
| chr9:131137636
|
C | T | 3 | a0006c0012t0001g0005a0006c0012t0001g0006a0006c0012t0001g0007 | 3 | HG01106.hp2 HG02723.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1005+1630C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 9/35 | chr9 | 131137636 | ||||||
| chr9:131137743
|
T | G | 97 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0174others(94): Show | 97 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.1006-1538T>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 9/35 | chr9 | 131137743 | ||||||
| chr9:131137753
|
G | C | 1 | a0002c0002t0001g0210 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1006-1528G>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 9/35 | chr9 | 131137753 | ||||||
| chr9:131137887
|
A | G | 111 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(108): Show | 111 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.1006-1394A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 9/35 | chr9 | 131137887 | ||||||
| chr9:131137933
|
A | T | 1 | a0002c0020t0012g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1006-1348A>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 9/35 | chr9 | 131137933 | ||||||
| chr9:131137957
|
T | C | 1 | a0011c0021t0001g0181 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1006-1324T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 9/35 | chr9 | 131137957 | ||||||
| chr9:131138043
|
C | T | 94 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0174others(91): Show | 94 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.1006-1238C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 9/35 | chr9 | 131138043 | ||||||
| chr9:131138162
|
T | A | 1 | a0001c0005t0002g0212 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1006-1119T>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 9/35 | chr9 | 131138162 | ||||||
| chr9:131138243
|
C | T | 94 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0174others(91): Show | 94 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.1006-1038C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 9/35 | chr9 | 131138243 | ||||||
| chr9:131138286
|
TCGGCTCA | T | 3 | a0006c0012t0001g0005a0006c0012t0001g0006a0006c0012t0001g0007 | 3 | HG01106.hp2 HG02723.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1006-993_1006-987d others(9): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 9/35 | INFO_REALIGN_3_PRIME | chr9 | 131138286 | |||||
| chr9:131138288
|
G | A | 3 | a0005c0008t0001g0021a0005c0008t0001g0022a0005c0008t0001g0109 | 3 | HG02109.hp2 HG02559.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1006-993G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 9/35 | chr9 | 131138288 | ||||||
| chr9:131138379
|
C | A | 94 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0174others(91): Show | 94 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.1006-902C>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 9/35 | chr9 | 131138379 | ||||||
| chr9:131138613
|
A | G | 103 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0174others(100): Show | 103 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.1006-668A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 9/35 | chr9 | 131138613 | ||||||
| chr9:131138652
|
C | T | 1 | a0002c0018t0002g0107 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1006-629C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 9/35 | chr9 | 131138652 | ||||||
| chr9:131139088
|
T | G | 94 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0174others(91): Show | 94 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.1006-193T>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 9/35 | chr9 | 131139088 | ||||||
| chr9:131139148
|
G | A | 104 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0174others(101): Show | 104 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.1006-133G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 9/35 | chr9 | 131139148 | ||||||
| chr9:131139205
|
C | A | 1 | a0002c0002t0001g0113 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1006-76C>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 9/35 | chr9 | 131139205 | ||||||
| chr9:131139255
|
C | CT | 10 | a0001c0001t0001g0233a0001c0005t0002g0205a0001c0005t0002g0212others(7): Show | 10 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(7): Show |
splice_acceptor_variant&intron_variant | HIGH | c.1006-3dupT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 9/35 | INFO_REALIGN_3_PRIME | chr9 | 131139255 | |||||
| chr9:131139255
|
CT | C | 18 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0024others(15): Show | 18 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(15): Show |
splice_region_variant&intron_variant | LOW | c.1006-3delT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 9/35 | INFO_REALIGN_3_PRIME | chr9 | 131139255 | |||||
| chr9:131139255
|
CTTTTTTT others(6): Show |
C | 2 | a0002c0002t0001g0162a0002c0002t0001g0163 | 2 | HG01981.hp1 NA19000.hp1 |
splice_region_variant&intron_variant | LOW | c.1006-15_1006-3delT others(12): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 9/35 | INFO_REALIGN_3_PRIME | chr9 | 131139255 | |||||
| chr9:131139259
|
T | C | 3 | a0001c0010t0003g0214a0001c0010t0003g0228a0001c0010t0003g0229 | 3 | HG01109.hp1 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1006-22T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 9/35 | chr9 | 131139259 | ||||||
| chr9:131139262
|
T | C | 3 | a0001c0010t0003g0214a0001c0010t0003g0228a0001c0010t0003g0229 | 3 | HG01109.hp1 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1006-19T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 9/35 | chr9 | 131139262 | ||||||
| chr9:131139464
|
A | G | 2 | a0001c0001t0001g0077a0001c0001t0001g0078 | 2 | HG01515.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1132+57A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 10/35 | chr9 | 131139464 | ||||||
| chr9:131139554
|
C | T | 219 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(216): Show | 219 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.1132+147C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 10/35 | chr9 | 131139554 | ||||||
| chr9:131139685
|
T | G | 25 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(22): Show | 25 | HG00099.hp1 HG00733.hp2 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.1132+278T>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 10/35 | chr9 | 131139685 | ||||||
| chr9:131139690
|
A | G | 1 | a0001c0001t0006g0076 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1132+283A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 10/35 | chr9 | 131139690 | ||||||
| chr9:131139802
|
A | G | 1 | a0001c0001t0001g0049 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1132+395A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 10/35 | chr9 | 131139802 | ||||||
| chr9:131139886
|
GTAGCTTG others(4): Show |
G | 4 | a0001c0007t0001g0065a0001c0007t0001g0088a0001c0007t0001g0089others(1): Show | 4 | HG02145.hp2 HG02897.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1132+482_1132+492d others(13): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 10/35 | INFO_REALIGN_3_PRIME | chr9 | 131139886 | |||||
| chr9:131140080
|
A | T | 94 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0174others(91): Show | 94 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.1133-469A>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 10/35 | chr9 | 131140080 | ||||||
| chr9:131140191
|
C | T | 2 | a0001c0004t0001g0137a0002c0002t0001g0136 | 2 | HG00733.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1133-358C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 10/35 | chr9 | 131140191 | ||||||
| chr9:131140394
|
A | G | 103 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0174others(100): Show | 103 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.1133-155A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 10/35 | chr9 | 131140394 | ||||||
| chr9:131140401
|
G | C | 2 | a0001c0001t0001g0018a0001c0001t0001g0053 | 2 | HG01109.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.1133-148G>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 10/35 | chr9 | 131140401 | ||||||
| chr9:131140419
|
A | G | 3 | a0006c0012t0001g0005a0006c0012t0001g0006a0006c0012t0001g0007 | 3 | HG01106.hp2 HG02723.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1133-130A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 10/35 | chr9 | 131140419 | ||||||
| chr9:131140512
|
C | G | 100 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0174others(97): Show | 100 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.1133-37C>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 10/35 | chr9 | 131140512 | ||||||
| chr9:131140734
|
C | T | 45 | a0001c0004t0001g0131a0001c0004t0001g0137a0001c0004t0001g0138others(42): Show | 45 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(42): Show |
intron_variant | MODIFIER | c.1294+24C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 11/35 | chr9 | 131140734 | ||||||
| chr9:131140862
|
A | G | 13 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(10): Show | 13 | HG00099.hp1 HG00733.hp2 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.1294+152A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 11/35 | chr9 | 131140862 | ||||||
| chr9:131140893
|
C | T | 94 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0174others(91): Show | 94 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.1294+183C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 11/35 | chr9 | 131140893 | ||||||
| chr9:131140994
|
T | G | 1 | a0001c0001t0001g0066 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1294+284T>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 11/35 | chr9 | 131140994 | ||||||
| chr9:131141138
|
C | CA | 101 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0114others(98): Show | 101 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.1294+441dupA | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 11/35 | INFO_REALIGN_3_PRIME | chr9 | 131141138 | |||||
| chr9:131141138
|
C | CAA | 6 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0213others(3): Show | 6 | HG01496.hp2 HG01891.hp2 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.1294+440_1294+441d others(4): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 11/35 | INFO_REALIGN_3_PRIME | chr9 | 131141138 | |||||
| chr9:131141139
|
A | C | 2 | a0001c0001t0001g0048a0001c0001t0001g0081 | 2 | HG00408.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.1294+429A>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 11/35 | chr9 | 131141139 | ||||||
| chr9:131141162
|
T | G | 103 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0174others(100): Show | 103 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.1294+452T>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 11/35 | chr9 | 131141162 | ||||||
| chr9:131141170
|
T | C | 103 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0174others(100): Show | 103 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.1294+460T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 11/35 | chr9 | 131141170 | ||||||
| chr9:131141263
|
G | C | 104 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0174others(101): Show | 104 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.1294+553G>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 11/35 | chr9 | 131141263 | ||||||
| chr9:131141336
|
A | G | 104 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0174others(101): Show | 104 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.1294+626A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 11/35 | chr9 | 131141336 | ||||||
| chr9:131141478
|
C | CT | 6 | a0001c0001t0001g0017a0001c0001t0001g0052a0001c0001t0001g0061others(3): Show | 6 | HG01081.hp2 HG01433.hp1 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.1294+788dupT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 11/35 | INFO_REALIGN_3_PRIME | chr9 | 131141478 | |||||
| chr9:131141478
|
C | CTT | 7 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0213others(4): Show | 7 | HG01169.hp1 HG01175.hp1 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.1294+787_1294+788d others(4): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 11/35 | INFO_REALIGN_3_PRIME | chr9 | 131141478 | |||||
| chr9:131141478
|
C | CTTT | 86 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0174others(83): Show | 86 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.1294+786_1294+788d others(5): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 11/35 | INFO_REALIGN_3_PRIME | chr9 | 131141478 | |||||
| chr9:131141478
|
C | CTTTT | 8 | a0001c0004t0001g0165a0001c0004t0001g0209a0002c0002t0001g0130others(5): Show | 8 | HG01993.hp1 HG02735.hp2 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.1294+785_1294+788d others(6): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 11/35 | INFO_REALIGN_3_PRIME | chr9 | 131141478 | |||||
| chr9:131141793
|
T | A | 104 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0174others(101): Show | 104 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.1294+1083T>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 11/35 | chr9 | 131141793 | ||||||
| chr9:131141917
|
T | C | 2 | a0001c0001t0001g0010a0001c0001t0001g0114 | 2 | HG03688.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1294+1207T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 11/35 | chr9 | 131141917 | ||||||
| chr9:131141936
|
T | G | 104 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0174others(101): Show | 104 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.1294+1226T>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 11/35 | chr9 | 131141936 | ||||||
| chr9:131142141
|
T | C | 1 | a0002c0002t0001g0179 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1294+1431T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 11/35 | chr9 | 131142141 | ||||||
| chr9:131142177
|
C | G | 1 | a0001c0001t0001g0083 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1294+1467C>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 11/35 | chr9 | 131142177 | ||||||
| chr9:131142191
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1294+1481C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 11/35 | chr9 | 131142191 | ||||||
| chr9:131142368
|
A | G | 1 | a0002c0020t0012g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1294+1658A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 11/35 | chr9 | 131142368 | ||||||
| chr9:131142885
|
A | G | 1 | a0002c0020t0012g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1295-1395A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 11/35 | chr9 | 131142885 | ||||||
| chr9:131142934
|
T | C | 223 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(220): Show | 223 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(220): Show |
intron_variant | MODIFIER | c.1295-1346T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 11/35 | chr9 | 131142934 | ||||||
| chr9:131143217
|
C | T | 1 | a0012c0022t0001g0112 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1295-1063C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 11/35 | chr9 | 131143217 | ||||||
| chr9:131143339
|
A | G | 1 | a0002c0020t0012g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1295-941A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 11/35 | chr9 | 131143339 | ||||||
| chr9:131143429
|
A | G | 107 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0174others(104): Show | 107 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.1295-851A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 11/35 | chr9 | 131143429 | ||||||
| chr9:131143628
|
GAGTT | G | 95 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0004t0001g0131others(92): Show | 95 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1295-647_1295-644d others(6): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 11/35 | INFO_REALIGN_3_PRIME | chr9 | 131143628 | |||||
| chr9:131143660
|
T | C | 94 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0004t0001g0131others(91): Show | 94 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.1295-620T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 11/35 | chr9 | 131143660 | ||||||
| chr9:131143988
|
G | C | 1 | a0013c0023t0005g0003 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1295-292G>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 11/35 | chr9 | 131143988 | ||||||
| chr9:131144881
|
C | G | 3 | a0001c0010t0003g0214a0001c0010t0003g0228a0001c0010t0003g0229 | 3 | HG01109.hp1 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1769+127C>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 12/35 | chr9 | 131144881 | ||||||
| chr9:131144925
|
A | C | 4 | a0001c0007t0001g0065a0001c0007t0001g0088a0001c0007t0001g0089others(1): Show | 4 | HG02145.hp2 HG02897.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1769+171A>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 12/35 | chr9 | 131144925 | ||||||
| chr9:131144929
|
A | G | 217 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(214): Show | 217 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.1769+175A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 12/35 | chr9 | 131144929 | ||||||
| chr9:131144930
|
A | G | 168 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.1769+176A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 12/35 | chr9 | 131144930 | ||||||
| chr9:131145123
|
C | G | 1 | a0001c0001t0001g0066 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1769+369C>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 12/35 | chr9 | 131145123 | ||||||
| chr9:131145177
|
G | A | 1 | a0001c0010t0003g0214 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1769+423G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 12/35 | chr9 | 131145177 | ||||||
| chr9:131145449
|
A | T | 4 | a0001c0005t0003g0211a0002c0018t0002g0107a0010c0017t0001g0108others(1): Show | 4 | HG01891.hp2 HG02145.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1770-680A>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 12/35 | chr9 | 131145449 | ||||||
| chr9:131145475
|
A | G | 1 | a0001c0001t0001g0001 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1770-654A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 12/35 | chr9 | 131145475 | ||||||
| chr9:131145527
|
C | A | 1 | a0001c0001t0001g0082 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1770-602C>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 12/35 | chr9 | 131145527 | ||||||
| chr9:131145539
|
A | G | 1 | a0002c0002t0001g0193 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1770-590A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 12/35 | chr9 | 131145539 | ||||||
| chr9:131145716
|
C | A | 1 | a0002c0018t0002g0107 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1770-413C>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 12/35 | chr9 | 131145716 | ||||||
| chr9:131145959
|
A | G | 1 | a0015c0028t0004g0207 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1770-170A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 12/35 | chr9 | 131145959 | ||||||
| chr9:131146576
|
A | G | 1 | a0002c0003t0001g0075 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1945+272A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 13/35 | chr9 | 131146576 | ||||||
| chr9:131146874
|
G | T | 7 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0212others(4): Show | 7 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1945+570G>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 13/35 | chr9 | 131146874 | ||||||
| chr9:131146928
|
C | CA | 112 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(109): Show | 112 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.1946-548dupA | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 13/35 | INFO_REALIGN_3_PRIME | chr9 | 131146928 | |||||
| chr9:131146928
|
C | CAA | 5 | a0001c0001t0001g0027a0001c0004t0001g0227a0001c0005t0003g0211others(2): Show | 5 | HG01891.hp2 HG02615.hp2 HG04204.hp2 others(2): Show |
intron_variant | MODIFIER | c.1946-549_1946-548d others(4): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 13/35 | INFO_REALIGN_3_PRIME | chr9 | 131146928 | |||||
| chr9:131147111
|
T | C | 106 | a0001c0001t0001g0067a0001c0001t0001g0174a0001c0001t0001g0189others(103): Show | 106 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.1946-379T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 13/35 | chr9 | 131147111 | ||||||
| chr9:131147248
|
A | G | 2 | a0001c0004t0001g0137a0002c0002t0001g0136 | 2 | HG00733.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1946-242A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 13/35 | chr9 | 131147248 | ||||||
| chr9:131147285
|
G | T | 2 | a0001c0001t0001g0102a0001c0001t0001g0103 | 2 | HG03540.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1946-205G>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 13/35 | chr9 | 131147285 | ||||||
| chr9:131147786
|
T | C | 1 | a0001c0001t0001g0230 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.2040+202T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 14/35 | chr9 | 131147786 | ||||||
| chr9:131148044
|
G | A | 1 | a0001c0001t0010g0234 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2040+460G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 14/35 | chr9 | 131148044 | ||||||
| chr9:131148190
|
T | TTTC | 110 | a0001c0001t0001g0067a0001c0001t0001g0174a0001c0001t0001g0189others(107): Show | 110 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.2040+608_2040+609i others(5): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 14/35 | INFO_REALIGN_3_PRIME | chr9 | 131148190 | |||||
| chr9:131148333
|
T | C | 1 | a0001c0001t0001g0083 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2040+749T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 14/35 | chr9 | 131148333 | ||||||
| chr9:131148421
|
C | G | 2 | a0001c0001t0001g0060a0001c0001t0001g0097 | 2 | HG02698.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.2040+837C>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 14/35 | chr9 | 131148421 | ||||||
| chr9:131148432
|
A | G | 1 | a0002c0020t0012g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2040+848A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 14/35 | chr9 | 131148432 | ||||||
| chr9:131148478
|
A | G | 110 | a0001c0001t0001g0067a0001c0001t0001g0174a0001c0001t0001g0189others(107): Show | 110 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.2040+894A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 14/35 | chr9 | 131148478 | ||||||
| chr9:131148620
|
A | C | 1 | a0001c0004t0001g0204 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.2040+1036A>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 14/35 | chr9 | 131148620 | ||||||
| chr9:131148869
|
T | C | 1 | a0001c0001t0001g0032 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.2040+1285T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 14/35 | chr9 | 131148869 | ||||||
| chr9:131148955
|
T | C | 1 | a0015c0028t0004g0207 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2041-1369T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 14/35 | chr9 | 131148955 | ||||||
| chr9:131149082
|
G | C | 3 | a0001c0004t0001g0202a0002c0002t0001g0200a0002c0002t0001g0201 | 3 | HG00099.hp2 HG01433.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.2041-1242G>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 14/35 | chr9 | 131149082 | ||||||
| chr9:131149084
|
G | C | 6 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0212others(3): Show | 6 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.2041-1240G>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 14/35 | chr9 | 131149084 | ||||||
| chr9:131149137
|
T | C | 220 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(217): Show | 220 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(217): Show |
intron_variant | MODIFIER | c.2041-1187T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 14/35 | chr9 | 131149137 | ||||||
| chr9:131149150
|
T | TCTC | 100 | a0001c0001t0001g0067a0001c0001t0001g0174a0001c0001t0001g0189others(97): Show | 100 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.2041-1174_2041-117 others(7): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 14/35 | chr9 | 131149150 | ||||||
| chr9:131149151
|
G | C | 100 | a0001c0001t0001g0067a0001c0001t0001g0174a0001c0001t0001g0189others(97): Show | 100 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.2041-1173G>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 14/35 | chr9 | 131149151 | ||||||
| chr9:131149302
|
TG | T | 100 | a0001c0001t0001g0067a0001c0001t0001g0174a0001c0001t0001g0189others(97): Show | 100 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.2041-1021delG | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 14/35 | chr9 | 131149302 | ||||||
| chr9:131149531
|
T | C | 3 | a0001c0010t0003g0214a0001c0010t0003g0228a0001c0010t0003g0229 | 3 | HG01109.hp1 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2041-793T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 14/35 | chr9 | 131149531 | ||||||
| chr9:131149542
|
A | G | 103 | a0001c0001t0001g0067a0001c0001t0001g0174a0001c0001t0001g0189others(100): Show | 103 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.2041-782A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 14/35 | chr9 | 131149542 | ||||||
| chr9:131149562
|
C | T | 1 | a0001c0001t0001g0174 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2041-762C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 14/35 | chr9 | 131149562 | ||||||
| chr9:131149698
|
C | T | 1 | a0002c0003t0001g0064 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2041-626C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 14/35 | chr9 | 131149698 | ||||||
| chr9:131149771
|
G | A | 1 | a0002c0002t0001g0187 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2041-553G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 14/35 | chr9 | 131149771 | ||||||
| chr9:131149787
|
T | C | 103 | a0001c0001t0001g0067a0001c0001t0001g0174a0001c0001t0001g0189others(100): Show | 103 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.2041-537T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 14/35 | chr9 | 131149787 | ||||||
| chr9:131149828
|
G | C | 1 | a0002c0018t0002g0107 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2041-496G>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 14/35 | chr9 | 131149828 | ||||||
| chr9:131149896
|
G | C | 11 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0212others(8): Show | 11 | HG01109.hp1 HG01496.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.2041-428G>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 14/35 | chr9 | 131149896 | ||||||
| chr9:131149985
|
G | A | 2 | a0001c0005t0002g0205a0001c0005t0002g0206 | 2 | HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.2041-339G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 14/35 | chr9 | 131149985 | ||||||
| chr9:131150096
|
A | G | 3 | a0001c0001t0001g0025a0001c0001t0001g0026a0008c0014t0001g0100 | 3 | HG02015.hp2 NA18983.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.2041-228A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 14/35 | chr9 | 131150096 | ||||||
| chr9:131150208
|
A | G | 51 | a0001c0004t0001g0131a0001c0004t0001g0137a0001c0004t0001g0138others(48): Show | 51 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(48): Show |
intron_variant | MODIFIER | c.2041-116A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 14/35 | chr9 | 131150208 | ||||||
| chr9:131150257
|
A | C | 1 | a0001c0001t0001g0004 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2041-67A>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 14/35 | chr9 | 131150257 | ||||||
| chr9:131150508
|
G | A | 1 | a0001c0001t0001g0069 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.2127+98G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 15/35 | chr9 | 131150508 | ||||||
| chr9:131150895
|
G | A | 1 | a0001c0001t0001g0033 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2277+130G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 16/35 | chr9 | 131150895 | ||||||
| chr9:131151031
|
T | C | 3 | a0001c0010t0003g0214a0001c0010t0003g0228a0001c0010t0003g0229 | 3 | HG01109.hp1 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2277+266T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 16/35 | chr9 | 131151031 | ||||||
| chr9:131151116
|
G | A | 3 | a0002c0003t0001g0019a0002c0003t0001g0070a0002c0003t0001g0098 | 3 | NA18949.hp1 NA19001.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.2277+351G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 16/35 | chr9 | 131151116 | ||||||
| chr9:131151324
|
G | A | 1 | a0011c0021t0001g0181 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2278-412G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 16/35 | chr9 | 131151324 | ||||||
| chr9:131151574
|
G | A | 1 | a0002c0020t0012g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2278-162G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 16/35 | chr9 | 131151574 | ||||||
| chr9:131151579
|
G | T | 10 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0212others(7): Show | 10 | HG01109.hp1 HG01496.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.2278-157G>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 16/35 | chr9 | 131151579 | ||||||
| chr9:131151606
|
C | T | 1 | a0002c0002t0001g0173 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2278-130C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 16/35 | chr9 | 131151606 | ||||||
| chr9:131151677
|
A | G | 2 | a0001c0001t0001g0067a0001c0001t0001g0189 | 2 | HG02965.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2278-59A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 16/35 | chr9 | 131151677 | ||||||
| chr9:131151693
|
C | T | 2 | a0002c0002t0001g0143a0002c0002t0001g0144 | 2 | NA18944.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.2278-43C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 16/35 | chr9 | 131151693 | ||||||
| chr9:131152104
|
AT | A | 11 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0212others(8): Show | 11 | HG01109.hp1 HG01496.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.2436+218delT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | INFO_REALIGN_3_PRIME | chr9 | 131152104 | |||||
| chr9:131152200
|
A | T | 107 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(104): Show | 107 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.2436+306A>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131152200 | ||||||
| chr9:131152305
|
T | C | 11 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0212others(8): Show | 11 | HG01109.hp1 HG01496.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.2436+411T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131152305 | ||||||
| chr9:131152331
|
A | G | 11 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0212others(8): Show | 11 | HG01109.hp1 HG01496.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.2436+437A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131152331 | ||||||
| chr9:131152400
|
C | A | 1 | a0001c0005t0003g0211 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2436+506C>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131152400 | ||||||
| chr9:131152401
|
G | A | 1 | a0005c0008t0001g0109 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2436+507G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131152401 | ||||||
| chr9:131152449
|
T | G | 1 | a0015c0028t0004g0207 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2436+555T>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131152449 | ||||||
| chr9:131152597
|
C | G | 1 | a0002c0018t0002g0107 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2436+703C>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131152597 | ||||||
| chr9:131152813
|
G | C | 3 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0003g0211 | 3 | HG01891.hp2 HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.2436+919G>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131152813 | ||||||
| chr9:131152919
|
G | T | 3 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0003g0211 | 3 | HG01891.hp2 HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.2436+1025G>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131152919 | ||||||
| chr9:131153211
|
G | A | 1 | a0006c0012t0001g0007 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2436+1317G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131153211 | ||||||
| chr9:131153469
|
T | C | 3 | a0001c0010t0003g0214a0001c0010t0003g0228a0001c0010t0003g0229 | 3 | HG01109.hp1 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2436+1575T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131153469 | ||||||
| chr9:131153837
|
C | G | 1 | a0002c0018t0002g0107 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2436+1943C>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131153837 | ||||||
| chr9:131153865
|
G | A | 1 | a0002c0002t0001g0166 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2436+1971G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131153865 | ||||||
| chr9:131153905
|
A | G | 1 | a0014c0025t0001g0086 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2436+2011A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131153905 | ||||||
| chr9:131153980
|
T | C | 2 | a0002c0002t0001g0175a0002c0002t0001g0184 | 2 | HG01175.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.2436+2086T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131153980 | ||||||
| chr9:131154075
|
G | A | 1 | a0003c0013t0001g0071 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2436+2181G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131154075 | ||||||
| chr9:131154091
|
G | C | 1 | a0005c0008t0001g0109 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2436+2197G>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131154091 | ||||||
| chr9:131154146
|
A | G | 1 | a0001c0001t0001g0027 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.2436+2252A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131154146 | ||||||
| chr9:131154334
|
T | C | 1 | a0002c0020t0012g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2436+2440T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131154334 | ||||||
| chr9:131154430
|
ATCTG | A | 2 | a0001c0007t0001g0065a0001c0007t0001g0089 | 2 | HG02897.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.2436+2552_2436+255 others(8): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | INFO_REALIGN_3_PRIME | chr9 | 131154430 | |||||
| chr9:131154446
|
GTCTA | G | 2 | a0001c0005t0002g0212a0001c0005t0002g0213 | 2 | HG01496.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.2436+2562_2436+256 others(8): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | INFO_REALIGN_3_PRIME | chr9 | 131154446 | |||||
| chr9:131154661
|
T | C | 3 | a0001c0010t0003g0214a0001c0010t0003g0228a0001c0010t0003g0229 | 3 | HG01109.hp1 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2436+2767T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131154661 | ||||||
| chr9:131154800
|
C | G | 2 | a0001c0006t0001g0168a0001c0006t0001g0169 | 2 | HG00408.hp2 HG00544.hp1 |
intron_variant | MODIFIER | c.2436+2906C>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131154800 | ||||||
| chr9:131154825
|
TTG | T | 50 | a0001c0004t0001g0131a0001c0004t0001g0137a0001c0004t0001g0140others(47): Show | 50 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(47): Show |
intron_variant | MODIFIER | c.2436+2948_2436+294 others(6): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | INFO_REALIGN_3_PRIME | chr9 | 131154825 | |||||
| chr9:131154825
|
TTGTG | T | 7 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0212others(4): Show | 7 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.2436+2946_2436+294 others(8): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | INFO_REALIGN_3_PRIME | chr9 | 131154825 | |||||
| chr9:131154840
|
T | TGTGCGC | 5 | a0001c0001t0001g0032a0001c0001t0001g0095a0001c0004t0001g0204others(2): Show | 5 | HG02027.hp1 HG02083.hp2 NA18952.hp2 others(2): Show |
intron_variant | MODIFIER | c.2436+2947_2436+295 others(10): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | INFO_REALIGN_3_PRIME | chr9 | 131154840 | |||||
| chr9:131154842
|
T | C | 1 | a0001c0004t0001g0138 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2436+2948T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131154842 | ||||||
| chr9:131154845
|
G | A | 1 | a0001c0004t0001g0138 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2436+2951G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131154845 | ||||||
| chr9:131154849
|
G | A | 1 | a0002c0018t0002g0107 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2436+2955G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131154849 | ||||||
| chr9:131155177
|
C | T | 1 | a0002c0018t0002g0107 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2436+3283C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131155177 | ||||||
| chr9:131155329
|
A | G | 3 | a0001c0005t0002g0212a0001c0005t0002g0213a0015c0028t0004g0207 | 3 | HG01496.hp2 HG02145.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.2436+3435A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131155329 | ||||||
| chr9:131155367
|
T | C | 1 | a0001c0005t0002g0212 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2436+3473T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131155367 | ||||||
| chr9:131155899
|
G | A | 1 | a0002c0002t0001g0183 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2437-3484G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131155899 | ||||||
| chr9:131155901
|
A | C | 2 | a0002c0002t0001g0157a0002c0002t0001g0164 | 2 | NA18968.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.2437-3482A>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131155901 | ||||||
| chr9:131156130
|
CT | C | 222 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(219): Show | 222 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(219): Show |
intron_variant | MODIFIER | c.2437-3233delT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | INFO_REALIGN_3_PRIME | chr9 | 131156130 | |||||
| chr9:131156130
|
CTT | C | 6 | a0001c0001t0001g0010a0001c0001t0001g0114a0002c0002t0001g0135others(3): Show | 6 | HG03195.hp1 HG03688.hp2 HG04199.hp1 others(3): Show |
intron_variant | MODIFIER | c.2437-3234_2437-323 others(6): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | INFO_REALIGN_3_PRIME | chr9 | 131156130 | |||||
| chr9:131156201
|
C | T | 34 | a0001c0004t0001g0165a0001c0004t0001g0196a0001c0004t0001g0197others(31): Show | 34 | HG00597.hp1 HG01175.hp1 HG02027.hp2 others(31): Show |
intron_variant | MODIFIER | c.2437-3182C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131156201 | ||||||
| chr9:131156208
|
C | CT | 3 | a0001c0010t0003g0214a0001c0010t0003g0228a0001c0010t0003g0229 | 3 | HG01109.hp1 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2437-3174dupT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | INFO_REALIGN_3_PRIME | chr9 | 131156208 | |||||
| chr9:131156278
|
G | A | 1 | a0001c0010t0003g0228 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2437-3105G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131156278 | ||||||
| chr9:131156379
|
G | A | 1 | a0002c0002t0001g0106 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2437-3004G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131156379 | ||||||
| chr9:131156479
|
G | A | 1 | a0001c0001t0006g0076 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2437-2904G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131156479 | ||||||
| chr9:131156656
|
A | G | 1 | a0013c0023t0005g0003 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2437-2727A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131156656 | ||||||
| chr9:131156738
|
T | C | 1 | a0015c0028t0004g0207 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2437-2645T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131156738 | ||||||
| chr9:131157034
|
A | G | 3 | a0001c0010t0003g0214a0001c0010t0003g0228a0001c0010t0003g0229 | 3 | HG01109.hp1 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2437-2349A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131157034 | ||||||
| chr9:131157121
|
C | T | 1 | a0006c0012t0001g0006 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2437-2262C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131157121 | ||||||
| chr9:131157140
|
G | GT | 110 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(107): Show | 110 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.2437-2232dupT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | INFO_REALIGN_3_PRIME | chr9 | 131157140 | |||||
| chr9:131157175
|
G | A | 1 | a0001c0001t0001g0090 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2437-2208G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131157175 | ||||||
| chr9:131157180
|
C | T | 3 | a0006c0012t0001g0005a0006c0012t0001g0006a0006c0012t0001g0007 | 3 | HG01106.hp2 HG02723.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2437-2203C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131157180 | ||||||
| chr9:131157310
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2437-2073G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131157310 | ||||||
| chr9:131157337
|
T | A | 1 | a0015c0028t0004g0207 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2437-2046T>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131157337 | ||||||
| chr9:131157459
|
G | GT | 94 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0044others(91): Show | 94 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.2437-1901dupT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | INFO_REALIGN_3_PRIME | chr9 | 131157459 | |||||
| chr9:131157459
|
G | GTT | 29 | a0001c0001t0001g0093a0001c0004t0001g0131a0001c0004t0001g0138others(26): Show | 29 | HG00544.hp1 HG00558.hp2 HG01175.hp1 others(26): Show |
intron_variant | MODIFIER | c.2437-1902_2437-190 others(6): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | INFO_REALIGN_3_PRIME | chr9 | 131157459 | |||||
| chr9:131157459
|
GT | G | 8 | a0001c0005t0002g0206a0001c0010t0003g0214a0001c0010t0003g0228others(5): Show | 8 | HG01106.hp2 HG01109.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.2437-1901delT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | INFO_REALIGN_3_PRIME | chr9 | 131157459 | |||||
| chr9:131157497
|
C | G | 1 | a0010c0017t0001g0108 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2437-1886C>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131157497 | ||||||
| chr9:131157527
|
C | T | 2 | a0001c0005t0002g0205a0001c0005t0002g0206 | 2 | HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.2437-1856C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131157527 | ||||||
| chr9:131157610
|
G | A | 10 | a0001c0004t0001g0220a0001c0004t0001g0227a0002c0002t0001g0104others(7): Show | 10 | HG01361.hp2 HG01884.hp2 HG01943.hp2 others(7): Show |
intron_variant | MODIFIER | c.2437-1773G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131157610 | ||||||
| chr9:131157791
|
G | A | 1 | a0002c0020t0012g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2437-1592G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131157791 | ||||||
| chr9:131157909
|
G | A | 7 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0212others(4): Show | 7 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.2437-1474G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131157909 | ||||||
| chr9:131157933
|
A | C | 3 | a0001c0010t0003g0214a0001c0010t0003g0228a0001c0010t0003g0229 | 3 | HG01109.hp1 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2437-1450A>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131157933 | ||||||
| chr9:131158224
|
A | G | 11 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0212others(8): Show | 11 | HG01109.hp1 HG01496.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.2437-1159A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131158224 | ||||||
| chr9:131158370
|
C | T | 2 | a0001c0001t0001g0048a0002c0003t0001g0125 | 2 | HG01884.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.2437-1013C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131158370 | ||||||
| chr9:131158371
|
G | A | 1 | a0001c0001t0001g0018 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.2437-1012G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131158371 | ||||||
| chr9:131158484
|
G | A | 2 | a0002c0003t0001g0072a0002c0003t0001g0075 | 2 | HG02723.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2437-899G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131158484 | ||||||
| chr9:131158521
|
G | T | 3 | a0001c0010t0003g0214a0001c0010t0003g0228a0001c0010t0003g0229 | 3 | HG01109.hp1 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2437-862G>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131158521 | ||||||
| chr9:131158667
|
G | A | 1 | a0002c0020t0012g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2437-716G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131158667 | ||||||
| chr9:131159052
|
A | C | 1 | a0002c0002t0001g0193 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.2437-331A>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131159052 | ||||||
| chr9:131159103
|
A | G | 1 | a0001c0001t0001g0053 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2437-280A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131159103 | ||||||
| chr9:131159324
|
C | T | 2 | a0002c0003t0001g0042a0002c0003t0001g0043 | 2 | HG01074.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.2437-59C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131159324 | ||||||
| chr9:131159563
|
T | C | 3 | a0002c0002t0001g0178a0002c0002t0001g0191a0002c0002t0001g0194 | 3 | HG01928.hp2 HG01993.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.2540+77T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 18/35 | chr9 | 131159563 | ||||||
| chr9:131159628
|
C | A | 3 | a0001c0007t0001g0065a0001c0007t0001g0088a0001c0007t0001g0089 | 3 | HG02145.hp2 HG02897.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.2540+142C>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 18/35 | chr9 | 131159628 | ||||||
| chr9:131159718
|
A | G | 3 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015 | 3 | HG00733.hp2 HG01074.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.2540+232A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 18/35 | chr9 | 131159718 | ||||||
| chr9:131159871
|
A | AG | 3 | a0006c0012t0001g0005a0006c0012t0001g0006a0006c0012t0001g0007 | 3 | HG01106.hp2 HG02723.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2540+385_2540+386i others(3): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 18/35 | chr9 | 131159871 | ||||||
| chr9:131159897
|
C | T | 1 | a0001c0001t0001g0049 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2540+411C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 18/35 | chr9 | 131159897 | ||||||
| chr9:131159979
|
A | C | 109 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(106): Show | 109 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.2540+493A>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 18/35 | chr9 | 131159979 | ||||||
| chr9:131160004
|
A | T | 1 | a0001c0001t0001g0090 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2540+518A>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 18/35 | chr9 | 131160004 | ||||||
| chr9:131160086
|
A | T | 1 | a0013c0023t0005g0003 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2540+600A>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 18/35 | chr9 | 131160086 | ||||||
| chr9:131160119
|
C | G | 3 | a0001c0010t0003g0214a0001c0010t0003g0228a0001c0010t0003g0229 | 3 | HG01109.hp1 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2540+633C>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 18/35 | chr9 | 131160119 | ||||||
| chr9:131160527
|
A | G | 3 | a0002c0002t0001g0115a0002c0002t0001g0116a0002c0002t0001g0119 | 3 | NA19000.hp2 NA19011.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.2540+1041A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 18/35 | chr9 | 131160527 | ||||||
| chr9:131160983
|
A | G | 3 | a0002c0002t0001g0146a0002c0002t0001g0154a0002c0002t0001g0155 | 3 | HG02738.hp2 HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.2540+1497A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 18/35 | chr9 | 131160983 | ||||||
| chr9:131161010
|
C | G | 1 | a0015c0028t0004g0207 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2540+1524C>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 18/35 | chr9 | 131161010 | ||||||
| chr9:131161259
|
C | CT | 9 | a0001c0001t0001g0074a0001c0001t0001g0216a0001c0001t0001g0217others(6): Show | 9 | HG01943.hp2 HG02055.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.2541-1716dupT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 18/35 | INFO_REALIGN_3_PRIME | chr9 | 131161259 | |||||
| chr9:131161259
|
CT | C | 35 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0014others(32): Show | 35 | HG00099.hp1 HG00438.hp1 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.2541-1716delT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 18/35 | INFO_REALIGN_3_PRIME | chr9 | 131161259 | |||||
| chr9:131161344
|
G | A | 7 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0212others(4): Show | 7 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.2541-1647G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 18/35 | chr9 | 131161344 | ||||||
| chr9:131161350
|
G | A | 2 | a0002c0002t0001g0143a0002c0002t0001g0144 | 2 | NA18944.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.2541-1641G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 18/35 | chr9 | 131161350 | ||||||
| chr9:131161796
|
C | T | 220 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(217): Show | 220 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(217): Show |
intron_variant | MODIFIER | c.2541-1195C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 18/35 | chr9 | 131161796 | ||||||
| chr9:131161840
|
A | G | 7 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0212others(4): Show | 7 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.2541-1151A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 18/35 | chr9 | 131161840 | ||||||
| chr9:131162031
|
T | C | 2 | a0001c0001t0001g0035a0001c0001t0001g0036 | 2 | HG03130.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2541-960T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 18/35 | chr9 | 131162031 | ||||||
| chr9:131162097
|
G | A | 1 | a0015c0028t0004g0207 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2541-894G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 18/35 | chr9 | 131162097 | ||||||
| chr9:131162177
|
A | G | 1 | a0001c0001t0001g0016 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.2541-814A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 18/35 | chr9 | 131162177 | ||||||
| chr9:131162191
|
C | G | 1 | a0001c0001t0001g0016 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.2541-800C>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 18/35 | chr9 | 131162191 | ||||||
| chr9:131162576
|
C | T | 4 | a0001c0007t0001g0065a0001c0007t0001g0088a0001c0007t0001g0089others(1): Show | 4 | HG02145.hp2 HG02897.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.2541-415C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 18/35 | chr9 | 131162576 | ||||||
| chr9:131162798
|
A | G | 1 | a0002c0003t0001g0019 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.2541-193A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 18/35 | chr9 | 131162798 | ||||||
| chr9:131162877
|
G | C | 1 | a0001c0004t0001g0131 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2541-114G>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 18/35 | chr9 | 131162877 | ||||||
| chr9:131163225
|
T | C | 1 | a0001c0001t0001g0016 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.2723+52T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 19/35 | chr9 | 131163225 | ||||||
| chr9:131163311
|
T | A | 108 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(105): Show | 108 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.2723+138T>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 19/35 | chr9 | 131163311 | ||||||
| chr9:131163336
|
A | G | 2 | a0001c0001t0001g0010a0001c0001t0001g0114 | 2 | HG03688.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.2723+163A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 19/35 | chr9 | 131163336 | ||||||
| chr9:131163434
|
T | C | 220 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(217): Show | 220 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(217): Show |
intron_variant | MODIFIER | c.2723+261T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 19/35 | chr9 | 131163434 | ||||||
| chr9:131163498
|
T | C | 1 | a0002c0003t0001g0120 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2723+325T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 19/35 | chr9 | 131163498 | ||||||
| chr9:131164208
|
C | T | 1 | a0001c0001t0001g0041 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.2893+64C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131164208 | ||||||
| chr9:131164212
|
C | T | 1 | a0001c0001t0001g0069 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.2893+68C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131164212 | ||||||
| chr9:131164590
|
C | G | 3 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0099 | 3 | HG01081.hp1 HG02055.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2893+446C>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131164590 | ||||||
| chr9:131164721
|
G | A | 1 | a0002c0020t0012g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2893+577G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131164721 | ||||||
| chr9:131164729
|
A | G | 2 | a0001c0001t0001g0102a0001c0001t0001g0103 | 2 | HG03540.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2893+585A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131164729 | ||||||
| chr9:131164855
|
T | G | 2 | a0001c0005t0002g0205a0001c0005t0002g0206 | 2 | HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.2893+711T>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131164855 | ||||||
| chr9:131165062
|
T | A | 220 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(217): Show | 220 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(217): Show |
intron_variant | MODIFIER | c.2893+918T>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131165062 | ||||||
| chr9:131165067
|
C | T | 223 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(220): Show | 223 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(220): Show |
intron_variant | MODIFIER | c.2893+923C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131165067 | ||||||
| chr9:131165647
|
A | G | 10 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0212others(7): Show | 10 | HG01109.hp1 HG01496.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.2893+1503A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131165647 | ||||||
| chr9:131165693
|
T | C | 1 | a0002c0002t0001g0080 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2893+1549T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131165693 | ||||||
| chr9:131165724
|
T | C | 1 | a0001c0005t0002g0212 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2893+1580T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131165724 | ||||||
| chr9:131165804
|
C | A | 1 | a0002c0002t0001g0193 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.2893+1660C>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131165804 | ||||||
| chr9:131166230
|
C | T | 3 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0099 | 3 | HG01081.hp1 HG02055.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2893+2086C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131166230 | ||||||
| chr9:131166241
|
C | T | 1 | a0001c0001t0001g0053 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2893+2097C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131166241 | ||||||
| chr9:131166670
|
C | T | 1 | a0001c0001t0001g0053 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2893+2526C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131166670 | ||||||
| chr9:131166682
|
G | A | 1 | a0002c0002t0001g0142 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2893+2538G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131166682 | ||||||
| chr9:131166836
|
C | T | 1 | a0002c0018t0002g0107 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2893+2692C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131166836 | ||||||
| chr9:131167097
|
C | G | 1 | a0015c0028t0004g0207 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2893+2953C>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131167097 | ||||||
| chr9:131167448
|
G | A | 2 | a0001c0001t0001g0061a0001c0001t0001g0062 | 2 | HG01081.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.2893+3304G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131167448 | ||||||
| chr9:131168105
|
A | G | 1 | a0002c0020t0012g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2893+3961A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131168105 | ||||||
| chr9:131168126
|
G | A | 7 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0212others(4): Show | 7 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.2893+3982G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131168126 | ||||||
| chr9:131168129
|
A | T | 1 | a0001c0001t0001g0090 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2893+3985A>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131168129 | ||||||
| chr9:131168426
|
T | A | 3 | a0001c0010t0003g0214a0001c0010t0003g0228a0001c0010t0003g0229 | 3 | HG01109.hp1 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2893+4282T>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131168426 | ||||||
| chr9:131168870
|
C | A | 7 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0212others(4): Show | 7 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.2893+4726C>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131168870 | ||||||
| chr9:131168907
|
C | T | 1 | a0001c0004t0001g0196 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2893+4763C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131168907 | ||||||
| chr9:131169034
|
G | GT | 205 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(202): Show | 205 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.2893+4906dupT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | INFO_REALIGN_3_PRIME | chr9 | 131169034 | |||||
| chr9:131169034
|
G | GTT | 13 | a0001c0001t0001g0036a0001c0001t0001g0092a0001c0001t0001g0095others(10): Show | 13 | HG00544.hp2 HG00741.hp1 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.2893+4905_2893+490 others(6): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | INFO_REALIGN_3_PRIME | chr9 | 131169034 | |||||
| chr9:131169318
|
G | A | 3 | a0006c0012t0001g0005a0006c0012t0001g0006a0006c0012t0001g0007 | 3 | HG01106.hp2 HG02723.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2894-4737G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131169318 | ||||||
| chr9:131169325
|
C | T | 1 | a0001c0001t0001g0031 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.2894-4730C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131169325 | ||||||
| chr9:131169356
|
A | C | 1 | a0015c0028t0004g0207 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2894-4699A>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131169356 | ||||||
| chr9:131169357
|
A | T | 1 | a0015c0028t0004g0207 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2894-4698A>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131169357 | ||||||
| chr9:131169362
|
G | A | 1 | a0001c0001t0001g0020 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2894-4693G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131169362 | ||||||
| chr9:131169446
|
G | A | 1 | a0001c0001t0001g0069 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.2894-4609G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131169446 | ||||||
| chr9:131169494
|
A | C | 7 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0212others(4): Show | 7 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.2894-4561A>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131169494 | ||||||
| chr9:131169679
|
G | T | 3 | a0001c0001t0001g0216a0001c0001t0001g0217a0001c0001t0001g0218 | 3 | HG02109.hp1 HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2894-4376G>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131169679 | ||||||
| chr9:131169992
|
G | A | 1 | a0002c0003t0001g0121 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2894-4063G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131169992 | ||||||
| chr9:131170147
|
A | G | 117 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(114): Show | 117 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.2894-3908A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131170147 | ||||||
| chr9:131170258
|
G | A | 1 | a0015c0028t0004g0207 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2894-3797G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131170258 | ||||||
| chr9:131170440
|
C | T | 1 | a0002c0003t0001g0098 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.2894-3615C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131170440 | ||||||
| chr9:131170496
|
T | C | 3 | a0001c0005t0002g0212a0001c0005t0002g0213a0015c0028t0004g0207 | 3 | HG01496.hp2 HG02145.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.2894-3559T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131170496 | ||||||
| chr9:131170592
|
T | C | 7 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0212others(4): Show | 7 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.2894-3463T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131170592 | ||||||
| chr9:131170698
|
G | A | 1 | a0001c0001t0001g0018 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.2894-3357G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131170698 | ||||||
| chr9:131170803
|
C | CATT | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(151): Show | 154 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.2894-3233_2894-323 others(7): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | INFO_REALIGN_3_PRIME | chr9 | 131170803 | |||||
| chr9:131170824
|
T | TA | 2 | a0002c0002t0001g0152a0002c0002t0001g0185 | 2 | HG04204.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.2894-3231_2894-323 others(5): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131170824 | ||||||
| chr9:131171268
|
G | A | 1 | a0014c0025t0001g0086 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2894-2787G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131171268 | ||||||
| chr9:131171547
|
CT | C | 125 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(122): Show | 125 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.2894-2490delT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | INFO_REALIGN_3_PRIME | chr9 | 131171547 | |||||
| chr9:131171547
|
CTT | C | 88 | a0001c0001t0001g0054a0001c0001t0001g0077a0001c0001t0001g0097others(85): Show | 88 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.2894-2491_2894-249 others(6): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | INFO_REALIGN_3_PRIME | chr9 | 131171547 | |||||
| chr9:131171616
|
A | G | 7 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0212others(4): Show | 7 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.2894-2439A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131171616 | ||||||
| chr9:131171651
|
C | T | 1 | a0001c0001t0001g0231 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2894-2404C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131171651 | ||||||
| chr9:131171682
|
T | G | 9 | a0001c0001t0001g0034a0001c0001t0001g0057a0001c0001t0001g0060others(6): Show | 9 | HG00438.hp1 HG00642.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.2894-2373T>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131171682 | ||||||
| chr9:131171834
|
G | A | 1 | a0001c0001t0001g0004 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2894-2221G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131171834 | ||||||
| chr9:131171875
|
A | G | 3 | a0001c0004t0001g0220a0002c0002t0001g0225a0002c0002t0001g0226 | 3 | HG01884.hp2 HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2894-2180A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131171875 | ||||||
| chr9:131171896
|
T | C | 4 | a0002c0002t0001g0011a0002c0002t0001g0028a0002c0002t0001g0068others(1): Show | 4 | HG00639.hp2 HG03239.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.2894-2159T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131171896 | ||||||
| chr9:131172124
|
G | A | 3 | a0001c0010t0003g0214a0001c0010t0003g0228a0001c0010t0003g0229 | 3 | HG01109.hp1 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2894-1931G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131172124 | ||||||
| chr9:131172254
|
C | T | 2 | a0002c0002t0001g0221a0002c0002t0001g0223 | 2 | HG01361.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.2894-1801C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131172254 | ||||||
| chr9:131172320
|
T | C | 1 | a0001c0005t0003g0211 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2894-1735T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131172320 | ||||||
| chr9:131172585
|
T | C | 11 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0212others(8): Show | 11 | HG01109.hp1 HG01496.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.2894-1470T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131172585 | ||||||
| chr9:131172622
|
A | G | 2 | a0002c0003t0001g0064a0002c0016t0001g0101 | 2 | HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2894-1433A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131172622 | ||||||
| chr9:131172660
|
A | G | 1 | a0002c0002t0001g0161 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.2894-1395A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131172660 | ||||||
| chr9:131172769
|
C | G | 1 | a0002c0018t0002g0107 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2894-1286C>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131172769 | ||||||
| chr9:131172996
|
C | T | 1 | a0002c0002t0001g0191 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.2894-1059C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131172996 | ||||||
| chr9:131173157
|
A | G | 1 | a0001c0001t0010g0234 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2894-898A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131173157 | ||||||
| chr9:131173196
|
A | G | 10 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0212others(7): Show | 10 | HG01109.hp1 HG01496.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.2894-859A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131173196 | ||||||
| chr9:131173287
|
T | A | 232 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(229): Show | 232 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.2894-768T>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131173287 | ||||||
| chr9:131173355
|
CT | C | 146 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(143): Show | 146 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.2894-676delT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | INFO_REALIGN_3_PRIME | chr9 | 131173355 | |||||
| chr9:131173355
|
CTT | C | 39 | a0001c0001t0001g0066a0001c0001t0001g0093a0001c0004t0001g0196others(36): Show | 39 | HG00597.hp1 HG01106.hp2 HG01175.hp1 others(36): Show |
intron_variant | MODIFIER | c.2894-677_2894-676d others(4): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | INFO_REALIGN_3_PRIME | chr9 | 131173355 | |||||
| chr9:131173355
|
CTTTTTTT others(3): Show |
C | 2 | a0001c0005t0002g0205a0001c0005t0002g0206 | 2 | HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.2894-685_2894-676d others(12): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | INFO_REALIGN_3_PRIME | chr9 | 131173355 | |||||
| chr9:131173455
|
C | T | 3 | a0006c0012t0001g0005a0006c0012t0001g0006a0006c0012t0001g0007 | 3 | HG01106.hp2 HG02723.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2894-600C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131173455 | ||||||
| chr9:131173537
|
T | C | 1 | a0002c0002t0001g0173 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2894-518T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131173537 | ||||||
| chr9:131173538
|
AT | A | 6 | a0001c0010t0003g0214a0001c0010t0003g0228a0001c0010t0003g0229others(3): Show | 6 | HG00597.hp2 HG01109.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.2894-505delT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | INFO_REALIGN_3_PRIME | chr9 | 131173538 | |||||
| chr9:131173616
|
C | T | 2 | a0002c0003t0001g0042a0002c0003t0001g0043 | 2 | HG01074.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.2894-439C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131173616 | ||||||
| chr9:131173893
|
A | G | 1 | a0005c0008t0001g0109 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2894-162A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131173893 | ||||||
| chr9:131173916
|
C | T | 2 | a0001c0005t0002g0205a0001c0005t0002g0206 | 2 | HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.2894-139C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131173916 | ||||||
| chr9:131174355
|
A | G | 1 | a0005c0008t0001g0022 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3157+37A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 22/35 | chr9 | 131174355 | ||||||
| chr9:131174431
|
A | C | 1 | a0002c0003t0001g0085 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.3157+113A>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 22/35 | chr9 | 131174431 | ||||||
| chr9:131174432
|
CT | C | 5 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0003g0211others(2): Show | 5 | HG01891.hp2 HG02145.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.3157+128delT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 22/35 | INFO_REALIGN_3_PRIME | chr9 | 131174432 | |||||
| chr9:131174446
|
T | C | 3 | a0001c0001t0001g0077a0002c0002t0001g0225a0002c0002t0001g0226 | 3 | HG01515.hp1 HG01884.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.3157+128T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 22/35 | chr9 | 131174446 | ||||||
| chr9:131174447
|
C | CT | 191 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(188): Show | 191 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(188): Show |
intron_variant | MODIFIER | c.3157+136dupT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 22/35 | INFO_REALIGN_3_PRIME | chr9 | 131174447 | |||||
| chr9:131174447
|
C | CTT | 9 | a0001c0001t0001g0017a0001c0004t0001g0209a0001c0004t0001g0220others(6): Show | 9 | HG01928.hp2 HG01981.hp2 HG01993.hp1 others(6): Show |
intron_variant | MODIFIER | c.3157+135_3157+136d others(4): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 22/35 | INFO_REALIGN_3_PRIME | chr9 | 131174447 | |||||
| chr9:131174447
|
C | T | 7 | a0001c0001t0001g0077a0001c0007t0001g0088a0001c0010t0003g0214others(4): Show | 7 | HG01109.hp1 HG01515.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.3157+129C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 22/35 | chr9 | 131174447 | ||||||
| chr9:131174453
|
TTC | T | 6 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0212others(3): Show | 6 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.3157+137_3157+138d others(4): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 22/35 | INFO_REALIGN_3_PRIME | chr9 | 131174453 | |||||
| chr9:131174455
|
C | T | 212 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(209): Show | 212 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(209): Show |
intron_variant | MODIFIER | c.3157+137C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 22/35 | chr9 | 131174455 | ||||||
| chr9:131174458
|
T | TC | 2 | a0002c0003t0001g0064a0002c0016t0001g0101 | 2 | HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.3157+140_3157+141i others(3): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 22/35 | chr9 | 131174458 | ||||||
| chr9:131174656
|
G | A | 1 | a0001c0005t0003g0211 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3157+338G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 22/35 | chr9 | 131174656 | ||||||
| chr9:131174732
|
G | A | 3 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015 | 3 | HG00733.hp2 HG01074.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.3157+414G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 22/35 | chr9 | 131174732 | ||||||
| chr9:131174876
|
A | G | 1 | a0002c0020t0012g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3157+558A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 22/35 | chr9 | 131174876 | ||||||
| chr9:131174897
|
C | G | 1 | a0001c0001t0001g0050 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3158-563C>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 22/35 | chr9 | 131174897 | ||||||
| chr9:131175265
|
G | A | 3 | a0002c0002t0001g0146a0002c0002t0001g0154a0002c0002t0001g0155 | 3 | HG02738.hp2 HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.3158-195G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 22/35 | chr9 | 131175265 | ||||||
| chr9:131175376
|
C | T | 7 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0212others(4): Show | 7 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.3158-84C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 22/35 | chr9 | 131175376 | ||||||
| chr9:131175908
|
A | T | 1 | a0002c0002t0001g0156 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.3319+287A>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 23/35 | chr9 | 131175908 | ||||||
| chr9:131176024
|
A | T | 3 | a0001c0001t0001g0067a0001c0001t0001g0174a0001c0001t0001g0189 | 3 | HG02451.hp1 HG02965.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.3319+403A>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 23/35 | chr9 | 131176024 | ||||||
| chr9:131176051
|
C | T | 1 | a0002c0002t0001g0135 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.3319+430C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 23/35 | chr9 | 131176051 | ||||||
| chr9:131176144
|
C | T | 1 | a0004c0009t0001g0045 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.3319+523C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 23/35 | chr9 | 131176144 | ||||||
| chr9:131176201
|
G | C | 7 | a0001c0004t0001g0227a0002c0002t0001g0104a0002c0002t0001g0219others(4): Show | 7 | HG01361.hp2 HG01943.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.3319+580G>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 23/35 | chr9 | 131176201 | ||||||
| chr9:131176387
|
G | A | 1 | a0015c0028t0004g0207 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3319+766G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 23/35 | chr9 | 131176387 | ||||||
| chr9:131176436
|
C | G | 1 | a0001c0001t0009g0073 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.3319+815C>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 23/35 | chr9 | 131176436 | ||||||
| chr9:131176446
|
CCTCCTGG others(4): Show |
C | 2 | a0004c0009t0001g0008a0004c0009t0001g0009 | 2 | HG00597.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.3319+828_3319+838d others(13): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 23/35 | INFO_REALIGN_3_PRIME | chr9 | 131176446 | |||||
| chr9:131176542
|
T | A | 1 | a0001c0001t0001g0049 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3319+921T>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 23/35 | chr9 | 131176542 | ||||||
| chr9:131176575
|
C | T | 2 | a0002c0002t0001g0159a0002c0002t0001g0160 | 2 | NA18945.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.3319+954C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 23/35 | chr9 | 131176575 | ||||||
| chr9:131176800
|
A | G | 1 | a0002c0002t0001g0208 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3319+1179A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 23/35 | chr9 | 131176800 | ||||||
| chr9:131176823
|
T | C | 3 | a0005c0008t0001g0021a0005c0008t0001g0022a0005c0008t0001g0109 | 3 | HG02109.hp2 HG02559.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.3319+1202T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 23/35 | chr9 | 131176823 | ||||||
| chr9:131176873
|
G | C | 11 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0212others(8): Show | 11 | HG01109.hp1 HG01496.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.3319+1252G>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 23/35 | chr9 | 131176873 | ||||||
| chr9:131176884
|
CT | C | 3 | a0001c0010t0003g0214a0001c0010t0003g0228a0001c0010t0003g0229 | 3 | HG01109.hp1 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.3319+1264delT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 23/35 | chr9 | 131176884 | ||||||
| chr9:131176971
|
C | T | 1 | a0001c0004t0001g0196 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.3320-1340C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 23/35 | chr9 | 131176971 | ||||||
| chr9:131177258
|
A | G | 2 | a0001c0001t0001g0024a0001c0001t0001g0039 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.3320-1053A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 23/35 | chr9 | 131177258 | ||||||
| chr9:131177335
|
T | C | 1 | a0001c0001t0001g0001 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3320-976T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 23/35 | chr9 | 131177335 | ||||||
| chr9:131177937
|
A | G | 2 | a0001c0001t0001g0230a0001c0001t0001g0232 | 2 | HG00642.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.3320-374A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 23/35 | chr9 | 131177937 | ||||||
| chr9:131177963
|
T | C | 1 | a0009c0019t0001g0141 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.3320-348T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 23/35 | chr9 | 131177963 | ||||||
| chr9:131178248
|
G | T | 2 | a0002c0003t0001g0072a0002c0003t0001g0075 | 2 | HG02723.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.3320-63G>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 23/35 | chr9 | 131178248 | ||||||
| chr9:131178522
|
T | C | 1 | a0001c0005t0002g0213 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.3419+112T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131178522 | ||||||
| chr9:131178565
|
A | G | 1 | a0001c0001t0010g0234 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.3419+155A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131178565 | ||||||
| chr9:131178703
|
A | AT | 101 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(98): Show | 101 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.3419+309dupT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | INFO_REALIGN_3_PRIME | chr9 | 131178703 | |||||
| chr9:131178703
|
AT | A | 14 | a0001c0001t0001g0016a0001c0001t0001g0074a0001c0005t0002g0205others(11): Show | 14 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.3419+309delT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | INFO_REALIGN_3_PRIME | chr9 | 131178703 | |||||
| chr9:131178719
|
T | A | 7 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0212others(4): Show | 7 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.3419+309T>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131178719 | ||||||
| chr9:131178993
|
T | G | 6 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0212others(3): Show | 6 | HG01891.hp2 HG02145.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.3419+583T>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131178993 | ||||||
| chr9:131179021
|
G | T | 1 | a0001c0001t0001g0230 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.3419+611G>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131179021 | ||||||
| chr9:131179241
|
A | G | 2 | a0002c0003t0001g0072a0002c0003t0001g0075 | 2 | HG02723.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.3419+831A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131179241 | ||||||
| chr9:131179287
|
C | G | 99 | a0001c0001t0001g0048a0001c0001t0001g0067a0001c0001t0001g0174others(96): Show | 99 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.3419+877C>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131179287 | ||||||
| chr9:131179395
|
C | T | 3 | a0001c0010t0003g0214a0001c0010t0003g0228a0001c0010t0003g0229 | 3 | HG01109.hp1 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.3419+985C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131179395 | ||||||
| chr9:131179446
|
C | T | 1 | a0010c0017t0001g0108 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3419+1036C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131179446 | ||||||
| chr9:131179812
|
C | T | 3 | a0001c0010t0003g0214a0001c0010t0003g0228a0001c0010t0003g0229 | 3 | HG01109.hp1 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.3419+1402C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131179812 | ||||||
| chr9:131180172
|
G | A | 4 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0003g0211others(1): Show | 4 | HG01891.hp2 HG02451.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.3419+1762G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131180172 | ||||||
| chr9:131180375
|
G | A | 3 | a0001c0010t0003g0214a0001c0010t0003g0228a0001c0010t0003g0229 | 3 | HG01109.hp1 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.3419+1965G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131180375 | ||||||
| chr9:131180433
|
A | T | 2 | a0001c0005t0002g0212a0001c0005t0002g0213 | 2 | HG01496.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.3419+2023A>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131180433 | ||||||
| chr9:131180485
|
C | A | 1 | a0001c0004t0001g0137 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3419+2075C>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131180485 | ||||||
| chr9:131180772
|
C | G | 2 | a0002c0002t0001g0221a0002c0002t0001g0223 | 2 | HG01361.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.3419+2362C>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131180772 | ||||||
| chr9:131180880
|
T | C | 1 | a0001c0001t0001g0031 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.3419+2470T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131180880 | ||||||
| chr9:131181014
|
A | G | 206 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(203): Show | 206 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(203): Show |
intron_variant | MODIFIER | c.3419+2604A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131181014 | ||||||
| chr9:131181244
|
T | C | 232 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(229): Show | 232 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.3419+2834T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131181244 | ||||||
| chr9:131181393
|
T | C | 1 | a0001c0001t0001g0017 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.3419+2983T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131181393 | ||||||
| chr9:131181809
|
G | A | 11 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0212others(8): Show | 11 | HG01109.hp1 HG01496.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.3419+3399G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131181809 | ||||||
| chr9:131181877
|
C | T | 1 | a0001c0001t0001g0004 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3419+3467C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131181877 | ||||||
| chr9:131181878
|
A | C | 2 | a0002c0002t0001g0143a0002c0002t0001g0144 | 2 | NA18944.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.3419+3468A>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131181878 | ||||||
| chr9:131182056
|
A | T | 1 | a0001c0005t0002g0212 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3419+3646A>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131182056 | ||||||
| chr9:131182149
|
T | C | 7 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0212others(4): Show | 7 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.3419+3739T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131182149 | ||||||
| chr9:131182221
|
A | C | 97 | a0001c0001t0001g0048a0001c0001t0001g0052a0001c0001t0001g0067others(94): Show | 97 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.3419+3811A>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131182221 | ||||||
| chr9:131182447
|
A | G | 1 | a0002c0020t0012g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3419+4037A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131182447 | ||||||
| chr9:131182550
|
G | A | 2 | a0001c0010t0003g0228a0001c0010t0003g0229 | 2 | HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.3419+4140G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131182550 | ||||||
| chr9:131182733
|
T | C | 220 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(217): Show | 220 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(217): Show |
intron_variant | MODIFIER | c.3419+4323T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131182733 | ||||||
| chr9:131182765
|
T | A | 3 | a0001c0024t0001g0056a0001c0026t0001g0055a0001c0027t0001g0087 | 3 | HG02056.hp2 NA18945.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.3419+4355T>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131182765 | ||||||
| chr9:131182950
|
A | G | 3 | a0001c0010t0003g0214a0001c0010t0003g0228a0001c0010t0003g0229 | 3 | HG01109.hp1 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.3420-4339A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131182950 | ||||||
| chr9:131183015
|
T | G | 3 | a0001c0010t0003g0214a0001c0010t0003g0228a0001c0010t0003g0229 | 3 | HG01109.hp1 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.3420-4274T>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131183015 | ||||||
| chr9:131183019
|
A | G | 2 | a0002c0002t0001g0221a0002c0002t0001g0223 | 2 | HG01361.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.3420-4270A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131183019 | ||||||
| chr9:131183051
|
C | T | 1 | a0002c0003t0001g0075 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3420-4238C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131183051 | ||||||
| chr9:131183228
|
G | A | 1 | a0001c0005t0002g0212 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3420-4061G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131183228 | ||||||
| chr9:131183233
|
C | T | 1 | a0010c0017t0001g0108 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3420-4056C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131183233 | ||||||
| chr9:131183682
|
C | G | 3 | a0001c0004t0001g0220a0002c0002t0001g0225a0002c0002t0001g0226 | 3 | HG01884.hp2 HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.3420-3607C>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131183682 | ||||||
| chr9:131183813
|
A | G | 3 | a0002c0002t0001g0011a0002c0002t0001g0028a0002c0002t0001g0068 | 3 | HG00639.hp2 HG03239.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.3420-3476A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131183813 | ||||||
| chr9:131183877
|
T | C | 1 | a0001c0001t0001g0083 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.3420-3412T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131183877 | ||||||
| chr9:131183952
|
C | T | 1 | a0001c0010t0003g0214 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.3420-3337C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131183952 | ||||||
| chr9:131184013
|
CTTTTTTC others(7): Show |
C | 1 | a0002c0002t0001g0190 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.3420-3269_3420-325 others(18): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | INFO_REALIGN_3_PRIME | chr9 | 131184013 | |||||
| chr9:131184014
|
TTTTTTCT others(5): Show |
T | 1 | a0015c0028t0004g0207 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3420-3269_3420-325 others(16): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | INFO_REALIGN_3_PRIME | chr9 | 131184014 | |||||
| chr9:131184026
|
C | CT | 12 | a0001c0001t0001g0010a0001c0001t0001g0018a0001c0001t0001g0026others(9): Show | 12 | HG00642.hp1 HG00642.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.3420-3241dupT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | INFO_REALIGN_3_PRIME | chr9 | 131184026 | |||||
| chr9:131184026
|
CT | C | 10 | a0001c0001t0001g0004a0001c0005t0002g0212a0001c0026t0001g0055others(7): Show | 10 | HG01943.hp2 HG02630.hp2 HG02735.hp2 others(7): Show |
intron_variant | MODIFIER | c.3420-3241delT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | INFO_REALIGN_3_PRIME | chr9 | 131184026 | |||||
| chr9:131184030
|
T | C | 1 | a0015c0028t0004g0207 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3420-3259T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131184030 | ||||||
| chr9:131184031
|
T | C | 5 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0213others(2): Show | 5 | HG01496.hp2 HG01891.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.3420-3258T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131184031 | ||||||
| chr9:131184032
|
T | C | 2 | a0001c0005t0002g0212a0002c0020t0012g0132 | 2 | HG02630.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.3420-3257T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131184032 | ||||||
| chr9:131184335
|
C | CT | 7 | a0001c0001t0001g0017a0001c0001t0001g0052a0001c0005t0002g0212others(4): Show | 7 | HG01943.hp2 HG01981.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.3420-2938dupT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | INFO_REALIGN_3_PRIME | chr9 | 131184335 | |||||
| chr9:131184444
|
A | G | 114 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(111): Show | 114 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.3420-2845A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131184444 | ||||||
| chr9:131184475
|
A | T | 3 | a0001c0010t0003g0214a0001c0010t0003g0228a0001c0010t0003g0229 | 3 | HG01109.hp1 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.3420-2814A>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131184475 | ||||||
| chr9:131184493
|
C | T | 7 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0212others(4): Show | 7 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.3420-2796C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131184493 | ||||||
| chr9:131184500
|
A | C | 3 | a0006c0012t0001g0005a0006c0012t0001g0006a0006c0012t0001g0007 | 3 | HG01106.hp2 HG02723.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.3420-2789A>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131184500 | ||||||
| chr9:131184536
|
A | G | 3 | a0002c0002t0001g0219a0002c0002t0001g0222a0002c0002t0001g0224 | 3 | HG01943.hp2 HG02559.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.3420-2753A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131184536 | ||||||
| chr9:131184556
|
G | A | 91 | a0001c0004t0001g0131a0001c0004t0001g0137a0001c0004t0001g0138others(88): Show | 91 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.3420-2733G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131184556 | ||||||
| chr9:131184577
|
A | C | 1 | a0001c0010t0003g0214 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.3420-2712A>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131184577 | ||||||
| chr9:131184627
|
T | C | 220 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(217): Show | 220 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(217): Show |
intron_variant | MODIFIER | c.3420-2662T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131184627 | ||||||
| chr9:131184674
|
A | G | 1 | a0001c0001t0010g0234 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.3420-2615A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131184674 | ||||||
| chr9:131184996
|
A | G | 2 | a0003c0013t0001g0040a0003c0013t0001g0071 | 2 | HG02615.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.3420-2293A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131184996 | ||||||
| chr9:131185008
|
T | G | 1 | a0002c0020t0012g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3420-2281T>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131185008 | ||||||
| chr9:131185226
|
A | C | 1 | a0002c0003t0001g0126 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3420-2063A>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131185226 | ||||||
| chr9:131185259
|
G | A | 1 | a0002c0002t0001g0145 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.3420-2030G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131185259 | ||||||
| chr9:131185336
|
A | T | 1 | a0002c0020t0012g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3420-1953A>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131185336 | ||||||
| chr9:131185399
|
A | G | 1 | a0001c0005t0002g0212 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3420-1890A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131185399 | ||||||
| chr9:131185559
|
C | T | 3 | a0001c0001t0001g0216a0001c0001t0001g0217a0001c0001t0001g0218 | 3 | HG02109.hp1 HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.3420-1730C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131185559 | ||||||
| chr9:131185583
|
C | G | 3 | a0002c0002t0001g0178a0002c0002t0001g0191a0002c0002t0001g0194 | 3 | HG01928.hp2 HG01993.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.3420-1706C>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131185583 | ||||||
| chr9:131185940
|
T | G | 1 | a0002c0020t0012g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3420-1349T>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131185940 | ||||||
| chr9:131186154
|
G | A | 3 | a0001c0004t0001g0137a0002c0002t0001g0136a0002c0002t0001g0208 | 3 | HG00733.hp1 HG01243.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.3420-1135G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131186154 | ||||||
| chr9:131186383
|
G | A | 1 | a0002c0002t0001g0142 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.3420-906G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131186383 | ||||||
| chr9:131186452
|
T | C | 1 | a0011c0021t0001g0181 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.3420-837T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131186452 | ||||||
| chr9:131186518
|
A | G | 1 | a0001c0005t0002g0213 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.3420-771A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131186518 | ||||||
| chr9:131187146
|
C | T | 3 | a0001c0010t0003g0214a0001c0010t0003g0228a0001c0010t0003g0229 | 3 | HG01109.hp1 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.3420-143C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131187146 | ||||||
| chr9:131187222
|
T | A | 2 | a0001c0001t0001g0060a0001c0001t0001g0170 | 2 | HG03017.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.3420-67T>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131187222 | ||||||
| chr9:131187383
|
C | CT | 57 | a0001c0001t0001g0015a0001c0001t0001g0044a0001c0001t0001g0049others(54): Show | 57 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.3495+40dupT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 25/35 | INFO_REALIGN_3_PRIME | chr9 | 131187383 | |||||
| chr9:131187383
|
C | CTT | 7 | a0001c0004t0001g0137a0001c0005t0002g0213a0001c0010t0003g0214others(4): Show | 7 | HG01109.hp1 HG01496.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.3495+39_3495+40dup others(2): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 25/35 | INFO_REALIGN_3_PRIME | chr9 | 131187383 | |||||
| chr9:131187383
|
CT | C | 9 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0096others(6): Show | 9 | HG00558.hp1 HG01169.hp2 HG01943.hp1 others(6): Show |
intron_variant | MODIFIER | c.3495+40delT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 25/35 | INFO_REALIGN_3_PRIME | chr9 | 131187383 | |||||
| chr9:131187453
|
C | G | 1 | a0001c0001t0001g0066 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3495+89C>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 25/35 | chr9 | 131187453 | ||||||
| chr9:131187487
|
A | G | 1 | a0013c0023t0005g0003 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3495+123A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 25/35 | chr9 | 131187487 | ||||||
| chr9:131187713
|
G | A | 1 | a0001c0001t0001g0035 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3495+349G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 25/35 | chr9 | 131187713 | ||||||
| chr9:131187801
|
C | T | 11 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0212others(8): Show | 11 | HG01109.hp1 HG01496.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.3495+437C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 25/35 | chr9 | 131187801 | ||||||
| chr9:131187829
|
A | G | 1 | a0001c0005t0003g0211 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3495+465A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 25/35 | chr9 | 131187829 | ||||||
| chr9:131187876
|
T | C | 1 | a0001c0001t0001g0002 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.3495+512T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 25/35 | chr9 | 131187876 | ||||||
| chr9:131188036
|
C | A | 2 | a0006c0012t0001g0005a0006c0012t0001g0007 | 2 | HG01106.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.3495+672C>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 25/35 | chr9 | 131188036 | ||||||
| chr9:131188112
|
C | T | 3 | a0001c0010t0003g0214a0001c0010t0003g0228a0001c0010t0003g0229 | 3 | HG01109.hp1 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.3495+748C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 25/35 | chr9 | 131188112 | ||||||
| chr9:131188252
|
G | T | 1 | a0001c0001t0001g0062 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.3496-801G>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 25/35 | chr9 | 131188252 | ||||||
| chr9:131188328
|
A | G | 3 | a0001c0010t0003g0214a0001c0010t0003g0228a0001c0010t0003g0229 | 3 | HG01109.hp1 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.3496-725A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 25/35 | chr9 | 131188328 | ||||||
| chr9:131188536
|
A | G | 50 | a0001c0004t0001g0131a0001c0004t0001g0137a0001c0004t0001g0138others(47): Show | 50 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(47): Show |
intron_variant | MODIFIER | c.3496-517A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 25/35 | chr9 | 131188536 | ||||||
| chr9:131188561
|
C | T | 1 | a0002c0020t0012g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3496-492C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 25/35 | chr9 | 131188561 | ||||||
| chr9:131188659
|
C | A | 1 | a0002c0003t0001g0019 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.3496-394C>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 25/35 | chr9 | 131188659 | ||||||
| chr9:131188957
|
T | C | 1 | a0001c0004t0001g0140 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.3496-96T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 25/35 | chr9 | 131188957 | ||||||
| chr9:131188958
|
T | C | 113 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(110): Show | 113 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.3496-95T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 25/35 | chr9 | 131188958 | ||||||
| chr9:131189341
|
A | G | 41 | a0001c0004t0001g0131a0001c0004t0001g0137a0001c0004t0001g0138others(38): Show | 41 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(38): Show |
intron_variant | MODIFIER | c.3574+210A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 26/35 | chr9 | 131189341 | ||||||
| chr9:131190193
|
G | A | 92 | a0001c0004t0001g0131a0001c0004t0001g0137a0001c0004t0001g0138others(89): Show | 92 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.3574+1062G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 26/35 | chr9 | 131190193 | ||||||
| chr9:131190619
|
A | G | 3 | a0001c0010t0003g0214a0001c0010t0003g0228a0001c0010t0003g0229 | 3 | HG01109.hp1 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.3574+1488A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 26/35 | chr9 | 131190619 | ||||||
| chr9:131190926
|
A | G | 2 | a0002c0003t0001g0072a0002c0003t0001g0075 | 2 | HG02723.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.3575-1282A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 26/35 | chr9 | 131190926 | ||||||
| chr9:131191047
|
CT | C | 3 | a0001c0001t0001g0216a0001c0001t0001g0217a0001c0001t0001g0218 | 3 | HG02109.hp1 HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.3575-1160delT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 26/35 | chr9 | 131191047 | ||||||
| chr9:131191186
|
A | C | 2 | a0001c0006t0001g0168a0001c0006t0001g0169 | 2 | HG00408.hp2 HG00544.hp1 |
intron_variant | MODIFIER | c.3575-1022A>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 26/35 | chr9 | 131191186 | ||||||
| chr9:131191296
|
T | A | 3 | a0001c0010t0003g0214a0001c0010t0003g0228a0001c0010t0003g0229 | 3 | HG01109.hp1 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.3575-912T>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 26/35 | chr9 | 131191296 | ||||||
| chr9:131191430
|
T | G | 1 | a0014c0025t0001g0086 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.3575-778T>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 26/35 | chr9 | 131191430 | ||||||
| chr9:131191619
|
G | A | 1 | a0001c0005t0002g0212 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3575-589G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 26/35 | chr9 | 131191619 | ||||||
| chr9:131192087
|
C | A | 108 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(105): Show | 108 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.3575-121C>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 26/35 | chr9 | 131192087 | ||||||
| chr9:131192169
|
C | CT | 165 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(162): Show | 165 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.3575-13dupT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 26/35 | INFO_REALIGN_3_PRIME | chr9 | 131192169 | |||||
| chr9:131192169
|
C | CTT | 16 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0031others(13): Show | 16 | HG00558.hp2 HG01884.hp2 HG01993.hp2 others(13): Show |
intron_variant | MODIFIER | c.3575-14_3575-13dup others(2): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 26/35 | INFO_REALIGN_3_PRIME | chr9 | 131192169 | |||||
| chr9:131192169
|
C | CTTT | 8 | a0001c0001t0001g0012a0001c0001t0001g0092a0001c0001t0007g0046others(5): Show | 8 | HG00639.hp1 HG00741.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.3575-15_3575-13dup others(3): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 26/35 | INFO_REALIGN_3_PRIME | chr9 | 131192169 | |||||
| chr9:131192169
|
CTTTTTTT others(3): Show |
C | 1 | a0002c0002t0001g0210 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.3575-22_3575-13del others(10): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 26/35 | INFO_REALIGN_3_PRIME | chr9 | 131192169 | |||||
| chr9:131192324
|
T | G | 2 | a0001c0005t0002g0205a0001c0005t0002g0206 | 2 | HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.3659+32T>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | chr9 | 131192324 | ||||||
| chr9:131192408
|
G | A | 223 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(220): Show | 223 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(220): Show |
intron_variant | MODIFIER | c.3659+116G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | chr9 | 131192408 | ||||||
| chr9:131192438
|
A | G | 223 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(220): Show | 223 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(220): Show |
intron_variant | MODIFIER | c.3659+146A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | chr9 | 131192438 | ||||||
| chr9:131192492
|
T | C | 1 | a0015c0028t0004g0207 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3659+200T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | chr9 | 131192492 | ||||||
| chr9:131192573
|
G | T | 1 | a0001c0001t0001g0066 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3659+281G>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | chr9 | 131192573 | ||||||
| chr9:131192731
|
A | G | 3 | a0001c0010t0003g0214a0001c0010t0003g0228a0001c0010t0003g0229 | 3 | HG01109.hp1 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.3659+439A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | chr9 | 131192731 | ||||||
| chr9:131192733
|
G | C | 1 | a0001c0005t0003g0211 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3659+441G>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | chr9 | 131192733 | ||||||
| chr9:131192818
|
A | G | 1 | a0003c0011t0001g0177 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.3659+526A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | chr9 | 131192818 | ||||||
| chr9:131192941
|
C | CA | 74 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(71): Show | 74 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.3659+676dupA | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr9 | 131192941 | |||||
| chr9:131192941
|
C | CAA | 12 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0053others(9): Show | 12 | HG00733.hp2 HG01109.hp2 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.3659+675_3659+676d others(4): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr9 | 131192941 | |||||
| chr9:131192941
|
CA | C | 29 | a0001c0001t0001g0033a0001c0004t0001g0197a0001c0004t0001g0198others(26): Show | 29 | HG01109.hp1 HG01175.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.3659+676delA | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr9 | 131192941 | |||||
| chr9:131192941
|
CAA | C | 7 | a0001c0005t0002g0206a0001c0005t0003g0211a0001c0010t0003g0228others(4): Show | 7 | HG01361.hp2 HG01891.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.3659+675_3659+676d others(4): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr9 | 131192941 | |||||
| chr9:131192969
|
G | A | 1 | a0002c0002t0001g0193 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.3659+677G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | chr9 | 131192969 | ||||||
| chr9:131192981
|
C | T | 6 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0213others(3): Show | 6 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.3659+689C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | chr9 | 131192981 | ||||||
| chr9:131193050
|
T | C | 1 | a0001c0001t0001g0053 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3659+758T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | chr9 | 131193050 | ||||||
| chr9:131193208
|
G | A | 1 | a0001c0001t0001g0004 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3659+916G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | chr9 | 131193208 | ||||||
| chr9:131193243
|
T | TCTCTTCC others(11): Show |
11 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0212others(8): Show | 11 | HG01109.hp1 HG01496.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.3659+951_3659+952i others(20): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | chr9 | 131193243 | ||||||
| chr9:131193502
|
T | C | 3 | a0001c0001t0001g0216a0001c0001t0001g0217a0001c0001t0001g0218 | 3 | HG02109.hp1 HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.3659+1210T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | chr9 | 131193502 | ||||||
| chr9:131193629
|
C | CT | 6 | a0001c0001t0001g0218a0002c0003t0001g0120a0002c0003t0001g0124others(3): Show | 6 | HG01884.hp1 HG02258.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.3659+1370dupT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr9 | 131193629 | |||||
| chr9:131193629
|
C | CTTTT | 5 | a0001c0001t0001g0060a0001c0001t0001g0230a0002c0003t0001g0085others(2): Show | 5 | HG00609.hp1 HG01516.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.3659+1367_3659+137 others(8): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr9 | 131193629 | |||||
| chr9:131193629
|
C | CTTTTT | 14 | a0001c0001t0001g0029a0001c0001t0001g0034a0001c0001t0001g0036others(11): Show | 14 | HG00423.hp1 HG01243.hp2 HG02132.hp2 others(11): Show |
intron_variant | MODIFIER | c.3659+1366_3659+137 others(9): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr9 | 131193629 | |||||
| chr9:131193629
|
C | CTTTTTT | 30 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0023others(27): Show | 30 | HG00408.hp1 HG00597.hp2 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.3659+1365_3659+137 others(10): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr9 | 131193629 | |||||
| chr9:131193629
|
C | CTTTTTTT | 17 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0026others(14): Show | 17 | HG00544.hp2 HG00639.hp1 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.3659+1364_3659+137 others(11): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr9 | 131193629 | |||||
| chr9:131193629
|
C | CTTTTTTT others(8): Show |
1 | a0003c0011t0001g0186 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.3659+1344_3659+134 others(19): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr9 | 131193629 | |||||
| chr9:131193629
|
C | CTTTTTTT others(1): Show |
14 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0020others(11): Show | 14 | HG00558.hp1 HG01074.hp1 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.3659+1363_3659+137 others(12): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr9 | 131193629 | |||||
| chr9:131193629
|
C | CTTTTTTT others(2): Show |
6 | a0001c0001t0001g0018a0001c0001t0001g0052a0001c0001t0001g0053others(3): Show | 6 | HG01109.hp2 HG01943.hp1 HG02027.hp1 others(3): Show |
intron_variant | MODIFIER | c.3659+1362_3659+137 others(13): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr9 | 131193629 | |||||
| chr9:131193629
|
C | CTTTTTTT others(3): Show |
4 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0059others(1): Show | 4 | HG00099.hp1 HG00733.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.3659+1361_3659+137 others(14): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr9 | 131193629 | |||||
| chr9:131193629
|
C | CTTTTTTT others(4): Show |
7 | a0001c0001t0001g0017a0001c0001t0001g0058a0001c0004t0001g0204others(4): Show | 7 | HG00408.hp2 HG00544.hp1 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.3659+1360_3659+137 others(15): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr9 | 131193629 | |||||
| chr9:131193629
|
C | CTTTTTTT others(5): Show |
10 | a0001c0004t0001g0202a0001c0006t0001g0182a0002c0002t0001g0147others(7): Show | 10 | HG01168.hp2 HG01516.hp2 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.3659+1359_3659+137 others(16): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr9 | 131193629 | |||||
| chr9:131193629
|
C | CTTTTTTT others(6): Show |
10 | a0001c0004t0001g0131a0001c0006t0001g0176a0002c0002t0001g0115others(7): Show | 10 | HG00423.hp2 HG01169.hp1 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.3659+1358_3659+137 others(17): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr9 | 131193629 | |||||
| chr9:131193629
|
C | CTTTTTTT others(7): Show |
4 | a0001c0004t0001g0209a0002c0002t0001g0175a0002c0002t0001g0194others(1): Show | 4 | HG01928.hp2 HG02698.hp1 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.3659+1357_3659+137 others(18): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr9 | 131193629 | |||||
| chr9:131193629
|
C | CTTTTTTT others(8): Show |
6 | a0001c0001t0001g0090a0001c0004t0001g0140a0002c0002t0001g0135others(3): Show | 6 | HG00558.hp2 HG00609.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.3659+1356_3659+137 others(19): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr9 | 131193629 | |||||
| chr9:131193629
|
C | CTTTTTTT others(9): Show |
3 | a0002c0002t0001g0080a0002c0002t0001g0143a0003c0011t0001g0192 | 3 | HG00642.hp1 HG04204.hp2 NA18944.hp2 |
intron_variant | MODIFIER | c.3659+1355_3659+137 others(20): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr9 | 131193629 | |||||
| chr9:131193629
|
C | CTTTTTTT others(10): Show |
1 | a0002c0002t0001g0028 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.3659+1354_3659+137 others(21): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr9 | 131193629 | |||||
| chr9:131193629
|
C | CTTTTTTT others(11): Show |
5 | a0001c0001t0001g0084a0002c0002t0001g0068a0002c0002t0001g0133others(2): Show | 5 | HG00099.hp2 HG02056.hp1 HG02135.hp1 others(2): Show |
intron_variant | MODIFIER | c.3659+1353_3659+137 others(22): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr9 | 131193629 | |||||
| chr9:131193629
|
C | CTTTTTTT others(12): Show |
3 | a0002c0002t0001g0011a0002c0002t0001g0164a0009c0019t0001g0141 | 3 | HG00639.hp2 NA18969.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.3659+1352_3659+137 others(23): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr9 | 131193629 | |||||
| chr9:131193629
|
C | CTTTTTTT others(13): Show |
2 | a0002c0002t0001g0079a0002c0003t0001g0019 | 2 | HG04228.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.3659+1351_3659+137 others(24): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr9 | 131193629 | |||||
| chr9:131193629
|
C | CTTTTTTT others(14): Show |
2 | a0001c0007t0001g0088a0002c0002t0001g0158 | 2 | HG00741.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.3659+1350_3659+137 others(25): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr9 | 131193629 | |||||
| chr9:131193629
|
C | CTTTTTTT others(15): Show |
3 | a0002c0002t0001g0139a0002c0003t0001g0070a0002c0003t0001g0098 | 3 | HG03927.hp1 NA18949.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.3659+1349_3659+137 others(26): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr9 | 131193629 | |||||
| chr9:131193629
|
C | CTTTTTTT others(17): Show |
2 | a0001c0001t0001g0016a0001c0001t0001g0074 | 2 | NA18944.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.3659+1347_3659+137 others(28): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr9 | 131193629 | |||||
| chr9:131193629
|
C | CTTTTTTT others(21): Show |
1 | a0001c0001t0001g0069 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.3659+1343_3659+137 others(32): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr9 | 131193629 | |||||
| chr9:131193629
|
C | T | 1 | a0001c0001t0001g0032 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.3659+1337C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | chr9 | 131193629 | ||||||
| chr9:131193629
|
CTTTT | C | 5 | a0001c0005t0002g0213a0001c0010t0003g0229a0002c0002t0001g0113others(2): Show | 5 | HG00733.hp1 HG01496.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.3659+1367_3659+137 others(8): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr9 | 131193629 | |||||
| chr9:131193629
|
CTTTTT | C | 10 | a0001c0004t0001g0137a0001c0005t0002g0212a0001c0005t0003g0211others(7): Show | 10 | HG01109.hp1 HG01243.hp1 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.3659+1366_3659+137 others(9): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr9 | 131193629 | |||||
| chr9:131193629
|
CTTTTTT | C | 8 | a0001c0004t0001g0227a0001c0005t0002g0205a0001c0005t0002g0206others(5): Show | 8 | HG01175.hp1 HG02027.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.3659+1365_3659+137 others(10): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr9 | 131193629 | |||||
| chr9:131193629
|
CTTTTTTT | C | 34 | a0001c0001t0001g0099a0001c0004t0001g0165a0001c0004t0001g0196others(31): Show | 34 | HG00597.hp1 HG01361.hp2 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.3659+1364_3659+137 others(11): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr9 | 131193629 | |||||
| chr9:131193629
|
CTTTTTTT others(5): Show |
C | 1 | a0002c0020t0012g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3659+1359_3659+137 others(16): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr9 | 131193629 | |||||
| chr9:131193636
|
T | C | 1 | a0015c0028t0004g0207 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3659+1344T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | chr9 | 131193636 | ||||||
| chr9:131193675
|
A | G | 1 | a0001c0001t0001g0066 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3659+1383A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | chr9 | 131193675 | ||||||
| chr9:131193687
|
C | T | 1 | a0002c0018t0002g0107 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.3659+1395C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | chr9 | 131193687 | ||||||
| chr9:131193867
|
T | TCTTGAAC others(7): Show |
11 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0212others(8): Show | 11 | HG01109.hp1 HG01496.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.3660-1363_3660-135 others(18): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr9 | 131193867 | |||||
| chr9:131193910
|
C | A | 1 | a0002c0020t0012g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3660-1323C>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | chr9 | 131193910 | ||||||
| chr9:131193932
|
C | T | 4 | a0001c0007t0001g0065a0001c0007t0001g0088a0001c0007t0001g0089others(1): Show | 4 | HG02145.hp2 HG02897.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.3660-1301C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | chr9 | 131193932 | ||||||
| chr9:131193985
|
G | A | 1 | a0007c0030t0001g0091 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3660-1248G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | chr9 | 131193985 | ||||||
| chr9:131194205
|
C | A | 1 | a0002c0018t0002g0107 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.3660-1028C>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | chr9 | 131194205 | ||||||
| chr9:131194205
|
C | CA | 205 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(202): Show | 205 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.3660-1015dupA | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr9 | 131194205 | |||||
| chr9:131194205
|
C | CAA | 6 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0212others(3): Show | 6 | HG01891.hp2 HG01981.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.3660-1016_3660-101 others(6): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr9 | 131194205 | |||||
| chr9:131194258
|
C | T | 11 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0212others(8): Show | 11 | HG01109.hp1 HG01496.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.3660-975C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | chr9 | 131194258 | ||||||
| chr9:131194654
|
A | C | 1 | a0001c0001t0001g0096 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.3660-579A>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | chr9 | 131194654 | ||||||
| chr9:131194691
|
G | A | 1 | a0002c0002t0001g0184 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.3660-542G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | chr9 | 131194691 | ||||||
| chr9:131194884
|
C | T | 3 | a0002c0002t0001g0178a0002c0002t0001g0191a0002c0002t0001g0194 | 3 | HG01928.hp2 HG01993.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.3660-349C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | chr9 | 131194884 | ||||||
| chr9:131195436
|
T | C | 1 | a0002c0018t0002g0107 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.3721+142T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | chr9 | 131195436 | ||||||
| chr9:131195494
|
G | T | 1 | a0004c0009t0001g0045 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.3721+200G>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | chr9 | 131195494 | ||||||
| chr9:131195598
|
T | A | 3 | a0001c0004t0001g0165a0002c0002t0001g0130a0002c0002t0001g0134 | 3 | HG02735.hp2 HG03490.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.3721+304T>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | chr9 | 131195598 | ||||||
| chr9:131195640
|
G | A | 1 | a0002c0002t0001g0190 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.3721+346G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | chr9 | 131195640 | ||||||
| chr9:131195669
|
C | T | 1 | a0001c0005t0002g0212 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3721+375C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | chr9 | 131195669 | ||||||
| chr9:131195711
|
C | T | 1 | a0001c0005t0003g0211 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3721+417C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | chr9 | 131195711 | ||||||
| chr9:131195751
|
C | T | 2 | a0001c0010t0003g0228a0001c0010t0003g0229 | 2 | HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.3721+457C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | chr9 | 131195751 | ||||||
| chr9:131195757
|
G | A | 5 | a0001c0001t0001g0017a0001c0001t0001g0052a0001c0001t0001g0061others(2): Show | 5 | HG01081.hp2 HG01433.hp1 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.3721+463G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | chr9 | 131195757 | ||||||
| chr9:131195775
|
C | T | 3 | a0002c0002t0001g0219a0002c0002t0001g0222a0002c0002t0001g0224 | 3 | HG01943.hp2 HG02559.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.3721+481C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | chr9 | 131195775 | ||||||
| chr9:131195893
|
C | T | 2 | a0001c0001t0001g0010a0001c0001t0001g0114 | 2 | HG03688.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.3721+599C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | chr9 | 131195893 | ||||||
| chr9:131195959
|
GGT | G | 6 | a0001c0004t0001g0227a0002c0002t0001g0219a0002c0002t0001g0221others(3): Show | 6 | HG01361.hp2 HG01943.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.3721+666_3721+667d others(4): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | chr9 | 131195959 | ||||||
| chr9:131196023
|
T | TCC | 6 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0213others(3): Show | 6 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.3721+729_3721+730i others(4): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | chr9 | 131196023 | ||||||
| chr9:131196023
|
T | TCCCCCCC others(3): Show |
1 | a0002c0020t0012g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3721+729_3721+730i others(12): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | chr9 | 131196023 | ||||||
| chr9:131196024
|
G | C | 3 | a0001c0010t0003g0214a0001c0010t0003g0228a0002c0020t0012g0132 | 3 | HG01109.hp1 HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.3721+730G>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | chr9 | 131196024 | ||||||
| chr9:131196024
|
G | GTCCC | 6 | a0001c0001t0001g0059a0001c0001t0001g0082a0001c0001t0001g0097others(3): Show | 6 | HG00099.hp1 HG02698.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.3721+731_3721+734d others(6): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr9 | 131196024 | |||||
| chr9:131196025
|
T | C | 3 | a0001c0010t0003g0214a0001c0010t0003g0228a0002c0020t0012g0132 | 3 | HG01109.hp1 HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.3721+731T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | chr9 | 131196025 | ||||||
| chr9:131196025
|
T | TCCCCCCC others(3): Show |
1 | a0006c0012t0001g0006 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3721+736_3721+745d others(12): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr9 | 131196025 | |||||
| chr9:131196025
|
T | TCCCCCCC others(5): Show |
1 | a0001c0005t0002g0212 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3721+734_3721+745d others(14): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr9 | 131196025 | |||||
| chr9:131196025
|
T | TCCCCCCC others(8): Show |
1 | a0006c0012t0001g0005 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.3721+745_3721+746i others(17): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr9 | 131196025 | |||||
| chr9:131196025
|
T | TCCCCCCC others(9): Show |
1 | a0006c0012t0001g0007 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.3721+745_3721+746i others(18): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr9 | 131196025 | |||||
| chr9:131196025
|
T | TCCCCCCC others(13): Show |
1 | a0013c0023t0005g0003 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3721+745_3721+746i others(22): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr9 | 131196025 | |||||
| chr9:131196025
|
T | TCCCCTCC others(12): Show |
1 | a0001c0001t0001g0096 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.3721+735_3721+736i others(21): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr9 | 131196025 | |||||
| chr9:131196025
|
T | TCCCTCCC others(3): Show |
5 | a0001c0001t0001g0051a0001c0001t0001g0066a0001c0001t0001g0230others(2): Show | 5 | HG01168.hp1 HG01516.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.3721+734_3721+735i others(12): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr9 | 131196025 | |||||
| chr9:131196025
|
T | TCCCTCCC others(4): Show |
6 | a0001c0001t0001g0034a0001c0001t0001g0074a0001c0001t0001g0189others(3): Show | 6 | HG00642.hp2 HG02293.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.3721+734_3721+735i others(13): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr9 | 131196025 | |||||
| chr9:131196025
|
T | TCCCTCCC others(5): Show |
7 | a0001c0001t0001g0004a0001c0001t0001g0054a0001c0001t0001g0060others(4): Show | 7 | HG02523.hp1 HG03017.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.3721+734_3721+735i others(14): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr9 | 131196025 | |||||
| chr9:131196025
|
T | TCCCTCCC others(6): Show |
7 | a0001c0001t0001g0057a0001c0001t0001g0067a0001c0001t0001g0084others(4): Show | 7 | HG02135.hp1 HG02897.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.3721+734_3721+735i others(15): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr9 | 131196025 | |||||
| chr9:131196025
|
T | TCCCTCCC others(7): Show |
6 | a0001c0001t0001g0062a0001c0001t0001g0174a0001c0007t0001g0088others(3): Show | 6 | HG01433.hp1 HG02109.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.3721+734_3721+735i others(16): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr9 | 131196025 | |||||
| chr9:131196025
|
T | TCCCTCCC others(8): Show |
6 | a0001c0001t0001g0010a0001c0001t0001g0052a0001c0001t0001g0058others(3): Show | 6 | HG00642.hp1 HG01081.hp2 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.3721+734_3721+735i others(17): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr9 | 131196025 | |||||
| chr9:131196025
|
T | TCCCTCCC others(9): Show |
2 | a0001c0001t0001g0016a0001c0001t0001g0114 | 2 | HG04199.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.3721+734_3721+735i others(18): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr9 | 131196025 | |||||
| chr9:131196025
|
T | TCCCTCCC others(12): Show |
2 | a0001c0001t0001g0018a0005c0008t0001g0109 | 2 | HG01943.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.3721+734_3721+735i others(21): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr9 | 131196025 | |||||
| chr9:131196025
|
T | TCCCTCCC others(19): Show |
1 | a0001c0001t0001g0017 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.3721+734_3721+735i others(28): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr9 | 131196025 | |||||
| chr9:131196025
|
T | TCCCTCCC others(6): Show |
1 | a0001c0001t0001g0090 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3721+734_3721+735i others(15): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr9 | 131196025 | |||||
| chr9:131196025
|
T | TCCCTCTC others(3): Show |
2 | a0001c0001t0001g0039a0008c0014t0001g0100 | 2 | HG03492.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.3721+734_3721+735i others(12): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr9 | 131196025 | |||||
| chr9:131196025
|
T | TCCCTCTC others(4): Show |
3 | a0001c0001t0001g0035a0001c0026t0001g0055a0004c0009t0001g0008 | 3 | HG03130.hp2 NA19055.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.3721+734_3721+735i others(13): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr9 | 131196025 | |||||
| chr9:131196025
|
T | TCCCTCTC others(5): Show |
5 | a0001c0001t0001g0027a0001c0001t0001g0081a0001c0001t0001g0110others(2): Show | 5 | HG00408.hp1 HG00597.hp2 NA18945.hp2 others(2): Show |
intron_variant | MODIFIER | c.3721+734_3721+735i others(14): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr9 | 131196025 | |||||
| chr9:131196025
|
T | TCCCTCTC others(6): Show |
4 | a0001c0001t0001g0025a0001c0001t0001g0030a0001c0001t0007g0046others(1): Show | 4 | HG01928.hp1 NA18983.hp1 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.3721+734_3721+735i others(15): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr9 | 131196025 | |||||
| chr9:131196025
|
T | TCCCTCTC others(7): Show |
6 | a0001c0001t0001g0036a0001c0001t0001g0041a0001c0001t0009g0073others(3): Show | 6 | HG00609.hp1 HG03942.hp2 HG04184.hp1 others(3): Show |
intron_variant | MODIFIER | c.3721+734_3721+735i others(16): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr9 | 131196025 | |||||
| chr9:131196025
|
T | TCCCTCTC others(8): Show |
5 | a0001c0001t0001g0012a0001c0001t0001g0078a0001c0001t0001g0092others(2): Show | 5 | HG00639.hp1 HG00741.hp1 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.3721+734_3721+735i others(17): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr9 | 131196025 | |||||
| chr9:131196025
|
T | TCCCTCTC others(9): Show |
1 | a0003c0013t0001g0071 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3721+734_3721+735i others(18): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr9 | 131196025 | |||||
| chr9:131196025
|
T | TCCCTCTC others(10): Show |
8 | a0001c0001t0001g0044a0001c0001t0001g0048a0001c0001t0001g0049others(5): Show | 8 | HG00423.hp1 HG00544.hp2 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.3721+734_3721+735i others(19): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr9 | 131196025 | |||||
| chr9:131196025
|
T | TCCCTCTC others(11): Show |
2 | a0001c0001t0001g0037a0001c0001t0001g0038 | 2 | HG02132.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.3721+734_3721+735i others(20): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr9 | 131196025 | |||||
| chr9:131196025
|
T | TCCCTCTC others(13): Show |
1 | a0001c0001t0001g0095 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.3721+734_3721+735i others(22): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr9 | 131196025 | |||||
| chr9:131196025
|
T | TCCCTCTC others(14): Show |
1 | a0001c0001t0001g0020 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.3721+734_3721+735i others(23): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr9 | 131196025 | |||||
| chr9:131196025
|
T | TCCCTCTC others(15): Show |
1 | a0001c0001t0001g0031 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.3721+734_3721+735i others(24): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr9 | 131196025 | |||||
| chr9:131196025
|
T | TCCCTCTC others(18): Show |
1 | a0002c0003t0001g0043 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3721+734_3721+735i others(27): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr9 | 131196025 | |||||
| chr9:131196025
|
T | TCCGTCCC | 17 | a0001c0004t0001g0138a0001c0004t0001g0140a0002c0002t0001g0068others(14): Show | 17 | HG00609.hp2 HG00741.hp2 HG02056.hp1 others(14): Show |
intron_variant | MODIFIER | c.3721+733_3721+734i others(9): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr9 | 131196025 | |||||
| chr9:131196025
|
T | TCCGTCCC others(1): Show |
15 | a0001c0001t0001g0093a0001c0004t0001g0209a0002c0002t0001g0011others(12): Show | 15 | HG00558.hp2 HG00639.hp2 HG00733.hp1 others(12): Show |
intron_variant | MODIFIER | c.3721+733_3721+734i others(10): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr9 | 131196025 | |||||
| chr9:131196025
|
T | TCCGTCCC others(2): Show |
18 | a0001c0004t0001g0131a0001c0004t0001g0137a0001c0004t0001g0198others(15): Show | 18 | HG00099.hp2 HG01243.hp1 HG01361.hp1 others(15): Show |
intron_variant | MODIFIER | c.3721+733_3721+734i others(11): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr9 | 131196025 | |||||
| chr9:131196025
|
T | TCCGTCCC others(3): Show |
7 | a0001c0001t0001g0029a0001c0004t0001g0227a0002c0002t0001g0145others(4): Show | 7 | HG01433.hp2 HG01928.hp2 HG01993.hp1 others(4): Show |
intron_variant | MODIFIER | c.3721+733_3721+734i others(12): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr9 | 131196025 | |||||
| chr9:131196025
|
T | TCCGTCCC others(4): Show |
7 | a0002c0002t0001g0130a0002c0002t0001g0146a0002c0002t0001g0162others(4): Show | 7 | HG01175.hp1 HG01361.hp2 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.3721+733_3721+734i others(13): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr9 | 131196025 | |||||
| chr9:131196025
|
T | TCCGTCCC others(5): Show |
5 | a0001c0006t0001g0176a0002c0002t0001g0134a0002c0002t0001g0191others(2): Show | 5 | HG01884.hp2 HG02135.hp2 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.3721+733_3721+734i others(14): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr9 | 131196025 | |||||
| chr9:131196025
|
T | TCCGTCCC others(6): Show |
8 | a0001c0004t0001g0165a0001c0006t0001g0168a0001c0006t0001g0169others(5): Show | 8 | HG00408.hp2 HG00544.hp1 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.3721+733_3721+734i others(15): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr9 | 131196025 | |||||
| chr9:131196025
|
T | TCCGTCCC others(7): Show |
3 | a0001c0004t0001g0197a0002c0002t0001g0193a0002c0002t0001g0224 | 3 | HG00423.hp2 HG01943.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.3721+733_3721+734i others(16): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr9 | 131196025 | |||||
| chr9:131196025
|
T | TCCGTCCC others(8): Show |
1 | a0001c0004t0001g0196 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.3721+733_3721+734i others(17): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr9 | 131196025 | |||||
| chr9:131196025
|
T | TCCGTCCC others(9): Show |
1 | a0002c0002t0001g0149 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.3721+733_3721+734i others(18): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr9 | 131196025 | |||||
| chr9:131196025
|
T | TCCGTCCC others(10): Show |
2 | a0002c0002t0001g0185a0002c0002t0001g0187 | 2 | HG02523.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.3721+733_3721+734i others(19): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr9 | 131196025 | |||||
| chr9:131196025
|
T | TCCGTCCC others(13): Show |
2 | a0002c0002t0001g0150a0002c0002t0008g0148 | 2 | HG00597.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.3721+733_3721+734i others(22): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr9 | 131196025 | |||||
| chr9:131196025
|
T | TCGTCCCC others(3): Show |
1 | a0002c0002t0001g0221 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3721+732_3721+733i others(12): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr9 | 131196025 | |||||
| chr9:131196028
|
C | T | 1 | a0002c0002t0001g0154 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.3721+734C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | chr9 | 131196028 | ||||||
| chr9:131196029
|
C | T | 2 | a0001c0001t0006g0076a0001c0001t0010g0234 | 2 | HG00438.hp1 HG00438.hp2 |
intron_variant | MODIFIER | c.3721+735C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | chr9 | 131196029 | ||||||
| chr9:131196032
|
C | G | 1 | a0002c0018t0002g0107 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.3721+738C>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | chr9 | 131196032 | ||||||
| chr9:131196039
|
C | CCCGCCCC others(3): Show |
2 | a0001c0010t0003g0214a0001c0010t0003g0228 | 2 | HG01109.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.3721+745_3721+746i others(12): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | chr9 | 131196039 | ||||||
| chr9:131196039
|
C | G | 1 | a0001c0010t0003g0229 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3721+745C>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | chr9 | 131196039 | ||||||
| chr9:131196040
|
G | C | 215 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(212): Show | 215 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(212): Show |
intron_variant | MODIFIER | c.3721+746G>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | chr9 | 131196040 | ||||||
| chr9:131196042
|
G | C | 1 | a0001c0001t0001g0031 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.3721+748G>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | chr9 | 131196042 | ||||||
| chr9:131196139
|
G | A | 1 | a0001c0001t0001g0036 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.3721+845G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | chr9 | 131196139 | ||||||
| chr9:131196377
|
G | C | 7 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0212others(4): Show | 7 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.3722-839G>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | chr9 | 131196377 | ||||||
| chr9:131196396
|
C | T | 50 | a0001c0004t0001g0131a0001c0004t0001g0137a0001c0004t0001g0138others(47): Show | 50 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(47): Show |
intron_variant | MODIFIER | c.3722-820C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | chr9 | 131196396 | ||||||
| chr9:131196450
|
C | T | 1 | a0001c0001t0001g0001 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3722-766C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | chr9 | 131196450 | ||||||
| chr9:131196506
|
A | G | 1 | a0001c0001t0001g0002 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.3722-710A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | chr9 | 131196506 | ||||||
| chr9:131196836
|
A | G | 1 | a0002c0020t0012g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3722-380A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | chr9 | 131196836 | ||||||
| chr9:131196856
|
T | A | 1 | a0001c0001t0001g0034 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.3722-360T>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | chr9 | 131196856 | ||||||
| chr9:131199126
|
A | G | 1 | a0001c0001t0001g0027 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.5521+111A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 29/35 | chr9 | 131199126 | ||||||
| chr9:131199369
|
TTA | T | 2 | a0006c0012t0001g0006a0006c0012t0001g0007 | 2 | HG01106.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.5521+357_5521+358d others(4): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 29/35 | INFO_REALIGN_3_PRIME | chr9 | 131199369 | |||||
| chr9:131199522
|
C | T | 7 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0212others(4): Show | 7 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.5521+507C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 29/35 | chr9 | 131199522 | ||||||
| chr9:131199782
|
G | T | 2 | a0002c0002t0001g0079a0002c0002t0001g0080 | 2 | HG00642.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.5521+767G>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 29/35 | chr9 | 131199782 | ||||||
| chr9:131199912
|
A | C | 2 | a0001c0005t0002g0205a0001c0005t0002g0206 | 2 | HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.5521+897A>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 29/35 | chr9 | 131199912 | ||||||
| chr9:131199922
|
G | A | 2 | a0001c0005t0002g0213a0015c0028t0004g0207 | 2 | HG01496.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.5521+907G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 29/35 | chr9 | 131199922 | ||||||
| chr9:131199933
|
GAC | G | 7 | a0001c0001t0001g0016a0001c0001t0001g0069a0001c0001t0001g0084others(4): Show | 7 | HG00642.hp1 HG02135.hp1 HG04228.hp1 others(4): Show |
intron_variant | MODIFIER | c.5521+920_5521+921d others(4): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 29/35 | INFO_REALIGN_3_PRIME | chr9 | 131199933 | |||||
| chr9:131199985
|
T | C | 11 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0212others(8): Show | 11 | HG01109.hp1 HG01496.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.5521+970T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 29/35 | chr9 | 131199985 | ||||||
| chr9:131200090
|
C | T | 1 | a0001c0005t0002g0212 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.5521+1075C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 29/35 | chr9 | 131200090 | ||||||
| chr9:131200254
|
T | C | 1 | a0002c0002t0001g0210 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.5521+1239T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 29/35 | chr9 | 131200254 | ||||||
| chr9:131200314
|
G | A | 7 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0212others(4): Show | 7 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.5521+1299G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 29/35 | chr9 | 131200314 | ||||||
| chr9:131200686
|
G | A | 1 | a0013c0023t0005g0003 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.5522-961G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 29/35 | chr9 | 131200686 | ||||||
| chr9:131200694
|
G | A | 1 | a0001c0001t0001g0217 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.5522-953G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 29/35 | chr9 | 131200694 | ||||||
| chr9:131201068
|
C | A | 1 | a0002c0002t0001g0179 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.5522-579C>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 29/35 | chr9 | 131201068 | ||||||
| chr9:131201360
|
C | T | 1 | a0001c0001t0001g0066 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.5522-287C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 29/35 | chr9 | 131201360 | ||||||
| chr9:131201362
|
C | T | 1 | a0015c0028t0004g0207 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.5522-285C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 29/35 | chr9 | 131201362 | ||||||
| chr9:131201523
|
C | T | 1 | a0002c0002t0001g0158 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.5522-124C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 29/35 | chr9 | 131201523 | ||||||
| chr9:131201563
|
C | CA | 130 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(127): Show | 130 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.5522-72dupA | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 29/35 | INFO_REALIGN_3_PRIME | chr9 | 131201563 | |||||
| chr9:131201576
|
C | A | 2 | a0002c0003t0001g0072a0002c0003t0001g0075 | 2 | HG02723.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.5522-71C>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 29/35 | chr9 | 131201576 | ||||||
| chr9:131201617
|
T | C | 1 | a0001c0005t0002g0213 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.5522-30T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 29/35 | chr9 | 131201617 | ||||||
| chr9:131201889
|
T | C | 11 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0212others(8): Show | 11 | HG01109.hp1 HG01496.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.5592+172T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131201889 | ||||||
| chr9:131201992
|
C | G | 1 | a0015c0028t0004g0207 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.5592+275C>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131201992 | ||||||
| chr9:131202116
|
A | G | 3 | a0001c0010t0003g0214a0001c0010t0003g0228a0001c0010t0003g0229 | 3 | HG01109.hp1 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.5592+399A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131202116 | ||||||
| chr9:131202173
|
G | A | 1 | a0002c0003t0001g0124 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.5592+456G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131202173 | ||||||
| chr9:131202219
|
C | T | 4 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0003g0211others(1): Show | 4 | HG01891.hp2 HG02451.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.5592+502C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131202219 | ||||||
| chr9:131202377
|
A | G | 1 | a0001c0001t0001g0058 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.5592+660A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131202377 | ||||||
| chr9:131202386
|
T | TACAC | 2 | a0001c0001t0001g0004a0002c0020t0012g0132 | 2 | HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.5592+683_5592+686d others(6): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | INFO_REALIGN_3_PRIME | chr9 | 131202386 | |||||
| chr9:131202404
|
T | C | 1 | a0002c0020t0012g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.5592+687T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131202404 | ||||||
| chr9:131202459
|
T | G | 1 | a0001c0005t0002g0212 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.5592+742T>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131202459 | ||||||
| chr9:131202577
|
C | T | 1 | a0001c0005t0002g0206 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.5592+860C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131202577 | ||||||
| chr9:131202580
|
C | G | 1 | a0002c0002t0001g0028 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.5592+863C>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131202580 | ||||||
| chr9:131202905
|
T | A | 1 | a0001c0001t0001g0016 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.5592+1188T>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131202905 | ||||||
| chr9:131203092
|
C | T | 1 | a0001c0005t0002g0213 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.5592+1375C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131203092 | ||||||
| chr9:131203167
|
G | C | 1 | a0001c0001t0001g0232 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.5592+1450G>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131203167 | ||||||
| chr9:131203237
|
A | G | 11 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0212others(8): Show | 11 | HG01109.hp1 HG01496.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.5592+1520A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131203237 | ||||||
| chr9:131203383
|
G | A | 11 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0212others(8): Show | 11 | HG01109.hp1 HG01496.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.5592+1666G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131203383 | ||||||
| chr9:131203388
|
C | T | 1 | a0001c0004t0001g0198 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.5592+1671C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131203388 | ||||||
| chr9:131203456
|
A | T | 14 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0014others(11): Show | 14 | HG00099.hp1 HG00733.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.5592+1739A>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131203456 | ||||||
| chr9:131203579
|
C | T | 1 | a0001c0001t0001g0217 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.5592+1862C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131203579 | ||||||
| chr9:131203849
|
T | C | 3 | a0001c0001t0001g0216a0001c0001t0001g0217a0001c0001t0001g0218 | 3 | HG02109.hp1 HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.5592+2132T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131203849 | ||||||
| chr9:131203993
|
A | G | 1 | a0001c0005t0002g0213 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.5592+2276A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131203993 | ||||||
| chr9:131204030
|
C | T | 1 | a0002c0020t0012g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.5592+2313C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131204030 | ||||||
| chr9:131204039
|
C | CG | 4 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0003g0211others(1): Show | 4 | HG01891.hp2 HG02451.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.5592+2323dupG | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | INFO_REALIGN_3_PRIME | chr9 | 131204039 | |||||
| chr9:131204188
|
C | T | 1 | a0002c0020t0012g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.5592+2471C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131204188 | ||||||
| chr9:131204500
|
C | T | 1 | a0001c0001t0001g0103 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.5592+2783C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131204500 | ||||||
| chr9:131204731
|
AAGAG | A | 2 | a0001c0001t0001g0081a0001c0006t0001g0168 | 2 | HG00408.hp1 HG00408.hp2 |
intron_variant | MODIFIER | c.5592+3018_5592+302 others(8): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | INFO_REALIGN_3_PRIME | chr9 | 131204731 | |||||
| chr9:131204763
|
C | A | 1 | a0002c0003t0001g0064 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.5592+3046C>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131204763 | ||||||
| chr9:131204808
|
G | A | 2 | a0001c0010t0003g0228a0001c0010t0003g0229 | 2 | HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.5592+3091G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131204808 | ||||||
| chr9:131204933
|
T | A | 3 | a0001c0004t0001g0220a0002c0002t0001g0225a0002c0002t0001g0226 | 3 | HG01884.hp2 HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.5592+3216T>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131204933 | ||||||
| chr9:131205641
|
T | A | 1 | a0002c0003t0001g0124 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.5592+3924T>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131205641 | ||||||
| chr9:131205717
|
C | T | 1 | a0002c0020t0012g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.5592+4000C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131205717 | ||||||
| chr9:131206015
|
A | G | 3 | a0001c0001t0001g0010a0001c0001t0001g0114a0002c0002t0001g0104 | 3 | HG03688.hp2 HG03942.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.5592+4298A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131206015 | ||||||
| chr9:131206148
|
C | CTTTTTTC others(13): Show |
1 | a0001c0007t0001g0088 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.5592+4437_5592+443 others(24): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | INFO_REALIGN_3_PRIME | chr9 | 131206148 | |||||
| chr9:131206148
|
C | CTTTTTTT others(5): Show |
1 | a0002c0002t0001g0173 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.5592+4434_5592+444 others(16): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | INFO_REALIGN_3_PRIME | chr9 | 131206148 | |||||
| chr9:131206148
|
C | CTTTTTTT others(6): Show |
2 | a0001c0001t0001g0058a0001c0005t0002g0206 | 2 | HG02451.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.5592+4433_5592+444 others(17): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | INFO_REALIGN_3_PRIME | chr9 | 131206148 | |||||
| chr9:131206148
|
C | CTTTTTTT others(7): Show |
6 | a0001c0005t0002g0205a0001c0005t0002g0213a0001c0005t0003g0211others(3): Show | 6 | HG01496.hp2 HG01891.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.5592+4432_5592+444 others(18): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | INFO_REALIGN_3_PRIME | chr9 | 131206148 | |||||
| chr9:131206148
|
C | CTTTTTTT others(8): Show |
4 | a0001c0001t0001g0216a0001c0001t0001g0217a0001c0001t0001g0218others(1): Show | 4 | HG02109.hp1 HG02818.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.5592+4445_5592+444 others(19): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | INFO_REALIGN_3_PRIME | chr9 | 131206148 | |||||
| chr9:131206148
|
C | CTTTTTTT others(9): Show |
3 | a0001c0001t0001g0049a0001c0010t0003g0214a0012c0022t0001g0112 | 3 | HG01109.hp1 HG02922.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.5592+4445_5592+444 others(20): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | INFO_REALIGN_3_PRIME | chr9 | 131206148 | |||||
| chr9:131206148
|
C | CTTTTTTT others(10): Show |
18 | a0001c0001t0001g0013a0001c0001t0001g0060a0001c0001t0001g0066others(15): Show | 18 | HG00642.hp1 HG00642.hp2 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.5592+4445_5592+444 others(21): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | INFO_REALIGN_3_PRIME | chr9 | 131206148 | |||||
| chr9:131206148
|
C | CTTTTTTT others(11): Show |
67 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(64): Show | 67 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.5592+4445_5592+444 others(22): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | INFO_REALIGN_3_PRIME | chr9 | 131206148 | |||||
| chr9:131206148
|
C | CTTTTTTT others(12): Show |
48 | a0001c0001t0001g0012a0001c0001t0001g0020a0001c0001t0001g0023others(45): Show | 48 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.5592+4445_5592+444 others(23): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | INFO_REALIGN_3_PRIME | chr9 | 131206148 | |||||
| chr9:131206148
|
C | CTTTTTTT others(13): Show |
23 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0039others(20): Show | 23 | HG00423.hp2 HG00741.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.5592+4445_5592+444 others(24): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | INFO_REALIGN_3_PRIME | chr9 | 131206148 | |||||
| chr9:131206148
|
C | CTTTTTTT others(14): Show |
11 | a0001c0001t0001g0081a0001c0001t0001g0170a0001c0001t0001g0189others(8): Show | 11 | HG00408.hp1 HG00408.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.5592+4445_5592+444 others(25): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | INFO_REALIGN_3_PRIME | chr9 | 131206148 | |||||
| chr9:131206148
|
C | CTTTTTTT others(15): Show |
2 | a0001c0004t0001g0220a0002c0002t0001g0166 | 2 | HG02055.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.5592+4445_5592+444 others(26): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | INFO_REALIGN_3_PRIME | chr9 | 131206148 | |||||
| chr9:131206148
|
CTT | C | 24 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0015others(21): Show | 24 | HG00099.hp1 HG01074.hp1 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.5592+4444_5592+444 others(6): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | INFO_REALIGN_3_PRIME | chr9 | 131206148 | |||||
| chr9:131206168
|
A | G | 7 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0212others(4): Show | 7 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.5592+4451A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131206168 | ||||||
| chr9:131206289
|
G | A | 1 | a0001c0001t0001g0069 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.5592+4572G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131206289 | ||||||
| chr9:131206643
|
G | A | 1 | a0001c0005t0002g0213 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.5592+4926G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131206643 | ||||||
| chr9:131206647
|
T | G | 1 | a0001c0001t0001g0083 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.5592+4930T>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131206647 | ||||||
| chr9:131206793
|
A | G | 7 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0212others(4): Show | 7 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.5592+5076A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131206793 | ||||||
| chr9:131207104
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.5592+5387G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131207104 | ||||||
| chr9:131207166
|
T | C | 1 | a0002c0002t0001g0166 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.5592+5449T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131207166 | ||||||
| chr9:131207171
|
G | A | 11 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0212others(8): Show | 11 | HG01109.hp1 HG01496.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.5592+5454G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131207171 | ||||||
| chr9:131207403
|
G | T | 2 | a0002c0002t0001g0175a0002c0002t0001g0184 | 2 | HG01175.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.5592+5686G>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131207403 | ||||||
| chr9:131207853
|
A | G | 7 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0212others(4): Show | 7 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.5592+6136A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131207853 | ||||||
| chr9:131207919
|
G | T | 2 | a0002c0002t0001g0157a0002c0002t0001g0164 | 2 | NA18968.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.5592+6202G>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131207919 | ||||||
| chr9:131208049
|
A | G | 1 | a0002c0020t0012g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.5592+6332A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131208049 | ||||||
| chr9:131208480
|
G | A | 7 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0212others(4): Show | 7 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.5593-6732G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131208480 | ||||||
| chr9:131208590
|
G | A | 1 | a0002c0020t0012g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.5593-6622G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131208590 | ||||||
| chr9:131208671
|
T | G | 1 | a0002c0018t0002g0107 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.5593-6541T>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131208671 | ||||||
| chr9:131208885
|
C | T | 1 | a0001c0005t0002g0213 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.5593-6327C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131208885 | ||||||
| chr9:131209268
|
C | T | 1 | a0001c0005t0002g0212 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.5593-5944C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131209268 | ||||||
| chr9:131209413
|
C | T | 1 | a0001c0001t0001g0066 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.5593-5799C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131209413 | ||||||
| chr9:131209435
|
T | C | 11 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0212others(8): Show | 11 | HG01109.hp1 HG01496.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.5593-5777T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131209435 | ||||||
| chr9:131209639
|
C | T | 1 | a0002c0002t0001g0173 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.5593-5573C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131209639 | ||||||
| chr9:131209724
|
T | C | 1 | a0001c0001t0001g0050 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.5593-5488T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131209724 | ||||||
| chr9:131209791
|
C | T | 1 | a0010c0017t0001g0108 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.5593-5421C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131209791 | ||||||
| chr9:131209890
|
C | G | 7 | a0001c0001t0001g0051a0001c0001t0001g0054a0001c0001t0001g0096others(4): Show | 7 | HG01168.hp1 HG01169.hp2 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.5593-5322C>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131209890 | ||||||
| chr9:131210181
|
A | G | 1 | a0005c0008t0001g0109 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.5593-5031A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131210181 | ||||||
| chr9:131210296
|
T | C | 3 | a0001c0010t0003g0214a0001c0010t0003g0228a0001c0010t0003g0229 | 3 | HG01109.hp1 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.5593-4916T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131210296 | ||||||
| chr9:131210394
|
C | T | 1 | a0001c0001t0001g0002 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.5593-4818C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131210394 | ||||||
| chr9:131210497
|
C | T | 1 | a0001c0004t0001g0227 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.5593-4715C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131210497 | ||||||
| chr9:131210626
|
C | CA | 9 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0001g0031others(6): Show | 9 | HG01109.hp1 HG02630.hp2 HG03486.hp1 others(6): Show |
intron_variant | MODIFIER | c.5593-4575dupA | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | INFO_REALIGN_3_PRIME | chr9 | 131210626 | |||||
| chr9:131210638
|
C | A | 11 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0212others(8): Show | 11 | HG01109.hp1 HG01496.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.5593-4574C>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131210638 | ||||||
| chr9:131210802
|
G | C | 3 | a0006c0012t0001g0005a0006c0012t0001g0006a0006c0012t0001g0007 | 3 | HG01106.hp2 HG02723.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.5593-4410G>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131210802 | ||||||
| chr9:131211009
|
C | T | 1 | a0002c0020t0012g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.5593-4203C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131211009 | ||||||
| chr9:131211577
|
G | A | 1 | a0001c0001t0001g0061 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.5593-3635G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131211577 | ||||||
| chr9:131211773
|
C | T | 11 | a0001c0001t0001g0110a0001c0010t0003g0214a0001c0010t0003g0228others(8): Show | 11 | HG00597.hp1 HG01109.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.5593-3439C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131211773 | ||||||
| chr9:131211821
|
G | A | 1 | a0002c0018t0002g0107 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.5593-3391G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131211821 | ||||||
| chr9:131211885
|
A | G | 1 | a0001c0001t0001g0066 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.5593-3327A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131211885 | ||||||
| chr9:131211923
|
A | G | 3 | a0006c0012t0001g0005a0006c0012t0001g0006a0006c0012t0001g0007 | 3 | HG01106.hp2 HG02723.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.5593-3289A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131211923 | ||||||
| chr9:131212040
|
C | T | 1 | a0002c0020t0012g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.5593-3172C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131212040 | ||||||
| chr9:131212195
|
TAGTC | T | 2 | a0001c0005t0002g0205a0001c0005t0002g0206 | 2 | HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.5593-3014_5593-301 others(8): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | INFO_REALIGN_3_PRIME | chr9 | 131212195 | |||||
| chr9:131212286
|
G | T | 1 | a0015c0028t0004g0207 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.5593-2926G>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131212286 | ||||||
| chr9:131212454
|
G | A | 1 | a0001c0005t0002g0213 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.5593-2758G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131212454 | ||||||
| chr9:131212964
|
TTTTTGTA others(19): Show |
T | 4 | a0001c0010t0003g0214a0001c0010t0003g0228a0001c0010t0003g0229others(1): Show | 4 | HG01109.hp1 HG02818.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.5593-2217_5593-219 others(30): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | INFO_REALIGN_3_PRIME | chr9 | 131212964 | |||||
| chr9:131213178
|
C | CT | 5 | a0001c0001t0001g0057a0001c0005t0002g0205a0001c0005t0002g0206others(2): Show | 5 | HG01109.hp1 HG02451.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.5593-2018dupT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | INFO_REALIGN_3_PRIME | chr9 | 131213178 | |||||
| chr9:131213220
|
G | T | 7 | a0001c0001t0001g0051a0001c0001t0001g0054a0001c0001t0001g0096others(4): Show | 7 | HG01168.hp1 HG01169.hp2 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.5593-1992G>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131213220 | ||||||
| chr9:131213270
|
G | A | 1 | a0002c0002t0001g0139 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.5593-1942G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131213270 | ||||||
| chr9:131213632
|
G | A | 1 | a0001c0005t0002g0213 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.5593-1580G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131213632 | ||||||
| chr9:131213751
|
C | CTGT | 80 | a0001c0001t0001g0012a0001c0001t0001g0020a0001c0001t0001g0023others(77): Show | 80 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.5593-1426_5593-142 others(7): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | INFO_REALIGN_3_PRIME | chr9 | 131213751 | |||||
| chr9:131213751
|
C | CTGTTGT | 68 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0026others(65): Show | 68 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.5593-1429_5593-142 others(10): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | INFO_REALIGN_3_PRIME | chr9 | 131213751 | |||||
| chr9:131213751
|
C | CTGTTGTT others(2): Show |
48 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(45): Show | 48 | HG00438.hp1 HG00642.hp2 HG00733.hp1 others(45): Show |
intron_variant | MODIFIER | c.5593-1432_5593-142 others(13): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | INFO_REALIGN_3_PRIME | chr9 | 131213751 | |||||
| chr9:131213751
|
C | CTGTTGTT others(5): Show |
5 | a0001c0001t0001g0058a0001c0001t0001g0060a0001c0001t0001g0102others(2): Show | 5 | HG03017.hp1 HG03491.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.5593-1435_5593-142 others(16): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | INFO_REALIGN_3_PRIME | chr9 | 131213751 | |||||
| chr9:131213751
|
CTGT | C | 4 | a0001c0001t0001g0216a0001c0001t0001g0217a0001c0001t0001g0218others(1): Show | 4 | HG02109.hp1 HG02976.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.5593-1426_5593-142 others(7): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | INFO_REALIGN_3_PRIME | chr9 | 131213751 | |||||
| chr9:131213751
|
CTGTTGTT others(5): Show |
C | 1 | a0001c0005t0002g0212 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.5593-1435_5593-142 others(16): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | INFO_REALIGN_3_PRIME | chr9 | 131213751 | |||||
| chr9:131213805
|
G | GA | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(207): Show | 210 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.5593-1399dupA | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | INFO_REALIGN_3_PRIME | chr9 | 131213805 | |||||
| chr9:131213805
|
G | GAA | 10 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0212others(7): Show | 10 | HG01109.hp1 HG01496.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.5593-1400_5593-139 others(6): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | INFO_REALIGN_3_PRIME | chr9 | 131213805 | |||||
| chr9:131213841
|
A | G | 11 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0212others(8): Show | 11 | HG01109.hp1 HG01496.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.5593-1371A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131213841 | ||||||
| chr9:131213870
|
T | C | 2 | a0001c0001t0001g0077a0001c0001t0001g0078 | 2 | HG01515.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.5593-1342T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131213870 | ||||||
| chr9:131213910
|
G | A | 1 | a0002c0003t0001g0064 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.5593-1302G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131213910 | ||||||
| chr9:131213988
|
G | A | 1 | a0002c0002t0001g0208 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.5593-1224G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131213988 | ||||||
| chr9:131214063
|
C | G | 1 | a0013c0023t0005g0003 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.5593-1149C>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131214063 | ||||||
| chr9:131214368
|
G | A | 11 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0212others(8): Show | 11 | HG01109.hp1 HG01496.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.5593-844G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131214368 | ||||||
| chr9:131214403
|
T | C | 1 | a0003c0011t0001g0192 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.5593-809T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131214403 | ||||||
| chr9:131214466
|
C | T | 11 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0212others(8): Show | 11 | HG01109.hp1 HG01496.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.5593-746C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131214466 | ||||||
| chr9:131214540
|
A | G | 2 | a0001c0001t0001g0051a0001c0001t0001g0096 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.5593-672A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131214540 | ||||||
| chr9:131214695
|
A | T | 1 | a0003c0013t0001g0040 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.5593-517A>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131214695 | ||||||
| chr9:131215059
|
A | G | 10 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0212others(7): Show | 10 | HG01109.hp1 HG01496.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.5593-153A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131215059 | ||||||
| chr9:131215063
|
T | G | 7 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0212others(4): Show | 7 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.5593-149T>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131215063 | ||||||
| chr9:131215068
|
T | G | 1 | a0001c0001t0001g0054 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.5593-144T>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131215068 | ||||||
| chr9:131215101
|
C | A | 1 | a0001c0001t0001g0090 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.5593-111C>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131215101 | ||||||
| chr9:131215386
|
T | C | 1 | a0002c0002t0001g0147 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.5749+18T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131215386 | ||||||
| chr9:131215537
|
T | C | 3 | a0006c0012t0001g0005a0006c0012t0001g0006a0006c0012t0001g0007 | 3 | HG01106.hp2 HG02723.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.5749+169T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131215537 | ||||||
| chr9:131215583
|
GC | G | 107 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(104): Show | 107 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.5749+216delC | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131215583 | ||||||
| chr9:131215616
|
C | T | 3 | a0002c0002t0001g0178a0002c0002t0001g0191a0002c0002t0001g0194 | 3 | HG01928.hp2 HG01993.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.5749+248C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131215616 | ||||||
| chr9:131215705
|
G | A | 1 | a0001c0005t0002g0212 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.5749+337G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131215705 | ||||||
| chr9:131215744
|
C | A | 1 | a0015c0028t0004g0207 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.5749+376C>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131215744 | ||||||
| chr9:131215897
|
A | AT | 26 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0016others(23): Show | 26 | HG00099.hp1 HG01106.hp2 HG01175.hp2 others(23): Show |
intron_variant | MODIFIER | c.5749+551dupT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | INFO_REALIGN_3_PRIME | chr9 | 131215897 | |||||
| chr9:131215897
|
AT | A | 15 | a0001c0001t0001g0004a0001c0001t0001g0096a0001c0001t0001g0102others(12): Show | 15 | HG00558.hp2 HG00609.hp1 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.5749+551delT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | INFO_REALIGN_3_PRIME | chr9 | 131215897 | |||||
| chr9:131215924
|
CAG | C | 7 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0212others(4): Show | 7 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.5749+559_5749+560d others(4): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | INFO_REALIGN_3_PRIME | chr9 | 131215924 | |||||
| chr9:131216180
|
A | G | 3 | a0001c0010t0003g0214a0001c0010t0003g0228a0001c0010t0003g0229 | 3 | HG01109.hp1 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.5749+812A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131216180 | ||||||
| chr9:131216213
|
CT | C | 15 | a0001c0001t0001g0016a0001c0005t0002g0205a0001c0005t0002g0206others(12): Show | 15 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.5749+861delT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | INFO_REALIGN_3_PRIME | chr9 | 131216213 | |||||
| chr9:131216286
|
G | A | 7 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0212others(4): Show | 7 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.5749+918G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131216286 | ||||||
| chr9:131216312
|
C | T | 3 | a0001c0001t0001g0051a0001c0001t0001g0096a0002c0002t0001g0161 | 3 | HG01168.hp1 HG01169.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.5749+944C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131216312 | ||||||
| chr9:131216385
|
C | T | 1 | a0001c0005t0003g0211 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.5749+1017C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131216385 | ||||||
| chr9:131216525
|
C | CT | 124 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0012others(121): Show | 124 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.5749+1172dupT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | INFO_REALIGN_3_PRIME | chr9 | 131216525 | |||||
| chr9:131216525
|
C | CTT | 15 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0053others(12): Show | 15 | HG00438.hp1 HG01109.hp2 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.5749+1171_5749+117 others(6): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | INFO_REALIGN_3_PRIME | chr9 | 131216525 | |||||
| chr9:131216557
|
G | A | 1 | a0013c0023t0005g0003 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.5749+1189G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131216557 | ||||||
| chr9:131216601
|
C | T | 1 | a0011c0021t0001g0181 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.5749+1233C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131216601 | ||||||
| chr9:131216797
|
G | T | 1 | a0002c0002t0001g0146 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.5749+1429G>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131216797 | ||||||
| chr9:131216824
|
G | A | 1 | a0001c0001t0006g0076 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.5749+1456G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131216824 | ||||||
| chr9:131217026
|
T | C | 3 | a0001c0010t0003g0214a0001c0010t0003g0228a0001c0010t0003g0229 | 3 | HG01109.hp1 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.5749+1658T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131217026 | ||||||
| chr9:131217134
|
T | C | 1 | a0001c0001t0001g0174 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.5749+1766T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131217134 | ||||||
| chr9:131217178
|
T | C | 1 | a0001c0001t0001g0044 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.5749+1810T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131217178 | ||||||
| chr9:131217189
|
A | G | 3 | a0001c0004t0001g0137a0002c0002t0001g0136a0002c0002t0001g0208 | 3 | HG00733.hp1 HG01243.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.5749+1821A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131217189 | ||||||
| chr9:131217450
|
G | A | 1 | a0002c0018t0002g0107 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.5749+2082G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131217450 | ||||||
| chr9:131217452
|
A | G | 1 | a0001c0005t0003g0211 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.5749+2084A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131217452 | ||||||
| chr9:131217705
|
G | C | 5 | a0001c0010t0003g0214a0001c0010t0003g0228a0001c0010t0003g0229others(2): Show | 5 | HG01109.hp1 HG02818.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.5749+2337G>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131217705 | ||||||
| chr9:131217919
|
T | A | 111 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(108): Show | 111 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.5749+2551T>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131217919 | ||||||
| chr9:131217926
|
A | G | 1 | a0002c0020t0012g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.5749+2558A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131217926 | ||||||
| chr9:131217928
|
C | T | 2 | a0001c0001t0001g0060a0001c0001t0001g0170 | 2 | HG03017.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.5749+2560C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131217928 | ||||||
| chr9:131218055
|
A | C | 1 | a0015c0028t0004g0207 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.5749+2687A>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131218055 | ||||||
| chr9:131218123
|
A | G | 1 | a0002c0020t0012g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.5749+2755A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131218123 | ||||||
| chr9:131218262
|
A | G | 2 | a0001c0004t0001g0196a0001c0004t0001g0198 | 2 | HG02165.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.5749+2894A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131218262 | ||||||
| chr9:131218579
|
C | T | 1 | a0013c0023t0005g0003 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.5749+3211C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131218579 | ||||||
| chr9:131219142
|
G | A | 1 | a0001c0005t0003g0211 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.5750-3636G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131219142 | ||||||
| chr9:131219415
|
C | T | 4 | a0001c0001t0001g0051a0001c0001t0001g0054a0001c0001t0001g0096others(1): Show | 4 | HG01168.hp1 HG01169.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.5750-3363C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131219415 | ||||||
| chr9:131219416
|
G | A | 1 | a0001c0001t0001g0231 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.5750-3362G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131219416 | ||||||
| chr9:131219584
|
A | G | 1 | a0001c0005t0002g0213 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.5750-3194A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131219584 | ||||||
| chr9:131219601
|
T | G | 7 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0212others(4): Show | 7 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.5750-3177T>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131219601 | ||||||
| chr9:131219704
|
A | G | 3 | a0001c0010t0003g0214a0001c0010t0003g0228a0001c0010t0003g0229 | 3 | HG01109.hp1 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.5750-3074A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131219704 | ||||||
| chr9:131219804
|
C | T | 1 | a0013c0023t0005g0003 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.5750-2974C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131219804 | ||||||
| chr9:131219816
|
G | A | 2 | a0001c0001t0001g0033a0001c0001t0001g0082 | 2 | HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.5750-2962G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131219816 | ||||||
| chr9:131219826
|
A | C | 1 | a0012c0022t0001g0112 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.5750-2952A>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131219826 | ||||||
| chr9:131220176
|
G | A | 1 | a0002c0020t0012g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.5750-2602G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131220176 | ||||||
| chr9:131220254
|
A | G | 1 | a0002c0020t0012g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.5750-2524A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131220254 | ||||||
| chr9:131220272
|
A | G | 1 | a0002c0002t0001g0080 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.5750-2506A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131220272 | ||||||
| chr9:131220376
|
A | C | 1 | a0015c0028t0004g0207 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.5750-2402A>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131220376 | ||||||
| chr9:131220628
|
C | T | 91 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0041others(88): Show | 91 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.5750-2150C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131220628 | ||||||
| chr9:131220722
|
G | C | 7 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0212others(4): Show | 7 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.5750-2056G>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131220722 | ||||||
| chr9:131220759
|
G | C | 1 | a0001c0001t0001g0049 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.5750-2019G>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131220759 | ||||||
| chr9:131220921
|
T | A | 1 | a0015c0028t0004g0207 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.5750-1857T>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131220921 | ||||||
| chr9:131221464
|
G | A | 1 | a0002c0002t0001g0193 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.5750-1314G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131221464 | ||||||
| chr9:131221841
|
C | T | 1 | a0013c0023t0005g0003 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.5750-937C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131221841 | ||||||
| chr9:131221842
|
G | A | 1 | a0001c0005t0002g0213 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.5750-936G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131221842 | ||||||
| chr9:131221854
|
C | CA | 34 | a0001c0001t0001g0030a0001c0001t0001g0074a0001c0001t0001g0110others(31): Show | 34 | HG00597.hp1 HG01175.hp1 HG02027.hp2 others(31): Show |
intron_variant | MODIFIER | c.5750-917dupA | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | INFO_REALIGN_3_PRIME | chr9 | 131221854 | |||||
| chr9:131222075
|
T | A | 2 | a0001c0005t0002g0205a0001c0005t0002g0206 | 2 | HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.5750-703T>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131222075 | ||||||
| chr9:131222138
|
C | G | 3 | a0001c0001t0001g0051a0001c0001t0001g0096a0002c0002t0001g0161 | 3 | HG01168.hp1 HG01169.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.5750-640C>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131222138 | ||||||
| chr9:131222146
|
C | A | 7 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0212others(4): Show | 7 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.5750-632C>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131222146 | ||||||
| chr9:131222304
|
T | A | 223 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(220): Show | 223 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(220): Show |
intron_variant | MODIFIER | c.5750-474T>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131222304 | ||||||
| chr9:131222511
|
C | T | 2 | a0001c0001t0001g0024a0001c0001t0001g0039 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.5750-267C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131222511 | ||||||
| chr9:131222665
|
C | T | 4 | a0002c0002t0001g0159a0002c0002t0001g0160a0002c0002t0001g0172others(1): Show | 4 | NA18945.hp1 NA19009.hp1 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.5750-113C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131222665 | ||||||
| chr9:131222712
|
G | C | 11 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0212others(8): Show | 11 | HG01109.hp1 HG01496.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.5750-66G>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131222712 | ||||||
| chr9:131222764
|
C | G | 1 | a0001c0001t0001g0092 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.5750-14C>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131222764 | ||||||
| chr9:131222970
|
G | T | 1 | a0001c0005t0002g0212 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.5902+40G>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131222970 | ||||||
| chr9:131223061
|
C | T | 4 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0003g0211others(1): Show | 4 | HG01891.hp2 HG02451.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.5902+131C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131223061 | ||||||
| chr9:131223162
|
A | AT | 11 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0212others(8): Show | 11 | HG01109.hp1 HG01496.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.5902+241dupT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223162 | |||||
| chr9:131223454
|
C | T | 1 | a0001c0001t0001g0111 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.5902+524C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131223454 | ||||||
| chr9:131223671
|
A | G | 4 | a0001c0010t0003g0214a0001c0010t0003g0228a0001c0010t0003g0229others(1): Show | 4 | HG01109.hp1 HG02818.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.5902+741A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131223671 | ||||||
| chr9:131223699
|
CT | C | 33 | a0001c0001t0001g0030a0001c0001t0001g0074a0001c0001t0001g0110others(30): Show | 33 | HG00597.hp1 HG01175.hp1 HG02027.hp2 others(30): Show |
intron_variant | MODIFIER | c.5902+778delT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223699 | |||||
| chr9:131223708
|
T | A | 1 | a0005c0008t0001g0109 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.5902+778T>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131223708 | ||||||
| chr9:131223723
|
A | ATTTATTT others(13): Show |
1 | a0001c0010t0003g0228 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.5902+808_5902+809i others(22): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223723 | |||||
| chr9:131223723
|
A | ATTTTTTT others(15): Show |
1 | a0001c0001t0001g0216 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.5902+796_5902+797i others(24): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223723 | |||||
| chr9:131223723
|
A | ATTTTTTT others(16): Show |
2 | a0001c0001t0001g0217a0002c0002t0001g0175 | 2 | HG02109.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.5902+796_5902+797i others(25): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223723 | |||||
| chr9:131223727
|
A | ATTTATTT others(3): Show |
1 | a0002c0002t0001g0225 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.5902+800_5902+801i others(12): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | |||||
| chr9:131223727
|
A | ATTTATTT others(21): Show |
1 | a0001c0004t0001g0138 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.5902+800_5902+801i others(30): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | |||||
| chr9:131223727
|
A | ATTTATTT others(14): Show |
1 | a0002c0003t0001g0064 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.5902+800_5902+801i others(23): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | |||||
| chr9:131223727
|
A | ATTTATTT others(18): Show |
1 | a0002c0002t0001g0079 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.5902+800_5902+801i others(27): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | |||||
| chr9:131223727
|
A | ATTTATTT others(19): Show |
4 | a0001c0001t0001g0027a0001c0001t0001g0038a0002c0002t0001g0149others(1): Show | 4 | HG02132.hp2 NA18960.hp2 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.5902+800_5902+801i others(28): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | |||||
| chr9:131223727
|
A | ATTTATTT others(20): Show |
1 | a0001c0001t0001g0031 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.5902+800_5902+801i others(29): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | |||||
| chr9:131223727
|
A | ATTTATTT others(19): Show |
6 | a0001c0001t0001g0026a0001c0001t0001g0067a0001c0001t0001g0174others(3): Show | 6 | HG02015.hp2 HG02451.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.5902+800_5902+801i others(28): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | |||||
| chr9:131223727
|
A | ATTTATTT others(20): Show |
4 | a0001c0001t0001g0023a0001c0001t0001g0035a0001c0006t0001g0168others(1): Show | 4 | HG00408.hp2 HG00544.hp2 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.5902+800_5902+801i others(29): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | |||||
| chr9:131223727
|
A | ATTTATTT others(21): Show |
2 | a0001c0001t0001g0083a0002c0002t0001g0183 | 2 | HG00423.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.5902+800_5902+801i others(30): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | |||||
| chr9:131223727
|
A | ATTTATTT others(22): Show |
2 | a0001c0001t0001g0095a0002c0003t0001g0043 | 2 | HG01243.hp2 HG02027.hp1 |
intron_variant | MODIFIER | c.5902+800_5902+801i others(31): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | |||||
| chr9:131223727
|
A | ATTTATTT others(16): Show |
1 | a0001c0001t0001g0001 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.5902+800_5902+801i others(25): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | |||||
| chr9:131223727
|
A | ATTTATTT others(17): Show |
1 | a0001c0001t0001g0058 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.5902+800_5902+801i others(26): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | |||||
| chr9:131223727
|
A | ATTTATTT others(18): Show |
1 | a0001c0001t0001g0050 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.5902+800_5902+801i others(27): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | |||||
| chr9:131223727
|
A | ATTTATTT others(19): Show |
1 | a0001c0001t0001g0099 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.5902+800_5902+801i others(28): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | |||||
| chr9:131223727
|
A | ATTTATTT others(14): Show |
1 | a0013c0023t0005g0003 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.5902+800_5902+801i others(23): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | |||||
| chr9:131223727
|
A | ATTTATTT others(15): Show |
1 | a0001c0001t0001g0002 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.5902+800_5902+801i others(24): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | |||||
| chr9:131223727
|
A | ATTTATTT others(16): Show |
2 | a0001c0001t0001g0057a0001c0001t0010g0234 | 2 | HG00438.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.5902+800_5902+801i others(25): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | |||||
| chr9:131223727
|
A | ATTTATTT others(17): Show |
2 | a0002c0002t0001g0163a0002c0002t0001g0184 | 2 | HG01175.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.5902+800_5902+801i others(26): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | |||||
| chr9:131223727
|
A | ATTTATTT others(18): Show |
2 | a0002c0002t0001g0080a0004c0009t0001g0009 | 2 | HG00597.hp2 HG00642.hp1 |
intron_variant | MODIFIER | c.5902+800_5902+801i others(27): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | |||||
| chr9:131223727
|
A | ATTTATTT others(19): Show |
9 | a0001c0001t0001g0012a0001c0001t0001g0020a0001c0001t0001g0025others(6): Show | 9 | HG00558.hp1 HG00639.hp1 HG00741.hp1 others(6): Show |
intron_variant | MODIFIER | c.5902+800_5902+801i others(28): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | |||||
| chr9:131223727
|
A | ATTTATTT others(20): Show |
4 | a0001c0001t0001g0048a0001c0001t0001g0111a0002c0003t0001g0085others(1): Show | 4 | HG01106.hp1 HG03209.hp1 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.5902+800_5902+801i others(29): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | |||||
| chr9:131223727
|
A | ATTTATTT others(21): Show |
3 | a0002c0002t0001g0118a0002c0003t0001g0042a0003c0011t0001g0186 | 3 | HG01074.hp2 NA18952.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.5902+800_5902+801i others(30): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | |||||
| chr9:131223727
|
A | ATTTATTT others(25): Show |
1 | a0001c0001t0001g0041 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.5902+800_5902+801i others(34): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | |||||
| chr9:131223727
|
A | ATTTATTT others(18): Show |
1 | a0003c0013t0001g0040 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.5902+800_5902+801i others(27): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | |||||
| chr9:131223727
|
A | ATTTATTT others(13): Show |
1 | a0001c0010t0003g0214 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.5902+800_5902+801i others(22): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | |||||
| chr9:131223727
|
A | ATTTATTT others(15): Show |
1 | a0002c0002t0001g0144 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.5902+800_5902+801i others(24): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | |||||
| chr9:131223727
|
A | ATTTATTT others(16): Show |
8 | a0001c0001t0001g0066a0001c0001t0001g0231a0001c0007t0001g0065others(5): Show | 8 | HG00733.hp1 HG01496.hp1 HG02083.hp2 others(5): Show |
intron_variant | MODIFIER | c.5902+800_5902+801i others(25): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | |||||
| chr9:131223727
|
A | ATTTATTT others(17): Show |
10 | a0001c0001t0001g0032a0001c0001t0001g0233a0001c0004t0001g0140others(7): Show | 10 | HG00609.hp2 HG02015.hp1 HG03831.hp2 others(7): Show |
intron_variant | MODIFIER | c.5902+800_5902+801i others(26): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | |||||
| chr9:131223727
|
A | ATTTATTT others(18): Show |
6 | a0001c0001t0001g0004a0001c0001t0001g0036a0001c0001t0001g0077others(3): Show | 6 | HG01515.hp1 HG01981.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.5902+800_5902+801i others(27): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | |||||
| chr9:131223727
|
A | ATTTATTT others(19): Show |
2 | a0002c0002t0001g0194a0004c0009t0001g0008 | 2 | HG01928.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.5902+800_5902+801i others(28): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | |||||
| chr9:131223727
|
A | ATTTATTT others(20): Show |
2 | a0001c0001t0001g0024a0001c0007t0001g0088 | 2 | HG02145.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.5902+800_5902+801i others(29): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | |||||
| chr9:131223727
|
A | ATTTATTT others(21): Show |
5 | a0001c0001t0001g0039a0001c0001t0001g0049a0001c0001t0001g0090others(2): Show | 5 | HG00609.hp1 HG01891.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.5902+800_5902+801i others(30): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | |||||
| chr9:131223727
|
A | ATTTATTT others(22): Show |
1 | a0005c0008t0001g0021 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.5902+800_5902+801i others(31): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | |||||
| chr9:131223727
|
A | ATTTATTT others(39): Show |
1 | a0002c0002t0001g0068 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.5902+800_5902+801i others(48): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | |||||
| chr9:131223727
|
A | ATTTATTT others(7): Show |
3 | a0001c0001t0001g0059a0001c0005t0003g0211a0001c0026t0001g0055 | 3 | HG00099.hp1 HG01891.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.5902+800_5902+801i others(16): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | |||||
| chr9:131223727
|
A | ATTTATTT others(15): Show |
1 | a0011c0021t0001g0181 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.5902+800_5902+801i others(24): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | |||||
| chr9:131223727
|
A | ATTTATTT others(16): Show |
7 | a0001c0001t0001g0034a0001c0001t0001g0114a0001c0001t0001g0230others(4): Show | 7 | HG00423.hp2 HG01169.hp1 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.5902+800_5902+801i others(25): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | |||||
| chr9:131223727
|
A | ATTTATTT others(17): Show |
10 | a0001c0001t0001g0016a0001c0001t0001g0069a0001c0001t0001g0189others(7): Show | 10 | HG00642.hp2 HG03490.hp2 HG03927.hp1 others(7): Show |
intron_variant | MODIFIER | c.5902+800_5902+801i others(26): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | |||||
| chr9:131223727
|
A | ATTTATTT others(18): Show |
6 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0084others(3): Show | 6 | HG01081.hp2 HG01433.hp1 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.5902+800_5902+801i others(27): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | |||||
| chr9:131223727
|
A | ATTTATTT others(19): Show |
2 | a0001c0001t0001g0103a0016c0029t0001g0063 | 2 | HG02523.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.5902+800_5902+801i others(28): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | |||||
| chr9:131223727
|
A | ATTTATTT others(20): Show |
1 | a0001c0001t0009g0073 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.5902+800_5902+801i others(29): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | |||||
| chr9:131223727
|
A | ATTTATTT others(21): Show |
2 | a0001c0001t0001g0053a0005c0008t0001g0022 | 2 | HG01109.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.5902+800_5902+801i others(30): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | |||||
| chr9:131223727
|
A | ATTTATTT others(23): Show |
2 | a0001c0004t0001g0196a0001c0004t0001g0198 | 2 | HG02165.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.5902+800_5902+801i others(32): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | |||||
| chr9:131223727
|
A | ATTTATTT others(29): Show |
1 | a0002c0002t0001g0210 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.5902+800_5902+801i others(38): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | |||||
| chr9:131223727
|
A | ATTTATTT others(30): Show |
1 | a0002c0002t0001g0113 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.5902+800_5902+801i others(39): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | |||||
| chr9:131223727
|
A | ATTTATTT others(4): Show |
2 | a0001c0001t0001g0018a0002c0002t0001g0173 | 2 | HG01943.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.5902+800_5902+801i others(13): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | |||||
| chr9:131223727
|
A | ATTTATTT others(5): Show |
1 | a0001c0005t0002g0212 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.5902+800_5902+801i others(14): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | |||||
| chr9:131223727
|
A | ATTTATTT others(7): Show |
2 | a0002c0003t0001g0075a0002c0020t0012g0132 | 2 | HG02723.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.5902+800_5902+801i others(16): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | |||||
| chr9:131223727
|
A | ATTTATTT others(8): Show |
4 | a0001c0004t0001g0131a0001c0024t0001g0056a0001c0027t0001g0087others(1): Show | 4 | HG00741.hp2 HG01361.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.5902+800_5902+801i others(17): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | |||||
| chr9:131223727
|
A | ATTTATTT others(16): Show |
8 | a0001c0001t0001g0010a0001c0001t0001g0074a0001c0001t0001g0170others(5): Show | 8 | HG00558.hp2 HG02027.hp2 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.5902+800_5902+801i others(25): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | |||||
| chr9:131223727
|
A | ATTTATTT others(17): Show |
10 | a0001c0001t0001g0110a0001c0006t0001g0182a0002c0002t0001g0116others(7): Show | 10 | HG00099.hp2 HG01243.hp1 HG02735.hp2 others(7): Show |
intron_variant | MODIFIER | c.5902+800_5902+801i others(26): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | |||||
| chr9:131223727
|
A | ATTTATTT others(18): Show |
5 | a0001c0004t0001g0202a0002c0002t0001g0115a0002c0002t0001g0133others(2): Show | 5 | HG01516.hp2 HG01993.hp1 HG02056.hp1 others(2): Show |
intron_variant | MODIFIER | c.5902+800_5902+801i others(27): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | |||||
| chr9:131223727
|
A | ATTTATTT others(19): Show |
1 | a0006c0012t0001g0006 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.5902+800_5902+801i others(28): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | |||||
| chr9:131223727
|
A | ATTTATTT others(21): Show |
4 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0033others(1): Show | 4 | HG00733.hp2 HG01074.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.5902+800_5902+801i others(30): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | |||||
| chr9:131223727
|
A | ATTTATTT others(23): Show |
2 | a0001c0001t0001g0015a0001c0001t0001g0030 | 2 | HG01175.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.5902+800_5902+801i others(32): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | |||||
| chr9:131223727
|
A | ATTTATTT others(32): Show |
1 | a0002c0002t0001g0226 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.5902+800_5902+801i others(41): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | |||||
| chr9:131223727
|
A | ATTTATTT others(36): Show |
1 | a0002c0002t0001g0028 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.5902+800_5902+801i others(45): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | |||||
| chr9:131223727
|
A | ATTTATTT others(38): Show |
1 | a0002c0002t0001g0011 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.5902+800_5902+801i others(47): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | |||||
| chr9:131223727
|
A | ATTTTTAT others(38): Show |
1 | a0002c0002t0001g0166 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.5902+802_5902+803i others(47): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | |||||
| chr9:131223727
|
A | ATTTTTTT others(18): Show |
1 | a0002c0002t0001g0200 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.5902+804_5902+805i others(27): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | |||||
| chr9:131223727
|
A | ATTTTTTT others(4): Show |
2 | a0002c0002t0001g0104a0002c0018t0002g0107 | 2 | HG03942.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.5902+812_5902+822d others(13): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | |||||
| chr9:131223727
|
A | ATTTTTTT others(5): Show |
1 | a0015c0028t0004g0207 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.5902+811_5902+822d others(14): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | |||||
| chr9:131223727
|
A | ATTTTTTT others(8): Show |
1 | a0001c0004t0001g0220 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.5902+808_5902+822d others(17): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | |||||
| chr9:131223727
|
A | ATTTTTTT others(10): Show |
1 | a0002c0003t0001g0072 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.5902+806_5902+822d others(19): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | |||||
| chr9:131223727
|
A | ATTTTTTT others(15): Show |
2 | a0001c0001t0001g0060a0001c0010t0003g0229 | 2 | HG02818.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.5902+801_5902+822d others(24): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | |||||
| chr9:131223727
|
A | ATTTTTTT others(16): Show |
4 | a0001c0001t0001g0218a0002c0002t0001g0151a0002c0002t0001g0179others(1): Show | 4 | HG02132.hp1 HG03195.hp2 NA18948.hp2 others(1): Show |
intron_variant | MODIFIER | c.5902+800_5902+822d others(25): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | |||||
| chr9:131223727
|
A | ATTTTTTT others(17): Show |
8 | a0001c0001t0001g0081a0001c0004t0001g0204a0001c0006t0001g0169others(5): Show | 8 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(5): Show |
intron_variant | MODIFIER | c.5902+799_5902+822d others(26): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | |||||
| chr9:131223727
|
A | ATTTTTTT others(18): Show |
1 | a0001c0001t0001g0052 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.5902+798_5902+822d others(27): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | |||||
| chr9:131223727
|
A | ATTTTTTT others(19): Show |
2 | a0002c0002t0001g0156a0006c0012t0001g0007 | 2 | HG01106.hp2 NA18949.hp2 |
intron_variant | MODIFIER | c.5902+822_5902+823i others(28): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | |||||
| chr9:131223727
|
A | ATTTTTTT others(20): Show |
2 | a0001c0001t0001g0017a0006c0012t0001g0005 | 2 | HG01981.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.5902+822_5902+823i others(29): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | |||||
| chr9:131223727
|
A | ATTTTTTT others(22): Show |
1 | a0002c0002t0001g0135 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.5902+822_5902+823i others(31): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | |||||
| chr9:131223727
|
A | ATTTTTTT others(25): Show |
1 | a0001c0001t0001g0082 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.5902+822_5902+823i others(34): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | |||||
| chr9:131223727
|
A | T | 4 | a0001c0001t0001g0216a0001c0001t0001g0217a0002c0002t0001g0175others(1): Show | 4 | HG02109.hp1 HG02698.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.5902+797A>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131223727 | ||||||
| chr9:131223729
|
T | TTATTTAT others(3): Show |
2 | a0001c0005t0002g0205a0001c0005t0002g0206 | 2 | HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.5902+800_5902+801i others(12): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223729 | |||||
| chr9:131223729
|
T | TTATTTAT others(19): Show |
1 | a0001c0001t0001g0029 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.5902+800_5902+801i others(28): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223729 | |||||
| chr9:131223730
|
T | TATTTTA | 2 | a0001c0001t0001g0054a0002c0002t0001g0161 | 2 | HG01515.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.5902+800_5902+801i others(8): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131223730 | ||||||
| chr9:131223731
|
T | A | 1 | a0002c0020t0012g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.5902+801T>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131223731 | ||||||
| chr9:131223732
|
T | A | 3 | a0002c0002t0001g0146a0002c0002t0001g0154a0002c0002t0001g0155 | 3 | HG02738.hp2 HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.5902+802T>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131223732 | ||||||
| chr9:131223733
|
T | A | 1 | a0001c0005t0002g0206 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.5902+803T>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131223733 | ||||||
| chr9:131223736
|
T | A | 1 | a0002c0002t0001g0146 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.5902+806T>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131223736 | ||||||
| chr9:131223737
|
T | A | 1 | a0001c0005t0002g0206 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.5902+807T>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131223737 | ||||||
| chr9:131223849
|
G | A | 3 | a0006c0012t0001g0005a0006c0012t0001g0006a0006c0012t0001g0007 | 3 | HG01106.hp2 HG02723.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.5902+919G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131223849 | ||||||
| chr9:131223892
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.5902+962G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131223892 | ||||||
| chr9:131223906
|
T | C | 7 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0212others(4): Show | 7 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.5902+976T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131223906 | ||||||
| chr9:131223966
|
C | T | 4 | a0001c0007t0001g0065a0001c0007t0001g0088a0001c0007t0001g0089others(1): Show | 4 | HG02145.hp2 HG02897.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.5902+1036C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131223966 | ||||||
| chr9:131223996
|
C | A | 220 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(217): Show | 220 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(217): Show |
intron_variant | MODIFIER | c.5902+1066C>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131223996 | ||||||
| chr9:131224060
|
G | A | 1 | a0001c0004t0001g0220 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.5902+1130G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131224060 | ||||||
| chr9:131224241
|
A | G | 1 | a0002c0002t0001g0225 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.5902+1311A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131224241 | ||||||
| chr9:131224284
|
A | G | 2 | a0010c0017t0001g0108a0012c0022t0001g0112 | 2 | HG02886.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.5902+1354A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131224284 | ||||||
| chr9:131224300
|
T | A | 7 | a0001c0001t0001g0110a0002c0002t0001g0135a0002c0002t0001g0150others(4): Show | 7 | HG00597.hp1 NA18948.hp2 NA18949.hp2 others(4): Show |
intron_variant | MODIFIER | c.5902+1370T>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131224300 | ||||||
| chr9:131224325
|
GTC | G | 6 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0213others(3): Show | 6 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.5902+1399_5902+140 others(6): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131224325 | |||||
| chr9:131224569
|
G | A | 2 | a0001c0001t0001g0010a0001c0001t0001g0114 | 2 | HG03688.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.5902+1639G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131224569 | ||||||
| chr9:131224674
|
G | A | 1 | a0001c0001t0001g0074 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.5902+1744G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131224674 | ||||||
| chr9:131224777
|
G | C | 7 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0212others(4): Show | 7 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.5902+1847G>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131224777 | ||||||
| chr9:131224870
|
A | G | 1 | a0001c0004t0001g0137 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.5902+1940A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131224870 | ||||||
| chr9:131224927
|
G | A | 207 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(204): Show | 207 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.5902+1997G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131224927 | ||||||
| chr9:131225241
|
C | T | 1 | a0013c0023t0005g0003 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.5902+2311C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131225241 | ||||||
| chr9:131225312
|
G | A | 1 | a0003c0013t0001g0071 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.5902+2382G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131225312 | ||||||
| chr9:131225488
|
A | G | 1 | a0001c0001t0001g0035 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.5902+2558A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131225488 | ||||||
| chr9:131225716
|
C | T | 3 | a0006c0012t0001g0005a0006c0012t0001g0006a0006c0012t0001g0007 | 3 | HG01106.hp2 HG02723.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.5903-2444C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131225716 | ||||||
| chr9:131225717
|
G | A | 2 | a0001c0005t0002g0213a0015c0028t0004g0207 | 2 | HG01496.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.5903-2443G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131225717 | ||||||
| chr9:131226385
|
C | T | 2 | a0002c0002t0001g0195a0002c0002t0001g0203 | 2 | HG01169.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.5903-1775C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131226385 | ||||||
| chr9:131226624
|
C | CT | 218 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(215): Show | 218 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(215): Show |
intron_variant | MODIFIER | c.5903-1526dupT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131226624 | |||||
| chr9:131226836
|
A | C | 1 | a0001c0007t0001g0089 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.5903-1324A>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131226836 | ||||||
| chr9:131226850
|
A | T | 3 | a0001c0001t0001g0032a0001c0004t0001g0140a0002c0002t0001g0139 | 3 | HG00609.hp2 HG03927.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.5903-1310A>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131226850 | ||||||
| chr9:131227040
|
C | T | 1 | a0002c0002t0001g0144 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.5903-1120C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131227040 | ||||||
| chr9:131227171
|
C | T | 1 | a0001c0007t0001g0089 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.5903-989C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131227171 | ||||||
| chr9:131227530
|
A | T | 2 | a0001c0005t0002g0205a0001c0005t0002g0206 | 2 | HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.5903-630A>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131227530 | ||||||
| chr9:131227539
|
G | A | 7 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0212others(4): Show | 7 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.5903-621G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131227539 | ||||||
| chr9:131227584
|
C | T | 2 | a0002c0002t0001g0159a0002c0002t0001g0160 | 2 | NA18945.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.5903-576C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131227584 | ||||||
| chr9:131227597
|
G | A | 2 | a0001c0005t0002g0213a0015c0028t0004g0207 | 2 | HG01496.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.5903-563G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131227597 | ||||||
| chr9:131227741
|
A | G | 13 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0212others(10): Show | 13 | HG01109.hp1 HG01496.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.5903-419A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131227741 | ||||||
| chr9:131227838
|
T | C | 1 | a0015c0028t0004g0207 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.5903-322T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131227838 | ||||||
| chr9:131227842
|
C | T | 4 | a0001c0001t0001g0048a0001c0001t0001g0095a0001c0004t0001g0138others(1): Show | 4 | HG02027.hp1 HG02083.hp1 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.5903-318C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131227842 | ||||||
| chr9:131227879
|
G | A | 3 | a0001c0010t0003g0214a0001c0010t0003g0228a0001c0010t0003g0229 | 3 | HG01109.hp1 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.5903-281G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131227879 | ||||||
| chr9:131227922
|
G | A | 7 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0212others(4): Show | 7 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.5903-238G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131227922 | ||||||
| chr9:131227976
|
A | G | 10 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0212others(7): Show | 10 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.5903-184A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131227976 | ||||||
| chr9:131227985
|
C | T | 1 | a0001c0004t0001g0227 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.5903-175C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131227985 | ||||||
| chr9:131227988
|
G | T | 1 | a0001c0001t0007g0046 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.5903-172G>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131227988 | ||||||
| chr9:131228087
|
GCTCAATG others(4): Show |
G | 2 | a0001c0007t0001g0065a0001c0007t0001g0089 | 2 | HG02897.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.5903-69_5903-59del others(11): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131228087 | |||||
| chr9:131228111
|
C | T | 1 | a0001c0001t0001g0054 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.5903-49C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131228111 | ||||||
| chr9:131228372
|
G | A | 48 | a0001c0001t0001g0032a0001c0001t0001g0041a0001c0001t0001g0069others(45): Show | 48 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(45): Show |
intron_variant | MODIFIER | c.6074+41G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 33/35 | chr9 | 131228372 | ||||||
| chr9:131228399
|
T | C | 2 | a0010c0017t0001g0108a0012c0022t0001g0112 | 2 | HG02886.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.6074+68T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 33/35 | chr9 | 131228399 | ||||||
| chr9:131228422
|
A | G | 1 | a0013c0023t0005g0003 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.6074+91A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 33/35 | chr9 | 131228422 | ||||||
| chr9:131228656
|
G | A | 10 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0212others(7): Show | 10 | HG01109.hp1 HG01496.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.6074+325G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 33/35 | chr9 | 131228656 | ||||||
| chr9:131228679
|
G | A | 1 | a0002c0002t0001g0219 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.6074+348G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 33/35 | chr9 | 131228679 | ||||||
| chr9:131228689
|
A | G | 1 | a0001c0001t0001g0030 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.6074+358A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 33/35 | chr9 | 131228689 | ||||||
| chr9:131228742
|
C | T | 1 | a0001c0005t0002g0212 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.6074+411C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 33/35 | chr9 | 131228742 | ||||||
| chr9:131228789
|
C | G | 7 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0212others(4): Show | 7 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.6074+458C>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 33/35 | chr9 | 131228789 | ||||||
| chr9:131228840
|
G | T | 2 | a0002c0003t0001g0042a0002c0003t0001g0043 | 2 | HG01074.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.6074+509G>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 33/35 | chr9 | 131228840 | ||||||
| chr9:131229006
|
A | G | 1 | a0002c0002t0001g0080 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.6074+675A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 33/35 | chr9 | 131229006 | ||||||
| chr9:131229406
|
G | A | 1 | a0001c0001t0001g0090 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.6074+1075G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 33/35 | chr9 | 131229406 | ||||||
| chr9:131229465
|
A | G | 9 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0212others(6): Show | 9 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.6074+1134A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 33/35 | chr9 | 131229465 | ||||||
| chr9:131229476
|
G | C | 1 | a0001c0005t0003g0211 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.6074+1145G>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 33/35 | chr9 | 131229476 | ||||||
| chr9:131229661
|
A | G | 9 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0212others(6): Show | 9 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.6075-969A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 33/35 | chr9 | 131229661 | ||||||
| chr9:131229773
|
G | A | 1 | a0001c0005t0003g0211 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.6075-857G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 33/35 | chr9 | 131229773 | ||||||
| chr9:131229817
|
C | A | 1 | a0002c0020t0012g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.6075-813C>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 33/35 | chr9 | 131229817 | ||||||
| chr9:131229848
|
A | G | 9 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0212others(6): Show | 9 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.6075-782A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 33/35 | chr9 | 131229848 | ||||||
| chr9:131229852
|
T | G | 7 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0212others(4): Show | 7 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.6075-778T>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 33/35 | chr9 | 131229852 | ||||||
| chr9:131229863
|
T | G | 7 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0212others(4): Show | 7 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.6075-767T>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 33/35 | chr9 | 131229863 | ||||||
| chr9:131229955
|
C | A | 3 | a0001c0001t0001g0216a0001c0001t0001g0217a0001c0001t0001g0218 | 3 | HG02109.hp1 HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.6075-675C>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 33/35 | chr9 | 131229955 | ||||||
| chr9:131229979
|
C | G | 1 | a0001c0005t0002g0212 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.6075-651C>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 33/35 | chr9 | 131229979 | ||||||
| chr9:131229979
|
C | T | 4 | a0001c0010t0003g0214a0001c0010t0003g0228a0001c0010t0003g0229others(1): Show | 4 | HG01109.hp1 HG02818.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.6075-651C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 33/35 | chr9 | 131229979 | ||||||
| chr9:131230057
|
G | T | 2 | a0001c0001t0001g0077a0001c0001t0001g0078 | 2 | HG01515.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.6075-573G>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 33/35 | chr9 | 131230057 | ||||||
| chr9:131230319
|
G | T | 3 | a0001c0010t0003g0214a0001c0010t0003g0228a0001c0010t0003g0229 | 3 | HG01109.hp1 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.6075-311G>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 33/35 | chr9 | 131230319 | ||||||
| chr9:131230552
|
A | G | 220 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(217): Show | 220 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(217): Show |
intron_variant | MODIFIER | c.6075-78A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 33/35 | chr9 | 131230552 | ||||||
| chr9:131230784
|
G | A | 3 | a0001c0010t0003g0214a0001c0010t0003g0228a0001c0010t0003g0229 | 3 | HG01109.hp1 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.6214+15G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 34/35 | chr9 | 131230784 | ||||||
| chr9:131230976
|
C | T | 1 | a0002c0002t0001g0185 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.6214+207C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 34/35 | chr9 | 131230976 | ||||||
| chr9:131231085
|
G | A | 1 | a0002c0002t0001g0200 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.6214+316G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 34/35 | chr9 | 131231085 | ||||||
| chr9:131231087
|
T | C | 1 | a0002c0002t0001g0226 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.6214+318T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 34/35 | chr9 | 131231087 | ||||||
| chr9:131231186
|
A | C | 7 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0212others(4): Show | 7 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.6214+417A>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 34/35 | chr9 | 131231186 | ||||||
| chr9:131231188
|
C | CATAT | 3 | a0002c0002t0001g0068a0013c0023t0005g0003a0015c0028t0004g0207 | 3 | HG02145.hp1 HG03579.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.6214+434_6214+437d others(6): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 34/35 | INFO_REALIGN_3_PRIME | chr9 | 131231188 | |||||
| chr9:131231188
|
CAT | C | 4 | a0001c0010t0003g0214a0001c0010t0003g0228a0001c0010t0003g0229others(1): Show | 4 | HG01109.hp1 HG02818.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.6214+436_6214+437d others(4): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 34/35 | INFO_REALIGN_3_PRIME | chr9 | 131231188 | |||||
| chr9:131231205
|
A | T | 4 | a0001c0010t0003g0214a0001c0010t0003g0228a0001c0010t0003g0229others(1): Show | 4 | HG01109.hp1 HG02818.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.6214+436A>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 34/35 | chr9 | 131231205 | ||||||
| chr9:131231410
|
C | T | 1 | a0001c0024t0001g0056 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.6214+641C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 34/35 | chr9 | 131231410 | ||||||
| chr9:131231779
|
C | T | 1 | a0001c0001t0001g0058 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.6215-505C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 34/35 | chr9 | 131231779 | ||||||
| chr9:131231818
|
C | T | 1 | a0002c0003t0001g0070 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.6215-466C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 34/35 | chr9 | 131231818 | ||||||
| chr9:131231829
|
A | T | 3 | a0001c0001t0001g0216a0001c0001t0001g0217a0001c0001t0001g0218 | 3 | HG02109.hp1 HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.6215-455A>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 34/35 | chr9 | 131231829 | ||||||
| chr9:131231912
|
C | CA | 24 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(21): Show | 24 | HG00558.hp1 HG00642.hp1 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.6215-350dupA | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 34/35 | INFO_REALIGN_3_PRIME | chr9 | 131231912 | |||||
| chr9:131231912
|
CA | C | 6 | a0001c0001t0001g0111a0001c0005t0002g0205a0001c0005t0002g0206others(3): Show | 6 | HG01106.hp1 HG01496.hp2 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.6215-350delA | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 34/35 | INFO_REALIGN_3_PRIME | chr9 | 131231912 | |||||
| chr9:131232015
|
G | A | 1 | a0010c0017t0001g0108 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.6215-269G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 34/35 | chr9 | 131232015 | ||||||
| chr9:131232212
|
A | G | 3 | a0001c0010t0003g0214a0001c0010t0003g0228a0001c0010t0003g0229 | 3 | HG01109.hp1 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.6215-72A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 34/35 | chr9 | 131232212 | ||||||
| chr9:131232246
|
G | A | 3 | a0001c0001t0001g0216a0001c0001t0001g0217a0001c0001t0001g0218 | 3 | HG02109.hp1 HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.6215-38G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 34/35 | chr9 | 131232246 | ||||||
| chr9:131232333
|
C | T | 1 | a0001c0001t0001g0083 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.6239+25C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 35/35 | chr9 | 131232333 | ||||||
| chr9:131232429
|
C | T | 2 | a0001c0001t0001g0077a0001c0001t0001g0078 | 2 | HG01515.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.6239+121C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 35/35 | chr9 | 131232429 | ||||||
| chr9:131232682
|
C | T | 1 | a0002c0002t0001g0147 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.6239+374C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 35/35 | chr9 | 131232682 | ||||||
| chr9:131232934
|
T | C | 4 | a0001c0010t0003g0214a0001c0010t0003g0228a0001c0010t0003g0229others(1): Show | 4 | HG01109.hp1 HG02818.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.6240-520T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 35/35 | chr9 | 131232934 | ||||||
| chr9:131233020
|
T | A | 216 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(213): Show | 216 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.6240-434T>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 35/35 | chr9 | 131233020 | ||||||
| chr9:131233178
|
A | C | 13 | a0001c0005t0002g0205a0001c0005t0002g0206a0001c0005t0002g0212others(10): Show | 13 | HG01109.hp1 HG01496.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.6240-276A>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 35/35 | chr9 | 131233178 |