Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 23511 |
| ensemblid | ENSG00000095319.14 |
| hgncid | 17859 |
| symbol | NUP188 |
| name | nucleoporin 188 |
| refseq_nuc | NM_015354.3 |
| refseq_prot | NP_056169.1 |
| ensembl_nuc | ENST00000372577.2 |
| ensembl_prot | ENSP00000361658.2 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 128947699 |
| end | 129007096 |
| strand | + |
| ver | v1.2 |
| region | chr9:128947699-129007096 |
| region5000 | chr9:128942699-129012096 |
| regionname0 | NUP188_chr9_128947699_129007096 |
| regionname5000 | NUP188_chr9_128942699_129012096 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1749 | 275 | 66 | 56 | 108 | 12 | 31 | 81 | NUP188_chr9_128942699_129012096 | NUP188 | MAAAA others(1744): Show |
chr9 | 128942699 | 129012096 |
| a0002 | 0/0 | 1749 | 6 | 5 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | MAAAA others(1744): Show |
chr9 | 128942699 | 129012096 |
| a0003 | 0/0 | 1749 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | MAAAA others(1744): Show |
chr9 | 128942699 | 129012096 |
| a0004 | 0/0 | 1749 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | MAAAA others(1744): Show |
chr9 | 128942699 | 129012096 |
| a0005 | 0/0 | 1749 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | MAAAA others(1744): Show |
chr9 | 128942699 | 129012096 |
| a0006 | 0/0 | 1749 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | MAAAA others(1744): Show |
chr9 | 128942699 | 129012096 |
| a0007 | 0/0 | 1749 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | MAAAA others(1744): Show |
chr9 | 128942699 | 129012096 |
| a0008 | 0/0 | 1749 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | MAAAA others(1744): Show |
chr9 | 128942699 | 129012096 |
| a0009 | 0/0 | 1749 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | MAAAA others(1744): Show |
chr9 | 128942699 | 129012096 |
| a0010 | 0/0 | 1749 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | MAAAA others(1744): Show |
chr9 | 128942699 | 129012096 |
| a0011 | 0/0 | 1749 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | MAAAA others(1744): Show |
chr9 | 128942699 | 129012096 |
| a0012 | 0/0 | 1749 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | MAAAA others(1744): Show |
chr9 | 128942699 | 129012096 |
| a0013 | 0/0 | 1749 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | MAAAA others(1744): Show |
chr9 | 128942699 | 129012096 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 5247 | 137 | 32 | 24 | 54 | 6 | 20 | NUP188_chr9_128942699_129012096 | NUP188 | ATGGC others(5242): Show |
chr9 | 128942699 | 129012096 | ||
| a0001c0002 | 0/1 | 5247 | 98 | 17 | 27 | 38 | 6 | 9 | NUP188_chr9_128942699_129012096 | NUP188 | ATGGC others(5242): Show |
chr9 | 128942699 | 129012096 | ||
| a0001c0003 | 0/0 | 5247 | 14 | 0 | 0 | 12 | 0 | 2 | NUP188_chr9_128942699_129012096 | NUP188 | ATGGC others(5242): Show |
chr9 | 128942699 | 129012096 | ||
| a0001c0004 | 0/0 | 5247 | 10 | 9 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | ATGGC others(5242): Show |
chr9 | 128942699 | 129012096 | ||
| a0001c0007 | 0/0 | 5247 | 2 | 2 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | ATGGC others(5242): Show |
chr9 | 128942699 | 129012096 | ||
| a0001c0008 | 0/0 | 5247 | 2 | 2 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | ATGGC others(5242): Show |
chr9 | 128942699 | 129012096 | ||
| a0001c0009 | 0/0 | 5247 | 2 | 2 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | ATGGC others(5242): Show |
chr9 | 128942699 | 129012096 | ||
| a0001c0013 | 0/0 | 5247 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | ATGGC others(5242): Show |
chr9 | 128942699 | 129012096 | ||
| a0001c0014 | 0/0 | 5247 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | ATGGC others(5242): Show |
chr9 | 128942699 | 129012096 | ||
| a0001c0017 | 0/0 | 5247 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | ATGGC others(5242): Show |
chr9 | 128942699 | 129012096 | ||
| a0001c0020 | 0/0 | 5247 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | ATGGC others(5242): Show |
chr9 | 128942699 | 129012096 | ||
| a0001c0021 | 0/0 | 5247 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | ATGGC others(5242): Show |
chr9 | 128942699 | 129012096 | ||
| a0001c0023 | 0/0 | 5247 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | ATGGC others(5242): Show |
chr9 | 128942699 | 129012096 | ||
| a0001c0025 | 0/0 | 5247 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | ATGGC others(5242): Show |
chr9 | 128942699 | 129012096 | ||
| a0001c0027 | 0/0 | 5247 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | ATGGC others(5242): Show |
chr9 | 128942699 | 129012096 | ||
| a0001c0028 | 0/0 | 5247 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | ATGGC others(5242): Show |
chr9 | 128942699 | 129012096 | ||
| a0001c0029 | 0/0 | 5247 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | ATGGC others(5242): Show |
chr9 | 128942699 | 129012096 | ||
| a0002c0005 | 0/0 | 5247 | 5 | 5 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | ATGGC others(5242): Show |
chr9 | 128942699 | 129012096 | ||
| a0002c0012 | 0/0 | 5247 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | ATGGC others(5242): Show |
chr9 | 128942699 | 129012096 | ||
| a0003c0006 | 0/0 | 5247 | 4 | 4 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | ATGGC others(5242): Show |
chr9 | 128942699 | 129012096 | ||
| a0004c0010 | 0/0 | 5247 | 2 | 0 | 2 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | ATGGC others(5242): Show |
chr9 | 128942699 | 129012096 | ||
| a0005c0011 | 0/0 | 5247 | 1 | 0 | 0 | 0 | 1 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | ATGGC others(5242): Show |
chr9 | 128942699 | 129012096 | ||
| a0006c0026 | 0/0 | 5247 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | ATGGC others(5242): Show |
chr9 | 128942699 | 129012096 | ||
| a0007c0015 | 0/0 | 5247 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | ATGGC others(5242): Show |
chr9 | 128942699 | 129012096 | ||
| a0008c0022 | 0/0 | 5247 | 1 | 0 | 0 | 0 | 1 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | ATGGC others(5242): Show |
chr9 | 128942699 | 129012096 | ||
| a0009c0018 | 0/0 | 5247 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | ATGGC others(5242): Show |
chr9 | 128942699 | 129012096 | ||
| a0010c0024 | 0/0 | 5247 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | ATGGC others(5242): Show |
chr9 | 128942699 | 129012096 | ||
| a0011c0030 | 0/0 | 5247 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | ATGGC others(5242): Show |
chr9 | 128942699 | 129012096 | ||
| a0012c0016 | 0/0 | 5247 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | ATGGC others(5242): Show |
chr9 | 128942699 | 129012096 | ||
| a0013c0019 | 0/0 | 5247 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | ATGGC others(5242): Show |
chr9 | 128942699 | 129012096 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 5689 | 129 | 30 | 24 | 53 | 6 | 15 | NUP188_chr9_128942699_129012096 | NUP188 | AGGGC others(5684): Show |
chr9 | 128942699 | 129012096 |
| a0001c0001t0003 | 0/0 | 5689 | 3 | 0 | 0 | 0 | 0 | 3 | NUP188_chr9_128942699_129012096 | NUP188 | AGGGC others(5684): Show |
chr9 | 128942699 | 129012096 |
| a0001c0001t0004 | 0/0 | 5689 | 2 | 2 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | AGGGC others(5684): Show |
chr9 | 128942699 | 129012096 |
| a0001c0001t0005 | 0/0 | 5689 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | AGGGC others(5684): Show |
chr9 | 128942699 | 129012096 |
| a0001c0001t0006 | 0/0 | 5689 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | AGGGC others(5684): Show |
chr9 | 128942699 | 129012096 |
| a0001c0001t0007 | 0/0 | 5689 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | AGGGC others(5684): Show |
chr9 | 128942699 | 129012096 |
| a0001c0002t0001 | 0/1 | 5689 | 98 | 17 | 27 | 38 | 6 | 9 | NUP188_chr9_128942699_129012096 | NUP188 | AGGGC others(5684): Show |
chr9 | 128942699 | 129012096 |
| a0001c0003t0002 | 0/0 | 5689 | 13 | 0 | 0 | 12 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | AGGGC others(5684): Show |
chr9 | 128942699 | 129012096 |
| a0001c0003t0009 | 0/0 | 5689 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | AGGGC others(5684): Show |
chr9 | 128942699 | 129012096 |
| a0001c0004t0001 | 0/0 | 5689 | 9 | 8 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | AGGGC others(5684): Show |
chr9 | 128942699 | 129012096 |
| a0001c0004t0008 | 0/0 | 5689 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | AGGGC others(5684): Show |
chr9 | 128942699 | 129012096 |
| a0001c0007t0001 | 0/0 | 5689 | 2 | 2 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | AGGGC others(5684): Show |
chr9 | 128942699 | 129012096 |
| a0001c0008t0001 | 0/0 | 5689 | 2 | 2 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | AGGGC others(5684): Show |
chr9 | 128942699 | 129012096 |
| a0001c0009t0001 | 0/0 | 5689 | 2 | 2 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | AGGGC others(5684): Show |
chr9 | 128942699 | 129012096 |
| a0001c0013t0001 | 0/0 | 5689 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | AGGGC others(5684): Show |
chr9 | 128942699 | 129012096 |
| a0001c0014t0001 | 0/0 | 5689 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | AGGGC others(5684): Show |
chr9 | 128942699 | 129012096 |
| a0001c0017t0001 | 0/0 | 5689 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | AGGGC others(5684): Show |
chr9 | 128942699 | 129012096 |
| a0001c0020t0001 | 0/0 | 5689 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | AGGGC others(5684): Show |
chr9 | 128942699 | 129012096 |
| a0001c0021t0001 | 0/0 | 5689 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | AGGGC others(5684): Show |
chr9 | 128942699 | 129012096 |
| a0001c0023t0001 | 0/0 | 5689 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | AGGGC others(5684): Show |
chr9 | 128942699 | 129012096 |
| a0001c0025t0001 | 0/0 | 5689 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | AGGGC others(5684): Show |
chr9 | 128942699 | 129012096 |
| a0001c0027t0001 | 0/0 | 5689 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | AGGGC others(5684): Show |
chr9 | 128942699 | 129012096 |
| a0001c0028t0001 | 0/0 | 5689 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | AGGGC others(5684): Show |
chr9 | 128942699 | 129012096 |
| a0001c0029t0001 | 0/0 | 5689 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | AGGGC others(5684): Show |
chr9 | 128942699 | 129012096 |
| a0002c0005t0001 | 0/0 | 5689 | 5 | 5 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | AGGGC others(5684): Show |
chr9 | 128942699 | 129012096 |
| a0002c0012t0001 | 0/0 | 5689 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | AGGGC others(5684): Show |
chr9 | 128942699 | 129012096 |
| a0003c0006t0001 | 0/0 | 5689 | 4 | 4 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | AGGGC others(5684): Show |
chr9 | 128942699 | 129012096 |
| a0004c0010t0001 | 0/0 | 5689 | 2 | 0 | 2 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | AGGGC others(5684): Show |
chr9 | 128942699 | 129012096 |
| a0005c0011t0001 | 0/0 | 5689 | 1 | 0 | 0 | 0 | 1 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | AGGGC others(5684): Show |
chr9 | 128942699 | 129012096 |
| a0006c0026t0001 | 0/0 | 5689 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | AGGGC others(5684): Show |
chr9 | 128942699 | 129012096 |
| a0007c0015t0001 | 0/0 | 5689 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | AGGGC others(5684): Show |
chr9 | 128942699 | 129012096 |
| a0008c0022t0001 | 0/0 | 5689 | 1 | 0 | 0 | 0 | 1 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | AGGGC others(5684): Show |
chr9 | 128942699 | 129012096 |
| a0009c0018t0001 | 0/0 | 5689 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | AGGGC others(5684): Show |
chr9 | 128942699 | 129012096 |
| a0010c0024t0001 | 0/0 | 5689 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | AGGGC others(5684): Show |
chr9 | 128942699 | 129012096 |
| a0011c0030t0001 | 0/0 | 5689 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | AGGGC others(5684): Show |
chr9 | 128942699 | 129012096 |
| a0012c0016t0001 | 0/0 | 5689 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | AGGGC others(5684): Show |
chr9 | 128942699 | 129012096 |
| a0013c0019t0001 | 0/0 | 5689 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | AGGGC others(5684): Show |
chr9 | 128942699 | 129012096 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0065 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0003g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0004g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0004g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0005g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0006g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0001t0007g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0231 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0002t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0003t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0003t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0003t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0003t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0003t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0003t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0003t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0003t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0003t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0003t0002g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0003t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0003t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0003t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0003t0009g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0004t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0004t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0004t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0004t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0004t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0004t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0004t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0004t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0004t0008g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0007t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0007t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0008t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0008t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0009t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0009t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0013t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0014t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0017t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0020t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0021t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0023t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0025t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0027t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0028t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0001c0029t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0002c0005t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0002c0005t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0002c0005t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0002c0005t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0002c0005t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0002c0012t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0003c0006t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0003c0006t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0003c0006t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0004c0010t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0004c0010t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0005c0011t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0006c0026t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0007c0015t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0008c0022t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0009c0018t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0010c0024t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0011c0030t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0012c0016t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| a0013c0019t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0226 | EUR | GBR | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0127 | EUR | GBR | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG00140 | hp1 | a0001 | c0002 | t0001 | g0235 | EUR | GBR | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG00140 | hp2 | a0005 | c0011 | t0001 | g0152 | EUR | GBR | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0110 | EUR | FIN | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG00280 | hp2 | a0001 | c0002 | t0001 | g0033 | EUR | FIN | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | CHS | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | CHS | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG00438 | hp1 | a0001 | c0002 | t0001 | g0220 | EAS | CHS | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0237 | EAS | CHS | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | CHS | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG00597 | hp1 | a0006 | c0026 | t0001 | g0116 | EAS | CHS | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | CHS | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG00642 | hp2 | a0004 | c0010 | t0001 | g0234 | AMR | PUR | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | CHS | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | CHS | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG00735 | hp1 | a0001 | c0013 | t0001 | g0199 | AMR | PUR | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG00738 | hp1 | a0001 | c0002 | t0001 | g0048 | AMR | PUR | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG00738 | hp2 | a0001 | c0002 | t0001 | g0219 | AMR | PUR | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG00741 | hp1 | a0001 | c0002 | t0001 | g0242 | AMR | PUR | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0067 | AMR | PUR | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG01069 | hp1 | a0001 | c0002 | t0001 | g0244 | AMR | PUR | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG01074 | hp1 | a0001 | c0002 | t0001 | g0099 | AMR | PUR | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG01099 | hp1 | a0001 | c0004 | t0001 | g0255 | AMR | PUR | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0240 | AMR | PUR | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG01167 | hp1 | a0002 | c0012 | t0001 | g0289 | AMR | PUR | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG01167 | hp2 | a0001 | c0002 | t0001 | g0177 | AMR | PUR | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0188 | AMR | PUR | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0215 | AMR | PUR | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0243 | AMR | PUR | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG01243 | hp2 | a0001 | c0021 | t0001 | g0135 | AMR | PUR | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0193 | AMR | CLM | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0027 | AMR | CLM | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | CLM | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG01256 | hp2 | a0004 | c0010 | t0001 | g0169 | AMR | CLM | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG01257 | hp1 | a0001 | c0002 | t0001 | g0024 | AMR | CLM | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG01257 | hp2 | a0001 | c0002 | t0001 | g0186 | AMR | CLM | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG01261 | hp1 | a0001 | c0002 | t0001 | g0209 | AMR | CLM | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | CLM | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG01346 | hp1 | a0007 | c0015 | t0001 | g0165 | AMR | CLM | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG01346 | hp2 | a0001 | c0002 | t0001 | g0224 | AMR | CLM | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | CLM | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | CLM | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0080 | AMR | CLM | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG01433 | hp2 | a0001 | c0020 | t0001 | g0085 | AMR | CLM | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0260 | AMR | CLM | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | CLM | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0112 | EUR | IBS | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0118 | EUR | IBS | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG01516 | hp1 | a0001 | c0002 | t0001 | g0189 | EUR | IBS | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG01516 | hp2 | a0008 | c0022 | t0001 | g0156 | EUR | IBS | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG01517 | hp1 | a0001 | c0002 | t0001 | g0191 | EUR | IBS | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0113 | EUR | IBS | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG01928 | hp1 | a0001 | c0002 | t0001 | g0214 | AMR | PEL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG01934 | hp1 | a0001 | c0002 | t0001 | g0236 | AMR | PEL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PEL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG01952 | hp1 | a0001 | c0002 | t0001 | g0225 | AMR | PEL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PEL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PEL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PEL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PEL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0206 | AMR | PEL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG02015 | hp1 | a0001 | c0002 | t0001 | g0175 | EAS | KHV | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | KHV | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG02027 | hp1 | a0001 | c0003 | t0002 | g0279 | EAS | KHV | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG02040 | hp1 | a0001 | c0002 | t0001 | g0020 | EAS | KHV | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG02040 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | KHV | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG02056 | hp2 | a0001 | c0002 | t0001 | g0196 | EAS | KHV | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | KHV | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0198 | EAS | KHV | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | KHV | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG02145 | hp1 | a0001 | c0002 | t0001 | g0246 | AFR | ACB | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | ACB | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | CDX | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0182 | EAS | CDX | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0223 | AFR | ACB | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | ACB | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG02258 | hp1 | a0001 | c0002 | t0001 | g0176 | AFR | ACB | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG02258 | hp2 | a0001 | c0004 | t0001 | g0253 | AFR | ACB | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG02273 | hp1 | a0001 | c0002 | t0001 | g0216 | AMR | PEL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG02273 | hp2 | a0001 | c0002 | t0001 | g0259 | AMR | PEL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | ACB | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG02280 | hp2 | a0001 | c0004 | t0008 | g0254 | AFR | ACB | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG02293 | hp1 | a0001 | c0002 | t0001 | g0171 | AMR | PEL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG02293 | hp2 | a0001 | c0002 | t0001 | g0258 | AMR | PEL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG02300 | hp1 | a0001 | c0025 | t0001 | g0197 | AMR | PEL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PEL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG02451 | hp1 | a0001 | c0009 | t0001 | g0265 | AFR | ACB | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG02451 | hp2 | a0002 | c0005 | t0001 | g0292 | AFR | ACB | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG02523 | hp1 | a0001 | c0002 | t0001 | g0021 | EAS | KHV | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0174 | EAS | KHV | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG02602 | hp2 | a0009 | c0018 | t0001 | g0089 | SAS | PJL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG02615 | hp1 | a0002 | c0005 | t0001 | g0293 | AFR | GWD | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG02622 | hp1 | a0001 | c0002 | t0001 | g0233 | AFR | GWD | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG02630 | hp1 | a0001 | c0007 | t0001 | g0261 | AFR | GWD | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG02647 | hp2 | a0001 | c0002 | t0001 | g0269 | AFR | GWD | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG02683 | hp1 | a0001 | c0002 | t0001 | g0208 | SAS | PJL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG02683 | hp2 | a0001 | c0001 | t0005 | g0064 | SAS | PJL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG02717 | hp2 | a0001 | c0008 | t0001 | g0161 | AFR | GWD | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG02886 | hp2 | a0001 | c0004 | t0001 | g0003 | AFR | GWD | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG02895 | hp2 | a0001 | c0002 | t0001 | g0264 | AFR | GWD | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG02896 | hp1 | a0001 | c0002 | t0001 | g0218 | AFR | GWD | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0286 | AFR | GWD | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG02897 | hp2 | a0001 | c0001 | t0004 | g0285 | AFR | GWD | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG02965 | hp2 | a0001 | c0004 | t0001 | g0247 | AFR | ESN | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG02970 | hp1 | a0001 | c0002 | t0001 | g0241 | AFR | ESN | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG02970 | hp2 | a0001 | c0002 | t0001 | g0267 | AFR | ESN | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | ESN | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG02976 | hp2 | a0001 | c0004 | t0001 | g0256 | AFR | ESN | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG03017 | hp1 | a0001 | c0001 | t0007 | g0088 | SAS | PJL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0190 | SAS | PJL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG03041 | hp1 | a0010 | c0024 | t0001 | g0250 | AFR | GWD | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG03041 | hp2 | a0002 | c0005 | t0001 | g0291 | AFR | GWD | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG03098 | hp1 | a0001 | c0007 | t0001 | g0123 | AFR | MSL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | MSL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG03130 | hp1 | a0001 | c0009 | t0001 | g0266 | AFR | ESN | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG03139 | hp1 | a0001 | c0008 | t0001 | g0137 | AFR | ESN | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG03139 | hp2 | a0001 | c0002 | t0001 | g0252 | AFR | ESN | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | ESN | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG03195 | hp2 | a0001 | c0004 | t0001 | g0251 | AFR | ESN | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | MSL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG03209 | hp2 | a0001 | c0002 | t0001 | g0217 | AFR | MSL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | MSL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG03225 | hp2 | a0002 | c0005 | t0001 | g0288 | AFR | MSL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG03453 | hp1 | a0003 | c0006 | t0001 | g0071 | AFR | MSL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG03453 | hp2 | a0001 | c0002 | t0001 | g0228 | AFR | MSL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG03486 | hp1 | a0001 | c0004 | t0001 | g0003 | AFR | MSL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG03486 | hp2 | a0003 | c0006 | t0001 | g0002 | AFR | MSL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0170 | SAS | PJL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0207 | SAS | PJL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG03579 | hp1 | a0001 | c0002 | t0001 | g0263 | AFR | MSL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG03579 | hp2 | a0003 | c0006 | t0001 | g0160 | AFR | MSL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG03654 | hp2 | a0011 | c0030 | t0001 | g0150 | SAS | PJL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG03688 | hp1 | a0012 | c0016 | t0001 | g0230 | SAS | STU | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | STU | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0205 | SAS | PJL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0032 | SAS | PJL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0130 | SAS | BEB | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG03834 | hp2 | a0001 | c0003 | t0002 | g0281 | SAS | BEB | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG03942 | hp1 | a0001 | c0002 | t0001 | g0179 | SAS | BEB | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0134 | SAS | BEB | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG04115 | hp1 | a0001 | c0003 | t0009 | g0274 | SAS | STU | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG04115 | hp2 | a0001 | c0002 | t0001 | g0212 | SAS | STU | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | STU | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0239 | SAS | STU | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0238 | SAS | STU | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | STU | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | CHB | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | CHB | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA18941 | hp2 | a0001 | c0003 | t0002 | g0273 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA18943 | hp1 | a0001 | c0002 | t0001 | g0184 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA18943 | hp2 | a0001 | c0002 | t0001 | g0162 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA18946 | hp2 | a0001 | c0002 | t0001 | g0229 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA18951 | hp2 | a0001 | c0003 | t0002 | g0277 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA18954 | hp1 | a0001 | c0001 | t0006 | g0022 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA18954 | hp2 | a0001 | c0002 | t0001 | g0023 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA18962 | hp2 | a0001 | c0023 | t0001 | g0168 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA18964 | hp1 | a0001 | c0002 | t0001 | g0081 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA18966 | hp1 | a0001 | c0002 | t0001 | g0040 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA18968 | hp2 | a0001 | c0017 | t0001 | g0211 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA18975 | hp1 | a0001 | c0003 | t0002 | g0275 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA18975 | hp2 | a0001 | c0002 | t0001 | g0025 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA18979 | hp1 | a0001 | c0002 | t0001 | g0096 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA18982 | hp1 | a0001 | c0002 | t0001 | g0187 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA18983 | hp2 | a0001 | c0002 | t0001 | g0201 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA18984 | hp1 | a0001 | c0002 | t0001 | g0183 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA18984 | hp2 | a0001 | c0002 | t0001 | g0034 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA18985 | hp2 | a0001 | c0003 | t0002 | g0280 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA18986 | hp1 | a0001 | c0003 | t0002 | g0276 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA18987 | hp1 | a0001 | c0029 | t0001 | g0185 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA18999 | hp1 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA18999 | hp2 | a0001 | c0002 | t0001 | g0203 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA19000 | hp2 | a0001 | c0002 | t0001 | g0083 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA19004 | hp1 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA19004 | hp2 | a0001 | c0003 | t0002 | g0282 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA19009 | hp1 | a0001 | c0002 | t0001 | g0202 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA19043 | hp1 | a0001 | c0002 | t0001 | g0210 | AFR | LWK | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA19043 | hp2 | a0001 | c0028 | t0001 | g0257 | AFR | LWK | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA19055 | hp1 | a0001 | c0002 | t0001 | g0222 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA19056 | hp1 | a0013 | c0019 | t0001 | g0092 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA19056 | hp2 | a0001 | c0002 | t0001 | g0178 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA19057 | hp1 | a0001 | c0002 | t0001 | g0172 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA19062 | hp1 | a0001 | c0003 | t0002 | g0272 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA19064 | hp2 | a0001 | c0002 | t0001 | g0192 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA19065 | hp1 | a0001 | c0003 | t0002 | g0271 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA19065 | hp2 | a0001 | c0002 | t0001 | g0195 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA19066 | hp2 | a0001 | c0002 | t0001 | g0245 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA19067 | hp2 | a0001 | c0002 | t0001 | g0232 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA19074 | hp2 | a0001 | c0003 | t0002 | g0278 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA19078 | hp2 | a0001 | c0014 | t0001 | g0180 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA19081 | hp1 | a0001 | c0003 | t0002 | g0284 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA19082 | hp1 | a0001 | c0003 | t0002 | g0283 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA19084 | hp2 | a0001 | c0002 | t0001 | g0227 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA19085 | hp1 | a0001 | c0002 | t0001 | g0181 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA19088 | hp2 | a0001 | c0002 | t0001 | g0213 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA19240 | hp1 | a0003 | c0006 | t0001 | g0002 | AFR | YRI | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA19240 | hp2 | a0001 | c0002 | t0001 | g0008 | AFR | YRI | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | ASW | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA20129 | hp2 | a0001 | c0002 | t0001 | g0194 | AFR | ASW | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0120 | EUR | TSI | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0204 | EUR | TSI | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | GIH | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0049 | SAS | GIH | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0200 | AMR | CLM | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | CLM | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | ACB | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG02109 | hp2 | a0001 | c0004 | t0001 | g0249 | AFR | ACB | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | ACB | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG02559 | hp2 | a0002 | c0005 | t0001 | g0290 | AFR | ACB | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | MSL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | MSL | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG06807 | hp1 | a0001 | c0002 | t0001 | g0268 | AFR | USA | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| HG06807 | hp2 | a0001 | c0027 | t0001 | g0287 | AFR | USA | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA18955 | hp2 | a0001 | c0002 | t0001 | g0173 | EAS | JPT | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA21309 | hp1 | a0001 | c0004 | t0001 | g0248 | AFR | LWK | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0270 | AFR | LWK | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0231 | REF | REF | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0065 | REF | REF | NUP188_chr9_128942699_129012096 | NUP188 | chr9 | 128942699 | 129012096 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:128947736 | G | C | 1 | a0005 | 1 | HG00140.hp2 | missense_variant | MODERATE | c.17G>C | p.Gly6Ala | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 1/44 | 38/5689 | 17/5250 | 6/1749 | chr9 | 128947736 | |||
| chr9:128947738 | G | A | 1 | a0002 | 6 | HG01167.hp1 HG02451.hp2 HG02559.hp2 others(3): Show |
missense_variant | MODERATE | c.19G>A | p.Gly7Arg | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 1/44 | 40/5689 | 19/5250 | 7/1749 | chr9 | 128947738 | |||
| chr9:128956378 | A | G | 1 | a0011 | 1 | HG03654.hp2 | missense_variant | MODERATE | c.190A>G | p.Asn64Asp | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 4/44 | 211/5689 | 190/5250 | 64/1749 | chr9 | 128956378 | |||
| chr9:128979263 | A | G | 1 | a0006 | 1 | HG00597.hp1 | missense_variant&splice_region_variant | MODERATE | c.1205A>G | p.Asp402Gly | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 13/44 | 1226/5689 | 1205/5250 | 402/1749 | chr9 | 128979263 | |||
| chr9:128993282 | T | C | 1 | a0007 | 1 | HG01346.hp1 | missense_variant | MODERATE | c.2726T>C | p.Ile909Thr | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 26/44 | 2747/5689 | 2726/5250 | 909/1749 | chr9 | 128993282 | |||
| chr9:128993643 | A | G | 1 | a0010 | 1 | HG03041.hp1 | missense_variant | MODERATE | c.2966A>G | p.His989Arg | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 27/44 | 2987/5689 | 2966/5250 | 989/1749 | chr9 | 128993643 | |||
| chr9:128998185 | G | A | 1 | a0012 | 1 | HG03688.hp1 | missense_variant | MODERATE | c.3386G>A | p.Arg1129His | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 31/44 | 3407/5689 | 3386/5250 | 1129/1749 | chr9 | 128998185 | |||
| chr9:128999742 | G | T | 1 | a0004 | 2 | HG00642.hp2 HG01256.hp2 |
missense_variant | MODERATE | c.3780G>T | p.Glu1260Asp | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 34/44 | 3801/5689 | 3780/5250 | 1260/1749 | chr9 | 128999742 | |||
| chr9:128999801 | A | G | 1 | a0003 | 4 | HG03453.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
missense_variant | MODERATE | c.3839A>G | p.Asp1280Gly | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 34/44 | 3860/5689 | 3839/5250 | 1280/1749 | chr9 | 128999801 | |||
| chr9:129001595 | C | G | 1 | a0008 | 1 | HG01516.hp2 | missense_variant | MODERATE | c.3910C>G | p.Leu1304Val | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 35/44 | 3931/5689 | 3910/5250 | 1304/1749 | chr9 | 129001595 | |||
| chr9:129001659 | G | A | 1 | a0009 | 1 | HG02602.hp2 | missense_variant | MODERATE | c.3974G>A | p.Arg1325His | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 35/44 | 3995/5689 | 3974/5250 | 1325/1749 | chr9 | 129001659 | |||
| chr9:129002931 | G | A | 1 | a0013 | 1 | NA19056.hp1 | missense_variant | MODERATE | c.4252G>A | p.Glu1418Lys | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 37/44 | 4273/5689 | 4252/5250 | 1418/1749 | chr9 | 129002931 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:128958885 | C | T | 2 | a0001c0029 a0002c0012 |
2 | HG01167.hp1 NA18987.hp1 |
synonymous_variant | LOW | c.456C>T | p.His152His | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 7/44 | 477/5689 | 456/5250 | 152/1749 | chr9 | 128958885 | |||
| chr9:128968607 | C | T | 1 | a0001c0028 | 1 | NA19043.hp2 | synonymous_variant | LOW | c.687C>T | p.Pro229Pro | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 9/44 | 708/5689 | 687/5250 | 229/1749 | chr9 | 128968607 | |||
| chr9:128969439 | C | T | 2 | a0001c0003 a0001c0027 |
15 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(12): Show |
synonymous_variant | LOW | c.837C>T | p.Ile279Ile | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 10/44 | 858/5689 | 837/5250 | 279/1749 | chr9 | 128969439 | |||
| chr9:128984936 | C | A | 1 | a0001c0013 | 1 | HG00735.hp1 | synonymous_variant | LOW | c.1998C>A | p.Leu666Leu | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 20/44 | 2019/5689 | 1998/5250 | 666/1749 | chr9 | 128984936 | |||
| chr9:128986834 | T | C | 2 | a0001c0007 a0001c0008 |
4 | HG02630.hp1 HG02717.hp2 HG03098.hp1 others(1): Show |
synonymous_variant | LOW | c.2223T>C | p.His741His | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 22/44 | 2244/5689 | 2223/5250 | 741/1749 | chr9 | 128986834 | |||
| chr9:128990166 | C | T | 1 | a0001c0025 | 1 | HG02300.hp1 | synonymous_variant | LOW | c.2580C>T | p.Tyr860Tyr | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 25/44 | 2601/5689 | 2580/5250 | 860/1749 | chr9 | 128990166 | |||
| chr9:128993262 | G | A | 1 | a0001c0014 | 1 | NA19078.hp2 | synonymous_variant | LOW | c.2706G>A | p.Leu902Leu | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 26/44 | 2727/5689 | 2706/5250 | 902/1749 | chr9 | 128993262 | |||
| chr9:128993391 | T | C | 1 | a0001c0027 | 1 | HG06807.hp2 | synonymous_variant | LOW | c.2835T>C | p.Ser945Ser | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 26/44 | 2856/5689 | 2835/5250 | 945/1749 | chr9 | 128993391 | |||
| chr9:128993612 | C | T | 3 | a0001c0004 a0001c0028 a0010c0024 |
12 | HG01099.hp1 HG02109.hp2 HG02258.hp2 others(9): Show |
synonymous_variant | LOW | c.2935C>T | p.Leu979Leu | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 27/44 | 2956/5689 | 2935/5250 | 979/1749 | chr9 | 128993612 | |||
| chr9:128995418 | C | T | 2 | a0001c0008 a0001c0023 |
3 | HG02717.hp2 HG03139.hp1 NA18962.hp2 |
synonymous_variant | LOW | c.3255C>T | p.His1085His | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 30/44 | 3276/5689 | 3255/5250 | 1085/1749 | chr9 | 128995418 | |||
| chr9:129001612 | G | A | 1 | a0001c0017 | 1 | NA18968.hp2 | synonymous_variant | LOW | c.3927G>A | p.Arg1309Arg | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 35/44 | 3948/5689 | 3927/5250 | 1309/1749 | chr9 | 129001612 | |||
| chr9:129005389 | A | C | 19 | a0001c0002 a0001c0003 a0001c0004 others(16): Show |
145 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(142): Show |
synonymous_variant | LOW | c.4596A>C | p.Ser1532Ser | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 40/44 | 4617/5689 | 4596/5250 | 1532/1749 | chr9 | 129005389 | |||
| chr9:129006094 | C | T | 1 | a0001c0021 | 1 | HG01243.hp2 | synonymous_variant | LOW | c.4914C>T | p.Ser1638Ser | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 42/44 | 4935/5689 | 4914/5250 | 1638/1749 | chr9 | 129006094 | |||
| chr9:129006507 | G | A | 1 | a0001c0020 | 1 | HG01433.hp2 | synonymous_variant | LOW | c.5079G>A | p.Thr1693Thr | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 44/44 | 5100/5689 | 5079/5250 | 1693/1749 | chr9 | 129006507 | |||
| chr9:129006643 | T | C | 1 | a0001c0009 | 2 | HG02451.hp1 HG03130.hp1 |
synonymous_variant | LOW | c.5215T>C | p.Leu1739Leu | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 44/44 | 5236/5689 | 5215/5250 | 1739/1749 | chr9 | 129006643 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:128947706 | G | A | 1 | a0001c0001t0005 | 1 | HG02683.hp2 | 5_prime_UTR_variant | MODIFIER | c.-14G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 1/44 | 14 | chr9 | 128947706 | ||||||
| chr9:128947707 | C | T | 2 | a0001c0003t0002 a0001c0003t0009 |
14 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(11): Show |
5_prime_UTR_variant | MODIFIER | c.-13C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 1/44 | 13 | chr9 | 128947707 | ||||||
| chr9:129006761 | C | T | 1 | a0001c0004t0008 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*83C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 44/44 | 83 | chr9 | 129006761 | ||||||
| chr9:129006769 | A | G | 1 | a0001c0001t0007 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*91A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 44/44 | 91 | chr9 | 129006769 | ||||||
| chr9:129006798 | C | T | 1 | a0001c0001t0006 | 1 | NA18954.hp1 | 3_prime_UTR_variant | MODIFIER | c.*120C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 44/44 | 120 | chr9 | 129006798 | ||||||
| chr9:129006832 | C | T | 2 | a0001c0003t0002 a0001c0003t0009 |
14 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*154C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 44/44 | 154 | chr9 | 129006832 | ||||||
| chr9:129006881 | A | G | 1 | a0001c0001t0004 | 2 | HG02896.hp2 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*203A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 44/44 | 203 | chr9 | 129006881 | ||||||
| chr9:129006964 | G | A | 1 | a0001c0001t0003 | 3 | HG03710.hp2 HG03834.hp1 HG03942.hp2 |
3_prime_UTR_variant | MODIFIER | c.*286G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 44/44 | 286 | chr9 | 129006964 | ||||||
| chr9:129006972 | G | T | 1 | a0001c0003t0009 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*294G>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 44/44 | 294 | chr9 | 129006972 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:128947846 | A | G | 31 | a0001c0001t0001g0270 a0001c0001t0004g0285 a0001c0001t0004g0286 others(28): Show |
31 | HG01167.hp1 HG02027.hp1 HG02451.hp1 others(28): Show |
intron_variant | MODIFIER | c.32+95A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 1/43 | chr9 | 128947846 | |||||||
| chr9:128947888 | G | A | 6 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(3): Show |
6 | HG01891.hp2 HG02055.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.32+137G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 1/43 | chr9 | 128947888 | |||||||
| chr9:128947907 | A | G | 3 | a0001c0001t0001g0260 a0001c0001t0001g0262 a0001c0007t0001g0261 |
3 | HG01496.hp1 HG02559.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.32+156A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 1/43 | chr9 | 128947907 | |||||||
| chr9:128948062 | C | T | 6 | a0002c0005t0001g0288 a0002c0005t0001g0290 a0002c0005t0001g0291 others(3): Show |
6 | HG01167.hp1 HG02451.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.32+311C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 1/43 | chr9 | 128948062 | |||||||
| chr9:128948127 | C | A | 13 | a0001c0002t0001g0263 a0001c0002t0001g0264 a0001c0002t0001g0267 others(10): Show |
13 | HG01167.hp1 HG02451.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.32+376C>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 1/43 | chr9 | 128948127 | |||||||
| chr9:128948272 | C | G | 2 | a0001c0002t0001g0258 a0001c0002t0001g0259 |
2 | HG02273.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.32+521C>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 1/43 | chr9 | 128948272 | |||||||
| chr9:128948530 | C | G | 1 | a0001c0027t0001g0287 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.33-659C>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 1/43 | chr9 | 128948530 | |||||||
| chr9:128948553 | A | G | 2 | a0001c0001t0004g0285 a0001c0001t0004g0286 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.33-636A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 1/43 | chr9 | 128948553 | |||||||
| chr9:128948555 | C | T | 12 | a0001c0002t0001g0252 a0001c0004t0001g0003 a0001c0004t0001g0247 others(9): Show |
13 | HG01099.hp1 HG02109.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.33-634C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 1/43 | chr9 | 128948555 | |||||||
| chr9:128948568 | A | G | 120 | a0001c0001t0001g0221 a0001c0001t0004g0285 a0001c0001t0004g0286 others(117): Show |
121 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.33-621A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 1/43 | chr9 | 128948568 | |||||||
| chr9:128948630 | T | C | 14 | a0001c0003t0002g0271 a0001c0003t0002g0272 a0001c0003t0002g0273 others(11): Show |
14 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(11): Show |
intron_variant | MODIFIER | c.33-559T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 1/43 | chr9 | 128948630 | |||||||
| chr9:128948673 | G | T | 1 | a0001c0027t0001g0287 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.33-516G>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 1/43 | chr9 | 128948673 | |||||||
| chr9:128948711 | C | CT | 74 | a0001c0001t0001g0009 a0001c0001t0001g0094 a0001c0001t0001g0095 others(71): Show |
74 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.33-446dupT | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr9 | 128948711 | ||||||
| chr9:128948711 | C | CTT | 23 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0155 others(20): Show |
24 | HG00423.hp2 HG00642.hp1 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.33-447_33-446dupTT | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr9 | 128948711 | ||||||
| chr9:128948711 | CT | C | 73 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(70): Show |
74 | HG00280.hp2 HG00558.hp2 HG00735.hp1 others(71): Show |
intron_variant | MODIFIER | c.33-446delT | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr9 | 128948711 | ||||||
| chr9:128948711 | CTT | C | 9 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0014 others(6): Show |
9 | HG01256.hp2 HG02040.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.33-447_33-446delTT | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr9 | 128948711 | ||||||
| chr9:128948711 | CTTTTTT | C | 7 | a0001c0002t0001g0252 a0001c0004t0001g0003 a0001c0004t0001g0247 others(4): Show |
8 | HG02109.hp2 HG02886.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.33-451_33-446delTT others(4): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr9 | 128948711 | ||||||
| chr9:128948711 | CTTTTTTT others(2): Show |
C | 13 | a0001c0002t0001g0263 a0001c0002t0001g0264 a0001c0002t0001g0267 others(10): Show |
13 | HG01167.hp1 HG02451.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.33-454_33-446delTT others(7): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr9 | 128948711 | ||||||
| chr9:128948711 | CTTTTTTT others(3): Show |
C | 1 | a0001c0027t0001g0287 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.33-455_33-446delTT others(8): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr9 | 128948711 | ||||||
| chr9:128948711 | CTTTTTTT others(8): Show |
C | 2 | a0001c0001t0004g0285 a0001c0001t0004g0286 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.33-460_33-446delTT others(13): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr9 | 128948711 | ||||||
| chr9:128948800 | A | T | 1 | a0001c0001t0001g0035 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.33-389A>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 1/43 | chr9 | 128948800 | |||||||
| chr9:128949039 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.33-150A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 1/43 | chr9 | 128949039 | |||||||
| chr9:128949098 | C | T | 1 | a0005c0011t0001g0152 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.33-91C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 1/43 | chr9 | 128949098 | |||||||
| chr9:128949257 | T | G | 14 | a0001c0003t0002g0271 a0001c0003t0002g0272 a0001c0003t0002g0273 others(11): Show |
14 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(11): Show |
intron_variant | MODIFIER | c.87+14T>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 2/43 | chr9 | 128949257 | |||||||
| chr9:128949300 | C | CA | 5 | a0001c0001t0001g0036 a0001c0001t0001g0094 a0001c0001t0001g0153 others(2): Show |
5 | HG02293.hp1 HG03225.hp1 NA18985.hp1 others(2): Show |
intron_variant | MODIFIER | c.87+65dupA | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 2/43 | INFO_REALIGN_3_PRIME | chr9 | 128949300 | ||||||
| chr9:128949519 | A | G | 1 | a0001c0002t0001g0240 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.87+276A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 2/43 | chr9 | 128949519 | |||||||
| chr9:128949900 | A | G | 14 | a0001c0003t0002g0271 a0001c0003t0002g0272 a0001c0003t0002g0273 others(11): Show |
14 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(11): Show |
intron_variant | MODIFIER | c.87+657A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 2/43 | chr9 | 128949900 | |||||||
| chr9:128949919 | C | CT | 14 | a0001c0001t0001g0036 a0001c0001t0001g0090 a0001c0001t0001g0091 others(11): Show |
14 | HG01175.hp2 HG01346.hp1 HG01952.hp2 others(11): Show |
intron_variant | MODIFIER | c.87+701dupT | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 2/43 | INFO_REALIGN_3_PRIME | chr9 | 128949919 | ||||||
| chr9:128949919 | CT | C | 137 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(134): Show |
139 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.87+701delT | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 2/43 | INFO_REALIGN_3_PRIME | chr9 | 128949919 | ||||||
| chr9:128950085 | G | A | 1 | a0001c0001t0001g0057 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.87+842G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 2/43 | chr9 | 128950085 | |||||||
| chr9:128950684 | T | A | 2 | a0001c0001t0001g0037 a0001c0001t0001g0095 |
2 | HG00673.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.87+1441T>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 2/43 | chr9 | 128950684 | |||||||
| chr9:128950689 | T | A | 12 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(9): Show |
13 | HG00558.hp2 HG00673.hp1 HG02080.hp1 others(10): Show |
intron_variant | MODIFIER | c.87+1446T>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 2/43 | chr9 | 128950689 | |||||||
| chr9:128950812 | C | T | 1 | a0001c0002t0001g0218 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.87+1569C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 2/43 | chr9 | 128950812 | |||||||
| chr9:128950822 | G | A | 1 | a0001c0002t0001g0269 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.87+1579G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 2/43 | chr9 | 128950822 | |||||||
| chr9:128950988 | G | C | 2 | a0001c0001t0004g0285 a0001c0001t0004g0286 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.87+1745G>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 2/43 | chr9 | 128950988 | |||||||
| chr9:128951028 | T | C | 2 | a0001c0001t0004g0285 a0001c0001t0004g0286 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.88-1745T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 2/43 | chr9 | 128951028 | |||||||
| chr9:128951200 | C | T | 6 | a0001c0001t0001g0147 a0002c0005t0001g0290 a0002c0005t0001g0291 others(3): Show |
6 | HG01167.hp1 HG02451.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.88-1573C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 2/43 | chr9 | 128951200 | |||||||
| chr9:128951306 | C | CA | 6 | a0001c0001t0001g0059 a0001c0001t0001g0260 a0001c0001t0001g0262 others(3): Show |
6 | HG01496.hp1 HG02040.hp1 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.88-1447dupA | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 2/43 | INFO_REALIGN_3_PRIME | chr9 | 128951306 | ||||||
| chr9:128951306 | CA | C | 107 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0056 others(104): Show |
108 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.88-1447delA | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 2/43 | INFO_REALIGN_3_PRIME | chr9 | 128951306 | ||||||
| chr9:128951306 | CAA | C | 16 | a0001c0003t0002g0271 a0001c0003t0002g0272 a0001c0003t0002g0273 others(13): Show |
16 | HG02027.hp1 HG03195.hp2 HG03834.hp2 others(13): Show |
intron_variant | MODIFIER | c.88-1448_88-1447del others(2): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 2/43 | INFO_REALIGN_3_PRIME | chr9 | 128951306 | ||||||
| chr9:128951439 | A | G | 1 | a0001c0027t0001g0287 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.88-1334A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 2/43 | chr9 | 128951439 | |||||||
| chr9:128951477 | T | C | 3 | a0001c0004t0001g0253 a0001c0004t0001g0255 a0001c0004t0008g0254 |
3 | HG01099.hp1 HG02258.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.88-1296T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 2/43 | chr9 | 128951477 | |||||||
| chr9:128951517 | T | A | 2 | a0001c0001t0001g0060 a0009c0018t0001g0089 |
2 | HG01496.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.88-1256T>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 2/43 | chr9 | 128951517 | |||||||
| chr9:128951597 | A | G | 3 | a0001c0001t0001g0060 a0001c0001t0001g0087 a0009c0018t0001g0089 |
3 | HG01069.hp2 HG01496.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.88-1176A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 2/43 | chr9 | 128951597 | |||||||
| chr9:128951670 | T | C | 1 | a0001c0002t0001g0021 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.88-1103T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 2/43 | chr9 | 128951670 | |||||||
| chr9:128951683 | A | G | 2 | a0001c0001t0004g0285 a0001c0001t0004g0286 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.88-1090A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 2/43 | chr9 | 128951683 | |||||||
| chr9:128951789 | T | G | 1 | a0001c0002t0001g0252 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.88-984T>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 2/43 | chr9 | 128951789 | |||||||
| chr9:128951791 | AT | A | 35 | a0001c0001t0001g0029 a0001c0001t0001g0104 a0001c0001t0001g0105 others(32): Show |
35 | HG01167.hp1 HG02027.hp1 HG02451.hp1 others(32): Show |
intron_variant | MODIFIER | c.88-964delT | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 2/43 | INFO_REALIGN_3_PRIME | chr9 | 128951791 | ||||||
| chr9:128951793 | T | C | 2 | a0001c0001t0004g0285 a0001c0001t0004g0286 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.88-980T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 2/43 | chr9 | 128951793 | |||||||
| chr9:128951814 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.88-959C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 2/43 | chr9 | 128951814 | |||||||
| chr9:128951917 | C | T | 1 | a0001c0001t0001g0102 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.88-856C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 2/43 | chr9 | 128951917 | |||||||
| chr9:128952044 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.88-729C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 2/43 | chr9 | 128952044 | |||||||
| chr9:128952073 | C | G | 16 | a0001c0001t0004g0285 a0001c0001t0004g0286 a0001c0003t0002g0271 others(13): Show |
16 | HG02027.hp1 HG02896.hp2 HG02897.hp2 others(13): Show |
intron_variant | MODIFIER | c.88-700C>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 2/43 | chr9 | 128952073 | |||||||
| chr9:128952084 | T | C | 2 | a0001c0001t0001g0061 a0001c0001t0001g0086 |
2 | HG02698.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.88-689T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 2/43 | chr9 | 128952084 | |||||||
| chr9:128952085 | G | T | 2 | a0001c0001t0004g0285 a0001c0001t0004g0286 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.88-688G>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 2/43 | chr9 | 128952085 | |||||||
| chr9:128952184 | T | G | 2 | a0001c0001t0004g0285 a0001c0001t0004g0286 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.88-589T>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 2/43 | chr9 | 128952184 | |||||||
| chr9:128952242 | C | CA | 20 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(17): Show |
21 | HG00558.hp2 HG00673.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.88-523dupA | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 2/43 | INFO_REALIGN_3_PRIME | chr9 | 128952242 | ||||||
| chr9:128952393 | C | T | 13 | a0001c0002t0001g0263 a0001c0002t0001g0264 a0001c0002t0001g0267 others(10): Show |
13 | HG01167.hp1 HG02451.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.88-380C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 2/43 | chr9 | 128952393 | |||||||
| chr9:128952398 | CA | C | 11 | a0001c0001t0001g0015 a0001c0001t0001g0140 a0001c0001t0001g0270 others(8): Show |
11 | HG01167.hp1 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.88-357delA | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 2/43 | INFO_REALIGN_3_PRIME | chr9 | 128952398 | ||||||
| chr9:128952461 | G | A | 11 | a0001c0004t0001g0003 a0001c0004t0001g0247 a0001c0004t0001g0248 others(8): Show |
12 | HG01099.hp1 HG02109.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.88-312G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 2/43 | chr9 | 128952461 | |||||||
| chr9:128952469 | T | C | 3 | a0001c0002t0001g0241 a0001c0002t0001g0244 a0001c0002t0001g0246 |
3 | HG01069.hp1 HG02145.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.88-304T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 2/43 | chr9 | 128952469 | |||||||
| chr9:128952496 | G | T | 1 | a0001c0004t0001g0255 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.88-277G>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 2/43 | chr9 | 128952496 | |||||||
| chr9:128952722 | C | CA | 7 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0004g0285 others(4): Show |
7 | HG02015.hp1 HG02055.hp1 HG02523.hp2 others(4): Show |
intron_variant | MODIFIER | c.88-36dupA | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 2/43 | INFO_REALIGN_3_PRIME | chr9 | 128952722 | ||||||
| chr9:128953108 | A | G | 1 | a0001c0002t0001g0020 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.161+262A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | chr9 | 128953108 | |||||||
| chr9:128953393 | G | A | 3 | a0001c0001t0001g0260 a0001c0001t0001g0262 a0001c0007t0001g0261 |
3 | HG01496.hp1 HG02559.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.161+547G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | chr9 | 128953393 | |||||||
| chr9:128953395 | G | T | 3 | a0001c0001t0001g0260 a0001c0001t0001g0262 a0001c0007t0001g0261 |
3 | HG01496.hp1 HG02559.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.161+549G>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | chr9 | 128953395 | |||||||
| chr9:128953564 | C | A | 14 | a0001c0003t0002g0271 a0001c0003t0002g0272 a0001c0003t0002g0273 others(11): Show |
14 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(11): Show |
intron_variant | MODIFIER | c.161+718C>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | chr9 | 128953564 | |||||||
| chr9:128953894 | A | G | 13 | a0001c0002t0001g0263 a0001c0002t0001g0264 a0001c0002t0001g0267 others(10): Show |
13 | HG01167.hp1 HG02451.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.161+1048A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | chr9 | 128953894 | |||||||
| chr9:128953922 | C | T | 1 | a0001c0002t0001g0210 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.161+1076C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | chr9 | 128953922 | |||||||
| chr9:128953986 | C | T | 76 | a0001c0001t0001g0221 a0001c0002t0001g0170 a0001c0002t0001g0171 others(73): Show |
76 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.161+1140C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | chr9 | 128953986 | |||||||
| chr9:128954249 | TTGTGGCC others(163): Show |
T | 3 | a0001c0002t0001g0096 a0001c0002t0001g0263 a0001c0002t0001g0264 |
3 | HG02895.hp2 HG03579.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.161+1501_161+1670d others(2): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | INFO_REALIGN_3_PRIME | chr9 | 128954249 | ||||||
| chr9:128954362 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.161+1516C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | chr9 | 128954362 | |||||||
| chr9:128954383 | C | CT | 11 | a0001c0001t0001g0016 a0001c0001t0001g0058 a0001c0001t0001g0117 others(8): Show |
11 | HG01261.hp1 HG02280.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.161+1556dupT | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | INFO_REALIGN_3_PRIME | chr9 | 128954383 | ||||||
| chr9:128954383 | CT | C | 7 | a0001c0001t0001g0125 a0001c0002t0001g0172 a0001c0002t0001g0217 others(4): Show |
7 | HG01069.hp1 HG02145.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.161+1556delT | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | INFO_REALIGN_3_PRIME | chr9 | 128954383 | ||||||
| chr9:128954406 | A | G | 2 | a0001c0001t0004g0285 a0001c0001t0004g0286 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.161+1560A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | chr9 | 128954406 | |||||||
| chr9:128954474 | T | A | 1 | a0001c0001t0001g0041 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.161+1628T>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | chr9 | 128954474 | |||||||
| chr9:128954517 | A | G | 5 | a0002c0005t0001g0290 a0002c0005t0001g0291 a0002c0005t0001g0292 others(2): Show |
5 | HG01167.hp1 HG02451.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.161+1671A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | chr9 | 128954517 | |||||||
| chr9:128954528 | G | T | 1 | a0001c0002t0001g0240 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.161+1682G>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | chr9 | 128954528 | |||||||
| chr9:128954576 | G | C | 1 | a0001c0001t0001g0109 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.161+1730G>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | chr9 | 128954576 | |||||||
| chr9:128954650 | C | T | 1 | a0001c0002t0001g0209 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.162-1700C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | chr9 | 128954650 | |||||||
| chr9:128954662 | G | A | 13 | a0001c0002t0001g0263 a0001c0002t0001g0264 a0001c0002t0001g0267 others(10): Show |
13 | HG01167.hp1 HG02451.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.162-1688G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | chr9 | 128954662 | |||||||
| chr9:128954902 | C | T | 3 | a0001c0001t0001g0139 a0001c0001t0001g0146 a0001c0001t0001g0163 |
3 | HG02145.hp2 HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.162-1448C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | chr9 | 128954902 | |||||||
| chr9:128954905 | G | A | 2 | a0001c0009t0001g0265 a0001c0009t0001g0266 |
2 | HG02451.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.162-1445G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | chr9 | 128954905 | |||||||
| chr9:128954910 | A | G | 120 | a0001c0001t0001g0221 a0001c0001t0004g0285 a0001c0001t0004g0286 others(117): Show |
121 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.162-1440A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | chr9 | 128954910 | |||||||
| chr9:128954913 | G | GTGCGATT others(9): Show |
1 | a0001c0002t0001g0027 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.162-1433_162-1418d others(18): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | INFO_REALIGN_3_PRIME | chr9 | 128954913 | ||||||
| chr9:128954938 | T | C | 120 | a0001c0001t0001g0221 a0001c0001t0004g0285 a0001c0001t0004g0286 others(117): Show |
121 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.162-1412T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | chr9 | 128954938 | |||||||
| chr9:128954950 | T | C | 14 | a0001c0003t0002g0271 a0001c0003t0002g0272 a0001c0003t0002g0273 others(11): Show |
14 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(11): Show |
intron_variant | MODIFIER | c.162-1400T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | chr9 | 128954950 | |||||||
| chr9:128955097 | C | T | 14 | a0001c0003t0002g0271 a0001c0003t0002g0272 a0001c0003t0002g0273 others(11): Show |
14 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(11): Show |
intron_variant | MODIFIER | c.162-1253C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | chr9 | 128955097 | |||||||
| chr9:128955125 | A | G | 1 | a0001c0002t0001g0264 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.162-1225A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | chr9 | 128955125 | |||||||
| chr9:128955158 | C | G | 1 | a0001c0027t0001g0287 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.162-1192C>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | chr9 | 128955158 | |||||||
| chr9:128955251 | A | G | 13 | a0001c0002t0001g0263 a0001c0002t0001g0264 a0001c0002t0001g0267 others(10): Show |
13 | HG01167.hp1 HG02451.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.162-1099A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | chr9 | 128955251 | |||||||
| chr9:128955437 | G | A | 2 | a0001c0009t0001g0265 a0001c0009t0001g0266 |
2 | HG02451.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.162-913G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | chr9 | 128955437 | |||||||
| chr9:128955614 | G | A | 14 | a0001c0003t0002g0271 a0001c0003t0002g0272 a0001c0003t0002g0273 others(11): Show |
14 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(11): Show |
intron_variant | MODIFIER | c.162-736G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | chr9 | 128955614 | |||||||
| chr9:128955752 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.162-598C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | chr9 | 128955752 | |||||||
| chr9:128955987 | C | CCTTT | 246 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(243): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.162-361_162-360ins others(4): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | INFO_REALIGN_3_PRIME | chr9 | 128955987 | ||||||
| chr9:128956017 | G | A | 1 | a0001c0002t0001g0220 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.162-333G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | chr9 | 128956017 | |||||||
| chr9:128956075 | A | G | 1 | a0001c0001t0001g0036 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.162-275A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | chr9 | 128956075 | |||||||
| chr9:128956121 | T | G | 1 | a0001c0002t0001g0220 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.162-229T>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | chr9 | 128956121 | |||||||
| chr9:128956182 | G | GGT | 68 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(65): Show |
69 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.162-140_162-139dup others(2): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | INFO_REALIGN_3_PRIME | chr9 | 128956182 | ||||||
| chr9:128956182 | G | GGTGT | 7 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(4): Show |
7 | HG01891.hp2 HG02040.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.162-142_162-139dup others(4): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | INFO_REALIGN_3_PRIME | chr9 | 128956182 | ||||||
| chr9:128956182 | GGT | G | 19 | a0001c0001t0001g0029 a0001c0001t0001g0035 a0001c0001t0001g0054 others(16): Show |
20 | HG01099.hp1 HG01109.hp2 HG01261.hp2 others(17): Show |
intron_variant | MODIFIER | c.162-140_162-139del others(2): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | INFO_REALIGN_3_PRIME | chr9 | 128956182 | ||||||
| chr9:128956182 | GGTGT | G | 3 | a0001c0001t0001g0069 a0001c0002t0001g0240 a0002c0005t0001g0293 |
3 | HG01109.hp1 HG02615.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.162-142_162-139del others(4): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | INFO_REALIGN_3_PRIME | chr9 | 128956182 | ||||||
| chr9:128956182 | GGTGTGT | G | 12 | a0001c0002t0001g0263 a0001c0002t0001g0264 a0001c0002t0001g0267 others(9): Show |
12 | HG01167.hp1 HG02451.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.162-144_162-139del others(6): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | INFO_REALIGN_3_PRIME | chr9 | 128956182 | ||||||
| chr9:128956186 | T | G | 1 | a0001c0028t0001g0257 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.162-164T>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | chr9 | 128956186 | |||||||
| chr9:128956208 | T | C | 3 | a0001c0001t0001g0110 a0001c0001t0004g0285 a0001c0001t0004g0286 |
3 | HG00280.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.162-142T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | chr9 | 128956208 | |||||||
| chr9:128956210 | T | TGC | 67 | a0001c0001t0001g0221 a0001c0002t0001g0171 a0001c0002t0001g0172 others(64): Show |
67 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.162-138_162-137dup others(2): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | INFO_REALIGN_3_PRIME | chr9 | 128956210 | ||||||
| chr9:128956210 | T | TGTGC | 8 | a0001c0002t0001g0170 a0001c0002t0001g0204 a0001c0002t0001g0205 others(5): Show |
8 | HG00738.hp2 HG01243.hp1 HG01993.hp2 others(5): Show |
intron_variant | MODIFIER | c.162-139_162-138ins others(4): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | INFO_REALIGN_3_PRIME | chr9 | 128956210 | ||||||
| chr9:128956214 | T | G | 1 | a0001c0002t0001g0027 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.162-136T>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | chr9 | 128956214 | |||||||
| chr9:128956216 | T | C | 1 | a0001c0002t0001g0240 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.162-134T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 3/43 | chr9 | 128956216 | |||||||
| chr9:128956449 | G | A | 2 | a0001c0001t0001g0061 a0001c0001t0001g0086 |
2 | HG02698.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.246+15G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 4/43 | chr9 | 128956449 | |||||||
| chr9:128956500 | A | C | 1 | a0001c0002t0001g0176 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.246+66A>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 4/43 | chr9 | 128956500 | |||||||
| chr9:128956665 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.246+231C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 4/43 | chr9 | 128956665 | |||||||
| chr9:128956819 | T | C | 2 | a0001c0001t0004g0285 a0001c0001t0004g0286 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.247-133T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 4/43 | chr9 | 128956819 | |||||||
| chr9:128957398 | T | G | 1 | a0001c0001t0001g0030 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.327+366T>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 5/43 | chr9 | 128957398 | |||||||
| chr9:128957527 | T | C | 2 | a0001c0001t0004g0285 a0001c0001t0004g0286 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.328-483T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 5/43 | chr9 | 128957527 | |||||||
| chr9:128957706 | C | T | 1 | a0011c0030t0001g0150 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.328-304C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 5/43 | chr9 | 128957706 | |||||||
| chr9:128958115 | C | T | 2 | a0001c0001t0004g0285 a0001c0001t0004g0286 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.372+61C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 6/43 | chr9 | 128958115 | |||||||
| chr9:128958196 | A | G | 17 | a0001c0001t0004g0285 a0001c0001t0004g0286 a0001c0003t0002g0271 others(14): Show |
17 | HG02027.hp1 HG02896.hp2 HG02897.hp2 others(14): Show |
intron_variant | MODIFIER | c.372+142A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 6/43 | chr9 | 128958196 | |||||||
| chr9:128958406 | T | G | 2 | a0001c0001t0004g0285 a0001c0001t0004g0286 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.372+352T>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 6/43 | chr9 | 128958406 | |||||||
| chr9:128958758 | A | G | 3 | a0001c0001t0001g0139 a0001c0001t0001g0146 a0001c0001t0001g0163 |
3 | HG02145.hp2 HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.373-44A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 6/43 | chr9 | 128958758 | |||||||
| chr9:128959294 | G | A | 2 | a0001c0001t0001g0029 a0001c0001t0001g0105 |
2 | NA18969.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.585+160G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128959294 | |||||||
| chr9:128959384 | C | T | 17 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(14): Show |
18 | HG00558.hp2 HG00673.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.585+250C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128959384 | |||||||
| chr9:128959427 | C | T | 2 | a0001c0001t0004g0285 a0001c0001t0004g0286 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.585+293C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128959427 | |||||||
| chr9:128959439 | G | A | 1 | a0001c0002t0001g0219 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.585+305G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128959439 | |||||||
| chr9:128959527 | C | CT | 16 | a0001c0001t0001g0016 a0001c0001t0001g0052 a0001c0001t0001g0053 others(13): Show |
16 | HG01099.hp1 HG01109.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.585+413dupT | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128959527 | ||||||
| chr9:128959527 | C | CTTTT | 13 | a0001c0003t0002g0271 a0001c0003t0002g0272 a0001c0003t0002g0275 others(10): Show |
13 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(10): Show |
intron_variant | MODIFIER | c.585+410_585+413dup others(4): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128959527 | ||||||
| chr9:128959527 | C | CTTTTTTT others(7): Show |
1 | a0001c0027t0001g0287 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.585+400_585+413dup others(14): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128959527 | ||||||
| chr9:128959527 | C | CTTTTTTT others(8): Show |
1 | a0001c0001t0004g0285 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.585+399_585+413dup others(15): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128959527 | ||||||
| chr9:128959527 | C | CTTTTTTT others(9): Show |
1 | a0001c0001t0004g0286 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.585+398_585+413dup others(16): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128959527 | ||||||
| chr9:128959625 | C | T | 1 | a0001c0001t0001g0066 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.585+491C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128959625 | |||||||
| chr9:128959748 | C | T | 1 | a0001c0001t0001g0066 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.585+614C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128959748 | |||||||
| chr9:128959759 | C | T | 90 | a0001c0001t0001g0221 a0001c0002t0001g0170 a0001c0002t0001g0171 others(87): Show |
91 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.585+625C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128959759 | |||||||
| chr9:128959803 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.585+669G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128959803 | |||||||
| chr9:128959864 | A | G | 3 | a0001c0001t0001g0051 a0001c0001t0001g0101 a0001c0001t0001g0136 |
3 | HG02647.hp1 HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.585+730A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128959864 | |||||||
| chr9:128960059 | C | CT | 27 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0012 others(24): Show |
27 | HG00438.hp1 HG00558.hp1 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.585+947dupT | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128960059 | ||||||
| chr9:128960059 | C | CTT | 13 | a0001c0001t0001g0100 a0001c0002t0001g0040 a0001c0002t0001g0096 others(10): Show |
13 | HG01167.hp1 HG02451.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.585+946_585+947dup others(2): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128960059 | ||||||
| chr9:128960059 | CT | C | 6 | a0001c0001t0001g0121 a0001c0002t0001g0172 a0001c0002t0001g0176 others(3): Show |
6 | HG01167.hp2 HG02258.hp1 NA18941.hp1 others(3): Show |
intron_variant | MODIFIER | c.585+947delT | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128960059 | ||||||
| chr9:128960230 | AT | A | 15 | a0001c0003t0002g0271 a0001c0003t0002g0272 a0001c0003t0002g0273 others(12): Show |
15 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(12): Show |
intron_variant | MODIFIER | c.585+1102delT | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128960230 | ||||||
| chr9:128960259 | G | GT | 11 | a0001c0004t0001g0003 a0001c0004t0001g0247 a0001c0004t0001g0248 others(8): Show |
12 | HG01099.hp1 HG02109.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.585+1134dupT | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128960259 | ||||||
| chr9:128960270 | G | A | 13 | a0001c0002t0001g0263 a0001c0002t0001g0264 a0001c0002t0001g0267 others(10): Show |
13 | HG01167.hp1 HG02451.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.585+1136G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128960270 | |||||||
| chr9:128960310 | A | G | 8 | a0001c0001t0001g0030 a0001c0001t0001g0076 a0001c0001t0001g0077 others(5): Show |
8 | HG00597.hp2 HG01099.hp2 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.585+1176A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128960310 | |||||||
| chr9:128960363 | G | A | 76 | a0001c0001t0001g0221 a0001c0002t0001g0170 a0001c0002t0001g0171 others(73): Show |
76 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.585+1229G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128960363 | |||||||
| chr9:128960376 | A | T | 2 | a0001c0004t0001g0253 a0001c0004t0008g0254 |
2 | HG02258.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.585+1242A>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128960376 | |||||||
| chr9:128960453 | A | C | 1 | a0001c0027t0001g0287 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.585+1319A>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128960453 | |||||||
| chr9:128960616 | G | A | 2 | a0001c0001t0004g0285 a0001c0001t0004g0286 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.585+1482G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128960616 | |||||||
| chr9:128960646 | G | C | 3 | a0001c0001t0001g0149 a0001c0001t0001g0166 a0007c0015t0001g0165 |
3 | HG01175.hp2 HG01346.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.585+1512G>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128960646 | |||||||
| chr9:128960882 | C | G | 1 | a0001c0027t0001g0287 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.585+1748C>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128960882 | |||||||
| chr9:128960888 | C | T | 2 | a0001c0001t0001g0118 a0001c0001t0001g0151 |
2 | HG01515.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.585+1754C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128960888 | |||||||
| chr9:128960912 | T | C | 120 | a0001c0001t0001g0221 a0001c0001t0004g0285 a0001c0001t0004g0286 others(117): Show |
121 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.585+1778T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128960912 | |||||||
| chr9:128960913 | C | T | 14 | a0001c0003t0002g0271 a0001c0003t0002g0272 a0001c0003t0002g0273 others(11): Show |
14 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(11): Show |
intron_variant | MODIFIER | c.585+1779C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128960913 | |||||||
| chr9:128960914 | G | A | 2 | a0001c0001t0004g0285 a0001c0001t0004g0286 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.585+1780G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128960914 | |||||||
| chr9:128961054 | C | T | 3 | a0001c0001t0001g0149 a0001c0001t0001g0166 a0007c0015t0001g0165 |
3 | HG01175.hp2 HG01346.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.585+1920C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128961054 | |||||||
| chr9:128961081 | G | T | 1 | a0001c0001t0001g0053 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.585+1947G>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128961081 | |||||||
| chr9:128961085 | C | CA | 50 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0036 others(47): Show |
50 | HG00140.hp2 HG00423.hp1 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.585+1969dupA | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128961085 | ||||||
| chr9:128961109 | A | G | 1 | a0001c0027t0001g0287 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.585+1975A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128961109 | |||||||
| chr9:128961169 | CA | C | 17 | a0001c0001t0004g0285 a0001c0001t0004g0286 a0001c0003t0002g0271 others(14): Show |
17 | HG02027.hp1 HG02896.hp2 HG02897.hp2 others(14): Show |
intron_variant | MODIFIER | c.585+2046delA | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128961169 | ||||||
| chr9:128961273 | T | G | 2 | a0001c0001t0001g0056 a0001c0001t0001g0103 |
2 | NA18955.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.585+2139T>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128961273 | |||||||
| chr9:128961389 | G | A | 1 | a0001c0008t0001g0137 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.585+2255G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128961389 | |||||||
| chr9:128961512 | AAAAT | A | 14 | a0001c0003t0002g0271 a0001c0003t0002g0272 a0001c0003t0002g0273 others(11): Show |
14 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(11): Show |
intron_variant | MODIFIER | c.585+2401_585+2404d others(6): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128961512 | ||||||
| chr9:128961572 | C | T | 1 | a0001c0001t0001g0132 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.585+2438C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128961572 | |||||||
| chr9:128961582 | C | CTAGATAG others(5): Show |
2 | a0001c0001t0004g0285 a0001c0001t0004g0286 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.585+2450_585+2451i others(14): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128961582 | ||||||
| chr9:128961585 | T | G | 5 | a0001c0001t0004g0285 a0001c0001t0004g0286 a0001c0002t0001g0267 others(2): Show |
5 | HG02647.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.585+2451T>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128961585 | |||||||
| chr9:128961586 | C | A | 5 | a0001c0001t0004g0285 a0001c0001t0004g0286 a0001c0002t0001g0267 others(2): Show |
5 | HG02647.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.585+2452C>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128961586 | |||||||
| chr9:128961586 | C | CTAGATAG others(1): Show |
3 | a0001c0001t0001g0005 a0001c0002t0001g0011 a0002c0005t0001g0290 |
3 | HG02559.hp2 HG02717.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.585+2454_585+2455i others(10): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128961586 | ||||||
| chr9:128961586 | C | CTAGATAG others(5): Show |
2 | a0001c0027t0001g0287 a0002c0005t0001g0288 |
2 | HG03225.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.585+2454_585+2455i others(14): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128961586 | ||||||
| chr9:128961589 | T | G | 18 | a0001c0001t0001g0005 a0001c0001t0001g0063 a0001c0001t0001g0112 others(15): Show |
18 | HG00639.hp2 HG01109.hp1 HG01361.hp1 others(15): Show |
intron_variant | MODIFIER | c.585+2455T>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128961589 | |||||||
| chr9:128961590 | C | A | 18 | a0001c0001t0001g0005 a0001c0001t0001g0063 a0001c0001t0001g0112 others(15): Show |
18 | HG00639.hp2 HG01109.hp1 HG01361.hp1 others(15): Show |
intron_variant | MODIFIER | c.585+2456C>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128961590 | |||||||
| chr9:128961590 | C | CTAGA | 24 | a0001c0001t0001g0031 a0001c0001t0001g0058 a0001c0001t0001g0072 others(21): Show |
24 | HG01123.hp2 HG01261.hp2 HG01928.hp2 others(21): Show |
intron_variant | MODIFIER | c.585+2486_585+2489d others(6): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128961590 | ||||||
| chr9:128961590 | C | CTAGATAG others(1): Show |
43 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0016 others(40): Show |
43 | HG00738.hp1 HG01109.hp2 HG01167.hp1 others(40): Show |
intron_variant | MODIFIER | c.585+2482_585+2489d others(10): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128961590 | ||||||
| chr9:128961590 | C | CTAGATAG others(5): Show |
27 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(24): Show |
29 | HG00558.hp2 HG00673.hp1 HG01433.hp1 others(26): Show |
intron_variant | MODIFIER | c.585+2478_585+2489d others(14): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128961590 | ||||||
| chr9:128961590 | C | CTAGATAG others(9): Show |
6 | a0001c0001t0001g0007 a0001c0001t0001g0043 a0001c0001t0001g0132 others(3): Show |
6 | HG00280.hp2 HG00639.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.585+2474_585+2489d others(18): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128961590 | ||||||
| chr9:128961590 | C | CTATCTAG others(5): Show |
8 | a0001c0004t0001g0003 a0001c0004t0001g0248 a0001c0004t0001g0249 others(5): Show |
9 | HG01099.hp1 HG02109.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.585+2458_585+2459i others(14): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128961590 | ||||||
| chr9:128961590 | C | CTATCTAG others(9): Show |
4 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0004t0001g0253 others(1): Show |
4 | HG02258.hp2 HG02280.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.585+2458_585+2459i others(18): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128961590 | ||||||
| chr9:128961590 | C | CTATCTAG others(13): Show |
1 | a0001c0004t0001g0247 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.585+2458_585+2459i others(22): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128961590 | ||||||
| chr9:128961590 | CTAGATAG others(1): Show |
C | 4 | a0001c0001t0001g0117 a0001c0001t0001g0260 a0001c0001t0001g0262 others(1): Show |
4 | HG01496.hp1 HG02280.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.585+2482_585+2489d others(10): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128961590 | ||||||
| chr9:128961622 | A | AT | 77 | a0001c0001t0001g0166 a0001c0001t0001g0221 a0001c0002t0001g0170 others(74): Show |
78 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.585+2504dupT | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128961622 | ||||||
| chr9:128961622 | A | ATAGAT | 10 | a0001c0002t0001g0172 a0001c0002t0001g0174 a0001c0002t0001g0181 others(7): Show |
10 | HG01109.hp1 HG02165.hp2 HG02523.hp2 others(7): Show |
intron_variant | MODIFIER | c.585+2489_585+2490i others(7): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128961622 | ||||||
| chr9:128961623 | T | TAGATAGA | 3 | a0001c0001t0006g0022 a0001c0002t0001g0023 a0001c0002t0001g0099 |
3 | HG01074.hp1 NA18954.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.585+2489_585+2490i others(9): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128961623 | |||||||
| chr9:128961661 | G | C | 14 | a0001c0003t0002g0271 a0001c0003t0002g0272 a0001c0003t0002g0273 others(11): Show |
14 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(11): Show |
intron_variant | MODIFIER | c.585+2527G>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128961661 | |||||||
| chr9:128961676 | C | T | 1 | a0001c0027t0001g0287 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.585+2542C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128961676 | |||||||
| chr9:128961755 | G | A | 2 | a0001c0001t0001g0061 a0001c0001t0001g0086 |
2 | HG02698.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.585+2621G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128961755 | |||||||
| chr9:128961940 | C | CT | 15 | a0001c0001t0001g0062 a0001c0003t0002g0271 a0001c0003t0002g0272 others(12): Show |
15 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(12): Show |
intron_variant | MODIFIER | c.585+2820dupT | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128961940 | ||||||
| chr9:128961958 | C | T | 2 | a0001c0002t0001g0228 a0001c0002t0001g0233 |
2 | HG02622.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.585+2824C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128961958 | |||||||
| chr9:128961959 | G | A | 1 | a0001c0001t0001g0044 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.585+2825G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128961959 | |||||||
| chr9:128961993 | A | G | 2 | a0001c0002t0001g0263 a0001c0002t0001g0264 |
2 | HG02895.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.585+2859A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128961993 | |||||||
| chr9:128962001 | A | G | 2 | a0001c0001t0004g0285 a0001c0001t0004g0286 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.585+2867A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128962001 | |||||||
| chr9:128962163 | G | C | 3 | a0001c0001t0001g0063 a0001c0001t0001g0112 a0001c0001t0001g0113 |
3 | HG01515.hp1 HG01517.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.585+3029G>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128962163 | |||||||
| chr9:128962248 | C | CT | 24 | a0001c0001t0001g0016 a0001c0001t0001g0133 a0001c0001t0001g0139 others(21): Show |
24 | HG00738.hp1 HG01069.hp1 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.585+3132dupT | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128962248 | ||||||
| chr9:128962248 | C | CTT | 14 | a0001c0003t0002g0271 a0001c0003t0002g0272 a0001c0003t0002g0273 others(11): Show |
14 | HG02027.hp1 HG03130.hp1 HG03834.hp2 others(11): Show |
intron_variant | MODIFIER | c.585+3131_585+3132d others(4): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128962248 | ||||||
| chr9:128962251 | T | G | 1 | a0001c0001t0001g0260 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.585+3117T>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128962251 | |||||||
| chr9:128962274 | A | G | 2 | a0001c0001t0004g0285 a0001c0001t0004g0286 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.585+3140A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128962274 | |||||||
| chr9:128962289 | C | G | 1 | a0001c0001t0001g0090 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.585+3155C>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128962289 | |||||||
| chr9:128962318 | G | T | 1 | a0001c0001t0001g0050 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.585+3184G>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128962318 | |||||||
| chr9:128962341 | C | A | 12 | a0001c0002t0001g0252 a0001c0004t0001g0003 a0001c0004t0001g0247 others(9): Show |
13 | HG01099.hp1 HG02109.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.585+3207C>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128962341 | |||||||
| chr9:128962405 | C | A | 1 | a0001c0001t0005g0064 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.585+3271C>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128962405 | |||||||
| chr9:128962476 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.585+3342C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128962476 | |||||||
| chr9:128962485 | C | G | 120 | a0001c0001t0001g0221 a0001c0001t0004g0285 a0001c0001t0004g0286 others(117): Show |
121 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.585+3351C>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128962485 | |||||||
| chr9:128962492 | A | C | 15 | a0001c0003t0002g0271 a0001c0003t0002g0272 a0001c0003t0002g0273 others(12): Show |
15 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(12): Show |
intron_variant | MODIFIER | c.585+3358A>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128962492 | |||||||
| chr9:128962493 | C | T | 2 | a0001c0001t0004g0285 a0001c0001t0004g0286 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.585+3359C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128962493 | |||||||
| chr9:128962524 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.585+3390C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128962524 | |||||||
| chr9:128962805 | T | C | 14 | a0001c0003t0002g0271 a0001c0003t0002g0272 a0001c0003t0002g0273 others(11): Show |
14 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(11): Show |
intron_variant | MODIFIER | c.585+3671T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128962805 | |||||||
| chr9:128963282 | A | AT | 7 | a0001c0001t0001g0090 a0001c0001t0001g0131 a0001c0001t0001g0143 others(4): Show |
7 | HG01169.hp2 HG01175.hp1 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.585+4169dupT | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128963282 | ||||||
| chr9:128963282 | A | ATT | 10 | a0001c0003t0002g0271 a0001c0003t0002g0275 a0001c0003t0002g0276 others(7): Show |
10 | HG02027.hp1 HG03834.hp2 NA18951.hp2 others(7): Show |
intron_variant | MODIFIER | c.585+4168_585+4169d others(4): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128963282 | ||||||
| chr9:128963282 | A | G | 1 | a0001c0002t0001g0237 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.585+4148A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128963282 | |||||||
| chr9:128963282 | AT | A | 10 | a0001c0001t0001g0014 a0001c0001t0001g0052 a0001c0001t0001g0132 others(7): Show |
10 | HG00639.hp1 HG00642.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.585+4169delT | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128963282 | ||||||
| chr9:128963282 | ATT | A | 13 | a0001c0001t0004g0286 a0001c0002t0001g0263 a0001c0002t0001g0267 others(10): Show |
13 | HG01167.hp1 HG02451.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.585+4168_585+4169d others(4): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128963282 | ||||||
| chr9:128963294 | T | C | 2 | a0001c0009t0001g0265 a0001c0009t0001g0266 |
2 | HG02451.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.585+4160T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128963294 | |||||||
| chr9:128963328 | C | T | 3 | a0001c0002t0001g0267 a0001c0002t0001g0268 a0001c0002t0001g0269 |
3 | HG02647.hp2 HG02970.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.585+4194C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128963328 | |||||||
| chr9:128963348 | C | T | 1 | a0003c0006t0001g0160 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.585+4214C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128963348 | |||||||
| chr9:128963509 | T | TG | 121 | a0001c0001t0001g0221 a0001c0001t0004g0285 a0001c0001t0004g0286 others(118): Show |
122 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.585+4376dupG | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128963509 | ||||||
| chr9:128963526 | A | T | 15 | a0001c0003t0002g0271 a0001c0003t0002g0272 a0001c0003t0002g0273 others(12): Show |
15 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(12): Show |
intron_variant | MODIFIER | c.585+4392A>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128963526 | |||||||
| chr9:128963814 | GT | G | 32 | a0001c0001t0001g0122 a0001c0001t0001g0142 a0001c0001t0004g0285 others(29): Show |
32 | HG00639.hp2 HG01167.hp1 HG01256.hp1 others(29): Show |
intron_variant | MODIFIER | c.586-4678delT | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128963814 | ||||||
| chr9:128963840 | G | A | 2 | a0001c0001t0001g0069 a0001c0001t0001g0125 |
2 | NA19009.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.586-4666G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128963840 | |||||||
| chr9:128964049 | T | C | 1 | a0001c0027t0001g0287 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.586-4457T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128964049 | |||||||
| chr9:128964171 | C | T | 2 | a0001c0001t0004g0285 a0001c0001t0004g0286 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.586-4335C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128964171 | |||||||
| chr9:128964252 | T | C | 1 | a0001c0027t0001g0287 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.586-4254T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128964252 | |||||||
| chr9:128964364 | CT | C | 17 | a0001c0001t0001g0140 a0001c0001t0004g0285 a0001c0001t0004g0286 others(14): Show |
18 | HG01099.hp1 HG02109.hp2 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.586-4127delT | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128964364 | ||||||
| chr9:128964404 | C | G | 9 | a0001c0001t0001g0062 a0001c0001t0001g0111 a0001c0001t0001g0143 others(6): Show |
9 | HG00642.hp1 HG01123.hp2 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.586-4102C>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128964404 | |||||||
| chr9:128964424 | G | A | 7 | a0001c0002t0001g0177 a0001c0002t0001g0188 a0001c0002t0001g0209 others(4): Show |
7 | HG00741.hp1 HG01167.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.586-4082G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128964424 | |||||||
| chr9:128964536 | A | ATT | 13 | a0001c0003t0002g0271 a0001c0003t0002g0272 a0001c0003t0002g0275 others(10): Show |
13 | HG02027.hp1 HG03834.hp2 HG06807.hp2 others(10): Show |
intron_variant | MODIFIER | c.586-3954_586-3953d others(4): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128964536 | ||||||
| chr9:128964536 | AT | A | 89 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0140 others(86): Show |
90 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.586-3953delT | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128964536 | ||||||
| chr9:128964706 | A | AT | 7 | a0001c0001t0001g0079 a0001c0001t0004g0286 a0001c0002t0001g0048 others(4): Show |
7 | HG00738.hp1 HG02300.hp2 HG02602.hp2 others(4): Show |
intron_variant | MODIFIER | c.586-3781dupT | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128964706 | ||||||
| chr9:128964706 | AT | A | 40 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0031 others(37): Show |
41 | HG01099.hp1 HG01109.hp1 HG01257.hp1 others(38): Show |
intron_variant | MODIFIER | c.586-3781delT | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128964706 | ||||||
| chr9:128964706 | ATT | A | 74 | a0001c0001t0001g0221 a0001c0002t0001g0011 a0001c0002t0001g0170 others(71): Show |
74 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.586-3782_586-3781d others(4): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128964706 | ||||||
| chr9:128964801 | G | A | 1 | a0001c0002t0001g0216 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.586-3705G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128964801 | |||||||
| chr9:128964828 | T | C | 1 | a0001c0002t0001g0025 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.586-3678T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128964828 | |||||||
| chr9:128964916 | C | T | 1 | a0001c0027t0001g0287 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.586-3590C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128964916 | |||||||
| chr9:128964953 | G | A | 2 | a0001c0001t0004g0285 a0001c0001t0004g0286 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.586-3553G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128964953 | |||||||
| chr9:128965022 | A | G | 1 | a0002c0005t0001g0288 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.586-3484A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128965022 | |||||||
| chr9:128965063 | T | G | 1 | a0001c0027t0001g0287 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.586-3443T>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128965063 | |||||||
| chr9:128965272 | A | G | 1 | a0001c0027t0001g0287 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.586-3234A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128965272 | |||||||
| chr9:128965681 | G | T | 1 | a0001c0001t0001g0042 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.586-2825G>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128965681 | |||||||
| chr9:128965804 | A | AT | 11 | a0001c0002t0001g0263 a0001c0002t0001g0267 a0001c0002t0001g0268 others(8): Show |
11 | HG01167.hp1 HG02451.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.586-2687dupT | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128965804 | ||||||
| chr9:128965804 | AT | A | 9 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0100 others(6): Show |
9 | HG02896.hp2 HG02897.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.586-2687delT | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128965804 | ||||||
| chr9:128965820 | A | T | 13 | a0001c0002t0001g0263 a0001c0002t0001g0264 a0001c0002t0001g0267 others(10): Show |
13 | HG01167.hp1 HG02451.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.586-2686A>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128965820 | |||||||
| chr9:128966046 | C | T | 6 | a0002c0005t0001g0288 a0002c0005t0001g0290 a0002c0005t0001g0291 others(3): Show |
6 | HG01167.hp1 HG02451.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.586-2460C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128966046 | |||||||
| chr9:128966128 | C | CGT | 10 | a0001c0001t0001g0009 a0001c0001t0001g0049 a0001c0001t0001g0112 others(7): Show |
10 | HG01515.hp1 HG01517.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.586-2338_586-2337d others(4): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128966128 | ||||||
| chr9:128966128 | CGT | C | 101 | a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0031 others(98): Show |
102 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.586-2338_586-2337d others(4): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128966128 | ||||||
| chr9:128966128 | CGTGT | C | 85 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(82): Show |
86 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.586-2340_586-2337d others(6): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128966128 | ||||||
| chr9:128966128 | CGTGTGT | C | 21 | a0001c0001t0001g0093 a0001c0001t0001g0102 a0001c0001t0001g0107 others(18): Show |
21 | HG00423.hp1 HG01109.hp2 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.586-2342_586-2337d others(8): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128966128 | ||||||
| chr9:128966128 | CGTGTGTG others(1): Show |
C | 13 | a0001c0001t0001g0115 a0001c0001t0001g0120 a0001c0001t0001g0142 others(10): Show |
14 | HG00140.hp2 HG00741.hp2 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.586-2344_586-2337d others(10): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128966128 | ||||||
| chr9:128966128 | CGTGTGTG others(3): Show |
C | 3 | a0001c0002t0001g0252 a0001c0004t0001g0248 a0001c0027t0001g0287 |
3 | HG03139.hp2 HG06807.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.586-2346_586-2337d others(12): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128966128 | ||||||
| chr9:128966128 | CGTGTGTG others(5): Show |
C | 8 | a0001c0003t0002g0273 a0001c0003t0002g0276 a0001c0003t0002g0277 others(5): Show |
8 | HG02027.hp1 NA18941.hp2 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.586-2348_586-2337d others(14): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128966128 | ||||||
| chr9:128966128 | CGTGTGTG others(7): Show |
C | 6 | a0001c0003t0002g0271 a0001c0003t0002g0272 a0001c0003t0002g0275 others(3): Show |
6 | HG03834.hp2 HG04115.hp1 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.586-2350_586-2337d others(16): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128966128 | ||||||
| chr9:128966168 | T | C | 1 | a0001c0001t0001g0005 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.586-2338T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128966168 | |||||||
| chr9:128966260 | C | CTG | 21 | a0001c0001t0001g0012 a0001c0001t0001g0043 a0001c0001t0001g0044 others(18): Show |
22 | HG00099.hp2 HG01099.hp1 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.586-2220_586-2219d others(4): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128966260 | ||||||
| chr9:128966260 | CTG | C | 78 | a0001c0001t0001g0072 a0001c0001t0001g0221 a0001c0002t0001g0170 others(75): Show |
78 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.586-2220_586-2219d others(4): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128966260 | ||||||
| chr9:128966260 | CTGTG | C | 8 | a0001c0002t0001g0176 a0001c0002t0001g0177 a0001c0002t0001g0188 others(5): Show |
8 | HG00741.hp1 HG01167.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.586-2222_586-2219d others(6): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128966260 | ||||||
| chr9:128966260 | CTGTGTG | C | 13 | a0001c0002t0001g0263 a0001c0002t0001g0264 a0001c0002t0001g0267 others(10): Show |
13 | HG02027.hp1 HG02647.hp2 HG02895.hp2 others(10): Show |
intron_variant | MODIFIER | c.586-2224_586-2219d others(8): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128966260 | ||||||
| chr9:128966262 | GTGTGTGT others(19): Show |
G | 1 | a0001c0001t0001g0097 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.586-2232_586-2207d others(28): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128966262 | ||||||
| chr9:128966286 | GT | G | 3 | a0001c0002t0001g0011 a0001c0002t0001g0172 a0001c0002t0001g0244 |
3 | HG01069.hp1 NA18999.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.586-2217delT | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128966286 | ||||||
| chr9:128966287 | T | TG | 4 | a0001c0001t0001g0114 a0001c0001t0001g0128 a0001c0001t0006g0022 others(1): Show |
4 | HG01361.hp1 HG02735.hp1 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.586-2219_586-2218i others(3): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128966287 | |||||||
| chr9:128966379 | T | C | 14 | a0001c0003t0002g0271 a0001c0003t0002g0272 a0001c0003t0002g0273 others(11): Show |
14 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(11): Show |
intron_variant | MODIFIER | c.586-2127T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128966379 | |||||||
| chr9:128966385 | T | G | 2 | a0001c0001t0004g0285 a0001c0001t0004g0286 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.586-2121T>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128966385 | |||||||
| chr9:128966504 | C | T | 1 | a0001c0002t0001g0238 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.586-2002C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128966504 | |||||||
| chr9:128966516 | A | T | 14 | a0001c0003t0002g0271 a0001c0003t0002g0272 a0001c0003t0002g0273 others(11): Show |
14 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(11): Show |
intron_variant | MODIFIER | c.586-1990A>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128966516 | |||||||
| chr9:128966565 | C | T | 1 | a0001c0001t0001g0148 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.586-1941C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128966565 | |||||||
| chr9:128966603 | G | A | 2 | a0001c0001t0001g0100 a0001c0001t0001g0141 |
2 | NA19055.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.586-1903G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128966603 | |||||||
| chr9:128967061 | A | T | 2 | a0004c0010t0001g0169 a0004c0010t0001g0234 |
2 | HG00642.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.586-1445A>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128967061 | |||||||
| chr9:128967190 | T | C | 2 | a0001c0001t0004g0285 a0001c0001t0004g0286 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.586-1316T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128967190 | |||||||
| chr9:128967285 | T | C | 1 | a0001c0002t0001g0240 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.586-1221T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128967285 | |||||||
| chr9:128967335 | C | T | 1 | a0001c0001t0001g0010 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.586-1171C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128967335 | |||||||
| chr9:128967350 | A | G | 15 | a0001c0003t0002g0271 a0001c0003t0002g0272 a0001c0003t0002g0273 others(12): Show |
15 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(12): Show |
intron_variant | MODIFIER | c.586-1156A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128967350 | |||||||
| chr9:128967504 | A | T | 2 | a0001c0001t0001g0057 a0001c0001t0001g0070 |
2 | NA18942.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.586-1002A>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128967504 | |||||||
| chr9:128967558 | G | A | 2 | a0001c0001t0004g0285 a0001c0001t0004g0286 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.586-948G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128967558 | |||||||
| chr9:128967646 | C | T | 6 | a0002c0005t0001g0288 a0002c0005t0001g0290 a0002c0005t0001g0291 others(3): Show |
6 | HG01167.hp1 HG02451.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.586-860C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128967646 | |||||||
| chr9:128967721 | C | T | 2 | a0001c0001t0004g0285 a0001c0001t0004g0286 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.586-785C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128967721 | |||||||
| chr9:128967747 | G | T | 1 | a0001c0001t0001g0052 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.586-759G>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128967747 | |||||||
| chr9:128967785 | C | T | 1 | a0001c0002t0001g0240 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.586-721C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128967785 | |||||||
| chr9:128967790 | CA | C | 7 | a0001c0002t0001g0190 a0001c0002t0001g0191 a0001c0002t0001g0267 others(4): Show |
7 | HG01517.hp1 HG02451.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.586-701delA | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128967790 | ||||||
| chr9:128967790 | CAA | C | 6 | a0002c0005t0001g0288 a0002c0005t0001g0290 a0002c0005t0001g0291 others(3): Show |
6 | HG01167.hp1 HG02451.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.586-702_586-701del others(2): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128967790 | ||||||
| chr9:128967832 | T | C | 1 | a0001c0002t0001g0242 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.586-674T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128967832 | |||||||
| chr9:128967908 | C | T | 1 | a0001c0001t0001g0105 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.586-598C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128967908 | |||||||
| chr9:128968037 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.586-469G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128968037 | |||||||
| chr9:128968225 | A | G | 1 | a0001c0002t0001g0176 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.586-281A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128968225 | |||||||
| chr9:128968273 | T | TA | 13 | a0001c0002t0001g0263 a0001c0002t0001g0264 a0001c0002t0001g0267 others(10): Show |
13 | HG01167.hp1 HG02451.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.586-222dupA | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 128968273 | ||||||
| chr9:128968361 | C | G | 1 | a0001c0001t0007g0088 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.586-145C>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 8/43 | chr9 | 128968361 | |||||||
| chr9:128968844 | C | T | 4 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(1): Show |
4 | HG01891.hp2 HG02055.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.797+127C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 9/43 | chr9 | 128968844 | |||||||
| chr9:128968858 | C | G | 1 | a0001c0027t0001g0287 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.797+141C>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 9/43 | chr9 | 128968858 | |||||||
| chr9:128968859 | A | G | 1 | a0001c0001t0001g0047 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.797+142A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 9/43 | chr9 | 128968859 | |||||||
| chr9:128969201 | G | A | 13 | a0001c0002t0001g0263 a0001c0002t0001g0264 a0001c0002t0001g0267 others(10): Show |
13 | HG01167.hp1 HG02451.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.798-199G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 9/43 | chr9 | 128969201 | |||||||
| chr9:128969236 | T | C | 12 | a0001c0002t0001g0252 a0001c0004t0001g0003 a0001c0004t0001g0247 others(9): Show |
13 | HG01099.hp1 HG02109.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.798-164T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 9/43 | chr9 | 128969236 | |||||||
| chr9:128969318 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.798-82C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 9/43 | chr9 | 128969318 | |||||||
| chr9:128969331 | A | T | 1 | a0001c0002t0001g0176 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.798-69A>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 9/43 | chr9 | 128969331 | |||||||
| chr9:128969572 | A | G | 2 | a0001c0002t0001g0263 a0001c0002t0001g0264 |
2 | HG02895.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.912+58A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 10/43 | chr9 | 128969572 | |||||||
| chr9:128969734 | A | G | 1 | a0001c0027t0001g0287 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.912+220A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 10/43 | chr9 | 128969734 | |||||||
| chr9:128969744 | C | G | 1 | a0001c0027t0001g0287 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.912+230C>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 10/43 | chr9 | 128969744 | |||||||
| chr9:128969904 | T | A | 6 | a0002c0005t0001g0288 a0002c0005t0001g0290 a0002c0005t0001g0291 others(3): Show |
6 | HG01167.hp1 HG02451.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.912+390T>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 10/43 | chr9 | 128969904 | |||||||
| chr9:128970085 | G | A | 1 | a0001c0002t0001g0267 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.912+571G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 10/43 | chr9 | 128970085 | |||||||
| chr9:128970225 | G | A | 2 | a0001c0009t0001g0265 a0001c0009t0001g0266 |
2 | HG02451.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.913-533G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 10/43 | chr9 | 128970225 | |||||||
| chr9:128970326 | A | G | 12 | a0001c0002t0001g0252 a0001c0004t0001g0003 a0001c0004t0001g0247 others(9): Show |
13 | HG01099.hp1 HG02109.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.913-432A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 10/43 | chr9 | 128970326 | |||||||
| chr9:128970392 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.913-366G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 10/43 | chr9 | 128970392 | |||||||
| chr9:128970585 | G | A | 2 | a0001c0001t0001g0139 a0001c0001t0001g0163 |
2 | HG02145.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.913-173G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 10/43 | chr9 | 128970585 | |||||||
| chr9:128970725 | C | T | 3 | a0001c0001t0001g0139 a0001c0001t0001g0146 a0001c0001t0001g0163 |
3 | HG02145.hp2 HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.913-33C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 10/43 | chr9 | 128970725 | |||||||
| chr9:128971174 | T | G | 14 | a0001c0003t0002g0271 a0001c0003t0002g0272 a0001c0003t0002g0273 others(11): Show |
14 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(11): Show |
intron_variant | MODIFIER | c.1113+216T>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 11/43 | chr9 | 128971174 | |||||||
| chr9:128971268 | A | G | 1 | a0001c0002t0001g0198 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1113+310A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 11/43 | chr9 | 128971268 | |||||||
| chr9:128971408 | CTTGT | C | 15 | a0001c0002t0001g0252 a0001c0003t0002g0271 a0001c0003t0002g0272 others(12): Show |
15 | HG02027.hp1 HG03139.hp2 HG03834.hp2 others(12): Show |
intron_variant | MODIFIER | c.1113+473_1113+476d others(6): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 11/43 | INFO_REALIGN_3_PRIME | chr9 | 128971408 | ||||||
| chr9:128971637 | C | A | 13 | a0001c0002t0001g0263 a0001c0002t0001g0264 a0001c0002t0001g0267 others(10): Show |
13 | HG01167.hp1 HG02451.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.1113+679C>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 11/43 | chr9 | 128971637 | |||||||
| chr9:128971879 | C | G | 1 | a0001c0001t0001g0141 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1113+921C>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 11/43 | chr9 | 128971879 | |||||||
| chr9:128971914 | G | A | 1 | a0001c0001t0001g0073 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1113+956G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 11/43 | chr9 | 128971914 | |||||||
| chr9:128972051 | T | C | 1 | a0001c0027t0001g0287 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1113+1093T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 11/43 | chr9 | 128972051 | |||||||
| chr9:128972462 | ACACAGAG others(5): Show |
A | 28 | a0001c0002t0001g0263 a0001c0002t0001g0264 a0001c0002t0001g0267 others(25): Show |
28 | HG01167.hp1 HG02027.hp1 HG02451.hp1 others(25): Show |
intron_variant | MODIFIER | c.1114-685_1114-674d others(14): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 11/43 | INFO_REALIGN_3_PRIME | chr9 | 128972462 | ||||||
| chr9:128972764 | A | G | 1 | a0001c0001t0001g0042 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1114-396A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 11/43 | chr9 | 128972764 | |||||||
| chr9:128972922 | G | A | 4 | a0001c0002t0001g0187 a0001c0002t0001g0192 a0001c0002t0001g0213 others(1): Show |
4 | NA18968.hp2 NA18982.hp1 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.1114-238G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 11/43 | chr9 | 128972922 | |||||||
| chr9:128973280 | T | C | 76 | a0001c0001t0001g0221 a0001c0002t0001g0170 a0001c0002t0001g0171 others(73): Show |
76 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.1203+31T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128973280 | |||||||
| chr9:128973371 | A | AT | 13 | a0001c0002t0001g0263 a0001c0002t0001g0264 a0001c0002t0001g0267 others(10): Show |
13 | HG01167.hp1 HG02451.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.1203+129dupT | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | INFO_REALIGN_3_PRIME | chr9 | 128973371 | ||||||
| chr9:128974094 | A | G | 15 | a0001c0003t0002g0271 a0001c0003t0002g0272 a0001c0003t0002g0273 others(12): Show |
15 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(12): Show |
intron_variant | MODIFIER | c.1203+845A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128974094 | |||||||
| chr9:128974262 | C | G | 2 | a0001c0001t0001g0014 a0001c0001t0001g0015 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1203+1013C>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128974262 | |||||||
| chr9:128974294 | A | C | 2 | a0001c0001t0001g0014 a0001c0001t0001g0015 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1203+1045A>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128974294 | |||||||
| chr9:128974303 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1203+1054C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128974303 | |||||||
| chr9:128974389 | G | GT | 54 | a0001c0001t0001g0016 a0001c0001t0001g0050 a0001c0001t0001g0054 others(51): Show |
54 | HG00423.hp2 HG00639.hp2 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.1203+1160dupT | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | INFO_REALIGN_3_PRIME | chr9 | 128974389 | ||||||
| chr9:128974389 | G | GTTT | 11 | a0001c0003t0002g0271 a0001c0003t0002g0272 a0001c0003t0002g0273 others(8): Show |
11 | HG02027.hp1 HG03834.hp2 NA18941.hp2 others(8): Show |
intron_variant | MODIFIER | c.1203+1158_1203+116 others(7): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | INFO_REALIGN_3_PRIME | chr9 | 128974389 | ||||||
| chr9:128974389 | G | T | 2 | a0001c0001t0001g0042 a0001c0003t0002g0280 |
2 | HG03688.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.1203+1140G>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128974389 | |||||||
| chr9:128974392 | T | G | 3 | a0001c0001t0001g0060 a0001c0001t0001g0087 a0009c0018t0001g0089 |
3 | HG01069.hp2 HG01496.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.1203+1143T>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128974392 | |||||||
| chr9:128974432 | C | T | 2 | a0001c0001t0001g0014 a0001c0001t0001g0015 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1203+1183C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128974432 | |||||||
| chr9:128974622 | A | T | 1 | a0001c0028t0001g0257 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1203+1373A>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128974622 | |||||||
| chr9:128974624 | C | G | 18 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(15): Show |
19 | HG00558.hp2 HG00673.hp1 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.1203+1375C>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128974624 | |||||||
| chr9:128974680 | T | C | 13 | a0001c0002t0001g0263 a0001c0002t0001g0264 a0001c0002t0001g0267 others(10): Show |
13 | HG01167.hp1 HG02451.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.1203+1431T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128974680 | |||||||
| chr9:128974773 | C | CT | 34 | a0001c0001t0001g0029 a0001c0001t0001g0031 a0001c0001t0001g0036 others(31): Show |
35 | HG00639.hp1 HG00673.hp2 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.1203+1539dupT | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | INFO_REALIGN_3_PRIME | chr9 | 128974773 | ||||||
| chr9:128974828 | G | A | 1 | a0001c0002t0001g0176 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1203+1579G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128974828 | |||||||
| chr9:128974898 | A | G | 14 | a0001c0003t0002g0271 a0001c0003t0002g0272 a0001c0003t0002g0273 others(11): Show |
14 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(11): Show |
intron_variant | MODIFIER | c.1203+1649A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128974898 | |||||||
| chr9:128975060 | T | C | 244 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(241): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.1203+1811T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128975060 | |||||||
| chr9:128975159 | T | G | 14 | a0001c0003t0002g0271 a0001c0003t0002g0272 a0001c0003t0002g0273 others(11): Show |
14 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(11): Show |
intron_variant | MODIFIER | c.1203+1910T>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128975159 | |||||||
| chr9:128975163 | G | T | 28 | a0001c0002t0001g0263 a0001c0002t0001g0264 a0001c0002t0001g0267 others(25): Show |
28 | HG01167.hp1 HG02027.hp1 HG02451.hp1 others(25): Show |
intron_variant | MODIFIER | c.1203+1914G>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128975163 | |||||||
| chr9:128975226 | C | CTTTTT | 12 | a0001c0003t0002g0271 a0001c0003t0002g0272 a0001c0003t0002g0273 others(9): Show |
12 | HG02027.hp1 HG03834.hp2 NA18941.hp2 others(9): Show |
intron_variant | MODIFIER | c.1203+1990_1203+199 others(9): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | INFO_REALIGN_3_PRIME | chr9 | 128975226 | ||||||
| chr9:128975235 | T | C | 1 | a0010c0024t0001g0250 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1203+1986T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128975235 | |||||||
| chr9:128975238 | T | C | 1 | a0001c0002t0001g0220 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1203+1989T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128975238 | |||||||
| chr9:128975323 | A | G | 14 | a0001c0002t0001g0176 a0001c0002t0001g0240 a0001c0002t0001g0252 others(11): Show |
15 | HG01099.hp1 HG01109.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1203+2074A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128975323 | |||||||
| chr9:128975362 | A | T | 28 | a0001c0002t0001g0263 a0001c0002t0001g0264 a0001c0002t0001g0267 others(25): Show |
28 | HG01167.hp1 HG02027.hp1 HG02451.hp1 others(25): Show |
intron_variant | MODIFIER | c.1203+2113A>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128975362 | |||||||
| chr9:128975405 | G | A | 2 | a0001c0002t0001g0263 a0001c0002t0001g0264 |
2 | HG02895.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1203+2156G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128975405 | |||||||
| chr9:128975468 | C | T | 75 | a0001c0001t0001g0221 a0001c0002t0001g0170 a0001c0002t0001g0171 others(72): Show |
75 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.1203+2219C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128975468 | |||||||
| chr9:128975511 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1203+2262C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128975511 | |||||||
| chr9:128975682 | G | A | 1 | a0001c0008t0001g0137 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1203+2433G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128975682 | |||||||
| chr9:128975896 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1203+2647G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128975896 | |||||||
| chr9:128975932 | C | T | 15 | a0001c0003t0002g0271 a0001c0003t0002g0272 a0001c0003t0002g0273 others(12): Show |
15 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(12): Show |
intron_variant | MODIFIER | c.1203+2683C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128975932 | |||||||
| chr9:128976012 | A | G | 1 | a0001c0001t0001g0046 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1203+2763A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128976012 | |||||||
| chr9:128976069 | T | C | 1 | a0001c0001t0001g0052 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1203+2820T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128976069 | |||||||
| chr9:128976250 | A | T | 13 | a0001c0002t0001g0263 a0001c0002t0001g0264 a0001c0002t0001g0267 others(10): Show |
13 | HG01167.hp1 HG02451.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.1203+3001A>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128976250 | |||||||
| chr9:128976359 | T | G | 1 | a0001c0027t0001g0287 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1204-2903T>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128976359 | |||||||
| chr9:128976950 | C | T | 1 | a0001c0001t0007g0088 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1204-2312C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128976950 | |||||||
| chr9:128976952 | C | T | 12 | a0001c0002t0001g0252 a0001c0004t0001g0003 a0001c0004t0001g0247 others(9): Show |
13 | HG01099.hp1 HG02109.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1204-2310C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128976952 | |||||||
| chr9:128977117 | A | AT | 23 | a0001c0001t0001g0007 a0001c0001t0001g0037 a0001c0001t0001g0045 others(20): Show |
23 | HG00642.hp1 HG00673.hp1 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.1204-2124dupT | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | INFO_REALIGN_3_PRIME | chr9 | 128977117 | ||||||
| chr9:128977117 | AT | A | 94 | a0001c0001t0001g0221 a0001c0002t0001g0170 a0001c0002t0001g0171 others(91): Show |
95 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.1204-2124delT | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | INFO_REALIGN_3_PRIME | chr9 | 128977117 | ||||||
| chr9:128977198 | C | T | 14 | a0001c0002t0001g0176 a0001c0002t0001g0240 a0001c0002t0001g0252 others(11): Show |
15 | HG01099.hp1 HG01109.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1204-2064C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128977198 | |||||||
| chr9:128977239 | C | A | 76 | a0001c0001t0001g0221 a0001c0002t0001g0170 a0001c0002t0001g0171 others(73): Show |
76 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.1204-2023C>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128977239 | |||||||
| chr9:128977306 | G | T | 1 | a0001c0001t0001g0103 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1204-1956G>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128977306 | |||||||
| chr9:128977773 | T | C | 1 | a0001c0001t0001g0042 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1204-1489T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128977773 | |||||||
| chr9:128978141 | C | A | 14 | a0001c0003t0002g0271 a0001c0003t0002g0272 a0001c0003t0002g0273 others(11): Show |
14 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(11): Show |
intron_variant | MODIFIER | c.1204-1121C>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128978141 | |||||||
| chr9:128978435 | C | T | 1 | a0001c0001t0001g0082 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1204-827C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128978435 | |||||||
| chr9:128978550 | G | A | 1 | a0001c0003t0002g0279 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1204-712G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128978550 | |||||||
| chr9:128978556 | C | CA | 50 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0062 others(47): Show |
51 | HG00597.hp2 HG00639.hp1 HG01099.hp1 others(48): Show |
intron_variant | MODIFIER | c.1204-683dupA | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | INFO_REALIGN_3_PRIME | chr9 | 128978556 | ||||||
| chr9:128978556 | C | CAA | 7 | a0001c0001t0001g0103 a0001c0003t0002g0272 a0001c0003t0002g0275 others(4): Show |
8 | HG03098.hp1 HG03453.hp1 HG03486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1204-684_1204-683d others(4): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | INFO_REALIGN_3_PRIME | chr9 | 128978556 | ||||||
| chr9:128978556 | CAAAA | C | 63 | a0001c0002t0001g0170 a0001c0002t0001g0171 a0001c0002t0001g0173 others(60): Show |
63 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.1204-686_1204-683d others(6): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | INFO_REALIGN_3_PRIME | chr9 | 128978556 | ||||||
| chr9:128978556 | CAAAAA | C | 8 | a0001c0001t0001g0221 a0001c0002t0001g0172 a0001c0002t0001g0181 others(5): Show |
8 | HG00423.hp1 HG06807.hp2 NA18943.hp1 others(5): Show |
intron_variant | MODIFIER | c.1204-687_1204-683d others(7): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | INFO_REALIGN_3_PRIME | chr9 | 128978556 | ||||||
| chr9:128978556 | CAAAAAAA others(8): Show |
C | 2 | a0001c0002t0001g0195 a0001c0029t0001g0185 |
2 | NA18987.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.1204-697_1204-683d others(17): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | INFO_REALIGN_3_PRIME | chr9 | 128978556 | ||||||
| chr9:128978584 | A | C | 13 | a0001c0002t0001g0263 a0001c0002t0001g0264 a0001c0002t0001g0267 others(10): Show |
13 | HG01167.hp1 HG02451.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.1204-678A>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128978584 | |||||||
| chr9:128978865 | C | T | 1 | a0001c0001t0001g0154 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1204-397C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128978865 | |||||||
| chr9:128978883 | G | A | 1 | a0001c0028t0001g0257 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1204-379G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128978883 | |||||||
| chr9:128979155 | T | C | 14 | a0001c0003t0002g0271 a0001c0003t0002g0272 a0001c0003t0002g0273 others(11): Show |
14 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(11): Show |
intron_variant | MODIFIER | c.1204-107T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128979155 | |||||||
| chr9:128979180 | T | C | 2 | a0001c0003t0002g0282 a0001c0003t0002g0283 |
2 | NA19004.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.1204-82T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128979180 | |||||||
| chr9:128979188 | A | G | 1 | a0001c0014t0001g0180 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1204-74A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 12/43 | chr9 | 128979188 | |||||||
| chr9:128979354 | A | G | 8 | a0001c0001t0001g0045 a0001c0001t0001g0051 a0001c0001t0001g0084 others(5): Show |
8 | HG02109.hp1 HG02622.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1269+27A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 13/43 | chr9 | 128979354 | |||||||
| chr9:128979587 | T | C | 1 | a0001c0002t0001g0204 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1269+260T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 13/43 | chr9 | 128979587 | |||||||
| chr9:128979616 | GT | G | 118 | a0001c0001t0001g0221 a0001c0002t0001g0026 a0001c0002t0001g0170 others(115): Show |
119 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.1269+300delT | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 13/43 | INFO_REALIGN_3_PRIME | chr9 | 128979616 | ||||||
| chr9:128979736 | A | G | 1 | a0001c0001t0001g0050 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1269+409A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 13/43 | chr9 | 128979736 | |||||||
| chr9:128979764 | C | G | 2 | a0001c0001t0004g0285 a0001c0001t0004g0286 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1269+437C>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 13/43 | chr9 | 128979764 | |||||||
| chr9:128979782 | G | A | 2 | a0001c0002t0001g0263 a0001c0002t0001g0264 |
2 | HG02895.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1269+455G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 13/43 | chr9 | 128979782 | |||||||
| chr9:128979867 | C | T | 2 | a0001c0002t0001g0013 a0001c0002t0001g0021 |
2 | HG02040.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.1269+540C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 13/43 | chr9 | 128979867 | |||||||
| chr9:128979868 | G | A | 1 | a0001c0001t0001g0018 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1269+541G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 13/43 | chr9 | 128979868 | |||||||
| chr9:128979901 | G | C | 1 | a0002c0005t0001g0288 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1269+574G>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 13/43 | chr9 | 128979901 | |||||||
| chr9:128980146 | A | G | 1 | a0001c0004t0008g0254 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1270-460A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 13/43 | chr9 | 128980146 | |||||||
| chr9:128980238 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1270-368G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 13/43 | chr9 | 128980238 | |||||||
| chr9:128980367 | A | G | 1 | a0001c0002t0001g0238 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1270-239A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 13/43 | chr9 | 128980367 | |||||||
| chr9:128980390 | G | A | 2 | a0001c0002t0001g0178 a0001c0002t0001g0203 |
2 | NA18999.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.1270-216G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 13/43 | chr9 | 128980390 | |||||||
| chr9:128980421 | C | T | 14 | a0001c0003t0002g0271 a0001c0003t0002g0272 a0001c0003t0002g0273 others(11): Show |
14 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(11): Show |
intron_variant | MODIFIER | c.1270-185C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 13/43 | chr9 | 128980421 | |||||||
| chr9:128980545 | T | C | 10 | a0001c0001t0001g0098 a0001c0001t0001g0132 a0001c0001t0001g0147 others(7): Show |
11 | HG00639.hp1 HG02615.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.1270-61T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 13/43 | chr9 | 128980545 | |||||||
| chr9:128980592 | C | T | 1 | a0001c0001t0001g0132 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1270-14C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 13/43 | chr9 | 128980592 | |||||||
| chr9:128980835 | T | C | 15 | a0001c0003t0002g0271 a0001c0003t0002g0272 a0001c0003t0002g0273 others(12): Show |
15 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(12): Show |
intron_variant | MODIFIER | c.1389+110T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 14/43 | chr9 | 128980835 | |||||||
| chr9:128980880 | A | G | 1 | a0001c0001t0001g0042 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1389+155A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 14/43 | chr9 | 128980880 | |||||||
| chr9:128981619 | A | G | 1 | a0001c0001t0001g0262 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1516+229A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 15/43 | chr9 | 128981619 | |||||||
| chr9:128981678 | C | T | 5 | a0002c0005t0001g0290 a0002c0005t0001g0291 a0002c0005t0001g0292 others(2): Show |
5 | HG01167.hp1 HG02451.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.1516+288C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 15/43 | chr9 | 128981678 | |||||||
| chr9:128981693 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1516+303C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 15/43 | chr9 | 128981693 | |||||||
| chr9:128981853 | G | A | 2 | a0001c0001t0001g0042 a0001c0001t0001g0119 |
2 | HG00597.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.1516+463G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 15/43 | chr9 | 128981853 | |||||||
| chr9:128981906 | C | T | 6 | a0002c0005t0001g0288 a0002c0005t0001g0290 a0002c0005t0001g0291 others(3): Show |
6 | HG01167.hp1 HG02451.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1516+516C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 15/43 | chr9 | 128981906 | |||||||
| chr9:128981907 | G | A | 76 | a0001c0001t0001g0221 a0001c0002t0001g0170 a0001c0002t0001g0171 others(73): Show |
76 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.1516+517G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 15/43 | chr9 | 128981907 | |||||||
| chr9:128982034 | G | A | 13 | a0001c0002t0001g0263 a0001c0002t0001g0264 a0001c0002t0001g0267 others(10): Show |
13 | HG01167.hp1 HG02451.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.1517-515G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 15/43 | chr9 | 128982034 | |||||||
| chr9:128982039 | T | C | 1 | a0001c0027t0001g0287 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1517-510T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 15/43 | chr9 | 128982039 | |||||||
| chr9:128982189 | G | A | 13 | a0001c0002t0001g0263 a0001c0002t0001g0264 a0001c0002t0001g0267 others(10): Show |
13 | HG01167.hp1 HG02451.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.1517-360G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 15/43 | chr9 | 128982189 | |||||||
| chr9:128982716 | C | T | 1 | a0001c0002t0001g0083 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1669+15C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 16/43 | chr9 | 128982716 | |||||||
| chr9:128982731 | C | T | 2 | a0001c0001t0007g0088 a0001c0027t0001g0287 |
2 | HG03017.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1669+30C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 16/43 | chr9 | 128982731 | |||||||
| chr9:128982823 | T | C | 13 | a0001c0003t0002g0271 a0001c0003t0002g0272 a0001c0003t0002g0275 others(10): Show |
13 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(10): Show |
intron_variant | MODIFIER | c.1670-79T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 16/43 | chr9 | 128982823 | |||||||
| chr9:128982872 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1670-30C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 16/43 | chr9 | 128982872 | |||||||
| chr9:128982883 | A | T | 1 | a0001c0001t0001g0120 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1670-19A>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 16/43 | chr9 | 128982883 | |||||||
| chr9:128983081 | T | C | 1 | a0001c0001t0001g0017 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1796+53T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 17/43 | chr9 | 128983081 | |||||||
| chr9:128983115 | A | C | 1 | a0001c0002t0001g0235 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1796+87A>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 17/43 | chr9 | 128983115 | |||||||
| chr9:128983130 | G | A | 2 | a0001c0001t0001g0056 a0001c0001t0001g0103 |
2 | NA18955.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.1796+102G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 17/43 | chr9 | 128983130 | |||||||
| chr9:128983269 | T | C | 84 | a0001c0001t0001g0031 a0001c0001t0001g0057 a0001c0001t0001g0069 others(81): Show |
84 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.1797-24T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 17/43 | chr9 | 128983269 | |||||||
| chr9:128983392 | G | C | 1 | a0001c0001t0001g0146 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1884+12G>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 18/43 | chr9 | 128983392 | |||||||
| chr9:128983573 | G | A | 1 | a0001c0001t0001g0072 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1961+23G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 19/43 | chr9 | 128983573 | |||||||
| chr9:128983599 | A | G | 1 | a0001c0002t0001g0096 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1961+49A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 19/43 | chr9 | 128983599 | |||||||
| chr9:128983686 | C | T | 5 | a0001c0002t0001g0241 a0001c0002t0001g0244 a0001c0002t0001g0246 others(2): Show |
5 | HG01069.hp1 HG02145.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1961+136C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 19/43 | chr9 | 128983686 | |||||||
| chr9:128983777 | G | A | 1 | a0001c0001t0001g0035 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1961+227G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 19/43 | chr9 | 128983777 | |||||||
| chr9:128983862 | C | T | 1 | a0001c0027t0001g0287 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1961+312C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 19/43 | chr9 | 128983862 | |||||||
| chr9:128983870 | G | T | 1 | a0001c0002t0001g0178 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1961+320G>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 19/43 | chr9 | 128983870 | |||||||
| chr9:128983936 | T | C | 1 | a0001c0002t0001g0237 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1961+386T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 19/43 | chr9 | 128983936 | |||||||
| chr9:128984037 | G | C | 1 | a0001c0027t0001g0287 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1961+487G>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 19/43 | chr9 | 128984037 | |||||||
| chr9:128984102 | G | A | 1 | a0001c0002t0001g0252 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1961+552G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 19/43 | chr9 | 128984102 | |||||||
| chr9:128984124 | A | AT | 24 | a0001c0001t0001g0050 a0001c0001t0001g0059 a0001c0001t0001g0078 others(21): Show |
24 | HG00438.hp2 HG00558.hp1 HG02027.hp1 others(21): Show |
intron_variant | MODIFIER | c.1961+593dupT | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 19/43 | INFO_REALIGN_3_PRIME | chr9 | 128984124 | ||||||
| chr9:128984124 | A | ATTTTTTT others(4): Show |
1 | a0001c0002t0001g0026 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1961+583_1961+593d others(13): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 19/43 | INFO_REALIGN_3_PRIME | chr9 | 128984124 | ||||||
| chr9:128984124 | A | ATTTTTTT others(5): Show |
1 | a0001c0027t0001g0287 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1961+582_1961+593d others(14): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 19/43 | INFO_REALIGN_3_PRIME | chr9 | 128984124 | ||||||
| chr9:128984124 | A | ATTTTTTT others(6): Show |
2 | a0002c0005t0001g0291 a0002c0005t0001g0293 |
2 | HG02615.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1961+581_1961+593d others(15): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 19/43 | INFO_REALIGN_3_PRIME | chr9 | 128984124 | ||||||
| chr9:128984124 | A | ATTTTTTT others(7): Show |
3 | a0002c0005t0001g0288 a0002c0005t0001g0292 a0002c0012t0001g0289 |
3 | HG01167.hp1 HG02451.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1961+580_1961+593d others(16): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 19/43 | INFO_REALIGN_3_PRIME | chr9 | 128984124 | ||||||
| chr9:128984124 | A | ATTTTTTT others(8): Show |
2 | a0001c0001t0001g0038 a0001c0002t0001g0020 |
2 | HG02040.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.1961+579_1961+593d others(17): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 19/43 | INFO_REALIGN_3_PRIME | chr9 | 128984124 | ||||||
| chr9:128984124 | A | ATTTTTTT others(10): Show |
3 | a0001c0002t0001g0263 a0001c0002t0001g0264 a0001c0002t0001g0268 |
3 | HG02895.hp2 HG03579.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1961+577_1961+593d others(19): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 19/43 | INFO_REALIGN_3_PRIME | chr9 | 128984124 | ||||||
| chr9:128984124 | A | ATTTTTTT others(11): Show |
2 | a0001c0002t0001g0267 a0001c0002t0001g0269 |
2 | HG02647.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1961+576_1961+593d others(20): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 19/43 | INFO_REALIGN_3_PRIME | chr9 | 128984124 | ||||||
| chr9:128984124 | A | ATTTTTTT others(13): Show |
9 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0051 others(6): Show |
9 | HG01074.hp1 HG02559.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1961+593_1961+594i others(22): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 19/43 | INFO_REALIGN_3_PRIME | chr9 | 128984124 | ||||||
| chr9:128984124 | A | ATTTTTTT others(14): Show |
12 | a0001c0001t0001g0012 a0001c0001t0001g0035 a0001c0001t0001g0041 others(9): Show |
12 | HG00738.hp1 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.1961+593_1961+594i others(23): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 19/43 | INFO_REALIGN_3_PRIME | chr9 | 128984124 | ||||||
| chr9:128984124 | A | ATTTTTTT others(15): Show |
9 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(6): Show |
9 | HG00673.hp1 HG01496.hp1 HG02080.hp1 others(6): Show |
intron_variant | MODIFIER | c.1961+593_1961+594i others(24): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 19/43 | INFO_REALIGN_3_PRIME | chr9 | 128984124 | ||||||
| chr9:128984124 | A | ATTTTTTT others(16): Show |
1 | a0001c0001t0001g0052 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1961+593_1961+594i others(25): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 19/43 | INFO_REALIGN_3_PRIME | chr9 | 128984124 | ||||||
| chr9:128984124 | A | ATTTTTTT others(17): Show |
4 | a0001c0001t0001g0005 a0001c0001t0001g0124 a0001c0002t0001g0013 others(1): Show |
4 | HG02040.hp2 HG02451.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1961+593_1961+594i others(26): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 19/43 | INFO_REALIGN_3_PRIME | chr9 | 128984124 | ||||||
| chr9:128984124 | A | ATTTTTTT others(18): Show |
3 | a0001c0002t0001g0011 a0001c0002t0001g0021 a0001c0002t0001g0027 |
3 | HG01255.hp2 HG02523.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.1961+593_1961+594i others(27): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 19/43 | INFO_REALIGN_3_PRIME | chr9 | 128984124 | ||||||
| chr9:128984124 | A | ATTTTTTT others(19): Show |
4 | a0001c0001t0001g0045 a0001c0002t0001g0024 a0001c0002t0001g0034 others(1): Show |
4 | HG01257.hp1 HG02886.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1961+593_1961+594i others(28): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 19/43 | INFO_REALIGN_3_PRIME | chr9 | 128984124 | ||||||
| chr9:128984124 | A | ATTTTTTT others(20): Show |
3 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0028 |
3 | NA18966.hp2 NA18969.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.1961+593_1961+594i others(29): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 19/43 | INFO_REALIGN_3_PRIME | chr9 | 128984124 | ||||||
| chr9:128984124 | A | ATTTTTTT others(21): Show |
4 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(1): Show |
5 | HG00558.hp2 HG02293.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1961+593_1961+594i others(30): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 19/43 | INFO_REALIGN_3_PRIME | chr9 | 128984124 | ||||||
| chr9:128984124 | A | ATTTTTTT others(22): Show |
3 | a0001c0001t0001g0058 a0001c0001t0001g0108 a0001c0002t0001g0008 |
3 | HG03540.hp1 NA19000.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1961+593_1961+594i others(31): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 19/43 | INFO_REALIGN_3_PRIME | chr9 | 128984124 | ||||||
| chr9:128984124 | A | ATTTTTTT others(23): Show |
5 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0002t0001g0025 others(2): Show |
5 | HG01433.hp1 HG01891.hp2 HG02273.hp2 others(2): Show |
intron_variant | MODIFIER | c.1961+593_1961+594i others(32): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 19/43 | INFO_REALIGN_3_PRIME | chr9 | 128984124 | ||||||
| chr9:128984124 | A | ATTTTTTT others(24): Show |
1 | a0001c0002t0001g0033 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1961+593_1961+594i others(33): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 19/43 | INFO_REALIGN_3_PRIME | chr9 | 128984124 | ||||||
| chr9:128984124 | A | ATTTTTTT others(25): Show |
1 | a0001c0002t0001g0083 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1961+593_1961+594i others(34): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 19/43 | INFO_REALIGN_3_PRIME | chr9 | 128984124 | ||||||
| chr9:128984124 | A | ATTTTTTT others(26): Show |
2 | a0001c0001t0001g0018 a0001c0002t0001g0096 |
2 | NA18747.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.1961+593_1961+594i others(35): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 19/43 | INFO_REALIGN_3_PRIME | chr9 | 128984124 | ||||||
| chr9:128984124 | A | ATTTTTTT others(31): Show |
1 | a0001c0001t0001g0107 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1961+593_1961+594i others(40): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 19/43 | INFO_REALIGN_3_PRIME | chr9 | 128984124 | ||||||
| chr9:128984124 | A | ATTTTTTT others(33): Show |
1 | a0001c0001t0001g0007 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1961+593_1961+594i others(42): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 19/43 | INFO_REALIGN_3_PRIME | chr9 | 128984124 | ||||||
| chr9:128984124 | A | ATTTTTTT others(40): Show |
1 | a0001c0002t0001g0023 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1961+593_1961+594i others(49): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 19/43 | INFO_REALIGN_3_PRIME | chr9 | 128984124 | ||||||
| chr9:128984124 | AT | A | 16 | a0001c0001t0001g0029 a0001c0001t0001g0131 a0001c0001t0001g0140 others(13): Show |
17 | HG01099.hp1 HG01169.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.1961+593delT | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 19/43 | INFO_REALIGN_3_PRIME | chr9 | 128984124 | ||||||
| chr9:128984157 | G | A | 2 | a0001c0002t0001g0217 a0001c0002t0001g0218 |
2 | HG02896.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1961+607G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 19/43 | chr9 | 128984157 | |||||||
| chr9:128984207 | A | G | 67 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(64): Show |
68 | HG00280.hp2 HG00558.hp2 HG00673.hp1 others(65): Show |
intron_variant | MODIFIER | c.1961+657A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 19/43 | chr9 | 128984207 | |||||||
| chr9:128984228 | G | A | 1 | a0006c0026t0001g0116 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1962-672G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 19/43 | chr9 | 128984228 | |||||||
| chr9:128984280 | C | G | 82 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(79): Show |
83 | HG00280.hp2 HG00558.hp2 HG00673.hp1 others(80): Show |
intron_variant | MODIFIER | c.1962-620C>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 19/43 | chr9 | 128984280 | |||||||
| chr9:128984468 | A | G | 2 | a0001c0002t0001g0178 a0001c0002t0001g0203 |
2 | NA18999.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.1962-432A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 19/43 | chr9 | 128984468 | |||||||
| chr9:128984617 | C | T | 1 | a0001c0001t0001g0133 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1962-283C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 19/43 | chr9 | 128984617 | |||||||
| chr9:128984651 | G | C | 28 | a0001c0002t0001g0263 a0001c0002t0001g0264 a0001c0002t0001g0267 others(25): Show |
28 | HG01167.hp1 HG02027.hp1 HG02451.hp1 others(25): Show |
intron_variant | MODIFIER | c.1962-249G>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 19/43 | chr9 | 128984651 | |||||||
| chr9:128985340 | T | C | 1 | a0001c0003t0009g0274 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2076+326T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 20/43 | chr9 | 128985340 | |||||||
| chr9:128985432 | A | G | 95 | a0001c0001t0001g0221 a0001c0002t0001g0067 a0001c0002t0001g0170 others(92): Show |
96 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.2076+418A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 20/43 | chr9 | 128985432 | |||||||
| chr9:128985710 | C | T | 1 | a0001c0002t0001g0176 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2076+696C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 20/43 | chr9 | 128985710 | |||||||
| chr9:128985805 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.2077-753C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 20/43 | chr9 | 128985805 | |||||||
| chr9:128986041 | G | A | 17 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(14): Show |
18 | HG00558.hp2 HG00673.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.2077-517G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 20/43 | chr9 | 128986041 | |||||||
| chr9:128986218 | C | T | 1 | a0003c0006t0001g0160 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2077-340C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 20/43 | chr9 | 128986218 | |||||||
| chr9:128986224 | A | G | 1 | a0001c0001t0001g0012 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.2077-334A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 20/43 | chr9 | 128986224 | |||||||
| chr9:128986265 | C | G | 1 | a0001c0028t0001g0257 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2077-293C>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 20/43 | chr9 | 128986265 | |||||||
| chr9:128986405 | A | C | 1 | a0001c0027t0001g0287 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2077-153A>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 20/43 | chr9 | 128986405 | |||||||
| chr9:128986424 | C | G | 1 | a0001c0001t0001g0124 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2077-134C>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 20/43 | chr9 | 128986424 | |||||||
| chr9:128986433 | C | A | 2 | a0001c0001t0001g0014 a0001c0001t0001g0015 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2077-125C>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 20/43 | chr9 | 128986433 | |||||||
| chr9:128986934 | C | A | 11 | a0001c0004t0001g0003 a0001c0004t0001g0247 a0001c0004t0001g0248 others(8): Show |
12 | HG01099.hp1 HG02109.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.2264+59C>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 22/43 | chr9 | 128986934 | |||||||
| chr9:128987064 | T | TGA | 46 | a0001c0001t0001g0029 a0001c0001t0001g0041 a0001c0001t0001g0045 others(43): Show |
46 | HG00140.hp1 HG00438.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.2264+213_2264+214d others(4): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 22/43 | INFO_REALIGN_3_PRIME | chr9 | 128987064 | ||||||
| chr9:128987064 | T | TGAGA | 15 | a0001c0001t0001g0124 a0001c0001t0001g0260 a0001c0001t0001g0262 others(12): Show |
15 | HG01069.hp1 HG01496.hp1 HG01934.hp1 others(12): Show |
intron_variant | MODIFIER | c.2264+211_2264+214d others(6): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 22/43 | INFO_REALIGN_3_PRIME | chr9 | 128987064 | ||||||
| chr9:128987064 | T | TGAGAGA | 3 | a0001c0002t0001g0204 a0001c0002t0001g0205 a0001c0014t0001g0180 |
3 | HG03710.hp1 NA19078.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.2264+209_2264+214d others(8): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 22/43 | INFO_REALIGN_3_PRIME | chr9 | 128987064 | ||||||
| chr9:128987064 | TGA | T | 32 | a0001c0001t0001g0005 a0001c0001t0001g0049 a0001c0001t0001g0056 others(29): Show |
32 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(29): Show |
intron_variant | MODIFIER | c.2264+213_2264+214d others(4): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 22/43 | INFO_REALIGN_3_PRIME | chr9 | 128987064 | ||||||
| chr9:128987084 | AGAGAGTG others(5): Show |
A | 5 | a0001c0002t0001g0263 a0001c0002t0001g0264 a0001c0002t0001g0269 others(2): Show |
5 | HG02451.hp1 HG02647.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.2264+211_2264+222d others(14): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 22/43 | INFO_REALIGN_3_PRIME | chr9 | 128987084 | ||||||
| chr9:128987084 | AGAGAGTG others(7): Show |
A | 3 | a0001c0002t0001g0267 a0001c0002t0001g0268 a0001c0027t0001g0287 |
3 | HG02970.hp2 HG06807.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2264+211_2264+224d others(16): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 22/43 | INFO_REALIGN_3_PRIME | chr9 | 128987084 | ||||||
| chr9:128987086 | A | AGT | 18 | a0001c0001t0001g0031 a0001c0001t0001g0059 a0001c0001t0001g0069 others(15): Show |
19 | HG00639.hp1 HG00673.hp2 HG01433.hp1 others(16): Show |
intron_variant | MODIFIER | c.2264+212_2264+213i others(4): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 22/43 | INFO_REALIGN_3_PRIME | chr9 | 128987086 | ||||||
| chr9:128987086 | A | AGTGT | 7 | a0001c0001t0001g0036 a0001c0001t0001g0060 a0001c0001t0001g0086 others(4): Show |
7 | HG01069.hp2 HG01496.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.2264+212_2264+213i others(6): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 22/43 | INFO_REALIGN_3_PRIME | chr9 | 128987086 | ||||||
| chr9:128987086 | A | T | 2 | a0001c0001t0001g0075 a0001c0001t0001g0159 |
2 | HG00423.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.2264+211A>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 22/43 | chr9 | 128987086 | |||||||
| chr9:128987086 | AGAGT | A | 3 | a0001c0001t0001g0148 a0001c0001t0001g0166 a0001c0001t0003g0134 |
3 | HG01175.hp2 HG02257.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.2264+213_2264+216d others(6): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 22/43 | INFO_REALIGN_3_PRIME | chr9 | 128987086 | ||||||
| chr9:128987086 | AGAGTGT | A | 3 | a0001c0001t0001g0114 a0001c0001t0001g0122 a0001c0001t0001g0151 |
3 | HG00639.hp2 HG01361.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.2264+213_2264+218d others(8): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 22/43 | INFO_REALIGN_3_PRIME | chr9 | 128987086 | ||||||
| chr9:128987088 | A | AGAGAGAG others(1): Show |
4 | a0001c0007t0001g0123 a0001c0007t0001g0261 a0001c0008t0001g0137 others(1): Show |
4 | HG02630.hp1 HG02717.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2264+214_2264+215i others(10): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 22/43 | INFO_REALIGN_3_PRIME | chr9 | 128987088 | ||||||
| chr9:128987088 | A | AGAGAGAG others(3): Show |
1 | a0001c0001t0001g0047 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2264+214_2264+215i others(12): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 22/43 | INFO_REALIGN_3_PRIME | chr9 | 128987088 | ||||||
| chr9:128987088 | A | AGAGAGTG others(3): Show |
1 | a0001c0001t0001g0042 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2264+214_2264+215i others(12): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 22/43 | INFO_REALIGN_3_PRIME | chr9 | 128987088 | ||||||
| chr9:128987088 | A | AGAGAGTG others(5): Show |
1 | a0001c0002t0001g0048 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2264+214_2264+215i others(14): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 22/43 | INFO_REALIGN_3_PRIME | chr9 | 128987088 | ||||||
| chr9:128987088 | A | AGAGT | 6 | a0001c0001t0001g0035 a0001c0001t0001g0044 a0001c0001t0001g0052 others(3): Show |
6 | HG01891.hp1 HG02015.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.2264+214_2264+215i others(6): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 22/43 | INFO_REALIGN_3_PRIME | chr9 | 128987088 | ||||||
| chr9:128987088 | A | AGAGTGTG others(9): Show |
1 | a0001c0002t0001g0099 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2264+214_2264+215i others(18): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 22/43 | INFO_REALIGN_3_PRIME | chr9 | 128987088 | ||||||
| chr9:128987088 | A | AGT | 16 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0038 others(13): Show |
16 | HG01109.hp2 HG02735.hp2 HG02886.hp2 others(13): Show |
intron_variant | MODIFIER | c.2264+256_2264+257d others(4): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 22/43 | INFO_REALIGN_3_PRIME | chr9 | 128987088 | ||||||
| chr9:128987088 | A | AGTGT | 3 | a0001c0001t0001g0017 a0001c0004t0001g0251 a0001c0020t0001g0085 |
3 | HG01433.hp2 HG03195.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.2264+254_2264+257d others(6): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 22/43 | INFO_REALIGN_3_PRIME | chr9 | 128987088 | ||||||
| chr9:128987088 | A | T | 46 | a0001c0001t0001g0031 a0001c0001t0001g0036 a0001c0001t0001g0050 others(43): Show |
47 | HG00280.hp2 HG00423.hp2 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.2264+213A>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 22/43 | chr9 | 128987088 | |||||||
| chr9:128987088 | AGT | A | 32 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(29): Show |
32 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.2264+256_2264+257d others(4): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 22/43 | INFO_REALIGN_3_PRIME | chr9 | 128987088 | ||||||
| chr9:128987088 | AGTGT | A | 5 | a0001c0001t0001g0111 a0001c0001t0001g0270 a0001c0002t0001g0218 others(2): Show |
5 | HG01109.hp1 HG01261.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.2264+254_2264+257d others(6): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 22/43 | INFO_REALIGN_3_PRIME | chr9 | 128987088 | ||||||
| chr9:128987088 | AGTGTGTG others(3): Show |
A | 6 | a0002c0005t0001g0288 a0002c0005t0001g0290 a0002c0005t0001g0291 others(3): Show |
6 | HG01167.hp1 HG02451.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.2264+248_2264+257d others(12): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 22/43 | INFO_REALIGN_3_PRIME | chr9 | 128987088 | ||||||
| chr9:128987088 | AGTGTGTG others(5): Show |
A | 13 | a0001c0003t0002g0271 a0001c0003t0002g0272 a0001c0003t0002g0273 others(10): Show |
13 | HG02027.hp1 HG04115.hp1 NA18941.hp2 others(10): Show |
intron_variant | MODIFIER | c.2264+246_2264+257d others(14): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 22/43 | INFO_REALIGN_3_PRIME | chr9 | 128987088 | ||||||
| chr9:128987090 | T | A | 71 | a0001c0001t0001g0012 a0001c0001t0001g0037 a0001c0001t0001g0041 others(68): Show |
71 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.2264+215T>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 22/43 | chr9 | 128987090 | |||||||
| chr9:128987092 | T | A | 74 | a0001c0001t0001g0012 a0001c0001t0001g0221 a0001c0002t0001g0008 others(71): Show |
74 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.2264+217T>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 22/43 | chr9 | 128987092 | |||||||
| chr9:128987094 | T | A | 70 | a0001c0001t0001g0221 a0001c0002t0001g0067 a0001c0002t0001g0170 others(67): Show |
70 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.2264+219T>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 22/43 | chr9 | 128987094 | |||||||
| chr9:128987096 | T | A | 11 | a0001c0002t0001g0183 a0001c0002t0001g0189 a0001c0002t0001g0191 others(8): Show |
11 | HG00438.hp1 HG00642.hp2 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.2264+221T>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 22/43 | chr9 | 128987096 | |||||||
| chr9:128987098 | T | A | 2 | a0001c0002t0001g0218 a0004c0010t0001g0234 |
2 | HG00642.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.2264+223T>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 22/43 | chr9 | 128987098 | |||||||
| chr9:128987100 | T | A | 1 | a0001c0002t0001g0218 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2264+225T>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 22/43 | chr9 | 128987100 | |||||||
| chr9:128987102 | T | A | 3 | a0001c0002t0001g0218 a0001c0003t0002g0283 a0001c0003t0009g0274 |
3 | HG02896.hp1 HG04115.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.2264+227T>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 22/43 | chr9 | 128987102 | |||||||
| chr9:128987119 | GTGTGTGT others(7): Show |
G | 1 | a0001c0003t0002g0281 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2264+250_2264+263d others(16): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 22/43 | INFO_REALIGN_3_PRIME | chr9 | 128987119 | ||||||
| chr9:128987127 | G | A | 1 | a0001c0001t0001g0049 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2264+252G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 22/43 | chr9 | 128987127 | |||||||
| chr9:128987296 | T | A | 14 | a0001c0003t0002g0271 a0001c0003t0002g0272 a0001c0003t0002g0273 others(11): Show |
14 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(11): Show |
intron_variant | MODIFIER | c.2265-293T>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 22/43 | chr9 | 128987296 | |||||||
| chr9:128987297 | G | T | 14 | a0001c0003t0002g0271 a0001c0003t0002g0272 a0001c0003t0002g0273 others(11): Show |
14 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(11): Show |
intron_variant | MODIFIER | c.2265-292G>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 22/43 | chr9 | 128987297 | |||||||
| chr9:128987331 | T | G | 1 | a0002c0005t0001g0288 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2265-258T>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 22/43 | chr9 | 128987331 | |||||||
| chr9:128987432 | G | A | 15 | a0001c0003t0002g0271 a0001c0003t0002g0272 a0001c0003t0002g0273 others(12): Show |
15 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(12): Show |
intron_variant | MODIFIER | c.2265-157G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 22/43 | chr9 | 128987432 | |||||||
| chr9:128987454 | G | T | 1 | a0001c0002t0001g0206 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.2265-135G>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 22/43 | chr9 | 128987454 | |||||||
| chr9:128987935 | C | T | 11 | a0001c0004t0001g0003 a0001c0004t0001g0247 a0001c0004t0001g0248 others(8): Show |
12 | HG01099.hp1 HG02109.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.2394-112C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 23/43 | chr9 | 128987935 | |||||||
| chr9:128988394 | A | G | 15 | a0001c0003t0002g0271 a0001c0003t0002g0272 a0001c0003t0002g0273 others(12): Show |
15 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(12): Show |
intron_variant | MODIFIER | c.2533+208A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 24/43 | chr9 | 128988394 | |||||||
| chr9:128988719 | A | AT | 32 | a0001c0001t0001g0007 a0001c0001t0001g0042 a0001c0001t0001g0051 others(29): Show |
32 | HG00140.hp2 HG00280.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.2533+560dupT | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 24/43 | INFO_REALIGN_3_PRIME | chr9 | 128988719 | ||||||
| chr9:128988719 | AT | A | 142 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0030 others(139): Show |
143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.2533+560delT | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 24/43 | INFO_REALIGN_3_PRIME | chr9 | 128988719 | ||||||
| chr9:128988719 | ATT | A | 20 | a0001c0001t0001g0029 a0001c0001t0001g0031 a0001c0001t0001g0068 others(17): Show |
20 | HG00423.hp2 HG00558.hp1 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.2533+559_2533+560d others(4): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 24/43 | INFO_REALIGN_3_PRIME | chr9 | 128988719 | ||||||
| chr9:128988719 | ATTTTTTT others(5): Show |
A | 2 | a0001c0004t0001g0253 a0001c0004t0008g0254 |
2 | HG02258.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.2533+549_2533+560d others(14): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 24/43 | INFO_REALIGN_3_PRIME | chr9 | 128988719 | ||||||
| chr9:128988719 | ATTTTTTT others(6): Show |
A | 12 | a0001c0002t0001g0176 a0001c0002t0001g0240 a0001c0002t0001g0252 others(9): Show |
13 | HG01099.hp1 HG01109.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.2533+548_2533+560d others(15): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 24/43 | INFO_REALIGN_3_PRIME | chr9 | 128988719 | ||||||
| chr9:128988764 | T | C | 1 | a0001c0027t0001g0287 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2533+578T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 24/43 | chr9 | 128988764 | |||||||
| chr9:128988796 | G | C | 13 | a0001c0002t0001g0263 a0001c0002t0001g0264 a0001c0002t0001g0267 others(10): Show |
13 | HG01167.hp1 HG02451.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.2533+610G>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 24/43 | chr9 | 128988796 | |||||||
| chr9:128989285 | C | A | 1 | a0001c0007t0001g0123 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2534-835C>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 24/43 | chr9 | 128989285 | |||||||
| chr9:128989726 | A | G | 122 | a0001c0001t0001g0221 a0001c0002t0001g0170 a0001c0002t0001g0171 others(119): Show |
123 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.2534-394A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 24/43 | chr9 | 128989726 | |||||||
| chr9:128989774 | G | A | 11 | a0001c0004t0001g0003 a0001c0004t0001g0247 a0001c0004t0001g0248 others(8): Show |
12 | HG01099.hp1 HG02109.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.2534-346G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 24/43 | chr9 | 128989774 | |||||||
| chr9:128989786 | C | T | 1 | a0001c0002t0001g0220 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2534-334C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 24/43 | chr9 | 128989786 | |||||||
| chr9:128989787 | G | A | 3 | a0001c0001t0001g0114 a0001c0001t0001g0122 a0001c0001t0001g0148 |
3 | HG00639.hp2 HG01361.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.2534-333G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 24/43 | chr9 | 128989787 | |||||||
| chr9:128990244 | G | GCA | 14 | a0001c0003t0002g0271 a0001c0003t0002g0272 a0001c0003t0002g0273 others(11): Show |
14 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(11): Show |
intron_variant | MODIFIER | c.2640+26_2640+27dup others(2): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 25/43 | INFO_REALIGN_3_PRIME | chr9 | 128990244 | ||||||
| chr9:128990316 | G | A | 1 | a0001c0002t0001g0190 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2640+90G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 25/43 | chr9 | 128990316 | |||||||
| chr9:128990541 | G | A | 12 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(9): Show |
13 | HG00558.hp2 HG00673.hp1 HG02080.hp1 others(10): Show |
intron_variant | MODIFIER | c.2640+315G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 25/43 | chr9 | 128990541 | |||||||
| chr9:128990602 | C | T | 2 | a0001c0001t0001g0061 a0001c0001t0001g0086 |
2 | HG02698.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.2640+376C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 25/43 | chr9 | 128990602 | |||||||
| chr9:128990603 | G | A | 1 | a0001c0002t0001g0220 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2640+377G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 25/43 | chr9 | 128990603 | |||||||
| chr9:128990613 | C | G | 1 | a0001c0029t0001g0185 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.2640+387C>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 25/43 | chr9 | 128990613 | |||||||
| chr9:128990662 | A | C | 1 | a0001c0001t0001g0053 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2640+436A>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 25/43 | chr9 | 128990662 | |||||||
| chr9:128990692 | T | A | 15 | a0001c0003t0002g0271 a0001c0003t0002g0272 a0001c0003t0002g0273 others(12): Show |
15 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(12): Show |
intron_variant | MODIFIER | c.2640+466T>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 25/43 | chr9 | 128990692 | |||||||
| chr9:128990788 | T | C | 289 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(286): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.2640+562T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 25/43 | chr9 | 128990788 | |||||||
| chr9:128990820 | G | A | 8 | a0001c0003t0002g0273 a0001c0003t0002g0276 a0001c0003t0002g0277 others(5): Show |
8 | HG02027.hp1 NA18941.hp2 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.2640+594G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 25/43 | chr9 | 128990820 | |||||||
| chr9:128990821 | C | T | 14 | a0001c0003t0002g0271 a0001c0003t0002g0272 a0001c0003t0002g0273 others(11): Show |
14 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(11): Show |
intron_variant | MODIFIER | c.2640+595C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 25/43 | chr9 | 128990821 | |||||||
| chr9:128990822 | G | A | 1 | a0001c0002t0001g0196 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2640+596G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 25/43 | chr9 | 128990822 | |||||||
| chr9:128990991 | C | G | 1 | a0001c0001t0001g0049 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2640+765C>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 25/43 | chr9 | 128990991 | |||||||
| chr9:128991012 | C | T | 6 | a0002c0005t0001g0288 a0002c0005t0001g0290 a0002c0005t0001g0291 others(3): Show |
6 | HG01167.hp1 HG02451.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.2640+786C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 25/43 | chr9 | 128991012 | |||||||
| chr9:128991162 | CT | C | 116 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0018 others(113): Show |
117 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.2640+956delT | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 25/43 | INFO_REALIGN_3_PRIME | chr9 | 128991162 | ||||||
| chr9:128991162 | CTT | C | 9 | a0001c0002t0001g0177 a0001c0002t0001g0178 a0001c0002t0001g0191 others(6): Show |
9 | HG00642.hp2 HG01069.hp1 HG01167.hp2 others(6): Show |
intron_variant | MODIFIER | c.2640+955_2640+956d others(4): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 25/43 | INFO_REALIGN_3_PRIME | chr9 | 128991162 | ||||||
| chr9:128991253 | G | A | 15 | a0001c0003t0002g0271 a0001c0003t0002g0272 a0001c0003t0002g0273 others(12): Show |
15 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(12): Show |
intron_variant | MODIFIER | c.2640+1027G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 25/43 | chr9 | 128991253 | |||||||
| chr9:128991298 | G | T | 1 | a0001c0002t0001g0212 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2640+1072G>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 25/43 | chr9 | 128991298 | |||||||
| chr9:128991568 | G | A | 12 | a0001c0002t0001g0252 a0001c0004t0001g0003 a0001c0004t0001g0247 others(9): Show |
13 | HG01099.hp1 HG02109.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.2640+1342G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 25/43 | chr9 | 128991568 | |||||||
| chr9:128991611 | G | T | 14 | a0001c0003t0002g0271 a0001c0003t0002g0272 a0001c0003t0002g0273 others(11): Show |
14 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(11): Show |
intron_variant | MODIFIER | c.2640+1385G>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 25/43 | chr9 | 128991611 | |||||||
| chr9:128991700 | G | A | 1 | a0001c0027t0001g0287 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2640+1474G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 25/43 | chr9 | 128991700 | |||||||
| chr9:128991707 | G | T | 1 | a0001c0002t0001g0176 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2640+1481G>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 25/43 | chr9 | 128991707 | |||||||
| chr9:128991830 | C | CA | 18 | a0001c0001t0001g0087 a0001c0001t0001g0094 a0001c0002t0001g0212 others(15): Show |
18 | HG00597.hp1 HG01069.hp2 HG01175.hp1 others(15): Show |
intron_variant | MODIFIER | c.2641-1351dupA | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 25/43 | INFO_REALIGN_3_PRIME | chr9 | 128991830 | ||||||
| chr9:128991907 | C | CT | 7 | a0001c0001t0001g0041 a0001c0001t0001g0044 a0001c0001t0001g0059 others(4): Show |
7 | HG01361.hp2 HG02027.hp2 HG02080.hp2 others(4): Show |
intron_variant | MODIFIER | c.2641-1272dupT | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 25/43 | INFO_REALIGN_3_PRIME | chr9 | 128991907 | ||||||
| chr9:128991907 | CT | C | 90 | a0001c0001t0001g0086 a0001c0001t0001g0106 a0001c0001t0001g0221 others(87): Show |
90 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.2641-1272delT | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 25/43 | INFO_REALIGN_3_PRIME | chr9 | 128991907 | ||||||
| chr9:128992032 | G | A | 1 | a0001c0002t0001g0240 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2641-1165G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 25/43 | chr9 | 128992032 | |||||||
| chr9:128992035 | T | G | 1 | a0001c0001t0001g0149 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.2641-1162T>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 25/43 | chr9 | 128992035 | |||||||
| chr9:128992157 | A | G | 2 | a0001c0002t0001g0204 a0001c0002t0001g0205 |
2 | HG03710.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.2641-1040A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 25/43 | chr9 | 128992157 | |||||||
| chr9:128992356 | C | A | 2 | a0001c0002t0001g0263 a0001c0002t0001g0264 |
2 | HG02895.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2641-841C>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 25/43 | chr9 | 128992356 | |||||||
| chr9:128992873 | C | T | 1 | a0001c0001t0001g0141 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.2641-324C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 25/43 | chr9 | 128992873 | |||||||
| chr9:128992886 | G | C | 121 | a0001c0001t0001g0221 a0001c0002t0001g0170 a0001c0002t0001g0171 others(118): Show |
122 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.2641-311G>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 25/43 | chr9 | 128992886 | |||||||
| chr9:128993001 | C | G | 1 | a0001c0001t0001g0109 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.2641-196C>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 25/43 | chr9 | 128993001 | |||||||
| chr9:128993146 | A | G | 14 | a0001c0003t0002g0271 a0001c0003t0002g0272 a0001c0003t0002g0273 others(11): Show |
14 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(11): Show |
intron_variant | MODIFIER | c.2641-51A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 25/43 | chr9 | 128993146 | |||||||
| chr9:128993767 | A | G | 1 | a0001c0001t0001g0045 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3017+73A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 27/43 | chr9 | 128993767 | |||||||
| chr9:128993790 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.3017+96G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 27/43 | chr9 | 128993790 | |||||||
| chr9:128993834 | A | G | 1 | a0001c0001t0001g0044 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.3017+140A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 27/43 | chr9 | 128993834 | |||||||
| chr9:128993848 | T | C | 4 | a0001c0007t0001g0123 a0001c0007t0001g0261 a0001c0008t0001g0137 others(1): Show |
4 | HG02630.hp1 HG02717.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.3017+154T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 27/43 | chr9 | 128993848 | |||||||
| chr9:128994019 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.3017+325C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 27/43 | chr9 | 128994019 | |||||||
| chr9:128994136 | G | A | 15 | a0001c0003t0002g0271 a0001c0003t0002g0272 a0001c0003t0002g0273 others(12): Show |
15 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(12): Show |
intron_variant | MODIFIER | c.3018-237G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 27/43 | chr9 | 128994136 | |||||||
| chr9:128994358 | T | G | 1 | a0001c0002t0001g0182 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.3018-15T>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 27/43 | chr9 | 128994358 | |||||||
| chr9:128994607 | T | C | 1 | a0001c0002t0001g0219 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.3087+165T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 28/43 | chr9 | 128994607 | |||||||
| chr9:128994687 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.3088-169C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 28/43 | chr9 | 128994687 | |||||||
| chr9:128994846 | A | G | 28 | a0001c0002t0001g0263 a0001c0002t0001g0264 a0001c0002t0001g0267 others(25): Show |
28 | HG01167.hp1 HG02027.hp1 HG02451.hp1 others(25): Show |
intron_variant | MODIFIER | c.3088-10A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 28/43 | chr9 | 128994846 | |||||||
| chr9:128995158 | C | T | 1 | a0001c0027t0001g0287 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3156-161C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 29/43 | chr9 | 128995158 | |||||||
| chr9:128995239 | C | T | 1 | a0001c0001t0001g0102 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3156-80C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 29/43 | chr9 | 128995239 | |||||||
| chr9:128995720 | GA | G | 14 | a0001c0003t0002g0271 a0001c0003t0002g0272 a0001c0003t0002g0273 others(11): Show |
14 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(11): Show |
intron_variant | MODIFIER | c.3351+208delA | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 30/43 | INFO_REALIGN_3_PRIME | chr9 | 128995720 | ||||||
| chr9:128996089 | C | T | 1 | a0001c0028t0001g0257 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3351+575C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 30/43 | chr9 | 128996089 | |||||||
| chr9:128996095 | G | A | 1 | a0001c0002t0001g0174 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.3351+581G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 30/43 | chr9 | 128996095 | |||||||
| chr9:128996134 | G | A | 2 | a0001c0001t0001g0061 a0001c0001t0001g0086 |
2 | HG02698.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.3351+620G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 30/43 | chr9 | 128996134 | |||||||
| chr9:128996149 | AT | A | 12 | a0001c0002t0001g0177 a0001c0002t0001g0252 a0001c0004t0001g0003 others(9): Show |
13 | HG01099.hp1 HG01167.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.3351+650delT | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 30/43 | INFO_REALIGN_3_PRIME | chr9 | 128996149 | ||||||
| chr9:128996240 | T | C | 120 | a0001c0002t0001g0048 a0001c0002t0001g0067 a0001c0002t0001g0099 others(117): Show |
121 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.3351+726T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 30/43 | chr9 | 128996240 | |||||||
| chr9:128996267 | A | G | 2 | a0001c0001t0001g0109 a0001c0001t0001g0133 |
2 | NA18968.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.3351+753A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 30/43 | chr9 | 128996267 | |||||||
| chr9:128996517 | T | G | 1 | a0001c0027t0001g0287 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3351+1003T>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 30/43 | chr9 | 128996517 | |||||||
| chr9:128996800 | T | A | 13 | a0001c0002t0001g0263 a0001c0002t0001g0264 a0001c0002t0001g0267 others(10): Show |
13 | HG01167.hp1 HG02451.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.3351+1286T>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 30/43 | chr9 | 128996800 | |||||||
| chr9:128996969 | C | T | 76 | a0001c0001t0001g0221 a0001c0002t0001g0170 a0001c0002t0001g0171 others(73): Show |
76 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.3352-1182C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 30/43 | chr9 | 128996969 | |||||||
| chr9:128997189 | G | T | 1 | a0001c0002t0001g0237 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.3352-962G>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 30/43 | chr9 | 128997189 | |||||||
| chr9:128997292 | A | C | 2 | a0001c0002t0001g0217 a0001c0002t0001g0218 |
2 | HG02896.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.3352-859A>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 30/43 | chr9 | 128997292 | |||||||
| chr9:128997470 | A | C | 3 | a0001c0001t0001g0063 a0001c0001t0001g0113 a0001c0001t0001g0118 |
3 | HG01515.hp2 HG01517.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.3352-681A>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 30/43 | chr9 | 128997470 | |||||||
| chr9:128997477 | C | A | 2 | a0001c0001t0001g0014 a0001c0001t0001g0015 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.3352-674C>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 30/43 | chr9 | 128997477 | |||||||
| chr9:128997502 | T | C | 1 | a0001c0027t0001g0287 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3352-649T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 30/43 | chr9 | 128997502 | |||||||
| chr9:128997590 | C | T | 1 | a0001c0001t0001g0073 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.3352-561C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 30/43 | chr9 | 128997590 | |||||||
| chr9:128997887 | AT | A | 6 | a0002c0005t0001g0288 a0002c0005t0001g0290 a0002c0005t0001g0291 others(3): Show |
6 | HG01167.hp1 HG02451.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.3352-259delT | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 30/43 | INFO_REALIGN_3_PRIME | chr9 | 128997887 | ||||||
| chr9:128997919 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.3352-232C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 30/43 | chr9 | 128997919 | |||||||
| chr9:128998261 | C | T | 1 | a0001c0001t0001g0017 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.3429+33C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 31/43 | chr9 | 128998261 | |||||||
| chr9:128998337 | G | A | 1 | a0001c0002t0001g0245 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.3429+109G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 31/43 | chr9 | 128998337 | |||||||
| chr9:128998338 | G | C | 1 | a0001c0002t0001g0245 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.3429+110G>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 31/43 | chr9 | 128998338 | |||||||
| chr9:128998361 | G | A | 1 | a0001c0001t0001g0010 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.3429+133G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 31/43 | chr9 | 128998361 | |||||||
| chr9:128998388 | G | C | 1 | a0001c0027t0001g0287 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3430-150G>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 31/43 | chr9 | 128998388 | |||||||
| chr9:128998419 | C | T | 4 | a0001c0007t0001g0123 a0001c0007t0001g0261 a0001c0008t0001g0137 others(1): Show |
4 | HG02630.hp1 HG02717.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.3430-119C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 31/43 | chr9 | 128998419 | |||||||
| chr9:128998494 | G | A | 1 | a0001c0002t0001g0259 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.3430-44G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 31/43 | chr9 | 128998494 | |||||||
| chr9:128998497 | T | C | 1 | a0001c0002t0001g0020 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.3430-41T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 31/43 | chr9 | 128998497 | |||||||
| chr9:128998711 | G | A | 2 | a0001c0001t0001g0014 a0001c0001t0001g0015 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.3515+88G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 32/43 | chr9 | 128998711 | |||||||
| chr9:128998856 | C | CT | 78 | a0001c0001t0001g0036 a0001c0001t0001g0098 a0001c0001t0001g0132 others(75): Show |
79 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.3515+251dupT | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 32/43 | INFO_REALIGN_3_PRIME | chr9 | 128998856 | ||||||
| chr9:128998896 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.3515+273G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 32/43 | chr9 | 128998896 | |||||||
| chr9:128998918 | G | A | 4 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0107 others(1): Show |
4 | HG01109.hp2 HG02055.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.3516-254G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 32/43 | chr9 | 128998918 | |||||||
| chr9:128998998 | G | A | 42 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(39): Show |
43 | HG00280.hp2 HG00558.hp2 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.3516-174G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 32/43 | chr9 | 128998998 | |||||||
| chr9:128999041 | CAG | C | 14 | a0001c0003t0002g0271 a0001c0003t0002g0272 a0001c0003t0002g0273 others(11): Show |
14 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(11): Show |
intron_variant | MODIFIER | c.3516-130_3516-129d others(4): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 32/43 | chr9 | 128999041 | |||||||
| chr9:128999145 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.3516-27G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 32/43 | chr9 | 128999145 | |||||||
| chr9:128999158 | A | G | 78 | a0001c0001t0001g0221 a0001c0002t0001g0048 a0001c0002t0001g0099 others(75): Show |
78 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.3516-14A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 32/43 | chr9 | 128999158 | |||||||
| chr9:128999325 | G | C | 1 | a0001c0027t0001g0287 | 1 | HG06807.hp2 | splice_region_variant&intron_variant | LOW | c.3661+8G>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 33/43 | chr9 | 128999325 | |||||||
| chr9:128999380 | A | G | 78 | a0001c0002t0001g0048 a0001c0002t0001g0099 a0001c0002t0001g0170 others(75): Show |
78 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.3661+63A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 33/43 | chr9 | 128999380 | |||||||
| chr9:128999437 | A | T | 93 | a0001c0001t0001g0221 a0001c0002t0001g0048 a0001c0002t0001g0099 others(90): Show |
93 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.3661+120A>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 33/43 | chr9 | 128999437 | |||||||
| chr9:128999438 | T | C | 1 | a0001c0001t0001g0141 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.3661+121T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 33/43 | chr9 | 128999438 | |||||||
| chr9:128999523 | G | A | 1 | a0012c0016t0001g0230 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.3662-101G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 33/43 | chr9 | 128999523 | |||||||
| chr9:128999620 | A | G | 93 | a0001c0001t0001g0221 a0001c0002t0001g0048 a0001c0002t0001g0099 others(90): Show |
93 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(90): Show |
splice_region_variant&intron_variant | LOW | c.3662-4A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 33/43 | chr9 | 128999620 | |||||||
| chr9:128999878 | G | C | 1 | a0001c0027t0001g0287 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3843+73G>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 34/43 | chr9 | 128999878 | |||||||
| chr9:129000101 | T | C | 78 | a0001c0001t0001g0221 a0001c0002t0001g0048 a0001c0002t0001g0099 others(75): Show |
78 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.3843+296T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 34/43 | chr9 | 129000101 | |||||||
| chr9:129000169 | C | G | 1 | a0001c0027t0001g0287 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3843+364C>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 34/43 | chr9 | 129000169 | |||||||
| chr9:129000231 | A | ACAGGCG | 78 | a0001c0001t0001g0221 a0001c0002t0001g0048 a0001c0002t0001g0099 others(75): Show |
78 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.3843+427_3843+432d others(8): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 34/43 | INFO_REALIGN_3_PRIME | chr9 | 129000231 | ||||||
| chr9:129000237 | G | A | 14 | a0001c0003t0002g0271 a0001c0003t0002g0272 a0001c0003t0002g0273 others(11): Show |
14 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(11): Show |
intron_variant | MODIFIER | c.3843+432G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 34/43 | chr9 | 129000237 | |||||||
| chr9:129000341 | A | G | 4 | a0001c0002t0001g0187 a0001c0002t0001g0192 a0001c0002t0001g0213 others(1): Show |
4 | NA18968.hp2 NA18982.hp1 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.3843+536A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 34/43 | chr9 | 129000341 | |||||||
| chr9:129000341 | A | T | 1 | a0001c0027t0001g0287 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3843+536A>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 34/43 | chr9 | 129000341 | |||||||
| chr9:129000431 | A | G | 80 | a0001c0001t0001g0047 a0001c0001t0001g0221 a0001c0002t0001g0048 others(77): Show |
80 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.3843+626A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 34/43 | chr9 | 129000431 | |||||||
| chr9:129000444 | G | A | 76 | a0001c0001t0001g0221 a0001c0002t0001g0170 a0001c0002t0001g0171 others(73): Show |
76 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.3843+639G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 34/43 | chr9 | 129000444 | |||||||
| chr9:129000479 | C | T | 1 | a0001c0002t0001g0217 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3843+674C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 34/43 | chr9 | 129000479 | |||||||
| chr9:129000576 | C | T | 2 | a0001c0001t0001g0090 a0001c0001t0005g0064 |
2 | HG02683.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.3843+771C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 34/43 | chr9 | 129000576 | |||||||
| chr9:129000634 | T | A | 3 | a0001c0002t0001g0170 a0001c0002t0001g0195 a0001c0002t0001g0207 |
3 | HG03491.hp2 HG03492.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.3843+829T>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 34/43 | chr9 | 129000634 | |||||||
| chr9:129000774 | A | C | 27 | a0001c0002t0001g0176 a0001c0002t0001g0240 a0001c0002t0001g0252 others(24): Show |
28 | HG01099.hp1 HG01109.hp1 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.3844-755A>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 34/43 | chr9 | 129000774 | |||||||
| chr9:129000776 | C | T | 1 | a0002c0005t0001g0288 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3844-753C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 34/43 | chr9 | 129000776 | |||||||
| chr9:129000991 | C | T | 1 | a0001c0021t0001g0135 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3844-538C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 34/43 | chr9 | 129000991 | |||||||
| chr9:129001145 | G | C | 2 | a0001c0002t0001g0189 a0001c0002t0001g0191 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.3844-384G>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 34/43 | chr9 | 129001145 | |||||||
| chr9:129001159 | G | A | 109 | a0001c0001t0001g0221 a0001c0002t0001g0048 a0001c0002t0001g0099 others(106): Show |
109 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.3844-370G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 34/43 | chr9 | 129001159 | |||||||
| chr9:129001239 | G | A | 1 | a0001c0002t0001g0252 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3844-290G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 34/43 | chr9 | 129001239 | |||||||
| chr9:129001266 | G | A | 1 | a0009c0018t0001g0089 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.3844-263G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 34/43 | chr9 | 129001266 | |||||||
| chr9:129001735 | A | C | 67 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(64): Show |
68 | HG00280.hp2 HG00558.hp2 HG00673.hp1 others(65): Show |
splice_region_variant&intron_variant | LOW | c.4044+6A>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 35/43 | chr9 | 129001735 | |||||||
| chr9:129001745 | G | A | 1 | a0001c0002t0001g0048 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.4044+16G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 35/43 | chr9 | 129001745 | |||||||
| chr9:129001836 | A | G | 6 | a0002c0005t0001g0288 a0002c0005t0001g0290 a0002c0005t0001g0291 others(3): Show |
6 | HG01167.hp1 HG02451.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.4045-48A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 35/43 | chr9 | 129001836 | |||||||
| chr9:129002099 | G | A | 1 | a0001c0002t0001g0245 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.4137+123G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 36/43 | chr9 | 129002099 | |||||||
| chr9:129002347 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.4137+371G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 36/43 | chr9 | 129002347 | |||||||
| chr9:129002541 | G | T | 1 | a0001c0002t0001g0162 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.4138-276G>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 36/43 | chr9 | 129002541 | |||||||
| chr9:129002578 | G | A | 78 | a0001c0001t0001g0221 a0001c0002t0001g0048 a0001c0002t0001g0099 others(75): Show |
78 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.4138-239G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 36/43 | chr9 | 129002578 | |||||||
| chr9:129002579 | C | T | 2 | a0001c0001t0001g0100 a0001c0001t0001g0141 |
2 | NA19055.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.4138-238C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 36/43 | chr9 | 129002579 | |||||||
| chr9:129002644 | T | C | 14 | a0001c0003t0002g0271 a0001c0003t0002g0272 a0001c0003t0002g0273 others(11): Show |
14 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(11): Show |
intron_variant | MODIFIER | c.4138-173T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 36/43 | chr9 | 129002644 | |||||||
| chr9:129002690 | A | G | 80 | a0001c0001t0001g0221 a0001c0002t0001g0048 a0001c0002t0001g0067 others(77): Show |
80 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.4138-127A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 36/43 | chr9 | 129002690 | |||||||
| chr9:129002705 | A | G | 4 | a0001c0002t0001g0170 a0001c0002t0001g0207 a0001c0002t0001g0219 others(1): Show |
4 | HG00738.hp2 HG01243.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.4138-112A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 36/43 | chr9 | 129002705 | |||||||
| chr9:129003051 | G | A | 6 | a0001c0002t0001g0172 a0001c0002t0001g0173 a0001c0002t0001g0181 others(3): Show |
6 | NA18943.hp1 NA18955.hp2 NA18962.hp2 others(3): Show |
intron_variant | MODIFIER | c.4296+76G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 37/43 | chr9 | 129003051 | |||||||
| chr9:129003070 | G | A | 2 | a0001c0001t0001g0077 a0001c0001t0001g0094 |
2 | NA18962.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.4296+95G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 37/43 | chr9 | 129003070 | |||||||
| chr9:129003099 | T | C | 79 | a0001c0001t0001g0221 a0001c0002t0001g0048 a0001c0002t0001g0099 others(76): Show |
79 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.4296+124T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 37/43 | chr9 | 129003099 | |||||||
| chr9:129003154 | G | A | 1 | a0001c0002t0001g0240 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.4297-163G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 37/43 | chr9 | 129003154 | |||||||
| chr9:129003269 | G | A | 1 | a0001c0027t0001g0287 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.4297-48G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 37/43 | chr9 | 129003269 | |||||||
| chr9:129003517 | G | T | 1 | a0001c0001t0001g0119 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.4434+63G>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 38/43 | chr9 | 129003517 | |||||||
| chr9:129003521 | C | T | 1 | a0001c0002t0001g0200 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.4434+67C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 38/43 | chr9 | 129003521 | |||||||
| chr9:129003532 | T | C | 1 | a0001c0027t0001g0287 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.4434+78T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 38/43 | chr9 | 129003532 | |||||||
| chr9:129003648 | T | C | 14 | a0001c0003t0002g0271 a0001c0003t0002g0272 a0001c0003t0002g0273 others(11): Show |
14 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(11): Show |
intron_variant | MODIFIER | c.4434+194T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 38/43 | chr9 | 129003648 | |||||||
| chr9:129003708 | T | C | 141 | a0001c0002t0001g0011 a0001c0002t0001g0013 a0001c0002t0001g0020 others(138): Show |
142 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.4434+254T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 38/43 | chr9 | 129003708 | |||||||
| chr9:129003978 | GA | G | 11 | a0001c0001t0001g0006 a0001c0001t0004g0285 a0001c0001t0004g0286 others(8): Show |
11 | HG02622.hp1 HG02630.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.4434+539delA | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 38/43 | INFO_REALIGN_3_PRIME | chr9 | 129003978 | ||||||
| chr9:129004073 | C | T | 75 | a0001c0002t0001g0170 a0001c0002t0001g0171 a0001c0002t0001g0172 others(72): Show |
75 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.4434+619C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 38/43 | chr9 | 129004073 | |||||||
| chr9:129004148 | A | G | 91 | a0001c0002t0001g0067 a0001c0002t0001g0170 a0001c0002t0001g0171 others(88): Show |
91 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.4434+694A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 38/43 | chr9 | 129004148 | |||||||
| chr9:129004281 | C | CA | 8 | a0001c0001t0001g0016 a0001c0001t0001g0031 a0001c0001t0001g0060 others(5): Show |
8 | HG01496.hp2 HG02056.hp1 NA18946.hp1 others(5): Show |
intron_variant | MODIFIER | c.4434+845dupA | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 38/43 | INFO_REALIGN_3_PRIME | chr9 | 129004281 | ||||||
| chr9:129004281 | CA | C | 20 | a0001c0001t0001g0059 a0001c0001t0001g0087 a0001c0002t0001g0034 others(17): Show |
20 | HG00738.hp2 HG01069.hp2 HG02027.hp1 others(17): Show |
intron_variant | MODIFIER | c.4434+845delA | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 38/43 | INFO_REALIGN_3_PRIME | chr9 | 129004281 | ||||||
| chr9:129004281 | CAA | C | 73 | a0001c0002t0001g0170 a0001c0002t0001g0171 a0001c0002t0001g0172 others(70): Show |
73 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.4434+844_4434+845d others(4): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 38/43 | INFO_REALIGN_3_PRIME | chr9 | 129004281 | ||||||
| chr9:129004290 | A | G | 2 | a0001c0009t0001g0265 a0001c0009t0001g0266 |
2 | HG02451.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.4434+836A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 38/43 | chr9 | 129004290 | |||||||
| chr9:129004501 | A | G | 1 | a0001c0009t0001g0266 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.4435-646A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 38/43 | chr9 | 129004501 | |||||||
| chr9:129004661 | C | T | 5 | a0002c0005t0001g0290 a0002c0005t0001g0291 a0002c0005t0001g0292 others(2): Show |
5 | HG01167.hp1 HG02451.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.4435-486C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 38/43 | chr9 | 129004661 | |||||||
| chr9:129004696 | G | A | 1 | a0001c0002t0001g0219 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.4435-451G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 38/43 | chr9 | 129004696 | |||||||
| chr9:129004791 | C | T | 1 | a0001c0001t0006g0022 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.4435-356C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 38/43 | chr9 | 129004791 | |||||||
| chr9:129004828 | C | G | 14 | a0001c0003t0002g0271 a0001c0003t0002g0272 a0001c0003t0002g0273 others(11): Show |
14 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(11): Show |
intron_variant | MODIFIER | c.4435-319C>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 38/43 | chr9 | 129004828 | |||||||
| chr9:129004945 | C | CAGGGGAG others(21): Show |
4 | a0001c0002t0001g0193 a0001c0002t0001g0214 a0001c0002t0001g0224 others(1): Show |
4 | HG01255.hp1 HG01346.hp2 HG01928.hp1 others(1): Show |
intron_variant | MODIFIER | c.4435-143_4435-116d others(30): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 38/43 | INFO_REALIGN_3_PRIME | chr9 | 129004945 | ||||||
| chr9:129004945 | C | CAGGGGAG others(49): Show |
3 | a0001c0002t0001g0181 a0001c0002t0001g0183 a0001c0023t0001g0168 |
3 | NA18962.hp2 NA18984.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.4435-171_4435-116d others(58): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 38/43 | INFO_REALIGN_3_PRIME | chr9 | 129004945 | ||||||
| chr9:129004945 | CAGGGGAG others(21): Show |
C | 4 | a0001c0002t0001g0187 a0001c0002t0001g0192 a0001c0002t0001g0213 others(1): Show |
4 | NA18968.hp2 NA18982.hp1 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.4435-143_4435-116d others(30): Show |
NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 38/43 | INFO_REALIGN_3_PRIME | chr9 | 129004945 | ||||||
| chr9:129004947 | G | A | 1 | a0001c0001t0001g0050 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.4435-200G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 38/43 | chr9 | 129004947 | |||||||
| chr9:129005566 | A | G | 1 | a0001c0027t0001g0287 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.4737+36A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 40/43 | chr9 | 129005566 | |||||||
| chr9:129005781 | G | A | 1 | a0001c0027t0001g0287 | 1 | HG06807.hp2 | splice_region_variant&intron_variant | LOW | c.4869+5G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 41/43 | chr9 | 129005781 | |||||||
| chr9:129005823 | C | T | 14 | a0001c0003t0002g0271 a0001c0003t0002g0272 a0001c0003t0002g0273 others(11): Show |
14 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(11): Show |
intron_variant | MODIFIER | c.4869+47C>T | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 41/43 | chr9 | 129005823 | |||||||
| chr9:129005912 | A | G | 28 | a0001c0001t0001g0012 a0001c0001t0001g0041 a0001c0001t0001g0042 others(25): Show |
28 | HG00423.hp1 HG00738.hp1 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.4869+136A>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 41/43 | chr9 | 129005912 | |||||||
| chr9:129005983 | G | A | 4 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(1): Show |
4 | HG01891.hp2 HG02055.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.4870-67G>A | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 41/43 | chr9 | 129005983 | |||||||
| chr9:129006461 | C | G | 2 | a0001c0002t0001g0217 a0001c0002t0001g0218 |
2 | HG02896.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.5074-41C>G | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 43/43 | chr9 | 129006461 | |||||||
| chr9:129006497 | T | C | 14 | a0001c0003t0002g0271 a0001c0003t0002g0272 a0001c0003t0002g0273 others(11): Show |
14 | HG02027.hp1 HG03834.hp2 HG04115.hp1 others(11): Show |
splice_region_variant&intron_variant | LOW | c.5074-5T>C | NUP188 | ENSG00000095319.14 | transcript | ENST00000372577.2 | protein_coding | 43/43 | chr9 | 129006497 |