Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 9688 |
|---|---|
| ensemblid | ENSG00000102900.13 |
| hgncid | 28958 |
| symbol | NUP93 |
| name | nucleoporin 93 |
| refseq_nuc | NM_014669.5 |
| refseq_prot | NP_055484.3 |
| ensembl_nuc | ENST00000308159.10 |
| ensembl_prot | ENSP00000310668.5 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 56730129 |
| end | 56850286 |
| strand | + |
| ver | v1.2 |
| region | chr16:56730129-56850286 |
| region5000 | chr16:56725129-56855286 |
| regionname0 | NUP93_chr16_56730129_56850286 |
| regionname5000 | NUP93_chr16_56725129_56855286 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 819 | 366 | 87 | 65 | 161 | 14 | 37 | 118 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0002 | 0/0 | 819 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0003 | 0/0 | 819 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0004 | 0/0 | 819 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0005 | 0/0 | 819 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0006 | 0/0 | 819 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0007 | 0/0 | 819 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0008 | 0/0 | 819 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0009 | 0/0 | 819 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0010 | 0/0 | 819 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 2460 | 189 | 42 | 29 | 88 | 9 | 21 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| c0002 | 0/0 | 2460 | 68 | 12 | 14 | 32 | 3 | 7 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| c0003 | 0/1 | 2460 | 42 | 4 | 11 | 24 | 1 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| c0004 | 1/0 | 2460 | 39 | 4 | 11 | 15 | 1 | 7 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| c0005 | 0/0 | 2460 | 8 | 8 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| c0006 | 0/0 | 2460 | 5 | 5 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| c0007 | 0/0 | 2460 | 4 | 4 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| c0008 | 0/0 | 2460 | 4 | 0 | 0 | 4 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| c0009 | 0/0 | 2460 | 2 | 2 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| c0010 | 0/0 | 2460 | 2 | 2 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| c0011 | 0/0 | 2460 | 2 | 2 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| c0012 | 0/0 | 2460 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| c0013 | 0/0 | 2460 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| c0014 | 0/0 | 2460 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| c0015 | 0/0 | 2460 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| c0016 | 0/0 | 2460 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| c0017 | 0/0 | 2460 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| c0018 | 0/0 | 2460 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| c0019 | 0/0 | 2460 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| c0020 | 0/0 | 2460 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| c0021 | 0/0 | 2460 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| c0022 | 0/0 | 2460 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| c0023 | 0/0 | 2460 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| c0024 | 0/0 | 2460 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 5776 | 155 | 32 | 16 | 79 | 10 | 18 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| t0002 | 0/1 | 5776 | 42 | 7 | 9 | 24 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| t0003 | 0/0 | 5748 | 26 | 2 | 10 | 11 | 1 | 2 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| t0004 | 0/0 | 5776 | 23 | 1 | 5 | 16 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| t0005 | 0/0 | 5771 | 22 | 0 | 6 | 15 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| t0006 | 0/0 | 5776 | 19 | 4 | 5 | 6 | 1 | 3 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| t0007 | 0/0 | 5750 | 12 | 8 | 2 | 0 | 0 | 2 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| t0008 | 0/0 | 5775 | 7 | 1 | 3 | 0 | 0 | 3 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| t0009 | 0/0 | 5777 | 5 | 5 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| t0010 | 0/0 | 5776 | 5 | 0 | 5 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| t0011 | 0/0 | 5776 | 5 | 5 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| t0012 | 0/0 | 5776 | 4 | 4 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| t0013 | 0/0 | 5776 | 3 | 3 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| t0014 | 0/0 | 5776 | 3 | 3 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| t0015 | 0/0 | 5776 | 3 | 3 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| t0016 | 0/0 | 5750 | 3 | 3 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| t0017 | 0/0 | 5776 | 3 | 0 | 0 | 3 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| t0018 | 0/0 | 5776 | 3 | 3 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| t0019 | 1/0 | 5775 | 3 | 0 | 0 | 0 | 0 | 2 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| t0020 | 0/0 | 5776 | 2 | 0 | 2 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| t0021 | 0/0 | 5776 | 2 | 0 | 0 | 2 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| t0022 | 0/0 | 5776 | 2 | 1 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| t0023 | 0/0 | 5776 | 2 | 0 | 0 | 2 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| t0024 | 0/0 | 5775 | 2 | 0 | 2 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| t0025 | 0/0 | 5776 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| t0026 | 0/0 | 5748 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| t0027 | 0/0 | 5748 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| t0028 | 0/0 | 5748 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| t0029 | 0/0 | 5776 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| t0030 | 0/0 | 5776 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| t0031 | 0/0 | 5776 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| t0032 | 0/0 | 5776 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| t0033 | 0/0 | 5776 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| t0034 | 0/0 | 5750 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| t0035 | 0/0 | 5776 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| t0036 | 0/0 | 5776 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| t0037 | 0/0 | 5776 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| t0038 | 0/0 | 5776 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| t0039 | 0/0 | 5776 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| t0040 | 0/0 | 5776 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| t0041 | 0/0 | 5776 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| t0042 | 0/0 | 5776 | 1 | 0 | 0 | 0 | 1 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| t0043 | 0/0 | 5776 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| t0044 | 0/0 | 5775 | 1 | 0 | 0 | 0 | 1 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| t0045 | 0/0 | 5775 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| t0046 | 0/0 | 5776 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0002 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0171 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0259 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0325 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0352 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0367 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0371 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0372 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0375 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| g0376 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2460 | 189 | 42 | 29 | 88 | 9 | 21 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0001c0002 | 0/0 | 2460 | 68 | 12 | 14 | 32 | 3 | 7 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0001c0003 | 0/1 | 2460 | 42 | 4 | 11 | 24 | 1 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0001c0004 | 1/0 | 2460 | 39 | 4 | 11 | 15 | 1 | 7 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0001c0005 | 0/0 | 2460 | 8 | 8 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0001c0006 | 0/0 | 2460 | 5 | 5 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0001c0007 | 0/0 | 2460 | 4 | 4 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0001c0009 | 0/0 | 2460 | 2 | 2 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0001c0010 | 0/0 | 2460 | 2 | 2 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0001c0011 | 0/0 | 2460 | 2 | 2 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0001c0012 | 0/0 | 2460 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0001c0014 | 0/0 | 2460 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0001c0016 | 0/0 | 2460 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0001c0017 | 0/0 | 2460 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0001c0019 | 0/0 | 2460 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0002c0008 | 0/0 | 2460 | 4 | 0 | 0 | 4 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0003c0024 | 0/0 | 2460 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0004c0023 | 0/0 | 2460 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0005c0022 | 0/0 | 2460 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0006c0021 | 0/0 | 2460 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0007c0020 | 0/0 | 2460 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0008c0018 | 0/0 | 2460 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0009c0015 | 0/0 | 2460 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0010c0013 | 0/0 | 2460 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 8235 | 86 | 15 | 8 | 45 | 7 | 11 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0001c0001t0002 | 0/0 | 8235 | 3 | 3 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0001c0001t0003 | 0/0 | 8207 | 26 | 2 | 10 | 11 | 1 | 2 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0001c0001t0004 | 0/0 | 8235 | 21 | 1 | 4 | 16 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0001c0001t0006 | 0/0 | 8235 | 19 | 4 | 5 | 6 | 1 | 3 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0001c0001t0007 | 0/0 | 8209 | 3 | 0 | 2 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0001c0001t0011 | 0/0 | 8235 | 5 | 5 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0001c0001t0013 | 0/0 | 8235 | 3 | 3 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0001c0001t0014 | 0/0 | 8235 | 3 | 3 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0001c0001t0016 | 0/0 | 8209 | 3 | 3 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0001c0001t0017 | 0/0 | 8235 | 3 | 0 | 0 | 3 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0001c0001t0023 | 0/0 | 8235 | 2 | 0 | 0 | 2 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0001c0001t0025 | 0/0 | 8235 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0001c0001t0027 | 0/0 | 8207 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0001c0001t0028 | 0/0 | 8207 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0001c0001t0029 | 0/0 | 8235 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0001c0001t0031 | 0/0 | 8235 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0001c0001t0034 | 0/0 | 8209 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0001c0001t0035 | 0/0 | 8235 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0001c0001t0036 | 0/0 | 8235 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0001c0001t0038 | 0/0 | 8235 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0001c0001t0039 | 0/0 | 8235 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0001c0001t0043 | 0/0 | 8235 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0001c0001t0046 | 0/0 | 8235 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0001c0002t0001 | 0/0 | 8235 | 60 | 11 | 8 | 32 | 3 | 6 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0001c0002t0010 | 0/0 | 8235 | 5 | 0 | 5 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0001c0002t0037 | 0/0 | 8235 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0001c0002t0040 | 0/0 | 8235 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0001c0002t0041 | 0/0 | 8235 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0001c0003t0002 | 0/1 | 8235 | 35 | 4 | 9 | 20 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0001c0003t0020 | 0/0 | 8235 | 2 | 0 | 2 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0001c0003t0021 | 0/0 | 8235 | 2 | 0 | 0 | 2 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0001c0003t0030 | 0/0 | 8235 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0001c0003t0032 | 0/0 | 8235 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0001c0003t0042 | 0/0 | 8235 | 1 | 0 | 0 | 0 | 1 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0001c0004t0005 | 0/0 | 8230 | 22 | 0 | 6 | 15 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0001c0004t0008 | 0/0 | 8234 | 7 | 1 | 3 | 0 | 0 | 3 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0001c0004t0015 | 0/0 | 8235 | 3 | 3 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0001c0004t0019 | 1/0 | 8234 | 3 | 0 | 0 | 0 | 0 | 2 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0001c0004t0024 | 0/0 | 8234 | 2 | 0 | 2 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0001c0004t0044 | 0/0 | 8234 | 1 | 0 | 0 | 0 | 1 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0001c0004t0045 | 0/0 | 8234 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0001c0005t0007 | 0/0 | 8209 | 8 | 8 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0001c0006t0009 | 0/0 | 8236 | 5 | 5 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0001c0007t0012 | 0/0 | 8235 | 4 | 4 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0001c0009t0018 | 0/0 | 8235 | 2 | 2 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0001c0010t0022 | 0/0 | 8235 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0001c0010t0033 | 0/0 | 8235 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0001c0011t0001 | 0/0 | 8235 | 2 | 2 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0001c0012t0001 | 0/0 | 8235 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0001c0014t0001 | 0/0 | 8235 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0001c0016t0001 | 0/0 | 8235 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0001c0017t0001 | 0/0 | 8235 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0001c0019t0001 | 0/0 | 8235 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0002c0008t0002 | 0/0 | 8235 | 4 | 0 | 0 | 4 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0003c0024t0018 | 0/0 | 8235 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0004c0023t0026 | 0/0 | 8207 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0005c0022t0022 | 0/0 | 8235 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0006c0021t0001 | 0/0 | 8235 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0007c0020t0001 | 0/0 | 8235 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0008c0018t0004 | 0/0 | 8235 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0009c0015t0004 | 0/0 | 8235 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| a0010c0013t0007 | 0/0 | 8209 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | copy fasta | chr16 | 56725129 | 56855286 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0002g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0002g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0002g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0003g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0003g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0003g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0003g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0003g0352 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0003g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0003g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0003g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0003g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0003g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0003g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0003g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0003g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0003g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0003g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0003g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0003g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0003g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0003g0367 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0003g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0003g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0003g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0003g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0003g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0003g0375 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0003g0376 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0004g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0004g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0004g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0004g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0004g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0004g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0004g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0004g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0004g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0004g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0004g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0004g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0004g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0004g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0004g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0004g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0004g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0004g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0004g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0004g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0004g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0006g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0006g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0006g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0006g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0006g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0006g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0006g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0006g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0006g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0006g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0006g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0006g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0006g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0006g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0006g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0006g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0006g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0006g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0006g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0007g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0007g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0007g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0011g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0011g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0011g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0011g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0011g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0013g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0013g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0013g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0014g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0014g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0014g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0016g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0016g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0016g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0017g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0017g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0017g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0023g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0023g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0025g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0027g0371 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0028g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0029g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0031g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0034g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0035g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0036g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0038g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0039g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0043g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0001t0046g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0002t0001g0001 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0002t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0002t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0002t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0002t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0002t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0002t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0002t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0002t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0002t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0002t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0002t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0002t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0002t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0002t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0002t0010g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0002t0010g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0002t0010g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0002t0010g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0002t0010g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0002t0037g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0002t0040g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0002t0041g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0003t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0003t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0003t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0003t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0003t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0003t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0003t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0003t0002g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0003t0002g0259 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0003t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0003t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0003t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0003t0002g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0003t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0003t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0003t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0003t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0003t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0003t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0003t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0003t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0003t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0003t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0003t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0003t0002g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0003t0002g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0003t0002g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0003t0002g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0003t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0003t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0003t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0003t0002g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0003t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0003t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0003t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0003t0020g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0003t0020g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0003t0021g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0003t0021g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0003t0030g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0003t0032g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0003t0042g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0004t0005g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0004t0005g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0004t0005g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0004t0005g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0004t0005g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0004t0005g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0004t0005g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0004t0005g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0004t0005g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0004t0005g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0004t0005g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0004t0005g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0004t0005g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0004t0005g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0004t0005g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0004t0005g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0004t0005g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0004t0005g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0004t0005g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0004t0005g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0004t0005g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0004t0005g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0004t0008g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0004t0008g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0004t0008g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0004t0008g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0004t0008g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0004t0008g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0004t0008g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0004t0015g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0004t0015g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0004t0015g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0004t0019g0171 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0004t0019g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0004t0019g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0004t0024g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0004t0024g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0004t0044g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0004t0045g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0005t0007g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0005t0007g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0005t0007g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0005t0007g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0005t0007g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0005t0007g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0005t0007g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0005t0007g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0006t0009g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0006t0009g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0006t0009g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0006t0009g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0006t0009g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0007t0012g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0007t0012g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0007t0012g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0007t0012g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0009t0018g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0009t0018g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0010t0022g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0010t0033g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0011t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0011t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0012t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0014t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0016t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0017t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0001c0019t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0002c0008t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0002c0008t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0002c0008t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0002c0008t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0003c0024t0018g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0004c0023t0026g0372 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0005c0022t0022g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0006c0021t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0007c0020t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0008c0018t0004g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0009c0015t0004g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| a0010c0013t0007g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0136 | EUR | GBR | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG00099 | hp2 | a0001 | c0004 | t0044 | g0179 | EUR | GBR | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG00140 | hp1 | a0001 | c0002 | t0001 | g0108 | EUR | GBR | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0305 | EUR | GBR | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0367 | EUR | FIN | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG00323 | hp2 | a0001 | c0002 | t0001 | g0070 | EUR | FIN | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG00408 | hp1 | a0001 | c0002 | t0001 | g0168 | EAS | CHS | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG00408 | hp2 | a0001 | c0001 | t0004 | g0234 | EAS | CHS | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG00423 | hp1 | a0001 | c0003 | t0021 | g0262 | EAS | CHS | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG00423 | hp2 | a0001 | c0004 | t0005 | g0043 | EAS | CHS | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0327 | EAS | CHS | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG00438 | hp2 | a0001 | c0004 | t0005 | g0040 | EAS | CHS | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0044 | EAS | CHS | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG00544 | hp2 | a0001 | c0003 | t0002 | g0288 | EAS | CHS | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | CHS | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG00558 | hp2 | a0001 | c0004 | t0005 | g0037 | EAS | CHS | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG00597 | hp1 | a0001 | c0003 | t0002 | g0293 | EAS | CHS | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG00597 | hp2 | a0001 | c0001 | t0004 | g0242 | EAS | CHS | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | CHS | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0095 | EAS | CHS | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | CHS | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG00621 | hp2 | a0001 | c0001 | t0017 | g0307 | EAS | CHS | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0365 | AMR | PUR | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG00639 | hp2 | a0001 | c0004 | t0024 | g0039 | AMR | PUR | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0170 | AMR | PUR | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG00642 | hp2 | a0001 | c0001 | t0007 | g0195 | AMR | PUR | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG00673 | hp1 | a0001 | c0003 | t0002 | g0289 | EAS | CHS | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG00673 | hp2 | a0001 | c0002 | t0001 | g0104 | EAS | CHS | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG00733 | hp1 | a0001 | c0001 | t0004 | g0220 | AMR | PUR | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG00733 | hp2 | a0001 | c0002 | t0010 | g0111 | AMR | PUR | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0322 | AMR | PUR | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG00741 | hp1 | a0001 | c0004 | t0008 | g0174 | AMR | PUR | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG00741 | hp2 | a0001 | c0004 | t0005 | g0034 | AMR | PUR | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG01069 | hp1 | a0001 | c0003 | t0002 | g0258 | AMR | PUR | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG01069 | hp2 | a0001 | c0002 | t0010 | g0049 | AMR | PUR | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0350 | AMR | PUR | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG01070 | hp2 | a0001 | c0001 | t0006 | g0212 | AMR | PUR | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0349 | AMR | PUR | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG01071 | hp2 | a0001 | c0003 | t0002 | g0257 | AMR | PUR | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0324 | AMR | PUR | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0366 | AMR | PUR | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG01099 | hp1 | a0001 | c0003 | t0002 | g0280 | AMR | PUR | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG01099 | hp2 | a0001 | c0004 | t0005 | g0030 | AMR | PUR | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG01106 | hp1 | a0001 | c0004 | t0008 | g0173 | AMR | PUR | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0304 | AMR | PUR | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG01109 | hp1 | a0001 | c0001 | t0007 | g0340 | AMR | PUR | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG01109 | hp2 | a0001 | c0003 | t0002 | g0255 | AMR | PUR | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG01167 | hp1 | a0001 | c0002 | t0010 | g0048 | AMR | PUR | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0376 | AMR | PUR | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG01168 | hp1 | a0001 | c0003 | t0020 | g0297 | AMR | PUR | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG01168 | hp2 | a0001 | c0001 | t0006 | g0216 | AMR | PUR | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG01169 | hp1 | a0001 | c0003 | t0020 | g0283 | AMR | PUR | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0375 | AMR | PUR | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG01175 | hp1 | a0001 | c0001 | t0004 | g0225 | AMR | PUR | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG01175 | hp2 | a0001 | c0003 | t0002 | g0281 | AMR | PUR | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG01243 | hp1 | a0001 | c0001 | t0006 | g0210 | AMR | PUR | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG01243 | hp2 | a0001 | c0003 | t0002 | g0264 | AMR | PUR | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG01255 | hp1 | a0001 | c0002 | t0010 | g0050 | AMR | CLM | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG01255 | hp2 | a0001 | c0001 | t0006 | g0211 | AMR | CLM | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG01258 | hp1 | a0001 | c0002 | t0001 | g0082 | AMR | CLM | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG01258 | hp2 | a0001 | c0004 | t0008 | g0177 | AMR | CLM | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG01261 | hp1 | a0001 | c0004 | t0005 | g0035 | AMR | CLM | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG01261 | hp2 | a0001 | c0003 | t0002 | g0248 | AMR | CLM | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG01346 | hp1 | a0001 | c0004 | t0005 | g0033 | AMR | CLM | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG01346 | hp2 | a0001 | c0002 | t0010 | g0112 | AMR | CLM | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG01358 | hp1 | a0001 | c0004 | t0024 | g0042 | AMR | CLM | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0318 | AMR | CLM | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG01361 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0348 | AMR | CLM | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | CLM | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG01433 | hp2 | a0001 | c0001 | t0004 | g0221 | AMR | CLM | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | CLM | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG01496 | hp2 | a0001 | c0001 | t0004 | g0236 | AMR | CLM | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG01515 | hp1 | a0001 | c0001 | t0006 | g0213 | EUR | IBS | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0134 | EUR | IBS | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0135 | EUR | IBS | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG01517 | hp2 | a0001 | c0002 | t0001 | g0001 | EUR | IBS | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG01884 | hp1 | a0001 | c0001 | t0011 | g0005 | AFR | ACB | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG01884 | hp2 | a0001 | c0001 | t0014 | g0217 | AFR | ACB | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG01891 | hp1 | a0001 | c0007 | t0012 | g0065 | AFR | ACB | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | ACB | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG01928 | hp1 | a0001 | c0003 | t0002 | g0266 | AMR | PEL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG01928 | hp2 | a0001 | c0001 | t0006 | g0215 | AMR | PEL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0363 | AMR | PEL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG01978 | hp2 | a0009 | c0015 | t0004 | g0235 | AMR | PEL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG01981 | hp1 | a0001 | c0002 | t0037 | g0084 | AMR | PEL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG01981 | hp2 | a0001 | c0001 | t0003 | g0362 | AMR | PEL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG01993 | hp1 | a0001 | c0004 | t0005 | g0031 | AMR | PEL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0074 | AMR | PEL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG02015 | hp1 | a0001 | c0001 | t0006 | g0202 | EAS | KHV | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0344 | EAS | KHV | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG02027 | hp1 | a0001 | c0001 | t0028 | g0360 | EAS | KHV | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG02027 | hp2 | a0001 | c0002 | t0001 | g0165 | EAS | KHV | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG02056 | hp1 | a0001 | c0003 | t0002 | g0291 | EAS | KHV | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG02056 | hp2 | a0001 | c0002 | t0001 | g0339 | EAS | KHV | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG02071 | hp2 | a0001 | c0002 | t0001 | g0076 | EAS | KHV | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0093 | EAS | KHV | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG02074 | hp2 | a0001 | c0003 | t0021 | g0294 | EAS | KHV | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG02080 | hp1 | a0001 | c0002 | t0001 | g0081 | EAS | KHV | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG02080 | hp2 | a0001 | c0003 | t0032 | g0271 | EAS | KHV | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG02083 | hp1 | a0001 | c0001 | t0006 | g0205 | EAS | KHV | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG02083 | hp2 | a0001 | c0002 | t0001 | g0088 | EAS | KHV | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0077 | EAS | KHV | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG02129 | hp2 | a0001 | c0002 | t0001 | g0058 | EAS | KHV | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0086 | EAS | KHV | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG02132 | hp2 | a0005 | c0022 | t0022 | g0254 | EAS | KHV | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG02145 | hp1 | a0001 | c0001 | t0029 | g0245 | AFR | ACB | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG02145 | hp2 | a0001 | c0007 | t0012 | g0345 | AFR | ACB | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG02148 | hp1 | a0001 | c0002 | t0001 | g0092 | AMR | PEL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG02148 | hp2 | a0001 | c0001 | t0003 | g0364 | AMR | PEL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG02155 | hp1 | a0001 | c0003 | t0002 | g0279 | EAS | CDX | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0338 | EAS | CDX | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | CDX | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0083 | EAS | CDX | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | ACB | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG02257 | hp2 | a0001 | c0005 | t0007 | g0183 | AFR | ACB | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG02258 | hp1 | a0001 | c0002 | t0001 | g0110 | AFR | ACB | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG02258 | hp2 | a0001 | c0001 | t0016 | g0193 | AFR | ACB | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0096 | AFR | ACB | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0284 | AFR | ACB | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG02293 | hp1 | a0001 | c0002 | t0001 | g0087 | AMR | PEL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG02293 | hp2 | a0001 | c0004 | t0005 | g0032 | AMR | PEL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG02300 | hp1 | a0001 | c0003 | t0002 | g0290 | AMR | PEL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG02300 | hp2 | a0001 | c0002 | t0001 | g0071 | AMR | PEL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | ACB | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG02451 | hp2 | a0003 | c0024 | t0018 | g0010 | AFR | ACB | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0064 | AFR | GWD | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG02572 | hp2 | a0001 | c0001 | t0034 | g0196 | AFR | GWD | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG02602 | hp1 | a0001 | c0004 | t0045 | g0182 | SAS | PJL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG02602 | hp2 | a0001 | c0002 | t0001 | g0101 | SAS | PJL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG02615 | hp1 | a0001 | c0003 | t0002 | g0273 | AFR | GWD | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG02615 | hp2 | a0001 | c0006 | t0009 | g0250 | AFR | GWD | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG02622 | hp1 | a0001 | c0002 | t0001 | g0069 | AFR | GWD | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG02622 | hp2 | a0001 | c0003 | t0002 | g0285 | AFR | GWD | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG02630 | hp1 | a0001 | c0001 | t0011 | g0009 | AFR | GWD | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG02630 | hp2 | a0001 | c0003 | t0002 | g0277 | AFR | GWD | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG02647 | hp2 | a0001 | c0002 | t0001 | g0068 | AFR | GWD | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG02698 | hp1 | a0001 | c0004 | t0008 | g0172 | SAS | PJL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0292 | AFR | GWD | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG02717 | hp2 | a0001 | c0005 | t0007 | g0188 | AFR | GWD | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG02738 | hp2 | a0001 | c0001 | t0007 | g0194 | SAS | PJL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0355 | AFR | GWD | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG02809 | hp2 | a0001 | c0005 | t0007 | g0185 | AFR | GWD | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG02818 | hp1 | a0001 | c0004 | t0015 | g0017 | AFR | GWD | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG02818 | hp2 | a0001 | c0006 | t0009 | g0252 | AFR | GWD | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0098 | AFR | GWD | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG02886 | hp2 | a0001 | c0007 | t0012 | g0347 | AFR | GWD | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG02895 | hp1 | a0001 | c0011 | t0001 | g0089 | AFR | GWD | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG02895 | hp2 | a0001 | c0014 | t0001 | g0137 | AFR | GWD | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG02896 | hp1 | a0001 | c0005 | t0007 | g0197 | AFR | GWD | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG02896 | hp2 | a0001 | c0006 | t0009 | g0253 | AFR | GWD | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG02897 | hp1 | a0001 | c0006 | t0009 | g0251 | AFR | GWD | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG02897 | hp2 | a0001 | c0011 | t0001 | g0090 | AFR | GWD | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG02922 | hp1 | a0001 | c0005 | t0007 | g0187 | AFR | ESN | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0295 | AFR | ESN | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG02965 | hp1 | a0007 | c0020 | t0001 | g0063 | AFR | ESN | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG02965 | hp2 | a0001 | c0004 | t0015 | g0016 | AFR | ESN | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG02970 | hp1 | a0001 | c0002 | t0040 | g0097 | AFR | ESN | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG02970 | hp2 | a0001 | c0001 | t0011 | g0007 | AFR | ESN | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | ESN | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG02976 | hp2 | a0001 | c0001 | t0006 | g0200 | AFR | ESN | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0335 | SAS | PJL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG03017 | hp2 | a0001 | c0004 | t0005 | g0021 | SAS | PJL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG03041 | hp1 | a0001 | c0001 | t0013 | g0013 | AFR | GWD | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG03041 | hp2 | a0001 | c0005 | t0007 | g0189 | AFR | GWD | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG03098 | hp1 | a0001 | c0001 | t0011 | g0004 | AFR | MSL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | ESN | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG03130 | hp2 | a0001 | c0001 | t0016 | g0191 | AFR | ESN | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG03139 | hp1 | a0001 | c0003 | t0002 | g0282 | AFR | ESN | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG03139 | hp2 | a0001 | c0010 | t0022 | g0260 | AFR | ESN | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | ESN | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG03195 | hp2 | a0001 | c0001 | t0006 | g0243 | AFR | ESN | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG03209 | hp1 | a0001 | c0009 | t0018 | g0018 | AFR | MSL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG03209 | hp2 | a0001 | c0002 | t0001 | g0094 | AFR | MSL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG03225 | hp1 | a0001 | c0001 | t0013 | g0014 | AFR | MSL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | MSL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG03239 | hp1 | a0001 | c0001 | t0006 | g0214 | SAS | PJL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG03239 | hp2 | a0001 | c0001 | t0036 | g0148 | SAS | PJL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG03453 | hp1 | a0001 | c0001 | t0014 | g0219 | AFR | MSL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG03453 | hp2 | a0001 | c0005 | t0007 | g0184 | AFR | MSL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG03486 | hp1 | a0001 | c0007 | t0012 | g0346 | AFR | MSL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG03486 | hp2 | a0001 | c0001 | t0011 | g0006 | AFR | MSL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0352 | SAS | PJL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG03491 | hp1 | a0001 | c0004 | t0019 | g0180 | SAS | PJL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG03491 | hp2 | a0001 | c0001 | t0006 | g0203 | SAS | PJL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG03492 | hp1 | a0001 | c0001 | t0006 | g0208 | SAS | PJL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0351 | SAS | PJL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0067 | AFR | ESN | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG03516 | hp2 | a0001 | c0009 | t0018 | g0019 | AFR | ESN | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG03540 | hp2 | a0001 | c0017 | t0001 | g0158 | AFR | GWD | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG03579 | hp1 | a0001 | c0010 | t0033 | g0261 | AFR | MSL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG03579 | hp2 | a0001 | c0002 | t0001 | g0100 | AFR | MSL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0310 | SAS | PJL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG03654 | hp2 | a0001 | c0002 | t0041 | g0113 | SAS | PJL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0332 | SAS | PJL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG03669 | hp2 | a0001 | c0004 | t0008 | g0176 | SAS | PJL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG03688 | hp1 | a0010 | c0013 | t0007 | g0190 | SAS | STU | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG03688 | hp2 | a0001 | c0002 | t0001 | g0105 | SAS | STU | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG03704 | hp1 | a0001 | c0016 | t0001 | g0117 | SAS | PJL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG03704 | hp2 | a0001 | c0004 | t0008 | g0178 | SAS | PJL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | BEB | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0336 | SAS | BEB | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0109 | SAS | BEB | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG03834 | hp2 | a0001 | c0003 | t0002 | g0047 | SAS | BEB | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG03927 | hp1 | a0001 | c0004 | t0019 | g0181 | SAS | BEB | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG03927 | hp2 | a0001 | c0002 | t0001 | g0051 | SAS | BEB | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG03942 | hp1 | a0001 | c0002 | t0001 | g0106 | SAS | BEB | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG03942 | hp2 | a0001 | c0001 | t0027 | g0371 | SAS | BEB | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG04184 | hp1 | a0001 | c0002 | t0001 | g0128 | SAS | BEB | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG04184 | hp2 | a0001 | c0001 | t0043 | g0154 | SAS | BEB | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | STU | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG04199 | hp2 | a0001 | c0001 | t0031 | g0209 | SAS | STU | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | STU | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG04204 | hp2 | a0004 | c0023 | t0026 | g0372 | SAS | STU | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA18522 | hp1 | a0001 | c0002 | t0001 | g0099 | AFR | YRI | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA18522 | hp2 | a0006 | c0021 | t0001 | g0011 | AFR | YRI | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA18612 | hp1 | a0001 | c0003 | t0002 | g0263 | EAS | CHB | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA18612 | hp2 | a0001 | c0004 | t0005 | g0025 | EAS | CHB | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA18747 | hp1 | a0001 | c0002 | t0001 | g0062 | EAS | CHB | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA18747 | hp2 | a0001 | c0001 | t0006 | g0204 | EAS | CHB | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA18906 | hp1 | a0001 | c0004 | t0015 | g0015 | AFR | YRI | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA18906 | hp2 | a0001 | c0001 | t0013 | g0012 | AFR | YRI | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA18939 | hp1 | a0001 | c0003 | t0002 | g0246 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA18940 | hp1 | a0001 | c0003 | t0002 | g0247 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA18941 | hp1 | a0001 | c0001 | t0035 | g0227 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA18941 | hp2 | a0001 | c0003 | t0002 | g0276 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0368 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA18942 | hp2 | a0001 | c0003 | t0002 | g0275 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA18943 | hp1 | a0001 | c0004 | t0005 | g0036 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA18944 | hp1 | a0001 | c0002 | t0001 | g0072 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA18945 | hp1 | a0001 | c0003 | t0002 | g0268 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA18945 | hp2 | a0001 | c0001 | t0004 | g0224 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA18946 | hp1 | a0001 | c0001 | t0039 | g0317 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA18948 | hp1 | a0001 | c0001 | t0006 | g0244 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA18948 | hp2 | a0001 | c0004 | t0005 | g0027 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA18949 | hp1 | a0001 | c0002 | t0001 | g0085 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA18949 | hp2 | a0001 | c0003 | t0002 | g0256 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA18951 | hp1 | a0001 | c0004 | t0005 | g0024 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA18952 | hp1 | a0001 | c0001 | t0004 | g0232 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA18952 | hp2 | a0001 | c0001 | t0003 | g0370 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA18953 | hp1 | a0001 | c0002 | t0001 | g0080 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA18954 | hp1 | a0002 | c0008 | t0002 | g0298 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA18954 | hp2 | a0001 | c0002 | t0001 | g0073 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA18959 | hp2 | a0001 | c0001 | t0004 | g0238 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA18961 | hp1 | a0001 | c0001 | t0003 | g0373 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0337 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA18965 | hp2 | a0001 | c0002 | t0001 | g0057 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA18966 | hp1 | a0002 | c0008 | t0002 | g0299 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA18967 | hp1 | a0001 | c0004 | t0005 | g0038 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA18967 | hp2 | a0001 | c0001 | t0004 | g0237 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA18969 | hp1 | a0001 | c0001 | t0017 | g0342 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA18969 | hp2 | a0001 | c0001 | t0003 | g0359 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA18970 | hp2 | a0001 | c0001 | t0006 | g0206 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA18971 | hp2 | a0001 | c0004 | t0005 | g0026 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA18972 | hp1 | a0001 | c0004 | t0005 | g0028 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA18972 | hp2 | a0001 | c0001 | t0004 | g0240 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA18977 | hp2 | a0001 | c0004 | t0005 | g0020 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA18979 | hp1 | a0001 | c0001 | t0003 | g0358 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA18981 | hp2 | a0001 | c0003 | t0002 | g0296 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA18982 | hp2 | a0001 | c0002 | t0001 | g0107 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA18983 | hp1 | a0001 | c0003 | t0002 | g0265 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA18983 | hp2 | a0001 | c0002 | t0001 | g0061 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA18984 | hp1 | a0001 | c0002 | t0001 | g0059 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA18988 | hp1 | a0001 | c0001 | t0038 | g0150 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA18988 | hp2 | a0001 | c0004 | t0005 | g0022 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA18989 | hp1 | a0001 | c0004 | t0005 | g0041 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA18989 | hp2 | a0001 | c0001 | t0004 | g0198 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA18990 | hp2 | a0001 | c0002 | t0001 | g0164 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA18991 | hp1 | a0001 | c0001 | t0023 | g0329 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA18992 | hp2 | a0001 | c0001 | t0004 | g0233 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA18999 | hp1 | a0001 | c0001 | t0003 | g0369 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA18999 | hp2 | a0001 | c0001 | t0004 | g0226 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA19000 | hp2 | a0001 | c0003 | t0002 | g0287 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA19001 | hp1 | a0001 | c0003 | t0002 | g0269 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA19002 | hp1 | a0001 | c0002 | t0001 | g0075 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA19004 | hp1 | a0001 | c0001 | t0004 | g0231 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA19005 | hp1 | a0001 | c0001 | t0003 | g0353 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA19010 | hp1 | a0001 | c0002 | t0001 | g0060 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0343 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA19011 | hp1 | a0001 | c0002 | t0001 | g0102 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA19011 | hp2 | a0001 | c0001 | t0017 | g0341 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA19012 | hp1 | a0001 | c0003 | t0002 | g0272 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA19057 | hp2 | a0001 | c0001 | t0025 | g0314 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA19062 | hp1 | a0001 | c0002 | t0001 | g0129 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA19062 | hp2 | a0001 | c0001 | t0003 | g0374 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA19064 | hp1 | a0001 | c0001 | t0003 | g0354 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA19066 | hp1 | a0001 | c0012 | t0001 | g0079 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA19066 | hp2 | a0001 | c0003 | t0002 | g0267 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA19068 | hp2 | a0001 | c0001 | t0023 | g0330 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA19070 | hp1 | a0001 | c0001 | t0004 | g0230 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA19070 | hp2 | a0001 | c0003 | t0030 | g0274 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA19074 | hp1 | a0001 | c0003 | t0002 | g0278 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA19077 | hp1 | a0001 | c0001 | t0004 | g0222 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA19077 | hp2 | a0001 | c0001 | t0003 | g0357 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA19079 | hp1 | a0001 | c0004 | t0005 | g0029 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA19079 | hp2 | a0002 | c0008 | t0002 | g0300 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA19080 | hp1 | a0001 | c0001 | t0004 | g0223 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA19080 | hp2 | a0001 | c0002 | t0001 | g0127 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA19081 | hp1 | a0001 | c0004 | t0005 | g0023 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA19081 | hp2 | a0001 | c0003 | t0002 | g0270 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA19083 | hp2 | a0001 | c0001 | t0004 | g0241 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA19084 | hp1 | a0001 | c0002 | t0001 | g0103 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0356 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA19085 | hp2 | a0001 | c0002 | t0001 | g0167 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA19087 | hp1 | a0001 | c0001 | t0006 | g0207 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA19087 | hp2 | a0001 | c0019 | t0001 | g0078 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA19090 | hp1 | a0002 | c0008 | t0002 | g0301 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA19090 | hp2 | a0001 | c0001 | t0004 | g0239 | EAS | JPT | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | YRI | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA19240 | hp2 | a0001 | c0001 | t0006 | g0199 | AFR | YRI | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA20129 | hp1 | a0001 | c0001 | t0004 | g0229 | AFR | ASW | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA20129 | hp2 | a0001 | c0002 | t0001 | g0066 | AFR | ASW | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA20752 | hp1 | a0001 | c0003 | t0042 | g0286 | EUR | TSI | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0325 | EUR | TSI | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0133 | EUR | TSI | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | GIH | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA20905 | hp2 | a0008 | c0018 | t0004 | g0228 | SAS | GIH | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0091 | AMR | CLM | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0323 | AMR | CLM | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | ACB | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG02109 | hp2 | a0001 | c0006 | t0009 | g0249 | AFR | ACB | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG02559 | hp1 | a0001 | c0001 | t0006 | g0201 | AFR | ACB | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG02559 | hp2 | a0001 | c0005 | t0007 | g0186 | AFR | ACB | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG03471 | hp1 | a0001 | c0001 | t0046 | g0008 | AFR | MSL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0361 | AFR | MSL | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG06807 | hp1 | a0001 | c0004 | t0008 | g0175 | AFR | USA | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | USA | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | USA | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA20300 | hp2 | a0001 | c0001 | t0016 | g0192 | AFR | USA | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA21309 | hp1 | a0001 | c0001 | t0014 | g0218 | AFR | LWK | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | LWK | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0003 | t0002 | g0259 | REF | REF | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| homoSapiens_grch38 | hp1 | a0001 | c0004 | t0019 | g0171 | REF | REF | NUP93_chr16_56725129_56855286 | NUP93 | chr16 | 56725129 | 56855286 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:56748383
|
C | T | 1 | a0003 | 1 | HG02451.hp2 | missense_variant | MODERATE | c.136C>T | p.Arg46Cys | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/22 | 233/8234 | 136/2460 | 46/819 | chr16 | 56748383 | ||
| chr16:56758644
|
A | G | 1 | a0004 | 1 | HG04204.hp2 | missense_variant | MODERATE | c.286A>G | p.Thr96Ala | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/22 | 383/8234 | 286/2460 | 96/819 | chr16 | 56758644 | ||
| chr16:56821545
|
G | C | 1 | a0005 | 1 | HG02132.hp2 | missense_variant | MODERATE | c.606G>C | p.Gln202His | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 7/22 | 703/8234 | 606/2460 | 202/819 | chr16 | 56821545 | ||
| chr16:56823768
|
C | T | 1 | a0006 | 1 | NA18522.hp2 | missense_variant | MODERATE | c.716C>T | p.Thr239Met | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/22 | 813/8234 | 716/2460 | 239/819 | chr16 | 56823768 | ||
| chr16:56823842
|
C | G | 1 | a0007 | 1 | HG02965.hp1 | missense_variant | MODERATE | c.790C>G | p.Gln264Glu | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/22 | 887/8234 | 790/2460 | 264/819 | chr16 | 56823842 | ||
| chr16:56830600
|
G | A | 1 | a0010 | 1 | HG03688.hp1 | missense_variant | MODERATE | c.1000G>A | p.Ala334Thr | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 10/22 | 1097/8234 | 1000/2460 | 334/819 | chr16 | 56830600 | ||
| chr16:56831966
|
A | G | 1 | a0008 | 1 | NA20905.hp2 | missense_variant | MODERATE | c.1210A>G | p.Ser404Gly | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 11/22 | 1307/8234 | 1210/2460 | 404/819 | chr16 | 56831966 | ||
| chr16:56836715
|
A | C | 1 | a0002 | 4 | NA18954.hp1 NA18966.hp1 NA19079.hp2 others(1): Show |
missense_variant&splice_region_variant | MODERATE | c.1897A>C | p.Lys633Gln | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 17/22 | 1994/8234 | 1897/2460 | 633/819 | chr16 | 56836715 | ||
| chr16:56837649
|
C | A | 1 | a0009 | 1 | HG01978.hp2 | missense_variant | MODERATE | c.1941C>A | p.Ser647Arg | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 18/22 | 2038/8234 | 1941/2460 | 647/819 | chr16 | 56837649 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:56748364
|
G | A | 1 | a0001c0006 | 5 | HG02109.hp2 HG02615.hp2 HG02818.hp2 others(2): Show |
synonymous_variant | LOW | c.117G>A | p.Ala39Ala | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/22 | 214/8234 | 117/2460 | 39/819 | chr16 | 56748364 | ||
| chr16:56805527
|
C | T | 3 | a0001c0003a0002c0008a0005c0022 | 47 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(44): Show |
synonymous_variant | LOW | c.384C>T | p.Tyr128Tyr | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/22 | 481/8234 | 384/2460 | 128/819 | chr16 | 56805527 | ||
| chr16:56818732
|
G | A | 1 | a0001c0005 | 8 | HG02257.hp2 HG02559.hp2 HG02717.hp2 others(5): Show |
synonymous_variant | LOW | c.558G>A | p.Ala186Ala | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 6/22 | 655/8234 | 558/2460 | 186/819 | chr16 | 56818732 | ||
| chr16:56821584
|
C | G | 21 | a0001c0001a0001c0002a0001c0003others(18): Show | 336 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(333): Show |
synonymous_variant | LOW | c.645C>G | p.Leu215Leu | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 7/22 | 742/8234 | 645/2460 | 215/819 | chr16 | 56821584 | ||
| chr16:56823748
|
C | T | 1 | a0001c0011 | 2 | HG02895.hp1 HG02897.hp2 |
synonymous_variant | LOW | c.696C>T | p.Asp232Asp | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/22 | 793/8234 | 696/2460 | 232/819 | chr16 | 56823748 | ||
| chr16:56823841
|
G | A | 1 | a0001c0007 | 4 | HG01891.hp1 HG02145.hp2 HG02886.hp2 others(1): Show |
synonymous_variant | LOW | c.789G>A | p.Glu263Glu | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/22 | 886/8234 | 789/2460 | 263/819 | chr16 | 56823841 | ||
| chr16:56830560
|
G | A | 1 | a0001c0012 | 1 | NA19066.hp1 | synonymous_variant | LOW | c.960G>A | p.Ala320Ala | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 10/22 | 1057/8234 | 960/2460 | 320/819 | chr16 | 56830560 | ||
| chr16:56831956
|
C | T | 1 | a0001c0019 | 1 | NA19087.hp2 | synonymous_variant | LOW | c.1200C>T | p.Thr400Thr | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 11/22 | 1297/8234 | 1200/2460 | 400/819 | chr16 | 56831956 | ||
| chr16:56832315
|
C | T | 1 | a0001c0017 | 1 | HG03540.hp2 | synonymous_variant | LOW | c.1272C>T | p.Asp424Asp | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 12/22 | 1369/8234 | 1272/2460 | 424/819 | chr16 | 56832315 | ||
| chr16:56833279
|
G | A | 1 | a0001c0014 | 1 | HG02895.hp2 | synonymous_variant | LOW | c.1410G>A | p.Ala470Ala | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 13/22 | 1507/8234 | 1410/2460 | 470/819 | chr16 | 56833279 | ||
| chr16:56833348
|
A | G | 1 | a0001c0010 | 2 | HG03139.hp2 HG03579.hp1 |
synonymous_variant | LOW | c.1479A>G | p.Ala493Ala | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 13/22 | 1576/8234 | 1479/2460 | 493/819 | chr16 | 56833348 | ||
| chr16:56834397
|
C | T | 2 | a0001c0009a0003c0024 | 3 | HG02451.hp2 HG03209.hp1 HG03516.hp2 |
synonymous_variant | LOW | c.1692C>T | p.Asn564Asn | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 15/22 | 1789/8234 | 1692/2460 | 564/819 | chr16 | 56834397 | ||
| chr16:56839583
|
C | T | 5 | a0001c0002a0001c0011a0001c0012others(2): Show | 73 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(70): Show |
synonymous_variant | LOW | c.2199C>T | p.Ala733Ala | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 20/22 | 2296/8234 | 2199/2460 | 733/819 | chr16 | 56839583 | ||
| chr16:56844549
|
A | G | 1 | a0001c0016 | 1 | HG03704.hp1 | synonymous_variant | LOW | c.2400A>G | p.Pro800Pro | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 2497/8234 | 2400/2460 | 800/819 | chr16 | 56844549 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:56730172
|
C | G | 2 | a0001c0001t0011a0001c0001t0046 | 6 | HG01884.hp1 HG02630.hp1 HG02970.hp2 others(3): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-54C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/22 | chr16 | 56730172 | ||||||
| chr16:56844630
|
C | G | 1 | a0001c0004t0045 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*21C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 21 | chr16 | 56844630 | |||||
| chr16:56844637
|
G | A | 2 | a0001c0001t0011a0001c0001t0046 | 6 | HG01884.hp1 HG02630.hp1 HG02970.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*28G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 28 | chr16 | 56844637 | |||||
| chr16:56844729
|
T | C | 1 | a0001c0001t0025 | 1 | NA19057.hp2 | 3_prime_UTR_variant | MODIFIER | c.*120T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 120 | chr16 | 56844729 | |||||
| chr16:56844802
|
T | TC | 58 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(55): Show | 364 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(361): Show |
3_prime_UTR_variant | MODIFIER | c.*194dupC | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 195 | INFO_REALIGN_3_PRIME | chr16 | 56844802 | ||||
| chr16:56844823
|
T | C | 1 | a0001c0001t0013 | 3 | HG03041.hp1 HG03225.hp1 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*214T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 214 | chr16 | 56844823 | |||||
| chr16:56845150
|
A | G | 2 | a0001c0001t0011a0001c0001t0046 | 6 | HG01884.hp1 HG02630.hp1 HG02970.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*541A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 541 | chr16 | 56845150 | |||||
| chr16:56845284
|
A | G | 1 | a0001c0001t0043 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*675A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 675 | chr16 | 56845284 | |||||
| chr16:56845290
|
T | C | 4 | a0001c0001t0003a0001c0001t0027a0001c0001t0028others(1): Show | 29 | HG00323.hp1 HG00639.hp1 HG01070.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*681T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 681 | chr16 | 56845290 | |||||
| chr16:56845302
|
C | T | 2 | a0001c0009t0018a0003c0024t0018 | 3 | HG02451.hp2 HG03209.hp1 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*693C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 693 | chr16 | 56845302 | |||||
| chr16:56845350
|
C | A | 1 | a0001c0003t0020 | 2 | HG01168.hp1 HG01169.hp1 |
3_prime_UTR_variant | MODIFIER | c.*741C>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 741 | chr16 | 56845350 | |||||
| chr16:56845364
|
C | T | 1 | a0001c0003t0042 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*755C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 755 | chr16 | 56845364 | |||||
| chr16:56845409
|
C | T | 1 | a0001c0002t0041 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*800C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 800 | chr16 | 56845409 | |||||
| chr16:56845413
|
C | T | 1 | a0001c0001t0023 | 2 | NA18991.hp1 NA19068.hp2 |
3_prime_UTR_variant | MODIFIER | c.*804C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 804 | chr16 | 56845413 | |||||
| chr16:56845516
|
C | A | 1 | a0001c0001t0014 | 3 | HG01884.hp2 HG03453.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*907C>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 907 | chr16 | 56845516 | |||||
| chr16:56845559
|
G | T | 2 | a0001c0009t0018a0003c0024t0018 | 3 | HG02451.hp2 HG03209.hp1 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*950G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 950 | chr16 | 56845559 | |||||
| chr16:56845620
|
G | A | 1 | a0001c0001t0046 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1011G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 1011 | chr16 | 56845620 | |||||
| chr16:56845659
|
G | C | 41 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(38): Show | 202 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(199): Show |
3_prime_UTR_variant | MODIFIER | c.*1050G>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 1050 | chr16 | 56845659 | |||||
| chr16:56845726
|
G | C | 7 | a0001c0001t0003a0001c0001t0007a0001c0001t0027others(4): Show | 41 | HG00323.hp1 HG00639.hp1 HG00642.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*1117G>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 1117 | chr16 | 56845726 | |||||
| chr16:56845948
|
C | G | 4 | a0001c0001t0004a0001c0001t0035a0008c0018t0004others(1): Show | 24 | HG00408.hp2 HG00597.hp2 HG00733.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*1339C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 1339 | chr16 | 56845948 | |||||
| chr16:56846187
|
GATCACC | G | 9 | a0001c0001t0003a0001c0001t0007a0001c0001t0016others(6): Show | 45 | HG00323.hp1 HG00639.hp1 HG00642.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*1579_*1584delATCA others(2): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 1579 | chr16 | 56846187 | |||||
| chr16:56846236
|
C | T | 1 | a0001c0001t0034 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1627C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 1627 | chr16 | 56846236 | |||||
| chr16:56846239
|
C | T | 1 | a0001c0007t0012 | 4 | HG01891.hp1 HG02145.hp2 HG02886.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1630C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 1630 | chr16 | 56846239 | |||||
| chr16:56846246
|
A | G | 22 | a0001c0001t0001a0001c0001t0017a0001c0001t0023others(19): Show | 176 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(173): Show |
3_prime_UTR_variant | MODIFIER | c.*1637A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 1637 | chr16 | 56846246 | |||||
| chr16:56846493
|
T | C | 9 | a0001c0001t0003a0001c0001t0007a0001c0001t0016others(6): Show | 45 | HG00323.hp1 HG00639.hp1 HG00642.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*1884T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 1884 | chr16 | 56846493 | |||||
| chr16:56846497
|
G | T | 1 | a0001c0001t0035 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1888G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 1888 | chr16 | 56846497 | |||||
| chr16:56846536
|
C | T | 2 | a0001c0001t0011a0001c0001t0046 | 6 | HG01884.hp1 HG02630.hp1 HG02970.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1927C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 1927 | chr16 | 56846536 | |||||
| chr16:56846659
|
G | A | 1 | a0001c0001t0029 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2050G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 2050 | chr16 | 56846659 | |||||
| chr16:56846700
|
G | T | 2 | a0001c0009t0018a0003c0024t0018 | 3 | HG02451.hp2 HG03209.hp1 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2091G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 2091 | chr16 | 56846700 | |||||
| chr16:56846924
|
C | G | 1 | a0001c0001t0028 | 1 | HG02027.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2315C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 2315 | chr16 | 56846924 | |||||
| chr16:56846925
|
T | G | 1 | a0001c0001t0028 | 1 | HG02027.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2316T>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 2316 | chr16 | 56846925 | |||||
| chr16:56846930
|
T | C | 59 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(56): Show | 366 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(363): Show |
3_prime_UTR_variant | MODIFIER | c.*2321T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 2321 | chr16 | 56846930 | |||||
| chr16:56846969
|
AGGTTCTT others(13): Show |
A | 9 | a0001c0001t0003a0001c0001t0007a0001c0001t0016others(6): Show | 45 | HG00323.hp1 HG00639.hp1 HG00642.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*2364_*2383delTCTT others(16): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 2364 | INFO_REALIGN_3_PRIME | chr16 | 56846969 | ||||
| chr16:56847045
|
G | A | 1 | a0001c0001t0016 | 3 | HG02258.hp2 HG03130.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2436G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 2436 | chr16 | 56847045 | |||||
| chr16:56847363
|
A | G | 1 | a0001c0010t0033 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2754A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 2754 | chr16 | 56847363 | |||||
| chr16:56847375
|
C | T | 1 | a0001c0003t0032 | 1 | HG02080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2766C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 2766 | chr16 | 56847375 | |||||
| chr16:56847479
|
A | G | 4 | a0001c0004t0005a0001c0004t0015a0001c0009t0018others(1): Show | 28 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*2870A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 2870 | chr16 | 56847479 | |||||
| chr16:56847518
|
C | G | 1 | a0001c0002t0040 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2909C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 2909 | chr16 | 56847518 | |||||
| chr16:56847732
|
T | A | 59 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(56): Show | 366 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(363): Show |
3_prime_UTR_variant | MODIFIER | c.*3123T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 3123 | chr16 | 56847732 | |||||
| chr16:56847804
|
C | T | 1 | a0001c0001t0031 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3195C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 3195 | chr16 | 56847804 | |||||
| chr16:56847822
|
G | A | 1 | a0001c0003t0021 | 2 | HG00423.hp1 HG02074.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3213G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 3213 | chr16 | 56847822 | |||||
| chr16:56847829
|
C | G | 1 | a0001c0001t0027 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3220C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 3220 | chr16 | 56847829 | |||||
| chr16:56847948
|
A | G | 1 | a0001c0001t0013 | 3 | HG03041.hp1 HG03225.hp1 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3339A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 3339 | chr16 | 56847948 | |||||
| chr16:56848237
|
G | C | 2 | a0001c0001t0011a0001c0001t0046 | 6 | HG01884.hp1 HG02630.hp1 HG02970.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3628G>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 3628 | chr16 | 56848237 | |||||
| chr16:56848277
|
C | G | 1 | a0001c0006t0009 | 5 | HG02109.hp2 HG02615.hp2 HG02818.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3668C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 3668 | chr16 | 56848277 | |||||
| chr16:56848298
|
G | A | 1 | a0001c0004t0044 | 1 | HG00099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3689G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 3689 | chr16 | 56848298 | |||||
| chr16:56848313
|
G | T | 1 | a0004c0023t0026 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3704G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 3704 | chr16 | 56848313 | |||||
| chr16:56848649
|
A | G | 1 | a0001c0001t0029 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4040A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 4040 | chr16 | 56848649 | |||||
| chr16:56848891
|
G | GT | 1 | a0001c0006t0009 | 5 | HG02109.hp2 HG02615.hp2 HG02818.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4289dupT | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 4290 | INFO_REALIGN_3_PRIME | chr16 | 56848891 | ||||
| chr16:56848952
|
AAG | A | 4 | a0001c0001t0003a0001c0001t0027a0001c0001t0028others(1): Show | 29 | HG00323.hp1 HG00639.hp1 HG01070.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*4346_*4347delAG | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 4346 | INFO_REALIGN_3_PRIME | chr16 | 56848952 | ||||
| chr16:56848958
|
A | G | 1 | a0001c0006t0009 | 5 | HG02109.hp2 HG02615.hp2 HG02818.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4349A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 4349 | chr16 | 56848958 | |||||
| chr16:56849027
|
C | G | 1 | a0001c0001t0017 | 3 | HG00621.hp2 NA18969.hp1 NA19011.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4418C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 4418 | chr16 | 56849027 | |||||
| chr16:56849057
|
T | C | 1 | a0001c0001t0014 | 3 | HG01884.hp2 HG03453.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4448T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 4448 | chr16 | 56849057 | |||||
| chr16:56849063
|
G | A | 1 | a0001c0001t0029 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4454G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 4454 | chr16 | 56849063 | |||||
| chr16:56849172
|
T | C | 4 | a0001c0001t0004a0001c0001t0035a0008c0018t0004others(1): Show | 24 | HG00408.hp2 HG00597.hp2 HG00733.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*4563T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 4563 | chr16 | 56849172 | |||||
| chr16:56849350
|
C | T | 1 | a0001c0001t0039 | 1 | NA18946.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4741C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 4741 | chr16 | 56849350 | |||||
| chr16:56849393
|
A | G | 1 | a0001c0001t0038 | 1 | NA18988.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4784A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 4784 | chr16 | 56849393 | |||||
| chr16:56849510
|
G | A | 1 | a0001c0001t0036 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4901G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 4901 | chr16 | 56849510 | |||||
| chr16:56849522
|
T | A | 1 | a0001c0002t0037 | 1 | HG01981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4913T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 4913 | chr16 | 56849522 | |||||
| chr16:56849526
|
G | A | 40 | a0001c0001t0001a0001c0001t0002a0001c0001t0013others(37): Show | 267 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(264): Show |
3_prime_UTR_variant | MODIFIER | c.*4917G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 4917 | chr16 | 56849526 | |||||
| chr16:56849574
|
G | C | 1 | a0004c0023t0026 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4965G>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 4965 | chr16 | 56849574 | |||||
| chr16:56849623
|
G | C | 4 | a0001c0001t0004a0001c0001t0035a0008c0018t0004others(1): Show | 24 | HG00408.hp2 HG00597.hp2 HG00733.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*5014G>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 5014 | chr16 | 56849623 | |||||
| chr16:56849649
|
GACACT | G | 1 | a0001c0004t0005 | 22 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*5041_*5045delACAC others(1): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 5041 | chr16 | 56849649 | |||||
| chr16:56849748
|
C | T | 2 | a0001c0002t0010a0001c0002t0041 | 6 | HG00733.hp2 HG01069.hp2 HG01167.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5139C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 5139 | chr16 | 56849748 | |||||
| chr16:56849792
|
C | T | 3 | a0001c0002t0010a0001c0002t0041a0001c0003t0030 | 7 | HG00733.hp2 HG01069.hp2 HG01167.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*5183C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 5183 | chr16 | 56849792 | |||||
| chr16:56849797
|
G | C | 21 | a0001c0001t0001a0001c0001t0017a0001c0001t0023others(18): Show | 173 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(170): Show |
3_prime_UTR_variant | MODIFIER | c.*5188G>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 5188 | chr16 | 56849797 | |||||
| chr16:56850012
|
A | G | 21 | a0001c0001t0001a0001c0001t0017a0001c0001t0023others(18): Show | 173 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(170): Show |
3_prime_UTR_variant | MODIFIER | c.*5403A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 5403 | chr16 | 56850012 | |||||
| chr16:56850169
|
G | C | 9 | a0001c0001t0002a0001c0003t0002a0001c0003t0020others(6): Show | 51 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*5560G>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 22/22 | 5560 | chr16 | 56850169 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:56730269
|
C | A | 1 | a0001c0001t0001g0003 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-15+58C>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56730269 | ||||||
| chr16:56730563
|
A | G | 29 | a0001c0001t0003g0348a0001c0001t0003g0349a0001c0001t0003g0350others(26): Show | 29 | HG00323.hp1 HG00639.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.-15+352A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56730563 | ||||||
| chr16:56730566
|
C | T | 3 | a0001c0007t0012g0345a0001c0007t0012g0346a0001c0007t0012g0347 | 3 | HG02145.hp2 HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-15+355C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56730566 | ||||||
| chr16:56730648
|
C | T | 1 | a0001c0002t0001g0344 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-15+437C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56730648 | ||||||
| chr16:56730749
|
A | T | 1 | a0001c0001t0001g0343 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-15+538A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56730749 | ||||||
| chr16:56730773
|
C | T | 2 | a0001c0001t0017g0341a0001c0001t0017g0342 | 2 | NA18969.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.-15+562C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56730773 | ||||||
| chr16:56730971
|
C | T | 1 | a0001c0001t0007g0340 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-15+760C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56730971 | ||||||
| chr16:56731087
|
A | G | 1 | a0001c0002t0001g0339 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-15+876A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56731087 | ||||||
| chr16:56731168
|
C | T | 97 | a0001c0001t0001g0002a0001c0001t0001g0302a0001c0001t0001g0303others(94): Show | 98 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.-15+957C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56731168 | ||||||
| chr16:56731191
|
T | C | 271 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0045others(268): Show | 273 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(270): Show |
intron_variant | MODIFIER | c.-15+980T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56731191 | ||||||
| chr16:56731202
|
C | T | 1 | a0001c0002t0001g0170 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-15+991C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56731202 | ||||||
| chr16:56731314
|
C | T | 168 | a0001c0001t0001g0003a0001c0001t0001g0045a0001c0001t0001g0046others(165): Show | 169 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.-15+1103C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56731314 | ||||||
| chr16:56731434
|
C | T | 3 | a0001c0007t0012g0345a0001c0007t0012g0346a0001c0007t0012g0347 | 3 | HG02145.hp2 HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-15+1223C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56731434 | ||||||
| chr16:56731650
|
C | T | 41 | a0001c0001t0001g0002a0001c0001t0001g0302a0001c0001t0001g0303others(38): Show | 42 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.-15+1439C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56731650 | ||||||
| chr16:56731774
|
A | T | 131 | a0001c0001t0001g0003a0001c0001t0001g0045a0001c0001t0001g0046others(128): Show | 132 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.-15+1563A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56731774 | ||||||
| chr16:56731890
|
C | T | 1 | a0001c0001t0001g0169 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-15+1679C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56731890 | ||||||
| chr16:56731915
|
A | G | 2 | a0001c0001t0001g0337a0001c0001t0001g0338 | 2 | HG02155.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.-15+1704A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56731915 | ||||||
| chr16:56732036
|
G | A | 1 | a0001c0002t0001g0044 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-15+1825G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56732036 | ||||||
| chr16:56732119
|
T | A | 2 | a0001c0001t0001g0045a0001c0001t0001g0046 | 2 | HG01433.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.-15+1908T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56732119 | ||||||
| chr16:56732146
|
C | T | 1 | a0001c0001t0029g0245 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-15+1935C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56732146 | ||||||
| chr16:56732522
|
G | A | 1 | a0003c0024t0018g0010 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-15+2311G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56732522 | ||||||
| chr16:56732576
|
C | T | 3 | a0001c0001t0001g0335a0001c0001t0001g0336a0001c0002t0001g0168 | 3 | HG00408.hp1 HG03017.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.-15+2365C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56732576 | ||||||
| chr16:56732581
|
A | G | 3 | a0001c0007t0012g0345a0001c0007t0012g0346a0001c0007t0012g0347 | 3 | HG02145.hp2 HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-15+2370A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56732581 | ||||||
| chr16:56732622
|
C | T | 1 | a0001c0002t0001g0167 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.-15+2411C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56732622 | ||||||
| chr16:56732692
|
G | A | 1 | a0001c0001t0001g0337 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-15+2481G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56732692 | ||||||
| chr16:56732919
|
C | T | 93 | a0001c0001t0003g0348a0001c0001t0003g0349a0001c0001t0003g0350others(90): Show | 93 | HG00323.hp1 HG00408.hp2 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.-15+2708C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56732919 | ||||||
| chr16:56733179
|
G | A | 45 | a0001c0001t0003g0348a0001c0001t0003g0349a0001c0001t0003g0350others(42): Show | 45 | HG00323.hp1 HG00639.hp1 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.-15+2968G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56733179 | ||||||
| chr16:56733213
|
T | A | 45 | a0001c0001t0003g0348a0001c0001t0003g0349a0001c0001t0003g0350others(42): Show | 45 | HG00323.hp1 HG00639.hp1 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.-15+3002T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56733213 | ||||||
| chr16:56733369
|
G | A | 2 | a0001c0003t0002g0246a0001c0003t0002g0247 | 2 | NA18939.hp1 NA18940.hp1 |
intron_variant | MODIFIER | c.-15+3158G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56733369 | ||||||
| chr16:56733424
|
AAGTAGAG others(1): Show |
A | 30 | a0001c0004t0005g0020a0001c0004t0005g0021a0001c0004t0005g0022others(27): Show | 30 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.-15+3214_-15+3221d others(10): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56733424 | ||||||
| chr16:56733469
|
G | A | 1 | a0001c0003t0002g0248 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-15+3258G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56733469 | ||||||
| chr16:56733687
|
G | T | 97 | a0001c0001t0001g0002a0001c0001t0001g0302a0001c0001t0001g0303others(94): Show | 98 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.-15+3476G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56733687 | ||||||
| chr16:56733873
|
G | A | 1 | a0001c0002t0001g0168 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-15+3662G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56733873 | ||||||
| chr16:56733890
|
C | T | 45 | a0001c0001t0003g0348a0001c0001t0003g0349a0001c0001t0003g0350others(42): Show | 45 | HG00323.hp1 HG00639.hp1 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.-15+3679C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56733890 | ||||||
| chr16:56733900
|
A | C | 3 | a0001c0001t0013g0012a0001c0001t0013g0013a0001c0001t0013g0014 | 3 | HG03041.hp1 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-15+3689A>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56733900 | ||||||
| chr16:56733916
|
T | A | 1 | a0001c0006t0009g0249 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-15+3705T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56733916 | ||||||
| chr16:56734635
|
CAT | C | 131 | a0001c0001t0001g0003a0001c0001t0001g0045a0001c0001t0001g0046others(128): Show | 132 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.-15+4425_-15+4426d others(4): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56734635 | ||||||
| chr16:56734967
|
G | A | 1 | a0001c0001t0003g0348 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-15+4756G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56734967 | ||||||
| chr16:56735103
|
A | G | 24 | a0001c0004t0005g0020a0001c0004t0005g0021a0001c0004t0005g0022others(21): Show | 24 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(21): Show |
intron_variant | MODIFIER | c.-15+4892A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56735103 | ||||||
| chr16:56735193
|
G | C | 2 | a0001c0001t0003g0349a0001c0001t0003g0350 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.-15+4982G>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56735193 | ||||||
| chr16:56735543
|
C | T | 1 | a0001c0001t0001g0166 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-15+5332C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56735543 | ||||||
| chr16:56735549
|
A | C | 4 | a0002c0008t0002g0298a0002c0008t0002g0299a0002c0008t0002g0300others(1): Show | 4 | NA18954.hp1 NA18966.hp1 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15+5338A>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56735549 | ||||||
| chr16:56735582
|
C | T | 1 | a0001c0001t0001g0334 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-15+5371C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56735582 | ||||||
| chr16:56735721
|
G | C | 1 | a0001c0007t0012g0345 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-15+5510G>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56735721 | ||||||
| chr16:56735828
|
C | CA | 134 | a0001c0001t0001g0003a0001c0001t0001g0045a0001c0001t0001g0046others(131): Show | 135 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.-15+5632dupA | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56735828 | |||||
| chr16:56735828
|
C | CAA | 7 | a0001c0002t0001g0051a0001c0002t0001g0167a0001c0002t0010g0048others(4): Show | 7 | HG01069.hp2 HG01167.hp1 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.-15+5631_-15+5632d others(4): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56735828 | |||||
| chr16:56735828
|
CA | C | 6 | a0001c0001t0001g0333a0001c0001t0003g0375a0001c0001t0003g0376others(3): Show | 6 | HG01167.hp2 HG01168.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.-15+5632delA | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56735828 | |||||
| chr16:56735990
|
A | G | 53 | a0001c0001t0002g0284a0001c0001t0002g0292a0001c0001t0002g0295others(50): Show | 53 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.-15+5779A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56735990 | ||||||
| chr16:56736059
|
G | T | 1 | a0001c0002t0001g0165 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-15+5848G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56736059 | ||||||
| chr16:56736081
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-15+5870G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56736081 | ||||||
| chr16:56736166
|
C | T | 1 | a0001c0002t0001g0164 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-15+5955C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56736166 | ||||||
| chr16:56736186
|
C | T | 2 | a0001c0001t0001g0162a0001c0001t0001g0163 | 2 | HG01891.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.-15+5975C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56736186 | ||||||
| chr16:56736258
|
G | A | 27 | a0001c0004t0005g0020a0001c0004t0005g0021a0001c0004t0005g0022others(24): Show | 27 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(24): Show |
intron_variant | MODIFIER | c.-15+6047G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56736258 | ||||||
| chr16:56736328
|
A | G | 1 | a0001c0004t0005g0043 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-15+6117A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56736328 | ||||||
| chr16:56736615
|
G | T | 1 | a0001c0004t0005g0021 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-15+6404G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56736615 | ||||||
| chr16:56736735
|
G | A | 3 | a0001c0007t0012g0345a0001c0007t0012g0346a0001c0007t0012g0347 | 3 | HG02145.hp2 HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-15+6524G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56736735 | ||||||
| chr16:56736739
|
A | C | 2 | a0001c0007t0012g0346a0001c0007t0012g0347 | 2 | HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-15+6528A>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56736739 | ||||||
| chr16:56737397
|
T | C | 1 | a0001c0007t0012g0346 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-15+7186T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56737397 | ||||||
| chr16:56737531
|
A | G | 30 | a0001c0004t0005g0020a0001c0004t0005g0021a0001c0004t0005g0022others(27): Show | 30 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.-15+7320A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56737531 | ||||||
| chr16:56737613
|
C | A | 24 | a0001c0004t0005g0020a0001c0004t0005g0021a0001c0004t0005g0022others(21): Show | 24 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(21): Show |
intron_variant | MODIFIER | c.-15+7402C>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56737613 | ||||||
| chr16:56737622
|
CT | C | 214 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0045others(211): Show | 216 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.-15+7423delT | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56737622 | |||||
| chr16:56737720
|
CTG | C | 30 | a0001c0004t0005g0020a0001c0004t0005g0021a0001c0004t0005g0022others(27): Show | 30 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.-15+7516_-15+7517d others(4): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56737720 | |||||
| chr16:56737879
|
T | C | 69 | a0001c0001t0003g0348a0001c0001t0003g0349a0001c0001t0003g0350others(66): Show | 69 | HG00323.hp1 HG00639.hp1 HG00642.hp2 others(66): Show |
intron_variant | MODIFIER | c.-15+7668T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56737879 | ||||||
| chr16:56738245
|
T | C | 131 | a0001c0001t0001g0003a0001c0001t0001g0045a0001c0001t0001g0046others(128): Show | 132 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.-15+8034T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56738245 | ||||||
| chr16:56738340
|
T | C | 1 | a0006c0021t0001g0011 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-15+8129T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56738340 | ||||||
| chr16:56738428
|
T | G | 14 | a0001c0004t0005g0022a0001c0004t0005g0023a0001c0004t0005g0024others(11): Show | 14 | HG00741.hp2 HG01099.hp2 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.-15+8217T>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56738428 | ||||||
| chr16:56738485
|
T | C | 3 | a0001c0009t0018g0018a0001c0009t0018g0019a0003c0024t0018g0010 | 3 | HG02451.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-15+8274T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56738485 | ||||||
| chr16:56738541
|
T | C | 364 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0045others(361): Show | 366 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(363): Show |
intron_variant | MODIFIER | c.-15+8330T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56738541 | ||||||
| chr16:56738600
|
A | G | 1 | a0001c0009t0018g0019 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-15+8389A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56738600 | ||||||
| chr16:56738643
|
CAAT | C | 6 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(3): Show | 6 | HG01884.hp1 HG02630.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.-15+8433_-15+8435d others(5): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56738643 | ||||||
| chr16:56738672
|
T | G | 3 | a0001c0005t0007g0183a0001c0005t0007g0184a0001c0005t0007g0185 | 3 | HG02257.hp2 HG02809.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-15+8461T>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56738672 | ||||||
| chr16:56738742
|
T | A | 2 | a0001c0001t0003g0351a0001c0001t0003g0352 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-15+8531T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56738742 | ||||||
| chr16:56738745
|
A | T | 1 | a0001c0001t0001g0161 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-15+8534A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56738745 | ||||||
| chr16:56738764
|
G | T | 3 | a0001c0001t0014g0217a0001c0001t0014g0218a0001c0001t0014g0219 | 3 | HG01884.hp2 HG03453.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-15+8553G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56738764 | ||||||
| chr16:56738835
|
A | T | 3 | a0001c0001t0013g0012a0001c0001t0013g0013a0001c0001t0013g0014 | 3 | HG03041.hp1 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-15+8624A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56738835 | ||||||
| chr16:56738893
|
G | T | 132 | a0001c0001t0001g0003a0001c0001t0001g0045a0001c0001t0001g0046others(129): Show | 133 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.-15+8682G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56738893 | ||||||
| chr16:56738945
|
C | CT | 94 | a0001c0001t0001g0002a0001c0001t0001g0045a0001c0001t0001g0302others(91): Show | 95 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.-15+8750dupT | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56738945 | |||||
| chr16:56738945
|
C | CTT | 92 | a0001c0001t0001g0003a0001c0001t0001g0046a0001c0001t0001g0114others(89): Show | 93 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.-15+8749_-15+8750d others(4): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56738945 | |||||
| chr16:56738945
|
C | CTTT | 32 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(29): Show | 32 | HG00099.hp1 HG00621.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.-15+8748_-15+8750d others(5): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56738945 | |||||
| chr16:56738945
|
C | CTTTT | 8 | a0001c0001t0001g0052a0001c0001t0001g0155a0001c0001t0001g0156others(5): Show | 8 | HG02109.hp1 HG02257.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.-15+8747_-15+8750d others(6): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56738945 | |||||
| chr16:56738945
|
CT | C | 54 | a0001c0001t0004g0198a0001c0001t0004g0220a0001c0001t0004g0221others(51): Show | 54 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.-15+8750delT | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56738945 | |||||
| chr16:56739130
|
C | T | 4 | a0001c0001t0002g0295a0001c0009t0018g0018a0001c0009t0018g0019others(1): Show | 4 | HG02451.hp2 HG02922.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-15+8919C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739130 | ||||||
| chr16:56739171
|
G | A | 2 | a0001c0001t0001g0162a0001c0001t0001g0163 | 2 | HG01891.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.-15+8960G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739171 | ||||||
| chr16:56739257
|
G | A | 1 | a0001c0001t0004g0220 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-14-8977G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739257 | ||||||
| chr16:56739322
|
G | A | 3 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055 | 3 | NA18939.hp2 NA18964.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.-14-8912G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739322 | ||||||
| chr16:56739326
|
C | T | 1 | a0001c0004t0005g0035 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-14-8908C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739326 | ||||||
| chr16:56739327
|
G | A | 6 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(3): Show | 6 | HG01884.hp1 HG02630.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.-14-8907G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739327 | ||||||
| chr16:56739339
|
A | G | 1 | a0001c0001t0034g0196 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-14-8895A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739339 | ||||||
| chr16:56739350
|
C | CCCCCCAA others(802): Show |
1 | a0001c0001t0001g0305 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-14-8879_-14-8878i others(811): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739350 | |||||
| chr16:56739350
|
C | CCCCCCCC others(835): Show |
11 | a0001c0001t0004g0220a0001c0001t0004g0221a0001c0001t0004g0222others(8): Show | 11 | HG00733.hp1 HG01175.hp1 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.-14-8864_-14-8863i others(844): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739350 | |||||
| chr16:56739350
|
C | CCCCCCCC others(786): Show |
2 | a0001c0001t0004g0231a0001c0001t0004g0232 | 2 | NA18952.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.-14-8864_-14-8863i others(795): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739350 | |||||
| chr16:56739350
|
C | CCCCCCCC others(836): Show |
1 | a0001c0001t0004g0233 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.-14-8864_-14-8863i others(845): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739350 | |||||
| chr16:56739350
|
C | CCCCCCCC others(836): Show |
3 | a0001c0001t0004g0234a0001c0001t0004g0236a0009c0015t0004g0235 | 3 | HG00408.hp2 HG01496.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.-14-8864_-14-8863i others(845): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739350 | |||||
| chr16:56739350
|
C | CCCCCCCC others(787): Show |
1 | a0001c0001t0004g0237 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-14-8864_-14-8863i others(796): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739350 | |||||
| chr16:56739350
|
C | CCCCCCCC others(835): Show |
3 | a0001c0001t0004g0238a0001c0001t0004g0239a0001c0001t0004g0240 | 3 | NA18959.hp2 NA18972.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.-14-8864_-14-8863i others(844): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739350 | |||||
| chr16:56739350
|
C | CCCCCCCC others(837): Show |
1 | a0001c0001t0004g0241 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-14-8864_-14-8863i others(846): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739350 | |||||
| chr16:56739350
|
C | CCCCCCCC others(657): Show |
1 | a0001c0001t0029g0245 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-14-8864_-14-8863i others(666): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739350 | |||||
| chr16:56739350
|
C | CCCCCCCC others(837): Show |
1 | a0001c0001t0004g0242 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-14-8864_-14-8863i others(846): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739350 | |||||
| chr16:56739350
|
C | CCCCCCCC others(835): Show |
1 | a0001c0001t0004g0198 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-14-8864_-14-8863i others(844): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739350 | |||||
| chr16:56739351
|
C | CCCCCCCA others(332): Show |
1 | a0001c0001t0003g0353 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-14-8864_-14-8863i others(341): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739351 | |||||
| chr16:56739351
|
C | CCCCCCCA others(332): Show |
43 | a0001c0001t0003g0348a0001c0001t0003g0349a0001c0001t0003g0350others(40): Show | 43 | HG00323.hp1 HG00639.hp1 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.-14-8864_-14-8863i others(341): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739351 | |||||
| chr16:56739351
|
C | CCCCCCCA others(332): Show |
3 | a0001c0001t0014g0217a0001c0001t0014g0218a0001c0001t0014g0219 | 3 | HG01884.hp2 HG03453.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-14-8864_-14-8863i others(341): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739351 | |||||
| chr16:56739351
|
C | CCCCCCCC others(333): Show |
20 | a0001c0001t0006g0199a0001c0001t0006g0200a0001c0001t0006g0201others(17): Show | 20 | HG01070.hp2 HG01168.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.-14-8877_-14-8876i others(342): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739351 | |||||
| chr16:56739351
|
C | T | 1 | a0001c0001t0034g0196 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-14-8883C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739351 | ||||||
| chr16:56739389
|
C | G | 1 | a0001c0001t0001g0130 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-14-8845C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739389 | ||||||
| chr16:56739389
|
C | T | 56 | a0001c0001t0001g0003a0001c0001t0001g0045a0001c0001t0001g0046others(53): Show | 56 | HG00099.hp1 HG00621.hp1 HG00735.hp1 others(53): Show |
intron_variant | MODIFIER | c.-14-8845C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739389 | ||||||
| chr16:56739397
|
T | C | 26 | a0001c0001t0001g0305a0001c0001t0004g0198a0001c0001t0004g0220others(23): Show | 26 | HG00140.hp2 HG00408.hp2 HG00597.hp2 others(23): Show |
intron_variant | MODIFIER | c.-14-8837T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739397 | ||||||
| chr16:56739401
|
C | A | 68 | a0001c0001t0003g0348a0001c0001t0003g0349a0001c0001t0003g0350others(65): Show | 68 | HG00323.hp1 HG00639.hp1 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.-14-8833C>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739401 | ||||||
| chr16:56739406
|
A | AACCTCCC others(673): Show |
1 | a0001c0001t0013g0012 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-14-8753_-14-8752i others(682): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739406 | |||||
| chr16:56739406
|
A | AACCTCCC others(673): Show |
2 | a0001c0001t0013g0013a0001c0001t0013g0014 | 2 | HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-14-8753_-14-8752i others(682): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739406 | |||||
| chr16:56739406
|
A | AACCTCCC others(855): Show |
1 | a0001c0004t0045g0182 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-14-8753_-14-8752i others(864): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739406 | |||||
| chr16:56739406
|
A | AACCTCCC others(676): Show |
3 | a0001c0007t0012g0345a0001c0007t0012g0346a0001c0007t0012g0347 | 3 | HG02145.hp2 HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-14-8753_-14-8752i others(685): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739406 | |||||
| chr16:56739406
|
A | AACCTCCC others(852): Show |
7 | a0001c0004t0008g0172a0001c0004t0008g0173a0001c0004t0008g0174others(4): Show | 7 | HG00741.hp1 HG01106.hp1 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.-14-8753_-14-8752i others(861): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739406 | |||||
| chr16:56739406
|
A | AACCTCCC others(852): Show |
1 | a0001c0004t0019g0180 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-14-8753_-14-8752i others(861): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739406 | |||||
| chr16:56739406
|
A | AACCTCCC others(836): Show |
6 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(3): Show | 6 | HG01884.hp1 HG02630.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.-14-8753_-14-8752i others(845): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739406 | |||||
| chr16:56739406
|
A | AACCTCCC others(349): Show |
3 | a0001c0002t0010g0111a0001c0002t0010g0112a0001c0002t0041g0113 | 3 | HG00733.hp2 HG01346.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.-14-8768_-14-8767i others(358): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739406 | |||||
| chr16:56739406
|
A | AACCTCCC others(1901): Show |
1 | a0001c0001t0001g0328 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-14-8789_-14-8788i others(1910): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739406 | |||||
| chr16:56739406
|
A | C | 95 | a0001c0001t0001g0305a0001c0001t0003g0348a0001c0001t0003g0349others(92): Show | 95 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.-14-8828A>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739406 | ||||||
| chr16:56739434
|
C | T | 1 | a0001c0002t0001g0129 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-14-8800C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739434 | ||||||
| chr16:56739471
|
C | T | 1 | a0001c0001t0034g0196 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-14-8763C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739471 | ||||||
| chr16:56739482
|
A | G | 327 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0045others(324): Show | 329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.-14-8752A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739482 | ||||||
| chr16:56739504
|
C | CGGCTGGC others(349): Show |
2 | a0001c0002t0001g0060a0001c0002t0001g0061 | 2 | NA18983.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.-14-8706_-14-8705i others(358): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739504 | |||||
| chr16:56739504
|
C | CGGCTGGC others(349): Show |
100 | a0001c0001t0001g0003a0001c0001t0001g0045a0001c0001t0001g0046others(97): Show | 101 | HG00099.hp1 HG00323.hp2 HG00609.hp2 others(98): Show |
intron_variant | MODIFIER | c.-14-8706_-14-8705i others(358): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739504 | |||||
| chr16:56739504
|
C | CGGCTGGC others(350): Show |
1 | a0001c0001t0001g0153 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.-14-8706_-14-8705i others(359): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739504 | |||||
| chr16:56739504
|
C | CGGCTGGC others(349): Show |
3 | a0001c0003t0002g0256a0001c0003t0002g0257a0001c0003t0002g0258 | 3 | HG01069.hp1 HG01071.hp2 NA18949.hp2 |
intron_variant | MODIFIER | c.-14-8706_-14-8705i others(358): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739504 | |||||
| chr16:56739504
|
C | CGGCTGGC others(171): Show |
1 | a0001c0001t0034g0196 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-14-8706_-14-8705i others(180): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739504 | |||||
| chr16:56739504
|
C | CGGCTGGC others(349): Show |
1 | a0001c0009t0018g0019 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-14-8706_-14-8705i others(358): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739504 | |||||
| chr16:56739504
|
C | CGGCTGGC others(349): Show |
21 | a0001c0004t0005g0020a0001c0004t0005g0021a0001c0004t0005g0022others(18): Show | 21 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(18): Show |
intron_variant | MODIFIER | c.-14-8706_-14-8705i others(358): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739504 | |||||
| chr16:56739504
|
C | CGGCTGGC others(348): Show |
6 | a0001c0004t0005g0030a0001c0004t0005g0031a0001c0004t0005g0032others(3): Show | 6 | HG00741.hp2 HG01099.hp2 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.-14-8706_-14-8705i others(357): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739504 | |||||
| chr16:56739504
|
C | CGGCTGGC others(171): Show |
3 | a0001c0002t0001g0108a0001c0002t0001g0109a0001c0002t0001g0128 | 3 | HG00140.hp1 HG03834.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.-14-8706_-14-8705i others(180): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739504 | |||||
| chr16:56739504
|
C | CGGCTGGC others(349): Show |
2 | a0001c0009t0018g0018a0003c0024t0018g0010 | 2 | HG02451.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-14-8706_-14-8705i others(358): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739504 | |||||
| chr16:56739504
|
C | CGGCTGGC others(350): Show |
1 | a0001c0002t0001g0110 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-14-8711_-14-8710i others(359): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739504 | |||||
| chr16:56739504
|
C | CGGGTGGC others(349): Show |
1 | a0001c0002t0001g0165 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-14-8728_-14-8727i others(358): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739504 | |||||
| chr16:56739504
|
C | T | 70 | a0001c0001t0003g0348a0001c0001t0003g0349a0001c0001t0003g0350others(67): Show | 70 | HG00323.hp1 HG00639.hp1 HG00642.hp2 others(67): Show |
intron_variant | MODIFIER | c.-14-8730C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739504 | ||||||
| chr16:56739516
|
C | CGGGGGGG others(350): Show |
1 | a0001c0002t0001g0129 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-14-8706_-14-8705i others(359): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739516 | |||||
| chr16:56739516
|
C | CGGGGGGG others(853): Show |
1 | a0001c0004t0019g0181 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-14-8706_-14-8705i others(862): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739516 | |||||
| chr16:56739516
|
C | T | 3 | a0001c0001t0001g0305a0001c0001t0001g0328a0001c0001t0029g0245 | 3 | HG00140.hp2 HG02145.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.-14-8718C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739516 | ||||||
| chr16:56739517
|
G | A | 3 | a0001c0001t0001g0305a0001c0001t0001g0328a0001c0002t0001g0058 | 3 | HG00140.hp2 HG02129.hp2 NA18953.hp2 |
intron_variant | MODIFIER | c.-14-8717G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739517 | ||||||
| chr16:56739517
|
G | GGGGGGGC others(801): Show |
1 | a0005c0022t0022g0254 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-14-8706_-14-8705i others(810): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739517 | |||||
| chr16:56739517
|
G | GGGGGGGC others(852): Show |
1 | a0001c0003t0002g0255 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-14-8706_-14-8705i others(861): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739517 | |||||
| chr16:56739517
|
G | GGGGGGGC others(525): Show |
1 | a0001c0001t0001g0334 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-14-8706_-14-8705i others(534): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739517 | |||||
| chr16:56739517
|
G | GGGGGGGC others(852): Show |
33 | a0001c0001t0001g0002a0001c0001t0001g0302a0001c0001t0001g0304others(30): Show | 34 | HG00609.hp1 HG00621.hp2 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.-14-8706_-14-8705i others(861): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739517 | |||||
| chr16:56739517
|
G | GGGGGGGC others(852): Show |
32 | a0001c0001t0002g0295a0001c0003t0002g0246a0001c0003t0002g0247others(29): Show | 32 | HG00423.hp1 HG01099.hp1 HG01168.hp1 others(29): Show |
intron_variant | MODIFIER | c.-14-8706_-14-8705i others(861): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739517 | |||||
| chr16:56739517
|
G | GGGGGGGC others(1857): Show |
1 | a0002c0008t0002g0300 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-14-8706_-14-8705i others(1866): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739517 | |||||
| chr16:56739517
|
G | GGGGGGGC others(853): Show |
1 | a0001c0001t0002g0284 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-14-8706_-14-8705i others(862): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739517 | |||||
| chr16:56739517
|
G | GGGGGGGC others(852): Show |
1 | a0001c0003t0002g0285 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-14-8706_-14-8705i others(861): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739517 | |||||
| chr16:56739517
|
G | GGGGGGGC others(853): Show |
1 | a0001c0003t0042g0286 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-14-8706_-14-8705i others(862): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739517 | |||||
| chr16:56739517
|
G | GGGGGGGC others(853): Show |
1 | a0001c0001t0001g0333 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-14-8706_-14-8705i others(862): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739517 | |||||
| chr16:56739517
|
G | GGGGGGGC others(853): Show |
3 | a0001c0003t0002g0287a0001c0003t0002g0296a0002c0008t0002g0301 | 3 | NA18981.hp2 NA19000.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.-14-8706_-14-8705i others(862): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739517 | |||||
| chr16:56739517
|
G | GGGGGGGC others(853): Show |
4 | a0001c0003t0002g0288a0001c0003t0002g0289a0001c0003t0002g0290others(1): Show | 4 | HG00544.hp2 HG00673.hp1 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.-14-8706_-14-8705i others(862): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739517 | |||||
| chr16:56739517
|
G | GGGGGGGC others(854): Show |
1 | a0001c0001t0001g0336 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-14-8706_-14-8705i others(863): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739517 | |||||
| chr16:56739517
|
G | GGGGGGGC others(856): Show |
1 | a0001c0001t0001g0303 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-14-8706_-14-8705i others(865): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739517 | |||||
| chr16:56739517
|
G | GGGGGGGC others(674): Show |
1 | a0001c0001t0002g0292 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-14-8706_-14-8705i others(683): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739517 | |||||
| chr16:56739517
|
G | GGGGGGGG others(856): Show |
1 | a0001c0003t0021g0294 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-14-8711_-14-8710i others(865): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739517 | |||||
| chr16:56739527
|
A | ACTCCCCC others(350): Show |
10 | a0001c0001t0001g0052a0001c0001t0001g0124a0001c0001t0001g0125others(7): Show | 10 | HG00408.hp1 HG00544.hp1 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.-14-8706_-14-8705i others(359): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739527 | |||||
| chr16:56739527
|
A | ACTCCCCC others(351): Show |
1 | a0001c0001t0001g0126 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-14-8706_-14-8705i others(360): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739527 | |||||
| chr16:56739527
|
A | ACTCCCCC others(351): Show |
1 | a0001c0002t0001g0170 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-14-8706_-14-8705i others(360): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739527 | |||||
| chr16:56739527
|
A | ACTCCCCC others(352): Show |
1 | a0001c0002t0001g0051 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-14-8706_-14-8705i others(361): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739527 | |||||
| chr16:56739527
|
A | ACTCCCCC others(352): Show |
1 | a0001c0001t0001g0130 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-14-8706_-14-8705i others(361): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739527 | |||||
| chr16:56739527
|
A | ACTCCCCC others(853): Show |
2 | a0001c0001t0001g0326a0001c0001t0001g0327 | 2 | HG00438.hp1 HG00558.hp1 |
intron_variant | MODIFIER | c.-14-8706_-14-8705i others(862): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739527 | |||||
| chr16:56739527
|
A | ACTCCCCC others(853): Show |
1 | a0001c0004t0044g0179 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-14-8706_-14-8705i others(862): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739527 | |||||
| chr16:56739527
|
A | ACTCCCCC others(853): Show |
3 | a0001c0003t0002g0282a0001c0003t0020g0283a0001c0006t0009g0249 | 3 | HG01169.hp1 HG02109.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-14-8706_-14-8705i others(862): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739527 | |||||
| chr16:56739527
|
A | ACTCCCCC others(856): Show |
1 | a0001c0003t0002g0248 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-14-8706_-14-8705i others(865): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739527 | |||||
| chr16:56739527
|
A | ACTCCCCC others(856): Show |
1 | a0001c0003t0002g0291 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-14-8706_-14-8705i others(865): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739527 | |||||
| chr16:56739527
|
A | ACTCCCCC others(857): Show |
1 | a0001c0003t0002g0293 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-14-8706_-14-8705i others(866): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739527 | |||||
| chr16:56739529
|
C | T | 1 | a0001c0001t0043g0154 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-14-8705C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739529 | ||||||
| chr16:56739530
|
C | T | 5 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(2): Show | 5 | NA18939.hp2 NA18964.hp2 NA18982.hp1 others(2): Show |
intron_variant | MODIFIER | c.-14-8704C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739530 | ||||||
| chr16:56739533
|
C | A | 1 | a0001c0001t0004g0234 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-14-8701C>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739533 | ||||||
| chr16:56739536
|
C | A | 1 | a0001c0002t0001g0062 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-14-8698C>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739536 | ||||||
| chr16:56739536
|
C | T | 1 | a0001c0002t0001g0107 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-14-8698C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739536 | ||||||
| chr16:56739547
|
C | T | 25 | a0001c0001t0004g0198a0001c0001t0004g0220a0001c0001t0004g0221others(22): Show | 25 | HG00408.hp2 HG00597.hp2 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.-14-8687C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739547 | ||||||
| chr16:56739552
|
G | A | 3 | a0001c0007t0012g0345a0001c0007t0012g0346a0001c0007t0012g0347 | 3 | HG02145.hp2 HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-14-8682G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739552 | ||||||
| chr16:56739556
|
C | T | 227 | a0001c0001t0001g0003a0001c0001t0001g0045a0001c0001t0001g0046others(224): Show | 228 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.-14-8678C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739556 | ||||||
| chr16:56739569
|
G | C | 6 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(3): Show | 6 | HG04184.hp2 NA18939.hp2 NA18964.hp2 others(3): Show |
intron_variant | MODIFIER | c.-14-8665G>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739569 | ||||||
| chr16:56739578
|
A | AC | 11 | a0001c0001t0001g0046a0001c0001t0001g0123a0001c0001t0001g0130others(8): Show | 11 | HG00642.hp2 HG01261.hp2 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.-14-8649dupC | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739578 | |||||
| chr16:56739578
|
A | ACACCCCC others(301): Show |
4 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(1): Show | 4 | NA18939.hp2 NA18964.hp2 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.-14-8655_-14-8654i others(310): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739578 | |||||
| chr16:56739578
|
A | ACACCCCC others(353): Show |
1 | a0001c0001t0043g0154 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-14-8655_-14-8654i others(362): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739578 | |||||
| chr16:56739580
|
C | A | 1 | a0001c0002t0001g0059 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-14-8654C>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739580 | ||||||
| chr16:56739600
|
T | C | 7 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(4): Show | 7 | NA18939.hp2 NA18964.hp2 NA18982.hp1 others(4): Show |
intron_variant | MODIFIER | c.-14-8634T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739600 | ||||||
| chr16:56739605
|
C | T | 4 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(1): Show | 4 | NA18939.hp2 NA18964.hp2 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.-14-8629C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739605 | ||||||
| chr16:56739614
|
G | A | 7 | a0001c0002t0001g0064a0001c0002t0001g0066a0001c0002t0001g0067others(4): Show | 7 | HG01891.hp1 HG02572.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-14-8620G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739614 | ||||||
| chr16:56739614
|
G | C | 6 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(3): Show | 6 | HG01884.hp1 HG02630.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.-14-8620G>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739614 | ||||||
| chr16:56739617
|
C | CAGAGGGG others(18): Show |
1 | a0001c0002t0001g0059 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-14-8617_-14-8616i others(27): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739617 | ||||||
| chr16:56739617
|
C | CG | 13 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0130others(10): Show | 13 | HG00642.hp2 HG01261.hp2 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.-14-8611dupG | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739617 | |||||
| chr16:56739617
|
C | T | 1 | a0006c0021t0001g0011 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-14-8617C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739617 | ||||||
| chr16:56739621
|
G | C | 1 | a0001c0002t0001g0059 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-14-8613G>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739621 | ||||||
| chr16:56739625
|
C | T | 4 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(1): Show | 4 | NA18939.hp2 NA18964.hp2 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.-14-8609C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739625 | ||||||
| chr16:56739628
|
C | G | 1 | a0001c0002t0001g0059 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-14-8606C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739628 | ||||||
| chr16:56739629
|
A | C | 4 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(1): Show | 4 | NA18939.hp2 NA18964.hp2 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.-14-8605A>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739629 | ||||||
| chr16:56739630
|
T | C | 4 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(1): Show | 4 | NA18939.hp2 NA18964.hp2 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.-14-8604T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739630 | ||||||
| chr16:56739630
|
T | G | 1 | a0001c0002t0001g0059 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-14-8604T>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739630 | ||||||
| chr16:56739630
|
T | TCCCCACC others(447): Show |
2 | a0001c0003t0002g0257a0001c0003t0002g0258 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-14-8568_-14-8567i others(456): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739630 | |||||
| chr16:56739631
|
C | G | 1 | a0001c0002t0001g0059 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-14-8603C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739631 | ||||||
| chr16:56739633
|
C | G | 1 | a0001c0002t0001g0059 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-14-8601C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739633 | ||||||
| chr16:56739635
|
A | C | 1 | a0001c0002t0001g0059 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-14-8599A>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739635 | ||||||
| chr16:56739646
|
G | A | 1 | a0001c0001t0029g0245 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-14-8588G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739646 | ||||||
| chr16:56739649
|
C | T | 4 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(1): Show | 4 | NA18939.hp2 NA18964.hp2 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.-14-8585C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739649 | ||||||
| chr16:56739654
|
C | CGGCTGGC others(170): Show |
1 | a0001c0001t0034g0196 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-14-8568_-14-8567i others(179): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739654 | |||||
| chr16:56739654
|
C | CGGCTGGC others(170): Show |
1 | a0001c0003t0002g0256 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-14-8568_-14-8567i others(179): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739654 | |||||
| chr16:56739654
|
C | CGGCTGGC others(172): Show |
1 | a0001c0001t0007g0194 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-14-8568_-14-8567i others(181): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739654 | |||||
| chr16:56739662
|
C | CGGGCAGG others(170): Show |
29 | a0001c0004t0005g0020a0001c0004t0005g0021a0001c0004t0005g0022others(26): Show | 29 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(26): Show |
intron_variant | MODIFIER | c.-14-8568_-14-8567i others(179): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739662 | |||||
| chr16:56739662
|
C | CGGGCAGG others(171): Show |
1 | a0001c0004t0005g0035 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-14-8568_-14-8567i others(180): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739662 | |||||
| chr16:56739662
|
CGGGCGGA others(5): Show |
C | 3 | a0001c0001t0013g0012a0001c0001t0013g0013a0001c0001t0013g0014 | 3 | HG03041.hp1 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-14-8570_-14-8559d others(14): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739662 | |||||
| chr16:56739666
|
C | G | 1 | a0001c0002t0001g0059 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-14-8568C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739666 | ||||||
| chr16:56739666
|
C | T | 6 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(3): Show | 6 | HG01884.hp1 HG02630.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.-14-8568C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739666 | ||||||
| chr16:56739667
|
G | A | 196 | a0001c0001t0001g0003a0001c0001t0001g0045a0001c0001t0001g0046others(193): Show | 197 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.-14-8567G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739667 | ||||||
| chr16:56739669
|
A | G | 198 | a0001c0001t0001g0003a0001c0001t0001g0045a0001c0001t0001g0046others(195): Show | 199 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.-14-8565A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739669 | ||||||
| chr16:56739674
|
T | C | 197 | a0001c0001t0001g0003a0001c0001t0001g0045a0001c0001t0001g0046others(194): Show | 198 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.-14-8560T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739674 | ||||||
| chr16:56739692
|
C | T | 3 | a0001c0001t0016g0191a0001c0001t0016g0192a0001c0001t0016g0193 | 3 | HG02258.hp2 HG03130.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-14-8542C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739692 | ||||||
| chr16:56739695
|
G | A | 6 | a0001c0002t0001g0001a0001c0002t0001g0051a0001c0002t0001g0070others(3): Show | 7 | HG00323.hp2 HG00642.hp1 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.-14-8539G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739695 | ||||||
| chr16:56739715
|
C | CG | 12 | a0001c0001t0001g0125a0001c0001t0001g0303a0001c0001t0001g0327others(9): Show | 12 | HG00438.hp1 HG00597.hp1 HG00642.hp1 others(9): Show |
intron_variant | MODIFIER | c.-14-8513dupG | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739715 | |||||
| chr16:56739723
|
C | CGATCCCC others(397): Show |
2 | a0001c0001t0014g0217a0001c0001t0014g0218 | 2 | HG01884.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-14-8509_-14-8508i others(406): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739723 | |||||
| chr16:56739723
|
C | CGATCCCC others(397): Show |
1 | a0001c0001t0014g0219 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-14-8509_-14-8508i others(406): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739723 | |||||
| chr16:56739723
|
C | CGATCCCC others(446): Show |
1 | a0001c0001t0006g0202 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-14-8509_-14-8508i others(455): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739723 | |||||
| chr16:56739723
|
C | CGATCCCC others(447): Show |
14 | a0001c0001t0006g0203a0001c0001t0006g0204a0001c0001t0006g0205others(11): Show | 14 | HG01070.hp2 HG01243.hp1 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.-14-8509_-14-8508i others(456): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739723 | |||||
| chr16:56739723
|
C | CGATCCCC others(448): Show |
1 | a0001c0001t0006g0216 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-14-8509_-14-8508i others(457): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739723 | |||||
| chr16:56739723
|
C | T | 1 | a0001c0002t0001g0059 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-14-8511C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739723 | ||||||
| chr16:56739725
|
A | AT | 176 | a0001c0001t0001g0003a0001c0001t0001g0045a0001c0001t0001g0046others(173): Show | 177 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.-14-8509_-14-8508i others(3): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739725 | ||||||
| chr16:56739727
|
C | A | 1 | a0001c0002t0001g0059 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-14-8507C>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739727 | ||||||
| chr16:56739728
|
C | T | 1 | a0001c0002t0001g0059 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-14-8506C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739728 | ||||||
| chr16:56739748
|
G | A | 47 | a0001c0001t0003g0348a0001c0001t0003g0349a0001c0001t0003g0350others(44): Show | 47 | HG00323.hp1 HG00639.hp1 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.-14-8486G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739748 | ||||||
| chr16:56739798
|
G | A | 9 | a0001c0001t0004g0198a0001c0001t0004g0231a0001c0001t0004g0232others(6): Show | 9 | HG00597.hp2 NA18952.hp1 NA18959.hp2 others(6): Show |
intron_variant | MODIFIER | c.-14-8436G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739798 | ||||||
| chr16:56739800
|
G | A | 47 | a0001c0001t0003g0348a0001c0001t0003g0349a0001c0001t0003g0350others(44): Show | 47 | HG00323.hp1 HG00639.hp1 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.-14-8434G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739800 | ||||||
| chr16:56739807
|
C | T | 2 | a0001c0001t0001g0123a0001c0001t0001g0125 | 2 | HG03831.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-14-8427C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739807 | ||||||
| chr16:56739808
|
G | A | 33 | a0001c0001t0007g0194a0001c0001t0034g0196a0001c0003t0002g0256others(30): Show | 33 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.-14-8426G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739808 | ||||||
| chr16:56739822
|
A | G | 34 | a0001c0001t0007g0194a0001c0001t0034g0196a0001c0002t0001g0059others(31): Show | 34 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.-14-8412A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739822 | ||||||
| chr16:56739825
|
C | T | 1 | a0001c0004t0024g0042 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-14-8409C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739825 | ||||||
| chr16:56739830
|
C | T | 44 | a0001c0001t0003g0348a0001c0001t0003g0349a0001c0001t0003g0350others(41): Show | 44 | HG00323.hp1 HG00639.hp1 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.-14-8404C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739830 | ||||||
| chr16:56739842
|
C | A | 1 | a0001c0003t0002g0256 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-14-8392C>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739842 | ||||||
| chr16:56739842
|
C | CG | 33 | a0001c0001t0007g0194a0001c0001t0034g0196a0001c0002t0001g0059others(30): Show | 33 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.-14-8390dupG | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739842 | |||||
| chr16:56739845
|
A | G | 34 | a0001c0001t0007g0194a0001c0001t0034g0196a0001c0002t0001g0059others(31): Show | 34 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.-14-8389A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739845 | ||||||
| chr16:56739850
|
T | TGA | 29 | a0001c0001t0034g0196a0001c0003t0002g0256a0001c0004t0005g0021others(26): Show | 29 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(26): Show |
intron_variant | MODIFIER | c.-14-8384_-14-8383i others(4): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739850 | ||||||
| chr16:56739850
|
T | TGAC | 4 | a0001c0001t0007g0194a0001c0004t0005g0020a0001c0004t0005g0034others(1): Show | 4 | HG00741.hp2 HG02738.hp2 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.-14-8384_-14-8383i others(5): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739850 | ||||||
| chr16:56739851
|
C | G | 44 | a0001c0001t0003g0348a0001c0001t0003g0349a0001c0001t0003g0350others(41): Show | 44 | HG00323.hp1 HG00639.hp1 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.-14-8383C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739851 | ||||||
| chr16:56739852
|
A | AC | 8 | a0001c0001t0001g0130a0001c0001t0001g0328a0001c0001t0004g0236others(5): Show | 8 | HG00597.hp1 HG00597.hp2 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.-14-8376dupC | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739852 | |||||
| chr16:56739852
|
A | C | 33 | a0001c0001t0007g0194a0001c0001t0034g0196a0001c0003t0002g0256others(30): Show | 33 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.-14-8382A>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739852 | ||||||
| chr16:56739855
|
C | CCCCCCAC others(271): Show |
1 | a0010c0013t0007g0190 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-14-8376_-14-8375i others(280): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739855 | |||||
| chr16:56739855
|
C | CCCCCCAC others(272): Show |
1 | a0001c0001t0007g0195 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-14-8376_-14-8375i others(281): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739855 | |||||
| chr16:56739855
|
C | CCCCCCCA others(93): Show |
1 | a0001c0002t0001g0059 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-14-8376_-14-8375i others(102): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739855 | |||||
| chr16:56739859
|
G | C | 364 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0045others(361): Show | 366 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(363): Show |
intron_variant | MODIFIER | c.-14-8375G>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739859 | ||||||
| chr16:56739870
|
C | T | 2 | a0001c0001t0007g0194a0001c0001t0034g0196 | 2 | HG02572.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.-14-8364C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739870 | ||||||
| chr16:56739879
|
C | T | 1 | a0001c0002t0001g0104 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-14-8355C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739879 | ||||||
| chr16:56739888
|
A | G | 211 | a0001c0001t0001g0003a0001c0001t0001g0045a0001c0001t0001g0046others(208): Show | 212 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.-14-8346A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739888 | ||||||
| chr16:56739892
|
G | A | 24 | a0001c0001t0004g0198a0001c0001t0004g0220a0001c0001t0004g0221others(21): Show | 24 | HG00408.hp2 HG00597.hp2 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.-14-8342G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739892 | ||||||
| chr16:56739894
|
G | A | 2 | a0001c0001t0007g0195a0010c0013t0007g0190 | 2 | HG00642.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.-14-8340G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739894 | ||||||
| chr16:56739894
|
G | GGGGCCGA others(270): Show |
39 | a0001c0001t0003g0348a0001c0001t0003g0349a0001c0001t0003g0350others(36): Show | 39 | HG00323.hp1 HG00639.hp1 HG01070.hp1 others(36): Show |
intron_variant | MODIFIER | c.-14-8336_-14-8335i others(279): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739894 | |||||
| chr16:56739894
|
G | GGGGCCGA others(271): Show |
1 | a0004c0023t0026g0372 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-14-8336_-14-8335i others(280): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739894 | |||||
| chr16:56739894
|
G | GGGGGCCG others(271): Show |
1 | a0001c0001t0003g0373 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-14-8337_-14-8336i others(280): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739894 | |||||
| chr16:56739899
|
T | C | 1 | a0001c0002t0001g0059 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-14-8335T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739899 | ||||||
| chr16:56739902
|
C | G | 3 | a0001c0004t0015g0015a0001c0004t0015g0016a0001c0004t0015g0017 | 3 | HG02818.hp1 HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-14-8332C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739902 | ||||||
| chr16:56739923
|
C | T | 4 | a0001c0001t0007g0194a0001c0001t0034g0196a0001c0002t0001g0164others(1): Show | 4 | HG02572.hp2 HG02738.hp2 NA18949.hp2 others(1): Show |
intron_variant | MODIFIER | c.-14-8311C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739923 | ||||||
| chr16:56739940
|
C | CG | 8 | a0001c0001t0001g0125a0001c0001t0001g0328a0001c0002t0001g0069others(5): Show | 8 | HG01175.hp2 HG01255.hp1 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.-14-8288dupG | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739940 | |||||
| chr16:56739940
|
CG | C | 6 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(3): Show | 6 | HG01884.hp1 HG02630.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.-14-8288delG | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739940 | |||||
| chr16:56739946
|
G | T | 6 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(3): Show | 6 | HG01884.hp1 HG02630.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.-14-8288G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739946 | ||||||
| chr16:56739950
|
A | AC | 27 | a0001c0001t0001g0045a0001c0001t0001g0123a0001c0001t0001g0125others(24): Show | 27 | HG00438.hp1 HG00558.hp1 HG00597.hp1 others(24): Show |
intron_variant | MODIFIER | c.-14-8276dupC | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739950 | |||||
| chr16:56739950
|
AC | A | 43 | a0001c0001t0003g0348a0001c0001t0003g0349a0001c0001t0003g0350others(40): Show | 43 | HG00323.hp1 HG00639.hp1 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.-14-8276delC | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56739950 | |||||
| chr16:56739951
|
C | CATCCCCA others(91): Show |
2 | a0001c0001t0034g0196a0001c0003t0002g0256 | 2 | HG02572.hp2 NA18949.hp2 |
intron_variant | MODIFIER | c.-14-8283_-14-8282i others(100): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739951 | ||||||
| chr16:56739951
|
C | CATCCCCA others(92): Show |
1 | a0001c0001t0007g0194 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-14-8283_-14-8282i others(101): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739951 | ||||||
| chr16:56739958
|
C | T | 3 | a0001c0009t0018g0018a0001c0009t0018g0019a0003c0024t0018g0010 | 3 | HG02451.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-14-8276C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739958 | ||||||
| chr16:56739960
|
C | A | 1 | a0001c0002t0010g0111 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-14-8274C>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739960 | ||||||
| chr16:56739986
|
C | T | 1 | a0001c0001t0001g0305 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-14-8248C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56739986 | ||||||
| chr16:56740012
|
G | T | 1 | a0001c0001t0029g0245 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-14-8222G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56740012 | ||||||
| chr16:56740023
|
G | C | 364 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0045others(361): Show | 366 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(363): Show |
intron_variant | MODIFIER | c.-14-8211G>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56740023 | ||||||
| chr16:56740067
|
G | T | 1 | a0001c0002t0001g0102 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-14-8167G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56740067 | ||||||
| chr16:56740089
|
T | C | 1 | a0001c0001t0004g0221 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-14-8145T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56740089 | ||||||
| chr16:56740100
|
C | T | 1 | a0001c0002t0001g0168 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-14-8134C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56740100 | ||||||
| chr16:56740111
|
G | A | 2 | a0001c0001t0023g0329a0001c0001t0023g0330 | 2 | NA18991.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.-14-8123G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56740111 | ||||||
| chr16:56740114
|
A | G | 132 | a0001c0001t0001g0003a0001c0001t0001g0045a0001c0001t0001g0046others(129): Show | 133 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.-14-8120A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56740114 | ||||||
| chr16:56740127
|
A | ACCC | 100 | a0001c0001t0001g0003a0001c0001t0001g0046a0001c0001t0001g0053others(97): Show | 101 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.-14-8102_-14-8100d others(5): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56740127 | |||||
| chr16:56740127
|
A | ACCCC | 28 | a0001c0001t0001g0045a0001c0001t0001g0052a0001c0001t0001g0120others(25): Show | 28 | HG00609.hp2 HG01433.hp1 HG02056.hp2 others(25): Show |
intron_variant | MODIFIER | c.-14-8103_-14-8100d others(6): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56740127 | |||||
| chr16:56740127
|
A | ACCCCCCC others(44): Show |
28 | a0001c0004t0005g0021a0001c0004t0005g0022a0001c0004t0005g0023others(25): Show | 28 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(25): Show |
intron_variant | MODIFIER | c.-14-8081_-14-8080i others(53): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56740127 | |||||
| chr16:56740127
|
A | ACCCCCCC others(45): Show |
4 | a0001c0004t0005g0020a0001c0004t0005g0035a0001c0007t0012g0346others(1): Show | 4 | HG01261.hp1 HG02886.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-14-8081_-14-8080i others(54): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56740127 | |||||
| chr16:56740127
|
A | ACCCCCCC others(46): Show |
1 | a0001c0007t0012g0345 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-14-8081_-14-8080i others(55): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56740127 | |||||
| chr16:56740195
|
GGCTGCCG others(33): Show |
G | 19 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(16): Show | 19 | HG00621.hp1 HG02071.hp1 HG03239.hp2 others(16): Show |
intron_variant | MODIFIER | c.-14-8024_-14-7985d others(42): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56740195 | |||||
| chr16:56740272
|
G | C | 3 | a0001c0009t0018g0018a0001c0009t0018g0019a0003c0024t0018g0010 | 3 | HG02451.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-14-7962G>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56740272 | ||||||
| chr16:56740318
|
C | T | 2 | a0001c0001t0016g0192a0001c0001t0016g0193 | 2 | HG02258.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-14-7916C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56740318 | ||||||
| chr16:56740346
|
C | T | 49 | a0001c0001t0002g0284a0001c0001t0002g0292a0001c0001t0002g0295others(46): Show | 49 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.-14-7888C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56740346 | ||||||
| chr16:56740386
|
T | C | 1 | a0001c0003t0002g0288 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-14-7848T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56740386 | ||||||
| chr16:56740405
|
C | T | 24 | a0001c0001t0004g0198a0001c0001t0004g0220a0001c0001t0004g0221others(21): Show | 24 | HG00408.hp2 HG00597.hp2 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.-14-7829C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56740405 | ||||||
| chr16:56740471
|
G | A | 30 | a0001c0004t0005g0020a0001c0004t0005g0021a0001c0004t0005g0022others(27): Show | 30 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.-14-7763G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56740471 | ||||||
| chr16:56740524
|
C | G | 1 | a0001c0001t0004g0234 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-14-7710C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56740524 | ||||||
| chr16:56740587
|
G | A | 3 | a0001c0001t0013g0012a0001c0001t0013g0013a0001c0001t0013g0014 | 3 | HG03041.hp1 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-14-7647G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56740587 | ||||||
| chr16:56740827
|
C | G | 1 | a0001c0001t0034g0196 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-14-7407C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56740827 | ||||||
| chr16:56740875
|
C | T | 97 | a0001c0001t0001g0002a0001c0001t0001g0302a0001c0001t0001g0303others(94): Show | 98 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.-14-7359C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56740875 | ||||||
| chr16:56740952
|
C | G | 1 | a0001c0017t0001g0158 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-14-7282C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56740952 | ||||||
| chr16:56740985
|
C | T | 2 | a0001c0007t0012g0346a0001c0007t0012g0347 | 2 | HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-14-7249C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56740985 | ||||||
| chr16:56741004
|
G | GGGGAGA | 161 | a0001c0001t0001g0003a0001c0001t0001g0045a0001c0001t0001g0046others(158): Show | 162 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.-14-7204_-14-7199d others(8): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56741004 | |||||
| chr16:56741004
|
G | GGGGAGAG others(5): Show |
5 | a0001c0001t0001g0126a0001c0001t0013g0012a0001c0001t0013g0013others(2): Show | 5 | HG03041.hp1 HG03225.hp1 HG04204.hp1 others(2): Show |
intron_variant | MODIFIER | c.-14-7210_-14-7199d others(14): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56741004 | |||||
| chr16:56741004
|
G | GGGGAGAG others(11): Show |
3 | a0001c0007t0012g0345a0001c0007t0012g0346a0001c0007t0012g0347 | 3 | HG02145.hp2 HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-14-7216_-14-7199d others(20): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56741004 | |||||
| chr16:56741004
|
GGGGAGA | G | 5 | a0001c0001t0029g0245a0001c0003t0002g0263a0001c0003t0021g0262others(2): Show | 5 | HG00423.hp1 HG02074.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.-14-7204_-14-7199d others(8): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56741004 | |||||
| chr16:56741006
|
G | A | 4 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(1): Show | 4 | HG01884.hp1 HG02970.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-14-7228G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56741006 | ||||||
| chr16:56741144
|
T | C | 6 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(3): Show | 6 | HG01884.hp1 HG02630.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.-14-7090T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56741144 | ||||||
| chr16:56741155
|
T | G | 1 | a0001c0003t0002g0285 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-14-7079T>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56741155 | ||||||
| chr16:56741205
|
A | G | 2 | a0001c0001t0001g0162a0001c0001t0001g0163 | 2 | HG01891.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.-14-7029A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56741205 | ||||||
| chr16:56741345
|
A | G | 1 | a0001c0001t0027g0371 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-14-6889A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56741345 | ||||||
| chr16:56741605
|
C | T | 364 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0045others(361): Show | 366 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(363): Show |
intron_variant | MODIFIER | c.-14-6629C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56741605 | ||||||
| chr16:56742048
|
A | G | 1 | a0001c0002t0001g0170 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-14-6186A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56742048 | ||||||
| chr16:56742096
|
C | A | 41 | a0001c0001t0001g0002a0001c0001t0001g0302a0001c0001t0001g0303others(38): Show | 42 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.-14-6138C>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56742096 | ||||||
| chr16:56742118
|
A | T | 2 | a0001c0010t0022g0260a0001c0010t0033g0261 | 2 | HG03139.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-14-6116A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56742118 | ||||||
| chr16:56742275
|
G | T | 364 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0045others(361): Show | 366 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(363): Show |
intron_variant | MODIFIER | c.-14-5959G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56742275 | ||||||
| chr16:56742371
|
A | G | 1 | a0001c0009t0018g0019 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-14-5863A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56742371 | ||||||
| chr16:56742643
|
A | G | 2 | a0001c0010t0022g0260a0001c0010t0033g0261 | 2 | HG03139.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-14-5591A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56742643 | ||||||
| chr16:56742744
|
C | T | 1 | a0001c0001t0014g0218 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-14-5490C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56742744 | ||||||
| chr16:56742868
|
C | T | 3 | a0001c0004t0015g0015a0001c0004t0015g0016a0001c0004t0015g0017 | 3 | HG02818.hp1 HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-14-5366C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56742868 | ||||||
| chr16:56742979
|
A | G | 5 | a0001c0006t0009g0249a0001c0006t0009g0250a0001c0006t0009g0251others(2): Show | 5 | HG02109.hp2 HG02615.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.-14-5255A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56742979 | ||||||
| chr16:56743113
|
G | A | 1 | a0001c0002t0001g0339 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-14-5121G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56743113 | ||||||
| chr16:56743125
|
A | C | 2 | a0001c0002t0001g0001a0001c0002t0001g0071 | 3 | HG01361.hp1 HG01517.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.-14-5109A>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56743125 | ||||||
| chr16:56743169
|
A | G | 1 | a0001c0002t0001g0165 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-14-5065A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56743169 | ||||||
| chr16:56743345
|
C | T | 1 | a0001c0001t0003g0370 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-14-4889C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56743345 | ||||||
| chr16:56743984
|
C | T | 1 | a0006c0021t0001g0011 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-14-4250C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56743984 | ||||||
| chr16:56744034
|
G | C | 3 | a0001c0001t0014g0217a0001c0001t0014g0218a0001c0001t0014g0219 | 3 | HG01884.hp2 HG03453.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-14-4200G>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56744034 | ||||||
| chr16:56744155
|
G | A | 130 | a0001c0001t0001g0003a0001c0001t0001g0045a0001c0001t0001g0046others(127): Show | 131 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.-14-4079G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56744155 | ||||||
| chr16:56744223
|
C | T | 3 | a0001c0001t0004g0221a0001c0001t0004g0229a0001c0001t0004g0236 | 3 | HG01433.hp2 HG01496.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-14-4011C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56744223 | ||||||
| chr16:56744374
|
G | T | 3 | a0001c0009t0018g0018a0001c0009t0018g0019a0003c0024t0018g0010 | 3 | HG02451.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-14-3860G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56744374 | ||||||
| chr16:56744589
|
C | T | 1 | a0001c0001t0007g0195 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-14-3645C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56744589 | ||||||
| chr16:56744701
|
G | A | 1 | a0001c0002t0001g0072 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-14-3533G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56744701 | ||||||
| chr16:56744706
|
C | A | 1 | a0001c0002t0001g0094 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-14-3528C>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56744706 | ||||||
| chr16:56744734
|
G | A | 30 | a0001c0004t0005g0020a0001c0004t0005g0021a0001c0004t0005g0022others(27): Show | 30 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.-14-3500G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56744734 | ||||||
| chr16:56744924
|
G | A | 4 | a0001c0001t0016g0191a0001c0001t0016g0192a0001c0001t0016g0193others(1): Show | 4 | HG02258.hp2 HG02572.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-14-3310G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56744924 | ||||||
| chr16:56744994
|
G | T | 2 | a0001c0001t0002g0292a0001c0014t0001g0137 | 2 | HG02717.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.-14-3240G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56744994 | ||||||
| chr16:56745009
|
A | G | 3 | a0001c0004t0015g0015a0001c0004t0015g0016a0001c0004t0015g0017 | 3 | HG02818.hp1 HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-14-3225A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56745009 | ||||||
| chr16:56745016
|
TG | T | 3 | a0001c0002t0001g0093a0001c0002t0001g0103a0001c0002t0001g0104 | 3 | HG00673.hp2 HG02074.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.-14-3215delG | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56745016 | |||||
| chr16:56745063
|
C | T | 3 | a0001c0004t0015g0015a0001c0004t0015g0016a0001c0004t0015g0017 | 3 | HG02818.hp1 HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-14-3171C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56745063 | ||||||
| chr16:56745350
|
GA | G | 6 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(3): Show | 6 | HG01884.hp1 HG02630.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.-14-2883delA | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56745350 | ||||||
| chr16:56745356
|
G | A | 131 | a0001c0001t0001g0003a0001c0001t0001g0045a0001c0001t0001g0046others(128): Show | 132 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.-14-2878G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56745356 | ||||||
| chr16:56745744
|
T | G | 2 | a0001c0001t0001g0123a0001c0001t0001g0125 | 2 | HG03831.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-14-2490T>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56745744 | ||||||
| chr16:56745796
|
T | C | 1 | a0001c0001t0003g0355 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-14-2438T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56745796 | ||||||
| chr16:56745888
|
A | G | 6 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(3): Show | 6 | HG01884.hp1 HG02630.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.-14-2346A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56745888 | ||||||
| chr16:56746214
|
C | G | 2 | a0001c0002t0001g0101a0001c0002t0001g0105 | 2 | HG02602.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.-14-2020C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56746214 | ||||||
| chr16:56746347
|
T | C | 1 | a0001c0007t0012g0345 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-14-1887T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56746347 | ||||||
| chr16:56746418
|
G | A | 3 | a0001c0009t0018g0018a0001c0009t0018g0019a0003c0024t0018g0010 | 3 | HG02451.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-14-1816G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56746418 | ||||||
| chr16:56746479
|
T | C | 93 | a0001c0001t0003g0348a0001c0001t0003g0349a0001c0001t0003g0350others(90): Show | 93 | HG00323.hp1 HG00408.hp2 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.-14-1755T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56746479 | ||||||
| chr16:56746997
|
A | AT | 8 | a0001c0001t0001g0336a0001c0001t0003g0370a0001c0002t0001g0106others(5): Show | 8 | HG01978.hp2 HG02145.hp2 HG03831.hp2 others(5): Show |
intron_variant | MODIFIER | c.-14-1221dupT | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56746997 | |||||
| chr16:56746997
|
AT | A | 10 | a0001c0001t0001g0302a0001c0001t0001g0306a0001c0001t0004g0238others(7): Show | 10 | HG00423.hp1 HG01993.hp2 HG02015.hp2 others(7): Show |
intron_variant | MODIFIER | c.-14-1221delT | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 56746997 | |||||
| chr16:56747019
|
A | G | 4 | a0001c0001t0001g0322a0001c0001t0001g0323a0001c0001t0001g0324others(1): Show | 4 | HG00735.hp2 HG01081.hp1 HG01123.hp2 others(1): Show |
intron_variant | MODIFIER | c.-14-1215A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56747019 | ||||||
| chr16:56747065
|
T | C | 5 | a0001c0006t0009g0249a0001c0006t0009g0250a0001c0006t0009g0251others(2): Show | 5 | HG02109.hp2 HG02615.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.-14-1169T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56747065 | ||||||
| chr16:56747123
|
C | T | 130 | a0001c0001t0001g0003a0001c0001t0001g0045a0001c0001t0001g0046others(127): Show | 131 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.-14-1111C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56747123 | ||||||
| chr16:56747350
|
G | A | 3 | a0001c0001t0014g0217a0001c0001t0014g0218a0001c0001t0014g0219 | 3 | HG01884.hp2 HG03453.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-14-884G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56747350 | ||||||
| chr16:56747384
|
A | G | 98 | a0001c0001t0001g0002a0001c0001t0001g0302a0001c0001t0001g0303others(95): Show | 99 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.-14-850A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56747384 | ||||||
| chr16:56747407
|
C | T | 1 | a0001c0001t0001g0136 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-14-827C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56747407 | ||||||
| chr16:56747411
|
A | G | 1 | a0001c0001t0006g0216 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-14-823A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56747411 | ||||||
| chr16:56747608
|
A | G | 1 | a0001c0001t0031g0209 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-14-626A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56747608 | ||||||
| chr16:56747820
|
A | G | 164 | a0001c0001t0001g0003a0001c0001t0001g0045a0001c0001t0001g0046others(161): Show | 165 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.-14-414A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56747820 | ||||||
| chr16:56747823
|
G | A | 9 | a0001c0001t0003g0353a0001c0001t0003g0354a0001c0001t0003g0356others(6): Show | 9 | HG02027.hp1 NA18961.hp1 NA18969.hp2 others(6): Show |
intron_variant | MODIFIER | c.-14-411G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56747823 | ||||||
| chr16:56747918
|
C | T | 364 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0045others(361): Show | 366 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(363): Show |
intron_variant | MODIFIER | c.-14-316C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56747918 | ||||||
| chr16:56748053
|
A | G | 23 | a0001c0001t0006g0199a0001c0001t0006g0200a0001c0001t0006g0201others(20): Show | 23 | HG01070.hp2 HG01168.hp2 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.-14-181A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | 56748053 | ||||||
| chr16:56748435
|
T | G | 1 | a0001c0001t0003g0355 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.179+9T>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56748435 | ||||||
| chr16:56748714
|
A | T | 1 | a0001c0001t0004g0221 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.179+288A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56748714 | ||||||
| chr16:56748732
|
A | G | 1 | a0001c0001t0001g0325 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.179+306A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56748732 | ||||||
| chr16:56748924
|
C | T | 1 | a0001c0001t0029g0245 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.179+498C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56748924 | ||||||
| chr16:56748990
|
G | A | 2 | a0001c0004t0005g0041a0001c0004t0005g0043 | 2 | HG00423.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.179+564G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56748990 | ||||||
| chr16:56749091
|
G | A | 1 | a0001c0001t0029g0245 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.179+665G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56749091 | ||||||
| chr16:56749154
|
A | G | 1 | a0001c0001t0001g0120 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.179+728A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56749154 | ||||||
| chr16:56749204
|
A | T | 3 | a0001c0001t0003g0368a0001c0001t0003g0369a0001c0001t0003g0370 | 3 | NA18942.hp1 NA18952.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.179+778A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56749204 | ||||||
| chr16:56749318
|
C | T | 1 | a0006c0021t0001g0011 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.179+892C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56749318 | ||||||
| chr16:56749465
|
G | A | 3 | a0001c0009t0018g0018a0001c0009t0018g0019a0003c0024t0018g0010 | 3 | HG02451.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.179+1039G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56749465 | ||||||
| chr16:56749476
|
G | A | 3 | a0001c0001t0017g0307a0001c0001t0017g0341a0001c0001t0017g0342 | 3 | HG00621.hp2 NA18969.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.179+1050G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56749476 | ||||||
| chr16:56749569
|
C | T | 364 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0045others(361): Show | 366 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(363): Show |
intron_variant | MODIFIER | c.179+1143C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56749569 | ||||||
| chr16:56749605
|
A | G | 1 | a0001c0001t0001g0122 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.179+1179A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56749605 | ||||||
| chr16:56749984
|
C | T | 3 | a0001c0007t0012g0345a0001c0007t0012g0346a0001c0007t0012g0347 | 3 | HG02145.hp2 HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.179+1558C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56749984 | ||||||
| chr16:56749985
|
C | T | 12 | a0001c0001t0003g0353a0001c0001t0003g0354a0001c0001t0003g0356others(9): Show | 12 | HG02027.hp1 NA18942.hp1 NA18952.hp2 others(9): Show |
intron_variant | MODIFIER | c.179+1559C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56749985 | ||||||
| chr16:56750273
|
A | G | 1 | a0001c0001t0004g0240 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.179+1847A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56750273 | ||||||
| chr16:56750489
|
A | G | 30 | a0001c0004t0005g0020a0001c0004t0005g0021a0001c0004t0005g0022others(27): Show | 30 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.179+2063A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56750489 | ||||||
| chr16:56750598
|
AT | A | 5 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(2): Show | 5 | NA18970.hp1 NA18988.hp1 NA18991.hp2 others(2): Show |
intron_variant | MODIFIER | c.179+2173delT | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56750598 | ||||||
| chr16:56750625
|
C | T | 1 | a0008c0018t0004g0228 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.179+2199C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56750625 | ||||||
| chr16:56750812
|
C | T | 1 | a0001c0002t0001g0092 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.179+2386C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56750812 | ||||||
| chr16:56750888
|
G | A | 11 | a0001c0002t0001g0059a0001c0002t0001g0073a0001c0002t0001g0075others(8): Show | 11 | HG02071.hp2 HG02080.hp1 HG02129.hp1 others(8): Show |
intron_variant | MODIFIER | c.179+2462G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56750888 | ||||||
| chr16:56750899
|
C | T | 5 | a0001c0006t0009g0249a0001c0006t0009g0250a0001c0006t0009g0251others(2): Show | 5 | HG02109.hp2 HG02615.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.179+2473C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56750899 | ||||||
| chr16:56750939
|
G | A | 1 | a0001c0002t0001g0170 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.179+2513G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56750939 | ||||||
| chr16:56751196
|
A | G | 130 | a0001c0001t0001g0003a0001c0001t0001g0045a0001c0001t0001g0046others(127): Show | 131 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.179+2770A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56751196 | ||||||
| chr16:56751211
|
C | A | 55 | a0001c0001t0001g0003a0001c0001t0001g0045a0001c0001t0001g0046others(52): Show | 55 | HG00099.hp1 HG00621.hp1 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.179+2785C>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56751211 | ||||||
| chr16:56751227
|
A | G | 1 | a0001c0002t0001g0091 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.179+2801A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56751227 | ||||||
| chr16:56751311
|
A | G | 1 | a0001c0001t0001g0321 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.179+2885A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56751311 | ||||||
| chr16:56751387
|
G | A | 6 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(3): Show | 6 | HG01884.hp1 HG02630.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.179+2961G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56751387 | ||||||
| chr16:56751407
|
C | T | 1 | a0001c0001t0003g0348 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.179+2981C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56751407 | ||||||
| chr16:56751408
|
G | A | 131 | a0001c0001t0001g0003a0001c0001t0001g0045a0001c0001t0001g0046others(128): Show | 132 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.179+2982G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56751408 | ||||||
| chr16:56751478
|
A | G | 131 | a0001c0001t0001g0003a0001c0001t0001g0045a0001c0001t0001g0046others(128): Show | 132 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.179+3052A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56751478 | ||||||
| chr16:56752120
|
T | C | 1 | a0001c0001t0001g0003 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.179+3694T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56752120 | ||||||
| chr16:56752668
|
A | G | 1 | a0001c0001t0029g0245 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.179+4242A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56752668 | ||||||
| chr16:56752880
|
G | T | 1 | a0001c0001t0001g0163 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.179+4454G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56752880 | ||||||
| chr16:56752937
|
G | A | 6 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(3): Show | 6 | HG01884.hp1 HG02630.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.179+4511G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56752937 | ||||||
| chr16:56753041
|
CAT | C | 6 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(3): Show | 6 | HG01884.hp1 HG02630.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.179+4618_179+4619d others(4): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr16 | 56753041 | |||||
| chr16:56753103
|
T | A | 3 | a0001c0001t0017g0307a0001c0001t0017g0341a0001c0001t0017g0342 | 3 | HG00621.hp2 NA18969.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.179+4677T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56753103 | ||||||
| chr16:56753195
|
T | C | 271 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0045others(268): Show | 273 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(270): Show |
intron_variant | MODIFIER | c.179+4769T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56753195 | ||||||
| chr16:56753249
|
A | G | 98 | a0001c0001t0001g0002a0001c0001t0001g0302a0001c0001t0001g0303others(95): Show | 99 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.179+4823A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56753249 | ||||||
| chr16:56753420
|
TATC | T | 24 | a0001c0004t0005g0020a0001c0004t0005g0021a0001c0004t0005g0022others(21): Show | 24 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(21): Show |
intron_variant | MODIFIER | c.179+4997_179+4999d others(5): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr16 | 56753420 | |||||
| chr16:56753434
|
T | C | 30 | a0001c0004t0005g0020a0001c0004t0005g0021a0001c0004t0005g0022others(27): Show | 30 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.179+5008T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56753434 | ||||||
| chr16:56753460
|
A | G | 5 | a0001c0006t0009g0249a0001c0006t0009g0250a0001c0006t0009g0251others(2): Show | 5 | HG02109.hp2 HG02615.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.179+5034A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56753460 | ||||||
| chr16:56753514
|
C | T | 1 | a0001c0002t0001g0081 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.180-5024C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56753514 | ||||||
| chr16:56753691
|
C | T | 1 | a0001c0006t0009g0252 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.180-4847C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56753691 | ||||||
| chr16:56753908
|
A | T | 1 | a0001c0001t0006g0216 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.180-4630A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56753908 | ||||||
| chr16:56753970
|
T | C | 23 | a0001c0001t0001g0003a0001c0001t0001g0045a0001c0001t0001g0046others(20): Show | 23 | HG01433.hp1 HG01496.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.180-4568T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56753970 | ||||||
| chr16:56753973
|
A | AT | 34 | a0001c0001t0001g0131a0001c0001t0011g0004a0001c0001t0011g0005others(31): Show | 34 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.180-4552dupT | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr16 | 56753973 | |||||
| chr16:56753973
|
AT | A | 8 | a0001c0001t0001g0115a0001c0001t0004g0240a0001c0001t0006g0203others(5): Show | 8 | HG02451.hp2 HG03209.hp1 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.180-4552delT | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr16 | 56753973 | |||||
| chr16:56753995
|
A | T | 24 | a0001c0001t0004g0198a0001c0001t0004g0220a0001c0001t0004g0221others(21): Show | 24 | HG00408.hp2 HG00597.hp2 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.180-4543A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56753995 | ||||||
| chr16:56754156
|
A | G | 3 | a0001c0007t0012g0345a0001c0007t0012g0346a0001c0007t0012g0347 | 3 | HG02145.hp2 HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.180-4382A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56754156 | ||||||
| chr16:56754209
|
CT | C | 30 | a0001c0004t0005g0020a0001c0004t0005g0021a0001c0004t0005g0022others(27): Show | 30 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.180-4327delT | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr16 | 56754209 | |||||
| chr16:56754279
|
G | T | 46 | a0001c0001t0001g0002a0001c0001t0001g0302a0001c0001t0001g0303others(43): Show | 47 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.180-4259G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56754279 | ||||||
| chr16:56754442
|
T | C | 1 | a0003c0024t0018g0010 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.180-4096T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56754442 | ||||||
| chr16:56754675
|
G | A | 3 | a0001c0007t0012g0345a0001c0007t0012g0346a0001c0007t0012g0347 | 3 | HG02145.hp2 HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.180-3863G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56754675 | ||||||
| chr16:56754842
|
G | A | 45 | a0001c0001t0003g0348a0001c0001t0003g0349a0001c0001t0003g0350others(42): Show | 45 | HG00323.hp1 HG00639.hp1 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.180-3696G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56754842 | ||||||
| chr16:56754879
|
T | C | 1 | a0001c0001t0002g0292 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.180-3659T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56754879 | ||||||
| chr16:56754922
|
C | T | 30 | a0001c0004t0005g0020a0001c0004t0005g0021a0001c0004t0005g0022others(27): Show | 30 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.180-3616C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56754922 | ||||||
| chr16:56754993
|
G | A | 1 | a0010c0013t0007g0190 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.180-3545G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56754993 | ||||||
| chr16:56754996
|
G | A | 3 | a0001c0009t0018g0018a0001c0009t0018g0019a0003c0024t0018g0010 | 3 | HG02451.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.180-3542G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56754996 | ||||||
| chr16:56755054
|
A | G | 1 | a0001c0002t0001g0101 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.180-3484A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56755054 | ||||||
| chr16:56755164
|
C | G | 41 | a0001c0001t0001g0002a0001c0001t0001g0302a0001c0001t0001g0303others(38): Show | 42 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.180-3374C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56755164 | ||||||
| chr16:56755252
|
G | A | 2 | a0001c0002t0010g0048a0001c0002t0010g0050 | 2 | HG01167.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.180-3286G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56755252 | ||||||
| chr16:56755427
|
A | G | 98 | a0001c0001t0001g0002a0001c0001t0001g0302a0001c0001t0001g0303others(95): Show | 99 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.180-3111A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56755427 | ||||||
| chr16:56755595
|
G | A | 2 | a0001c0007t0012g0346a0001c0007t0012g0347 | 2 | HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.180-2943G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56755595 | ||||||
| chr16:56755677
|
C | G | 1 | a0001c0001t0001g0124 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.180-2861C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56755677 | ||||||
| chr16:56756200
|
A | T | 3 | a0001c0001t0001g0114a0001c0001t0001g0120a0001c0001t0001g0121 | 3 | HG03195.hp1 HG03225.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.180-2338A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56756200 | ||||||
| chr16:56756295
|
G | GC | 72 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0125others(69): Show | 72 | HG00423.hp2 HG00558.hp2 HG00609.hp2 others(69): Show |
intron_variant | MODIFIER | c.180-2229dupC | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr16 | 56756295 | |||||
| chr16:56756295
|
G | GCC | 65 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0052others(62): Show | 65 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.180-2230_180-2229d others(4): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr16 | 56756295 | |||||
| chr16:56756295
|
G | GCCC | 24 | a0001c0001t0001g0126a0001c0001t0006g0202a0001c0001t0006g0204others(21): Show | 24 | HG01070.hp2 HG01109.hp2 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.180-2231_180-2229d others(5): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr16 | 56756295 | |||||
| chr16:56756295
|
GC | G | 27 | a0001c0001t0001g0121a0001c0001t0001g0308a0001c0001t0002g0292others(24): Show | 27 | HG00323.hp1 HG00642.hp1 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.180-2229delC | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr16 | 56756295 | |||||
| chr16:56756295
|
GCC | G | 46 | a0001c0001t0001g0002a0001c0001t0001g0302a0001c0001t0001g0303others(43): Show | 47 | HG00099.hp2 HG00438.hp1 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.180-2230_180-2229d others(4): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr16 | 56756295 | |||||
| chr16:56756299
|
C | G | 9 | a0001c0001t0003g0353a0001c0001t0003g0354a0001c0001t0003g0356others(6): Show | 9 | HG02027.hp1 NA18961.hp1 NA18969.hp2 others(6): Show |
intron_variant | MODIFIER | c.180-2239C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56756299 | ||||||
| chr16:56756300
|
C | G | 1 | a0001c0003t0002g0280 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.180-2238C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56756300 | ||||||
| chr16:56756302
|
C | G | 1 | a0001c0001t0029g0245 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.180-2236C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56756302 | ||||||
| chr16:56756303
|
C | A | 1 | a0001c0003t0002g0264 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.180-2235C>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56756303 | ||||||
| chr16:56756303
|
C | CG | 24 | a0001c0001t0004g0198a0001c0001t0004g0220a0001c0001t0004g0221others(21): Show | 24 | HG00408.hp2 HG00597.hp2 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.180-2235_180-2234i others(3): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56756303 | ||||||
| chr16:56756304
|
C | G | 4 | a0001c0001t0002g0292a0001c0001t0013g0012a0001c0001t0013g0013others(1): Show | 4 | HG02717.hp1 HG03041.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.180-2234C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56756304 | ||||||
| chr16:56756305
|
C | G | 16 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(13): Show | 16 | HG00621.hp1 NA18943.hp2 NA18946.hp2 others(13): Show |
intron_variant | MODIFIER | c.180-2233C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56756305 | ||||||
| chr16:56756306
|
C | T | 1 | a0001c0004t0005g0034 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.180-2232C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56756306 | ||||||
| chr16:56756310
|
G | A | 1 | a0001c0001t0001g0116 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.180-2228G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56756310 | ||||||
| chr16:56756368
|
G | A | 6 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(3): Show | 6 | HG01884.hp1 HG02630.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.180-2170G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56756368 | ||||||
| chr16:56756375
|
T | C | 4 | a0002c0008t0002g0298a0002c0008t0002g0299a0002c0008t0002g0300others(1): Show | 4 | NA18954.hp1 NA18966.hp1 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.180-2163T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56756375 | ||||||
| chr16:56756431
|
A | G | 50 | a0001c0001t0002g0284a0001c0001t0002g0292a0001c0001t0002g0295others(47): Show | 50 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.180-2107A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56756431 | ||||||
| chr16:56756440
|
A | G | 364 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0045others(361): Show | 366 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(363): Show |
intron_variant | MODIFIER | c.180-2098A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56756440 | ||||||
| chr16:56756545
|
G | A | 1 | a0001c0001t0001g0124 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.180-1993G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56756545 | ||||||
| chr16:56756596
|
G | A | 5 | a0001c0006t0009g0249a0001c0006t0009g0250a0001c0006t0009g0251others(2): Show | 5 | HG02109.hp2 HG02615.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.180-1942G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56756596 | ||||||
| chr16:56756795
|
C | T | 1 | a0001c0004t0008g0177 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.180-1743C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56756795 | ||||||
| chr16:56756966
|
T | C | 2 | a0001c0002t0001g0108a0001c0002t0001g0109 | 2 | HG00140.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.180-1572T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56756966 | ||||||
| chr16:56757304
|
A | G | 1 | a0001c0001t0029g0245 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.180-1234A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56757304 | ||||||
| chr16:56757471
|
C | G | 3 | a0001c0001t0013g0012a0001c0001t0013g0013a0001c0001t0013g0014 | 3 | HG03041.hp1 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.180-1067C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56757471 | ||||||
| chr16:56757482
|
C | T | 1 | a0001c0001t0003g0374 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.180-1056C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56757482 | ||||||
| chr16:56757540
|
T | C | 2 | a0001c0003t0002g0257a0001c0003t0002g0258 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.180-998T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56757540 | ||||||
| chr16:56757568
|
T | C | 24 | a0001c0004t0005g0020a0001c0004t0005g0021a0001c0004t0005g0022others(21): Show | 24 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(21): Show |
intron_variant | MODIFIER | c.180-970T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56757568 | ||||||
| chr16:56757572
|
A | G | 3 | a0001c0007t0012g0345a0001c0007t0012g0346a0001c0007t0012g0347 | 3 | HG02145.hp2 HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.180-966A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56757572 | ||||||
| chr16:56757687
|
C | T | 1 | a0001c0009t0018g0018 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.180-851C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56757687 | ||||||
| chr16:56757767
|
A | G | 17 | a0001c0001t0006g0202a0001c0001t0006g0203a0001c0001t0006g0204others(14): Show | 17 | HG01070.hp2 HG01168.hp2 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.180-771A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56757767 | ||||||
| chr16:56757829
|
C | A | 2 | a0001c0010t0022g0260a0001c0010t0033g0261 | 2 | HG03139.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.180-709C>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56757829 | ||||||
| chr16:56757856
|
C | T | 1 | a0001c0001t0034g0196 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.180-682C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56757856 | ||||||
| chr16:56757951
|
T | C | 7 | a0001c0002t0001g0064a0001c0002t0001g0066a0001c0002t0001g0067others(4): Show | 7 | HG01891.hp1 HG02572.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.180-587T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56757951 | ||||||
| chr16:56757963
|
C | T | 20 | a0001c0001t0006g0199a0001c0001t0006g0200a0001c0001t0006g0201others(17): Show | 20 | HG01070.hp2 HG01168.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.180-575C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56757963 | ||||||
| chr16:56757971
|
T | C | 1 | a0001c0001t0029g0245 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.180-567T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56757971 | ||||||
| chr16:56758020
|
G | A | 3 | a0001c0004t0015g0015a0001c0004t0015g0016a0001c0004t0015g0017 | 3 | HG02818.hp1 HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.180-518G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56758020 | ||||||
| chr16:56758071
|
AG | A | 131 | a0001c0001t0001g0003a0001c0001t0001g0045a0001c0001t0001g0046others(128): Show | 132 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.180-466delG | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56758071 | ||||||
| chr16:56758087
|
T | C | 3 | a0001c0001t0013g0012a0001c0001t0013g0013a0001c0001t0013g0014 | 3 | HG03041.hp1 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.180-451T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56758087 | ||||||
| chr16:56758087
|
T | G | 131 | a0001c0001t0003g0348a0001c0001t0003g0349a0001c0001t0003g0350others(128): Show | 131 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.180-451T>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56758087 | ||||||
| chr16:56758104
|
A | G | 164 | a0001c0001t0001g0003a0001c0001t0001g0045a0001c0001t0001g0046others(161): Show | 165 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.180-434A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56758104 | ||||||
| chr16:56758527
|
T | A | 6 | a0001c0001t0006g0202a0001c0001t0006g0204a0001c0001t0006g0205others(3): Show | 6 | HG02015.hp1 HG02083.hp1 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.180-11T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 2/21 | chr16 | 56758527 | ||||||
| chr16:56758973
|
C | T | 1 | a0001c0006t0009g0249 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.297+318C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56758973 | ||||||
| chr16:56759015
|
C | T | 24 | a0001c0001t0004g0198a0001c0001t0004g0220a0001c0001t0004g0221others(21): Show | 24 | HG00408.hp2 HG00597.hp2 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.297+360C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56759015 | ||||||
| chr16:56759045
|
T | A | 24 | a0001c0001t0004g0198a0001c0001t0004g0220a0001c0001t0004g0221others(21): Show | 24 | HG00408.hp2 HG00597.hp2 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.297+390T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56759045 | ||||||
| chr16:56759155
|
G | T | 1 | a0001c0014t0001g0137 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.297+500G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56759155 | ||||||
| chr16:56759192
|
A | G | 27 | a0001c0004t0005g0020a0001c0004t0005g0021a0001c0004t0005g0022others(24): Show | 27 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(24): Show |
intron_variant | MODIFIER | c.297+537A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56759192 | ||||||
| chr16:56759357
|
G | T | 2 | a0001c0001t0006g0203a0001c0001t0006g0208 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.297+702G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56759357 | ||||||
| chr16:56759434
|
C | A | 103 | a0001c0001t0001g0002a0001c0001t0001g0302a0001c0001t0001g0303others(100): Show | 104 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.297+779C>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56759434 | ||||||
| chr16:56759713
|
C | T | 2 | a0001c0003t0002g0246a0001c0003t0002g0247 | 2 | NA18939.hp1 NA18940.hp1 |
intron_variant | MODIFIER | c.297+1058C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56759713 | ||||||
| chr16:56759720
|
C | G | 1 | a0001c0003t0002g0272 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.297+1065C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56759720 | ||||||
| chr16:56759721
|
G | A | 1 | a0001c0001t0006g0216 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.297+1066G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56759721 | ||||||
| chr16:56759838
|
T | C | 1 | a0001c0001t0001g0120 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.297+1183T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56759838 | ||||||
| chr16:56759903
|
A | G | 1 | a0001c0001t0001g0126 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.297+1248A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56759903 | ||||||
| chr16:56760354
|
C | A | 2 | a0001c0002t0001g0096a0001c0002t0001g0110 | 2 | HG02258.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.297+1699C>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56760354 | ||||||
| chr16:56760403
|
G | C | 24 | a0001c0004t0005g0020a0001c0004t0005g0021a0001c0004t0005g0022others(21): Show | 24 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(21): Show |
intron_variant | MODIFIER | c.297+1748G>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56760403 | ||||||
| chr16:56760678
|
C | G | 27 | a0001c0004t0005g0020a0001c0004t0005g0021a0001c0004t0005g0022others(24): Show | 27 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(24): Show |
intron_variant | MODIFIER | c.297+2023C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56760678 | ||||||
| chr16:56760770
|
C | T | 3 | a0001c0001t0013g0012a0001c0001t0013g0013a0001c0001t0013g0014 | 3 | HG03041.hp1 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.297+2115C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56760770 | ||||||
| chr16:56760841
|
G | A | 3 | a0001c0001t0013g0012a0001c0001t0013g0013a0001c0001t0013g0014 | 3 | HG03041.hp1 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.297+2186G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56760841 | ||||||
| chr16:56760967
|
C | A | 21 | a0001c0001t0001g0309a0001c0001t0006g0199a0001c0001t0006g0200others(18): Show | 21 | HG01070.hp2 HG01168.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.297+2312C>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56760967 | ||||||
| chr16:56761025
|
A | G | 104 | a0001c0001t0001g0002a0001c0001t0001g0302a0001c0001t0001g0303others(101): Show | 105 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.297+2370A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56761025 | ||||||
| chr16:56761209
|
T | C | 5 | a0001c0001t0006g0210a0001c0001t0006g0211a0001c0001t0006g0212others(2): Show | 5 | HG01070.hp2 HG01243.hp1 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.297+2554T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56761209 | ||||||
| chr16:56761380
|
T | C | 25 | a0001c0001t0004g0198a0001c0001t0004g0220a0001c0001t0004g0221others(22): Show | 25 | HG00408.hp2 HG00597.hp2 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.297+2725T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56761380 | ||||||
| chr16:56761421
|
T | C | 3 | a0001c0001t0016g0191a0001c0001t0016g0192a0001c0001t0016g0193 | 3 | HG02258.hp2 HG03130.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.297+2766T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56761421 | ||||||
| chr16:56761423
|
A | C | 1 | a0001c0002t0001g0128 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.297+2768A>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56761423 | ||||||
| chr16:56761561
|
A | AT | 349 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0045others(346): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.297+2916dupT | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56761561 | |||||
| chr16:56761561
|
A | ATT | 14 | a0001c0001t0001g0166a0001c0001t0013g0012a0001c0001t0013g0013others(11): Show | 14 | HG00741.hp1 HG01106.hp1 HG01258.hp2 others(11): Show |
intron_variant | MODIFIER | c.297+2915_297+2916d others(4): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56761561 | |||||
| chr16:56761694
|
G | A | 30 | a0001c0004t0005g0020a0001c0004t0005g0021a0001c0004t0005g0022others(27): Show | 30 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.297+3039G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56761694 | ||||||
| chr16:56761711
|
A | C | 2 | a0001c0001t0001g0149a0001c0001t0001g0159 | 2 | NA18961.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.297+3056A>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56761711 | ||||||
| chr16:56762169
|
T | C | 8 | a0001c0005t0007g0183a0001c0005t0007g0184a0001c0005t0007g0185others(5): Show | 8 | HG02257.hp2 HG02559.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.297+3514T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56762169 | ||||||
| chr16:56762848
|
G | T | 3 | a0001c0001t0003g0366a0001c0001t0003g0375a0001c0001t0003g0376 | 3 | HG01081.hp2 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.297+4193G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56762848 | ||||||
| chr16:56762877
|
G | A | 1 | a0001c0002t0001g0096 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.297+4222G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56762877 | ||||||
| chr16:56762992
|
A | G | 47 | a0001c0001t0001g0169a0001c0001t0043g0154a0001c0002t0001g0044others(44): Show | 47 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.297+4337A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56762992 | ||||||
| chr16:56763059
|
T | C | 8 | a0001c0005t0007g0183a0001c0005t0007g0184a0001c0005t0007g0185others(5): Show | 8 | HG02257.hp2 HG02559.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.297+4404T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56763059 | ||||||
| chr16:56763289
|
A | G | 1 | a0001c0002t0001g0074 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.297+4634A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56763289 | ||||||
| chr16:56763455
|
G | A | 3 | a0001c0001t0014g0217a0001c0001t0014g0218a0001c0001t0014g0219 | 3 | HG01884.hp2 HG03453.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.297+4800G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56763455 | ||||||
| chr16:56763495
|
T | G | 3 | a0001c0001t0013g0012a0001c0001t0013g0013a0001c0001t0013g0014 | 3 | HG03041.hp1 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.297+4840T>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56763495 | ||||||
| chr16:56763503
|
G | GGT | 3 | a0001c0001t0003g0366a0001c0001t0003g0375a0001c0001t0003g0376 | 3 | HG01081.hp2 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.297+4859_297+4860d others(4): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56763503 | |||||
| chr16:56763503
|
G | T | 1 | a0001c0003t0002g0268 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.297+4848G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56763503 | ||||||
| chr16:56763503
|
GGTGTGTG others(17): Show |
G | 14 | a0001c0002t0001g0001a0001c0002t0001g0051a0001c0002t0001g0070others(11): Show | 15 | HG00323.hp2 HG00642.hp1 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.297+4865_297+4888d others(26): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56763503 | |||||
| chr16:56763892
|
A | G | 1 | a0001c0001t0029g0245 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.297+5237A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56763892 | ||||||
| chr16:56764004
|
A | G | 1 | a0003c0024t0018g0010 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.297+5349A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56764004 | ||||||
| chr16:56764268
|
A | C | 2 | a0001c0001t0003g0354a0001c0001t0003g0374 | 2 | NA19062.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.297+5613A>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56764268 | ||||||
| chr16:56764276
|
A | T | 1 | a0001c0001t0001g0320 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.297+5621A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56764276 | ||||||
| chr16:56764319
|
G | T | 1 | a0001c0001t0001g0334 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.297+5664G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56764319 | ||||||
| chr16:56764377
|
C | G | 2 | a0001c0001t0016g0192a0001c0001t0016g0193 | 2 | HG02258.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.297+5722C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56764377 | ||||||
| chr16:56764707
|
T | TG | 3 | a0001c0009t0018g0018a0001c0009t0018g0019a0003c0024t0018g0010 | 3 | HG02451.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.297+6054dupG | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56764707 | |||||
| chr16:56765163
|
G | A | 1 | a0001c0002t0001g0058 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.297+6508G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56765163 | ||||||
| chr16:56765315
|
C | T | 2 | a0001c0002t0001g0096a0001c0002t0001g0110 | 2 | HG02258.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.297+6660C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56765315 | ||||||
| chr16:56765379
|
A | T | 131 | a0001c0001t0001g0003a0001c0001t0001g0045a0001c0001t0001g0046others(128): Show | 132 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.297+6724A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56765379 | ||||||
| chr16:56765441
|
A | G | 1 | a0001c0001t0007g0340 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.297+6786A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56765441 | ||||||
| chr16:56765838
|
G | A | 1 | a0001c0001t0003g0361 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.297+7183G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56765838 | ||||||
| chr16:56765893
|
T | G | 24 | a0001c0001t0004g0198a0001c0001t0004g0220a0001c0001t0004g0221others(21): Show | 24 | HG00408.hp2 HG00597.hp2 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.297+7238T>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56765893 | ||||||
| chr16:56765973
|
T | TTAAAAAT others(13): Show |
11 | a0001c0004t0008g0172a0001c0004t0008g0173a0001c0004t0008g0174others(8): Show | 11 | HG00099.hp2 HG00741.hp1 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.297+7328_297+7347d others(22): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56765973 | |||||
| chr16:56766006
|
G | A | 2 | a0001c0001t0001g0310a0001c0003t0002g0288 | 2 | HG00544.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.297+7351G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56766006 | ||||||
| chr16:56766130
|
A | G | 1 | a0001c0001t0029g0245 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.297+7475A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56766130 | ||||||
| chr16:56766139
|
G | T | 1 | a0001c0003t0002g0293 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.297+7484G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56766139 | ||||||
| chr16:56766193
|
G | A | 4 | a0001c0001t0006g0204a0001c0001t0006g0205a0001c0001t0006g0206others(1): Show | 4 | HG02083.hp1 NA18747.hp2 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.297+7538G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56766193 | ||||||
| chr16:56766271
|
A | T | 6 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(3): Show | 6 | HG01884.hp1 HG02630.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.297+7616A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56766271 | ||||||
| chr16:56766415
|
C | T | 1 | a0001c0001t0001g0321 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.297+7760C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56766415 | ||||||
| chr16:56766421
|
T | A | 330 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0045others(327): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.297+7766T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56766421 | ||||||
| chr16:56766599
|
G | T | 1 | a0001c0001t0003g0369 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.297+7944G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56766599 | ||||||
| chr16:56766715
|
C | T | 2 | a0001c0002t0001g0108a0001c0002t0001g0109 | 2 | HG00140.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.297+8060C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56766715 | ||||||
| chr16:56766731
|
C | A | 1 | a0001c0002t0001g0082 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.297+8076C>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56766731 | ||||||
| chr16:56766831
|
GA | G | 3 | a0001c0002t0010g0048a0001c0002t0010g0049a0001c0002t0010g0050 | 3 | HG01069.hp2 HG01167.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.297+8177delA | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56766831 | ||||||
| chr16:56767135
|
C | T | 30 | a0001c0004t0005g0020a0001c0004t0005g0021a0001c0004t0005g0022others(27): Show | 30 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.297+8480C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56767135 | ||||||
| chr16:56767370
|
A | T | 3 | a0001c0001t0013g0012a0001c0001t0013g0013a0001c0001t0013g0014 | 3 | HG03041.hp1 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.297+8715A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56767370 | ||||||
| chr16:56767467
|
T | G | 1 | a0001c0001t0034g0196 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.297+8812T>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56767467 | ||||||
| chr16:56767514
|
T | A | 1 | a0001c0009t0018g0019 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.297+8859T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56767514 | ||||||
| chr16:56767695
|
G | A | 41 | a0001c0001t0001g0002a0001c0001t0001g0302a0001c0001t0001g0303others(38): Show | 42 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.297+9040G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56767695 | ||||||
| chr16:56767783
|
C | T | 1 | a0001c0001t0006g0212 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.297+9128C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56767783 | ||||||
| chr16:56767784
|
G | A | 98 | a0001c0001t0001g0002a0001c0001t0001g0302a0001c0001t0001g0303others(95): Show | 99 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.297+9129G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56767784 | ||||||
| chr16:56767848
|
C | T | 2 | a0001c0001t0016g0192a0001c0001t0016g0193 | 2 | HG02258.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.297+9193C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56767848 | ||||||
| chr16:56767946
|
A | T | 3 | a0001c0001t0013g0012a0001c0001t0013g0013a0001c0001t0013g0014 | 3 | HG03041.hp1 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.297+9291A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56767946 | ||||||
| chr16:56768013
|
A | G | 3 | a0001c0004t0015g0015a0001c0004t0015g0016a0001c0004t0015g0017 | 3 | HG02818.hp1 HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.297+9358A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56768013 | ||||||
| chr16:56768080
|
A | T | 1 | a0001c0001t0001g0327 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.297+9425A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56768080 | ||||||
| chr16:56768180
|
A | G | 30 | a0001c0004t0005g0020a0001c0004t0005g0021a0001c0004t0005g0022others(27): Show | 30 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.297+9525A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56768180 | ||||||
| chr16:56768259
|
G | A | 2 | a0001c0001t0001g0003a0001c0001t0001g0116 | 2 | HG03098.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.297+9604G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56768259 | ||||||
| chr16:56768301
|
C | T | 126 | a0001c0001t0001g0003a0001c0001t0001g0045a0001c0001t0001g0046others(123): Show | 127 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.297+9646C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56768301 | ||||||
| chr16:56768302
|
G | T | 1 | a0001c0001t0011g0006 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.297+9647G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56768302 | ||||||
| chr16:56768334
|
T | G | 49 | a0001c0001t0002g0284a0001c0001t0002g0295a0001c0003t0002g0047others(46): Show | 49 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.297+9679T>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56768334 | ||||||
| chr16:56768432
|
G | A | 4 | a0001c0003t0002g0257a0001c0003t0002g0258a0001c0003t0002g0265others(1): Show | 4 | HG01069.hp1 HG01071.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.297+9777G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56768432 | ||||||
| chr16:56768450
|
C | T | 28 | a0001c0004t0005g0020a0001c0004t0005g0021a0001c0004t0005g0022others(25): Show | 28 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(25): Show |
intron_variant | MODIFIER | c.297+9795C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56768450 | ||||||
| chr16:56768455
|
C | T | 2 | a0001c0004t0019g0180a0001c0004t0019g0181 | 2 | HG03491.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.297+9800C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56768455 | ||||||
| chr16:56768519
|
C | T | 1 | a0001c0001t0014g0217 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.297+9864C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56768519 | ||||||
| chr16:56768574
|
A | T | 2 | a0001c0001t0006g0211a0001c0001t0006g0215 | 2 | HG01255.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.297+9919A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56768574 | ||||||
| chr16:56768575
|
T | A | 6 | a0001c0001t0014g0217a0001c0001t0014g0218a0001c0001t0014g0219others(3): Show | 6 | HG01884.hp2 HG02818.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.297+9920T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56768575 | ||||||
| chr16:56768602
|
T | C | 42 | a0001c0001t0001g0002a0001c0001t0001g0138a0001c0001t0001g0302others(39): Show | 43 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.297+9947T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56768602 | ||||||
| chr16:56768638
|
G | A | 1 | a0001c0007t0012g0346 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.297+9983G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56768638 | ||||||
| chr16:56768683
|
G | A | 24 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0007g0194others(21): Show | 24 | HG00642.hp2 HG01109.hp1 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.297+10028G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56768683 | ||||||
| chr16:56768693
|
T | C | 14 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(11): Show | 14 | HG00621.hp1 NA18943.hp2 NA18961.hp2 others(11): Show |
intron_variant | MODIFIER | c.297+10038T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56768693 | ||||||
| chr16:56768702
|
TA | T | 15 | a0001c0001t0001g0052a0001c0001t0001g0130a0001c0001t0001g0132others(12): Show | 15 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.297+10053delA | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56768702 | |||||
| chr16:56768724
|
T | A | 2 | a0001c0011t0001g0089a0001c0011t0001g0090 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.297+10069T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56768724 | ||||||
| chr16:56768724
|
T | G | 14 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(11): Show | 14 | HG00621.hp1 NA18943.hp2 NA18961.hp2 others(11): Show |
intron_variant | MODIFIER | c.297+10069T>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56768724 | ||||||
| chr16:56768727
|
T | C | 14 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(11): Show | 14 | HG00621.hp1 NA18943.hp2 NA18961.hp2 others(11): Show |
intron_variant | MODIFIER | c.297+10072T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56768727 | ||||||
| chr16:56768728
|
G | A | 13 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(10): Show | 13 | HG00621.hp1 NA18943.hp2 NA18961.hp2 others(10): Show |
intron_variant | MODIFIER | c.297+10073G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56768728 | ||||||
| chr16:56768736
|
G | A | 28 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0004g0198others(25): Show | 28 | HG00408.hp2 HG00597.hp2 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.297+10081G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56768736 | ||||||
| chr16:56768759
|
C | T | 4 | a0001c0006t0009g0249a0001c0006t0009g0250a0001c0006t0009g0251others(1): Show | 4 | HG02109.hp2 HG02615.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.297+10104C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56768759 | ||||||
| chr16:56768866
|
C | CAA | 8 | a0001c0001t0001g0304a0001c0001t0001g0305a0001c0001t0001g0322others(5): Show | 8 | HG00140.hp2 HG00735.hp2 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.297+10225_297+1022 others(6): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56768866 | |||||
| chr16:56768866
|
C | CAAA | 243 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0045others(240): Show | 245 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(242): Show |
intron_variant | MODIFIER | c.297+10224_297+1022 others(7): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56768866 | |||||
| chr16:56768866
|
C | CAAAA | 42 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0303others(39): Show | 42 | HG00423.hp2 HG00558.hp2 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.297+10223_297+1022 others(8): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56768866 | |||||
| chr16:56768866
|
CA | C | 25 | a0001c0001t0004g0198a0001c0001t0004g0220a0001c0001t0004g0221others(22): Show | 25 | HG00408.hp2 HG00597.hp2 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.297+10226delA | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56768866 | |||||
| chr16:56769113
|
A | G | 4 | a0001c0004t0008g0174a0001c0004t0008g0175a0001c0004t0008g0176others(1): Show | 4 | HG00099.hp2 HG00741.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.297+10458A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56769113 | ||||||
| chr16:56769209
|
A | G | 2 | a0001c0002t0001g0167a0001c0012t0001g0079 | 2 | NA19066.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.297+10554A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56769209 | ||||||
| chr16:56769226
|
A | G | 6 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(3): Show | 6 | HG01884.hp1 HG02630.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.297+10571A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56769226 | ||||||
| chr16:56769287
|
C | T | 24 | a0001c0001t0004g0198a0001c0001t0004g0220a0001c0001t0004g0221others(21): Show | 24 | HG00408.hp2 HG00597.hp2 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.297+10632C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56769287 | ||||||
| chr16:56769288
|
G | A | 7 | a0001c0002t0001g0064a0001c0002t0001g0066a0001c0002t0001g0067others(4): Show | 7 | HG01891.hp1 HG02572.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.297+10633G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56769288 | ||||||
| chr16:56769379
|
G | A | 1 | a0001c0001t0036g0148 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.297+10724G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56769379 | ||||||
| chr16:56769590
|
A | AG | 24 | a0001c0001t0003g0362a0001c0001t0006g0199a0001c0001t0006g0200others(21): Show | 24 | HG01070.hp2 HG01168.hp2 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.297+10937dupG | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56769590 | |||||
| chr16:56769717
|
C | T | 2 | a0001c0001t0001g0118a0001c0001t0001g0126 | 2 | HG04204.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.297+11062C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56769717 | ||||||
| chr16:56769746
|
T | C | 3 | a0001c0001t0014g0217a0001c0001t0014g0218a0001c0001t0014g0219 | 3 | HG01884.hp2 HG03453.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.297+11091T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56769746 | ||||||
| chr16:56769794
|
A | C | 98 | a0001c0001t0001g0002a0001c0001t0001g0302a0001c0001t0001g0303others(95): Show | 99 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.297+11139A>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56769794 | ||||||
| chr16:56770128
|
G | A | 1 | a0001c0002t0001g0104 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.297+11473G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56770128 | ||||||
| chr16:56770282
|
G | A | 24 | a0001c0001t0004g0198a0001c0001t0004g0220a0001c0001t0004g0221others(21): Show | 24 | HG00408.hp2 HG00597.hp2 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.297+11627G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56770282 | ||||||
| chr16:56770492
|
G | A | 2 | a0001c0002t0001g0098a0001c0002t0040g0097 | 2 | HG02886.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.297+11837G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56770492 | ||||||
| chr16:56770526
|
C | T | 1 | a0001c0001t0006g0213 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.297+11871C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56770526 | ||||||
| chr16:56770565
|
T | C | 1 | a0001c0016t0001g0117 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.297+11910T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56770565 | ||||||
| chr16:56770780
|
T | A | 2 | a0001c0001t0023g0329a0001c0001t0023g0330 | 2 | NA18991.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.297+12125T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56770780 | ||||||
| chr16:56770907
|
T | TA | 97 | a0001c0001t0001g0002a0001c0001t0001g0302a0001c0001t0001g0303others(94): Show | 98 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.297+12263dupA | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56770907 | |||||
| chr16:56770982
|
G | C | 4 | a0001c0002t0001g0076a0001c0002t0001g0081a0001c0002t0001g0167others(1): Show | 4 | HG02071.hp2 HG02080.hp1 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.297+12327G>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56770982 | ||||||
| chr16:56770999
|
C | T | 1 | a0001c0001t0007g0340 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.297+12344C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56770999 | ||||||
| chr16:56771162
|
G | A | 1 | a0001c0009t0018g0019 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.297+12507G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56771162 | ||||||
| chr16:56771453
|
G | A | 12 | a0001c0002t0001g0001a0001c0002t0001g0051a0001c0002t0001g0070others(9): Show | 13 | HG00323.hp2 HG00642.hp1 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.297+12798G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56771453 | ||||||
| chr16:56771563
|
G | A | 2 | a0001c0010t0022g0260a0001c0010t0033g0261 | 2 | HG03139.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.297+12908G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56771563 | ||||||
| chr16:56771566
|
G | A | 2 | a0001c0001t0011g0009a0001c0001t0046g0008 | 2 | HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.297+12911G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56771566 | ||||||
| chr16:56771598
|
A | T | 98 | a0001c0001t0001g0002a0001c0001t0001g0302a0001c0001t0001g0303others(95): Show | 99 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.297+12943A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56771598 | ||||||
| chr16:56771642
|
A | G | 3 | a0001c0001t0016g0191a0001c0001t0016g0192a0001c0001t0016g0193 | 3 | HG02258.hp2 HG03130.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.297+12987A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56771642 | ||||||
| chr16:56771670
|
A | G | 41 | a0001c0001t0001g0002a0001c0001t0001g0302a0001c0001t0001g0303others(38): Show | 42 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.297+13015A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56771670 | ||||||
| chr16:56772167
|
G | A | 30 | a0001c0004t0005g0020a0001c0004t0005g0021a0001c0004t0005g0022others(27): Show | 30 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.297+13512G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56772167 | ||||||
| chr16:56772358
|
C | T | 3 | a0001c0004t0015g0015a0001c0004t0015g0016a0001c0004t0015g0017 | 3 | HG02818.hp1 HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.297+13703C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56772358 | ||||||
| chr16:56772549
|
T | C | 3 | a0001c0001t0016g0191a0001c0001t0016g0192a0001c0001t0016g0193 | 3 | HG02258.hp2 HG03130.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.297+13894T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56772549 | ||||||
| chr16:56772627
|
T | C | 1 | a0001c0002t0001g0127 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.297+13972T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56772627 | ||||||
| chr16:56772788
|
G | T | 1 | a0006c0021t0001g0011 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.297+14133G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56772788 | ||||||
| chr16:56772879
|
T | C | 1 | a0001c0002t0001g0080 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.297+14224T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56772879 | ||||||
| chr16:56772890
|
G | A | 1 | a0001c0003t0002g0268 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.297+14235G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56772890 | ||||||
| chr16:56773016
|
A | C | 2 | a0001c0011t0001g0089a0001c0011t0001g0090 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.297+14361A>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56773016 | ||||||
| chr16:56773051
|
A | G | 1 | a0001c0001t0036g0148 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.297+14396A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56773051 | ||||||
| chr16:56773461
|
T | C | 1 | a0001c0009t0018g0018 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.297+14806T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56773461 | ||||||
| chr16:56773478
|
T | G | 1 | a0007c0020t0001g0063 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.297+14823T>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56773478 | ||||||
| chr16:56773667
|
G | C | 164 | a0001c0001t0001g0003a0001c0001t0001g0045a0001c0001t0001g0046others(161): Show | 165 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.297+15012G>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56773667 | ||||||
| chr16:56773718
|
G | A | 6 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(3): Show | 6 | HG01884.hp1 HG02630.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.297+15063G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56773718 | ||||||
| chr16:56773984
|
C | A | 3 | a0001c0001t0013g0012a0001c0001t0013g0013a0001c0001t0013g0014 | 3 | HG03041.hp1 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.297+15329C>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56773984 | ||||||
| chr16:56774445
|
T | C | 1 | a0001c0003t0002g0273 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.297+15790T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56774445 | ||||||
| chr16:56774624
|
A | G | 4 | a0001c0002t0001g0066a0001c0002t0001g0067a0001c0002t0001g0068others(1): Show | 4 | HG02622.hp1 HG02647.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.297+15969A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56774624 | ||||||
| chr16:56774700
|
T | C | 131 | a0001c0001t0001g0003a0001c0001t0001g0045a0001c0001t0001g0046others(128): Show | 132 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.297+16045T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56774700 | ||||||
| chr16:56774731
|
G | A | 19 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(16): Show | 19 | HG00621.hp1 HG02071.hp1 HG03239.hp2 others(16): Show |
intron_variant | MODIFIER | c.297+16076G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56774731 | ||||||
| chr16:56774891
|
G | T | 4 | a0001c0001t0006g0199a0001c0001t0006g0200a0001c0001t0006g0201others(1): Show | 4 | HG02559.hp1 HG02976.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.297+16236G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56774891 | ||||||
| chr16:56774903
|
G | GT | 32 | a0001c0001t0001g0052a0001c0001t0001g0147a0001c0001t0001g0333others(29): Show | 32 | HG00408.hp2 HG00597.hp2 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.297+16262dupT | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56774903 | |||||
| chr16:56774903
|
GT | G | 7 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(4): Show | 7 | HG01884.hp1 HG02630.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.297+16262delT | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56774903 | |||||
| chr16:56774909
|
T | G | 1 | a0001c0001t0034g0196 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.297+16254T>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56774909 | ||||||
| chr16:56774931
|
G | A | 98 | a0001c0001t0001g0002a0001c0001t0001g0302a0001c0001t0001g0303others(95): Show | 99 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.297+16276G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56774931 | ||||||
| chr16:56775422
|
T | C | 2 | a0001c0001t0001g0303a0001c0001t0001g0311 | 2 | NA18971.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.297+16767T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56775422 | ||||||
| chr16:56775521
|
G | A | 3 | a0001c0005t0007g0183a0001c0005t0007g0184a0001c0005t0007g0185 | 3 | HG02257.hp2 HG02809.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.297+16866G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56775521 | ||||||
| chr16:56775541
|
AG | A | 131 | a0001c0001t0001g0003a0001c0001t0001g0045a0001c0001t0001g0046others(128): Show | 132 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.297+16887delG | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56775541 | ||||||
| chr16:56775718
|
A | G | 1 | a0001c0010t0033g0261 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.297+17063A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56775718 | ||||||
| chr16:56775834
|
G | T | 23 | a0001c0001t0006g0199a0001c0001t0006g0200a0001c0001t0006g0201others(20): Show | 23 | HG01070.hp2 HG01168.hp2 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.297+17179G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56775834 | ||||||
| chr16:56775945
|
T | G | 4 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(1): Show | 4 | NA18939.hp2 NA18964.hp2 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.297+17290T>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56775945 | ||||||
| chr16:56776058
|
AT | A | 160 | a0001c0001t0001g0003a0001c0001t0001g0045a0001c0001t0001g0046others(157): Show | 161 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.297+17414delT | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56776058 | |||||
| chr16:56776219
|
T | C | 1 | a0001c0001t0029g0245 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.297+17564T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56776219 | ||||||
| chr16:56776223
|
GT | G | 98 | a0001c0001t0001g0002a0001c0001t0001g0302a0001c0001t0001g0303others(95): Show | 99 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.297+17574delT | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56776223 | |||||
| chr16:56776360
|
T | C | 1 | a0001c0002t0001g0339 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.297+17705T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56776360 | ||||||
| chr16:56776633
|
G | A | 1 | a0001c0003t0002g0047 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.297+17978G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56776633 | ||||||
| chr16:56776810
|
C | G | 1 | a0001c0001t0003g0374 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.297+18155C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56776810 | ||||||
| chr16:56777022
|
G | C | 1 | a0001c0001t0001g0332 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.297+18367G>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56777022 | ||||||
| chr16:56777038
|
G | A | 3 | a0001c0001t0003g0349a0001c0001t0003g0350a0001c0001t0003g0355 | 3 | HG01070.hp1 HG01071.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.297+18383G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56777038 | ||||||
| chr16:56777149
|
G | A | 1 | a0001c0001t0016g0191 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.297+18494G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56777149 | ||||||
| chr16:56777275
|
A | G | 11 | a0001c0001t0007g0194a0001c0001t0007g0195a0001c0005t0007g0183others(8): Show | 11 | HG00642.hp2 HG02257.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.297+18620A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56777275 | ||||||
| chr16:56777362
|
C | CT | 3 | a0001c0001t0014g0217a0001c0001t0014g0218a0001c0001t0014g0219 | 3 | HG01884.hp2 HG03453.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.297+18708dupT | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56777362 | |||||
| chr16:56777501
|
C | A | 3 | a0001c0009t0018g0018a0001c0009t0018g0019a0003c0024t0018g0010 | 3 | HG02451.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.297+18846C>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56777501 | ||||||
| chr16:56777506
|
C | CT | 6 | a0001c0001t0006g0210a0001c0001t0006g0211a0001c0001t0006g0212others(3): Show | 6 | HG01070.hp2 HG01243.hp1 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.297+18859dupT | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56777506 | |||||
| chr16:56777549
|
A | C | 57 | a0001c0001t0001g0003a0001c0001t0001g0045a0001c0001t0001g0046others(54): Show | 57 | HG00099.hp1 HG00621.hp1 HG00735.hp1 others(54): Show |
intron_variant | MODIFIER | c.297+18894A>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56777549 | ||||||
| chr16:56777603
|
T | G | 2 | a0001c0002t0001g0083a0001c0002t0001g0344 | 2 | HG02015.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.297+18948T>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56777603 | ||||||
| chr16:56777677
|
C | T | 1 | a0001c0004t0005g0028 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.297+19022C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56777677 | ||||||
| chr16:56777692
|
G | A | 3 | a0001c0001t0014g0217a0001c0001t0014g0218a0001c0001t0014g0219 | 3 | HG01884.hp2 HG03453.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.297+19037G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56777692 | ||||||
| chr16:56777717
|
A | G | 1 | a0001c0001t0017g0307 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.297+19062A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56777717 | ||||||
| chr16:56777780
|
T | C | 167 | a0001c0001t0001g0003a0001c0001t0001g0045a0001c0001t0001g0046others(164): Show | 168 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.297+19125T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56777780 | ||||||
| chr16:56777913
|
G | A | 1 | a0001c0001t0006g0216 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.297+19258G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56777913 | ||||||
| chr16:56777955
|
T | C | 1 | a0001c0003t0002g0256 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.297+19300T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56777955 | ||||||
| chr16:56778076
|
A | G | 6 | a0001c0001t0004g0198a0001c0001t0004g0238a0001c0001t0004g0239others(3): Show | 6 | HG00597.hp2 NA18959.hp2 NA18972.hp2 others(3): Show |
intron_variant | MODIFIER | c.297+19421A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56778076 | ||||||
| chr16:56778101
|
C | T | 1 | a0006c0021t0001g0011 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.297+19446C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56778101 | ||||||
| chr16:56778102
|
G | A | 1 | a0001c0002t0001g0096 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.297+19447G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56778102 | ||||||
| chr16:56778199
|
A | G | 3 | a0001c0003t0002g0267a0001c0003t0002g0275a0001c0003t0002g0296 | 3 | NA18942.hp2 NA18981.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.297+19544A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56778199 | ||||||
| chr16:56778388
|
C | T | 167 | a0001c0001t0001g0003a0001c0001t0001g0045a0001c0001t0001g0046others(164): Show | 168 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.297+19733C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56778388 | ||||||
| chr16:56778441
|
A | G | 1 | a0001c0001t0001g0310 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.297+19786A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56778441 | ||||||
| chr16:56778559
|
G | T | 1 | a0001c0001t0001g0045 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.297+19904G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56778559 | ||||||
| chr16:56778765
|
A | C | 6 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(3): Show | 6 | HG01884.hp1 HG02630.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.298-19711A>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56778765 | ||||||
| chr16:56778862
|
C | T | 1 | a0001c0003t0002g0256 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.298-19614C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56778862 | ||||||
| chr16:56779653
|
A | G | 3 | a0001c0001t0013g0012a0001c0001t0013g0013a0001c0001t0013g0014 | 3 | HG03041.hp1 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.298-18823A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56779653 | ||||||
| chr16:56779752
|
C | A | 1 | a0001c0001t0001g0163 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.298-18724C>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56779752 | ||||||
| chr16:56780413
|
A | T | 57 | a0001c0001t0002g0284a0001c0001t0002g0292a0001c0001t0002g0295others(54): Show | 57 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.298-18063A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56780413 | ||||||
| chr16:56780583
|
A | C | 27 | a0001c0004t0005g0020a0001c0004t0005g0021a0001c0004t0005g0022others(24): Show | 27 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(24): Show |
intron_variant | MODIFIER | c.298-17893A>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56780583 | ||||||
| chr16:56780927
|
G | A | 1 | a0001c0001t0003g0355 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.298-17549G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56780927 | ||||||
| chr16:56780935
|
G | A | 181 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0045others(178): Show | 183 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.298-17541G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56780935 | ||||||
| chr16:56780994
|
C | T | 2 | a0001c0001t0001g0145a0001c0001t0001g0146 | 2 | NA18946.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.298-17482C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56780994 | ||||||
| chr16:56781052
|
T | C | 1 | a0001c0001t0016g0191 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.298-17424T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56781052 | ||||||
| chr16:56781288
|
A | G | 11 | a0001c0004t0008g0172a0001c0004t0008g0173a0001c0004t0008g0174others(8): Show | 11 | HG00099.hp2 HG00741.hp1 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.298-17188A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56781288 | ||||||
| chr16:56781646
|
C | T | 3 | a0001c0001t0014g0217a0001c0001t0014g0218a0001c0001t0014g0219 | 3 | HG01884.hp2 HG03453.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.298-16830C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56781646 | ||||||
| chr16:56781708
|
G | A | 2 | a0001c0004t0019g0180a0001c0004t0019g0181 | 2 | HG03491.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.298-16768G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56781708 | ||||||
| chr16:56781809
|
C | A | 1 | a0001c0001t0001g0332 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.298-16667C>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56781809 | ||||||
| chr16:56782170
|
G | A | 2 | a0001c0001t0003g0368a0001c0001t0003g0369 | 2 | NA18942.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.298-16306G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56782170 | ||||||
| chr16:56782183
|
G | A | 1 | a0001c0002t0001g0339 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.298-16293G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56782183 | ||||||
| chr16:56782540
|
T | G | 1 | a0001c0001t0034g0196 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.298-15936T>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56782540 | ||||||
| chr16:56783154
|
G | T | 1 | a0001c0003t0002g0266 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.298-15322G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56783154 | ||||||
| chr16:56783250
|
C | T | 130 | a0001c0001t0001g0003a0001c0001t0001g0045a0001c0001t0001g0046others(127): Show | 131 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.298-15226C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56783250 | ||||||
| chr16:56783383
|
C | T | 2 | a0001c0002t0001g0083a0001c0002t0001g0344 | 2 | HG02015.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.298-15093C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56783383 | ||||||
| chr16:56783465
|
A | T | 2 | a0001c0001t0006g0203a0001c0001t0006g0208 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.298-15011A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56783465 | ||||||
| chr16:56783585
|
A | G | 1 | a0001c0001t0003g0354 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.298-14891A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56783585 | ||||||
| chr16:56783727
|
C | G | 1 | a0001c0001t0036g0148 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.298-14749C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56783727 | ||||||
| chr16:56783757
|
G | C | 1 | a0001c0004t0005g0030 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.298-14719G>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56783757 | ||||||
| chr16:56783992
|
C | T | 1 | a0001c0001t0002g0292 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.298-14484C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56783992 | ||||||
| chr16:56784003
|
AT | A | 11 | a0001c0004t0008g0172a0001c0004t0008g0173a0001c0004t0008g0174others(8): Show | 11 | HG00099.hp2 HG00741.hp1 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.298-14464delT | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56784003 | |||||
| chr16:56784329
|
A | G | 3 | a0001c0004t0015g0015a0001c0004t0015g0016a0001c0004t0015g0017 | 3 | HG02818.hp1 HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.298-14147A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56784329 | ||||||
| chr16:56784347
|
A | C | 49 | a0001c0001t0002g0284a0001c0001t0002g0295a0001c0003t0002g0047others(46): Show | 49 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.298-14129A>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56784347 | ||||||
| chr16:56784438
|
T | C | 1 | a0001c0010t0033g0261 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.298-14038T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56784438 | ||||||
| chr16:56784635
|
T | G | 330 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0045others(327): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.298-13841T>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56784635 | ||||||
| chr16:56784671
|
G | T | 1 | a0001c0001t0006g0213 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.298-13805G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56784671 | ||||||
| chr16:56784879
|
G | A | 1 | a0001c0001t0003g0355 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.298-13597G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56784879 | ||||||
| chr16:56784942
|
G | A | 3 | a0001c0001t0017g0307a0001c0001t0017g0341a0001c0001t0017g0342 | 3 | HG00621.hp2 NA18969.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.298-13534G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56784942 | ||||||
| chr16:56785075
|
A | G | 130 | a0001c0001t0001g0003a0001c0001t0001g0045a0001c0001t0001g0046others(127): Show | 131 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.298-13401A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56785075 | ||||||
| chr16:56785107
|
G | A | 1 | a0006c0021t0001g0011 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.298-13369G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56785107 | ||||||
| chr16:56785259
|
T | G | 330 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0045others(327): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.298-13217T>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56785259 | ||||||
| chr16:56785328
|
G | A | 1 | a0001c0001t0001g0325 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.298-13148G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56785328 | ||||||
| chr16:56785359
|
T | G | 2 | a0001c0004t0005g0030a0001c0004t0005g0032 | 2 | HG01099.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.298-13117T>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56785359 | ||||||
| chr16:56785565
|
A | G | 1 | a0001c0001t0002g0295 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.298-12911A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56785565 | ||||||
| chr16:56785671
|
T | C | 2 | a0001c0001t0001g0123a0001c0001t0001g0125 | 2 | HG03831.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.298-12805T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56785671 | ||||||
| chr16:56786007
|
C | T | 57 | a0001c0001t0002g0284a0001c0001t0002g0292a0001c0001t0002g0295others(54): Show | 57 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.298-12469C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56786007 | ||||||
| chr16:56786024
|
G | A | 1 | a0001c0001t0023g0329 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.298-12452G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56786024 | ||||||
| chr16:56786505
|
G | A | 1 | a0001c0006t0009g0252 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.298-11971G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56786505 | ||||||
| chr16:56786625
|
C | G | 3 | a0001c0001t0004g0231a0001c0001t0004g0232a0001c0001t0004g0237 | 3 | NA18952.hp1 NA18967.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.298-11851C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56786625 | ||||||
| chr16:56786647
|
A | G | 2 | a0001c0001t0001g0003a0001c0001t0001g0116 | 2 | HG03098.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.298-11829A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56786647 | ||||||
| chr16:56786690
|
T | C | 1 | a0001c0002t0001g0081 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.298-11786T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56786690 | ||||||
| chr16:56786728
|
G | A | 282 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0045others(279): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.298-11748G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56786728 | ||||||
| chr16:56786967
|
T | C | 3 | a0001c0004t0015g0015a0001c0004t0015g0016a0001c0004t0015g0017 | 3 | HG02818.hp1 HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.298-11509T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56786967 | ||||||
| chr16:56787084
|
G | A | 2 | a0001c0001t0003g0356a0001c0001t0003g0373 | 2 | NA18961.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.298-11392G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56787084 | ||||||
| chr16:56787204
|
GAAAGAAT others(8): Show |
G | 23 | a0001c0001t0006g0199a0001c0001t0006g0200a0001c0001t0006g0201others(20): Show | 23 | HG01070.hp2 HG01168.hp2 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.298-11269_298-1125 others(19): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56787204 | |||||
| chr16:56787360
|
G | C | 1 | a0001c0001t0029g0245 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.298-11116G>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56787360 | ||||||
| chr16:56787508
|
T | G | 1 | a0001c0004t0005g0030 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.298-10968T>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56787508 | ||||||
| chr16:56787557
|
T | C | 1 | a0001c0001t0001g0122 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.298-10919T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56787557 | ||||||
| chr16:56787607
|
C | G | 8 | a0001c0005t0007g0183a0001c0005t0007g0184a0001c0005t0007g0185others(5): Show | 8 | HG02257.hp2 HG02559.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.298-10869C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56787607 | ||||||
| chr16:56787747
|
G | A | 6 | a0001c0001t0001g0130a0001c0001t0001g0132a0001c0001t0001g0133others(3): Show | 6 | HG00099.hp1 HG00735.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.298-10729G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56787747 | ||||||
| chr16:56788081
|
C | T | 2 | a0001c0003t0002g0257a0001c0003t0002g0258 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.298-10395C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56788081 | ||||||
| chr16:56788082
|
G | A | 1 | a0001c0001t0001g0124 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.298-10394G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56788082 | ||||||
| chr16:56788127
|
G | C | 3 | a0001c0009t0018g0018a0001c0009t0018g0019a0003c0024t0018g0010 | 3 | HG02451.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.298-10349G>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56788127 | ||||||
| chr16:56788156
|
C | T | 1 | a0001c0001t0029g0245 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.298-10320C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56788156 | ||||||
| chr16:56788233
|
G | T | 1 | a0001c0003t0002g0272 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.298-10243G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56788233 | ||||||
| chr16:56788497
|
C | A | 1 | a0001c0003t0042g0286 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.298-9979C>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56788497 | ||||||
| chr16:56788581
|
G | A | 2 | a0001c0002t0001g0064a0001c0007t0012g0065 | 2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.298-9895G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56788581 | ||||||
| chr16:56788699
|
C | G | 1 | a0001c0001t0001g0318 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.298-9777C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56788699 | ||||||
| chr16:56788730
|
C | A | 24 | a0001c0001t0004g0198a0001c0001t0004g0220a0001c0001t0004g0221others(21): Show | 24 | HG00408.hp2 HG00597.hp2 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.298-9746C>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56788730 | ||||||
| chr16:56788737
|
G | A | 1 | a0001c0001t0002g0284 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.298-9739G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56788737 | ||||||
| chr16:56788761
|
C | G | 3 | a0001c0002t0010g0111a0001c0002t0010g0112a0001c0002t0041g0113 | 3 | HG00733.hp2 HG01346.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.298-9715C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56788761 | ||||||
| chr16:56789000
|
G | A | 4 | a0001c0002t0001g0044a0001c0002t0010g0048a0001c0002t0010g0049others(1): Show | 4 | HG00544.hp1 HG01069.hp2 HG01167.hp1 others(1): Show |
intron_variant | MODIFIER | c.298-9476G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56789000 | ||||||
| chr16:56789089
|
T | G | 6 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(3): Show | 6 | HG01884.hp1 HG02630.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.298-9387T>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56789089 | ||||||
| chr16:56789324
|
T | A | 1 | a0005c0022t0022g0254 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.298-9152T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56789324 | ||||||
| chr16:56789325
|
A | G | 2 | a0001c0003t0002g0257a0001c0003t0002g0258 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.298-9151A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56789325 | ||||||
| chr16:56789419
|
T | G | 2 | a0001c0001t0004g0239a0001c0001t0004g0241 | 2 | NA19083.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.298-9057T>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56789419 | ||||||
| chr16:56789444
|
C | T | 1 | a0001c0014t0001g0137 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.298-9032C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56789444 | ||||||
| chr16:56789614
|
C | T | 16 | a0001c0001t0006g0202a0001c0001t0006g0203a0001c0001t0006g0204others(13): Show | 16 | HG01070.hp2 HG01168.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.298-8862C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56789614 | ||||||
| chr16:56789765
|
C | A | 2 | a0001c0004t0024g0039a0001c0004t0024g0042 | 2 | HG00639.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.298-8711C>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56789765 | ||||||
| chr16:56789785
|
G | A | 1 | a0001c0001t0001g0122 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.298-8691G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56789785 | ||||||
| chr16:56789799
|
G | T | 3 | a0001c0007t0012g0345a0001c0007t0012g0346a0001c0007t0012g0347 | 3 | HG02145.hp2 HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.298-8677G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56789799 | ||||||
| chr16:56789815
|
A | G | 1 | a0001c0001t0001g0319 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.298-8661A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56789815 | ||||||
| chr16:56789836
|
C | T | 2 | a0001c0009t0018g0018a0003c0024t0018g0010 | 2 | HG02451.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.298-8640C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56789836 | ||||||
| chr16:56789946
|
A | G | 6 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(3): Show | 6 | HG01884.hp1 HG02630.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.298-8530A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56789946 | ||||||
| chr16:56789970
|
G | A | 1 | a0001c0001t0001g0332 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.298-8506G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56789970 | ||||||
| chr16:56790096
|
T | TCAAAA | 90 | a0001c0001t0001g0002a0001c0001t0001g0302a0001c0001t0001g0303others(87): Show | 91 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.298-8349_298-8345d others(7): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56790096 | |||||
| chr16:56790096
|
T | TCAAAACA others(3): Show |
64 | a0001c0001t0001g0311a0001c0001t0002g0284a0001c0001t0003g0354others(61): Show | 64 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.298-8354_298-8345d others(12): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56790096 | |||||
| chr16:56790096
|
T | TCAAAACA others(8): Show |
11 | a0001c0001t0002g0295a0001c0003t0002g0256a0001c0003t0002g0275others(8): Show | 11 | HG01175.hp2 HG02109.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.298-8359_298-8345d others(17): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56790096 | |||||
| chr16:56790096
|
TCAAAA | T | 137 | a0001c0001t0001g0003a0001c0001t0001g0045a0001c0001t0001g0046others(134): Show | 138 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.298-8349_298-8345d others(7): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56790096 | |||||
| chr16:56790115
|
A | AACAAAAC others(3): Show |
1 | a0001c0001t0029g0245 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.298-8352_298-8351i others(12): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56790115 | |||||
| chr16:56790271
|
T | G | 373 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0045others(370): Show | 375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.298-8205T>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56790271 | ||||||
| chr16:56790407
|
A | T | 3 | a0001c0007t0012g0345a0001c0007t0012g0346a0001c0007t0012g0347 | 3 | HG02145.hp2 HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.298-8069A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56790407 | ||||||
| chr16:56790633
|
T | A | 41 | a0001c0001t0001g0002a0001c0001t0001g0302a0001c0001t0001g0303others(38): Show | 42 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.298-7843T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56790633 | ||||||
| chr16:56790794
|
T | G | 1 | a0001c0007t0012g0345 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.298-7682T>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56790794 | ||||||
| chr16:56791012
|
C | T | 2 | a0001c0001t0017g0341a0001c0001t0017g0342 | 2 | NA18969.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.298-7464C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56791012 | ||||||
| chr16:56791046
|
A | G | 1 | a0001c0002t0001g0067 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.298-7430A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56791046 | ||||||
| chr16:56791149
|
C | T | 1 | a0001c0002t0001g0075 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.298-7327C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56791149 | ||||||
| chr16:56791523
|
C | T | 6 | a0001c0001t0006g0210a0001c0001t0006g0211a0001c0001t0006g0212others(3): Show | 6 | HG01070.hp2 HG01243.hp1 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.298-6953C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56791523 | ||||||
| chr16:56791668
|
G | A | 1 | a0001c0001t0029g0245 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.298-6808G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56791668 | ||||||
| chr16:56791754
|
G | A | 64 | a0001c0002t0001g0001a0001c0002t0001g0044a0001c0002t0001g0051others(61): Show | 65 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.298-6722G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56791754 | ||||||
| chr16:56791818
|
G | C | 1 | a0001c0003t0030g0274 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.298-6658G>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56791818 | ||||||
| chr16:56791983
|
A | G | 1 | a0001c0001t0003g0368 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.298-6493A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56791983 | ||||||
| chr16:56791989
|
A | G | 1 | a0001c0002t0001g0082 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.298-6487A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56791989 | ||||||
| chr16:56792129
|
G | A | 1 | a0001c0001t0043g0154 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.298-6347G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56792129 | ||||||
| chr16:56792335
|
G | GA | 24 | a0001c0004t0005g0020a0001c0004t0005g0021a0001c0004t0005g0022others(21): Show | 24 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(21): Show |
intron_variant | MODIFIER | c.298-6140dupA | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56792335 | |||||
| chr16:56792450
|
A | C | 57 | a0001c0001t0002g0284a0001c0001t0002g0292a0001c0001t0002g0295others(54): Show | 57 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.298-6026A>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56792450 | ||||||
| chr16:56792521
|
G | A | 20 | a0001c0001t0006g0199a0001c0001t0006g0200a0001c0001t0006g0201others(17): Show | 20 | HG01070.hp2 HG01168.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.298-5955G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56792521 | ||||||
| chr16:56792531
|
A | G | 1 | a0001c0003t0002g0280 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.298-5945A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56792531 | ||||||
| chr16:56792544
|
G | A | 1 | a0001c0001t0001g0310 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.298-5932G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56792544 | ||||||
| chr16:56792665
|
C | T | 6 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(3): Show | 6 | HG01884.hp1 HG02630.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.298-5811C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56792665 | ||||||
| chr16:56792706
|
A | C | 3 | a0001c0001t0013g0012a0001c0001t0013g0013a0001c0001t0013g0014 | 3 | HG03041.hp1 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.298-5770A>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56792706 | ||||||
| chr16:56792854
|
T | C | 172 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0045others(169): Show | 174 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.298-5622T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56792854 | ||||||
| chr16:56793011
|
A | G | 3 | a0001c0001t0013g0012a0001c0001t0013g0013a0001c0001t0013g0014 | 3 | HG03041.hp1 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.298-5465A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56793011 | ||||||
| chr16:56793133
|
A | C | 1 | a0001c0003t0002g0047 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.298-5343A>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56793133 | ||||||
| chr16:56793350
|
C | CTT | 5 | a0001c0006t0009g0249a0001c0006t0009g0250a0001c0006t0009g0251others(2): Show | 5 | HG02109.hp2 HG02615.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.298-5125_298-5124d others(4): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56793350 | |||||
| chr16:56793455
|
C | G | 1 | a0001c0001t0003g0361 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.298-5021C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56793455 | ||||||
| chr16:56793458
|
C | T | 2 | a0001c0001t0001g0003a0001c0001t0001g0116 | 2 | HG03098.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.298-5018C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56793458 | ||||||
| chr16:56793542
|
T | C | 271 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0045others(268): Show | 273 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(270): Show |
intron_variant | MODIFIER | c.298-4934T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56793542 | ||||||
| chr16:56793786
|
G | C | 1 | a0001c0001t0006g0199 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.298-4690G>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56793786 | ||||||
| chr16:56793839
|
T | C | 4 | a0001c0004t0005g0031a0001c0004t0005g0033a0001c0004t0005g0034others(1): Show | 4 | HG00741.hp2 HG01261.hp1 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.298-4637T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56793839 | ||||||
| chr16:56793858
|
G | A | 2 | a0001c0001t0006g0199a0001c0001t0006g0200 | 2 | HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.298-4618G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56793858 | ||||||
| chr16:56794034
|
G | A | 1 | a0001c0001t0003g0362 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.298-4442G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56794034 | ||||||
| chr16:56794070
|
A | G | 3 | a0001c0009t0018g0018a0001c0009t0018g0019a0003c0024t0018g0010 | 3 | HG02451.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.298-4406A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56794070 | ||||||
| chr16:56794070
|
ATAGG | A | 127 | a0001c0001t0001g0003a0001c0001t0001g0120a0001c0001t0001g0121others(124): Show | 128 | HG00323.hp1 HG00438.hp1 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.298-4386_298-4383d others(6): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56794070 | |||||
| chr16:56794074
|
G | A | 1 | a0001c0001t0004g0224 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.298-4402G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56794074 | ||||||
| chr16:56794082
|
GTAGGTAG others(5): Show |
G | 22 | a0001c0004t0005g0021a0001c0004t0005g0022a0001c0004t0005g0023others(19): Show | 22 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(19): Show |
intron_variant | MODIFIER | c.298-4390_298-4379d others(14): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56794082 | |||||
| chr16:56794082
|
GTAGGTAG others(9): Show |
G | 4 | a0001c0004t0005g0033a0001c0009t0018g0018a0001c0009t0018g0019others(1): Show | 4 | HG01346.hp1 HG02451.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.298-4390_298-4375d others(18): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56794082 | |||||
| chr16:56794082
|
GTAGGTAG others(13): Show |
G | 2 | a0001c0004t0015g0015a0001c0004t0015g0017 | 2 | HG02818.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.298-4390_298-4371d others(22): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56794082 | |||||
| chr16:56794086
|
G | GTAGA | 19 | a0001c0001t0001g0116a0001c0001t0001g0141a0001c0001t0011g0007others(16): Show | 19 | HG01123.hp1 HG01175.hp2 HG01258.hp1 others(16): Show |
intron_variant | MODIFIER | c.298-4387_298-4386i others(6): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56794086 | |||||
| chr16:56794086
|
GTAGGTAG others(1): Show |
G | 74 | a0001c0001t0001g0002a0001c0001t0001g0052a0001c0001t0001g0114others(71): Show | 75 | HG00099.hp1 HG00609.hp1 HG00621.hp2 others(72): Show |
intron_variant | MODIFIER | c.298-4386_298-4379d others(10): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56794086 | |||||
| chr16:56794086
|
GTAGGTAG others(5): Show |
G | 23 | a0001c0001t0004g0198a0001c0001t0004g0220a0001c0001t0004g0221others(20): Show | 23 | HG00408.hp2 HG00597.hp2 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.298-4386_298-4375d others(14): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56794086 | |||||
| chr16:56794090
|
G | A | 86 | a0001c0001t0001g0116a0001c0001t0001g0119a0001c0001t0001g0141others(83): Show | 86 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.298-4386G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56794090 | ||||||
| chr16:56794090
|
G | GTAGA | 9 | a0001c0002t0001g0064a0001c0004t0008g0175a0001c0006t0009g0249others(6): Show | 9 | HG01891.hp1 HG02109.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.298-4348_298-4345d others(6): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56794090 | |||||
| chr16:56794090
|
G | GTAGATAG others(5): Show |
2 | a0001c0004t0008g0174a0001c0004t0008g0177 | 2 | HG00741.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.298-4356_298-4345d others(14): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56794090 | |||||
| chr16:56794090
|
GTAGA | G | 13 | a0001c0001t0001g0045a0001c0001t0001g0053a0001c0001t0001g0054others(10): Show | 13 | HG00099.hp2 HG01106.hp1 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.298-4348_298-4345d others(6): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56794090 | |||||
| chr16:56794136
|
T | A | 1 | a0006c0021t0001g0011 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.298-4340T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56794136 | ||||||
| chr16:56794148
|
A | C | 1 | a0001c0004t0005g0020 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.298-4328A>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56794148 | ||||||
| chr16:56794409
|
A | ATATTT | 364 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0045others(361): Show | 366 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(363): Show |
intron_variant | MODIFIER | c.298-4065_298-4064i others(7): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56794409 | |||||
| chr16:56794421
|
G | T | 2 | a0001c0001t0003g0364a0001c0001t0003g0365 | 2 | HG00639.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.298-4055G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56794421 | ||||||
| chr16:56794563
|
G | A | 41 | a0001c0001t0001g0002a0001c0001t0001g0302a0001c0001t0001g0303others(38): Show | 42 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.298-3913G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56794563 | ||||||
| chr16:56794584
|
T | G | 2 | a0001c0001t0001g0123a0001c0001t0001g0125 | 2 | HG03831.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.298-3892T>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56794584 | ||||||
| chr16:56794584
|
T | TAG | 8 | a0001c0001t0001g0305a0001c0001t0011g0004a0001c0001t0011g0005others(5): Show | 8 | HG00140.hp2 HG01884.hp1 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.298-3864_298-3863d others(4): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56794584 | |||||
| chr16:56794584
|
TAG | T | 72 | a0001c0001t0001g0045a0001c0001t0003g0348a0001c0001t0003g0349others(69): Show | 72 | HG00323.hp1 HG00408.hp2 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.298-3864_298-3863d others(4): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56794584 | |||||
| chr16:56794584
|
TAGAG | T | 107 | a0001c0001t0001g0130a0001c0001t0001g0132a0001c0001t0001g0133others(104): Show | 107 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.298-3866_298-3863d others(6): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56794584 | |||||
| chr16:56794584
|
TAGAGAG | T | 7 | a0001c0001t0001g0334a0001c0001t0003g0369a0001c0007t0012g0346others(4): Show | 7 | HG02451.hp2 HG02886.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.298-3868_298-3863d others(8): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56794584 | |||||
| chr16:56794584
|
TAGAGAGA others(1): Show |
T | 45 | a0001c0001t0001g0169a0001c0002t0001g0044a0001c0002t0001g0057others(42): Show | 45 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.298-3870_298-3863d others(10): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56794584 | |||||
| chr16:56794584
|
TAGAGAGA others(3): Show |
T | 20 | a0001c0001t0006g0199a0001c0001t0006g0200a0001c0001t0006g0201others(17): Show | 20 | HG01070.hp2 HG01168.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.298-3872_298-3863d others(12): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56794584 | |||||
| chr16:56794592
|
G | C | 1 | a0001c0002t0001g0129 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.298-3884G>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56794592 | ||||||
| chr16:56794604
|
G | A | 1 | a0001c0001t0001g0155 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.298-3872G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56794604 | ||||||
| chr16:56794710
|
C | T | 1 | a0001c0002t0001g0051 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.298-3766C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56794710 | ||||||
| chr16:56794785
|
G | A | 1 | a0001c0001t0006g0244 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.298-3691G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56794785 | ||||||
| chr16:56794811
|
C | T | 131 | a0001c0001t0001g0003a0001c0001t0001g0045a0001c0001t0001g0046others(128): Show | 132 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.298-3665C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56794811 | ||||||
| chr16:56794826
|
G | A | 6 | a0001c0001t0006g0210a0001c0001t0006g0211a0001c0001t0006g0212others(3): Show | 6 | HG01070.hp2 HG01243.hp1 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.298-3650G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56794826 | ||||||
| chr16:56794853
|
G | A | 1 | a0001c0001t0006g0212 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.298-3623G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56794853 | ||||||
| chr16:56794858
|
G | A | 24 | a0001c0004t0005g0020a0001c0004t0005g0021a0001c0004t0005g0022others(21): Show | 24 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(21): Show |
intron_variant | MODIFIER | c.298-3618G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56794858 | ||||||
| chr16:56794927
|
CAAAA | C | 20 | a0001c0001t0004g0220a0001c0001t0004g0221a0001c0001t0004g0222others(17): Show | 20 | HG00408.hp2 HG00597.hp2 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.298-3520_298-3517d others(6): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56794927 | |||||
| chr16:56794927
|
CAAAAAAA | C | 40 | a0001c0001t0001g0002a0001c0001t0001g0302a0001c0001t0001g0303others(37): Show | 41 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.298-3523_298-3517d others(9): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56794927 | |||||
| chr16:56794927
|
CAAAAAAA others(1): Show |
C | 22 | a0001c0001t0001g0169a0001c0001t0043g0154a0001c0002t0001g0064others(19): Show | 22 | HG01099.hp1 HG02080.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.298-3524_298-3517d others(10): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56794927 | |||||
| chr16:56794927
|
CAAAAAAA others(2): Show |
C | 161 | a0001c0001t0001g0045a0001c0001t0001g0139a0001c0001t0001g0140others(158): Show | 162 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.298-3525_298-3517d others(11): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56794927 | |||||
| chr16:56794927
|
CAAAAAAA others(3): Show |
C | 57 | a0001c0001t0001g0003a0001c0001t0001g0046a0001c0001t0001g0052others(54): Show | 57 | HG00099.hp1 HG00621.hp1 HG00735.hp1 others(54): Show |
intron_variant | MODIFIER | c.298-3526_298-3517d others(12): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56794927 | |||||
| chr16:56794927
|
CAAAAAAA others(4): Show |
C | 13 | a0001c0001t0007g0194a0001c0001t0011g0004a0001c0001t0011g0005others(10): Show | 13 | HG01884.hp1 HG02258.hp2 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.298-3527_298-3517d others(13): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56794927 | |||||
| chr16:56794927
|
CAAAAAAA others(5): Show |
C | 40 | a0001c0001t0003g0348a0001c0001t0003g0349a0001c0001t0003g0350others(37): Show | 40 | HG00323.hp1 HG00639.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.298-3528_298-3517d others(14): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56794927 | |||||
| chr16:56794927
|
CAAAAAAA others(6): Show |
C | 1 | a0001c0005t0007g0189 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.298-3529_298-3517d others(15): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56794927 | |||||
| chr16:56795116
|
C | CA | 5 | a0001c0006t0009g0249a0001c0006t0009g0250a0001c0006t0009g0251others(2): Show | 5 | HG02109.hp2 HG02615.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.298-3360_298-3359i others(3): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56795116 | ||||||
| chr16:56795212
|
A | G | 1 | a0001c0001t0001g0310 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.298-3264A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56795212 | ||||||
| chr16:56795246
|
C | T | 1 | a0001c0001t0001g0124 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.298-3230C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56795246 | ||||||
| chr16:56795266
|
G | A | 20 | a0001c0001t0006g0199a0001c0001t0006g0200a0001c0001t0006g0201others(17): Show | 20 | HG01070.hp2 HG01168.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.298-3210G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56795266 | ||||||
| chr16:56795380
|
C | G | 1 | a0001c0001t0001g0309 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.298-3096C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56795380 | ||||||
| chr16:56795417
|
T | A | 3 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0152 | 3 | NA18992.hp1 NA19005.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.298-3059T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56795417 | ||||||
| chr16:56795510
|
T | C | 6 | a0001c0001t0004g0198a0001c0001t0004g0238a0001c0001t0004g0239others(3): Show | 6 | HG00597.hp2 NA18959.hp2 NA18972.hp2 others(3): Show |
intron_variant | MODIFIER | c.298-2966T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56795510 | ||||||
| chr16:56795628
|
G | A | 68 | a0001c0001t0003g0348a0001c0001t0003g0349a0001c0001t0003g0350others(65): Show | 68 | HG00323.hp1 HG00639.hp1 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.298-2848G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56795628 | ||||||
| chr16:56795630
|
A | ATATTTT | 156 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0052others(153): Show | 157 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.298-2814_298-2809d others(8): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56795630 | |||||
| chr16:56795630
|
A | ATATTTTT others(5): Show |
2 | a0001c0001t0001g0003a0001c0002t0001g0075 | 2 | HG03098.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.298-2820_298-2809d others(14): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56795630 | |||||
| chr16:56795630
|
ATATTTTT others(5): Show |
A | 1 | a0001c0002t0001g0167 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.298-2820_298-2809d others(14): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 56795630 | |||||
| chr16:56795698
|
G | A | 24 | a0001c0001t0004g0198a0001c0001t0004g0220a0001c0001t0004g0221others(21): Show | 24 | HG00408.hp2 HG00597.hp2 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.298-2778G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56795698 | ||||||
| chr16:56795771
|
C | T | 5 | a0001c0006t0009g0249a0001c0006t0009g0250a0001c0006t0009g0251others(2): Show | 5 | HG02109.hp2 HG02615.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.298-2705C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56795771 | ||||||
| chr16:56795791
|
C | T | 2 | a0001c0007t0012g0346a0001c0007t0012g0347 | 2 | HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.298-2685C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56795791 | ||||||
| chr16:56795838
|
G | T | 1 | a0001c0003t0002g0285 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.298-2638G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56795838 | ||||||
| chr16:56795893
|
C | T | 3 | a0001c0001t0013g0012a0001c0001t0013g0013a0001c0001t0013g0014 | 3 | HG03041.hp1 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.298-2583C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56795893 | ||||||
| chr16:56796067
|
T | C | 3 | a0001c0001t0013g0012a0001c0001t0013g0013a0001c0001t0013g0014 | 3 | HG03041.hp1 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.298-2409T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56796067 | ||||||
| chr16:56796437
|
C | A | 27 | a0001c0004t0005g0020a0001c0004t0005g0021a0001c0004t0005g0022others(24): Show | 27 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(24): Show |
intron_variant | MODIFIER | c.298-2039C>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56796437 | ||||||
| chr16:56796481
|
C | G | 2 | a0001c0002t0001g0096a0001c0002t0001g0110 | 2 | HG02258.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.298-1995C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56796481 | ||||||
| chr16:56796867
|
G | C | 70 | a0001c0001t0003g0348a0001c0001t0003g0349a0001c0001t0003g0350others(67): Show | 70 | HG00323.hp1 HG00639.hp1 HG00642.hp2 others(67): Show |
intron_variant | MODIFIER | c.298-1609G>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56796867 | ||||||
| chr16:56796987
|
A | G | 41 | a0001c0001t0001g0002a0001c0001t0001g0302a0001c0001t0001g0303others(38): Show | 42 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.298-1489A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56796987 | ||||||
| chr16:56797234
|
C | T | 130 | a0001c0001t0001g0003a0001c0001t0001g0045a0001c0001t0001g0046others(127): Show | 131 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.298-1242C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56797234 | ||||||
| chr16:56797254
|
A | G | 2 | a0001c0002t0001g0001a0001c0002t0001g0071 | 3 | HG01361.hp1 HG01517.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.298-1222A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56797254 | ||||||
| chr16:56797386
|
A | G | 1 | a0001c0001t0001g0147 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.298-1090A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56797386 | ||||||
| chr16:56797415
|
C | A | 2 | a0001c0001t0016g0192a0001c0001t0016g0193 | 2 | HG02258.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.298-1061C>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56797415 | ||||||
| chr16:56797480
|
C | T | 1 | a0001c0001t0001g0116 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.298-996C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56797480 | ||||||
| chr16:56797650
|
A | G | 14 | a0001c0004t0005g0022a0001c0004t0005g0023a0001c0004t0005g0024others(11): Show | 14 | HG00741.hp2 HG01099.hp2 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.298-826A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56797650 | ||||||
| chr16:56797659
|
C | T | 1 | a0001c0002t0001g0064 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.298-817C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56797659 | ||||||
| chr16:56797757
|
G | A | 2 | a0001c0003t0002g0265a0001c0003t0002g0287 | 2 | NA18983.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.298-719G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56797757 | ||||||
| chr16:56797830
|
A | G | 1 | a0001c0002t0041g0113 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.298-646A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56797830 | ||||||
| chr16:56797924
|
C | T | 27 | a0001c0004t0005g0020a0001c0004t0005g0021a0001c0004t0005g0023others(24): Show | 27 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(24): Show |
intron_variant | MODIFIER | c.298-552C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56797924 | ||||||
| chr16:56798299
|
T | G | 1 | a0001c0001t0014g0218 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.298-177T>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56798299 | ||||||
| chr16:56798381
|
T | C | 4 | a0001c0007t0012g0065a0001c0007t0012g0345a0001c0007t0012g0346others(1): Show | 4 | HG01891.hp1 HG02145.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.298-95T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56798381 | ||||||
| chr16:56798390
|
C | T | 55 | a0001c0001t0001g0003a0001c0001t0001g0045a0001c0001t0001g0046others(52): Show | 55 | HG00099.hp1 HG00621.hp1 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.298-86C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 3/21 | chr16 | 56798390 | ||||||
| chr16:56798594
|
G | A | 1 | a0001c0016t0001g0117 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.360+56G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56798594 | ||||||
| chr16:56798679
|
G | A | 4 | a0001c0007t0012g0065a0001c0007t0012g0345a0001c0007t0012g0346others(1): Show | 4 | HG01891.hp1 HG02145.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.360+141G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56798679 | ||||||
| chr16:56798741
|
C | T | 3 | a0001c0001t0013g0012a0001c0001t0013g0013a0001c0001t0013g0014 | 3 | HG03041.hp1 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.360+203C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56798741 | ||||||
| chr16:56798844
|
G | A | 1 | a0001c0001t0001g0332 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.360+306G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56798844 | ||||||
| chr16:56798871
|
C | CA | 7 | a0001c0001t0006g0205a0001c0001t0013g0012a0001c0003t0002g0255others(4): Show | 7 | HG01109.hp2 HG02083.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.360+349dupA | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr16 | 56798871 | |||||
| chr16:56798871
|
CA | C | 30 | a0001c0001t0001g0133a0001c0001t0004g0198a0001c0001t0004g0220others(27): Show | 30 | HG00408.hp2 HG00597.hp2 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.360+349delA | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr16 | 56798871 | |||||
| chr16:56799583
|
G | A | 3 | a0001c0001t0013g0012a0001c0001t0013g0013a0001c0001t0013g0014 | 3 | HG03041.hp1 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.360+1045G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56799583 | ||||||
| chr16:56799904
|
C | G | 1 | a0001c0001t0001g0325 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.360+1366C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56799904 | ||||||
| chr16:56800041
|
G | A | 3 | a0001c0007t0012g0065a0001c0007t0012g0346a0001c0007t0012g0347 | 3 | HG01891.hp1 HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.360+1503G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56800041 | ||||||
| chr16:56800051
|
C | T | 1 | a0001c0003t0002g0280 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.360+1513C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56800051 | ||||||
| chr16:56800124
|
A | G | 1 | a0001c0003t0002g0280 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.360+1586A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56800124 | ||||||
| chr16:56800184
|
A | G | 170 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0045others(167): Show | 172 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.360+1646A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56800184 | ||||||
| chr16:56800295
|
G | GT | 9 | a0001c0001t0003g0366a0001c0001t0003g0373a0001c0001t0028g0360others(6): Show | 9 | HG01081.hp2 HG01106.hp1 HG02027.hp1 others(6): Show |
intron_variant | MODIFIER | c.360+1765dupT | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr16 | 56800295 | |||||
| chr16:56800322
|
G | A | 57 | a0001c0001t0002g0284a0001c0001t0002g0292a0001c0001t0002g0295others(54): Show | 57 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.360+1784G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56800322 | ||||||
| chr16:56800342
|
C | G | 57 | a0001c0001t0002g0284a0001c0001t0002g0292a0001c0001t0002g0295others(54): Show | 57 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.360+1804C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56800342 | ||||||
| chr16:56800416
|
C | T | 1 | a0001c0001t0001g0321 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.360+1878C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56800416 | ||||||
| chr16:56800570
|
A | G | 1 | a0001c0009t0018g0018 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.360+2032A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56800570 | ||||||
| chr16:56801028
|
C | T | 3 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0152 | 3 | NA18992.hp1 NA19005.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.360+2490C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56801028 | ||||||
| chr16:56801081
|
C | T | 2 | a0001c0007t0012g0346a0001c0007t0012g0347 | 2 | HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.360+2543C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56801081 | ||||||
| chr16:56801213
|
CATT | C | 3 | a0001c0003t0002g0267a0001c0003t0002g0275a0001c0003t0002g0296 | 3 | NA18942.hp2 NA18981.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.360+2677_360+2679d others(5): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr16 | 56801213 | |||||
| chr16:56801298
|
C | G | 1 | a0001c0003t0002g0275 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.360+2760C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56801298 | ||||||
| chr16:56801570
|
G | A | 1 | a0001c0001t0007g0194 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.360+3032G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56801570 | ||||||
| chr16:56801635
|
A | G | 2 | a0001c0005t0007g0186a0001c0005t0007g0187 | 2 | HG02559.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.360+3097A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56801635 | ||||||
| chr16:56801799
|
C | T | 1 | a0001c0001t0001g0308 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.360+3261C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56801799 | ||||||
| chr16:56801800
|
G | T | 134 | a0001c0001t0001g0003a0001c0001t0001g0045a0001c0001t0001g0046others(131): Show | 135 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.360+3262G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56801800 | ||||||
| chr16:56801983
|
T | G | 2 | a0001c0009t0018g0018a0003c0024t0018g0010 | 2 | HG02451.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.360+3445T>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56801983 | ||||||
| chr16:56802077
|
G | A | 24 | a0001c0001t0004g0198a0001c0001t0004g0220a0001c0001t0004g0221others(21): Show | 24 | HG00408.hp2 HG00597.hp2 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.361-3427G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56802077 | ||||||
| chr16:56802140
|
C | T | 1 | a0001c0001t0029g0245 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.361-3364C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56802140 | ||||||
| chr16:56802196
|
T | C | 172 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0045others(169): Show | 174 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.361-3308T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56802196 | ||||||
| chr16:56802305
|
C | A | 24 | a0001c0004t0005g0020a0001c0004t0005g0021a0001c0004t0005g0022others(21): Show | 24 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(21): Show |
intron_variant | MODIFIER | c.361-3199C>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56802305 | ||||||
| chr16:56802410
|
G | A | 1 | a0001c0004t0005g0022 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.361-3094G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56802410 | ||||||
| chr16:56802588
|
CA | C | 364 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0045others(361): Show | 366 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(363): Show |
intron_variant | MODIFIER | c.361-2915delA | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56802588 | ||||||
| chr16:56802647
|
A | G | 3 | a0001c0009t0018g0018a0001c0009t0018g0019a0003c0024t0018g0010 | 3 | HG02451.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.361-2857A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56802647 | ||||||
| chr16:56802826
|
G | A | 2 | a0001c0002t0001g0001a0001c0002t0001g0071 | 3 | HG01361.hp1 HG01517.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.361-2678G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56802826 | ||||||
| chr16:56802849
|
G | C | 1 | a0001c0002t0001g0081 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.361-2655G>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56802849 | ||||||
| chr16:56802910
|
A | G | 1 | a0001c0001t0001g0306 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.361-2594A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56802910 | ||||||
| chr16:56803238
|
C | T | 30 | a0001c0004t0005g0020a0001c0004t0005g0021a0001c0004t0005g0022others(27): Show | 30 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.361-2266C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56803238 | ||||||
| chr16:56803326
|
G | A | 1 | a0001c0002t0001g0170 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.361-2178G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56803326 | ||||||
| chr16:56803382
|
A | G | 3 | a0001c0001t0014g0217a0001c0001t0014g0218a0001c0001t0014g0219 | 3 | HG01884.hp2 HG03453.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.361-2122A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56803382 | ||||||
| chr16:56803456
|
T | A | 4 | a0001c0003t0002g0276a0001c0004t0005g0020a0001c0004t0005g0040others(1): Show | 4 | HG00438.hp2 NA18522.hp2 NA18941.hp2 others(1): Show |
intron_variant | MODIFIER | c.361-2048T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56803456 | ||||||
| chr16:56803676
|
A | C | 1 | a0001c0010t0033g0261 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.361-1828A>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56803676 | ||||||
| chr16:56803745
|
AAAAT | A | 3 | a0001c0009t0018g0018a0001c0009t0018g0019a0003c0024t0018g0010 | 3 | HG02451.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.361-1757_361-1754d others(6): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr16 | 56803745 | |||||
| chr16:56803747
|
AAT | A | 7 | a0001c0001t0014g0217a0001c0001t0014g0218a0001c0001t0014g0219others(4): Show | 7 | HG00423.hp1 HG01884.hp2 HG02074.hp2 others(4): Show |
intron_variant | MODIFIER | c.361-1738_361-1737d others(4): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr16 | 56803747 | |||||
| chr16:56803747
|
AATAT | A | 354 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0045others(351): Show | 356 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(353): Show |
intron_variant | MODIFIER | c.361-1740_361-1737d others(6): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr16 | 56803747 | |||||
| chr16:56803749
|
T | A | 1 | a0001c0004t0008g0177 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.361-1755T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56803749 | ||||||
| chr16:56803810
|
C | T | 5 | a0001c0006t0009g0249a0001c0006t0009g0250a0001c0006t0009g0251others(2): Show | 5 | HG02109.hp2 HG02615.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.361-1694C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56803810 | ||||||
| chr16:56803831
|
A | G | 4 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(1): Show | 4 | NA18939.hp2 NA18964.hp2 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.361-1673A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56803831 | ||||||
| chr16:56803867
|
G | T | 2 | a0001c0001t0023g0329a0001c0001t0023g0330 | 2 | NA18991.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.361-1637G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56803867 | ||||||
| chr16:56803963
|
G | A | 1 | a0001c0002t0001g0102 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.361-1541G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56803963 | ||||||
| chr16:56804157
|
C | T | 1 | a0001c0002t0010g0050 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.361-1347C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56804157 | ||||||
| chr16:56804187
|
CCTTGCAG others(5): Show |
C | 4 | a0001c0001t0016g0191a0001c0001t0016g0192a0001c0001t0016g0193others(1): Show | 4 | HG02258.hp2 HG02572.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.361-1301_361-1290d others(14): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr16 | 56804187 | |||||
| chr16:56804189
|
T | A | 30 | a0001c0004t0005g0020a0001c0004t0005g0021a0001c0004t0005g0022others(27): Show | 30 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.361-1315T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56804189 | ||||||
| chr16:56804595
|
A | G | 4 | a0001c0002t0001g0044a0001c0002t0001g0085a0001c0002t0001g0088others(1): Show | 4 | HG00544.hp1 HG00609.hp2 HG02083.hp2 others(1): Show |
intron_variant | MODIFIER | c.361-909A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56804595 | ||||||
| chr16:56804675
|
G | A | 93 | a0001c0001t0003g0348a0001c0001t0003g0349a0001c0001t0003g0350others(90): Show | 93 | HG00323.hp1 HG00408.hp2 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.361-829G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56804675 | ||||||
| chr16:56804691
|
C | T | 41 | a0001c0001t0001g0002a0001c0001t0001g0302a0001c0001t0001g0303others(38): Show | 42 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.361-813C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56804691 | ||||||
| chr16:56804767
|
G | A | 4 | a0002c0008t0002g0298a0002c0008t0002g0299a0002c0008t0002g0300others(1): Show | 4 | NA18954.hp1 NA18966.hp1 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.361-737G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56804767 | ||||||
| chr16:56804861
|
G | A | 1 | a0001c0001t0006g0211 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.361-643G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56804861 | ||||||
| chr16:56804905
|
C | CA | 7 | a0001c0001t0001g0309a0001c0001t0003g0355a0001c0001t0023g0329others(4): Show | 7 | HG00140.hp1 HG02257.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.361-583dupA | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr16 | 56804905 | |||||
| chr16:56804905
|
CA | C | 7 | a0001c0001t0001g0161a0001c0002t0001g0129a0001c0003t0002g0272others(4): Show | 7 | HG02895.hp2 NA18940.hp2 NA18967.hp1 others(4): Show |
intron_variant | MODIFIER | c.361-583delA | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr16 | 56804905 | |||||
| chr16:56804957
|
A | G | 1 | a0001c0001t0043g0154 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.361-547A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56804957 | ||||||
| chr16:56805015
|
A | T | 3 | a0001c0002t0001g0085a0001c0002t0001g0088a0001c0002t0001g0095 | 3 | HG00609.hp2 HG02083.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.361-489A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56805015 | ||||||
| chr16:56805040
|
C | G | 3 | a0001c0004t0008g0172a0001c0004t0008g0173a0001c0004t0008g0178 | 3 | HG01106.hp1 HG02698.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.361-464C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56805040 | ||||||
| chr16:56805066
|
T | G | 205 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0045others(202): Show | 207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.361-438T>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56805066 | ||||||
| chr16:56805107
|
G | A | 1 | a0001c0001t0001g0318 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.361-397G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56805107 | ||||||
| chr16:56805114
|
A | G | 2 | a0001c0001t0043g0154a0001c0002t0001g0100 | 2 | HG03579.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.361-390A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56805114 | ||||||
| chr16:56805124
|
C | T | 3 | a0001c0001t0013g0012a0001c0001t0013g0013a0001c0001t0013g0014 | 3 | HG03041.hp1 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.361-380C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56805124 | ||||||
| chr16:56805284
|
G | A | 1 | a0005c0022t0022g0254 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.361-220G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56805284 | ||||||
| chr16:56805434
|
T | A | 3 | a0001c0004t0015g0015a0001c0004t0015g0016a0001c0004t0015g0017 | 3 | HG02818.hp1 HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.361-70T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 4/21 | chr16 | 56805434 | ||||||
| chr16:56805725
|
C | A | 3 | a0001c0001t0014g0217a0001c0001t0014g0218a0001c0001t0014g0219 | 3 | HG01884.hp2 HG03453.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.489+93C>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56805725 | ||||||
| chr16:56805908
|
C | T | 27 | a0001c0004t0005g0020a0001c0004t0005g0021a0001c0004t0005g0022others(24): Show | 27 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(24): Show |
intron_variant | MODIFIER | c.489+276C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56805908 | ||||||
| chr16:56806115
|
T | C | 41 | a0001c0001t0001g0002a0001c0001t0001g0302a0001c0001t0001g0303others(38): Show | 42 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.489+483T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56806115 | ||||||
| chr16:56806259
|
A | G | 171 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0045others(168): Show | 173 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.489+627A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56806259 | ||||||
| chr16:56806309
|
A | G | 1 | a0001c0001t0001g0141 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.489+677A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56806309 | ||||||
| chr16:56806416
|
G | A | 68 | a0001c0001t0003g0348a0001c0001t0003g0349a0001c0001t0003g0350others(65): Show | 68 | HG00323.hp1 HG00639.hp1 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.489+784G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56806416 | ||||||
| chr16:56806527
|
G | A | 1 | a0001c0002t0001g0075 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.489+895G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56806527 | ||||||
| chr16:56806963
|
C | T | 7 | a0001c0001t0039g0317a0001c0002t0001g0064a0001c0002t0001g0066others(4): Show | 7 | HG02572.hp1 HG02622.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.489+1331C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56806963 | ||||||
| chr16:56807042
|
A | C | 1 | a0001c0001t0001g0310 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.489+1410A>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56807042 | ||||||
| chr16:56807056
|
C | T | 1 | a0001c0001t0001g0310 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.489+1424C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56807056 | ||||||
| chr16:56807067
|
G | C | 1 | a0001c0010t0033g0261 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.489+1435G>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56807067 | ||||||
| chr16:56807293
|
C | T | 1 | a0001c0001t0002g0284 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.489+1661C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56807293 | ||||||
| chr16:56807356
|
T | G | 6 | a0001c0001t0001g0304a0001c0001t0001g0305a0001c0001t0001g0322others(3): Show | 6 | HG00140.hp2 HG00735.hp2 HG01081.hp1 others(3): Show |
intron_variant | MODIFIER | c.489+1724T>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56807356 | ||||||
| chr16:56807748
|
C | T | 3 | a0001c0001t0013g0012a0001c0001t0013g0013a0001c0001t0013g0014 | 3 | HG03041.hp1 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.489+2116C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56807748 | ||||||
| chr16:56807802
|
C | T | 169 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0045others(166): Show | 171 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.489+2170C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56807802 | ||||||
| chr16:56807881
|
G | A | 1 | a0001c0001t0014g0217 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.489+2249G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56807881 | ||||||
| chr16:56807966
|
T | G | 3 | a0001c0001t0014g0217a0001c0001t0014g0218a0001c0001t0014g0219 | 3 | HG01884.hp2 HG03453.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.489+2334T>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56807966 | ||||||
| chr16:56808016
|
C | T | 3 | a0001c0001t0013g0012a0001c0001t0013g0013a0001c0001t0013g0014 | 3 | HG03041.hp1 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.489+2384C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808016 | ||||||
| chr16:56808100
|
C | A | 4 | a0002c0008t0002g0298a0002c0008t0002g0299a0002c0008t0002g0300others(1): Show | 4 | NA18954.hp1 NA18966.hp1 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.489+2468C>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808100 | ||||||
| chr16:56808115
|
A | ATTATATA others(15): Show |
4 | a0001c0001t0011g0004a0001c0001t0011g0006a0001c0001t0011g0009others(1): Show | 4 | HG02630.hp1 HG03098.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.489+2499_489+2520d others(24): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808115 | |||||
| chr16:56808124
|
C | A | 159 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0045others(156): Show | 160 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.489+2492C>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808124 | ||||||
| chr16:56808131
|
A | AAAT | 54 | a0001c0001t0002g0284a0001c0001t0002g0295a0001c0002t0001g0088others(51): Show | 54 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.489+2500_489+2501i others(5): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808131 | |||||
| chr16:56808131
|
A | AAATATAT others(394): Show |
1 | a0001c0003t0002g0264 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.489+2500_489+2501i others(403): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808131 | |||||
| chr16:56808131
|
A | AAATATAT others(286): Show |
1 | a0001c0001t0002g0292 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.489+2500_489+2501i others(295): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808131 | |||||
| chr16:56808131
|
A | AAATATAT others(21): Show |
2 | a0001c0003t0002g0285a0001c0003t0042g0286 | 2 | HG02622.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.489+2500_489+2501i others(30): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808131 | |||||
| chr16:56808131
|
A | AAATATAT others(344): Show |
1 | a0001c0003t0002g0247 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.489+2500_489+2501i others(353): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808131 | |||||
| chr16:56808131
|
A | AAATATAT others(369): Show |
1 | a0001c0003t0002g0248 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.489+2500_489+2501i others(378): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808131 | |||||
| chr16:56808137
|
T | G | 60 | a0001c0001t0002g0284a0001c0001t0002g0292a0001c0001t0002g0295others(57): Show | 60 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.489+2505T>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808137 | ||||||
| chr16:56808137
|
T | TTTATATA others(43): Show |
3 | a0001c0004t0015g0015a0001c0004t0015g0016a0001c0004t0015g0017 | 3 | HG02818.hp1 HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.489+2520_489+2521i others(52): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808137 | |||||
| chr16:56808137
|
T | TTTATATA others(143): Show |
1 | a0001c0009t0018g0019 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.489+2520_489+2521i others(152): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808137 | |||||
| chr16:56808137
|
T | TTTATATA others(168): Show |
1 | a0001c0009t0018g0018 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.489+2520_489+2521i others(177): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808137 | |||||
| chr16:56808141
|
T | C | 3 | a0001c0001t0002g0292a0001c0003t0002g0259a0001c0003t0002g0264 | 3 | HG01243.hp2 HG02717.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.489+2509T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808141 | ||||||
| chr16:56808142
|
A | G | 4 | a0001c0001t0002g0292a0001c0003t0002g0247a0001c0003t0002g0248others(1): Show | 4 | HG01243.hp2 HG01261.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.489+2510A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808142 | ||||||
| chr16:56808146
|
CT | C | 3 | a0001c0004t0008g0174a0001c0004t0008g0175a0001c0004t0008g0176 | 3 | HG00741.hp1 HG03669.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.489+2515delT | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808146 | ||||||
| chr16:56808153
|
T | A | 269 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0045others(266): Show | 271 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.489+2521T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808153 | ||||||
| chr16:56808153
|
T | TAATATAT others(143): Show |
1 | a0001c0001t0029g0245 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.489+2584_489+2585i others(152): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808153 | |||||
| chr16:56808153
|
T | TAATATAT others(68): Show |
3 | a0001c0001t0003g0361a0001c0001t0003g0374a0004c0023t0026g0372 | 3 | HG03471.hp2 HG04204.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.489+2570_489+2571i others(77): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808153 | |||||
| chr16:56808153
|
T | TAATATAT others(93): Show |
1 | a0001c0001t0003g0373 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.489+2570_489+2571i others(102): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808153 | |||||
| chr16:56808153
|
T | TAATATAT others(93): Show |
2 | a0001c0001t0003g0351a0001c0001t0003g0352 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.489+2545_489+2546i others(102): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808153 | |||||
| chr16:56808153
|
T | TTTTATAT others(18): Show |
1 | a0001c0001t0004g0230 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.489+2521_489+2522i others(27): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808153 | ||||||
| chr16:56808153
|
T | TTTTATAT others(18): Show |
19 | a0001c0001t0004g0198a0001c0001t0004g0220a0001c0001t0004g0222others(16): Show | 19 | HG00408.hp2 HG00597.hp2 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.489+2521_489+2522i others(27): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808153 | ||||||
| chr16:56808153
|
T | TTTTATAT others(68): Show |
1 | a0001c0001t0004g0229 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.489+2521_489+2522i others(77): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808153 | ||||||
| chr16:56808153
|
T | TTTTATAT others(93): Show |
3 | a0001c0001t0004g0221a0001c0001t0004g0232a0001c0001t0004g0236 | 3 | HG01433.hp2 HG01496.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.489+2521_489+2522i others(102): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808153 | ||||||
| chr16:56808155
|
A | ATATATAG others(43): Show |
17 | a0001c0001t0003g0348a0001c0001t0003g0349a0001c0001t0003g0350others(14): Show | 17 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.489+2570_489+2571i others(52): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808155 | |||||
| chr16:56808166
|
T | C | 6 | a0001c0001t0002g0292a0001c0003t0002g0259a0001c0003t0002g0264others(3): Show | 6 | HG01243.hp2 HG02132.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.489+2534T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808166 | ||||||
| chr16:56808167
|
A | ATAACTAT others(18): Show |
1 | a0001c0004t0008g0176 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.489+2559_489+2560i others(27): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808167 | |||||
| chr16:56808167
|
A | G | 16 | a0001c0001t0002g0292a0001c0001t0004g0221a0001c0001t0004g0229others(13): Show | 16 | HG01243.hp2 HG01261.hp2 HG01433.hp2 others(13): Show |
intron_variant | MODIFIER | c.489+2535A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808167 | ||||||
| chr16:56808180
|
A | ATATATAG others(18): Show |
4 | a0001c0001t0003g0362a0001c0001t0003g0366a0001c0001t0003g0375others(1): Show | 4 | HG01081.hp2 HG01167.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.489+2570_489+2571i others(27): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808180 | |||||
| chr16:56808181
|
TATATAGT others(116): Show |
T | 1 | a0001c0001t0006g0206 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.489+2555_489+2677d others(2): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808181 | |||||
| chr16:56808182
|
A | ATATAGTT others(16): Show |
1 | a0010c0013t0007g0190 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.489+2570_489+2571i others(25): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808182 | |||||
| chr16:56808191
|
T | C | 6 | a0001c0001t0002g0292a0001c0003t0002g0259a0001c0003t0002g0264others(3): Show | 6 | HG01243.hp2 HG02132.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.489+2559T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808191 | ||||||
| chr16:56808192
|
A | ATAACTAT others(218): Show |
1 | a0001c0001t0011g0005 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.489+2583_489+2584i others(227): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808192 | |||||
| chr16:56808192
|
A | ATAACTAT others(68): Show |
1 | a0001c0007t0012g0345 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.489+2583_489+2584i others(77): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808192 | |||||
| chr16:56808192
|
A | ATAACTAT others(168): Show |
1 | a0003c0024t0018g0010 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.489+2584_489+2585i others(177): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808192 | |||||
| chr16:56808192
|
A | ATAACTAT others(391): Show |
2 | a0001c0003t0002g0277a0001c0003t0002g0282 | 2 | HG02630.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.489+2584_489+2585i others(400): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808192 | |||||
| chr16:56808192
|
A | ATAACTAT others(466): Show |
2 | a0001c0003t0002g0257a0001c0003t0002g0258 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.489+2584_489+2585i others(475): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808192 | |||||
| chr16:56808192
|
A | ATAACTAT others(341): Show |
1 | a0001c0003t0002g0288 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.489+2584_489+2585i others(350): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808192 | |||||
| chr16:56808192
|
A | ATAACTAT others(316): Show |
1 | a0001c0003t0002g0287 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.489+2584_489+2585i others(325): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808192 | |||||
| chr16:56808192
|
A | ATAACTAT others(291): Show |
1 | a0001c0003t0002g0278 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.489+2584_489+2585i others(300): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808192 | |||||
| chr16:56808192
|
A | ATAACTAT others(291): Show |
1 | a0001c0003t0002g0272 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.489+2584_489+2585i others(300): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808192 | |||||
| chr16:56808192
|
A | ATAACTAT others(316): Show |
1 | a0001c0003t0002g0289 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.489+2584_489+2585i others(325): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808192 | |||||
| chr16:56808192
|
A | ATAACTAT others(341): Show |
2 | a0001c0003t0002g0263a0001c0003t0002g0279 | 2 | HG02155.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.489+2584_489+2585i others(350): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808192 | |||||
| chr16:56808192
|
A | ATAACTAT others(391): Show |
1 | a0001c0003t0002g0267 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.489+2584_489+2585i others(400): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808192 | |||||
| chr16:56808192
|
A | ATAACTAT others(416): Show |
2 | a0001c0003t0002g0256a0001c0003t0002g0275 | 2 | NA18942.hp2 NA18949.hp2 |
intron_variant | MODIFIER | c.489+2584_489+2585i others(425): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808192 | |||||
| chr16:56808192
|
A | ATAACTAT others(341): Show |
1 | a0001c0003t0002g0293 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.489+2584_489+2585i others(350): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808192 | |||||
| chr16:56808192
|
A | ATAACTAT others(343): Show |
1 | a0001c0003t0021g0262 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.489+2584_489+2585i others(352): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808192 | |||||
| chr16:56808192
|
A | ATAACTAT others(368): Show |
1 | a0001c0003t0021g0294 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.489+2584_489+2585i others(377): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808192 | |||||
| chr16:56808192
|
A | ATAACTAT others(18): Show |
6 | a0001c0004t0008g0172a0001c0004t0008g0173a0001c0004t0008g0174others(3): Show | 6 | HG00099.hp2 HG00741.hp1 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.489+2819_489+2843d others(27): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808192 | |||||
| chr16:56808192
|
A | ATAACTAT others(43): Show |
1 | a0001c0004t0019g0181 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.489+2794_489+2843d others(52): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808192 | |||||
| chr16:56808192
|
A | ATAACTAT others(366): Show |
1 | a0001c0003t0002g0265 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.489+2793_489+2794i others(375): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808192 | |||||
| chr16:56808192
|
A | ATAACTAT others(341): Show |
2 | a0001c0003t0002g0285a0001c0003t0030g0274 | 2 | HG02622.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.489+2818_489+2819i others(350): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808192 | |||||
| chr16:56808192
|
A | ATAACTAT others(366): Show |
2 | a0001c0003t0002g0246a0001c0003t0002g0280 | 2 | HG01099.hp1 NA18939.hp1 |
intron_variant | MODIFIER | c.489+2818_489+2819i others(375): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808192 | |||||
| chr16:56808192
|
A | ATAACTAT others(391): Show |
2 | a0001c0003t0002g0281a0002c0008t0002g0298 | 2 | HG01175.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.489+2870_489+2871i others(400): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808192 | |||||
| chr16:56808192
|
A | ATAACTAT others(416): Show |
1 | a0002c0008t0002g0299 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.489+2870_489+2871i others(425): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808192 | |||||
| chr16:56808192
|
A | ATAACTAT others(566): Show |
1 | a0001c0003t0002g0296 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.489+2870_489+2871i others(575): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808192 | |||||
| chr16:56808192
|
A | ATAACTAT others(468): Show |
1 | a0001c0003t0002g0273 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.489+2843_489+2844i others(477): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808192 | |||||
| chr16:56808192
|
A | ATAACTAT others(43): Show |
1 | a0001c0001t0003g0367 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.489+2570_489+2571i others(52): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808192 | |||||
| chr16:56808192
|
A | G | 25 | a0001c0001t0002g0292a0001c0001t0004g0221a0001c0001t0004g0229others(22): Show | 25 | HG01109.hp2 HG01243.hp2 HG01261.hp2 others(22): Show |
intron_variant | MODIFIER | c.489+2560A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808192 | ||||||
| chr16:56808192
|
ATAACTAT others(18): Show |
A | 1 | a0001c0004t0045g0182 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.489+2819_489+2843d others(27): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808192 | |||||
| chr16:56808198
|
A | ATATAAAA others(391): Show |
1 | a0001c0001t0002g0284 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.489+2584_489+2585i others(400): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808198 | |||||
| chr16:56808203
|
A | T | 12 | a0001c0001t0007g0194a0001c0001t0007g0195a0001c0001t0007g0340others(9): Show | 12 | HG00642.hp2 HG01109.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.489+2571A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808203 | ||||||
| chr16:56808204
|
A | T | 12 | a0001c0001t0007g0194a0001c0001t0007g0195a0001c0001t0007g0340others(9): Show | 12 | HG00642.hp2 HG01109.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.489+2572A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808204 | ||||||
| chr16:56808205
|
A | ATATATAG others(18): Show |
1 | a0001c0001t0016g0191 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.489+2584_489+2585i others(27): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808205 | |||||
| chr16:56808205
|
A | T | 10 | a0001c0001t0007g0194a0001c0001t0007g0195a0001c0001t0007g0340others(7): Show | 10 | HG00642.hp2 HG01109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.489+2573A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808205 | ||||||
| chr16:56808216
|
T | C | 8 | a0001c0001t0002g0292a0001c0001t0011g0005a0001c0003t0002g0259others(5): Show | 8 | HG01243.hp2 HG01884.hp1 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.489+2584T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808216 | ||||||
| chr16:56808217
|
G | A | 263 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0045others(260): Show | 265 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.489+2585G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808217 | ||||||
| chr16:56808217
|
G | GTAACTAT others(18): Show |
1 | a0001c0001t0002g0295 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.489+2609_489+2610i others(27): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808217 | |||||
| chr16:56808221
|
CTA | C | 19 | a0001c0001t0006g0199a0001c0001t0006g0200a0001c0001t0006g0201others(16): Show | 19 | HG01070.hp2 HG01168.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.489+2594_489+2595d others(4): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808221 | |||||
| chr16:56808223
|
A | ATATAAAA others(266): Show |
1 | a0005c0022t0022g0254 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.489+2608_489+2609i others(275): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808223 | |||||
| chr16:56808223
|
A | ATATAAAA others(441): Show |
1 | a0001c0003t0002g0259 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.489+2608_489+2609i others(450): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808223 | |||||
| chr16:56808223
|
A | ATATAAAA others(16): Show |
1 | a0001c0002t0001g0088 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.489+2609_489+2610i others(25): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808223 | |||||
| chr16:56808228
|
A | T | 3 | a0001c0001t0016g0192a0001c0001t0016g0193a0001c0001t0034g0196 | 3 | HG02258.hp2 HG02572.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.489+2596A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808228 | ||||||
| chr16:56808229
|
A | T | 3 | a0001c0001t0016g0192a0001c0001t0016g0193a0001c0001t0034g0196 | 3 | HG02258.hp2 HG02572.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.489+2597A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808229 | ||||||
| chr16:56808230
|
A | T | 3 | a0001c0001t0016g0192a0001c0001t0016g0193a0001c0001t0034g0196 | 3 | HG02258.hp2 HG02572.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.489+2598A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808230 | ||||||
| chr16:56808231
|
T | TATATAGT others(41): Show |
1 | a0001c0004t0005g0038 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.489+2609_489+2610i others(50): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808231 | |||||
| chr16:56808231
|
T | TATATAGT others(285): Show |
1 | a0001c0002t0001g0081 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.489+2609_489+2610i others(294): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808231 | |||||
| chr16:56808233
|
T | A | 1 | a0001c0001t0007g0195 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.489+2601T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808233 | ||||||
| chr16:56808241
|
T | C | 16 | a0001c0001t0002g0292a0001c0001t0007g0194a0001c0003t0002g0259others(13): Show | 16 | HG01243.hp2 HG02132.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.489+2609T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808241 | ||||||
| chr16:56808242
|
G | A | 251 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0045others(248): Show | 253 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.489+2610G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808242 | ||||||
| chr16:56808256
|
T | TATATAGT others(164): Show |
1 | a0001c0001t0001g0336 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.489+2634_489+2635i others(173): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808256 | |||||
| chr16:56808256
|
T | TATATAGT others(212): Show |
1 | a0001c0002t0001g0108 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.489+2634_489+2635i others(221): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808256 | |||||
| chr16:56808256
|
T | TATATAGT others(237): Show |
1 | a0001c0002t0001g0109 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.489+2634_489+2635i others(246): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808256 | |||||
| chr16:56808256
|
T | TATATAGT others(212): Show |
1 | a0001c0002t0001g0086 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.489+2634_489+2635i others(221): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808256 | |||||
| chr16:56808266
|
T | C | 16 | a0001c0001t0002g0292a0001c0001t0007g0194a0001c0003t0002g0259others(13): Show | 16 | HG01243.hp2 HG02132.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.489+2634T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808266 | ||||||
| chr16:56808267
|
G | A | 232 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0045others(229): Show | 234 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.489+2635G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808267 | ||||||
| chr16:56808281
|
T | TATAGTTA others(185): Show |
1 | a0001c0002t0001g0083 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.489+2652_489+2653i others(194): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808281 | |||||
| chr16:56808281
|
T | TATATAGT others(235): Show |
1 | a0001c0002t0001g0059 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.489+2659_489+2660i others(244): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808281 | |||||
| chr16:56808281
|
T | TATATAGT others(187): Show |
5 | a0001c0002t0001g0072a0001c0002t0001g0105a0001c0002t0001g0164others(2): Show | 5 | HG00408.hp1 HG02027.hp2 HG03688.hp2 others(2): Show |
intron_variant | MODIFIER | c.489+2659_489+2660i others(196): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808281 | |||||
| chr16:56808281
|
T | TATATAGT others(212): Show |
3 | a0001c0002t0001g0076a0001c0002t0001g0080a0001c0002t0001g0339 | 3 | HG02056.hp2 HG02071.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.489+2659_489+2660i others(221): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808281 | |||||
| chr16:56808281
|
T | TATATAGT others(235): Show |
2 | a0001c0002t0001g0075a0001c0012t0001g0079 | 2 | NA19002.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.489+2659_489+2660i others(244): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808281 | |||||
| chr16:56808288
|
T | TTATATAA others(37): Show |
3 | a0001c0001t0014g0217a0001c0001t0014g0218a0001c0001t0014g0219 | 3 | HG01884.hp2 HG03453.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.489+2659_489+2660i others(46): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808288 | |||||
| chr16:56808291
|
T | C | 16 | a0001c0001t0002g0292a0001c0001t0007g0194a0001c0003t0002g0259others(13): Show | 16 | HG01243.hp2 HG02132.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.489+2659T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808291 | ||||||
| chr16:56808292
|
G | A | 215 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0045others(212): Show | 217 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.489+2660G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808292 | ||||||
| chr16:56808304
|
AATATATA others(45): Show |
A | 1 | a0001c0001t0001g0136 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.489+2678_489+2729d others(54): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808304 | |||||
| chr16:56808306
|
T | TATATAGT others(114): Show |
1 | a0001c0001t0001g0163 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.489+2684_489+2685i others(123): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808306 | |||||
| chr16:56808306
|
T | TATATAGT others(39): Show |
1 | a0001c0002t0001g0088 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.489+2684_489+2685i others(48): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808306 | |||||
| chr16:56808306
|
T | TATATAGT others(210): Show |
5 | a0001c0002t0001g0094a0001c0002t0001g0098a0001c0002t0001g0099others(2): Show | 5 | HG02886.hp1 HG02970.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.489+2684_489+2685i others(219): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808306 | |||||
| chr16:56808316
|
T | C | 16 | a0001c0001t0002g0292a0001c0001t0007g0194a0001c0003t0002g0259others(13): Show | 16 | HG01243.hp2 HG02132.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.489+2684T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808316 | ||||||
| chr16:56808317
|
G | A | 199 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0045others(196): Show | 201 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.489+2685G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808317 | ||||||
| chr16:56808321
|
CTA | C | 17 | a0001c0001t0001g0302a0001c0001t0001g0303a0001c0001t0001g0305others(14): Show | 17 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(14): Show |
intron_variant | MODIFIER | c.489+2694_489+2695d others(4): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808321 | |||||
| chr16:56808331
|
T | TATATAGT others(162): Show |
2 | a0001c0001t0001g0323a0001c0001t0023g0330 | 2 | HG01123.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.489+2709_489+2710i others(171): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808331 | |||||
| chr16:56808331
|
T | TATATAGT others(162): Show |
3 | a0001c0001t0017g0307a0001c0001t0017g0341a0001c0001t0017g0342 | 3 | HG00621.hp2 NA18969.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.489+2709_489+2710i others(171): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808331 | |||||
| chr16:56808331
|
T | TATATAGT others(187): Show |
1 | a0001c0001t0001g0321 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.489+2709_489+2710i others(196): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808331 | |||||
| chr16:56808331
|
T | TATATAGT others(212): Show |
1 | a0001c0001t0001g0343 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.489+2709_489+2710i others(221): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808331 | |||||
| chr16:56808331
|
T | TATATAGT others(235): Show |
1 | a0001c0002t0001g0110 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.489+2709_489+2710i others(244): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808331 | |||||
| chr16:56808341
|
T | C | 15 | a0001c0001t0002g0292a0001c0001t0007g0194a0001c0003t0002g0259others(12): Show | 15 | HG01243.hp2 HG02132.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.489+2709T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808341 | ||||||
| chr16:56808342
|
G | A | 199 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0045others(196): Show | 201 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.489+2710G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808342 | ||||||
| chr16:56808346
|
CTA | C | 29 | a0001c0001t0001g0002a0001c0001t0001g0122a0001c0001t0001g0123others(26): Show | 29 | HG00544.hp1 HG00609.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.489+2719_489+2720d others(4): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808346 | |||||
| chr16:56808348
|
A | ATAAAATA others(185): Show |
1 | a0001c0002t0037g0084 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.489+2718_489+2719i others(194): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808348 | |||||
| chr16:56808348
|
A | ATAAAATA others(185): Show |
2 | a0001c0001t0001g0002a0001c0001t0001g0318 | 2 | HG01358.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.489+2718_489+2719i others(194): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808348 | |||||
| chr16:56808353
|
A | T | 3 | a0001c0001t0001g0002a0001c0001t0001g0318a0001c0002t0037g0084 | 3 | HG01358.hp2 HG01981.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.489+2721A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808353 | ||||||
| chr16:56808354
|
AAT | A | 7 | a0001c0001t0001g0163a0001c0001t0001g0336a0001c0002t0001g0108others(4): Show | 7 | HG00140.hp1 HG01891.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.489+2728_489+2729d others(4): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808354 | |||||
| chr16:56808356
|
T | A | 3 | a0001c0001t0001g0002a0001c0001t0001g0318a0001c0002t0037g0084 | 3 | HG01358.hp2 HG01981.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.489+2724T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808356 | ||||||
| chr16:56808356
|
T | TATATAGT others(114): Show |
1 | a0001c0001t0001g0147 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.489+2734_489+2735i others(123): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808356 | |||||
| chr16:56808356
|
T | TATATAGT others(162): Show |
7 | a0001c0001t0001g0046a0001c0001t0001g0053a0001c0001t0001g0054others(4): Show | 7 | HG01496.hp1 HG02451.hp1 HG03490.hp1 others(4): Show |
intron_variant | MODIFIER | c.489+2734_489+2735i others(171): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808356 | |||||
| chr16:56808356
|
T | TATATAGT others(187): Show |
3 | a0001c0001t0001g0045a0001c0001t0001g0116a0001c0001t0001g0124 | 3 | HG01433.hp1 HG02647.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.489+2734_489+2735i others(196): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808356 | |||||
| chr16:56808356
|
T | TATATAGT others(187): Show |
1 | a0001c0001t0001g0119 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.489+2734_489+2735i others(196): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808356 | |||||
| chr16:56808356
|
T | TATATAGT others(212): Show |
5 | a0001c0001t0001g0003a0001c0001t0001g0132a0001c0001t0001g0133others(2): Show | 5 | HG00735.hp1 HG01515.hp2 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.489+2734_489+2735i others(221): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808356 | |||||
| chr16:56808366
|
T | C | 15 | a0001c0001t0002g0292a0001c0001t0007g0194a0001c0003t0002g0259others(12): Show | 15 | HG01243.hp2 HG02132.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.489+2734T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808366 | ||||||
| chr16:56808366
|
T | TATAACTA others(235): Show |
1 | a0001c0002t0001g0060 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.489+2734_489+2735i others(244): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808366 | ||||||
| chr16:56808366
|
T | TATAACTA others(308): Show |
1 | a0001c0002t0001g0061 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.489+2734_489+2735i others(317): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808366 | ||||||
| chr16:56808367
|
G | A | 194 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0045others(191): Show | 196 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.489+2735G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808367 | ||||||
| chr16:56808371
|
CTA | C | 21 | a0001c0001t0001g0125a0001c0001t0001g0138a0001c0001t0001g0139others(18): Show | 21 | HG00621.hp1 HG01069.hp2 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.489+2744_489+2745d others(4): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808371 | |||||
| chr16:56808371
|
CTATATAA others(70): Show |
C | 2 | a0001c0001t0006g0203a0001c0001t0006g0208 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.489+2744_489+2820d others(79): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808371 | |||||
| chr16:56808373
|
A | ATAAAATA others(83): Show |
1 | a0006c0021t0001g0011 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.489+2743_489+2744i others(92): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808373 | |||||
| chr16:56808373
|
A | ATAAAATA others(185): Show |
2 | a0001c0002t0001g0066a0007c0020t0001g0063 | 2 | HG02965.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.489+2743_489+2744i others(194): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808373 | |||||
| chr16:56808373
|
A | ATAAAATA others(210): Show |
1 | a0001c0002t0001g0093 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.489+2743_489+2744i others(219): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808373 | |||||
| chr16:56808373
|
A | ATAAAATA others(306): Show |
2 | a0001c0002t0001g0073a0001c0019t0001g0078 | 2 | NA18954.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.489+2743_489+2744i others(315): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808373 | |||||
| chr16:56808373
|
A | ATAAAATA others(235): Show |
2 | a0001c0002t0001g0101a0001c0002t0001g0129 | 2 | HG02602.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.489+2743_489+2744i others(244): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808373 | |||||
| chr16:56808373
|
A | ATAAATAT others(135): Show |
1 | a0001c0001t0001g0161 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.489+2743_489+2744i others(144): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808373 | |||||
| chr16:56808378
|
A | T | 8 | a0001c0001t0001g0161a0001c0002t0001g0066a0001c0002t0001g0073others(5): Show | 8 | HG02074.hp1 HG02602.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.489+2746A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808378 | ||||||
| chr16:56808379
|
AAT | A | 25 | a0001c0001t0001g0321a0001c0001t0001g0323a0001c0001t0001g0343others(22): Show | 25 | HG00140.hp1 HG00408.hp1 HG00621.hp2 others(22): Show |
intron_variant | MODIFIER | c.489+2753_489+2754d others(4): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808379 | |||||
| chr16:56808381
|
T | A | 8 | a0001c0001t0001g0161a0001c0002t0001g0066a0001c0002t0001g0073others(5): Show | 8 | HG02074.hp1 HG02602.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.489+2749T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808381 | ||||||
| chr16:56808381
|
T | TATATAGT others(283): Show |
1 | a0001c0002t0001g0104 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.489+2759_489+2760i others(292): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808381 | |||||
| chr16:56808381
|
T | TATATAGT others(185): Show |
1 | a0001c0002t0001g0067 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.489+2759_489+2760i others(194): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808381 | |||||
| chr16:56808381
|
T | TATATAGT others(137): Show |
1 | a0001c0001t0043g0154 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.489+2759_489+2760i others(146): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808381 | |||||
| chr16:56808381
|
T | TATATAGT others(210): Show |
1 | a0001c0002t0001g0064 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.489+2759_489+2760i others(219): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808381 | |||||
| chr16:56808381
|
T | TATATAGT others(285): Show |
1 | a0001c0002t0001g0062 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.489+2759_489+2760i others(294): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808381 | |||||
| chr16:56808381
|
T | TATATAGT others(162): Show |
1 | a0001c0001t0001g0126 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.489+2759_489+2760i others(171): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808381 | |||||
| chr16:56808381
|
T | TATATAGT others(281): Show |
1 | a0001c0002t0001g0102 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.489+2759_489+2760i others(290): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808381 | |||||
| chr16:56808381
|
T | TATATAGT others(187): Show |
1 | a0001c0001t0001g0118 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.489+2759_489+2760i others(196): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808381 | |||||
| chr16:56808381
|
T | TATATAGT others(187): Show |
1 | a0001c0001t0001g0169 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.489+2759_489+2760i others(196): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808381 | |||||
| chr16:56808381
|
T | TATATAGT others(237): Show |
1 | a0001c0002t0001g0107 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.489+2759_489+2760i others(246): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808381 | |||||
| chr16:56808381
|
T | TATATAGT others(41): Show |
1 | a0001c0004t0005g0021 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.489+2759_489+2760i others(50): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808381 | |||||
| chr16:56808381
|
T | TATATAGT others(231): Show |
1 | a0001c0002t0001g0167 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.489+2759_489+2760i others(240): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808381 | |||||
| chr16:56808381
|
T | TATATAGT others(185): Show |
2 | a0001c0002t0001g0074a0001c0002t0001g0091 | 2 | HG01123.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.489+2759_489+2760i others(194): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808381 | |||||
| chr16:56808381
|
T | TATATAGT others(212): Show |
1 | a0001c0017t0001g0158 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.489+2759_489+2760i others(221): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808381 | |||||
| chr16:56808381
|
T | TATATAGT others(210): Show |
4 | a0001c0002t0001g0082a0001c0002t0001g0087a0001c0002t0001g0092others(1): Show | 4 | HG01258.hp1 HG02148.hp1 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.489+2759_489+2760i others(219): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808381 | |||||
| chr16:56808381
|
T | TATATAGT others(162): Show |
6 | a0001c0001t0001g0303a0001c0001t0001g0311a0001c0001t0001g0312others(3): Show | 6 | NA18944.hp2 NA18971.hp1 NA18984.hp2 others(3): Show |
intron_variant | MODIFIER | c.489+2759_489+2760i others(171): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808381 | |||||
| chr16:56808381
|
T | TATATAGT others(262): Show |
1 | a0001c0001t0001g0120 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.489+2759_489+2760i others(271): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808381 | |||||
| chr16:56808381
|
T | TATATAGT others(116): Show |
1 | a0001c0004t0005g0029 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.489+2759_489+2760i others(125): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808381 | |||||
| chr16:56808391
|
T | C | 17 | a0001c0001t0002g0292a0001c0001t0007g0194a0001c0002t0001g0060others(14): Show | 17 | HG01243.hp2 HG02132.hp2 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.489+2759T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808391 | ||||||
| chr16:56808392
|
G | A | 178 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0045others(175): Show | 179 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.489+2760G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808392 | ||||||
| chr16:56808396
|
CTA | C | 6 | a0001c0001t0001g0002a0001c0001t0001g0316a0001c0001t0001g0318others(3): Show | 6 | HG00609.hp1 HG01358.hp2 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.489+2769_489+2770d others(4): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808396 | |||||
| chr16:56808398
|
A | ATAAAATA others(137): Show |
1 | a0001c0001t0001g0159 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.489+2768_489+2769i others(146): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808398 | |||||
| chr16:56808398
|
A | ATAAAATA others(233): Show |
1 | a0001c0002t0001g0096 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.489+2768_489+2769i others(242): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808398 | |||||
| chr16:56808403
|
A | T | 2 | a0001c0001t0001g0159a0001c0002t0001g0096 | 2 | HG02280.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.489+2771A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808403 | ||||||
| chr16:56808404
|
AAT | A | 5 | a0001c0001t0001g0147a0001c0002t0001g0110a0001c0004t0015g0015others(2): Show | 5 | HG02258.hp1 HG02818.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.489+2778_489+2779d others(4): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808404 | |||||
| chr16:56808406
|
T | A | 2 | a0001c0001t0001g0159a0001c0002t0001g0096 | 2 | HG02280.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.489+2774T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808406 | ||||||
| chr16:56808416
|
T | C | 17 | a0001c0001t0002g0292a0001c0001t0007g0194a0001c0001t0007g0195others(14): Show | 17 | HG00642.hp2 HG01243.hp2 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.489+2784T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808416 | ||||||
| chr16:56808417
|
G | A | 148 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0045others(145): Show | 149 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.489+2785G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808417 | ||||||
| chr16:56808421
|
CTA | C | 18 | a0001c0001t0001g0002a0001c0001t0001g0303a0001c0001t0001g0311others(15): Show | 18 | HG00621.hp2 HG01123.hp2 HG01358.hp2 others(15): Show |
intron_variant | MODIFIER | c.489+2794_489+2795d others(4): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808421 | |||||
| chr16:56808421
|
CTATATAA others(20): Show |
C | 18 | a0001c0001t0006g0199a0001c0001t0006g0200a0001c0001t0006g0201others(15): Show | 18 | HG01070.hp2 HG01109.hp1 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.489+2794_489+2820d others(29): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808421 | |||||
| chr16:56808423
|
A | ATAAAATA others(187): Show |
1 | a0001c0001t0001g0141 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.489+2793_489+2794i others(196): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808423 | |||||
| chr16:56808423
|
A | ATAAAATA others(308): Show |
1 | a0001c0002t0001g0070 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.489+2793_489+2794i others(317): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808423 | |||||
| chr16:56808423
|
A | ATATAAAA others(135): Show |
5 | a0001c0001t0001g0302a0001c0001t0001g0305a0001c0001t0001g0306others(2): Show | 5 | HG00140.hp2 NA18946.hp1 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.489+2802_489+2803i others(144): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808423 | |||||
| chr16:56808423
|
A | ATATAAAA others(137): Show |
1 | a0001c0001t0001g0335 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.489+2802_489+2803i others(146): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808423 | |||||
| chr16:56808441
|
T | C | 14 | a0001c0001t0002g0292a0001c0001t0007g0194a0001c0001t0007g0195others(11): Show | 14 | HG00642.hp2 HG02257.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.489+2809T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808441 | ||||||
| chr16:56808442
|
G | A | 103 | a0001c0001t0001g0002a0001c0001t0001g0052a0001c0001t0001g0114others(100): Show | 104 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.489+2810G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808442 | ||||||
| chr16:56808446
|
CTA | C | 143 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0045others(140): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.489+2819_489+2820d others(4): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808446 | |||||
| chr16:56808448
|
A | ATAAAATA others(256): Show |
1 | a0001c0001t0001g0114 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.489+2818_489+2819i others(265): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808448 | |||||
| chr16:56808448
|
A | ATAAAATA others(235): Show |
1 | a0001c0001t0001g0130 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.489+2818_489+2819i others(244): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808448 | |||||
| chr16:56808448
|
A | ATAAAATA others(283): Show |
3 | a0001c0002t0001g0001a0001c0002t0001g0071a0001c0002t0001g0170 | 4 | HG00642.hp1 HG01361.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.489+2818_489+2819i others(292): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808448 | |||||
| chr16:56808448
|
A | ATAAAATA others(306): Show |
1 | a0001c0002t0001g0106 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.489+2818_489+2819i others(315): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808448 | |||||
| chr16:56808448
|
A | ATAAAATA others(39): Show |
1 | a0001c0001t0027g0371 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.489+2818_489+2819i others(48): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808448 | |||||
| chr16:56808448
|
A | ATATAAAA others(185): Show |
9 | a0001c0002t0001g0044a0001c0002t0001g0057a0001c0002t0001g0058others(6): Show | 9 | HG00544.hp1 HG00609.hp2 HG02015.hp2 others(6): Show |
intron_variant | MODIFIER | c.489+2827_489+2828i others(194): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808448 | |||||
| chr16:56808448
|
A | ATATAAAA others(158): Show |
1 | a0001c0001t0001g0123 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.489+2827_489+2828i others(167): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808448 | |||||
| chr16:56808448
|
A | ATATAAAA others(231): Show |
1 | a0001c0001t0025g0314 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.489+2827_489+2828i others(240): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808448 | |||||
| chr16:56808448
|
A | ATATAAAA others(158): Show |
10 | a0001c0001t0001g0304a0001c0001t0001g0315a0001c0001t0001g0319others(7): Show | 10 | HG00438.hp1 HG00558.hp1 HG00735.hp2 others(7): Show |
intron_variant | MODIFIER | c.489+2827_489+2828i others(167): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808448 | |||||
| chr16:56808448
|
A | ATATAAAA others(181): Show |
1 | a0001c0001t0001g0002 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.489+2827_489+2828i others(190): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808448 | |||||
| chr16:56808448
|
A | ATATAAAA others(158): Show |
1 | a0001c0001t0001g0333 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.489+2827_489+2828i others(167): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808448 | |||||
| chr16:56808448
|
A | ATATAAAA others(137): Show |
1 | a0001c0016t0001g0117 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.489+2827_489+2828i others(146): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808448 | |||||
| chr16:56808448
|
A | ATATAAAA others(160): Show |
1 | a0001c0001t0001g0122 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.489+2827_489+2828i others(169): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808448 | |||||
| chr16:56808448
|
A | ATATAAAA others(112): Show |
1 | a0001c0001t0001g0144 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.489+2827_489+2828i others(121): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808448 | |||||
| chr16:56808448
|
A | ATATAAAA others(135): Show |
2 | a0001c0001t0001g0145a0001c0001t0001g0146 | 2 | NA18946.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.489+2827_489+2828i others(144): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808448 | |||||
| chr16:56808448
|
A | ATATAAAA others(110): Show |
2 | a0001c0001t0001g0337a0001c0001t0001g0338 | 2 | HG02155.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.489+2827_489+2828i others(119): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808448 | |||||
| chr16:56808448
|
A | ATATAAAA others(64): Show |
1 | a0001c0004t0005g0038 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.489+2827_489+2828i others(73): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808448 | |||||
| chr16:56808448
|
A | ATATAAAA others(16): Show |
1 | a0001c0005t0007g0186 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.489+2833_489+2834i others(25): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808448 | |||||
| chr16:56808448
|
A | ATATAAAA others(64): Show |
1 | a0001c0001t0007g0194 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.489+2833_489+2834i others(73): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808448 | |||||
| chr16:56808448
|
A | ATATAAAA others(260): Show |
4 | a0001c0001t0001g0052a0001c0001t0001g0131a0001c0001t0001g0157others(1): Show | 4 | HG02257.hp1 HG03130.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.489+2834_489+2835i others(269): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808448 | |||||
| chr16:56808448
|
A | ATATAAAA others(308): Show |
1 | a0001c0002t0010g0111 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.489+2834_489+2835i others(317): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808448 | |||||
| chr16:56808448
|
A | ATATAAAA others(185): Show |
2 | a0001c0002t0001g0068a0001c0002t0001g0069 | 2 | HG02622.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.489+2834_489+2835i others(194): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808448 | |||||
| chr16:56808448
|
A | ATATAAAA others(135): Show |
1 | a0001c0001t0036g0148 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.489+2834_489+2835i others(144): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808448 | |||||
| chr16:56808448
|
A | ATATAAAA others(160): Show |
1 | a0001c0001t0001g0125 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.489+2834_489+2835i others(169): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808448 | |||||
| chr16:56808448
|
A | ATATAAAA others(160): Show |
2 | a0001c0001t0001g0310a0001c0001t0001g0328 | 2 | HG03654.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.489+2834_489+2835i others(169): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808448 | |||||
| chr16:56808448
|
A | ATATAAAA others(183): Show |
2 | a0001c0001t0001g0309a0001c0001t0001g0325 | 2 | NA19002.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.489+2834_489+2835i others(192): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808448 | |||||
| chr16:56808448
|
A | ATATAAAA others(137): Show |
10 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(7): Show | 10 | HG00621.hp1 NA18943.hp2 NA18970.hp1 others(7): Show |
intron_variant | MODIFIER | c.489+2834_489+2835i others(146): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808448 | |||||
| chr16:56808448
|
A | ATATAAAA others(112): Show |
1 | a0001c0001t0001g0149 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.489+2834_489+2835i others(121): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808448 | |||||
| chr16:56808448
|
A | ATATAAAA others(89): Show |
1 | a0001c0004t0024g0039 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.489+2834_489+2835i others(98): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808448 | |||||
| chr16:56808448
|
A | ATATAAAA others(285): Show |
2 | a0001c0001t0001g0155a0001c0001t0001g0156 | 2 | HG02109.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.489+2834_489+2835i others(294): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808448 | |||||
| chr16:56808448
|
A | ATATAAAA others(356): Show |
1 | a0001c0002t0010g0112 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.489+2834_489+2835i others(365): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808448 | |||||
| chr16:56808448
|
A | ATATAAAA others(333): Show |
2 | a0001c0011t0001g0089a0001c0011t0001g0090 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.489+2834_489+2835i others(342): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808448 | |||||
| chr16:56808448
|
A | ATATAAAA others(208): Show |
1 | a0001c0001t0001g0316 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.489+2834_489+2835i others(217): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808448 | |||||
| chr16:56808448
|
A | ATATAAAA others(114): Show |
12 | a0001c0004t0005g0020a0001c0004t0005g0022a0001c0004t0005g0023others(9): Show | 12 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(9): Show |
intron_variant | MODIFIER | c.489+2834_489+2835i others(123): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808448 | |||||
| chr16:56808448
|
A | ATATAAAA others(139): Show |
7 | a0001c0004t0005g0025a0001c0004t0005g0027a0001c0004t0005g0028others(4): Show | 7 | HG00741.hp2 HG01261.hp1 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.489+2834_489+2835i others(148): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808448 | |||||
| chr16:56808448
|
A | ATATAAAA others(260): Show |
1 | a0001c0002t0001g0051 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.489+2834_489+2835i others(269): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808448 | |||||
| chr16:56808448
|
A | ATATAAAA others(189): Show |
1 | a0001c0004t0005g0031 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.489+2834_489+2835i others(198): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808448 | |||||
| chr16:56808448
|
A | ATATAAAA others(285): Show |
1 | a0001c0002t0041g0113 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.489+2834_489+2835i others(294): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808448 | |||||
| chr16:56808448
|
A | ATATAAAA others(110): Show |
1 | a0001c0001t0013g0014 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.489+2834_489+2835i others(119): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808448 | |||||
| chr16:56808448
|
A | ATATAAAA others(133): Show |
1 | a0001c0001t0013g0013 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.489+2834_489+2835i others(142): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808448 | |||||
| chr16:56808448
|
A | ATATAAAA others(16): Show |
1 | a0001c0001t0001g0120 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.489+2844_489+2866d others(25): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808448 | |||||
| chr16:56808448
|
A | ATATAAAA others(85): Show |
1 | a0001c0001t0013g0012 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.489+2866_489+2867i others(94): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808448 | |||||
| chr16:56808448
|
A | ATATAAAA others(66): Show |
7 | a0001c0001t0004g0198a0001c0001t0004g0230a0001c0001t0004g0238others(4): Show | 7 | HG00597.hp2 NA18959.hp2 NA18972.hp2 others(4): Show |
intron_variant | MODIFIER | c.489+2843_489+2844i others(75): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808448 | |||||
| chr16:56808450
|
A | ATAAAATA others(137): Show |
1 | a0001c0007t0012g0346 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.489+2843_489+2844i others(146): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808450 | |||||
| chr16:56808450
|
A | ATAAAATA others(162): Show |
2 | a0001c0007t0012g0065a0001c0007t0012g0347 | 2 | HG01891.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.489+2843_489+2844i others(171): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808450 | |||||
| chr16:56808456
|
T | TATATAGT others(260): Show |
1 | a0001c0014t0001g0137 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.489+2834_489+2835i others(269): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808456 | |||||
| chr16:56808456
|
T | TATATAGT others(14): Show |
2 | a0001c0004t0015g0015a0001c0004t0015g0017 | 2 | HG02818.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.489+2830_489+2850d others(23): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808456 | |||||
| chr16:56808456
|
T | TATATAGT others(216): Show |
1 | a0001c0001t0011g0004 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.489+2843_489+2844i others(225): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808456 | |||||
| chr16:56808456
|
T | TATATAGT others(241): Show |
1 | a0001c0001t0011g0006 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.489+2843_489+2844i others(250): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808456 | |||||
| chr16:56808466
|
T | C | 6 | a0001c0001t0001g0114a0001c0001t0002g0292a0001c0002t0001g0060others(3): Show | 6 | HG02559.hp2 HG02717.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.489+2834T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808466 | ||||||
| chr16:56808467
|
G | A | 4 | a0001c0001t0001g0121a0001c0002t0010g0048a0001c0002t0010g0049others(1): Show | 4 | HG01069.hp2 HG01167.hp1 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.489+2835G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808467 | ||||||
| chr16:56808471
|
C | CTA | 15 | a0001c0001t0002g0284a0001c0001t0002g0292a0001c0001t0011g0007others(12): Show | 15 | HG00597.hp1 HG00673.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.489+2842_489+2843d others(4): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808471 | |||||
| chr16:56808471
|
C | CTATAAAA others(366): Show |
1 | a0001c0003t0032g0271 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.489+2866_489+2867i others(375): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808471 | |||||
| chr16:56808471
|
C | CTATAAAA others(343): Show |
2 | a0001c0003t0002g0255a0001c0003t0002g0290 | 2 | HG01109.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.489+2870_489+2871i others(352): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808471 | |||||
| chr16:56808471
|
C | CTATAAAA others(368): Show |
2 | a0001c0003t0002g0266a0001c0003t0002g0276 | 2 | HG01928.hp1 NA18941.hp2 |
intron_variant | MODIFIER | c.489+2870_489+2871i others(377): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808471 | |||||
| chr16:56808471
|
C | CTATATAA others(20): Show |
1 | a0001c0003t0002g0263 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.489+2843_489+2844i others(29): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808471 | |||||
| chr16:56808471
|
C | CTATATAA others(391): Show |
1 | a0001c0003t0002g0047 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.489+2843_489+2844i others(400): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808471 | |||||
| chr16:56808471
|
C | CTATATAA others(466): Show |
1 | a0002c0008t0002g0300 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.489+2843_489+2844i others(475): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808471 | |||||
| chr16:56808471
|
C | CTATATAA others(45): Show |
3 | a0001c0006t0009g0251a0001c0006t0009g0252a0001c0006t0009g0253 | 3 | HG02818.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.489+2843_489+2844i others(54): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808471 | |||||
| chr16:56808471
|
C | CTATATAA others(466): Show |
1 | a0001c0003t0002g0269 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.489+2843_489+2844i others(475): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808471 | |||||
| chr16:56808471
|
C | CTATATAA others(70): Show |
2 | a0001c0006t0009g0249a0001c0006t0009g0250 | 2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.489+2843_489+2844i others(79): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808471 | |||||
| chr16:56808471
|
C | CTATATAA others(91): Show |
7 | a0001c0001t0004g0220a0001c0001t0004g0225a0001c0001t0004g0231others(4): Show | 7 | HG00408.hp2 HG00733.hp1 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.489+2843_489+2844i others(100): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808471 | |||||
| chr16:56808471
|
C | CTATATAA others(116): Show |
6 | a0001c0001t0004g0222a0001c0001t0004g0223a0001c0001t0004g0224others(3): Show | 6 | NA18941.hp1 NA18945.hp2 NA18992.hp2 others(3): Show |
intron_variant | MODIFIER | c.489+2843_489+2844i others(125): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808471 | |||||
| chr16:56808471
|
C | CTATATAA others(116): Show |
2 | a0001c0001t0011g0009a0001c0001t0046g0008 | 2 | HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.489+2843_489+2844i others(125): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808471 | |||||
| chr16:56808471
|
C | CTATATAA others(493): Show |
1 | a0001c0001t0002g0295 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.489+2843_489+2844i others(502): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808471 | |||||
| chr16:56808471
|
C | CTATATAA others(318): Show |
2 | a0001c0003t0020g0283a0001c0003t0020g0297 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.489+2843_489+2844i others(327): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808471 | |||||
| chr16:56808471
|
C | CTATATAA others(370): Show |
1 | a0001c0003t0002g0270 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.489+2843_489+2844i others(379): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808471 | |||||
| chr16:56808471
|
C | CTATATAA others(395): Show |
2 | a0001c0010t0022g0260a0001c0010t0033g0261 | 2 | HG03139.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.489+2843_489+2844i others(404): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808471 | |||||
| chr16:56808475
|
A | AT | 4 | a0001c0001t0001g0123a0001c0001t0001g0145a0001c0001t0001g0146others(1): Show | 4 | HG03239.hp1 HG04199.hp1 NA18946.hp2 others(1): Show |
intron_variant | MODIFIER | c.489+2843_489+2844i others(3): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808475 | ||||||
| chr16:56808476
|
A | T | 2 | a0001c0009t0018g0018a0001c0009t0018g0019 | 2 | HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.489+2844A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808476 | ||||||
| chr16:56808479
|
T | A | 2 | a0001c0009t0018g0018a0001c0009t0018g0019 | 2 | HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.489+2847T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808479 | ||||||
| chr16:56808479
|
T | TATAGTTA others(12): Show |
1 | a0001c0004t0015g0016 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.489+2850_489+2851i others(21): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808479 | |||||
| chr16:56808489
|
T | C | 3 | a0001c0001t0001g0114a0001c0001t0002g0292a0006c0021t0001g0011 | 3 | HG02717.hp1 HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.489+2857T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808489 | ||||||
| chr16:56808489
|
T | TATAACTA others(331): Show |
1 | a0001c0001t0001g0121 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.489+2857_489+2858i others(340): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808489 | ||||||
| chr16:56808490
|
G | A | 42 | a0001c0001t0003g0348a0001c0001t0003g0349a0001c0001t0003g0350others(39): Show | 42 | HG00323.hp1 HG00642.hp2 HG01069.hp2 others(39): Show |
intron_variant | MODIFIER | c.489+2858G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808490 | ||||||
| chr16:56808498
|
AT | A | 3 | a0001c0001t0004g0221a0001c0001t0004g0229a0001c0001t0004g0236 | 3 | HG01433.hp2 HG01496.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.489+2867delT | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808498 | ||||||
| chr16:56808499
|
T | TA | 6 | a0001c0001t0002g0292a0001c0001t0011g0007a0001c0009t0018g0018others(3): Show | 6 | HG02451.hp2 HG02717.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.489+2870dupA | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808499 | |||||
| chr16:56808499
|
T | TAAAATAT others(17): Show |
1 | a0001c0003t0002g0279 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.489+2870_489+2871i others(26): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808499 | |||||
| chr16:56808499
|
T | TAAAATAT others(417): Show |
1 | a0002c0008t0002g0301 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.489+2870_489+2871i others(426): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808499 | |||||
| chr16:56808501
|
A | AAATATAT others(392): Show |
2 | a0001c0003t0002g0268a0001c0003t0002g0291 | 2 | HG02056.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.489+2870_489+2871i others(401): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808501 | |||||
| chr16:56808501
|
A | AAATATAT others(293): Show |
1 | a0001c0003t0042g0286 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.489+2870_489+2871i others(302): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808501 | |||||
| chr16:56808501
|
A | AAATATAT others(18): Show |
1 | a0001c0003t0030g0274 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.489+2870_489+2871i others(27): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808501 | |||||
| chr16:56808501
|
A | T | 45 | a0001c0002t0001g0044a0001c0002t0001g0057a0001c0002t0001g0058others(42): Show | 45 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.489+2869A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808501 | ||||||
| chr16:56808502
|
AT | A | 3 | a0001c0002t0010g0048a0001c0002t0010g0049a0001c0002t0010g0050 | 3 | HG01069.hp2 HG01167.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.489+2871delT | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808502 | ||||||
| chr16:56808503
|
T | A | 49 | a0001c0002t0001g0044a0001c0002t0001g0057a0001c0002t0001g0058others(46): Show | 49 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.489+2871T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808503 | ||||||
| chr16:56808503
|
T | TATATAGT others(17): Show |
10 | a0001c0003t0002g0255a0001c0003t0002g0266a0001c0003t0002g0270others(7): Show | 10 | HG01109.hp2 HG01928.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.489+2882_489+2905d others(26): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808503 | |||||
| chr16:56808513
|
T | C | 4 | a0001c0001t0001g0114a0001c0001t0001g0120a0001c0001t0001g0121others(1): Show | 4 | HG02717.hp1 HG03195.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.489+2881T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808513 | ||||||
| chr16:56808514
|
G | A | 3 | a0001c0002t0010g0048a0001c0002t0010g0049a0001c0002t0010g0050 | 3 | HG01069.hp2 HG01167.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.489+2882G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808514 | ||||||
| chr16:56808524
|
AT | A | 5 | a0001c0002t0010g0048a0001c0002t0010g0049a0001c0002t0010g0050others(2): Show | 5 | HG01069.hp2 HG01167.hp1 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.489+2893delT | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808524 | ||||||
| chr16:56808525
|
T | A | 28 | a0001c0001t0004g0198a0001c0001t0004g0220a0001c0001t0004g0221others(25): Show | 28 | HG00408.hp2 HG00597.hp2 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.489+2893T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808525 | ||||||
| chr16:56808527
|
A | T | 27 | a0001c0001t0004g0198a0001c0001t0004g0220a0001c0001t0004g0221others(24): Show | 27 | HG00408.hp2 HG00597.hp2 HG00733.hp1 others(24): Show |
intron_variant | MODIFIER | c.489+2895A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808527 | ||||||
| chr16:56808537
|
T | C | 1 | a0001c0001t0002g0292 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.489+2905T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808537 | ||||||
| chr16:56808538
|
A | G | 107 | a0001c0001t0002g0284a0001c0001t0002g0292a0001c0001t0002g0295others(104): Show | 107 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.489+2906A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808538 | ||||||
| chr16:56808545
|
T | TATA | 6 | a0001c0001t0011g0007a0001c0002t0010g0048a0001c0002t0010g0049others(3): Show | 6 | HG01069.hp2 HG01167.hp1 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.489+2914_489+2915i others(5): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808545 | |||||
| chr16:56808552
|
A | ATAGTTAT others(192): Show |
3 | a0001c0002t0010g0048a0001c0002t0010g0049a0001c0002t0010g0050 | 3 | HG01069.hp2 HG01167.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.489+2922_489+2923i others(201): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808552 | |||||
| chr16:56808552
|
A | ATAGTTAT others(221): Show |
1 | a0001c0001t0011g0007 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.489+2922_489+2923i others(230): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808552 | |||||
| chr16:56808554
|
A | AGTTACGT others(50): Show |
1 | a0003c0024t0018g0010 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.489+2922_489+2923i others(59): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808554 | ||||||
| chr16:56808554
|
A | AGTTATGT others(50): Show |
1 | a0001c0009t0018g0019 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.489+2922_489+2923i others(59): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808554 | ||||||
| chr16:56808555
|
A | AAAATATA others(25): Show |
12 | a0001c0001t0001g0119a0001c0001t0001g0122a0001c0001t0003g0362others(9): Show | 12 | HG00438.hp2 HG01884.hp2 HG01981.hp2 others(9): Show |
intron_variant | MODIFIER | c.489+2984_489+3015d others(34): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808555 | |||||
| chr16:56808555
|
A | AAAATATA others(57): Show |
1 | a0001c0007t0012g0345 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.489+2952_489+3015d others(66): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808555 | |||||
| chr16:56808555
|
A | AAAATATA others(53): Show |
3 | a0001c0007t0012g0065a0001c0007t0012g0346a0001c0007t0012g0347 | 3 | HG01891.hp1 HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.489+2964_489+2965i others(62): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808555 | |||||
| chr16:56808555
|
A | T | 3 | a0001c0009t0018g0018a0001c0009t0018g0019a0003c0024t0018g0010 | 3 | HG02451.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.489+2923A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808555 | ||||||
| chr16:56808556
|
A | C | 4 | a0001c0001t0011g0007a0001c0002t0010g0048a0001c0002t0010g0049others(1): Show | 4 | HG01069.hp2 HG01167.hp1 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.489+2924A>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808556 | ||||||
| chr16:56808557
|
A | T | 6 | a0001c0001t0011g0007a0001c0002t0010g0048a0001c0002t0010g0049others(3): Show | 6 | HG01069.hp2 HG01167.hp1 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.489+2925A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808557 | ||||||
| chr16:56808558
|
A | C | 1 | a0001c0009t0018g0018 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.489+2926A>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808558 | ||||||
| chr16:56808565
|
A | G | 2 | a0001c0009t0018g0019a0003c0024t0018g0010 | 2 | HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.489+2933A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808565 | ||||||
| chr16:56808565
|
A | T | 1 | a0001c0009t0018g0018 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.489+2933A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808565 | ||||||
| chr16:56808566
|
A | T | 2 | a0001c0009t0018g0019a0003c0024t0018g0010 | 2 | HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.489+2934A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808566 | ||||||
| chr16:56808569
|
C | G | 1 | a0001c0009t0018g0018 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.489+2937C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808569 | ||||||
| chr16:56808569
|
C | T | 6 | a0001c0001t0011g0007a0001c0002t0010g0048a0001c0002t0010g0049others(3): Show | 6 | HG01069.hp2 HG01167.hp1 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.489+2937C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808569 | ||||||
| chr16:56808570
|
A | T | 1 | a0001c0009t0018g0018 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.489+2938A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808570 | ||||||
| chr16:56808571
|
T | G | 4 | a0001c0001t0011g0007a0001c0002t0010g0048a0001c0002t0010g0049others(1): Show | 4 | HG01069.hp2 HG01167.hp1 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.489+2939T>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808571 | ||||||
| chr16:56808572
|
T | A | 3 | a0001c0009t0018g0018a0001c0009t0018g0019a0003c0024t0018g0010 | 3 | HG02451.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.489+2940T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808572 | ||||||
| chr16:56808573
|
T | A | 2 | a0001c0009t0018g0019a0003c0024t0018g0010 | 2 | HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.489+2941T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808573 | ||||||
| chr16:56808574
|
A | ATATAAC | 4 | a0001c0001t0011g0007a0001c0002t0010g0048a0001c0002t0010g0049others(1): Show | 4 | HG01069.hp2 HG01167.hp1 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.489+2947_489+2948i others(8): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808574 | |||||
| chr16:56808574
|
A | C | 2 | a0001c0009t0018g0019a0003c0024t0018g0010 | 2 | HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.489+2942A>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808574 | ||||||
| chr16:56808584
|
T | A | 7 | a0001c0001t0011g0007a0001c0002t0010g0048a0001c0002t0010g0049others(4): Show | 7 | HG01069.hp2 HG01167.hp1 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.489+2952T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808584 | ||||||
| chr16:56808584
|
T | TTATAAAT others(25): Show |
1 | a0006c0021t0001g0011 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.489+2983_489+2984i others(34): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808584 | |||||
| chr16:56808587
|
T | A | 7 | a0001c0001t0011g0007a0001c0002t0010g0048a0001c0002t0010g0049others(4): Show | 7 | HG01069.hp2 HG01167.hp1 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.489+2955T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808587 | ||||||
| chr16:56808590
|
A | ATATATAA others(39): Show |
5 | a0001c0006t0009g0249a0001c0006t0009g0250a0001c0006t0009g0251others(2): Show | 5 | HG02109.hp2 HG02615.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.489+2969_489+3014d others(48): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808590 | |||||
| chr16:56808623
|
T | A | 4 | a0001c0002t0001g0076a0001c0002t0001g0081a0001c0002t0001g0167others(1): Show | 4 | HG02071.hp2 HG02080.hp1 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.489+2991T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808623 | ||||||
| chr16:56808631
|
T | TACATTTA others(15): Show |
6 | a0001c0001t0001g0316a0001c0001t0001g0320a0001c0001t0001g0321others(3): Show | 6 | HG00609.hp1 NA18946.hp1 NA18953.hp2 others(3): Show |
intron_variant | MODIFIER | c.489+3001_489+3022d others(24): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808631 | |||||
| chr16:56808650
|
AAAAATAC others(18): Show |
A | 2 | a0001c0004t0024g0039a0001c0004t0024g0042 | 2 | HG00639.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.489+3048_489+3072d others(27): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808650 | |||||
| chr16:56808700
|
TA | T | 171 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0045others(168): Show | 173 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.489+3073delA | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808700 | |||||
| chr16:56808724
|
TAAATACA others(6): Show |
T | 1 | a0007c0020t0001g0063 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.489+3108_489+3120d others(15): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808724 | |||||
| chr16:56808736
|
T | TA | 362 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0045others(359): Show | 364 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(361): Show |
intron_variant | MODIFIER | c.489+3108dupA | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808736 | |||||
| chr16:56808847
|
C | CAT | 3 | a0001c0001t0004g0230a0001c0001t0013g0013a0001c0001t0013g0014 | 3 | HG03041.hp1 HG03225.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.489+3224_489+3225d others(4): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56808847 | |||||
| chr16:56808871
|
A | G | 3 | a0001c0007t0012g0065a0001c0007t0012g0346a0001c0007t0012g0347 | 3 | HG01891.hp1 HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.489+3239A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808871 | ||||||
| chr16:56808997
|
G | T | 1 | a0001c0001t0001g0161 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.489+3365G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808997 | ||||||
| chr16:56808999
|
G | T | 1 | a0001c0001t0001g0161 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.489+3367G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56808999 | ||||||
| chr16:56809002
|
T | A | 1 | a0001c0001t0001g0161 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.489+3370T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56809002 | ||||||
| chr16:56809003
|
G | T | 1 | a0001c0001t0001g0161 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.489+3371G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56809003 | ||||||
| chr16:56809004
|
T | A | 1 | a0001c0001t0001g0161 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.489+3372T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56809004 | ||||||
| chr16:56809005
|
A | G | 1 | a0001c0001t0001g0161 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.489+3373A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56809005 | ||||||
| chr16:56809006
|
T | C | 3 | a0001c0006t0009g0250a0001c0006t0009g0251a0001c0006t0009g0253 | 3 | HG02615.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.489+3374T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56809006 | ||||||
| chr16:56809008
|
T | A | 1 | a0001c0001t0001g0161 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.489+3376T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56809008 | ||||||
| chr16:56809010
|
C | G | 1 | a0001c0001t0001g0161 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.489+3378C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56809010 | ||||||
| chr16:56809049
|
A | C | 271 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0045others(268): Show | 273 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(270): Show |
intron_variant | MODIFIER | c.489+3417A>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56809049 | ||||||
| chr16:56809086
|
G | A | 23 | a0001c0001t0006g0199a0001c0001t0006g0200a0001c0001t0006g0201others(20): Show | 23 | HG01070.hp2 HG01168.hp2 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.489+3454G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56809086 | ||||||
| chr16:56809107
|
A | G | 3 | a0001c0001t0003g0368a0001c0001t0003g0369a0001c0001t0003g0370 | 3 | NA18942.hp1 NA18952.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.489+3475A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56809107 | ||||||
| chr16:56809351
|
A | G | 5 | a0001c0006t0009g0249a0001c0006t0009g0250a0001c0006t0009g0251others(2): Show | 5 | HG02109.hp2 HG02615.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.489+3719A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56809351 | ||||||
| chr16:56809414
|
T | TA | 364 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0045others(361): Show | 366 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(363): Show |
intron_variant | MODIFIER | c.489+3786dupA | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56809414 | |||||
| chr16:56809531
|
G | A | 62 | a0001c0001t0002g0284a0001c0001t0002g0292a0001c0001t0002g0295others(59): Show | 62 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.489+3899G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56809531 | ||||||
| chr16:56809613
|
G | C | 3 | a0001c0009t0018g0018a0001c0009t0018g0019a0003c0024t0018g0010 | 3 | HG02451.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.489+3981G>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56809613 | ||||||
| chr16:56809651
|
AC | A | 3 | a0001c0007t0012g0065a0001c0007t0012g0346a0001c0007t0012g0347 | 3 | HG01891.hp1 HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.489+4020delC | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56809651 | ||||||
| chr16:56810111
|
C | T | 4 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(1): Show | 4 | NA18939.hp2 NA18964.hp2 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.489+4479C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56810111 | ||||||
| chr16:56810189
|
G | C | 1 | a0001c0001t0001g0120 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.489+4557G>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56810189 | ||||||
| chr16:56810252
|
C | T | 364 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0045others(361): Show | 366 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(363): Show |
intron_variant | MODIFIER | c.489+4620C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56810252 | ||||||
| chr16:56810331
|
G | A | 2 | a0001c0001t0001g0002a0001c0001t0001g0318 | 3 | HG01358.hp2 HG02698.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.489+4699G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56810331 | ||||||
| chr16:56810457
|
C | T | 2 | a0001c0005t0007g0188a0001c0005t0007g0197 | 2 | HG02717.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.489+4825C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56810457 | ||||||
| chr16:56810547
|
G | A | 4 | a0001c0007t0012g0065a0001c0007t0012g0345a0001c0007t0012g0346others(1): Show | 4 | HG01891.hp1 HG02145.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.489+4915G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56810547 | ||||||
| chr16:56810659
|
T | A | 5 | a0001c0006t0009g0249a0001c0006t0009g0250a0001c0006t0009g0251others(2): Show | 5 | HG02109.hp2 HG02615.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.489+5027T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56810659 | ||||||
| chr16:56810727
|
TACCAGCG others(33): Show |
T | 41 | a0001c0001t0003g0348a0001c0001t0003g0349a0001c0001t0003g0350others(38): Show | 41 | HG00323.hp1 HG00639.hp1 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.489+5140_489+5179d others(42): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56810727 | |||||
| chr16:56810762
|
C | A | 1 | a0001c0001t0029g0245 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.489+5130C>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56810762 | ||||||
| chr16:56811048
|
T | C | 1 | a0001c0001t0034g0196 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.489+5416T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56811048 | ||||||
| chr16:56811207
|
A | C | 2 | a0001c0002t0001g0059a0001c0002t0001g0062 | 2 | NA18747.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.489+5575A>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56811207 | ||||||
| chr16:56811263
|
C | A | 4 | a0001c0007t0012g0065a0001c0007t0012g0345a0001c0007t0012g0346others(1): Show | 4 | HG01891.hp1 HG02145.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.489+5631C>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56811263 | ||||||
| chr16:56811388
|
A | T | 13 | a0001c0001t0001g0052a0001c0001t0001g0130a0001c0001t0001g0131others(10): Show | 13 | HG00099.hp1 HG00735.hp1 HG01515.hp2 others(10): Show |
intron_variant | MODIFIER | c.489+5756A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56811388 | ||||||
| chr16:56811478
|
A | C | 2 | a0001c0001t0006g0210a0001c0001t0006g0212 | 2 | HG01070.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.489+5846A>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56811478 | ||||||
| chr16:56811517
|
G | GT | 46 | a0001c0001t0001g0002a0001c0001t0001g0302a0001c0001t0001g0304others(43): Show | 47 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.489+5896dupT | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56811517 | |||||
| chr16:56811562
|
G | C | 1 | a0001c0004t0005g0030 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.489+5930G>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56811562 | ||||||
| chr16:56812118
|
C | T | 2 | a0001c0002t0001g0001a0001c0002t0001g0071 | 3 | HG01361.hp1 HG01517.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.489+6486C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56812118 | ||||||
| chr16:56812308
|
A | G | 3 | a0001c0001t0014g0217a0001c0001t0014g0218a0001c0001t0014g0219 | 3 | HG01884.hp2 HG03453.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.490-6356A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56812308 | ||||||
| chr16:56812500
|
C | T | 1 | a0001c0007t0012g0345 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.490-6164C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56812500 | ||||||
| chr16:56812595
|
G | A | 1 | a0001c0002t0001g0106 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.490-6069G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56812595 | ||||||
| chr16:56812624
|
T | C | 45 | a0001c0001t0003g0348a0001c0001t0003g0349a0001c0001t0003g0350others(42): Show | 45 | HG00323.hp1 HG00639.hp1 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.490-6040T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56812624 | ||||||
| chr16:56812644
|
C | G | 1 | a0001c0017t0001g0158 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.490-6020C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56812644 | ||||||
| chr16:56812852
|
C | T | 12 | a0001c0002t0001g0001a0001c0002t0001g0051a0001c0002t0001g0070others(9): Show | 13 | HG00323.hp2 HG00642.hp1 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.490-5812C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56812852 | ||||||
| chr16:56812892
|
C | T | 52 | a0001c0001t0002g0284a0001c0001t0002g0292a0001c0001t0002g0295others(49): Show | 52 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.490-5772C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56812892 | ||||||
| chr16:56813003
|
A | G | 5 | a0001c0002t0001g0094a0001c0002t0001g0098a0001c0002t0001g0099others(2): Show | 5 | HG02886.hp1 HG02970.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.490-5661A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56813003 | ||||||
| chr16:56813358
|
G | A | 41 | a0001c0001t0003g0348a0001c0001t0003g0349a0001c0001t0003g0350others(38): Show | 41 | HG00323.hp1 HG00639.hp1 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.490-5306G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56813358 | ||||||
| chr16:56813472
|
G | A | 30 | a0001c0004t0005g0020a0001c0004t0005g0021a0001c0004t0005g0022others(27): Show | 30 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.490-5192G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56813472 | ||||||
| chr16:56813655
|
G | C | 1 | a0006c0021t0001g0011 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.490-5009G>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56813655 | ||||||
| chr16:56813676
|
C | T | 1 | a0001c0002t0001g0057 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.490-4988C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56813676 | ||||||
| chr16:56813838
|
C | T | 2 | a0001c0001t0006g0201a0001c0001t0006g0243 | 2 | HG02559.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.490-4826C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56813838 | ||||||
| chr16:56814017
|
C | A | 364 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0045others(361): Show | 366 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(363): Show |
intron_variant | MODIFIER | c.490-4647C>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56814017 | ||||||
| chr16:56814121
|
A | T | 2 | a0001c0011t0001g0089a0001c0011t0001g0090 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.490-4543A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56814121 | ||||||
| chr16:56814157
|
G | A | 41 | a0001c0001t0001g0002a0001c0001t0001g0302a0001c0001t0001g0303others(38): Show | 42 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.490-4507G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56814157 | ||||||
| chr16:56814330
|
C | T | 3 | a0001c0002t0010g0048a0001c0002t0010g0049a0001c0002t0010g0050 | 3 | HG01069.hp2 HG01167.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.490-4334C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56814330 | ||||||
| chr16:56814332
|
C | T | 1 | a0001c0001t0007g0194 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.490-4332C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56814332 | ||||||
| chr16:56814443
|
G | A | 1 | a0001c0001t0001g0119 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.490-4221G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56814443 | ||||||
| chr16:56814613
|
C | T | 2 | a0001c0001t0006g0204a0001c0001t0006g0205 | 2 | HG02083.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.490-4051C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56814613 | ||||||
| chr16:56814665
|
C | T | 1 | a0001c0003t0002g0277 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.490-3999C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56814665 | ||||||
| chr16:56814731
|
G | A | 1 | a0001c0004t0005g0035 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.490-3933G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56814731 | ||||||
| chr16:56814959
|
G | A | 56 | a0001c0001t0002g0284a0001c0001t0002g0292a0001c0001t0002g0295others(53): Show | 56 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.490-3705G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56814959 | ||||||
| chr16:56815074
|
A | G | 1 | a0001c0001t0001g0304 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.490-3590A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56815074 | ||||||
| chr16:56815181
|
TACA | T | 24 | a0001c0004t0005g0020a0001c0004t0005g0021a0001c0004t0005g0022others(21): Show | 24 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(21): Show |
intron_variant | MODIFIER | c.490-3477_490-3475d others(5): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56815181 | |||||
| chr16:56815202
|
A | G | 27 | a0001c0004t0005g0020a0001c0004t0005g0021a0001c0004t0005g0022others(24): Show | 27 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(24): Show |
intron_variant | MODIFIER | c.490-3462A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56815202 | ||||||
| chr16:56815206
|
TG | T | 3 | a0001c0001t0014g0217a0001c0001t0014g0218a0001c0001t0014g0219 | 3 | HG01884.hp2 HG03453.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.490-3457delG | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56815206 | ||||||
| chr16:56815247
|
C | G | 6 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(3): Show | 6 | HG01884.hp1 HG02630.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.490-3417C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56815247 | ||||||
| chr16:56815517
|
T | C | 3 | a0001c0001t0014g0217a0001c0001t0014g0218a0001c0001t0014g0219 | 3 | HG01884.hp2 HG03453.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.490-3147T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56815517 | ||||||
| chr16:56815548
|
CTGT | C | 6 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(3): Show | 6 | HG01884.hp1 HG02630.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.490-3109_490-3107d others(5): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56815548 | |||||
| chr16:56815584
|
G | A | 175 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0045others(172): Show | 177 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.490-3080G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56815584 | ||||||
| chr16:56815678
|
A | C | 2 | a0001c0004t0015g0015a0001c0004t0015g0017 | 2 | HG02818.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.490-2986A>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56815678 | ||||||
| chr16:56815743
|
A | G | 1 | a0001c0007t0012g0345 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.490-2921A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56815743 | ||||||
| chr16:56815865
|
A | ACTG | 95 | a0001c0001t0002g0284a0001c0001t0002g0292a0001c0001t0002g0295others(92): Show | 95 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(92): Show |
intron_variant | MODIFIER | c.490-2768_490-2766d others(5): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56815865 | |||||
| chr16:56815865
|
A | ACTGCTG | 139 | a0001c0001t0001g0002a0001c0001t0001g0045a0001c0001t0001g0046others(136): Show | 140 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.490-2771_490-2766d others(8): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56815865 | |||||
| chr16:56815865
|
A | ACTGCTGC others(2): Show |
27 | a0001c0001t0001g0003a0001c0001t0001g0116a0001c0001t0001g0138others(24): Show | 27 | HG00621.hp1 HG01346.hp2 HG02071.hp1 others(24): Show |
intron_variant | MODIFIER | c.490-2774_490-2766d others(11): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56815865 | |||||
| chr16:56815865
|
A | ACTGCTGC others(11): Show |
2 | a0001c0001t0001g0337a0001c0001t0001g0338 | 2 | HG02155.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.490-2788_490-2787i others(20): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56815865 | |||||
| chr16:56815865
|
A | ACTGCTGC others(5): Show |
3 | a0001c0001t0001g0149a0001c0009t0018g0018a0001c0009t0018g0019 | 3 | HG03209.hp1 HG03516.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.490-2777_490-2766d others(14): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56815865 | |||||
| chr16:56815865
|
A | ACTGCTGC others(8): Show |
6 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(3): Show | 6 | HG01884.hp1 HG02630.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.490-2780_490-2766d others(17): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56815865 | |||||
| chr16:56815865
|
A | ACTGCTGC others(11): Show |
12 | a0001c0004t0005g0020a0001c0004t0005g0021a0001c0004t0005g0037others(9): Show | 12 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(9): Show |
intron_variant | MODIFIER | c.490-2783_490-2766d others(20): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56815865 | |||||
| chr16:56815865
|
A | ACTGCTGC others(14): Show |
2 | a0001c0004t0005g0036a0003c0024t0018g0010 | 2 | HG02451.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.490-2786_490-2766d others(23): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56815865 | |||||
| chr16:56815865
|
A | ACTGCTGC others(17): Show |
1 | a0001c0004t0005g0026 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.490-2789_490-2766d others(26): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56815865 | |||||
| chr16:56815865
|
A | ACTGCTGC others(29): Show |
1 | a0001c0004t0005g0034 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.490-2766_490-2765i others(38): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56815865 | |||||
| chr16:56815865
|
A | ACTGCTGC others(32): Show |
6 | a0001c0004t0005g0023a0001c0004t0005g0025a0001c0004t0005g0027others(3): Show | 6 | HG01261.hp1 HG01993.hp1 HG02293.hp2 others(3): Show |
intron_variant | MODIFIER | c.490-2766_490-2765i others(41): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56815865 | |||||
| chr16:56815865
|
A | ACTGCTGC others(35): Show |
3 | a0001c0004t0005g0022a0001c0004t0005g0030a0001c0004t0005g0033 | 3 | HG01099.hp2 HG01346.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.490-2766_490-2765i others(44): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56815865 | |||||
| chr16:56815865
|
ACTGCTG | A | 3 | a0001c0001t0013g0012a0001c0001t0013g0013a0001c0001t0013g0014 | 3 | HG03041.hp1 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.490-2771_490-2766d others(8): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56815865 | |||||
| chr16:56815865
|
ACTGCTGC others(5): Show |
A | 2 | a0001c0001t0036g0148a0001c0003t0002g0290 | 2 | HG02300.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.490-2777_490-2766d others(14): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56815865 | |||||
| chr16:56815865
|
ACTGCTGC others(8): Show |
A | 10 | a0001c0003t0002g0269a0001c0006t0009g0249a0001c0006t0009g0250others(7): Show | 10 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.490-2780_490-2766d others(17): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56815865 | |||||
| chr16:56815881
|
C | CTGCTGCT others(17): Show |
1 | a0001c0002t0041g0113 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.490-2766_490-2765i others(26): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56815881 | |||||
| chr16:56815881
|
C | CTGCTGCT others(14): Show |
11 | a0001c0001t0003g0355a0001c0001t0003g0356a0001c0001t0003g0357others(8): Show | 11 | HG00323.hp1 HG00639.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.490-2766_490-2765i others(23): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56815881 | |||||
| chr16:56815881
|
CTGCTGCT others(11): Show |
C | 6 | a0001c0002t0001g0001a0001c0002t0001g0051a0001c0002t0001g0070others(3): Show | 7 | HG00323.hp2 HG00642.hp1 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.490-2751_490-2734d others(20): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56815881 | |||||
| chr16:56815896
|
C | CTGG | 4 | a0001c0001t0006g0199a0001c0001t0006g0200a0001c0001t0006g0201others(1): Show | 4 | HG02559.hp1 HG02976.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.490-2765_490-2763d others(5): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56815896 | |||||
| chr16:56815899
|
G | C | 4 | a0001c0004t0005g0029a0001c0009t0018g0018a0001c0009t0018g0019others(1): Show | 4 | HG02451.hp2 HG03209.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.490-2765G>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56815899 | ||||||
| chr16:56815899
|
G | GTGC | 11 | a0001c0001t0003g0355a0001c0001t0003g0356a0001c0001t0003g0357others(8): Show | 11 | HG00323.hp1 HG00639.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.490-2750_490-2748d others(5): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56815899 | |||||
| chr16:56815899
|
G | GTGCTGCT others(14): Show |
34 | a0001c0001t0003g0348a0001c0001t0003g0349a0001c0001t0003g0350others(31): Show | 34 | HG00642.hp2 HG01070.hp1 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.490-2754_490-2734d others(23): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56815899 | |||||
| chr16:56815899
|
GTGC | G | 26 | a0001c0004t0005g0020a0001c0004t0005g0021a0001c0004t0005g0022others(23): Show | 26 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(23): Show |
intron_variant | MODIFIER | c.490-2750_490-2748d others(5): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56815899 | |||||
| chr16:56815902
|
C | CTGCTGCT others(32): Show |
1 | a0001c0004t0005g0029 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.490-2748_490-2747i others(41): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 56815902 | |||||
| chr16:56815922
|
G | A | 1 | a0001c0001t0031g0209 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.490-2742G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56815922 | ||||||
| chr16:56815947
|
C | T | 27 | a0001c0004t0005g0020a0001c0004t0005g0021a0001c0004t0005g0022others(24): Show | 27 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(24): Show |
intron_variant | MODIFIER | c.490-2717C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56815947 | ||||||
| chr16:56815968
|
A | C | 1 | a0001c0001t0011g0005 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.490-2696A>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56815968 | ||||||
| chr16:56815973
|
T | A | 1 | a0001c0001t0029g0245 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.490-2691T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56815973 | ||||||
| chr16:56816087
|
T | C | 2 | a0001c0010t0022g0260a0001c0010t0033g0261 | 2 | HG03139.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.490-2577T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56816087 | ||||||
| chr16:56816448
|
A | T | 2 | a0001c0011t0001g0089a0001c0011t0001g0090 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.490-2216A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56816448 | ||||||
| chr16:56816548
|
T | C | 5 | a0001c0006t0009g0249a0001c0006t0009g0250a0001c0006t0009g0251others(2): Show | 5 | HG02109.hp2 HG02615.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.490-2116T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56816548 | ||||||
| chr16:56816611
|
A | G | 58 | a0001c0001t0001g0003a0001c0001t0001g0045a0001c0001t0001g0046others(55): Show | 58 | HG00099.hp1 HG00621.hp1 HG00735.hp1 others(55): Show |
intron_variant | MODIFIER | c.490-2053A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56816611 | ||||||
| chr16:56816690
|
A | G | 173 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0045others(170): Show | 175 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.490-1974A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56816690 | ||||||
| chr16:56816939
|
G | A | 1 | a0001c0004t0005g0037 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.490-1725G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56816939 | ||||||
| chr16:56817000
|
A | G | 1 | a0001c0001t0001g0126 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.490-1664A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56817000 | ||||||
| chr16:56817075
|
G | A | 1 | a0001c0001t0001g0161 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.490-1589G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56817075 | ||||||
| chr16:56817175
|
A | C | 2 | a0001c0010t0022g0260a0001c0010t0033g0261 | 2 | HG03139.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.490-1489A>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56817175 | ||||||
| chr16:56817180
|
A | T | 1 | a0001c0003t0002g0264 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.490-1484A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56817180 | ||||||
| chr16:56817352
|
C | T | 1 | a0001c0002t0001g0110 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.490-1312C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56817352 | ||||||
| chr16:56817504
|
T | C | 14 | a0001c0002t0001g0001a0001c0002t0001g0051a0001c0002t0001g0070others(11): Show | 15 | HG00323.hp2 HG00642.hp1 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.490-1160T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56817504 | ||||||
| chr16:56817534
|
C | T | 1 | a0001c0007t0012g0345 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.490-1130C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56817534 | ||||||
| chr16:56817655
|
CTG | C | 24 | a0001c0004t0005g0020a0001c0004t0005g0021a0001c0004t0005g0022others(21): Show | 24 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(21): Show |
intron_variant | MODIFIER | c.490-1008_490-1007d others(4): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56817655 | ||||||
| chr16:56817723
|
G | A | 5 | a0001c0006t0009g0249a0001c0006t0009g0250a0001c0006t0009g0251others(2): Show | 5 | HG02109.hp2 HG02615.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.490-941G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56817723 | ||||||
| chr16:56817893
|
T | A | 4 | a0001c0001t0003g0349a0001c0001t0003g0350a0001c0001t0003g0355others(1): Show | 4 | HG01070.hp1 HG01071.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.490-771T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56817893 | ||||||
| chr16:56817921
|
C | T | 1 | a0001c0002t0001g0101 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.490-743C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56817921 | ||||||
| chr16:56818399
|
A | C | 334 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0045others(331): Show | 336 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(333): Show |
intron_variant | MODIFIER | c.490-265A>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56818399 | ||||||
| chr16:56818427
|
G | T | 1 | a0001c0003t0002g0282 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.490-237G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56818427 | ||||||
| chr16:56818430
|
G | A | 1 | a0004c0023t0026g0372 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.490-234G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56818430 | ||||||
| chr16:56818456
|
A | G | 3 | a0001c0001t0013g0012a0001c0001t0013g0013a0001c0001t0013g0014 | 3 | HG03041.hp1 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.490-208A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56818456 | ||||||
| chr16:56818477
|
T | C | 93 | a0001c0001t0003g0348a0001c0001t0003g0349a0001c0001t0003g0350others(90): Show | 93 | HG00323.hp1 HG00408.hp2 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.490-187T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 5/21 | chr16 | 56818477 | ||||||
| chr16:56818853
|
AT | A | 3 | a0001c0005t0007g0183a0001c0005t0007g0184a0001c0005t0007g0185 | 3 | HG02257.hp2 HG02809.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.564+118delT | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr16 | 56818853 | |||||
| chr16:56818910
|
G | T | 170 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0045others(167): Show | 172 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.564+172G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 6/21 | chr16 | 56818910 | ||||||
| chr16:56819530
|
G | T | 1 | a0001c0001t0034g0196 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.564+792G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 6/21 | chr16 | 56819530 | ||||||
| chr16:56819572
|
A | G | 1 | a0001c0003t0002g0291 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.564+834A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 6/21 | chr16 | 56819572 | ||||||
| chr16:56819644
|
A | G | 2 | a0001c0002t0001g0001a0001c0002t0001g0071 | 3 | HG01361.hp1 HG01517.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.564+906A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 6/21 | chr16 | 56819644 | ||||||
| chr16:56819845
|
C | T | 1 | a0001c0002t0001g0344 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.564+1107C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 6/21 | chr16 | 56819845 | ||||||
| chr16:56820090
|
C | A | 3 | a0001c0001t0013g0012a0001c0001t0013g0013a0001c0001t0013g0014 | 3 | HG03041.hp1 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.564+1352C>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 6/21 | chr16 | 56820090 | ||||||
| chr16:56820093
|
T | G | 1 | a0001c0005t0007g0184 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.564+1355T>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 6/21 | chr16 | 56820093 | ||||||
| chr16:56820184
|
C | T | 1 | a0001c0004t0005g0037 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.565-1320C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 6/21 | chr16 | 56820184 | ||||||
| chr16:56820240
|
A | C | 1 | a0001c0014t0001g0137 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.565-1264A>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 6/21 | chr16 | 56820240 | ||||||
| chr16:56820372
|
C | T | 93 | a0001c0001t0003g0348a0001c0001t0003g0349a0001c0001t0003g0350others(90): Show | 93 | HG00323.hp1 HG00408.hp2 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.565-1132C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 6/21 | chr16 | 56820372 | ||||||
| chr16:56820508
|
G | A | 2 | a0001c0003t0002g0256a0001c0003t0002g0281 | 2 | HG01175.hp2 NA18949.hp2 |
intron_variant | MODIFIER | c.565-996G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 6/21 | chr16 | 56820508 | ||||||
| chr16:56820615
|
C | T | 3 | a0001c0007t0012g0065a0001c0007t0012g0346a0001c0007t0012g0347 | 3 | HG01891.hp1 HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.565-889C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 6/21 | chr16 | 56820615 | ||||||
| chr16:56820837
|
A | G | 3 | a0001c0009t0018g0018a0001c0009t0018g0019a0003c0024t0018g0010 | 3 | HG02451.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.565-667A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 6/21 | chr16 | 56820837 | ||||||
| chr16:56820953
|
C | T | 4 | a0001c0001t0001g0322a0001c0001t0001g0323a0001c0001t0001g0324others(1): Show | 4 | HG00735.hp2 HG01081.hp1 HG01123.hp2 others(1): Show |
intron_variant | MODIFIER | c.565-551C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 6/21 | chr16 | 56820953 | ||||||
| chr16:56821112
|
C | T | 2 | a0001c0005t0007g0183a0001c0005t0007g0184 | 2 | HG02257.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.565-392C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 6/21 | chr16 | 56821112 | ||||||
| chr16:56821280
|
C | T | 52 | a0001c0001t0002g0284a0001c0001t0002g0292a0001c0001t0002g0295others(49): Show | 52 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.565-224C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 6/21 | chr16 | 56821280 | ||||||
| chr16:56821399
|
A | G | 1 | a0001c0003t0002g0278 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.565-105A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 6/21 | chr16 | 56821399 | ||||||
| chr16:56821637
|
TC | T | 57 | a0001c0001t0002g0284a0001c0001t0002g0292a0001c0001t0002g0295others(54): Show | 57 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.654+46delC | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr16 | 56821637 | |||||
| chr16:56822098
|
C | CA | 18 | a0001c0001t0001g0161a0001c0001t0001g0343a0001c0001t0003g0365others(15): Show | 18 | HG00609.hp2 HG00639.hp1 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.654+523dupA | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr16 | 56822098 | |||||
| chr16:56822116
|
A | G | 5 | a0001c0003t0002g0273a0001c0007t0012g0065a0001c0007t0012g0346others(2): Show | 5 | HG01891.hp1 HG02615.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.654+523A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 7/21 | chr16 | 56822116 | ||||||
| chr16:56822442
|
G | A | 1 | a0001c0002t0001g0066 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.654+849G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 7/21 | chr16 | 56822442 | ||||||
| chr16:56822446
|
C | A | 364 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0045others(361): Show | 366 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(363): Show |
intron_variant | MODIFIER | c.654+853C>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 7/21 | chr16 | 56822446 | ||||||
| chr16:56822564
|
C | CT | 159 | a0001c0001t0001g0335a0001c0001t0002g0284a0001c0001t0002g0292others(156): Show | 159 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.654+984dupT | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr16 | 56822564 | |||||
| chr16:56822564
|
C | CTT | 170 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0045others(167): Show | 172 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.654+983_654+984dup others(2): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr16 | 56822564 | |||||
| chr16:56822564
|
CT | C | 24 | a0001c0004t0005g0020a0001c0004t0005g0021a0001c0004t0005g0022others(21): Show | 24 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(21): Show |
intron_variant | MODIFIER | c.654+984delT | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr16 | 56822564 | |||||
| chr16:56822660
|
A | G | 72 | a0001c0002t0001g0001a0001c0002t0001g0044a0001c0002t0001g0051others(69): Show | 73 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.655-1047A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 7/21 | chr16 | 56822660 | ||||||
| chr16:56822933
|
C | T | 1 | a0001c0001t0007g0340 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.655-774C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 7/21 | chr16 | 56822933 | ||||||
| chr16:56822936
|
G | T | 27 | a0001c0004t0005g0020a0001c0004t0005g0021a0001c0004t0005g0022others(24): Show | 27 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(24): Show |
intron_variant | MODIFIER | c.655-771G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 7/21 | chr16 | 56822936 | ||||||
| chr16:56822998
|
C | T | 1 | a0001c0004t0005g0033 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.655-709C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 7/21 | chr16 | 56822998 | ||||||
| chr16:56823043
|
G | A | 52 | a0001c0001t0002g0284a0001c0001t0002g0292a0001c0001t0002g0295others(49): Show | 52 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.655-664G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 7/21 | chr16 | 56823043 | ||||||
| chr16:56823059
|
C | A | 367 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0045others(364): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.655-648C>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 7/21 | chr16 | 56823059 | ||||||
| chr16:56823059
|
C | G | 6 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(3): Show | 6 | HG01884.hp1 HG02630.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.655-648C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 7/21 | chr16 | 56823059 | ||||||
| chr16:56823155
|
T | C | 1 | a0001c0001t0004g0234 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.655-552T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 7/21 | chr16 | 56823155 | ||||||
| chr16:56823318
|
A | G | 2 | a0001c0001t0001g0002a0001c0001t0001g0318 | 3 | HG01358.hp2 HG02698.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.655-389A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 7/21 | chr16 | 56823318 | ||||||
| chr16:56823319
|
T | C | 27 | a0001c0004t0005g0020a0001c0004t0005g0021a0001c0004t0005g0022others(24): Show | 27 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(24): Show |
intron_variant | MODIFIER | c.655-388T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 7/21 | chr16 | 56823319 | ||||||
| chr16:56824042
|
G | A | 1 | a0001c0001t0034g0196 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.794+196G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56824042 | ||||||
| chr16:56824098
|
C | G | 2 | a0001c0001t0003g0354a0001c0001t0003g0374 | 2 | NA19062.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.794+252C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56824098 | ||||||
| chr16:56824257
|
G | A | 1 | a0001c0003t0002g0277 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.794+411G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56824257 | ||||||
| chr16:56824298
|
CA | C | 6 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(3): Show | 6 | HG01884.hp1 HG02630.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.794+453delA | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56824298 | ||||||
| chr16:56824436
|
G | A | 1 | a0001c0001t0003g0356 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.794+590G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56824436 | ||||||
| chr16:56824782
|
TGA | T | 39 | a0001c0001t0001g0002a0001c0001t0001g0302a0001c0001t0001g0303others(36): Show | 40 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.794+940_794+941del others(2): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr16 | 56824782 | |||||
| chr16:56825205
|
C | CT | 40 | a0001c0001t0003g0364a0001c0001t0004g0234a0001c0001t0004g0237others(37): Show | 40 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(37): Show |
intron_variant | MODIFIER | c.794+1382dupT | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr16 | 56825205 | |||||
| chr16:56825205
|
CT | C | 207 | a0001c0001t0001g0002a0001c0001t0001g0045a0001c0001t0001g0046others(204): Show | 209 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.794+1382delT | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr16 | 56825205 | |||||
| chr16:56825205
|
CTT | C | 7 | a0001c0001t0001g0052a0001c0001t0001g0155a0001c0001t0001g0156others(4): Show | 7 | HG02109.hp1 HG02257.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.794+1381_794+1382d others(4): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr16 | 56825205 | |||||
| chr16:56825304
|
C | T | 68 | a0001c0001t0003g0348a0001c0001t0003g0349a0001c0001t0003g0350others(65): Show | 68 | HG00323.hp1 HG00639.hp1 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.794+1458C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56825304 | ||||||
| chr16:56825475
|
G | A | 13 | a0001c0003t0002g0255a0001c0003t0002g0266a0001c0003t0002g0268others(10): Show | 13 | HG00597.hp1 HG00673.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.794+1629G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56825475 | ||||||
| chr16:56825509
|
AT | A | 24 | a0001c0004t0005g0020a0001c0004t0005g0021a0001c0004t0005g0022others(21): Show | 24 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(21): Show |
intron_variant | MODIFIER | c.794+1671delT | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr16 | 56825509 | |||||
| chr16:56825598
|
T | C | 1 | a0001c0002t0001g0104 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.794+1752T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56825598 | ||||||
| chr16:56825683
|
G | A | 171 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0045others(168): Show | 173 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.794+1837G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56825683 | ||||||
| chr16:56825985
|
A | G | 1 | a0001c0001t0007g0195 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.794+2139A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56825985 | ||||||
| chr16:56826021
|
G | A | 1 | a0001c0002t0001g0106 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.794+2175G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56826021 | ||||||
| chr16:56826141
|
T | C | 1 | a0001c0002t0001g0110 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.794+2295T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56826141 | ||||||
| chr16:56826311
|
A | G | 27 | a0001c0004t0005g0020a0001c0004t0005g0021a0001c0004t0005g0022others(24): Show | 27 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(24): Show |
intron_variant | MODIFIER | c.794+2465A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56826311 | ||||||
| chr16:56826350
|
A | G | 5 | a0001c0006t0009g0249a0001c0006t0009g0250a0001c0006t0009g0251others(2): Show | 5 | HG02109.hp2 HG02615.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.794+2504A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56826350 | ||||||
| chr16:56826467
|
G | T | 1 | a0001c0001t0001g0138 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.795-2510G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56826467 | ||||||
| chr16:56826514
|
TA | T | 238 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0045others(235): Show | 240 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.795-2445delA | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr16 | 56826514 | |||||
| chr16:56826514
|
TAA | T | 24 | a0001c0001t0003g0350a0001c0001t0006g0199a0001c0001t0006g0200others(21): Show | 24 | HG01070.hp1 HG01070.hp2 HG01168.hp2 others(21): Show |
intron_variant | MODIFIER | c.795-2446_795-2445d others(4): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr16 | 56826514 | |||||
| chr16:56826827
|
C | T | 1 | a0001c0001t0003g0365 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.795-2150C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56826827 | ||||||
| chr16:56826882
|
C | T | 1 | a0001c0001t0029g0245 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.795-2095C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56826882 | ||||||
| chr16:56827039
|
C | T | 3 | a0001c0001t0014g0217a0001c0001t0014g0218a0001c0001t0014g0219 | 3 | HG01884.hp2 HG03453.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.795-1938C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56827039 | ||||||
| chr16:56827040
|
G | A | 1 | a0007c0020t0001g0063 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.795-1937G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56827040 | ||||||
| chr16:56827044
|
C | CAAAAA | 29 | a0001c0001t0001g0002a0001c0001t0001g0302a0001c0001t0001g0303others(26): Show | 30 | HG00140.hp2 HG00558.hp1 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.795-1912_795-1908d others(7): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr16 | 56827044 | |||||
| chr16:56827044
|
C | CAAAAAA | 16 | a0001c0001t0001g0055a0001c0001t0001g0304a0001c0001t0001g0306others(13): Show | 16 | HG00438.hp1 HG00735.hp2 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.795-1913_795-1908d others(8): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr16 | 56827044 | |||||
| chr16:56827044
|
C | CAAAAAAA | 34 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0052others(31): Show | 34 | HG00099.hp1 HG00735.hp1 HG01433.hp1 others(31): Show |
intron_variant | MODIFIER | c.795-1914_795-1908d others(9): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr16 | 56827044 | |||||
| chr16:56827044
|
C | CAAAAAAA others(1): Show |
20 | a0001c0001t0001g0056a0001c0001t0001g0120a0001c0001t0001g0126others(17): Show | 20 | HG01070.hp2 HG01515.hp1 HG02071.hp1 others(17): Show |
intron_variant | MODIFIER | c.795-1915_795-1908d others(10): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr16 | 56827044 | |||||
| chr16:56827044
|
C | CAAAAAAA others(2): Show |
23 | a0001c0001t0001g0139a0001c0001t0001g0142a0001c0001t0001g0144others(20): Show | 24 | HG00642.hp1 HG01069.hp2 HG01167.hp1 others(21): Show |
intron_variant | MODIFIER | c.795-1916_795-1908d others(11): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr16 | 56827044 | |||||
| chr16:56827044
|
C | CAAAAAAA others(3): Show |
28 | a0001c0001t0001g0116a0001c0001t0001g0124a0001c0001t0001g0147others(25): Show | 28 | HG00323.hp2 HG00544.hp1 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.795-1917_795-1908d others(12): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr16 | 56827044 | |||||
| chr16:56827044
|
C | CAAAAAAA others(4): Show |
27 | a0001c0001t0001g0003a0001c0001t0001g0149a0001c0001t0001g0151others(24): Show | 27 | HG00140.hp1 HG00609.hp2 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.795-1918_795-1908d others(13): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr16 | 56827044 | |||||
| chr16:56827044
|
C | CAAAAAAA others(5): Show |
10 | a0001c0001t0001g0166a0001c0002t0001g0074a0001c0002t0001g0082others(7): Show | 10 | HG01258.hp1 HG01981.hp1 HG01993.hp2 others(7): Show |
intron_variant | MODIFIER | c.795-1919_795-1908d others(14): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr16 | 56827044 | |||||
| chr16:56827044
|
C | CAAAAAAA others(6): Show |
8 | a0001c0001t0029g0245a0001c0002t0001g0060a0001c0002t0001g0086others(5): Show | 8 | HG00408.hp1 HG02132.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.795-1920_795-1908d others(15): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr16 | 56827044 | |||||
| chr16:56827044
|
C | CAAAAAAA others(11): Show |
1 | a0001c0010t0033g0261 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.795-1925_795-1908d others(20): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr16 | 56827044 | |||||
| chr16:56827044
|
C | CAAAAAAA others(14): Show |
1 | a0001c0001t0007g0340 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.795-1928_795-1908d others(23): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr16 | 56827044 | |||||
| chr16:56827044
|
C | CAAAAAAA others(16): Show |
1 | a0001c0001t0016g0191 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.795-1930_795-1908d others(25): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr16 | 56827044 | |||||
| chr16:56827044
|
C | CAAAAAAA others(17): Show |
4 | a0001c0005t0007g0183a0001c0005t0007g0184a0001c0005t0007g0186others(1): Show | 4 | HG02257.hp2 HG02559.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.795-1931_795-1908d others(26): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr16 | 56827044 | |||||
| chr16:56827044
|
C | CAAAAAAA others(19): Show |
1 | a0001c0005t0007g0185 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.795-1908_795-1907i others(28): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr16 | 56827044 | |||||
| chr16:56827044
|
C | CAAAAAAA others(21): Show |
2 | a0001c0001t0007g0195a0001c0001t0016g0192 | 2 | HG00642.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.795-1908_795-1907i others(30): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr16 | 56827044 | |||||
| chr16:56827044
|
C | CAAAAAAA others(25): Show |
1 | a0001c0001t0016g0193 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.795-1908_795-1907i others(34): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr16 | 56827044 | |||||
| chr16:56827044
|
CAA | C | 8 | a0001c0001t0011g0005a0001c0001t0011g0006a0001c0001t0011g0007others(5): Show | 8 | HG00423.hp2 HG01884.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.795-1909_795-1908d others(4): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr16 | 56827044 | |||||
| chr16:56827044
|
CAAA | C | 27 | a0001c0001t0011g0009a0001c0004t0005g0020a0001c0004t0005g0021others(24): Show | 27 | HG00438.hp2 HG00558.hp2 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.795-1910_795-1908d others(5): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr16 | 56827044 | |||||
| chr16:56827044
|
CAAAAAA | C | 55 | a0001c0001t0002g0284a0001c0001t0002g0292a0001c0001t0002g0295others(52): Show | 55 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.795-1913_795-1908d others(8): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr16 | 56827044 | |||||
| chr16:56827064
|
AAAAAAT | A | 24 | a0001c0001t0004g0198a0001c0001t0004g0220a0001c0001t0004g0221others(21): Show | 24 | HG00408.hp2 HG00597.hp2 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.795-1912_795-1907d others(8): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56827064 | ||||||
| chr16:56827069
|
A | AAAAAAAA others(26): Show |
1 | a0001c0001t0003g0368 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.795-1908_795-1907i others(35): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56827069 | ||||||
| chr16:56827069
|
A | AAAAAAAA others(19): Show |
1 | a0001c0001t0003g0370 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.795-1908_795-1907i others(28): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56827069 | ||||||
| chr16:56827069
|
A | AAAAAAAA others(16): Show |
1 | a0001c0001t0003g0367 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.795-1908_795-1907i others(25): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56827069 | ||||||
| chr16:56827069
|
A | AAAAAAAA others(15): Show |
2 | a0001c0001t0003g0353a0001c0001t0003g0357 | 2 | NA19005.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.795-1908_795-1907i others(24): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56827069 | ||||||
| chr16:56827069
|
A | AAAAAAAA others(14): Show |
2 | a0001c0001t0003g0358a0001c0001t0003g0374 | 2 | NA18979.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.795-1908_795-1907i others(23): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56827069 | ||||||
| chr16:56827069
|
A | AAAAAAAA others(13): Show |
2 | a0001c0001t0003g0354a0001c0001t0003g0373 | 2 | NA18961.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.795-1908_795-1907i others(22): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56827069 | ||||||
| chr16:56827069
|
A | AAAAAAAA others(12): Show |
2 | a0001c0001t0003g0351a0001c0001t0003g0362 | 2 | HG01981.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.795-1908_795-1907i others(21): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56827069 | ||||||
| chr16:56827069
|
A | AAAAAAAA others(11): Show |
9 | a0001c0001t0003g0349a0001c0001t0003g0350a0001c0001t0003g0352others(6): Show | 9 | HG01070.hp1 HG01071.hp1 HG01978.hp1 others(6): Show |
intron_variant | MODIFIER | c.795-1908_795-1907i others(20): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56827069 | ||||||
| chr16:56827069
|
A | AAAAAAAA others(10): Show |
4 | a0001c0001t0003g0348a0001c0001t0003g0365a0001c0001t0027g0371others(1): Show | 4 | HG00639.hp1 HG01361.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.795-1908_795-1907i others(19): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56827069 | ||||||
| chr16:56827069
|
A | AAAAAAAA others(9): Show |
2 | a0001c0001t0003g0366a0001c0001t0003g0375 | 2 | HG01081.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.795-1908_795-1907i others(18): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56827069 | ||||||
| chr16:56827069
|
A | AAAAAAAA others(8): Show |
1 | a0001c0001t0003g0376 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.795-1908_795-1907i others(17): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56827069 | ||||||
| chr16:56827069
|
A | T | 2 | a0001c0001t0028g0360a0001c0007t0012g0345 | 2 | HG02027.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.795-1908A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56827069 | ||||||
| chr16:56827070
|
T | A | 7 | a0001c0002t0001g0064a0001c0002t0001g0066a0001c0002t0001g0067others(4): Show | 7 | HG02572.hp1 HG02622.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.795-1907T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56827070 | ||||||
| chr16:56827071
|
T | A | 3 | a0001c0002t0001g0066a0001c0002t0001g0068a0001c0002t0001g0069 | 3 | HG02622.hp1 HG02647.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.795-1906T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56827071 | ||||||
| chr16:56827171
|
C | T | 1 | a0001c0001t0011g0004 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.795-1806C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56827171 | ||||||
| chr16:56827246
|
C | G | 1 | a0001c0001t0006g0210 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.795-1731C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56827246 | ||||||
| chr16:56827389
|
T | C | 1 | a0001c0003t0002g0273 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.795-1588T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56827389 | ||||||
| chr16:56827532
|
G | C | 20 | a0001c0001t0006g0199a0001c0001t0006g0200a0001c0001t0006g0201others(17): Show | 20 | HG01070.hp2 HG01168.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.795-1445G>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56827532 | ||||||
| chr16:56827533
|
T | G | 2 | a0001c0001t0006g0203a0001c0001t0006g0208 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.795-1444T>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56827533 | ||||||
| chr16:56827614
|
A | G | 1 | a0001c0010t0033g0261 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.795-1363A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56827614 | ||||||
| chr16:56827631
|
G | T | 4 | a0001c0004t0008g0174a0001c0004t0008g0175a0001c0004t0008g0176others(1): Show | 4 | HG00099.hp2 HG00741.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.795-1346G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56827631 | ||||||
| chr16:56827660
|
T | C | 1 | a0001c0001t0001g0323 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.795-1317T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56827660 | ||||||
| chr16:56827763
|
A | C | 1 | a0001c0006t0009g0252 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.795-1214A>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56827763 | ||||||
| chr16:56827805
|
T | G | 1 | a0004c0023t0026g0372 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.795-1172T>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56827805 | ||||||
| chr16:56827881
|
A | C | 20 | a0001c0001t0006g0199a0001c0001t0006g0200a0001c0001t0006g0201others(17): Show | 20 | HG01070.hp2 HG01168.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.795-1096A>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56827881 | ||||||
| chr16:56827969
|
A | G | 1 | a0001c0001t0001g0126 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.795-1008A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56827969 | ||||||
| chr16:56827981
|
G | A | 1 | a0001c0002t0001g0091 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.795-996G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56827981 | ||||||
| chr16:56828083
|
C | G | 174 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0045others(171): Show | 176 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.795-894C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56828083 | ||||||
| chr16:56828117
|
C | T | 1 | a0001c0004t0005g0028 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.795-860C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56828117 | ||||||
| chr16:56828184
|
C | T | 1 | a0001c0001t0034g0196 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.795-793C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56828184 | ||||||
| chr16:56828194
|
T | TA | 16 | a0001c0001t0001g0120a0001c0001t0001g0157a0001c0001t0011g0004others(13): Show | 16 | HG00323.hp2 HG01884.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.795-763dupA | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr16 | 56828194 | |||||
| chr16:56828194
|
T | TAA | 219 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0045others(216): Show | 221 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.795-764_795-763dup others(2): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr16 | 56828194 | |||||
| chr16:56828194
|
TA | T | 7 | a0001c0001t0003g0350a0001c0001t0003g0359a0001c0001t0003g0376others(4): Show | 7 | HG01070.hp1 HG01167.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.795-763delA | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr16 | 56828194 | |||||
| chr16:56828210
|
A | T | 20 | a0001c0001t0006g0199a0001c0001t0006g0200a0001c0001t0006g0201others(17): Show | 20 | HG01070.hp2 HG01168.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.795-767A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56828210 | ||||||
| chr16:56828231
|
GA | G | 174 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0045others(171): Show | 176 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.795-745delA | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56828231 | ||||||
| chr16:56828854
|
G | T | 16 | a0001c0001t0006g0202a0001c0001t0006g0203a0001c0001t0006g0204others(13): Show | 16 | HG01070.hp2 HG01168.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.795-123G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 8/21 | chr16 | 56828854 | ||||||
| chr16:56829115
|
G | A | 21 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(18): Show | 21 | HG00621.hp1 HG02071.hp1 HG03239.hp2 others(18): Show |
splice_region_variant&intron_variant | LOW | c.927+6G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 9/21 | chr16 | 56829115 | ||||||
| chr16:56829160
|
C | T | 20 | a0001c0001t0006g0199a0001c0001t0006g0200a0001c0001t0006g0201others(17): Show | 20 | HG01070.hp2 HG01168.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.927+51C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 9/21 | chr16 | 56829160 | ||||||
| chr16:56829303
|
C | T | 41 | a0001c0001t0001g0002a0001c0001t0001g0302a0001c0001t0001g0303others(38): Show | 42 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.927+194C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 9/21 | chr16 | 56829303 | ||||||
| chr16:56829317
|
T | C | 59 | a0001c0001t0002g0284a0001c0001t0002g0292a0001c0001t0002g0295others(56): Show | 59 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.927+208T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 9/21 | chr16 | 56829317 | ||||||
| chr16:56829555
|
A | T | 2 | a0001c0001t0001g0162a0001c0001t0001g0163 | 2 | HG01891.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.927+446A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 9/21 | chr16 | 56829555 | ||||||
| chr16:56829584
|
T | C | 6 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(3): Show | 6 | HG01884.hp1 HG02630.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.927+475T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 9/21 | chr16 | 56829584 | ||||||
| chr16:56829708
|
A | G | 4 | a0001c0007t0012g0065a0001c0007t0012g0345a0001c0007t0012g0346others(1): Show | 4 | HG01891.hp1 HG02145.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.927+599A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 9/21 | chr16 | 56829708 | ||||||
| chr16:56829770
|
C | T | 3 | a0001c0007t0012g0065a0001c0007t0012g0346a0001c0007t0012g0347 | 3 | HG01891.hp1 HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.927+661C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 9/21 | chr16 | 56829770 | ||||||
| chr16:56830089
|
G | A | 1 | a0001c0007t0012g0345 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.928-439G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 9/21 | chr16 | 56830089 | ||||||
| chr16:56830146
|
C | T | 1 | a0001c0001t0011g0009 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.928-382C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 9/21 | chr16 | 56830146 | ||||||
| chr16:56830178
|
G | A | 1 | a0001c0002t0001g0070 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.928-350G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 9/21 | chr16 | 56830178 | ||||||
| chr16:56830202
|
C | T | 1 | a0001c0001t0029g0245 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.928-326C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 9/21 | chr16 | 56830202 | ||||||
| chr16:56830382
|
G | A | 5 | a0001c0002t0001g0094a0001c0002t0001g0098a0001c0002t0001g0099others(2): Show | 5 | HG02886.hp1 HG02970.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.928-146G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 9/21 | chr16 | 56830382 | ||||||
| chr16:56830486
|
C | T | 271 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0045others(268): Show | 273 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(270): Show |
intron_variant | MODIFIER | c.928-42C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 9/21 | chr16 | 56830486 | ||||||
| chr16:56830487
|
T | C | 6 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(3): Show | 6 | HG01884.hp1 HG02630.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.928-41T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 9/21 | chr16 | 56830487 | ||||||
| chr16:56830706
|
C | T | 203 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0045others(200): Show | 205 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.1085+21C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 10/21 | chr16 | 56830706 | ||||||
| chr16:56830775
|
G | T | 1 | a0001c0002t0001g0128 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1085+90G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 10/21 | chr16 | 56830775 | ||||||
| chr16:56830900
|
C | T | 1 | a0001c0001t0036g0148 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1085+215C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 10/21 | chr16 | 56830900 | ||||||
| chr16:56830938
|
G | A | 24 | a0001c0001t0004g0198a0001c0001t0004g0220a0001c0001t0004g0221others(21): Show | 24 | HG00408.hp2 HG00597.hp2 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.1085+253G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 10/21 | chr16 | 56830938 | ||||||
| chr16:56831259
|
A | G | 3 | a0001c0001t0006g0204a0001c0001t0006g0205a0001c0001t0006g0244 | 3 | HG02083.hp1 NA18747.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.1085+574A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 10/21 | chr16 | 56831259 | ||||||
| chr16:56831337
|
C | A | 202 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0045others(199): Show | 204 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.1086-505C>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 10/21 | chr16 | 56831337 | ||||||
| chr16:56831345
|
A | G | 1 | a0001c0010t0033g0261 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1086-497A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 10/21 | chr16 | 56831345 | ||||||
| chr16:56831462
|
G | A | 59 | a0001c0001t0002g0284a0001c0001t0002g0292a0001c0001t0002g0295others(56): Show | 59 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.1086-380G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 10/21 | chr16 | 56831462 | ||||||
| chr16:56831506
|
G | A | 1 | a0001c0004t0019g0180 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1086-336G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 10/21 | chr16 | 56831506 | ||||||
| chr16:56831633
|
G | A | 1 | a0005c0022t0022g0254 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1086-209G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 10/21 | chr16 | 56831633 | ||||||
| chr16:56831793
|
G | T | 2 | a0001c0001t0011g0009a0001c0001t0046g0008 | 2 | HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1086-49G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 10/21 | chr16 | 56831793 | ||||||
| chr16:56831816
|
A | G | 1 | a0001c0002t0001g0165 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1086-26A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 10/21 | chr16 | 56831816 | ||||||
| chr16:56832142
|
A | AT | 59 | a0001c0001t0002g0284a0001c0001t0002g0292a0001c0001t0002g0295others(56): Show | 59 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.1251+141dupT | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr16 | 56832142 | |||||
| chr16:56832284
|
T | C | 59 | a0001c0001t0002g0284a0001c0001t0002g0292a0001c0001t0002g0295others(56): Show | 59 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.1252-11T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 11/21 | chr16 | 56832284 | ||||||
| chr16:56832590
|
T | C | 45 | a0001c0001t0003g0348a0001c0001t0003g0349a0001c0001t0003g0350others(42): Show | 45 | HG00323.hp1 HG00639.hp1 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.1345+202T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 12/21 | chr16 | 56832590 | ||||||
| chr16:56832591
|
A | G | 1 | a0001c0004t0005g0030 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1345+203A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 12/21 | chr16 | 56832591 | ||||||
| chr16:56832638
|
A | G | 3 | a0001c0007t0012g0065a0001c0007t0012g0346a0001c0007t0012g0347 | 3 | HG01891.hp1 HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1345+250A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 12/21 | chr16 | 56832638 | ||||||
| chr16:56832737
|
CCTTT | C | 3 | a0001c0009t0018g0018a0001c0009t0018g0019a0003c0024t0018g0010 | 3 | HG02451.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1345+353_1345+356d others(6): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr16 | 56832737 | |||||
| chr16:56832848
|
C | T | 1 | a0001c0002t0001g0058 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1346-367C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 12/21 | chr16 | 56832848 | ||||||
| chr16:56832889
|
G | T | 45 | a0001c0001t0003g0348a0001c0001t0003g0349a0001c0001t0003g0350others(42): Show | 45 | HG00323.hp1 HG00639.hp1 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.1346-326G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 12/21 | chr16 | 56832889 | ||||||
| chr16:56833501
|
G | A | 2 | a0001c0001t0004g0239a0001c0001t0004g0241 | 2 | NA19083.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1537+95G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 13/21 | chr16 | 56833501 | ||||||
| chr16:56833865
|
A | C | 10 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(7): Show | 10 | HG01884.hp1 HG02145.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1538-263A>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 13/21 | chr16 | 56833865 | ||||||
| chr16:56833892
|
C | T | 363 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0045others(360): Show | 365 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(362): Show |
intron_variant | MODIFIER | c.1538-236C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 13/21 | chr16 | 56833892 | ||||||
| chr16:56833977
|
A | G | 3 | a0001c0009t0018g0018a0001c0009t0018g0019a0003c0024t0018g0010 | 3 | HG02451.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1538-151A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 13/21 | chr16 | 56833977 | ||||||
| chr16:56834558
|
T | C | 3 | a0001c0001t0001g0052a0001c0001t0001g0131a0001c0001t0001g0160 | 3 | HG03130.hp1 HG03540.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1737+116T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 15/21 | chr16 | 56834558 | ||||||
| chr16:56834653
|
C | T | 1 | a0001c0001t0001g0119 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1738-81C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 15/21 | chr16 | 56834653 | ||||||
| chr16:56834687
|
T | G | 1 | a0001c0003t0002g0247 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1738-47T>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 15/21 | chr16 | 56834687 | ||||||
| chr16:56834788
|
A | G | 200 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0045others(197): Show | 202 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.1782+10A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 16/21 | chr16 | 56834788 | ||||||
| chr16:56834821
|
G | A | 1 | a0001c0002t0001g0096 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1782+43G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 16/21 | chr16 | 56834821 | ||||||
| chr16:56835107
|
G | T | 6 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(3): Show | 6 | HG01884.hp1 HG02630.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1782+329G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 16/21 | chr16 | 56835107 | ||||||
| chr16:56835485
|
T | C | 2 | a0001c0004t0005g0030a0001c0004t0005g0032 | 2 | HG01099.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.1782+707T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 16/21 | chr16 | 56835485 | ||||||
| chr16:56835517
|
G | A | 2 | a0001c0002t0001g0083a0001c0002t0001g0344 | 2 | HG02015.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.1782+739G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 16/21 | chr16 | 56835517 | ||||||
| chr16:56835518
|
T | C | 363 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0045others(360): Show | 365 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(362): Show |
intron_variant | MODIFIER | c.1782+740T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 16/21 | chr16 | 56835518 | ||||||
| chr16:56835544
|
G | T | 3 | a0001c0007t0012g0065a0001c0007t0012g0346a0001c0007t0012g0347 | 3 | HG01891.hp1 HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1782+766G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 16/21 | chr16 | 56835544 | ||||||
| chr16:56835635
|
G | T | 4 | a0001c0002t0001g0096a0001c0004t0015g0015a0001c0004t0015g0016others(1): Show | 4 | HG02280.hp1 HG02818.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1782+857G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 16/21 | chr16 | 56835635 | ||||||
| chr16:56835704
|
G | A | 3 | a0001c0001t0013g0012a0001c0001t0013g0013a0001c0001t0013g0014 | 3 | HG03041.hp1 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1783-897G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 16/21 | chr16 | 56835704 | ||||||
| chr16:56835803
|
T | A | 74 | a0001c0002t0001g0001a0001c0002t0001g0044a0001c0002t0001g0051others(71): Show | 75 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.1783-798T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 16/21 | chr16 | 56835803 | ||||||
| chr16:56835850
|
C | T | 1 | a0001c0001t0006g0216 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1783-751C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 16/21 | chr16 | 56835850 | ||||||
| chr16:56835902
|
G | T | 2 | a0001c0001t0016g0192a0001c0001t0016g0193 | 2 | HG02258.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1783-699G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 16/21 | chr16 | 56835902 | ||||||
| chr16:56836128
|
C | CAAA | 49 | a0001c0001t0002g0284a0001c0001t0002g0295a0001c0003t0002g0047others(46): Show | 49 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.1783-460_1783-458d others(5): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 56836128 | |||||
| chr16:56836171
|
G | GT | 41 | a0001c0001t0003g0348a0001c0001t0003g0349a0001c0001t0003g0350others(38): Show | 41 | HG00323.hp1 HG00639.hp1 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.1783-424dupT | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr16 | 56836171 | |||||
| chr16:56836233
|
A | G | 1 | a0001c0017t0001g0158 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1783-368A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 16/21 | chr16 | 56836233 | ||||||
| chr16:56836526
|
G | T | 1 | a0001c0001t0002g0292 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1783-75G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 16/21 | chr16 | 56836526 | ||||||
| chr16:56836541
|
A | G | 1 | a0001c0001t0001g0332 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1783-60A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 16/21 | chr16 | 56836541 | ||||||
| chr16:56836863
|
G | T | 1 | a0001c0001t0001g0337 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1899+146G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 17/21 | chr16 | 56836863 | ||||||
| chr16:56836955
|
A | C | 1 | a0001c0002t0001g0051 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1899+238A>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 17/21 | chr16 | 56836955 | ||||||
| chr16:56837004
|
G | T | 16 | a0001c0001t0006g0202a0001c0001t0006g0203a0001c0001t0006g0204others(13): Show | 16 | HG01070.hp2 HG01168.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.1899+287G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 17/21 | chr16 | 56837004 | ||||||
| chr16:56837260
|
G | A | 3 | a0001c0001t0014g0217a0001c0001t0014g0218a0001c0001t0014g0219 | 3 | HG01884.hp2 HG03453.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1900-348G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 17/21 | chr16 | 56837260 | ||||||
| chr16:56837489
|
G | C | 1 | a0001c0001t0003g0374 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1900-119G>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 17/21 | chr16 | 56837489 | ||||||
| chr16:56837557
|
TTTTATTG others(5): Show |
T | 58 | a0001c0001t0001g0003a0001c0001t0001g0045a0001c0001t0001g0046others(55): Show | 58 | HG00099.hp1 HG00621.hp1 HG00735.hp1 others(55): Show |
intron_variant | MODIFIER | c.1900-40_1900-29del others(12): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr16 | 56837557 | |||||
| chr16:56837574
|
T | C | 1 | a0002c0008t0002g0299 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1900-34T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 17/21 | chr16 | 56837574 | ||||||
| chr16:56837764
|
C | A | 2 | a0001c0001t0006g0199a0001c0001t0006g0200 | 2 | HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2018+38C>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 18/21 | chr16 | 56837764 | ||||||
| chr16:56837784
|
C | T | 3 | a0001c0007t0012g0065a0001c0007t0012g0346a0001c0007t0012g0347 | 3 | HG01891.hp1 HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2018+58C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 18/21 | chr16 | 56837784 | ||||||
| chr16:56837893
|
C | T | 3 | a0001c0001t0013g0012a0001c0001t0013g0013a0001c0001t0013g0014 | 3 | HG03041.hp1 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2018+167C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 18/21 | chr16 | 56837893 | ||||||
| chr16:56838014
|
G | A | 3 | a0001c0001t0016g0191a0001c0001t0016g0192a0001c0001t0016g0193 | 3 | HG02258.hp2 HG03130.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2018+288G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 18/21 | chr16 | 56838014 | ||||||
| chr16:56838030
|
A | G | 1 | a0001c0001t0001g0316 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2018+304A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 18/21 | chr16 | 56838030 | ||||||
| chr16:56838347
|
C | T | 2 | a0001c0001t0001g0335a0001c0001t0001g0336 | 2 | HG03017.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.2019-605C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 18/21 | chr16 | 56838347 | ||||||
| chr16:56838804
|
A | G | 1 | a0001c0004t0005g0036 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.2019-148A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 18/21 | chr16 | 56838804 | ||||||
| chr16:56838810
|
C | T | 57 | a0001c0001t0001g0003a0001c0001t0001g0045a0001c0001t0001g0046others(54): Show | 57 | HG00099.hp1 HG00621.hp1 HG00735.hp1 others(54): Show |
intron_variant | MODIFIER | c.2019-142C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 18/21 | chr16 | 56838810 | ||||||
| chr16:56838866
|
T | G | 3 | a0001c0001t0013g0012a0001c0001t0013g0013a0001c0001t0013g0014 | 3 | HG03041.hp1 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2019-86T>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 18/21 | chr16 | 56838866 | ||||||
| chr16:56838912
|
G | A | 59 | a0001c0001t0002g0284a0001c0001t0002g0292a0001c0001t0002g0295others(56): Show | 59 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.2019-40G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 18/21 | chr16 | 56838912 | ||||||
| chr16:56839233
|
C | CT | 60 | a0001c0001t0001g0002a0001c0001t0001g0161a0001c0001t0001g0302others(57): Show | 61 | HG00323.hp1 HG00639.hp1 HG00642.hp2 others(58): Show |
intron_variant | MODIFIER | c.2136+191dupT | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr16 | 56839233 | |||||
| chr16:56839233
|
C | CTT | 12 | a0001c0001t0003g0363a0001c0001t0003g0364a0001c0001t0003g0366others(9): Show | 12 | HG01081.hp2 HG01167.hp2 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.2136+190_2136+191d others(4): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr16 | 56839233 | |||||
| chr16:56839233
|
CT | C | 163 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0052others(160): Show | 164 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.2136+191delT | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr16 | 56839233 | |||||
| chr16:56839233
|
CTT | C | 8 | a0001c0002t0001g0096a0001c0006t0009g0249a0001c0006t0009g0251others(5): Show | 8 | HG01891.hp1 HG02109.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.2136+190_2136+191d others(4): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr16 | 56839233 | |||||
| chr16:56839260
|
T | G | 19 | a0001c0001t0004g0198a0001c0001t0004g0220a0001c0001t0004g0221others(16): Show | 19 | HG00408.hp2 HG00597.hp2 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.2136+191T>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 19/21 | chr16 | 56839260 | ||||||
| chr16:56839260
|
T | TG | 5 | a0001c0001t0004g0225a0001c0001t0004g0230a0001c0001t0004g0232others(2): Show | 5 | HG01175.hp1 HG01978.hp2 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.2136+192dupG | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr16 | 56839260 | |||||
| chr16:56839622
|
G | A | 1 | a0001c0001t0003g0348 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2220+18G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 20/21 | chr16 | 56839622 | ||||||
| chr16:56839701
|
T | TA | 54 | a0001c0001t0002g0284a0001c0001t0002g0292a0001c0001t0002g0295others(51): Show | 54 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.2220+98dupA | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr16 | 56839701 | |||||
| chr16:56839703
|
C | T | 1 | a0001c0001t0046g0008 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2220+99C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 20/21 | chr16 | 56839703 | ||||||
| chr16:56839877
|
T | C | 59 | a0001c0001t0002g0284a0001c0001t0002g0292a0001c0001t0002g0295others(56): Show | 59 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.2220+273T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 20/21 | chr16 | 56839877 | ||||||
| chr16:56839902
|
A | G | 5 | a0001c0001t0001g0130a0001c0001t0001g0132a0001c0001t0001g0133others(2): Show | 5 | HG00735.hp1 HG01515.hp2 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.2220+298A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 20/21 | chr16 | 56839902 | ||||||
| chr16:56839928
|
G | A | 72 | a0001c0002t0001g0001a0001c0002t0001g0044a0001c0002t0001g0051others(69): Show | 73 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.2220+324G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 20/21 | chr16 | 56839928 | ||||||
| chr16:56839961
|
T | C | 8 | a0001c0001t0003g0353a0001c0001t0003g0354a0001c0001t0003g0356others(5): Show | 8 | NA18961.hp1 NA18969.hp2 NA18979.hp1 others(5): Show |
intron_variant | MODIFIER | c.2220+357T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 20/21 | chr16 | 56839961 | ||||||
| chr16:56840060
|
A | G | 370 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0045others(367): Show | 372 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(369): Show |
intron_variant | MODIFIER | c.2220+456A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 20/21 | chr16 | 56840060 | ||||||
| chr16:56840109
|
C | G | 3 | a0001c0003t0002g0267a0001c0003t0002g0275a0001c0003t0002g0296 | 3 | NA18942.hp2 NA18981.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.2220+505C>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 20/21 | chr16 | 56840109 | ||||||
| chr16:56840178
|
G | T | 3 | a0001c0009t0018g0018a0001c0009t0018g0019a0003c0024t0018g0010 | 3 | HG02451.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2220+574G>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 20/21 | chr16 | 56840178 | ||||||
| chr16:56840179
|
C | T | 3 | a0001c0009t0018g0018a0001c0009t0018g0019a0003c0024t0018g0010 | 3 | HG02451.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2220+575C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 20/21 | chr16 | 56840179 | ||||||
| chr16:56840272
|
G | A | 72 | a0001c0002t0001g0001a0001c0002t0001g0044a0001c0002t0001g0051others(69): Show | 73 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.2220+668G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 20/21 | chr16 | 56840272 | ||||||
| chr16:56840285
|
G | A | 171 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0045others(168): Show | 173 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.2220+681G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 20/21 | chr16 | 56840285 | ||||||
| chr16:56840299
|
C | T | 1 | a0001c0001t0003g0364 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.2220+695C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 20/21 | chr16 | 56840299 | ||||||
| chr16:56840356
|
C | T | 3 | a0001c0002t0001g0073a0001c0002t0001g0102a0001c0019t0001g0078 | 3 | NA18954.hp2 NA19011.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.2220+752C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 20/21 | chr16 | 56840356 | ||||||
| chr16:56840360
|
G | C | 364 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0045others(361): Show | 366 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(363): Show |
intron_variant | MODIFIER | c.2220+756G>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 20/21 | chr16 | 56840360 | ||||||
| chr16:56840564
|
A | G | 25 | a0001c0004t0005g0020a0001c0004t0005g0021a0001c0004t0005g0022others(22): Show | 25 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(22): Show |
intron_variant | MODIFIER | c.2220+960A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 20/21 | chr16 | 56840564 | ||||||
| chr16:56840681
|
T | C | 1 | a0010c0013t0007g0190 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2221-1024T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 20/21 | chr16 | 56840681 | ||||||
| chr16:56840788
|
G | A | 1 | a0001c0003t0002g0047 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2221-917G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 20/21 | chr16 | 56840788 | ||||||
| chr16:56840945
|
C | T | 171 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0045others(168): Show | 173 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.2221-760C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 20/21 | chr16 | 56840945 | ||||||
| chr16:56840976
|
G | A | 3 | a0001c0001t0016g0191a0001c0001t0016g0192a0001c0001t0016g0193 | 3 | HG02258.hp2 HG03130.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2221-729G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 20/21 | chr16 | 56840976 | ||||||
| chr16:56840991
|
T | C | 364 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0045others(361): Show | 366 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(363): Show |
intron_variant | MODIFIER | c.2221-714T>C | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 20/21 | chr16 | 56840991 | ||||||
| chr16:56840996
|
C | CA | 48 | a0001c0001t0001g0002a0001c0001t0001g0045a0001c0001t0001g0153others(45): Show | 49 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.2221-692dupA | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr16 | 56840996 | |||||
| chr16:56840996
|
CA | C | 11 | a0001c0001t0001g0143a0001c0001t0004g0233a0001c0003t0002g0246others(8): Show | 11 | HG00597.hp1 HG00673.hp1 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.2221-692delA | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr16 | 56840996 | |||||
| chr16:56841018
|
C | T | 28 | a0001c0004t0005g0020a0001c0004t0005g0021a0001c0004t0005g0022others(25): Show | 28 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(25): Show |
intron_variant | MODIFIER | c.2221-687C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 20/21 | chr16 | 56841018 | ||||||
| chr16:56841041
|
C | T | 1 | a0001c0007t0012g0345 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2221-664C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 20/21 | chr16 | 56841041 | ||||||
| chr16:56841060
|
G | A | 2 | a0001c0001t0001g0145a0001c0001t0001g0146 | 2 | NA18946.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.2221-645G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 20/21 | chr16 | 56841060 | ||||||
| chr16:56841222
|
C | T | 1 | a0001c0001t0029g0245 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2221-483C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 20/21 | chr16 | 56841222 | ||||||
| chr16:56841223
|
G | A | 1 | a0001c0007t0012g0347 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2221-482G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 20/21 | chr16 | 56841223 | ||||||
| chr16:56841291
|
G | A | 2 | a0001c0001t0001g0155a0001c0001t0001g0156 | 2 | HG02109.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2221-414G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 20/21 | chr16 | 56841291 | ||||||
| chr16:56841323
|
C | T | 4 | a0001c0003t0002g0280a0001c0003t0002g0281a0001c0003t0020g0283others(1): Show | 4 | HG01099.hp1 HG01168.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.2221-382C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 20/21 | chr16 | 56841323 | ||||||
| chr16:56841360
|
A | AT | 171 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0045others(168): Show | 173 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.2221-343dupT | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr16 | 56841360 | |||||
| chr16:56841367
|
T | G | 1 | a0001c0001t0001g0120 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2221-338T>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 20/21 | chr16 | 56841367 | ||||||
| chr16:56841370
|
A | T | 1 | a0001c0002t0001g0105 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2221-335A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 20/21 | chr16 | 56841370 | ||||||
| chr16:56841371
|
A | T | 1 | a0001c0001t0001g0120 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2221-334A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 20/21 | chr16 | 56841371 | ||||||
| chr16:56841383
|
G | A | 25 | a0001c0004t0005g0020a0001c0004t0005g0021a0001c0004t0005g0022others(22): Show | 25 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(22): Show |
intron_variant | MODIFIER | c.2221-322G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 20/21 | chr16 | 56841383 | ||||||
| chr16:56841390
|
C | A | 1 | a0001c0001t0029g0245 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2221-315C>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 20/21 | chr16 | 56841390 | ||||||
| chr16:56841472
|
A | T | 1 | a0001c0002t0001g0108 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2221-233A>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 20/21 | chr16 | 56841472 | ||||||
| chr16:56841664
|
G | A | 1 | a0001c0003t0002g0263 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2221-41G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 20/21 | chr16 | 56841664 | ||||||
| chr16:56842086
|
CTAATTTC others(39): Show |
C | 1 | a0001c0001t0001g0143 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.2349+257_2349+302d others(48): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr16 | 56842086 | |||||
| chr16:56842141
|
T | TTTTGGGG others(39): Show |
1 | a0001c0001t0001g0143 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.2349+312_2349+313i others(48): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr16 | 56842141 | |||||
| chr16:56842332
|
C | T | 1 | a0001c0001t0001g0306 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.2349+499C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 21/21 | chr16 | 56842332 | ||||||
| chr16:56842417
|
C | T | 1 | a0001c0001t0006g0202 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2349+584C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 21/21 | chr16 | 56842417 | ||||||
| chr16:56842448
|
A | G | 3 | a0001c0009t0018g0018a0001c0009t0018g0019a0003c0024t0018g0010 | 3 | HG02451.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2349+615A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 21/21 | chr16 | 56842448 | ||||||
| chr16:56842488
|
C | T | 1 | a0001c0001t0029g0245 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2349+655C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 21/21 | chr16 | 56842488 | ||||||
| chr16:56842555
|
CT | C | 261 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0045others(258): Show | 263 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.2349+737delT | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr16 | 56842555 | |||||
| chr16:56842616
|
G | A | 1 | a0001c0001t0001g0114 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2349+783G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 21/21 | chr16 | 56842616 | ||||||
| chr16:56842699
|
C | T | 1 | a0001c0007t0012g0345 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2349+866C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 21/21 | chr16 | 56842699 | ||||||
| chr16:56842933
|
T | G | 59 | a0001c0001t0002g0284a0001c0001t0002g0292a0001c0001t0002g0295others(56): Show | 59 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.2349+1100T>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 21/21 | chr16 | 56842933 | ||||||
| chr16:56842963
|
A | G | 1 | a0001c0002t0001g0051 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2349+1130A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 21/21 | chr16 | 56842963 | ||||||
| chr16:56842983
|
C | T | 2 | a0001c0004t0015g0015a0001c0004t0015g0017 | 2 | HG02818.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2349+1150C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 21/21 | chr16 | 56842983 | ||||||
| chr16:56843173
|
C | T | 28 | a0001c0004t0005g0020a0001c0004t0005g0021a0001c0004t0005g0022others(25): Show | 28 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(25): Show |
intron_variant | MODIFIER | c.2350-1326C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 21/21 | chr16 | 56843173 | ||||||
| chr16:56843240
|
A | G | 1 | a0001c0001t0001g0333 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2350-1259A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 21/21 | chr16 | 56843240 | ||||||
| chr16:56843565
|
C | T | 28 | a0001c0004t0005g0020a0001c0004t0005g0021a0001c0004t0005g0022others(25): Show | 28 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(25): Show |
intron_variant | MODIFIER | c.2350-934C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 21/21 | chr16 | 56843565 | ||||||
| chr16:56843742
|
G | A | 2 | a0001c0001t0001g0162a0001c0001t0001g0163 | 2 | HG01891.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.2350-757G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 21/21 | chr16 | 56843742 | ||||||
| chr16:56843906
|
A | G | 3 | a0001c0001t0003g0366a0001c0001t0003g0375a0001c0001t0003g0376 | 3 | HG01081.hp2 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.2350-593A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 21/21 | chr16 | 56843906 | ||||||
| chr16:56843909
|
C | A | 3 | a0001c0001t0016g0191a0001c0001t0016g0192a0001c0001t0016g0193 | 3 | HG02258.hp2 HG03130.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2350-590C>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 21/21 | chr16 | 56843909 | ||||||
| chr16:56843938
|
G | A | 1 | a0001c0001t0011g0007 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2350-561G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 21/21 | chr16 | 56843938 | ||||||
| chr16:56844161
|
T | A | 25 | a0001c0004t0005g0020a0001c0004t0005g0021a0001c0004t0005g0022others(22): Show | 25 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(22): Show |
intron_variant | MODIFIER | c.2350-338T>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 21/21 | chr16 | 56844161 | ||||||
| chr16:56844196
|
A | G | 6 | a0001c0001t0006g0202a0001c0001t0006g0204a0001c0001t0006g0205others(3): Show | 6 | HG02015.hp1 HG02083.hp1 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.2350-303A>G | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 21/21 | chr16 | 56844196 | ||||||
| chr16:56844302
|
C | T | 1 | a0001c0001t0013g0012 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2350-197C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 21/21 | chr16 | 56844302 | ||||||
| chr16:56844303
|
G | A | 3 | a0001c0007t0012g0065a0001c0007t0012g0346a0001c0007t0012g0347 | 3 | HG01891.hp1 HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2350-196G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 21/21 | chr16 | 56844303 | ||||||
| chr16:56844438
|
G | A | 2 | a0001c0010t0022g0260a0001c0010t0033g0261 | 2 | HG03139.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2350-61G>A | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 21/21 | chr16 | 56844438 | ||||||
| chr16:56844466
|
C | T | 28 | a0001c0004t0005g0020a0001c0004t0005g0021a0001c0004t0005g0022others(25): Show | 28 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(25): Show |
intron_variant | MODIFIER | c.2350-33C>T | NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 21/21 | chr16 | 56844466 |