Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 8021 |
| ensemblid | ENSG00000126883.19 |
| hgncid | 8064 |
| symbol | NUP214 |
| name | nucleoporin 214 |
| refseq_nuc | NM_005085.4 |
| refseq_prot | NP_005076.3 |
| ensembl_nuc | ENST00000359428.10 |
| ensembl_prot | ENSP00000352400.5 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 131125586 |
| end | 131234663 |
| strand | + |
| ver | v1.2 |
| region | chr9:131125586-131234663 |
| region5000 | chr9:131120586-131239663 |
| regionname0 | NUP214_chr9_131125586_131234663 |
| regionname5000 | NUP214_chr9_131120586_131239663 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 2090 | 112 | 31 | 22 | 39 | 5 | 14 | 23 | NUP214_chr9_131120586_131239663 | NUP214 | MGDEM others(2085): Show |
chr9 | 131120586 | 131239663 |
| a0002 | 1/0 | 2090 | 98 | 21 | 17 | 40 | 3 | 16 | 30 | NUP214_chr9_131120586_131239663 | NUP214 | MGDEM others(2085): Show |
chr9 | 131120586 | 131239663 |
| a0003 | 0/0 | 2090 | 5 | 2 | 0 | 0 | 0 | 3 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | MGDEM others(2085): Show |
chr9 | 131120586 | 131239663 |
| a0004 | 0/0 | 2090 | 3 | 0 | 0 | 3 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | MGDEM others(2085): Show |
chr9 | 131120586 | 131239663 |
| a0005 | 0/0 | 2090 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | MGDEM others(2085): Show |
chr9 | 131120586 | 131239663 |
| a0006 | 0/0 | 2090 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | MGDEM others(2085): Show |
chr9 | 131120586 | 131239663 |
| a0007 | 0/0 | 2090 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | MGDEM others(2085): Show |
chr9 | 131120586 | 131239663 |
| a0008 | 0/0 | 2090 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | MGDEM others(2085): Show |
chr9 | 131120586 | 131239663 |
| a0009 | 0/0 | 2090 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | MGDEM others(2085): Show |
chr9 | 131120586 | 131239663 |
| a0010 | 0/0 | 2090 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | MGDEM others(2085): Show |
chr9 | 131120586 | 131239663 |
| a0011 | 0/0 | 2090 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | MGDEM others(2085): Show |
chr9 | 131120586 | 131239663 |
| a0012 | 0/0 | 2090 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | MGDEM others(2085): Show |
chr9 | 131120586 | 131239663 |
| a0013 | 0/0 | 2090 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | MGDEM others(2085): Show |
chr9 | 131120586 | 131239663 |
| a0014 | 0/0 | 2090 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | MGDEM others(2085): Show |
chr9 | 131120586 | 131239663 |
| a0015 | 0/0 | 2090 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | MGDEM others(2085): Show |
chr9 | 131120586 | 131239663 |
| a0016 | 0/0 | 2090 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | MGDEM others(2085): Show |
chr9 | 131120586 | 131239663 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 6270 | 80 | 19 | 19 | 25 | 4 | 12 | NUP214_chr9_131120586_131239663 | NUP214 | ATGGG others(6265): Show |
chr9 | 131120586 | 131239663 | ||
| a0001c0004 | 0/0 | 6270 | 13 | 3 | 1 | 6 | 1 | 2 | NUP214_chr9_131120586_131239663 | NUP214 | ATGGG others(6265): Show |
chr9 | 131120586 | 131239663 | ||
| a0001c0005 | 0/0 | 6270 | 5 | 4 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | ATGGG others(6265): Show |
chr9 | 131120586 | 131239663 | ||
| a0001c0006 | 0/0 | 6270 | 4 | 0 | 0 | 4 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | ATGGG others(6265): Show |
chr9 | 131120586 | 131239663 | ||
| a0001c0007 | 0/0 | 6270 | 3 | 3 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | ATGGG others(6265): Show |
chr9 | 131120586 | 131239663 | ||
| a0001c0010 | 0/0 | 6270 | 3 | 2 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | ATGGG others(6265): Show |
chr9 | 131120586 | 131239663 | ||
| a0001c0015 | 0/0 | 6270 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | ATGGG others(6265): Show |
chr9 | 131120586 | 131239663 | ||
| a0001c0024 | 0/0 | 6270 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | ATGGG others(6265): Show |
chr9 | 131120586 | 131239663 | ||
| a0001c0026 | 0/0 | 6270 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | ATGGG others(6265): Show |
chr9 | 131120586 | 131239663 | ||
| a0001c0027 | 0/0 | 6270 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | ATGGG others(6265): Show |
chr9 | 131120586 | 131239663 | ||
| a0002c0002 | 0/0 | 6270 | 74 | 6 | 15 | 35 | 3 | 15 | NUP214_chr9_131120586_131239663 | NUP214 | ATGGG others(6265): Show |
chr9 | 131120586 | 131239663 | ||
| a0002c0003 | 1/0 | 6270 | 21 | 13 | 2 | 5 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | ATGGG others(6265): Show |
chr9 | 131120586 | 131239663 | ||
| a0002c0016 | 0/0 | 6270 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | ATGGG others(6265): Show |
chr9 | 131120586 | 131239663 | ||
| a0002c0018 | 0/0 | 6270 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | ATGGG others(6265): Show |
chr9 | 131120586 | 131239663 | ||
| a0002c0020 | 0/0 | 6270 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | ATGGG others(6265): Show |
chr9 | 131120586 | 131239663 | ||
| a0003c0011 | 0/0 | 6270 | 3 | 1 | 0 | 0 | 0 | 2 | NUP214_chr9_131120586_131239663 | NUP214 | ATGGG others(6265): Show |
chr9 | 131120586 | 131239663 | ||
| a0003c0013 | 0/0 | 6270 | 2 | 1 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | ATGGG others(6265): Show |
chr9 | 131120586 | 131239663 | ||
| a0004c0009 | 0/0 | 6270 | 3 | 0 | 0 | 3 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | ATGGG others(6265): Show |
chr9 | 131120586 | 131239663 | ||
| a0005c0012 | 0/0 | 6270 | 3 | 2 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | ATGGG others(6265): Show |
chr9 | 131120586 | 131239663 | ||
| a0006c0008 | 0/0 | 6270 | 3 | 3 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | ATGGG others(6265): Show |
chr9 | 131120586 | 131239663 | ||
| a0007c0025 | 0/0 | 6270 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | ATGGG others(6265): Show |
chr9 | 131120586 | 131239663 | ||
| a0008c0028 | 0/0 | 6270 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | ATGGG others(6265): Show |
chr9 | 131120586 | 131239663 | ||
| a0009c0029 | 0/0 | 6270 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | ATGGG others(6265): Show |
chr9 | 131120586 | 131239663 | ||
| a0010c0017 | 0/0 | 6270 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | ATGGG others(6265): Show |
chr9 | 131120586 | 131239663 | ||
| a0011c0030 | 0/0 | 6270 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | ATGGG others(6265): Show |
chr9 | 131120586 | 131239663 | ||
| a0012c0023 | 0/0 | 6270 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | ATGGG others(6265): Show |
chr9 | 131120586 | 131239663 | ||
| a0013c0021 | 0/0 | 6270 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | ATGGG others(6265): Show |
chr9 | 131120586 | 131239663 | ||
| a0014c0014 | 0/0 | 6270 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | ATGGG others(6265): Show |
chr9 | 131120586 | 131239663 | ||
| a0015c0019 | 0/0 | 6270 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | ATGGG others(6265): Show |
chr9 | 131120586 | 131239663 | ||
| a0016c0022 | 0/0 | 6270 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | ATGGG others(6265): Show |
chr9 | 131120586 | 131239663 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 7568 | 76 | 19 | 18 | 23 | 4 | 11 | NUP214_chr9_131120586_131239663 | NUP214 | GAGGT others(7563): Show |
chr9 | 131120586 | 131239663 |
| a0001c0001t0006 | 0/0 | 7568 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | GAGGT others(7563): Show |
chr9 | 131120586 | 131239663 |
| a0001c0001t0007 | 0/0 | 7568 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | GAGGT others(7563): Show |
chr9 | 131120586 | 131239663 |
| a0001c0001t0009 | 0/0 | 7568 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | GAGGT others(7563): Show |
chr9 | 131120586 | 131239663 |
| a0001c0001t0010 | 0/0 | 7568 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | GAGGT others(7563): Show |
chr9 | 131120586 | 131239663 |
| a0001c0004t0001 | 0/0 | 7568 | 13 | 3 | 1 | 6 | 1 | 2 | NUP214_chr9_131120586_131239663 | NUP214 | GAGGT others(7563): Show |
chr9 | 131120586 | 131239663 |
| a0001c0005t0002 | 0/0 | 7567 | 4 | 3 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | GAGGT others(7562): Show |
chr9 | 131120586 | 131239663 |
| a0001c0005t0003 | 0/0 | 7568 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | GAGGT others(7563): Show |
chr9 | 131120586 | 131239663 |
| a0001c0006t0001 | 0/0 | 7568 | 4 | 0 | 0 | 4 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | GAGGT others(7563): Show |
chr9 | 131120586 | 131239663 |
| a0001c0007t0001 | 0/0 | 7568 | 3 | 3 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | GAGGT others(7563): Show |
chr9 | 131120586 | 131239663 |
| a0001c0010t0003 | 0/0 | 7568 | 3 | 2 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | GAGGT others(7563): Show |
chr9 | 131120586 | 131239663 |
| a0001c0015t0001 | 0/0 | 7568 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | GAGGT others(7563): Show |
chr9 | 131120586 | 131239663 |
| a0001c0024t0001 | 0/0 | 7568 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | GAGGT others(7563): Show |
chr9 | 131120586 | 131239663 |
| a0001c0026t0001 | 0/0 | 7568 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | GAGGT others(7563): Show |
chr9 | 131120586 | 131239663 |
| a0001c0027t0001 | 0/0 | 7568 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | GAGGT others(7563): Show |
chr9 | 131120586 | 131239663 |
| a0002c0002t0001 | 0/0 | 7568 | 72 | 6 | 15 | 33 | 3 | 15 | NUP214_chr9_131120586_131239663 | NUP214 | GAGGT others(7563): Show |
chr9 | 131120586 | 131239663 |
| a0002c0002t0008 | 0/0 | 7567 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | GAGGT others(7562): Show |
chr9 | 131120586 | 131239663 |
| a0002c0002t0011 | 0/0 | 7568 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | GAGGT others(7563): Show |
chr9 | 131120586 | 131239663 |
| a0002c0003t0001 | 1/0 | 7568 | 21 | 13 | 2 | 5 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | GAGGT others(7563): Show |
chr9 | 131120586 | 131239663 |
| a0002c0016t0001 | 0/0 | 7568 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | GAGGT others(7563): Show |
chr9 | 131120586 | 131239663 |
| a0002c0018t0002 | 0/0 | 7567 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | GAGGT others(7562): Show |
chr9 | 131120586 | 131239663 |
| a0002c0020t0012 | 0/0 | 7568 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | GAGGT others(7563): Show |
chr9 | 131120586 | 131239663 |
| a0003c0011t0001 | 0/0 | 7568 | 3 | 1 | 0 | 0 | 0 | 2 | NUP214_chr9_131120586_131239663 | NUP214 | GAGGT others(7563): Show |
chr9 | 131120586 | 131239663 |
| a0003c0013t0001 | 0/0 | 7568 | 2 | 1 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | GAGGT others(7563): Show |
chr9 | 131120586 | 131239663 |
| a0004c0009t0001 | 0/0 | 7568 | 3 | 0 | 0 | 3 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | GAGGT others(7563): Show |
chr9 | 131120586 | 131239663 |
| a0005c0012t0001 | 0/0 | 7568 | 3 | 2 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | GAGGT others(7563): Show |
chr9 | 131120586 | 131239663 |
| a0006c0008t0001 | 0/0 | 7568 | 3 | 3 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | GAGGT others(7563): Show |
chr9 | 131120586 | 131239663 |
| a0007c0025t0001 | 0/0 | 7568 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | GAGGT others(7563): Show |
chr9 | 131120586 | 131239663 |
| a0008c0028t0004 | 0/0 | 7567 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | GAGGT others(7562): Show |
chr9 | 131120586 | 131239663 |
| a0009c0029t0001 | 0/0 | 7568 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | GAGGT others(7563): Show |
chr9 | 131120586 | 131239663 |
| a0010c0017t0001 | 0/0 | 7568 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | GAGGT others(7563): Show |
chr9 | 131120586 | 131239663 |
| a0011c0030t0001 | 0/0 | 7568 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | GAGGT others(7563): Show |
chr9 | 131120586 | 131239663 |
| a0012c0023t0005 | 0/0 | 7568 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | GAGGT others(7563): Show |
chr9 | 131120586 | 131239663 |
| a0013c0021t0001 | 0/0 | 7568 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | GAGGT others(7563): Show |
chr9 | 131120586 | 131239663 |
| a0014c0014t0001 | 0/0 | 7568 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | GAGGT others(7563): Show |
chr9 | 131120586 | 131239663 |
| a0015c0019t0001 | 0/0 | 7568 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | GAGGT others(7563): Show |
chr9 | 131120586 | 131239663 |
| a0016c0022t0001 | 0/0 | 7568 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | GAGGT others(7563): Show |
chr9 | 131120586 | 131239663 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0101 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0006g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0007g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0009g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0001t0010g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0004t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0004t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0004t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0004t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0004t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0004t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0004t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0004t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0004t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0004t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0004t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0004t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0004t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0005t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0005t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0005t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0005t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0005t0003g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0006t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0006t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0006t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0006t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0007t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0007t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0007t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0010t0003g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0010t0003g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0010t0003g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0015t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0024t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0026t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0001c0027t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0008g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0002t0011g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0003t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0003t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0003t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0003t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0003t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0003t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0003t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0003t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0003t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0003t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0003t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0003t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0003t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0003t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0003t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0003t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0003t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0003t0001g0127 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0003t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0003t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0003t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0016t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0018t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0002c0020t0012g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0003c0011t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0003c0011t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0003c0011t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0003c0013t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0003c0013t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0004c0009t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0004c0009t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0004c0009t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0005c0012t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0005c0012t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0005c0012t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0006c0008t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0006c0008t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0006c0008t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0007c0025t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0008c0028t0004g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0009c0029t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0010c0017t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0011c0030t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0012c0023t0005g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0013c0021t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0014c0014t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0015c0019t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| a0016c0022t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0057 | EUR | GBR | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG00099 | hp2 | a0002 | c0002 | t0001 | g0202 | EUR | GBR | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | CHS | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG00408 | hp2 | a0001 | c0006 | t0001 | g0169 | EAS | CHS | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | CHS | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG00423 | hp2 | a0002 | c0002 | t0001 | g0193 | EAS | CHS | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG00438 | hp1 | a0001 | c0001 | t0010 | g0234 | EAS | CHS | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG00438 | hp2 | a0001 | c0001 | t0006 | g0075 | EAS | CHS | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG00544 | hp1 | a0001 | c0006 | t0001 | g0168 | EAS | CHS | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG00544 | hp2 | a0007 | c0025 | t0001 | g0084 | EAS | CHS | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG00558 | hp2 | a0002 | c0002 | t0001 | g0144 | EAS | CHS | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG00597 | hp1 | a0002 | c0002 | t0001 | g0150 | EAS | CHS | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG00597 | hp2 | a0004 | c0009 | t0001 | g0030 | EAS | CHS | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG00609 | hp1 | a0004 | c0009 | t0001 | g0039 | EAS | CHS | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG00609 | hp2 | a0001 | c0004 | t0001 | g0140 | EAS | CHS | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG00639 | hp2 | a0002 | c0002 | t0001 | g0009 | AMR | PUR | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG00642 | hp1 | a0002 | c0002 | t0001 | g0078 | AMR | PUR | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG00733 | hp1 | a0002 | c0002 | t0001 | g0136 | AMR | PUR | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG00741 | hp2 | a0002 | c0002 | t0001 | g0158 | AMR | PUR | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG01074 | hp2 | a0002 | c0003 | t0001 | g0044 | AMR | PUR | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG01106 | hp2 | a0005 | c0012 | t0001 | g0007 | AMR | PUR | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG01109 | hp1 | a0001 | c0010 | t0003 | g0214 | AMR | PUR | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG01168 | hp2 | a0002 | c0002 | t0001 | g0199 | AMR | PUR | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG01169 | hp1 | a0002 | c0002 | t0001 | g0195 | AMR | PUR | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG01175 | hp1 | a0002 | c0002 | t0001 | g0184 | AMR | PUR | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG01243 | hp1 | a0002 | c0002 | t0001 | g0208 | AMR | PUR | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG01243 | hp2 | a0002 | c0003 | t0001 | g0045 | AMR | PUR | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG01361 | hp1 | a0001 | c0004 | t0001 | g0131 | AMR | CLM | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG01361 | hp2 | a0002 | c0002 | t0001 | g0222 | AMR | CLM | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | CLM | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG01433 | hp2 | a0002 | c0002 | t0001 | g0200 | AMR | CLM | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | CLM | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG01496 | hp2 | a0001 | c0005 | t0002 | g0213 | AMR | CLM | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0076 | EUR | IBS | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG01515 | hp2 | a0002 | c0002 | t0001 | g0161 | EUR | IBS | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0230 | EUR | IBS | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG01516 | hp2 | a0001 | c0004 | t0001 | g0201 | EUR | IBS | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG01884 | hp1 | a0002 | c0003 | t0001 | g0126 | AFR | ACB | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG01884 | hp2 | a0002 | c0002 | t0001 | g0225 | AFR | ACB | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | ACB | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG01891 | hp2 | a0001 | c0005 | t0003 | g0211 | AFR | ACB | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG01928 | hp1 | a0001 | c0001 | t0007 | g0042 | AMR | PEL | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG01928 | hp2 | a0002 | c0002 | t0001 | g0194 | AMR | PEL | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG01943 | hp2 | a0002 | c0002 | t0001 | g0224 | AMR | PEL | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG01981 | hp1 | a0002 | c0002 | t0001 | g0166 | AMR | PEL | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG01993 | hp1 | a0002 | c0002 | t0001 | g0180 | AMR | PEL | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02015 | hp1 | a0002 | c0002 | t0001 | g0165 | EAS | KHV | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | KHV | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02027 | hp2 | a0002 | c0002 | t0001 | g0188 | EAS | KHV | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02055 | hp1 | a0002 | c0002 | t0001 | g0163 | AFR | ACB | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | ACB | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02056 | hp1 | a0002 | c0002 | t0001 | g0133 | EAS | KHV | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02056 | hp2 | a0001 | c0027 | t0001 | g0085 | EAS | KHV | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02083 | hp1 | a0002 | c0002 | t0001 | g0183 | EAS | KHV | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02083 | hp2 | a0001 | c0015 | t0001 | g0046 | EAS | KHV | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02132 | hp1 | a0002 | c0002 | t0001 | g0181 | EAS | KHV | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | KHV | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02135 | hp2 | a0002 | c0002 | t0001 | g0210 | EAS | KHV | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02145 | hp1 | a0008 | c0028 | t0004 | g0207 | AFR | ACB | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02145 | hp2 | a0001 | c0007 | t0001 | g0086 | AFR | ACB | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | CDX | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02165 | hp2 | a0001 | c0004 | t0001 | g0198 | EAS | CDX | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02258 | hp1 | a0002 | c0003 | t0001 | g0125 | AFR | ACB | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02293 | hp1 | a0002 | c0002 | t0001 | g0192 | AMR | PEL | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | ACB | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02451 | hp2 | a0001 | c0005 | t0002 | g0206 | AFR | ACB | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02523 | hp1 | a0009 | c0029 | t0001 | g0062 | EAS | KHV | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02523 | hp2 | a0002 | c0002 | t0001 | g0187 | EAS | KHV | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02615 | hp1 | a0003 | c0013 | t0001 | g0070 | AFR | GWD | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02615 | hp2 | a0001 | c0004 | t0001 | g0227 | AFR | GWD | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02630 | hp1 | a0002 | c0003 | t0001 | g0123 | AFR | GWD | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02630 | hp2 | a0001 | c0005 | t0002 | g0212 | AFR | GWD | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0177 | SAS | PJL | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02723 | hp1 | a0002 | c0003 | t0001 | g0074 | AFR | GWD | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02723 | hp2 | a0005 | c0012 | t0001 | g0006 | AFR | GWD | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02735 | hp2 | a0002 | c0002 | t0001 | g0130 | SAS | PJL | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02738 | hp1 | a0002 | c0002 | t0001 | g0147 | SAS | PJL | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02738 | hp2 | a0002 | c0002 | t0001 | g0143 | SAS | PJL | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02809 | hp1 | a0002 | c0002 | t0001 | g0221 | AFR | GWD | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02809 | hp2 | a0002 | c0003 | t0001 | g0124 | AFR | GWD | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02818 | hp1 | a0001 | c0010 | t0003 | g0229 | AFR | GWD | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02818 | hp2 | a0002 | c0002 | t0001 | g0226 | AFR | GWD | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02886 | hp1 | a0010 | c0017 | t0001 | g0108 | AFR | GWD | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02886 | hp2 | a0001 | c0010 | t0003 | g0228 | AFR | GWD | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02897 | hp1 | a0005 | c0012 | t0001 | g0005 | AFR | GWD | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02897 | hp2 | a0001 | c0007 | t0001 | g0088 | AFR | GWD | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02922 | hp1 | a0002 | c0002 | t0001 | g0223 | AFR | ESN | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | ESN | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | ESN | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | ESN | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | ESN | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02970 | hp2 | a0001 | c0005 | t0002 | g0205 | AFR | ESN | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | ESN | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02976 | hp2 | a0002 | c0003 | t0001 | g0121 | AFR | ESN | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG03041 | hp1 | a0002 | c0003 | t0001 | g0063 | AFR | GWD | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG03041 | hp2 | a0001 | c0007 | t0001 | g0064 | AFR | GWD | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG03130 | hp1 | a0002 | c0003 | t0001 | g0128 | AFR | ESN | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG03195 | hp1 | a0002 | c0003 | t0001 | g0071 | AFR | ESN | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | ESN | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG03209 | hp1 | a0011 | c0030 | t0001 | g0091 | AFR | MSL | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG03209 | hp2 | a0002 | c0003 | t0001 | g0122 | AFR | MSL | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG03239 | hp1 | a0003 | c0013 | t0001 | g0041 | SAS | PJL | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG03239 | hp2 | a0002 | c0002 | t0001 | g0021 | SAS | PJL | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG03486 | hp1 | a0002 | c0020 | t0012 | g0132 | AFR | MSL | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG03486 | hp2 | a0002 | c0003 | t0001 | g0218 | AFR | MSL | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG03490 | hp2 | a0002 | c0002 | t0001 | g0134 | SAS | PJL | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG03491 | hp2 | a0002 | c0002 | t0001 | g0154 | SAS | PJL | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG03492 | hp1 | a0002 | c0002 | t0001 | g0155 | SAS | PJL | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG03540 | hp1 | a0001 | c0004 | t0001 | g0219 | AFR | GWD | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG03579 | hp1 | a0012 | c0023 | t0005 | g0003 | AFR | MSL | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG03579 | hp2 | a0002 | c0016 | t0001 | g0100 | AFR | MSL | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG03688 | hp1 | a0003 | c0011 | t0001 | g0178 | SAS | STU | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | STU | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG03704 | hp1 | a0002 | c0002 | t0001 | g0067 | SAS | PJL | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0050 | SAS | PJL | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG03831 | hp1 | a0013 | c0021 | t0001 | g0173 | SAS | BEB | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0233 | SAS | BEB | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG03927 | hp1 | a0002 | c0002 | t0001 | g0139 | SAS | BEB | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG03927 | hp2 | a0001 | c0004 | t0001 | g0162 | SAS | BEB | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG03942 | hp1 | a0002 | c0002 | t0001 | g0175 | SAS | BEB | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG03942 | hp2 | a0002 | c0002 | t0001 | g0104 | SAS | BEB | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG04184 | hp1 | a0001 | c0001 | t0009 | g0072 | SAS | BEB | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG04184 | hp2 | a0001 | c0004 | t0001 | g0209 | SAS | BEB | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | STU | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG04199 | hp2 | a0002 | c0002 | t0001 | g0113 | SAS | STU | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG04204 | hp1 | a0002 | c0002 | t0001 | g0185 | SAS | STU | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG04204 | hp2 | a0003 | c0011 | t0001 | g0191 | SAS | STU | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG04228 | hp1 | a0002 | c0002 | t0001 | g0077 | SAS | STU | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG04228 | hp2 | a0002 | c0018 | t0002 | g0107 | SAS | STU | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA18522 | hp1 | a0006 | c0008 | t0001 | g0109 | AFR | YRI | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | YRI | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA18944 | hp2 | a0002 | c0002 | t0001 | g0145 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA18945 | hp1 | a0002 | c0002 | t0001 | g0159 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA18945 | hp2 | a0001 | c0024 | t0001 | g0056 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA18948 | hp2 | a0002 | c0002 | t0001 | g0151 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA18949 | hp1 | a0002 | c0003 | t0001 | g0097 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA18949 | hp2 | a0002 | c0002 | t0001 | g0156 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA18952 | hp1 | a0002 | c0002 | t0001 | g0118 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA18952 | hp2 | a0001 | c0004 | t0001 | g0204 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA18953 | hp1 | a0002 | c0002 | t0001 | g0135 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA18953 | hp2 | a0002 | c0002 | t0001 | g0149 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA18960 | hp2 | a0002 | c0002 | t0001 | g0152 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA18961 | hp1 | a0001 | c0004 | t0001 | g0138 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA18962 | hp1 | a0002 | c0003 | t0001 | g0093 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA18968 | hp1 | a0002 | c0002 | t0001 | g0157 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA18968 | hp2 | a0002 | c0002 | t0001 | g0142 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA18969 | hp2 | a0002 | c0002 | t0001 | g0167 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA18971 | hp1 | a0002 | c0002 | t0001 | g0117 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA18983 | hp2 | a0001 | c0004 | t0001 | g0197 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA18991 | hp1 | a0001 | c0006 | t0001 | g0174 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA19000 | hp1 | a0002 | c0002 | t0001 | g0164 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA19000 | hp2 | a0002 | c0002 | t0001 | g0115 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA19001 | hp1 | a0002 | c0002 | t0001 | g0190 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA19001 | hp2 | a0002 | c0003 | t0001 | g0069 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA19002 | hp2 | a0002 | c0002 | t0011 | g0105 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA19009 | hp1 | a0002 | c0002 | t0001 | g0172 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA19009 | hp2 | a0014 | c0014 | t0001 | g0099 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA19010 | hp1 | a0002 | c0002 | t0001 | g0160 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA19010 | hp2 | a0002 | c0003 | t0001 | g0083 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA19011 | hp1 | a0002 | c0002 | t0001 | g0116 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | LWK | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA19030 | hp2 | a0001 | c0004 | t0001 | g0137 | AFR | LWK | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | LWK | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA19054 | hp1 | a0002 | c0002 | t0001 | g0153 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA19055 | hp1 | a0004 | c0009 | t0001 | g0031 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA19055 | hp2 | a0002 | c0002 | t0008 | g0148 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA19060 | hp1 | a0001 | c0004 | t0001 | g0196 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA19060 | hp2 | a0001 | c0006 | t0001 | g0179 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA19074 | hp1 | a0002 | c0002 | t0001 | g0119 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA19074 | hp2 | a0001 | c0026 | t0001 | g0055 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA19080 | hp1 | a0002 | c0002 | t0001 | g0146 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA19081 | hp1 | a0002 | c0003 | t0001 | g0016 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA19081 | hp2 | a0002 | c0002 | t0001 | g0182 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA19084 | hp1 | a0002 | c0002 | t0001 | g0106 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA19091 | hp1 | a0015 | c0019 | t0001 | g0141 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA19240 | hp1 | a0002 | c0003 | t0001 | g0120 | AFR | YRI | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA19240 | hp2 | a0016 | c0022 | t0001 | g0112 | AFR | YRI | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0051 | EUR | TSI | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA20805 | hp2 | a0002 | c0002 | t0001 | g0203 | EUR | TSI | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | ACB | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02109 | hp2 | a0006 | c0008 | t0001 | g0040 | AFR | ACB | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02559 | hp1 | a0006 | c0008 | t0001 | g0032 | AFR | ACB | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG02559 | hp2 | a0002 | c0002 | t0001 | g0220 | AFR | ACB | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | USA | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| HG06807 | hp2 | a0002 | c0003 | t0001 | g0129 | AFR | USA | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA20300 | hp1 | a0003 | c0011 | t0001 | g0186 | AFR | USA | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | USA | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0101 | REF | REF | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| homoSapiens | grch38p0 | a0002 | c0003 | t0001 | g0127 | REF | REF | NUP214_chr9_131120586_131239663 | NUP214 | chr9 | 131120586 | 131239663 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:131127647 | A | C | 1 | a0011 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.169A>C | p.Ser57Arg | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 2/36 | 288/7568 | 169/6273 | 57/2090 | chr9 | 131127647 | |||
| chr9:131128416 | C | T | 1 | a0005 | 3 | HG01106.hp2 HG02723.hp2 HG02897.hp1 |
missense_variant | MODERATE | c.326C>T | p.Ala109Val | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 3/36 | 445/7568 | 326/6273 | 109/2090 | chr9 | 131128416 | |||
| chr9:131140677 | T | G | 1 | a0014 | 1 | NA19009.hp2 | missense_variant | MODERATE | c.1261T>G | p.Ser421Ala | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 11/36 | 1380/7568 | 1261/6273 | 421/2090 | chr9 | 131140677 | |||
| chr9:131144699 | A | G | 2 | a0003 a0009 |
6 | HG02523.hp1 HG02615.hp1 HG03239.hp1 others(3): Show |
missense_variant | MODERATE | c.1714A>G | p.Met572Val | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 12/36 | 1833/7568 | 1714/6273 | 572/2090 | chr9 | 131144699 | |||
| chr9:131144705 | C | T | 11 | a0001 a0004 a0005 others(8): Show |
127 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(124): Show |
missense_variant | MODERATE | c.1720C>T | p.Pro574Ser | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 12/36 | 1839/7568 | 1720/6273 | 574/2090 | chr9 | 131144705 | |||
| chr9:131150710 | G | T | 1 | a0004 | 3 | HG00597.hp2 HG00609.hp1 NA19055.hp1 |
missense_variant | MODERATE | c.2222G>T | p.Arg741Leu | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 16/36 | 2341/7568 | 2222/6273 | 741/2090 | chr9 | 131150710 | |||
| chr9:131151751 | A | G | 1 | a0013 | 1 | HG03831.hp1 | missense_variant | MODERATE | c.2293A>G | p.Ile765Val | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/36 | 2412/7568 | 2293/6273 | 765/2090 | chr9 | 131151751 | |||
| chr9:131163116 | A | G | 1 | a0008 | 1 | HG02145.hp1 | missense_variant | MODERATE | c.2666A>G | p.Lys889Arg | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 19/36 | 2785/7568 | 2666/6273 | 889/2090 | chr9 | 131163116 | |||
| chr9:131175568 | C | T | 1 | a0015 | 1 | NA19091.hp1 | missense_variant | MODERATE | c.3266C>T | p.Pro1089Leu | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 23/36 | 3385/7568 | 3266/6273 | 1089/2090 | chr9 | 131175568 | |||
| chr9:131198269 | G | C | 3 | a0010 a0012 a0016 |
3 | HG02886.hp1 HG03579.hp1 NA19240.hp2 |
missense_variant | MODERATE | c.4775G>C | p.Gly1592Ala | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 29/36 | 4894/7568 | 4775/6273 | 1592/2090 | chr9 | 131198269 | |||
| chr9:131198511 | G | C | 1 | a0006 | 3 | HG02109.hp2 HG02559.hp1 NA18522.hp1 |
missense_variant | MODERATE | c.5017G>C | p.Val1673Leu | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 29/36 | 5136/7568 | 5017/6273 | 1673/2090 | chr9 | 131198511 | |||
| chr9:131198701 | C | T | 1 | a0012 | 1 | HG03579.hp1 | missense_variant | MODERATE | c.5207C>T | p.Ala1736Val | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 29/36 | 5326/7568 | 5207/6273 | 1736/2090 | chr9 | 131198701 | |||
| chr9:131198745 | A | G | 1 | a0007 | 1 | HG00544.hp2 | missense_variant | MODERATE | c.5251A>G | p.Ser1751Gly | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 29/36 | 5370/7568 | 5251/6273 | 1751/2090 | chr9 | 131198745 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:131144593 | G | A | 1 | a0001c0015 | 1 | HG02083.hp2 | synonymous_variant | LOW | c.1608G>A | p.Ala536Ala | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 12/36 | 1727/7568 | 1608/6273 | 536/2090 | chr9 | 131144593 | |||
| chr9:131146243 | A | G | 12 | a0001c0004 a0001c0005 a0001c0006 others(9): Show |
108 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(105): Show |
synonymous_variant | LOW | c.1884A>G | p.Thr628Thr | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 13/36 | 2003/7568 | 1884/6273 | 628/2090 | chr9 | 131146243 | |||
| chr9:131150637 | T | C | 1 | a0001c0006 | 4 | HG00408.hp2 HG00544.hp1 NA18991.hp1 others(1): Show |
synonymous_variant | LOW | c.2149T>C | p.Leu717Leu | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 16/36 | 2268/7568 | 2149/6273 | 717/2090 | chr9 | 131150637 | |||
| chr9:131163096 | T | G | 2 | a0001c0007 a0002c0016 |
4 | HG02145.hp2 HG02897.hp2 HG03041.hp2 others(1): Show |
synonymous_variant | LOW | c.2646T>G | p.Leu882Leu | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 19/36 | 2765/7568 | 2646/6273 | 882/2090 | chr9 | 131163096 | |||
| chr9:131174212 | C | T | 1 | a0002c0020 | 1 | HG03486.hp1 | synonymous_variant | LOW | c.3051C>T | p.Pro1017Pro | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 22/36 | 3170/7568 | 3051/6273 | 1017/2090 | chr9 | 131174212 | |||
| chr9:131178336 | G | T | 1 | a0001c0026 | 1 | NA19074.hp2 | synonymous_variant | LOW | c.3345G>T | p.Thr1115Thr | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/36 | 3464/7568 | 3345/6273 | 1115/2090 | chr9 | 131178336 | |||
| chr9:131187346 | T | C | 5 | a0001c0005 a0001c0010 a0002c0018 others(2): Show |
11 | HG01109.hp1 HG01496.hp2 HG01891.hp2 others(8): Show |
synonymous_variant | LOW | c.3477T>C | p.Ala1159Ala | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 25/36 | 3596/7568 | 3477/6273 | 1159/2090 | chr9 | 131187346 | |||
| chr9:131198420 | A | G | 3 | a0001c0005 a0002c0018 a0008c0028 |
7 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(4): Show |
synonymous_variant | LOW | c.4926A>G | p.Ser1642Ser | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 29/36 | 5045/7568 | 4926/6273 | 1642/2090 | chr9 | 131198420 | |||
| chr9:131233457 | T | C | 3 | a0001c0024 a0001c0026 a0001c0027 |
3 | HG02056.hp2 NA18945.hp2 NA19074.hp2 |
synonymous_variant | LOW | c.6243T>C | p.Ser2081Ser | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 36/36 | 6362/7568 | 6243/6273 | 2081/2090 | chr9 | 131233457 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:131125667 | G | T | 1 | a0002c0020t0012 | 1 | HG03486.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-38G>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 1/36 | chr9 | 131125667 | |||||||
| chr9:131125677 | G | A | 2 | a0008c0028t0004 a0012c0023t0005 |
2 | HG02145.hp1 HG03579.hp1 |
5_prime_UTR_variant | MODIFIER | c.-28G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 1/36 | 28 | chr9 | 131125677 | ||||||
| chr9:131233491 | C | T | 1 | a0002c0002t0011 | 1 | NA19002.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 36/36 | 4 | chr9 | 131233491 | ||||||
| chr9:131233509 | G | A | 1 | a0002c0020t0012 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*22G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 36/36 | 22 | chr9 | 131233509 | ||||||
| chr9:131233538 | T | G | 1 | a0001c0001t0006 | 1 | HG00438.hp2 | 3_prime_UTR_variant | MODIFIER | c.*51T>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 36/36 | 51 | chr9 | 131233538 | ||||||
| chr9:131233612 | A | C | 1 | a0001c0001t0010 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*125A>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 36/36 | 125 | chr9 | 131233612 | ||||||
| chr9:131233671 | T | C | 1 | a0002c0020t0012 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*184T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 36/36 | 184 | chr9 | 131233671 | ||||||
| chr9:131233894 | A | G | 1 | a0001c0001t0009 | 1 | HG04184.hp1 | 3_prime_UTR_variant | MODIFIER | c.*407A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 36/36 | 407 | chr9 | 131233894 | ||||||
| chr9:131233936 | T | C | 6 | a0001c0005t0002 a0001c0005t0003 a0001c0010t0003 others(3): Show |
11 | HG01109.hp1 HG01496.hp2 HG01891.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*449T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 36/36 | 449 | chr9 | 131233936 | ||||||
| chr9:131233981 | T | G | 1 | a0001c0001t0007 | 1 | HG01928.hp1 | 3_prime_UTR_variant | MODIFIER | c.*494T>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 36/36 | 494 | chr9 | 131233981 | ||||||
| chr9:131234587 | AT | A | 4 | a0001c0005t0002 a0002c0002t0008 a0002c0018t0002 others(1): Show |
7 | HG01496.hp2 HG02145.hp1 HG02451.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1111delT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 36/36 | 1111 | INFO_REALIGN_3_PRIME | chr9 | 131234587 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:131125771 | C | G | 5 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0232 others(2): Show |
5 | HG00438.hp1 HG00642.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.45+22C>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 1/35 | chr9 | 131125771 | |||||||
| chr9:131125777 | C | T | 2 | a0001c0010t0003g0228 a0001c0010t0003g0229 |
2 | HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.45+28C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 1/35 | chr9 | 131125777 | |||||||
| chr9:131125865 | C | T | 13 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0217 others(10): Show |
13 | HG01361.hp2 HG01884.hp2 HG01943.hp2 others(10): Show |
intron_variant | MODIFIER | c.45+116C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 1/35 | chr9 | 131125865 | |||||||
| chr9:131125900 | C | T | 3 | a0001c0010t0003g0214 a0001c0010t0003g0228 a0001c0010t0003g0229 |
3 | HG01109.hp1 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.45+151C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 1/35 | chr9 | 131125900 | |||||||
| chr9:131125988 | C | T | 1 | a0001c0005t0002g0213 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.45+239C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 1/35 | chr9 | 131125988 | |||||||
| chr9:131126419 | G | C | 123 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(120): Show |
123 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.45+670G>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 1/35 | chr9 | 131126419 | |||||||
| chr9:131126550 | A | AT | 13 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0114 others(10): Show |
13 | HG01106.hp1 HG01361.hp1 HG02735.hp2 others(10): Show |
intron_variant | MODIFIER | c.45+816dupT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 1/35 | INFO_REALIGN_3_PRIME | chr9 | 131126550 | ||||||
| chr9:131126550 | A | ATT | 86 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0176 others(83): Show |
86 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.45+815_45+816dupTT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 1/35 | INFO_REALIGN_3_PRIME | chr9 | 131126550 | ||||||
| chr9:131126550 | A | ATTT | 5 | a0001c0004t0001g0209 a0001c0005t0002g0212 a0001c0005t0002g0213 others(2): Show |
5 | HG01496.hp2 HG01891.hp2 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.45+814_45+816dupTT others(1): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 1/35 | INFO_REALIGN_3_PRIME | chr9 | 131126550 | ||||||
| chr9:131126692 | C | T | 1 | a0002c0002t0001g0208 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.46-832C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 1/35 | chr9 | 131126692 | |||||||
| chr9:131126713 | A | G | 1 | a0010c0017t0001g0108 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.46-811A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 1/35 | chr9 | 131126713 | |||||||
| chr9:131126732 | T | C | 1 | a0001c0001t0001g0001 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.46-792T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 1/35 | chr9 | 131126732 | |||||||
| chr9:131126995 | C | A | 3 | a0001c0010t0003g0214 a0001c0010t0003g0228 a0001c0010t0003g0229 |
3 | HG01109.hp1 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.46-529C>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 1/35 | chr9 | 131126995 | |||||||
| chr9:131127109 | T | C | 90 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0176 others(87): Show |
90 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.46-415T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 1/35 | chr9 | 131127109 | |||||||
| chr9:131127240 | G | A | 1 | a0001c0001t0001g0002 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.46-284G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 1/35 | chr9 | 131127240 | |||||||
| chr9:131127519 | A | G | 1 | a0008c0028t0004g0207 | 1 | HG02145.hp1 | splice_region_variant&intron_variant | LOW | c.46-5A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 1/35 | chr9 | 131127519 | |||||||
| chr9:131127817 | A | G | 1 | a0002c0018t0002g0107 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.241+98A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 2/35 | chr9 | 131127817 | |||||||
| chr9:131127876 | C | T | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(115): Show |
118 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.241+157C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 2/35 | chr9 | 131127876 | |||||||
| chr9:131128214 | T | C | 6 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0212 others(3): Show |
6 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.242-118T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 2/35 | chr9 | 131128214 | |||||||
| chr9:131128513 | A | G | 85 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0176 others(82): Show |
85 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.393+30A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 3/35 | chr9 | 131128513 | |||||||
| chr9:131128607 | T | TA | 6 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0212 others(3): Show |
6 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.393+133dupA | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 3/35 | INFO_REALIGN_3_PRIME | chr9 | 131128607 | ||||||
| chr9:131129525 | A | C | 97 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0176 others(94): Show |
97 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.592+48A>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 4/35 | chr9 | 131129525 | |||||||
| chr9:131129575 | G | GT | 6 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0010t0003g0214 others(3): Show |
6 | HG01109.hp1 HG02818.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.592+108dupT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr9 | 131129575 | ||||||
| chr9:131129575 | G | T | 6 | a0001c0004t0001g0131 a0001c0004t0001g0201 a0002c0002t0001g0199 others(3): Show |
6 | HG00099.hp2 HG01168.hp2 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.592+98G>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 4/35 | chr9 | 131129575 | |||||||
| chr9:131129713 | C | T | 1 | a0001c0004t0001g0227 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.592+236C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 4/35 | chr9 | 131129713 | |||||||
| chr9:131129753 | G | A | 1 | a0002c0002t0001g0133 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.592+276G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 4/35 | chr9 | 131129753 | |||||||
| chr9:131130132 | G | GTTTTGTT others(6): Show |
2 | a0001c0004t0001g0138 a0002c0002t0001g0139 |
2 | HG03927.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.593-629_593-617dup others(13): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr9 | 131130132 | ||||||
| chr9:131130132 | G | GTTTTTTT others(3): Show |
1 | a0008c0028t0004g0207 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.593-630_593-629ins others(10): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr9 | 131130132 | ||||||
| chr9:131130137 | G | GT | 91 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(88): Show |
91 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.593-616dupT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr9 | 131130137 | ||||||
| chr9:131130137 | G | GTT | 24 | a0001c0001t0001g0001 a0001c0001t0001g0089 a0001c0001t0001g0090 others(21): Show |
24 | HG00438.hp1 HG00741.hp1 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.593-617_593-616dup others(2): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr9 | 131130137 | ||||||
| chr9:131130137 | G | GTTTTGTT others(8): Show |
1 | a0002c0002t0001g0134 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.593-625_593-624ins others(15): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr9 | 131130137 | ||||||
| chr9:131130137 | G | GTTTTGTT others(9): Show |
1 | a0002c0002t0001g0130 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.593-625_593-624ins others(16): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr9 | 131130137 | ||||||
| chr9:131130137 | G | GTTTTTGT others(5): Show |
1 | a0002c0002t0001g0135 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.593-624_593-623ins others(12): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr9 | 131130137 | ||||||
| chr9:131130137 | G | GTTTTTTT others(6): Show |
1 | a0002c0002t0001g0136 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.593-618_593-617ins others(13): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr9 | 131130137 | ||||||
| chr9:131130137 | G | GTTTTTTT others(7): Show |
2 | a0001c0004t0001g0137 a0002c0002t0001g0208 |
2 | HG01243.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.593-618_593-617ins others(14): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr9 | 131130137 | ||||||
| chr9:131130137 | G | GTTTTTTT others(5): Show |
1 | a0002c0002t0001g0157 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.593-627_593-616dup others(12): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr9 | 131130137 | ||||||
| chr9:131130137 | G | GTTTTTTT others(7): Show |
1 | a0001c0004t0001g0140 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.593-617_593-616ins others(14): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr9 | 131130137 | ||||||
| chr9:131130137 | G | GTTTTTTT others(10): Show |
1 | a0015c0019t0001g0141 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.593-617_593-616ins others(17): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr9 | 131130137 | ||||||
| chr9:131130137 | G | GTTTTTTT others(6): Show |
2 | a0002c0002t0001g0158 a0002c0002t0001g0159 |
2 | HG00741.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.593-628_593-616dup others(13): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr9 | 131130137 | ||||||
| chr9:131130137 | G | GTTTTTTT others(7): Show |
7 | a0001c0004t0001g0201 a0001c0004t0001g0204 a0002c0002t0001g0160 others(4): Show |
7 | HG00099.hp2 HG01433.hp2 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.593-616_593-615ins others(14): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr9 | 131130137 | ||||||
| chr9:131130137 | G | GTTTTTTT others(8): Show |
16 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0004t0001g0131 others(13): Show |
16 | HG00408.hp2 HG00544.hp1 HG01361.hp1 others(13): Show |
intron_variant | MODIFIER | c.593-616_593-615ins others(15): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr9 | 131130137 | ||||||
| chr9:131130137 | G | GTTTTTTT others(9): Show |
13 | a0001c0001t0001g0176 a0001c0006t0001g0174 a0001c0006t0001g0179 others(10): Show |
13 | HG01943.hp2 HG01993.hp1 HG02132.hp1 others(10): Show |
intron_variant | MODIFIER | c.593-616_593-615ins others(16): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr9 | 131130137 | ||||||
| chr9:131130137 | G | GTTTTTTT others(10): Show |
9 | a0001c0001t0001g0189 a0002c0002t0001g0106 a0002c0002t0001g0116 others(6): Show |
9 | HG01175.hp1 HG02027.hp2 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.593-616_593-615ins others(17): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr9 | 131130137 | ||||||
| chr9:131130137 | G | GTTTTTTT others(11): Show |
9 | a0001c0005t0002g0212 a0002c0002t0001g0117 a0002c0002t0001g0118 others(6): Show |
9 | HG01884.hp2 HG02293.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.593-616_593-615ins others(18): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr9 | 131130137 | ||||||
| chr9:131130137 | G | GTTTTTTT others(13): Show |
1 | a0001c0004t0001g0209 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.593-616_593-615ins others(20): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr9 | 131130137 | ||||||
| chr9:131130137 | G | GTTTTTTT others(15): Show |
1 | a0001c0005t0002g0205 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.593-616_593-615ins others(22): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr9 | 131130137 | ||||||
| chr9:131130137 | G | GTTTTTTT others(17): Show |
3 | a0002c0002t0001g0193 a0002c0002t0001g0194 a0002c0002t0001g0210 |
3 | HG00423.hp2 HG01928.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.593-616_593-615ins others(24): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr9 | 131130137 | ||||||
| chr9:131130137 | G | GTTTTTTT others(18): Show |
1 | a0002c0002t0001g0195 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.593-616_593-615ins others(25): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr9 | 131130137 | ||||||
| chr9:131130137 | G | GTTTTTTT others(21): Show |
1 | a0001c0004t0001g0196 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.593-616_593-615ins others(28): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr9 | 131130137 | ||||||
| chr9:131130137 | G | GTTTTTTT others(22): Show |
2 | a0001c0004t0001g0197 a0001c0005t0002g0206 |
2 | HG02451.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.593-616_593-615ins others(29): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr9 | 131130137 | ||||||
| chr9:131130137 | G | GTTTTTTT others(23): Show |
1 | a0001c0004t0001g0198 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.593-616_593-615ins others(30): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr9 | 131130137 | ||||||
| chr9:131130137 | G | T | 2 | a0001c0005t0002g0213 a0008c0028t0004g0207 |
2 | HG01496.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.593-629G>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 4/35 | chr9 | 131130137 | |||||||
| chr9:131130138 | T | G | 1 | a0001c0004t0001g0227 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.593-628T>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 4/35 | chr9 | 131130138 | |||||||
| chr9:131130141 | TTTTTTTT others(3): Show |
T | 1 | a0001c0001t0001g0102 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.593-615_593-606del others(10): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr9 | 131130141 | ||||||
| chr9:131130151 | G | T | 212 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(209): Show |
212 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(209): Show |
intron_variant | MODIFIER | c.593-615G>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 4/35 | chr9 | 131130151 | |||||||
| chr9:131130239 | G | A | 3 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 |
3 | HG00733.hp2 HG01074.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.593-527G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 4/35 | chr9 | 131130239 | |||||||
| chr9:131130271 | G | A | 1 | a0002c0002t0001g0183 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.593-495G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 4/35 | chr9 | 131130271 | |||||||
| chr9:131130289 | G | A | 1 | a0002c0002t0001g0184 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.593-477G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 4/35 | chr9 | 131130289 | |||||||
| chr9:131130437 | G | A | 7 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0212 others(4): Show |
7 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.593-329G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 4/35 | chr9 | 131130437 | |||||||
| chr9:131130575 | G | T | 2 | a0002c0002t0001g0115 a0002c0002t0001g0119 |
2 | NA19000.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.593-191G>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 4/35 | chr9 | 131130575 | |||||||
| chr9:131130671 | C | T | 1 | a0002c0018t0002g0107 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.593-95C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 4/35 | chr9 | 131130671 | |||||||
| chr9:131130903 | G | A | 1 | a0015c0019t0001g0141 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.663+67G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 5/35 | chr9 | 131130903 | |||||||
| chr9:131131094 | T | G | 106 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0176 others(103): Show |
106 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.663+258T>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 5/35 | chr9 | 131131094 | |||||||
| chr9:131131133 | G | A | 7 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0212 others(4): Show |
7 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.663+297G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 5/35 | chr9 | 131131133 | |||||||
| chr9:131131241 | T | C | 3 | a0001c0010t0003g0214 a0001c0010t0003g0228 a0001c0010t0003g0229 |
3 | HG01109.hp1 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.663+405T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 5/35 | chr9 | 131131241 | |||||||
| chr9:131131271 | A | G | 1 | a0001c0001t0010g0234 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.663+435A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 5/35 | chr9 | 131131271 | |||||||
| chr9:131131374 | A | T | 7 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0212 others(4): Show |
7 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.663+538A>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 5/35 | chr9 | 131131374 | |||||||
| chr9:131131597 | A | G | 1 | a0002c0002t0001g0172 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.663+761A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 5/35 | chr9 | 131131597 | |||||||
| chr9:131131632 | T | C | 1 | a0002c0020t0012g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.663+796T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 5/35 | chr9 | 131131632 | |||||||
| chr9:131131674 | T | A | 1 | a0002c0002t0001g0133 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.663+838T>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 5/35 | chr9 | 131131674 | |||||||
| chr9:131131695 | T | A | 94 | a0001c0001t0001g0014 a0001c0001t0001g0170 a0001c0001t0001g0171 others(91): Show |
94 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.663+859T>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 5/35 | chr9 | 131131695 | |||||||
| chr9:131131777 | C | T | 1 | a0001c0004t0001g0196 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.664-819C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 5/35 | chr9 | 131131777 | |||||||
| chr9:131131816 | G | C | 1 | a0001c0001t0001g0015 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.664-780G>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 5/35 | chr9 | 131131816 | |||||||
| chr9:131131933 | C | T | 1 | a0002c0018t0002g0107 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.664-663C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 5/35 | chr9 | 131131933 | |||||||
| chr9:131132025 | G | A | 1 | a0002c0018t0002g0107 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.664-571G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 5/35 | chr9 | 131132025 | |||||||
| chr9:131132030 | G | A | 3 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0217 |
3 | HG02109.hp1 HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.664-566G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 5/35 | chr9 | 131132030 | |||||||
| chr9:131132054 | T | C | 1 | a0002c0020t0012g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.664-542T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 5/35 | chr9 | 131132054 | |||||||
| chr9:131132115 | C | CT | 110 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(107): Show |
110 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.664-478dupT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 5/35 | INFO_REALIGN_3_PRIME | chr9 | 131132115 | ||||||
| chr9:131132115 | C | CTT | 6 | a0001c0001t0001g0001 a0001c0007t0001g0086 a0001c0027t0001g0085 others(3): Show |
6 | HG02056.hp2 HG02145.hp2 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.664-479_664-478dup others(2): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 5/35 | INFO_REALIGN_3_PRIME | chr9 | 131132115 | ||||||
| chr9:131132115 | CTTTCTTT others(5): Show |
C | 1 | a0001c0001t0001g0087 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.664-477_664-466del others(12): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 5/35 | INFO_REALIGN_3_PRIME | chr9 | 131132115 | ||||||
| chr9:131132118 | TC | T | 92 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0176 others(89): Show |
92 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.664-477delC | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 5/35 | chr9 | 131132118 | |||||||
| chr9:131132119 | C | T | 124 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(121): Show |
124 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.664-477C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 5/35 | chr9 | 131132119 | |||||||
| chr9:131132126 | T | C | 5 | a0001c0004t0001g0209 a0001c0005t0002g0205 a0001c0005t0002g0206 others(2): Show |
5 | HG01496.hp2 HG02451.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.664-470T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 5/35 | chr9 | 131132126 | |||||||
| chr9:131132261 | G | A | 1 | a0012c0023t0005g0003 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.664-335G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 5/35 | chr9 | 131132261 | |||||||
| chr9:131132274 | A | G | 104 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0176 others(101): Show |
104 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.664-322A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 5/35 | chr9 | 131132274 | |||||||
| chr9:131132495 | T | C | 1 | a0016c0022t0001g0112 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.664-101T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 5/35 | chr9 | 131132495 | |||||||
| chr9:131132740 | C | T | 1 | a0007c0025t0001g0084 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.727+81C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 6/35 | chr9 | 131132740 | |||||||
| chr9:131133004 | A | AT | 8 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0212 others(5): Show |
8 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.728-92dupT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 6/35 | INFO_REALIGN_3_PRIME | chr9 | 131133004 | ||||||
| chr9:131133304 | G | GT | 9 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 others(6): Show |
9 | HG00423.hp1 HG01106.hp1 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.831+113dupT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 7/35 | INFO_REALIGN_3_PRIME | chr9 | 131133304 | ||||||
| chr9:131133304 | G | GTTT | 88 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0176 others(85): Show |
88 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.831+111_831+113dup others(3): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 7/35 | INFO_REALIGN_3_PRIME | chr9 | 131133304 | ||||||
| chr9:131133304 | GT | G | 6 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0212 others(3): Show |
6 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.831+113delT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 7/35 | INFO_REALIGN_3_PRIME | chr9 | 131133304 | ||||||
| chr9:131133333 | C | G | 97 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0176 others(94): Show |
97 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.831+124C>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 7/35 | chr9 | 131133333 | |||||||
| chr9:131133343 | C | T | 3 | a0005c0012t0001g0005 a0005c0012t0001g0006 a0005c0012t0001g0007 |
3 | HG01106.hp2 HG02723.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.831+134C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 7/35 | chr9 | 131133343 | |||||||
| chr9:131133374 | A | G | 219 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(216): Show |
219 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.831+165A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 7/35 | chr9 | 131133374 | |||||||
| chr9:131133390 | G | C | 6 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0212 others(3): Show |
6 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.831+181G>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 7/35 | chr9 | 131133390 | |||||||
| chr9:131133559 | T | C | 104 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0176 others(101): Show |
104 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.831+350T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 7/35 | chr9 | 131133559 | |||||||
| chr9:131133762 | A | G | 104 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0176 others(101): Show |
104 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.831+553A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 7/35 | chr9 | 131133762 | |||||||
| chr9:131133839 | G | A | 97 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0176 others(94): Show |
97 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.831+630G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 7/35 | chr9 | 131133839 | |||||||
| chr9:131133876 | A | G | 1 | a0001c0005t0003g0211 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.831+667A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 7/35 | chr9 | 131133876 | |||||||
| chr9:131134071 | C | T | 2 | a0001c0001t0001g0170 a0001c0001t0001g0171 |
2 | HG03017.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.832-827C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 7/35 | chr9 | 131134071 | |||||||
| chr9:131134192 | C | T | 7 | a0002c0002t0001g0149 a0002c0002t0001g0150 a0002c0002t0001g0151 others(4): Show |
7 | HG00597.hp1 NA18948.hp2 NA18949.hp2 others(4): Show |
intron_variant | MODIFIER | c.832-706C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 7/35 | chr9 | 131134192 | |||||||
| chr9:131134654 | A | G | 1 | a0001c0001t0001g0079 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.832-244A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 7/35 | chr9 | 131134654 | |||||||
| chr9:131134771 | C | T | 2 | a0002c0002t0001g0172 a0002c0002t0001g0182 |
2 | NA19009.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.832-127C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 7/35 | chr9 | 131134771 | |||||||
| chr9:131134849 | T | C | 101 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0176 others(98): Show |
101 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.832-49T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 7/35 | chr9 | 131134849 | |||||||
| chr9:131135344 | A | G | 1 | a0001c0001t0001g0189 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.938+340A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 8/35 | chr9 | 131135344 | |||||||
| chr9:131135470 | A | G | 1 | a0001c0005t0002g0213 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.938+466A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 8/35 | chr9 | 131135470 | |||||||
| chr9:131136033 | G | A | 1 | a0012c0023t0005g0003 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1005+27G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 9/35 | chr9 | 131136033 | |||||||
| chr9:131136162 | C | G | 6 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0212 others(3): Show |
6 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.1005+156C>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 9/35 | chr9 | 131136162 | |||||||
| chr9:131136185 | G | A | 3 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0002c0002t0001g0175 |
3 | HG03017.hp2 HG03491.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1005+179G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 9/35 | chr9 | 131136185 | |||||||
| chr9:131136197 | A | G | 104 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0176 others(101): Show |
104 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.1005+191A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 9/35 | chr9 | 131136197 | |||||||
| chr9:131136237 | G | A | 94 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0176 others(91): Show |
94 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.1005+231G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 9/35 | chr9 | 131136237 | |||||||
| chr9:131136535 | C | A | 97 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0176 others(94): Show |
97 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.1005+529C>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 9/35 | chr9 | 131136535 | |||||||
| chr9:131136565 | T | C | 1 | a0002c0018t0002g0107 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1005+559T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 9/35 | chr9 | 131136565 | |||||||
| chr9:131136593 | A | T | 94 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0176 others(91): Show |
94 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.1005+587A>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 9/35 | chr9 | 131136593 | |||||||
| chr9:131136772 | T | A | 1 | a0013c0021t0001g0173 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1005+766T>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 9/35 | chr9 | 131136772 | |||||||
| chr9:131136793 | C | T | 2 | a0002c0002t0001g0077 a0002c0002t0001g0078 |
2 | HG00642.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1005+787C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 9/35 | chr9 | 131136793 | |||||||
| chr9:131136907 | A | G | 6 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0212 others(3): Show |
6 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.1005+901A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 9/35 | chr9 | 131136907 | |||||||
| chr9:131137148 | T | C | 104 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0176 others(101): Show |
104 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.1005+1142T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 9/35 | chr9 | 131137148 | |||||||
| chr9:131137368 | T | A | 1 | a0008c0028t0004g0207 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1005+1362T>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 9/35 | chr9 | 131137368 | |||||||
| chr9:131137414 | C | T | 2 | a0002c0003t0001g0083 a0002c0020t0012g0132 |
2 | HG03486.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.1005+1408C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 9/35 | chr9 | 131137414 | |||||||
| chr9:131137535 | C | T | 94 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0176 others(91): Show |
94 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.1005+1529C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 9/35 | chr9 | 131137535 | |||||||
| chr9:131137552 | C | CT | 7 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0098 others(4): Show |
7 | HG00642.hp1 HG01175.hp2 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.1005+1569dupT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 9/35 | INFO_REALIGN_3_PRIME | chr9 | 131137552 | ||||||
| chr9:131137552 | CT | C | 139 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0018 others(136): Show |
139 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.1005+1569delT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 9/35 | INFO_REALIGN_3_PRIME | chr9 | 131137552 | ||||||
| chr9:131137552 | CTT | C | 8 | a0001c0001t0001g0017 a0001c0005t0002g0205 a0001c0005t0002g0206 others(5): Show |
8 | HG00558.hp1 HG01496.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.1005+1568_1005+156 others(6): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 9/35 | INFO_REALIGN_3_PRIME | chr9 | 131137552 | ||||||
| chr9:131137636 | C | T | 3 | a0005c0012t0001g0005 a0005c0012t0001g0006 a0005c0012t0001g0007 |
3 | HG01106.hp2 HG02723.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1005+1630C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 9/35 | chr9 | 131137636 | |||||||
| chr9:131137743 | T | G | 97 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0176 others(94): Show |
97 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.1006-1538T>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 9/35 | chr9 | 131137743 | |||||||
| chr9:131137753 | G | C | 1 | a0002c0002t0001g0210 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1006-1528G>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 9/35 | chr9 | 131137753 | |||||||
| chr9:131137887 | A | G | 110 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(107): Show |
110 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.1006-1394A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 9/35 | chr9 | 131137887 | |||||||
| chr9:131137933 | A | T | 1 | a0002c0020t0012g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1006-1348A>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 9/35 | chr9 | 131137933 | |||||||
| chr9:131137957 | T | C | 1 | a0013c0021t0001g0173 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1006-1324T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 9/35 | chr9 | 131137957 | |||||||
| chr9:131138043 | C | T | 94 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0176 others(91): Show |
94 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.1006-1238C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 9/35 | chr9 | 131138043 | |||||||
| chr9:131138162 | T | A | 1 | a0001c0005t0002g0212 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1006-1119T>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 9/35 | chr9 | 131138162 | |||||||
| chr9:131138243 | C | T | 94 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0176 others(91): Show |
94 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.1006-1038C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 9/35 | chr9 | 131138243 | |||||||
| chr9:131138286 | TCGGCTCA | T | 3 | a0005c0012t0001g0005 a0005c0012t0001g0006 a0005c0012t0001g0007 |
3 | HG01106.hp2 HG02723.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1006-993_1006-987d others(9): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 9/35 | INFO_REALIGN_3_PRIME | chr9 | 131138286 | ||||||
| chr9:131138288 | G | A | 3 | a0006c0008t0001g0032 a0006c0008t0001g0040 a0006c0008t0001g0109 |
3 | HG02109.hp2 HG02559.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1006-993G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 9/35 | chr9 | 131138288 | |||||||
| chr9:131138379 | C | A | 94 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0176 others(91): Show |
94 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.1006-902C>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 9/35 | chr9 | 131138379 | |||||||
| chr9:131138613 | A | G | 103 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0176 others(100): Show |
103 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.1006-668A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 9/35 | chr9 | 131138613 | |||||||
| chr9:131138652 | C | T | 1 | a0002c0018t0002g0107 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1006-629C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 9/35 | chr9 | 131138652 | |||||||
| chr9:131139088 | T | G | 94 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0176 others(91): Show |
94 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.1006-193T>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 9/35 | chr9 | 131139088 | |||||||
| chr9:131139148 | G | A | 104 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0176 others(101): Show |
104 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.1006-133G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 9/35 | chr9 | 131139148 | |||||||
| chr9:131139205 | C | A | 1 | a0002c0002t0001g0113 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1006-76C>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 9/35 | chr9 | 131139205 | |||||||
| chr9:131139255 | C | CT | 10 | a0001c0001t0001g0233 a0001c0005t0002g0205 a0001c0005t0002g0212 others(7): Show |
10 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(7): Show |
splice_acceptor_variant&intron_variant | HIGH | c.1006-3dupT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 9/35 | INFO_REALIGN_3_PRIME | chr9 | 131139255 | ||||||
| chr9:131139255 | CT | C | 18 | a0001c0001t0001g0017 a0001c0001t0001g0035 a0001c0001t0001g0037 others(15): Show |
18 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(15): Show |
splice_region_variant&intron_variant | LOW | c.1006-3delT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 9/35 | INFO_REALIGN_3_PRIME | chr9 | 131139255 | ||||||
| chr9:131139255 | CTTTTTTT others(6): Show |
C | 2 | a0002c0002t0001g0164 a0002c0002t0001g0166 |
2 | HG01981.hp1 NA19000.hp1 |
splice_region_variant&intron_variant | LOW | c.1006-15_1006-3delT others(12): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 9/35 | INFO_REALIGN_3_PRIME | chr9 | 131139255 | ||||||
| chr9:131139259 | T | C | 3 | a0001c0010t0003g0214 a0001c0010t0003g0228 a0001c0010t0003g0229 |
3 | HG01109.hp1 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1006-22T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 9/35 | chr9 | 131139259 | |||||||
| chr9:131139262 | T | C | 3 | a0001c0010t0003g0214 a0001c0010t0003g0228 a0001c0010t0003g0229 |
3 | HG01109.hp1 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1006-19T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 9/35 | chr9 | 131139262 | |||||||
| chr9:131139464 | A | G | 1 | a0001c0001t0001g0076 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1132+57A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 10/35 | chr9 | 131139464 | |||||||
| chr9:131139554 | C | T | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(215): Show |
218 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(215): Show |
intron_variant | MODIFIER | c.1132+147C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 10/35 | chr9 | 131139554 | |||||||
| chr9:131139685 | T | G | 25 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(22): Show |
25 | HG00099.hp1 HG00733.hp2 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.1132+278T>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 10/35 | chr9 | 131139685 | |||||||
| chr9:131139690 | A | G | 1 | a0001c0001t0006g0075 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1132+283A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 10/35 | chr9 | 131139690 | |||||||
| chr9:131139802 | A | G | 1 | a0001c0001t0001g0048 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1132+395A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 10/35 | chr9 | 131139802 | |||||||
| chr9:131139886 | GTAGCTTG others(4): Show |
G | 4 | a0001c0007t0001g0064 a0001c0007t0001g0086 a0001c0007t0001g0088 others(1): Show |
4 | HG02145.hp2 HG02897.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1132+482_1132+492d others(13): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 10/35 | INFO_REALIGN_3_PRIME | chr9 | 131139886 | ||||||
| chr9:131140080 | A | T | 94 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0176 others(91): Show |
94 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.1133-469A>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 10/35 | chr9 | 131140080 | |||||||
| chr9:131140191 | C | T | 2 | a0001c0004t0001g0137 a0002c0002t0001g0136 |
2 | HG00733.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1133-358C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 10/35 | chr9 | 131140191 | |||||||
| chr9:131140394 | A | G | 103 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0176 others(100): Show |
103 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.1133-155A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 10/35 | chr9 | 131140394 | |||||||
| chr9:131140401 | G | C | 2 | a0001c0001t0001g0049 a0001c0001t0001g0087 |
2 | HG01109.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.1133-148G>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 10/35 | chr9 | 131140401 | |||||||
| chr9:131140419 | A | G | 3 | a0005c0012t0001g0005 a0005c0012t0001g0006 a0005c0012t0001g0007 |
3 | HG01106.hp2 HG02723.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1133-130A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 10/35 | chr9 | 131140419 | |||||||
| chr9:131140512 | C | G | 100 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0176 others(97): Show |
100 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.1133-37C>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 10/35 | chr9 | 131140512 | |||||||
| chr9:131140734 | C | T | 45 | a0001c0004t0001g0131 a0001c0004t0001g0137 a0001c0004t0001g0138 others(42): Show |
45 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(42): Show |
intron_variant | MODIFIER | c.1294+24C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 11/35 | chr9 | 131140734 | |||||||
| chr9:131140862 | A | G | 13 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(10): Show |
13 | HG00099.hp1 HG00733.hp2 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.1294+152A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 11/35 | chr9 | 131140862 | |||||||
| chr9:131140893 | C | T | 94 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0176 others(91): Show |
94 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.1294+183C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 11/35 | chr9 | 131140893 | |||||||
| chr9:131140994 | T | G | 1 | a0001c0001t0001g0065 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1294+284T>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 11/35 | chr9 | 131140994 | |||||||
| chr9:131141138 | C | CA | 101 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0114 others(98): Show |
101 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.1294+441dupA | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 11/35 | INFO_REALIGN_3_PRIME | chr9 | 131141138 | ||||||
| chr9:131141138 | C | CAA | 6 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0213 others(3): Show |
6 | HG01496.hp2 HG01891.hp2 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.1294+440_1294+441d others(4): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 11/35 | INFO_REALIGN_3_PRIME | chr9 | 131141138 | ||||||
| chr9:131141139 | A | C | 2 | a0001c0001t0001g0047 a0001c0001t0001g0079 |
2 | HG00408.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.1294+429A>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 11/35 | chr9 | 131141139 | |||||||
| chr9:131141162 | T | G | 103 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0176 others(100): Show |
103 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.1294+452T>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 11/35 | chr9 | 131141162 | |||||||
| chr9:131141170 | T | C | 103 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0176 others(100): Show |
103 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.1294+460T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 11/35 | chr9 | 131141170 | |||||||
| chr9:131141263 | G | C | 104 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0176 others(101): Show |
104 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.1294+553G>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 11/35 | chr9 | 131141263 | |||||||
| chr9:131141336 | A | G | 104 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0176 others(101): Show |
104 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.1294+626A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 11/35 | chr9 | 131141336 | |||||||
| chr9:131141478 | C | CT | 6 | a0001c0001t0001g0015 a0001c0001t0001g0059 a0001c0001t0001g0060 others(3): Show |
6 | HG01081.hp2 HG01433.hp1 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.1294+788dupT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 11/35 | INFO_REALIGN_3_PRIME | chr9 | 131141478 | ||||||
| chr9:131141478 | C | CTT | 7 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0213 others(4): Show |
7 | HG01169.hp1 HG01175.hp1 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.1294+787_1294+788d others(4): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 11/35 | INFO_REALIGN_3_PRIME | chr9 | 131141478 | ||||||
| chr9:131141478 | C | CTTT | 86 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0176 others(83): Show |
86 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.1294+786_1294+788d others(5): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 11/35 | INFO_REALIGN_3_PRIME | chr9 | 131141478 | ||||||
| chr9:131141478 | C | CTTTT | 8 | a0001c0004t0001g0162 a0001c0004t0001g0209 a0002c0002t0001g0130 others(5): Show |
8 | HG01993.hp1 HG02735.hp2 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.1294+785_1294+788d others(6): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 11/35 | INFO_REALIGN_3_PRIME | chr9 | 131141478 | ||||||
| chr9:131141793 | T | A | 104 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0176 others(101): Show |
104 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.1294+1083T>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 11/35 | chr9 | 131141793 | |||||||
| chr9:131141917 | T | C | 2 | a0001c0001t0001g0008 a0001c0001t0001g0114 |
2 | HG03688.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1294+1207T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 11/35 | chr9 | 131141917 | |||||||
| chr9:131141936 | T | G | 104 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0176 others(101): Show |
104 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.1294+1226T>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 11/35 | chr9 | 131141936 | |||||||
| chr9:131142141 | T | C | 1 | a0002c0002t0001g0181 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1294+1431T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 11/35 | chr9 | 131142141 | |||||||
| chr9:131142177 | C | G | 1 | a0001c0001t0001g0081 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1294+1467C>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 11/35 | chr9 | 131142177 | |||||||
| chr9:131142191 | C | T | 1 | a0001c0001t0001g0079 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1294+1481C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 11/35 | chr9 | 131142191 | |||||||
| chr9:131142368 | A | G | 1 | a0002c0020t0012g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1294+1658A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 11/35 | chr9 | 131142368 | |||||||
| chr9:131142885 | A | G | 1 | a0002c0020t0012g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1295-1395A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 11/35 | chr9 | 131142885 | |||||||
| chr9:131142934 | T | C | 222 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(219): Show |
222 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(219): Show |
intron_variant | MODIFIER | c.1295-1346T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 11/35 | chr9 | 131142934 | |||||||
| chr9:131143217 | C | T | 1 | a0016c0022t0001g0112 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1295-1063C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 11/35 | chr9 | 131143217 | |||||||
| chr9:131143339 | A | G | 1 | a0002c0020t0012g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1295-941A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 11/35 | chr9 | 131143339 | |||||||
| chr9:131143429 | A | G | 107 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0176 others(104): Show |
107 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.1295-851A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 11/35 | chr9 | 131143429 | |||||||
| chr9:131143628 | GAGTT | G | 95 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0004t0001g0131 others(92): Show |
95 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1295-647_1295-644d others(6): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 11/35 | INFO_REALIGN_3_PRIME | chr9 | 131143628 | ||||||
| chr9:131143660 | T | C | 94 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0004t0001g0131 others(91): Show |
94 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.1295-620T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 11/35 | chr9 | 131143660 | |||||||
| chr9:131143988 | G | C | 1 | a0012c0023t0005g0003 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1295-292G>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 11/35 | chr9 | 131143988 | |||||||
| chr9:131144881 | C | G | 3 | a0001c0010t0003g0214 a0001c0010t0003g0228 a0001c0010t0003g0229 |
3 | HG01109.hp1 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1769+127C>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 12/35 | chr9 | 131144881 | |||||||
| chr9:131144925 | A | C | 4 | a0001c0007t0001g0064 a0001c0007t0001g0086 a0001c0007t0001g0088 others(1): Show |
4 | HG02145.hp2 HG02897.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1769+171A>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 12/35 | chr9 | 131144925 | |||||||
| chr9:131144929 | A | G | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(213): Show |
216 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.1769+175A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 12/35 | chr9 | 131144929 | |||||||
| chr9:131144930 | A | G | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(164): Show |
167 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.1769+176A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 12/35 | chr9 | 131144930 | |||||||
| chr9:131145123 | C | G | 1 | a0001c0001t0001g0065 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1769+369C>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 12/35 | chr9 | 131145123 | |||||||
| chr9:131145177 | G | A | 1 | a0001c0010t0003g0214 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1769+423G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 12/35 | chr9 | 131145177 | |||||||
| chr9:131145449 | A | T | 4 | a0001c0005t0003g0211 a0002c0018t0002g0107 a0008c0028t0004g0207 others(1): Show |
4 | HG01891.hp2 HG02145.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1770-680A>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 12/35 | chr9 | 131145449 | |||||||
| chr9:131145475 | A | G | 1 | a0001c0001t0001g0001 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1770-654A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 12/35 | chr9 | 131145475 | |||||||
| chr9:131145527 | C | A | 1 | a0001c0001t0001g0080 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1770-602C>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 12/35 | chr9 | 131145527 | |||||||
| chr9:131145539 | A | G | 1 | a0002c0002t0001g0193 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1770-590A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 12/35 | chr9 | 131145539 | |||||||
| chr9:131145716 | C | A | 1 | a0002c0018t0002g0107 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1770-413C>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 12/35 | chr9 | 131145716 | |||||||
| chr9:131145959 | A | G | 1 | a0008c0028t0004g0207 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1770-170A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 12/35 | chr9 | 131145959 | |||||||
| chr9:131146576 | A | G | 1 | a0002c0003t0001g0074 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1945+272A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 13/35 | chr9 | 131146576 | |||||||
| chr9:131146874 | G | T | 7 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0212 others(4): Show |
7 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1945+570G>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 13/35 | chr9 | 131146874 | |||||||
| chr9:131146928 | C | CA | 112 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(109): Show |
112 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.1946-548dupA | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 13/35 | INFO_REALIGN_3_PRIME | chr9 | 131146928 | ||||||
| chr9:131146928 | C | CAA | 5 | a0001c0001t0001g0020 a0001c0004t0001g0227 a0001c0005t0003g0211 others(2): Show |
5 | HG01891.hp2 HG02615.hp2 HG04204.hp2 others(2): Show |
intron_variant | MODIFIER | c.1946-549_1946-548d others(4): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 13/35 | INFO_REALIGN_3_PRIME | chr9 | 131146928 | ||||||
| chr9:131147111 | T | C | 106 | a0001c0001t0001g0066 a0001c0001t0001g0176 a0001c0001t0001g0189 others(103): Show |
106 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.1946-379T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 13/35 | chr9 | 131147111 | |||||||
| chr9:131147248 | A | G | 2 | a0001c0004t0001g0137 a0002c0002t0001g0136 |
2 | HG00733.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1946-242A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 13/35 | chr9 | 131147248 | |||||||
| chr9:131147285 | G | T | 2 | a0001c0001t0001g0102 a0001c0001t0001g0103 |
2 | HG03540.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1946-205G>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 13/35 | chr9 | 131147285 | |||||||
| chr9:131147786 | T | C | 1 | a0001c0001t0001g0230 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.2040+202T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 14/35 | chr9 | 131147786 | |||||||
| chr9:131148044 | G | A | 1 | a0001c0001t0010g0234 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2040+460G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 14/35 | chr9 | 131148044 | |||||||
| chr9:131148190 | T | TTTC | 110 | a0001c0001t0001g0066 a0001c0001t0001g0176 a0001c0001t0001g0189 others(107): Show |
110 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.2040+608_2040+609i others(5): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 14/35 | INFO_REALIGN_3_PRIME | chr9 | 131148190 | ||||||
| chr9:131148333 | T | C | 1 | a0001c0001t0001g0081 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2040+749T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 14/35 | chr9 | 131148333 | |||||||
| chr9:131148421 | C | G | 2 | a0001c0001t0001g0058 a0001c0001t0001g0096 |
2 | HG02698.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.2040+837C>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 14/35 | chr9 | 131148421 | |||||||
| chr9:131148432 | A | G | 1 | a0002c0020t0012g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2040+848A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 14/35 | chr9 | 131148432 | |||||||
| chr9:131148478 | A | G | 110 | a0001c0001t0001g0066 a0001c0001t0001g0176 a0001c0001t0001g0189 others(107): Show |
110 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.2040+894A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 14/35 | chr9 | 131148478 | |||||||
| chr9:131148620 | A | C | 1 | a0001c0004t0001g0204 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.2040+1036A>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 14/35 | chr9 | 131148620 | |||||||
| chr9:131148869 | T | C | 1 | a0001c0001t0001g0025 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.2040+1285T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 14/35 | chr9 | 131148869 | |||||||
| chr9:131148955 | T | C | 1 | a0008c0028t0004g0207 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2041-1369T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 14/35 | chr9 | 131148955 | |||||||
| chr9:131149082 | G | C | 3 | a0001c0004t0001g0201 a0002c0002t0001g0200 a0002c0002t0001g0202 |
3 | HG00099.hp2 HG01433.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.2041-1242G>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 14/35 | chr9 | 131149082 | |||||||
| chr9:131149084 | G | C | 6 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0212 others(3): Show |
6 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.2041-1240G>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 14/35 | chr9 | 131149084 | |||||||
| chr9:131149137 | T | C | 219 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(216): Show |
219 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.2041-1187T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 14/35 | chr9 | 131149137 | |||||||
| chr9:131149150 | T | TCTC | 100 | a0001c0001t0001g0066 a0001c0001t0001g0176 a0001c0001t0001g0189 others(97): Show |
100 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.2041-1174_2041-117 others(7): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 14/35 | chr9 | 131149150 | |||||||
| chr9:131149151 | G | C | 100 | a0001c0001t0001g0066 a0001c0001t0001g0176 a0001c0001t0001g0189 others(97): Show |
100 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.2041-1173G>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 14/35 | chr9 | 131149151 | |||||||
| chr9:131149302 | TG | T | 100 | a0001c0001t0001g0066 a0001c0001t0001g0176 a0001c0001t0001g0189 others(97): Show |
100 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.2041-1021delG | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 14/35 | chr9 | 131149302 | |||||||
| chr9:131149531 | T | C | 3 | a0001c0010t0003g0214 a0001c0010t0003g0228 a0001c0010t0003g0229 |
3 | HG01109.hp1 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2041-793T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 14/35 | chr9 | 131149531 | |||||||
| chr9:131149542 | A | G | 103 | a0001c0001t0001g0066 a0001c0001t0001g0176 a0001c0001t0001g0189 others(100): Show |
103 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.2041-782A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 14/35 | chr9 | 131149542 | |||||||
| chr9:131149562 | C | T | 1 | a0001c0001t0001g0176 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2041-762C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 14/35 | chr9 | 131149562 | |||||||
| chr9:131149698 | C | T | 1 | a0002c0003t0001g0063 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2041-626C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 14/35 | chr9 | 131149698 | |||||||
| chr9:131149771 | G | A | 1 | a0002c0002t0001g0187 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2041-553G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 14/35 | chr9 | 131149771 | |||||||
| chr9:131149787 | T | C | 103 | a0001c0001t0001g0066 a0001c0001t0001g0176 a0001c0001t0001g0189 others(100): Show |
103 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.2041-537T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 14/35 | chr9 | 131149787 | |||||||
| chr9:131149828 | G | C | 1 | a0002c0018t0002g0107 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2041-496G>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 14/35 | chr9 | 131149828 | |||||||
| chr9:131149896 | G | C | 11 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0212 others(8): Show |
11 | HG01109.hp1 HG01496.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.2041-428G>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 14/35 | chr9 | 131149896 | |||||||
| chr9:131149985 | G | A | 2 | a0001c0005t0002g0205 a0001c0005t0002g0206 |
2 | HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.2041-339G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 14/35 | chr9 | 131149985 | |||||||
| chr9:131150096 | A | G | 3 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0014c0014t0001g0099 |
3 | HG02015.hp2 NA18983.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.2041-228A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 14/35 | chr9 | 131150096 | |||||||
| chr9:131150208 | A | G | 51 | a0001c0004t0001g0131 a0001c0004t0001g0137 a0001c0004t0001g0138 others(48): Show |
51 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(48): Show |
intron_variant | MODIFIER | c.2041-116A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 14/35 | chr9 | 131150208 | |||||||
| chr9:131150257 | A | C | 1 | a0001c0001t0001g0004 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2041-67A>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 14/35 | chr9 | 131150257 | |||||||
| chr9:131150508 | G | A | 1 | a0001c0001t0001g0068 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.2127+98G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 15/35 | chr9 | 131150508 | |||||||
| chr9:131150895 | G | A | 1 | a0001c0001t0001g0026 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2277+130G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 16/35 | chr9 | 131150895 | |||||||
| chr9:131151031 | T | C | 3 | a0001c0010t0003g0214 a0001c0010t0003g0228 a0001c0010t0003g0229 |
3 | HG01109.hp1 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2277+266T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 16/35 | chr9 | 131151031 | |||||||
| chr9:131151116 | G | A | 3 | a0002c0003t0001g0016 a0002c0003t0001g0069 a0002c0003t0001g0097 |
3 | NA18949.hp1 NA19001.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.2277+351G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 16/35 | chr9 | 131151116 | |||||||
| chr9:131151324 | G | A | 1 | a0013c0021t0001g0173 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2278-412G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 16/35 | chr9 | 131151324 | |||||||
| chr9:131151574 | G | A | 1 | a0002c0020t0012g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2278-162G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 16/35 | chr9 | 131151574 | |||||||
| chr9:131151579 | G | T | 10 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0212 others(7): Show |
10 | HG01109.hp1 HG01496.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.2278-157G>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 16/35 | chr9 | 131151579 | |||||||
| chr9:131151606 | C | T | 1 | a0002c0002t0001g0175 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2278-130C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 16/35 | chr9 | 131151606 | |||||||
| chr9:131151677 | A | G | 2 | a0001c0001t0001g0066 a0001c0001t0001g0189 |
2 | HG02965.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2278-59A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 16/35 | chr9 | 131151677 | |||||||
| chr9:131151693 | C | T | 2 | a0002c0002t0001g0145 a0002c0002t0001g0146 |
2 | NA18944.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.2278-43C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 16/35 | chr9 | 131151693 | |||||||
| chr9:131152104 | AT | A | 11 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0212 others(8): Show |
11 | HG01109.hp1 HG01496.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.2436+218delT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | INFO_REALIGN_3_PRIME | chr9 | 131152104 | ||||||
| chr9:131152200 | A | T | 106 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(103): Show |
106 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.2436+306A>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131152200 | |||||||
| chr9:131152305 | T | C | 11 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0212 others(8): Show |
11 | HG01109.hp1 HG01496.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.2436+411T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131152305 | |||||||
| chr9:131152331 | A | G | 11 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0212 others(8): Show |
11 | HG01109.hp1 HG01496.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.2436+437A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131152331 | |||||||
| chr9:131152400 | C | A | 1 | a0001c0005t0003g0211 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2436+506C>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131152400 | |||||||
| chr9:131152401 | G | A | 1 | a0006c0008t0001g0109 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2436+507G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131152401 | |||||||
| chr9:131152449 | T | G | 1 | a0008c0028t0004g0207 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2436+555T>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131152449 | |||||||
| chr9:131152597 | C | G | 1 | a0002c0018t0002g0107 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2436+703C>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131152597 | |||||||
| chr9:131152813 | G | C | 3 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0003g0211 |
3 | HG01891.hp2 HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.2436+919G>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131152813 | |||||||
| chr9:131152919 | G | T | 3 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0003g0211 |
3 | HG01891.hp2 HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.2436+1025G>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131152919 | |||||||
| chr9:131153211 | G | A | 1 | a0005c0012t0001g0007 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2436+1317G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131153211 | |||||||
| chr9:131153469 | T | C | 3 | a0001c0010t0003g0214 a0001c0010t0003g0228 a0001c0010t0003g0229 |
3 | HG01109.hp1 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2436+1575T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131153469 | |||||||
| chr9:131153837 | C | G | 1 | a0002c0018t0002g0107 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2436+1943C>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131153837 | |||||||
| chr9:131153865 | G | A | 1 | a0002c0002t0001g0163 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2436+1971G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131153865 | |||||||
| chr9:131153905 | A | G | 1 | a0007c0025t0001g0084 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2436+2011A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131153905 | |||||||
| chr9:131153980 | T | C | 2 | a0002c0002t0001g0177 a0002c0002t0001g0184 |
2 | HG01175.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.2436+2086T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131153980 | |||||||
| chr9:131154075 | G | A | 1 | a0003c0013t0001g0070 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2436+2181G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131154075 | |||||||
| chr9:131154091 | G | C | 1 | a0006c0008t0001g0109 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2436+2197G>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131154091 | |||||||
| chr9:131154146 | A | G | 1 | a0001c0001t0001g0020 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.2436+2252A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131154146 | |||||||
| chr9:131154334 | T | C | 1 | a0002c0020t0012g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2436+2440T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131154334 | |||||||
| chr9:131154430 | ATCTG | A | 2 | a0001c0007t0001g0064 a0001c0007t0001g0088 |
2 | HG02897.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.2436+2552_2436+255 others(8): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | INFO_REALIGN_3_PRIME | chr9 | 131154430 | ||||||
| chr9:131154446 | GTCTA | G | 2 | a0001c0005t0002g0212 a0001c0005t0002g0213 |
2 | HG01496.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.2436+2562_2436+256 others(8): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | INFO_REALIGN_3_PRIME | chr9 | 131154446 | ||||||
| chr9:131154661 | T | C | 3 | a0001c0010t0003g0214 a0001c0010t0003g0228 a0001c0010t0003g0229 |
3 | HG01109.hp1 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2436+2767T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131154661 | |||||||
| chr9:131154800 | C | G | 2 | a0001c0006t0001g0168 a0001c0006t0001g0169 |
2 | HG00408.hp2 HG00544.hp1 |
intron_variant | MODIFIER | c.2436+2906C>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131154800 | |||||||
| chr9:131154825 | TTG | T | 50 | a0001c0004t0001g0131 a0001c0004t0001g0137 a0001c0004t0001g0140 others(47): Show |
50 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(47): Show |
intron_variant | MODIFIER | c.2436+2948_2436+294 others(6): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | INFO_REALIGN_3_PRIME | chr9 | 131154825 | ||||||
| chr9:131154825 | TTGTG | T | 7 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0212 others(4): Show |
7 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.2436+2946_2436+294 others(8): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | INFO_REALIGN_3_PRIME | chr9 | 131154825 | ||||||
| chr9:131154840 | T | TGTGCGC | 5 | a0001c0001t0001g0025 a0001c0001t0001g0094 a0001c0004t0001g0204 others(2): Show |
5 | HG02027.hp1 HG02083.hp2 NA18952.hp2 others(2): Show |
intron_variant | MODIFIER | c.2436+2947_2436+295 others(10): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | INFO_REALIGN_3_PRIME | chr9 | 131154840 | ||||||
| chr9:131154842 | T | C | 1 | a0001c0004t0001g0138 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2436+2948T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131154842 | |||||||
| chr9:131154845 | G | A | 1 | a0001c0004t0001g0138 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2436+2951G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131154845 | |||||||
| chr9:131154849 | G | A | 1 | a0002c0018t0002g0107 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2436+2955G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131154849 | |||||||
| chr9:131155177 | C | T | 1 | a0002c0018t0002g0107 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2436+3283C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131155177 | |||||||
| chr9:131155329 | A | G | 3 | a0001c0005t0002g0212 a0001c0005t0002g0213 a0008c0028t0004g0207 |
3 | HG01496.hp2 HG02145.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.2436+3435A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131155329 | |||||||
| chr9:131155367 | T | C | 1 | a0001c0005t0002g0212 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2436+3473T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131155367 | |||||||
| chr9:131155899 | G | A | 1 | a0002c0002t0001g0183 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2437-3484G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131155899 | |||||||
| chr9:131155901 | A | C | 2 | a0002c0002t0001g0157 a0002c0002t0001g0167 |
2 | NA18968.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.2437-3482A>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131155901 | |||||||
| chr9:131156130 | CT | C | 221 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(218): Show |
221 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(218): Show |
intron_variant | MODIFIER | c.2437-3233delT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | INFO_REALIGN_3_PRIME | chr9 | 131156130 | ||||||
| chr9:131156130 | CTT | C | 6 | a0001c0001t0001g0008 a0001c0001t0001g0114 a0002c0002t0001g0135 others(3): Show |
6 | HG03195.hp1 HG03688.hp2 HG04199.hp1 others(3): Show |
intron_variant | MODIFIER | c.2437-3234_2437-323 others(6): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | INFO_REALIGN_3_PRIME | chr9 | 131156130 | ||||||
| chr9:131156201 | C | T | 34 | a0001c0004t0001g0162 a0001c0004t0001g0196 a0001c0004t0001g0197 others(31): Show |
34 | HG00597.hp1 HG01175.hp1 HG02027.hp2 others(31): Show |
intron_variant | MODIFIER | c.2437-3182C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131156201 | |||||||
| chr9:131156208 | C | CT | 3 | a0001c0010t0003g0214 a0001c0010t0003g0228 a0001c0010t0003g0229 |
3 | HG01109.hp1 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2437-3174dupT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | INFO_REALIGN_3_PRIME | chr9 | 131156208 | ||||||
| chr9:131156278 | G | A | 1 | a0001c0010t0003g0228 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2437-3105G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131156278 | |||||||
| chr9:131156379 | G | A | 1 | a0002c0002t0001g0106 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2437-3004G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131156379 | |||||||
| chr9:131156479 | G | A | 1 | a0001c0001t0006g0075 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2437-2904G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131156479 | |||||||
| chr9:131156656 | A | G | 1 | a0012c0023t0005g0003 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2437-2727A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131156656 | |||||||
| chr9:131156738 | T | C | 1 | a0008c0028t0004g0207 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2437-2645T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131156738 | |||||||
| chr9:131157034 | A | G | 3 | a0001c0010t0003g0214 a0001c0010t0003g0228 a0001c0010t0003g0229 |
3 | HG01109.hp1 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2437-2349A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131157034 | |||||||
| chr9:131157121 | C | T | 1 | a0005c0012t0001g0006 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2437-2262C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131157121 | |||||||
| chr9:131157140 | G | GT | 109 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(106): Show |
109 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.2437-2232dupT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | INFO_REALIGN_3_PRIME | chr9 | 131157140 | ||||||
| chr9:131157175 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2437-2208G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131157175 | |||||||
| chr9:131157180 | C | T | 3 | a0005c0012t0001g0005 a0005c0012t0001g0006 a0005c0012t0001g0007 |
3 | HG01106.hp2 HG02723.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2437-2203C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131157180 | |||||||
| chr9:131157310 | G | A | 1 | a0001c0001t0001g0059 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2437-2073G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131157310 | |||||||
| chr9:131157337 | T | A | 1 | a0008c0028t0004g0207 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2437-2046T>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131157337 | |||||||
| chr9:131157459 | G | GT | 94 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0036 others(91): Show |
94 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.2437-1901dupT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | INFO_REALIGN_3_PRIME | chr9 | 131157459 | ||||||
| chr9:131157459 | G | GTT | 29 | a0001c0001t0001g0090 a0001c0004t0001g0131 a0001c0004t0001g0138 others(26): Show |
29 | HG00544.hp1 HG00558.hp2 HG01175.hp1 others(26): Show |
intron_variant | MODIFIER | c.2437-1902_2437-190 others(6): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | INFO_REALIGN_3_PRIME | chr9 | 131157459 | ||||||
| chr9:131157459 | GT | G | 8 | a0001c0005t0002g0206 a0001c0010t0003g0214 a0001c0010t0003g0228 others(5): Show |
8 | HG01106.hp2 HG01109.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.2437-1901delT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | INFO_REALIGN_3_PRIME | chr9 | 131157459 | ||||||
| chr9:131157497 | C | G | 1 | a0010c0017t0001g0108 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2437-1886C>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131157497 | |||||||
| chr9:131157527 | C | T | 2 | a0001c0005t0002g0205 a0001c0005t0002g0206 |
2 | HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.2437-1856C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131157527 | |||||||
| chr9:131157610 | G | A | 10 | a0001c0004t0001g0219 a0001c0004t0001g0227 a0002c0002t0001g0104 others(7): Show |
10 | HG01361.hp2 HG01884.hp2 HG01943.hp2 others(7): Show |
intron_variant | MODIFIER | c.2437-1773G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131157610 | |||||||
| chr9:131157791 | G | A | 1 | a0002c0020t0012g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2437-1592G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131157791 | |||||||
| chr9:131157909 | G | A | 7 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0212 others(4): Show |
7 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.2437-1474G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131157909 | |||||||
| chr9:131157933 | A | C | 3 | a0001c0010t0003g0214 a0001c0010t0003g0228 a0001c0010t0003g0229 |
3 | HG01109.hp1 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2437-1450A>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131157933 | |||||||
| chr9:131158224 | A | G | 11 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0212 others(8): Show |
11 | HG01109.hp1 HG01496.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.2437-1159A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131158224 | |||||||
| chr9:131158370 | C | T | 2 | a0001c0001t0001g0047 a0002c0003t0001g0126 |
2 | HG01884.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.2437-1013C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131158370 | |||||||
| chr9:131158371 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.2437-1012G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131158371 | |||||||
| chr9:131158484 | G | A | 2 | a0002c0003t0001g0071 a0002c0003t0001g0074 |
2 | HG02723.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2437-899G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131158484 | |||||||
| chr9:131158521 | G | T | 3 | a0001c0010t0003g0214 a0001c0010t0003g0228 a0001c0010t0003g0229 |
3 | HG01109.hp1 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2437-862G>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131158521 | |||||||
| chr9:131158667 | G | A | 1 | a0002c0020t0012g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2437-716G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131158667 | |||||||
| chr9:131159052 | A | C | 1 | a0002c0002t0001g0193 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.2437-331A>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131159052 | |||||||
| chr9:131159103 | A | G | 1 | a0001c0001t0001g0049 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2437-280A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131159103 | |||||||
| chr9:131159324 | C | T | 2 | a0002c0003t0001g0044 a0002c0003t0001g0045 |
2 | HG01074.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.2437-59C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 17/35 | chr9 | 131159324 | |||||||
| chr9:131159563 | T | C | 3 | a0002c0002t0001g0180 a0002c0002t0001g0192 a0002c0002t0001g0194 |
3 | HG01928.hp2 HG01993.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.2540+77T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 18/35 | chr9 | 131159563 | |||||||
| chr9:131159628 | C | A | 3 | a0001c0007t0001g0064 a0001c0007t0001g0086 a0001c0007t0001g0088 |
3 | HG02145.hp2 HG02897.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.2540+142C>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 18/35 | chr9 | 131159628 | |||||||
| chr9:131159718 | A | G | 3 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 |
3 | HG00733.hp2 HG01074.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.2540+232A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 18/35 | chr9 | 131159718 | |||||||
| chr9:131159871 | A | AG | 3 | a0005c0012t0001g0005 a0005c0012t0001g0006 a0005c0012t0001g0007 |
3 | HG01106.hp2 HG02723.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2540+385_2540+386i others(3): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 18/35 | chr9 | 131159871 | |||||||
| chr9:131159897 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2540+411C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 18/35 | chr9 | 131159897 | |||||||
| chr9:131159979 | A | C | 108 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(105): Show |
108 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.2540+493A>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 18/35 | chr9 | 131159979 | |||||||
| chr9:131160004 | A | T | 1 | a0001c0001t0001g0089 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2540+518A>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 18/35 | chr9 | 131160004 | |||||||
| chr9:131160086 | A | T | 1 | a0012c0023t0005g0003 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2540+600A>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 18/35 | chr9 | 131160086 | |||||||
| chr9:131160119 | C | G | 3 | a0001c0010t0003g0214 a0001c0010t0003g0228 a0001c0010t0003g0229 |
3 | HG01109.hp1 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2540+633C>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 18/35 | chr9 | 131160119 | |||||||
| chr9:131160527 | A | G | 3 | a0002c0002t0001g0115 a0002c0002t0001g0116 a0002c0002t0001g0119 |
3 | NA19000.hp2 NA19011.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.2540+1041A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 18/35 | chr9 | 131160527 | |||||||
| chr9:131160983 | A | G | 3 | a0002c0002t0001g0143 a0002c0002t0001g0154 a0002c0002t0001g0155 |
3 | HG02738.hp2 HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.2540+1497A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 18/35 | chr9 | 131160983 | |||||||
| chr9:131161010 | C | G | 1 | a0008c0028t0004g0207 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2540+1524C>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 18/35 | chr9 | 131161010 | |||||||
| chr9:131161259 | C | CT | 9 | a0001c0001t0001g0073 a0001c0001t0001g0215 a0001c0001t0001g0216 others(6): Show |
9 | HG01943.hp2 HG02055.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.2541-1716dupT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 18/35 | INFO_REALIGN_3_PRIME | chr9 | 131161259 | ||||||
| chr9:131161259 | CT | C | 35 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(32): Show |
35 | HG00099.hp1 HG00438.hp1 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.2541-1716delT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 18/35 | INFO_REALIGN_3_PRIME | chr9 | 131161259 | ||||||
| chr9:131161344 | G | A | 7 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0212 others(4): Show |
7 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.2541-1647G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 18/35 | chr9 | 131161344 | |||||||
| chr9:131161350 | G | A | 2 | a0002c0002t0001g0145 a0002c0002t0001g0146 |
2 | NA18944.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.2541-1641G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 18/35 | chr9 | 131161350 | |||||||
| chr9:131161796 | C | T | 219 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(216): Show |
219 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.2541-1195C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 18/35 | chr9 | 131161796 | |||||||
| chr9:131161840 | A | G | 7 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0212 others(4): Show |
7 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.2541-1151A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 18/35 | chr9 | 131161840 | |||||||
| chr9:131162031 | T | C | 2 | a0001c0001t0001g0028 a0001c0001t0001g0029 |
2 | HG03130.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2541-960T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 18/35 | chr9 | 131162031 | |||||||
| chr9:131162097 | G | A | 1 | a0008c0028t0004g0207 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2541-894G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 18/35 | chr9 | 131162097 | |||||||
| chr9:131162177 | A | G | 1 | a0001c0001t0001g0014 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.2541-814A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 18/35 | chr9 | 131162177 | |||||||
| chr9:131162191 | C | G | 1 | a0001c0001t0001g0014 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.2541-800C>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 18/35 | chr9 | 131162191 | |||||||
| chr9:131162576 | C | T | 4 | a0001c0007t0001g0064 a0001c0007t0001g0086 a0001c0007t0001g0088 others(1): Show |
4 | HG02145.hp2 HG02897.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.2541-415C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 18/35 | chr9 | 131162576 | |||||||
| chr9:131162798 | A | G | 1 | a0002c0003t0001g0016 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.2541-193A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 18/35 | chr9 | 131162798 | |||||||
| chr9:131162877 | G | C | 1 | a0001c0004t0001g0131 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2541-114G>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 18/35 | chr9 | 131162877 | |||||||
| chr9:131163225 | T | C | 1 | a0001c0001t0001g0014 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.2723+52T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 19/35 | chr9 | 131163225 | |||||||
| chr9:131163311 | T | A | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(104): Show |
107 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.2723+138T>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 19/35 | chr9 | 131163311 | |||||||
| chr9:131163336 | A | G | 2 | a0001c0001t0001g0008 a0001c0001t0001g0114 |
2 | HG03688.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.2723+163A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 19/35 | chr9 | 131163336 | |||||||
| chr9:131163434 | T | C | 219 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(216): Show |
219 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.2723+261T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 19/35 | chr9 | 131163434 | |||||||
| chr9:131163498 | T | C | 1 | a0002c0003t0001g0120 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2723+325T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 19/35 | chr9 | 131163498 | |||||||
| chr9:131164208 | C | T | 1 | a0001c0001t0001g0043 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.2893+64C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131164208 | |||||||
| chr9:131164212 | C | T | 1 | a0001c0001t0001g0068 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.2893+68C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131164212 | |||||||
| chr9:131164590 | C | G | 3 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0098 |
3 | HG01081.hp1 HG02055.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2893+446C>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131164590 | |||||||
| chr9:131164721 | G | A | 1 | a0002c0020t0012g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2893+577G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131164721 | |||||||
| chr9:131164729 | A | G | 2 | a0001c0001t0001g0102 a0001c0001t0001g0103 |
2 | HG03540.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2893+585A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131164729 | |||||||
| chr9:131164855 | T | G | 2 | a0001c0005t0002g0205 a0001c0005t0002g0206 |
2 | HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.2893+711T>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131164855 | |||||||
| chr9:131165062 | T | A | 219 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(216): Show |
219 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.2893+918T>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131165062 | |||||||
| chr9:131165067 | C | T | 222 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(219): Show |
222 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(219): Show |
intron_variant | MODIFIER | c.2893+923C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131165067 | |||||||
| chr9:131165647 | A | G | 10 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0212 others(7): Show |
10 | HG01109.hp1 HG01496.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.2893+1503A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131165647 | |||||||
| chr9:131165693 | T | C | 1 | a0002c0002t0001g0078 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2893+1549T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131165693 | |||||||
| chr9:131165724 | T | C | 1 | a0001c0005t0002g0212 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2893+1580T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131165724 | |||||||
| chr9:131165804 | C | A | 1 | a0002c0002t0001g0193 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.2893+1660C>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131165804 | |||||||
| chr9:131166230 | C | T | 3 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0098 |
3 | HG01081.hp1 HG02055.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2893+2086C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131166230 | |||||||
| chr9:131166241 | C | T | 1 | a0001c0001t0001g0049 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2893+2097C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131166241 | |||||||
| chr9:131166670 | C | T | 1 | a0001c0001t0001g0049 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2893+2526C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131166670 | |||||||
| chr9:131166682 | G | A | 1 | a0002c0002t0001g0144 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2893+2538G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131166682 | |||||||
| chr9:131166836 | C | T | 1 | a0002c0018t0002g0107 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2893+2692C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131166836 | |||||||
| chr9:131167097 | C | G | 1 | a0008c0028t0004g0207 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2893+2953C>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131167097 | |||||||
| chr9:131167448 | G | A | 2 | a0001c0001t0001g0060 a0001c0001t0001g0061 |
2 | HG01081.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.2893+3304G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131167448 | |||||||
| chr9:131168105 | A | G | 1 | a0002c0020t0012g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2893+3961A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131168105 | |||||||
| chr9:131168126 | G | A | 7 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0212 others(4): Show |
7 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.2893+3982G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131168126 | |||||||
| chr9:131168129 | A | T | 1 | a0001c0001t0001g0089 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2893+3985A>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131168129 | |||||||
| chr9:131168426 | T | A | 3 | a0001c0010t0003g0214 a0001c0010t0003g0228 a0001c0010t0003g0229 |
3 | HG01109.hp1 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2893+4282T>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131168426 | |||||||
| chr9:131168870 | C | A | 7 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0212 others(4): Show |
7 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.2893+4726C>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131168870 | |||||||
| chr9:131168907 | C | T | 1 | a0001c0004t0001g0196 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2893+4763C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131168907 | |||||||
| chr9:131169034 | G | GT | 204 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(201): Show |
204 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.2893+4906dupT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | INFO_REALIGN_3_PRIME | chr9 | 131169034 | ||||||
| chr9:131169034 | G | GTT | 13 | a0001c0001t0001g0029 a0001c0001t0001g0092 a0001c0001t0001g0094 others(10): Show |
13 | HG00544.hp2 HG00741.hp1 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.2893+4905_2893+490 others(6): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | INFO_REALIGN_3_PRIME | chr9 | 131169034 | ||||||
| chr9:131169318 | G | A | 3 | a0005c0012t0001g0005 a0005c0012t0001g0006 a0005c0012t0001g0007 |
3 | HG01106.hp2 HG02723.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2894-4737G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131169318 | |||||||
| chr9:131169325 | C | T | 1 | a0001c0001t0001g0024 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.2894-4730C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131169325 | |||||||
| chr9:131169356 | A | C | 1 | a0008c0028t0004g0207 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2894-4699A>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131169356 | |||||||
| chr9:131169357 | A | T | 1 | a0008c0028t0004g0207 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2894-4698A>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131169357 | |||||||
| chr9:131169362 | G | A | 1 | a0001c0001t0001g0017 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2894-4693G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131169362 | |||||||
| chr9:131169446 | G | A | 1 | a0001c0001t0001g0068 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.2894-4609G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131169446 | |||||||
| chr9:131169494 | A | C | 7 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0212 others(4): Show |
7 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.2894-4561A>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131169494 | |||||||
| chr9:131169679 | G | T | 3 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0217 |
3 | HG02109.hp1 HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2894-4376G>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131169679 | |||||||
| chr9:131169992 | G | A | 1 | a0002c0003t0001g0121 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2894-4063G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131169992 | |||||||
| chr9:131170147 | A | G | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(113): Show |
116 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.2894-3908A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131170147 | |||||||
| chr9:131170258 | G | A | 1 | a0008c0028t0004g0207 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2894-3797G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131170258 | |||||||
| chr9:131170440 | C | T | 1 | a0002c0003t0001g0097 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.2894-3615C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131170440 | |||||||
| chr9:131170496 | T | C | 3 | a0001c0005t0002g0212 a0001c0005t0002g0213 a0008c0028t0004g0207 |
3 | HG01496.hp2 HG02145.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.2894-3559T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131170496 | |||||||
| chr9:131170592 | T | C | 7 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0212 others(4): Show |
7 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.2894-3463T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131170592 | |||||||
| chr9:131170698 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.2894-3357G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131170698 | |||||||
| chr9:131170803 | C | CATT | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(150): Show |
153 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.2894-3233_2894-323 others(7): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | INFO_REALIGN_3_PRIME | chr9 | 131170803 | ||||||
| chr9:131170824 | T | TA | 2 | a0002c0002t0001g0149 a0002c0002t0001g0185 |
2 | HG04204.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.2894-3231_2894-323 others(5): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131170824 | |||||||
| chr9:131171268 | G | A | 1 | a0007c0025t0001g0084 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2894-2787G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131171268 | |||||||
| chr9:131171547 | CT | C | 124 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(121): Show |
124 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.2894-2490delT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | INFO_REALIGN_3_PRIME | chr9 | 131171547 | ||||||
| chr9:131171547 | CTT | C | 88 | a0001c0001t0001g0050 a0001c0001t0001g0076 a0001c0001t0001g0096 others(85): Show |
88 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.2894-2491_2894-249 others(6): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | INFO_REALIGN_3_PRIME | chr9 | 131171547 | ||||||
| chr9:131171616 | A | G | 7 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0212 others(4): Show |
7 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.2894-2439A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131171616 | |||||||
| chr9:131171651 | C | T | 1 | a0001c0001t0001g0231 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2894-2404C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131171651 | |||||||
| chr9:131171682 | T | G | 9 | a0001c0001t0001g0027 a0001c0001t0001g0051 a0001c0001t0001g0058 others(6): Show |
9 | HG00438.hp1 HG00642.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.2894-2373T>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131171682 | |||||||
| chr9:131171834 | G | A | 1 | a0001c0001t0001g0004 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2894-2221G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131171834 | |||||||
| chr9:131171875 | A | G | 3 | a0001c0004t0001g0219 a0002c0002t0001g0225 a0002c0002t0001g0226 |
3 | HG01884.hp2 HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2894-2180A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131171875 | |||||||
| chr9:131171896 | T | C | 4 | a0002c0002t0001g0009 a0002c0002t0001g0021 a0002c0002t0001g0067 others(1): Show |
4 | HG00639.hp2 HG03239.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.2894-2159T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131171896 | |||||||
| chr9:131172124 | G | A | 3 | a0001c0010t0003g0214 a0001c0010t0003g0228 a0001c0010t0003g0229 |
3 | HG01109.hp1 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2894-1931G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131172124 | |||||||
| chr9:131172254 | C | T | 2 | a0002c0002t0001g0221 a0002c0002t0001g0222 |
2 | HG01361.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.2894-1801C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131172254 | |||||||
| chr9:131172320 | T | C | 1 | a0001c0005t0003g0211 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2894-1735T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131172320 | |||||||
| chr9:131172585 | T | C | 11 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0212 others(8): Show |
11 | HG01109.hp1 HG01496.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.2894-1470T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131172585 | |||||||
| chr9:131172622 | A | G | 2 | a0002c0003t0001g0063 a0002c0016t0001g0100 |
2 | HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2894-1433A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131172622 | |||||||
| chr9:131172660 | A | G | 1 | a0002c0002t0001g0161 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.2894-1395A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131172660 | |||||||
| chr9:131172769 | C | G | 1 | a0002c0018t0002g0107 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2894-1286C>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131172769 | |||||||
| chr9:131172996 | C | T | 1 | a0002c0002t0001g0192 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.2894-1059C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131172996 | |||||||
| chr9:131173157 | A | G | 1 | a0001c0001t0010g0234 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2894-898A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131173157 | |||||||
| chr9:131173196 | A | G | 10 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0212 others(7): Show |
10 | HG01109.hp1 HG01496.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.2894-859A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131173196 | |||||||
| chr9:131173287 | T | A | 231 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(228): Show |
231 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(228): Show |
intron_variant | MODIFIER | c.2894-768T>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131173287 | |||||||
| chr9:131173355 | CT | C | 145 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(142): Show |
145 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.2894-676delT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | INFO_REALIGN_3_PRIME | chr9 | 131173355 | ||||||
| chr9:131173355 | CTT | C | 39 | a0001c0001t0001g0065 a0001c0001t0001g0090 a0001c0004t0001g0196 others(36): Show |
39 | HG00597.hp1 HG01106.hp2 HG01175.hp1 others(36): Show |
intron_variant | MODIFIER | c.2894-677_2894-676d others(4): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | INFO_REALIGN_3_PRIME | chr9 | 131173355 | ||||||
| chr9:131173355 | CTTTTTTT others(3): Show |
C | 2 | a0001c0005t0002g0205 a0001c0005t0002g0206 |
2 | HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.2894-685_2894-676d others(12): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | INFO_REALIGN_3_PRIME | chr9 | 131173355 | ||||||
| chr9:131173455 | C | T | 3 | a0005c0012t0001g0005 a0005c0012t0001g0006 a0005c0012t0001g0007 |
3 | HG01106.hp2 HG02723.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2894-600C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131173455 | |||||||
| chr9:131173537 | T | C | 1 | a0002c0002t0001g0175 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2894-518T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131173537 | |||||||
| chr9:131173538 | AT | A | 6 | a0001c0010t0003g0214 a0001c0010t0003g0228 a0001c0010t0003g0229 others(3): Show |
6 | HG00597.hp2 HG01109.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.2894-505delT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | INFO_REALIGN_3_PRIME | chr9 | 131173538 | ||||||
| chr9:131173616 | C | T | 2 | a0002c0003t0001g0044 a0002c0003t0001g0045 |
2 | HG01074.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.2894-439C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131173616 | |||||||
| chr9:131173893 | A | G | 1 | a0006c0008t0001g0109 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2894-162A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131173893 | |||||||
| chr9:131173916 | C | T | 2 | a0001c0005t0002g0205 a0001c0005t0002g0206 |
2 | HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.2894-139C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 21/35 | chr9 | 131173916 | |||||||
| chr9:131174355 | A | G | 1 | a0006c0008t0001g0040 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3157+37A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 22/35 | chr9 | 131174355 | |||||||
| chr9:131174431 | A | C | 1 | a0002c0003t0001g0083 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.3157+113A>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 22/35 | chr9 | 131174431 | |||||||
| chr9:131174432 | CT | C | 5 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0003g0211 others(2): Show |
5 | HG01891.hp2 HG02145.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.3157+128delT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 22/35 | INFO_REALIGN_3_PRIME | chr9 | 131174432 | ||||||
| chr9:131174446 | T | C | 3 | a0001c0001t0001g0076 a0002c0002t0001g0225 a0002c0002t0001g0226 |
3 | HG01515.hp1 HG01884.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.3157+128T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 22/35 | chr9 | 131174446 | |||||||
| chr9:131174447 | C | CT | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(187): Show |
190 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(187): Show |
intron_variant | MODIFIER | c.3157+136dupT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 22/35 | INFO_REALIGN_3_PRIME | chr9 | 131174447 | ||||||
| chr9:131174447 | C | CTT | 9 | a0001c0001t0001g0015 a0001c0004t0001g0209 a0001c0004t0001g0219 others(6): Show |
9 | HG01928.hp2 HG01981.hp2 HG01993.hp1 others(6): Show |
intron_variant | MODIFIER | c.3157+135_3157+136d others(4): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 22/35 | INFO_REALIGN_3_PRIME | chr9 | 131174447 | ||||||
| chr9:131174447 | C | T | 7 | a0001c0001t0001g0076 a0001c0007t0001g0086 a0001c0010t0003g0214 others(4): Show |
7 | HG01109.hp1 HG01515.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.3157+129C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 22/35 | chr9 | 131174447 | |||||||
| chr9:131174453 | TTC | T | 6 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0212 others(3): Show |
6 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.3157+137_3157+138d others(4): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 22/35 | INFO_REALIGN_3_PRIME | chr9 | 131174453 | ||||||
| chr9:131174455 | C | T | 211 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(208): Show |
211 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.3157+137C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 22/35 | chr9 | 131174455 | |||||||
| chr9:131174458 | T | TC | 2 | a0002c0003t0001g0063 a0002c0016t0001g0100 |
2 | HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.3157+140_3157+141i others(3): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 22/35 | chr9 | 131174458 | |||||||
| chr9:131174656 | G | A | 1 | a0001c0005t0003g0211 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3157+338G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 22/35 | chr9 | 131174656 | |||||||
| chr9:131174732 | G | A | 3 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 |
3 | HG00733.hp2 HG01074.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.3157+414G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 22/35 | chr9 | 131174732 | |||||||
| chr9:131174876 | A | G | 1 | a0002c0020t0012g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3157+558A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 22/35 | chr9 | 131174876 | |||||||
| chr9:131174897 | C | G | 1 | a0001c0001t0001g0054 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3158-563C>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 22/35 | chr9 | 131174897 | |||||||
| chr9:131175265 | G | A | 3 | a0002c0002t0001g0143 a0002c0002t0001g0154 a0002c0002t0001g0155 |
3 | HG02738.hp2 HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.3158-195G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 22/35 | chr9 | 131175265 | |||||||
| chr9:131175376 | C | T | 7 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0212 others(4): Show |
7 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.3158-84C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 22/35 | chr9 | 131175376 | |||||||
| chr9:131175908 | A | T | 1 | a0002c0002t0001g0156 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.3319+287A>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 23/35 | chr9 | 131175908 | |||||||
| chr9:131176024 | A | T | 3 | a0001c0001t0001g0066 a0001c0001t0001g0176 a0001c0001t0001g0189 |
3 | HG02451.hp1 HG02965.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.3319+403A>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 23/35 | chr9 | 131176024 | |||||||
| chr9:131176051 | C | T | 1 | a0002c0002t0001g0135 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.3319+430C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 23/35 | chr9 | 131176051 | |||||||
| chr9:131176144 | C | T | 1 | a0004c0009t0001g0039 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.3319+523C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 23/35 | chr9 | 131176144 | |||||||
| chr9:131176201 | G | C | 7 | a0001c0004t0001g0227 a0002c0002t0001g0104 a0002c0002t0001g0220 others(4): Show |
7 | HG01361.hp2 HG01943.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.3319+580G>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 23/35 | chr9 | 131176201 | |||||||
| chr9:131176387 | G | A | 1 | a0008c0028t0004g0207 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3319+766G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 23/35 | chr9 | 131176387 | |||||||
| chr9:131176436 | C | G | 1 | a0001c0001t0009g0072 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.3319+815C>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 23/35 | chr9 | 131176436 | |||||||
| chr9:131176446 | CCTCCTGG others(4): Show |
C | 2 | a0004c0009t0001g0030 a0004c0009t0001g0031 |
2 | HG00597.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.3319+828_3319+838d others(13): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 23/35 | INFO_REALIGN_3_PRIME | chr9 | 131176446 | ||||||
| chr9:131176542 | T | A | 1 | a0001c0001t0001g0048 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3319+921T>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 23/35 | chr9 | 131176542 | |||||||
| chr9:131176575 | C | T | 2 | a0002c0002t0001g0159 a0002c0002t0001g0160 |
2 | NA18945.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.3319+954C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 23/35 | chr9 | 131176575 | |||||||
| chr9:131176800 | A | G | 1 | a0002c0002t0001g0208 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3319+1179A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 23/35 | chr9 | 131176800 | |||||||
| chr9:131176823 | T | C | 3 | a0006c0008t0001g0032 a0006c0008t0001g0040 a0006c0008t0001g0109 |
3 | HG02109.hp2 HG02559.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.3319+1202T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 23/35 | chr9 | 131176823 | |||||||
| chr9:131176873 | G | C | 11 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0212 others(8): Show |
11 | HG01109.hp1 HG01496.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.3319+1252G>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 23/35 | chr9 | 131176873 | |||||||
| chr9:131176884 | CT | C | 3 | a0001c0010t0003g0214 a0001c0010t0003g0228 a0001c0010t0003g0229 |
3 | HG01109.hp1 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.3319+1264delT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 23/35 | chr9 | 131176884 | |||||||
| chr9:131176971 | C | T | 1 | a0001c0004t0001g0196 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.3320-1340C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 23/35 | chr9 | 131176971 | |||||||
| chr9:131177258 | A | G | 2 | a0001c0001t0001g0037 a0001c0001t0001g0038 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.3320-1053A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 23/35 | chr9 | 131177258 | |||||||
| chr9:131177335 | T | C | 1 | a0001c0001t0001g0001 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3320-976T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 23/35 | chr9 | 131177335 | |||||||
| chr9:131177937 | A | G | 2 | a0001c0001t0001g0230 a0001c0001t0001g0232 |
2 | HG00642.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.3320-374A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 23/35 | chr9 | 131177937 | |||||||
| chr9:131177963 | T | C | 1 | a0015c0019t0001g0141 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.3320-348T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 23/35 | chr9 | 131177963 | |||||||
| chr9:131178248 | G | T | 2 | a0002c0003t0001g0071 a0002c0003t0001g0074 |
2 | HG02723.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.3320-63G>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 23/35 | chr9 | 131178248 | |||||||
| chr9:131178522 | T | C | 1 | a0001c0005t0002g0213 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.3419+112T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131178522 | |||||||
| chr9:131178565 | A | G | 1 | a0001c0001t0010g0234 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.3419+155A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131178565 | |||||||
| chr9:131178703 | A | AT | 100 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(97): Show |
100 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.3419+309dupT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | INFO_REALIGN_3_PRIME | chr9 | 131178703 | ||||||
| chr9:131178703 | AT | A | 14 | a0001c0001t0001g0014 a0001c0001t0001g0073 a0001c0005t0002g0205 others(11): Show |
14 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.3419+309delT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | INFO_REALIGN_3_PRIME | chr9 | 131178703 | ||||||
| chr9:131178719 | T | A | 7 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0212 others(4): Show |
7 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.3419+309T>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131178719 | |||||||
| chr9:131178993 | T | G | 6 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0212 others(3): Show |
6 | HG01891.hp2 HG02145.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.3419+583T>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131178993 | |||||||
| chr9:131179021 | G | T | 1 | a0001c0001t0001g0230 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.3419+611G>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131179021 | |||||||
| chr9:131179241 | A | G | 2 | a0002c0003t0001g0071 a0002c0003t0001g0074 |
2 | HG02723.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.3419+831A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131179241 | |||||||
| chr9:131179287 | C | G | 99 | a0001c0001t0001g0047 a0001c0001t0001g0066 a0001c0001t0001g0176 others(96): Show |
99 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.3419+877C>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131179287 | |||||||
| chr9:131179395 | C | T | 3 | a0001c0010t0003g0214 a0001c0010t0003g0228 a0001c0010t0003g0229 |
3 | HG01109.hp1 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.3419+985C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131179395 | |||||||
| chr9:131179446 | C | T | 1 | a0010c0017t0001g0108 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3419+1036C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131179446 | |||||||
| chr9:131179812 | C | T | 3 | a0001c0010t0003g0214 a0001c0010t0003g0228 a0001c0010t0003g0229 |
3 | HG01109.hp1 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.3419+1402C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131179812 | |||||||
| chr9:131180172 | G | A | 4 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0003g0211 others(1): Show |
4 | HG01891.hp2 HG02451.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.3419+1762G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131180172 | |||||||
| chr9:131180375 | G | A | 3 | a0001c0010t0003g0214 a0001c0010t0003g0228 a0001c0010t0003g0229 |
3 | HG01109.hp1 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.3419+1965G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131180375 | |||||||
| chr9:131180433 | A | T | 2 | a0001c0005t0002g0212 a0001c0005t0002g0213 |
2 | HG01496.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.3419+2023A>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131180433 | |||||||
| chr9:131180485 | C | A | 1 | a0001c0004t0001g0137 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3419+2075C>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131180485 | |||||||
| chr9:131180772 | C | G | 2 | a0002c0002t0001g0221 a0002c0002t0001g0222 |
2 | HG01361.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.3419+2362C>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131180772 | |||||||
| chr9:131180880 | T | C | 1 | a0001c0001t0001g0024 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.3419+2470T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131180880 | |||||||
| chr9:131181014 | A | G | 205 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(202): Show |
205 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.3419+2604A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131181014 | |||||||
| chr9:131181244 | T | C | 231 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(228): Show |
231 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(228): Show |
intron_variant | MODIFIER | c.3419+2834T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131181244 | |||||||
| chr9:131181393 | T | C | 1 | a0001c0001t0001g0015 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.3419+2983T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131181393 | |||||||
| chr9:131181809 | G | A | 11 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0212 others(8): Show |
11 | HG01109.hp1 HG01496.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.3419+3399G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131181809 | |||||||
| chr9:131181877 | C | T | 1 | a0001c0001t0001g0004 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3419+3467C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131181877 | |||||||
| chr9:131181878 | A | C | 2 | a0002c0002t0001g0145 a0002c0002t0001g0146 |
2 | NA18944.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.3419+3468A>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131181878 | |||||||
| chr9:131182056 | A | T | 1 | a0001c0005t0002g0212 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3419+3646A>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131182056 | |||||||
| chr9:131182149 | T | C | 7 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0212 others(4): Show |
7 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.3419+3739T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131182149 | |||||||
| chr9:131182221 | A | C | 97 | a0001c0001t0001g0047 a0001c0001t0001g0059 a0001c0001t0001g0066 others(94): Show |
97 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.3419+3811A>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131182221 | |||||||
| chr9:131182447 | A | G | 1 | a0002c0020t0012g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3419+4037A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131182447 | |||||||
| chr9:131182550 | G | A | 2 | a0001c0010t0003g0228 a0001c0010t0003g0229 |
2 | HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.3419+4140G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131182550 | |||||||
| chr9:131182733 | T | C | 219 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(216): Show |
219 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.3419+4323T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131182733 | |||||||
| chr9:131182765 | T | A | 3 | a0001c0024t0001g0056 a0001c0026t0001g0055 a0001c0027t0001g0085 |
3 | HG02056.hp2 NA18945.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.3419+4355T>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131182765 | |||||||
| chr9:131182950 | A | G | 3 | a0001c0010t0003g0214 a0001c0010t0003g0228 a0001c0010t0003g0229 |
3 | HG01109.hp1 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.3420-4339A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131182950 | |||||||
| chr9:131183015 | T | G | 3 | a0001c0010t0003g0214 a0001c0010t0003g0228 a0001c0010t0003g0229 |
3 | HG01109.hp1 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.3420-4274T>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131183015 | |||||||
| chr9:131183019 | A | G | 2 | a0002c0002t0001g0221 a0002c0002t0001g0222 |
2 | HG01361.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.3420-4270A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131183019 | |||||||
| chr9:131183051 | C | T | 1 | a0002c0003t0001g0074 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3420-4238C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131183051 | |||||||
| chr9:131183228 | G | A | 1 | a0001c0005t0002g0212 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3420-4061G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131183228 | |||||||
| chr9:131183233 | C | T | 1 | a0010c0017t0001g0108 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3420-4056C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131183233 | |||||||
| chr9:131183682 | C | G | 3 | a0001c0004t0001g0219 a0002c0002t0001g0225 a0002c0002t0001g0226 |
3 | HG01884.hp2 HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.3420-3607C>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131183682 | |||||||
| chr9:131183813 | A | G | 3 | a0002c0002t0001g0009 a0002c0002t0001g0021 a0002c0002t0001g0067 |
3 | HG00639.hp2 HG03239.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.3420-3476A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131183813 | |||||||
| chr9:131183877 | T | C | 1 | a0001c0001t0001g0081 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.3420-3412T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131183877 | |||||||
| chr9:131183952 | C | T | 1 | a0001c0010t0003g0214 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.3420-3337C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131183952 | |||||||
| chr9:131184013 | CTTTTTTC others(7): Show |
C | 1 | a0002c0002t0001g0190 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.3420-3269_3420-325 others(18): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | INFO_REALIGN_3_PRIME | chr9 | 131184013 | ||||||
| chr9:131184014 | TTTTTTCT others(5): Show |
T | 1 | a0008c0028t0004g0207 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3420-3269_3420-325 others(16): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | INFO_REALIGN_3_PRIME | chr9 | 131184014 | ||||||
| chr9:131184026 | C | CT | 12 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0027 others(9): Show |
12 | HG00642.hp1 HG00642.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.3420-3241dupT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | INFO_REALIGN_3_PRIME | chr9 | 131184026 | ||||||
| chr9:131184026 | CT | C | 10 | a0001c0001t0001g0004 a0001c0005t0002g0212 a0001c0026t0001g0055 others(7): Show |
10 | HG01943.hp2 HG02630.hp2 HG02735.hp2 others(7): Show |
intron_variant | MODIFIER | c.3420-3241delT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | INFO_REALIGN_3_PRIME | chr9 | 131184026 | ||||||
| chr9:131184030 | T | C | 1 | a0008c0028t0004g0207 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3420-3259T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131184030 | |||||||
| chr9:131184031 | T | C | 5 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0213 others(2): Show |
5 | HG01496.hp2 HG01891.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.3420-3258T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131184031 | |||||||
| chr9:131184032 | T | C | 2 | a0001c0005t0002g0212 a0002c0020t0012g0132 |
2 | HG02630.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.3420-3257T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131184032 | |||||||
| chr9:131184335 | C | CT | 7 | a0001c0001t0001g0015 a0001c0001t0001g0059 a0001c0005t0002g0212 others(4): Show |
7 | HG01943.hp2 HG01981.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.3420-2938dupT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | INFO_REALIGN_3_PRIME | chr9 | 131184335 | ||||||
| chr9:131184444 | A | G | 113 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(110): Show |
113 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.3420-2845A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131184444 | |||||||
| chr9:131184475 | A | T | 3 | a0001c0010t0003g0214 a0001c0010t0003g0228 a0001c0010t0003g0229 |
3 | HG01109.hp1 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.3420-2814A>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131184475 | |||||||
| chr9:131184493 | C | T | 7 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0212 others(4): Show |
7 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.3420-2796C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131184493 | |||||||
| chr9:131184500 | A | C | 3 | a0005c0012t0001g0005 a0005c0012t0001g0006 a0005c0012t0001g0007 |
3 | HG01106.hp2 HG02723.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.3420-2789A>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131184500 | |||||||
| chr9:131184536 | A | G | 3 | a0002c0002t0001g0220 a0002c0002t0001g0223 a0002c0002t0001g0224 |
3 | HG01943.hp2 HG02559.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.3420-2753A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131184536 | |||||||
| chr9:131184556 | G | A | 91 | a0001c0004t0001g0131 a0001c0004t0001g0137 a0001c0004t0001g0138 others(88): Show |
91 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.3420-2733G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131184556 | |||||||
| chr9:131184577 | A | C | 1 | a0001c0010t0003g0214 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.3420-2712A>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131184577 | |||||||
| chr9:131184627 | T | C | 219 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(216): Show |
219 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.3420-2662T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131184627 | |||||||
| chr9:131184674 | A | G | 1 | a0001c0001t0010g0234 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.3420-2615A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131184674 | |||||||
| chr9:131184996 | A | G | 2 | a0003c0013t0001g0041 a0003c0013t0001g0070 |
2 | HG02615.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.3420-2293A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131184996 | |||||||
| chr9:131185008 | T | G | 1 | a0002c0020t0012g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3420-2281T>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131185008 | |||||||
| chr9:131185226 | A | C | 1 | a0002c0003t0001g0125 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3420-2063A>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131185226 | |||||||
| chr9:131185259 | G | A | 1 | a0002c0002t0001g0142 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.3420-2030G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131185259 | |||||||
| chr9:131185336 | A | T | 1 | a0002c0020t0012g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3420-1953A>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131185336 | |||||||
| chr9:131185399 | A | G | 1 | a0001c0005t0002g0212 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3420-1890A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131185399 | |||||||
| chr9:131185559 | C | T | 3 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0217 |
3 | HG02109.hp1 HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.3420-1730C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131185559 | |||||||
| chr9:131185583 | C | G | 3 | a0002c0002t0001g0180 a0002c0002t0001g0192 a0002c0002t0001g0194 |
3 | HG01928.hp2 HG01993.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.3420-1706C>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131185583 | |||||||
| chr9:131185940 | T | G | 1 | a0002c0020t0012g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3420-1349T>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131185940 | |||||||
| chr9:131186154 | G | A | 3 | a0001c0004t0001g0137 a0002c0002t0001g0136 a0002c0002t0001g0208 |
3 | HG00733.hp1 HG01243.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.3420-1135G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131186154 | |||||||
| chr9:131186383 | G | A | 1 | a0002c0002t0001g0144 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.3420-906G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131186383 | |||||||
| chr9:131186452 | T | C | 1 | a0013c0021t0001g0173 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.3420-837T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131186452 | |||||||
| chr9:131186518 | A | G | 1 | a0001c0005t0002g0213 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.3420-771A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131186518 | |||||||
| chr9:131187146 | C | T | 3 | a0001c0010t0003g0214 a0001c0010t0003g0228 a0001c0010t0003g0229 |
3 | HG01109.hp1 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.3420-143C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131187146 | |||||||
| chr9:131187222 | T | A | 2 | a0001c0001t0001g0058 a0001c0001t0001g0170 |
2 | HG03017.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.3420-67T>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 24/35 | chr9 | 131187222 | |||||||
| chr9:131187383 | C | CT | 57 | a0001c0001t0001g0013 a0001c0001t0001g0036 a0001c0001t0001g0048 others(54): Show |
57 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.3495+40dupT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 25/35 | INFO_REALIGN_3_PRIME | chr9 | 131187383 | ||||||
| chr9:131187383 | C | CTT | 7 | a0001c0004t0001g0137 a0001c0005t0002g0213 a0001c0010t0003g0214 others(4): Show |
7 | HG01109.hp1 HG01496.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.3495+39_3495+40dup others(2): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 25/35 | INFO_REALIGN_3_PRIME | chr9 | 131187383 | ||||||
| chr9:131187383 | CT | C | 9 | a0001c0001t0001g0017 a0001c0001t0001g0087 a0001c0001t0001g0095 others(6): Show |
9 | HG00558.hp1 HG01169.hp2 HG01943.hp1 others(6): Show |
intron_variant | MODIFIER | c.3495+40delT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 25/35 | INFO_REALIGN_3_PRIME | chr9 | 131187383 | ||||||
| chr9:131187453 | C | G | 1 | a0001c0001t0001g0065 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3495+89C>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 25/35 | chr9 | 131187453 | |||||||
| chr9:131187487 | A | G | 1 | a0012c0023t0005g0003 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3495+123A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 25/35 | chr9 | 131187487 | |||||||
| chr9:131187713 | G | A | 1 | a0001c0001t0001g0028 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3495+349G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 25/35 | chr9 | 131187713 | |||||||
| chr9:131187801 | C | T | 11 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0212 others(8): Show |
11 | HG01109.hp1 HG01496.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.3495+437C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 25/35 | chr9 | 131187801 | |||||||
| chr9:131187829 | A | G | 1 | a0001c0005t0003g0211 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3495+465A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 25/35 | chr9 | 131187829 | |||||||
| chr9:131187876 | T | C | 1 | a0001c0001t0001g0002 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.3495+512T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 25/35 | chr9 | 131187876 | |||||||
| chr9:131188036 | C | A | 2 | a0005c0012t0001g0005 a0005c0012t0001g0007 |
2 | HG01106.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.3495+672C>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 25/35 | chr9 | 131188036 | |||||||
| chr9:131188112 | C | T | 3 | a0001c0010t0003g0214 a0001c0010t0003g0228 a0001c0010t0003g0229 |
3 | HG01109.hp1 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.3495+748C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 25/35 | chr9 | 131188112 | |||||||
| chr9:131188252 | G | T | 1 | a0001c0001t0001g0061 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.3496-801G>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 25/35 | chr9 | 131188252 | |||||||
| chr9:131188328 | A | G | 3 | a0001c0010t0003g0214 a0001c0010t0003g0228 a0001c0010t0003g0229 |
3 | HG01109.hp1 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.3496-725A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 25/35 | chr9 | 131188328 | |||||||
| chr9:131188536 | A | G | 50 | a0001c0004t0001g0131 a0001c0004t0001g0137 a0001c0004t0001g0138 others(47): Show |
50 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(47): Show |
intron_variant | MODIFIER | c.3496-517A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 25/35 | chr9 | 131188536 | |||||||
| chr9:131188561 | C | T | 1 | a0002c0020t0012g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3496-492C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 25/35 | chr9 | 131188561 | |||||||
| chr9:131188659 | C | A | 1 | a0002c0003t0001g0016 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.3496-394C>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 25/35 | chr9 | 131188659 | |||||||
| chr9:131188957 | T | C | 1 | a0001c0004t0001g0140 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.3496-96T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 25/35 | chr9 | 131188957 | |||||||
| chr9:131188958 | T | C | 112 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(109): Show |
112 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.3496-95T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 25/35 | chr9 | 131188958 | |||||||
| chr9:131189341 | A | G | 41 | a0001c0004t0001g0131 a0001c0004t0001g0137 a0001c0004t0001g0138 others(38): Show |
41 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(38): Show |
intron_variant | MODIFIER | c.3574+210A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 26/35 | chr9 | 131189341 | |||||||
| chr9:131190193 | G | A | 92 | a0001c0004t0001g0131 a0001c0004t0001g0137 a0001c0004t0001g0138 others(89): Show |
92 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.3574+1062G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 26/35 | chr9 | 131190193 | |||||||
| chr9:131190619 | A | G | 3 | a0001c0010t0003g0214 a0001c0010t0003g0228 a0001c0010t0003g0229 |
3 | HG01109.hp1 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.3574+1488A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 26/35 | chr9 | 131190619 | |||||||
| chr9:131190926 | A | G | 2 | a0002c0003t0001g0071 a0002c0003t0001g0074 |
2 | HG02723.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.3575-1282A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 26/35 | chr9 | 131190926 | |||||||
| chr9:131191047 | CT | C | 3 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0217 |
3 | HG02109.hp1 HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.3575-1160delT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 26/35 | chr9 | 131191047 | |||||||
| chr9:131191186 | A | C | 2 | a0001c0006t0001g0168 a0001c0006t0001g0169 |
2 | HG00408.hp2 HG00544.hp1 |
intron_variant | MODIFIER | c.3575-1022A>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 26/35 | chr9 | 131191186 | |||||||
| chr9:131191296 | T | A | 3 | a0001c0010t0003g0214 a0001c0010t0003g0228 a0001c0010t0003g0229 |
3 | HG01109.hp1 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.3575-912T>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 26/35 | chr9 | 131191296 | |||||||
| chr9:131191430 | T | G | 1 | a0007c0025t0001g0084 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.3575-778T>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 26/35 | chr9 | 131191430 | |||||||
| chr9:131191619 | G | A | 1 | a0001c0005t0002g0212 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3575-589G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 26/35 | chr9 | 131191619 | |||||||
| chr9:131192087 | C | A | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(104): Show |
107 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.3575-121C>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 26/35 | chr9 | 131192087 | |||||||
| chr9:131192169 | C | CT | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(161): Show |
164 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.3575-13dupT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 26/35 | INFO_REALIGN_3_PRIME | chr9 | 131192169 | ||||||
| chr9:131192169 | C | CTT | 16 | a0001c0001t0001g0024 a0001c0001t0001g0035 a0001c0001t0001g0037 others(13): Show |
16 | HG00558.hp2 HG01884.hp2 HG01993.hp2 others(13): Show |
intron_variant | MODIFIER | c.3575-14_3575-13dup others(2): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 26/35 | INFO_REALIGN_3_PRIME | chr9 | 131192169 | ||||||
| chr9:131192169 | C | CTTT | 8 | a0001c0001t0001g0010 a0001c0001t0001g0092 a0001c0001t0007g0042 others(5): Show |
8 | HG00639.hp1 HG00741.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.3575-15_3575-13dup others(3): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 26/35 | INFO_REALIGN_3_PRIME | chr9 | 131192169 | ||||||
| chr9:131192169 | CTTTTTTT others(3): Show |
C | 1 | a0002c0002t0001g0210 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.3575-22_3575-13del others(10): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 26/35 | INFO_REALIGN_3_PRIME | chr9 | 131192169 | ||||||
| chr9:131192324 | T | G | 2 | a0001c0005t0002g0205 a0001c0005t0002g0206 |
2 | HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.3659+32T>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | chr9 | 131192324 | |||||||
| chr9:131192408 | G | A | 222 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(219): Show |
222 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(219): Show |
intron_variant | MODIFIER | c.3659+116G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | chr9 | 131192408 | |||||||
| chr9:131192438 | A | G | 222 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(219): Show |
222 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(219): Show |
intron_variant | MODIFIER | c.3659+146A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | chr9 | 131192438 | |||||||
| chr9:131192492 | T | C | 1 | a0008c0028t0004g0207 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3659+200T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | chr9 | 131192492 | |||||||
| chr9:131192573 | G | T | 1 | a0001c0001t0001g0065 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3659+281G>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | chr9 | 131192573 | |||||||
| chr9:131192731 | A | G | 3 | a0001c0010t0003g0214 a0001c0010t0003g0228 a0001c0010t0003g0229 |
3 | HG01109.hp1 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.3659+439A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | chr9 | 131192731 | |||||||
| chr9:131192733 | G | C | 1 | a0001c0005t0003g0211 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3659+441G>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | chr9 | 131192733 | |||||||
| chr9:131192818 | A | G | 1 | a0003c0011t0001g0178 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.3659+526A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | chr9 | 131192818 | |||||||
| chr9:131192941 | C | CA | 73 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(70): Show |
73 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.3659+676dupA | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr9 | 131192941 | ||||||
| chr9:131192941 | C | CAA | 12 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0049 others(9): Show |
12 | HG00733.hp2 HG01109.hp2 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.3659+675_3659+676d others(4): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr9 | 131192941 | ||||||
| chr9:131192941 | CA | C | 29 | a0001c0001t0001g0026 a0001c0004t0001g0197 a0001c0004t0001g0198 others(26): Show |
29 | HG01109.hp1 HG01175.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.3659+676delA | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr9 | 131192941 | ||||||
| chr9:131192941 | CAA | C | 7 | a0001c0005t0002g0206 a0001c0005t0003g0211 a0001c0010t0003g0228 others(4): Show |
7 | HG01361.hp2 HG01891.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.3659+675_3659+676d others(4): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr9 | 131192941 | ||||||
| chr9:131192969 | G | A | 1 | a0002c0002t0001g0193 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.3659+677G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | chr9 | 131192969 | |||||||
| chr9:131192981 | C | T | 6 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0213 others(3): Show |
6 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.3659+689C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | chr9 | 131192981 | |||||||
| chr9:131193050 | T | C | 1 | a0001c0001t0001g0049 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3659+758T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | chr9 | 131193050 | |||||||
| chr9:131193208 | G | A | 1 | a0001c0001t0001g0004 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3659+916G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | chr9 | 131193208 | |||||||
| chr9:131193243 | T | TCTCTTCC others(11): Show |
11 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0212 others(8): Show |
11 | HG01109.hp1 HG01496.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.3659+951_3659+952i others(20): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | chr9 | 131193243 | |||||||
| chr9:131193502 | T | C | 3 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0217 |
3 | HG02109.hp1 HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.3659+1210T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | chr9 | 131193502 | |||||||
| chr9:131193629 | C | CT | 6 | a0001c0001t0001g0217 a0002c0003t0001g0120 a0002c0003t0001g0124 others(3): Show |
6 | HG01884.hp1 HG02258.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.3659+1370dupT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr9 | 131193629 | ||||||
| chr9:131193629 | C | CTTTT | 5 | a0001c0001t0001g0058 a0001c0001t0001g0230 a0002c0003t0001g0083 others(2): Show |
5 | HG00609.hp1 HG01516.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.3659+1367_3659+137 others(8): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr9 | 131193629 | ||||||
| chr9:131193629 | C | CTTTTT | 13 | a0001c0001t0001g0022 a0001c0001t0001g0027 a0001c0001t0001g0029 others(10): Show |
13 | HG00423.hp1 HG01243.hp2 HG02132.hp2 others(10): Show |
intron_variant | MODIFIER | c.3659+1366_3659+137 others(9): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr9 | 131193629 | ||||||
| chr9:131193629 | C | CTTTTTT | 30 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0023 others(27): Show |
30 | HG00408.hp1 HG00597.hp2 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.3659+1365_3659+137 others(10): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr9 | 131193629 | ||||||
| chr9:131193629 | C | CTTTTTTT | 17 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0019 others(14): Show |
17 | HG00544.hp2 HG00639.hp1 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.3659+1364_3659+137 others(11): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr9 | 131193629 | ||||||
| chr9:131193629 | C | CTTTTTTT others(8): Show |
1 | a0003c0011t0001g0186 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.3659+1344_3659+134 others(19): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr9 | 131193629 | ||||||
| chr9:131193629 | C | CTTTTTTT others(1): Show |
14 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0017 others(11): Show |
14 | HG00558.hp1 HG01074.hp1 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.3659+1363_3659+137 others(12): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr9 | 131193629 | ||||||
| chr9:131193629 | C | CTTTTTTT others(2): Show |
6 | a0001c0001t0001g0049 a0001c0001t0001g0059 a0001c0001t0001g0087 others(3): Show |
6 | HG01109.hp2 HG01943.hp1 HG02027.hp1 others(3): Show |
intron_variant | MODIFIER | c.3659+1362_3659+137 others(13): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr9 | 131193629 | ||||||
| chr9:131193629 | C | CTTTTTTT others(3): Show |
4 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0057 others(1): Show |
4 | HG00099.hp1 HG00733.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.3659+1361_3659+137 others(14): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr9 | 131193629 | ||||||
| chr9:131193629 | C | CTTTTTTT others(4): Show |
7 | a0001c0001t0001g0015 a0001c0001t0001g0053 a0001c0004t0001g0204 others(4): Show |
7 | HG00408.hp2 HG00544.hp1 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.3659+1360_3659+137 others(15): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr9 | 131193629 | ||||||
| chr9:131193629 | C | CTTTTTTT others(5): Show |
10 | a0001c0004t0001g0201 a0001c0006t0001g0174 a0002c0002t0001g0147 others(7): Show |
10 | HG01168.hp2 HG01516.hp2 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.3659+1359_3659+137 others(16): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr9 | 131193629 | ||||||
| chr9:131193629 | C | CTTTTTTT others(6): Show |
10 | a0001c0004t0001g0131 a0001c0006t0001g0179 a0002c0002t0001g0115 others(7): Show |
10 | HG00423.hp2 HG01169.hp1 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.3659+1358_3659+137 others(17): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr9 | 131193629 | ||||||
| chr9:131193629 | C | CTTTTTTT others(7): Show |
4 | a0001c0004t0001g0209 a0002c0002t0001g0177 a0002c0002t0001g0194 others(1): Show |
4 | HG01928.hp2 HG02698.hp1 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.3659+1357_3659+137 others(18): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr9 | 131193629 | ||||||
| chr9:131193629 | C | CTTTTTTT others(8): Show |
6 | a0001c0001t0001g0089 a0001c0004t0001g0140 a0002c0002t0001g0135 others(3): Show |
6 | HG00558.hp2 HG00609.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.3659+1356_3659+137 others(19): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr9 | 131193629 | ||||||
| chr9:131193629 | C | CTTTTTTT others(9): Show |
3 | a0002c0002t0001g0078 a0002c0002t0001g0145 a0003c0011t0001g0191 |
3 | HG00642.hp1 HG04204.hp2 NA18944.hp2 |
intron_variant | MODIFIER | c.3659+1355_3659+137 others(20): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr9 | 131193629 | ||||||
| chr9:131193629 | C | CTTTTTTT others(10): Show |
1 | a0002c0002t0001g0021 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.3659+1354_3659+137 others(21): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr9 | 131193629 | ||||||
| chr9:131193629 | C | CTTTTTTT others(11): Show |
5 | a0001c0001t0001g0082 a0002c0002t0001g0067 a0002c0002t0001g0133 others(2): Show |
5 | HG00099.hp2 HG02056.hp1 HG02135.hp1 others(2): Show |
intron_variant | MODIFIER | c.3659+1353_3659+137 others(22): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr9 | 131193629 | ||||||
| chr9:131193629 | C | CTTTTTTT others(12): Show |
3 | a0002c0002t0001g0009 a0002c0002t0001g0167 a0015c0019t0001g0141 |
3 | HG00639.hp2 NA18969.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.3659+1352_3659+137 others(23): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr9 | 131193629 | ||||||
| chr9:131193629 | C | CTTTTTTT others(13): Show |
2 | a0002c0002t0001g0077 a0002c0003t0001g0016 |
2 | HG04228.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.3659+1351_3659+137 others(24): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr9 | 131193629 | ||||||
| chr9:131193629 | C | CTTTTTTT others(14): Show |
2 | a0001c0007t0001g0086 a0002c0002t0001g0158 |
2 | HG00741.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.3659+1350_3659+137 others(25): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr9 | 131193629 | ||||||
| chr9:131193629 | C | CTTTTTTT others(15): Show |
3 | a0002c0002t0001g0139 a0002c0003t0001g0069 a0002c0003t0001g0097 |
3 | HG03927.hp1 NA18949.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.3659+1349_3659+137 others(26): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr9 | 131193629 | ||||||
| chr9:131193629 | C | CTTTTTTT others(17): Show |
2 | a0001c0001t0001g0014 a0001c0001t0001g0073 |
2 | NA18944.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.3659+1347_3659+137 others(28): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr9 | 131193629 | ||||||
| chr9:131193629 | C | CTTTTTTT others(21): Show |
1 | a0001c0001t0001g0068 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.3659+1343_3659+137 others(32): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr9 | 131193629 | ||||||
| chr9:131193629 | C | T | 1 | a0001c0001t0001g0025 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.3659+1337C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | chr9 | 131193629 | |||||||
| chr9:131193629 | CTTTT | C | 5 | a0001c0005t0002g0213 a0001c0010t0003g0229 a0002c0002t0001g0113 others(2): Show |
5 | HG00733.hp1 HG01496.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.3659+1367_3659+137 others(8): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr9 | 131193629 | ||||||
| chr9:131193629 | CTTTTT | C | 10 | a0001c0004t0001g0137 a0001c0005t0002g0212 a0001c0005t0003g0211 others(7): Show |
10 | HG01109.hp1 HG01243.hp1 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.3659+1366_3659+137 others(9): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr9 | 131193629 | ||||||
| chr9:131193629 | CTTTTTT | C | 8 | a0001c0004t0001g0227 a0001c0005t0002g0205 a0001c0005t0002g0206 others(5): Show |
8 | HG01175.hp1 HG02027.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.3659+1365_3659+137 others(10): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr9 | 131193629 | ||||||
| chr9:131193629 | CTTTTTTT | C | 34 | a0001c0001t0001g0098 a0001c0004t0001g0162 a0001c0004t0001g0196 others(31): Show |
34 | HG00597.hp1 HG01361.hp2 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.3659+1364_3659+137 others(11): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr9 | 131193629 | ||||||
| chr9:131193629 | CTTTTTTT others(5): Show |
C | 1 | a0002c0020t0012g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3659+1359_3659+137 others(16): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr9 | 131193629 | ||||||
| chr9:131193636 | T | C | 1 | a0008c0028t0004g0207 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3659+1344T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | chr9 | 131193636 | |||||||
| chr9:131193675 | A | G | 1 | a0001c0001t0001g0065 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3659+1383A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | chr9 | 131193675 | |||||||
| chr9:131193687 | C | T | 1 | a0002c0018t0002g0107 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.3659+1395C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | chr9 | 131193687 | |||||||
| chr9:131193867 | T | TCTTGAAC others(7): Show |
11 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0212 others(8): Show |
11 | HG01109.hp1 HG01496.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.3660-1363_3660-135 others(18): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr9 | 131193867 | ||||||
| chr9:131193910 | C | A | 1 | a0002c0020t0012g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3660-1323C>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | chr9 | 131193910 | |||||||
| chr9:131193932 | C | T | 4 | a0001c0007t0001g0064 a0001c0007t0001g0086 a0001c0007t0001g0088 others(1): Show |
4 | HG02145.hp2 HG02897.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.3660-1301C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | chr9 | 131193932 | |||||||
| chr9:131193985 | G | A | 1 | a0011c0030t0001g0091 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3660-1248G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | chr9 | 131193985 | |||||||
| chr9:131194205 | C | A | 1 | a0002c0018t0002g0107 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.3660-1028C>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | chr9 | 131194205 | |||||||
| chr9:131194205 | C | CA | 204 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(201): Show |
204 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.3660-1015dupA | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr9 | 131194205 | ||||||
| chr9:131194205 | C | CAA | 6 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0212 others(3): Show |
6 | HG01891.hp2 HG01981.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.3660-1016_3660-101 others(6): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr9 | 131194205 | ||||||
| chr9:131194258 | C | T | 11 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0212 others(8): Show |
11 | HG01109.hp1 HG01496.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.3660-975C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | chr9 | 131194258 | |||||||
| chr9:131194654 | A | C | 1 | a0001c0001t0001g0095 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.3660-579A>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | chr9 | 131194654 | |||||||
| chr9:131194691 | G | A | 1 | a0002c0002t0001g0184 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.3660-542G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | chr9 | 131194691 | |||||||
| chr9:131194884 | C | T | 3 | a0002c0002t0001g0180 a0002c0002t0001g0192 a0002c0002t0001g0194 |
3 | HG01928.hp2 HG01993.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.3660-349C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 27/35 | chr9 | 131194884 | |||||||
| chr9:131195436 | T | C | 1 | a0002c0018t0002g0107 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.3721+142T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | chr9 | 131195436 | |||||||
| chr9:131195494 | G | T | 1 | a0004c0009t0001g0039 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.3721+200G>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | chr9 | 131195494 | |||||||
| chr9:131195598 | T | A | 3 | a0001c0004t0001g0162 a0002c0002t0001g0130 a0002c0002t0001g0134 |
3 | HG02735.hp2 HG03490.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.3721+304T>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | chr9 | 131195598 | |||||||
| chr9:131195640 | G | A | 1 | a0002c0002t0001g0190 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.3721+346G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | chr9 | 131195640 | |||||||
| chr9:131195669 | C | T | 1 | a0001c0005t0002g0212 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3721+375C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | chr9 | 131195669 | |||||||
| chr9:131195711 | C | T | 1 | a0001c0005t0003g0211 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3721+417C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | chr9 | 131195711 | |||||||
| chr9:131195751 | C | T | 2 | a0001c0010t0003g0228 a0001c0010t0003g0229 |
2 | HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.3721+457C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | chr9 | 131195751 | |||||||
| chr9:131195757 | G | A | 5 | a0001c0001t0001g0015 a0001c0001t0001g0059 a0001c0001t0001g0060 others(2): Show |
5 | HG01081.hp2 HG01433.hp1 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.3721+463G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | chr9 | 131195757 | |||||||
| chr9:131195775 | C | T | 3 | a0002c0002t0001g0220 a0002c0002t0001g0223 a0002c0002t0001g0224 |
3 | HG01943.hp2 HG02559.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.3721+481C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | chr9 | 131195775 | |||||||
| chr9:131195893 | C | T | 2 | a0001c0001t0001g0008 a0001c0001t0001g0114 |
2 | HG03688.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.3721+599C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | chr9 | 131195893 | |||||||
| chr9:131195959 | GGT | G | 6 | a0001c0004t0001g0227 a0002c0002t0001g0220 a0002c0002t0001g0221 others(3): Show |
6 | HG01361.hp2 HG01943.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.3721+666_3721+667d others(4): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | chr9 | 131195959 | |||||||
| chr9:131196023 | T | TCC | 6 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0213 others(3): Show |
6 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.3721+729_3721+730i others(4): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | chr9 | 131196023 | |||||||
| chr9:131196023 | T | TCCCCCCC others(3): Show |
1 | a0002c0020t0012g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3721+729_3721+730i others(12): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | chr9 | 131196023 | |||||||
| chr9:131196024 | G | C | 3 | a0001c0010t0003g0214 a0001c0010t0003g0228 a0002c0020t0012g0132 |
3 | HG01109.hp1 HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.3721+730G>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | chr9 | 131196024 | |||||||
| chr9:131196024 | G | GTCCC | 6 | a0001c0001t0001g0057 a0001c0001t0001g0080 a0001c0001t0001g0096 others(3): Show |
6 | HG00099.hp1 HG02698.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.3721+731_3721+734d others(6): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr9 | 131196024 | ||||||
| chr9:131196025 | T | C | 3 | a0001c0010t0003g0214 a0001c0010t0003g0228 a0002c0020t0012g0132 |
3 | HG01109.hp1 HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.3721+731T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | chr9 | 131196025 | |||||||
| chr9:131196025 | T | TCCCCCCC others(3): Show |
1 | a0005c0012t0001g0006 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3721+736_3721+745d others(12): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr9 | 131196025 | ||||||
| chr9:131196025 | T | TCCCCCCC others(5): Show |
1 | a0001c0005t0002g0212 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3721+734_3721+745d others(14): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr9 | 131196025 | ||||||
| chr9:131196025 | T | TCCCCCCC others(8): Show |
1 | a0005c0012t0001g0005 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.3721+745_3721+746i others(17): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr9 | 131196025 | ||||||
| chr9:131196025 | T | TCCCCCCC others(9): Show |
1 | a0005c0012t0001g0007 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.3721+745_3721+746i others(18): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr9 | 131196025 | ||||||
| chr9:131196025 | T | TCCCCCCC others(13): Show |
1 | a0012c0023t0005g0003 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3721+745_3721+746i others(22): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr9 | 131196025 | ||||||
| chr9:131196025 | T | TCCCCTCC others(12): Show |
1 | a0001c0001t0001g0095 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.3721+735_3721+736i others(21): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr9 | 131196025 | ||||||
| chr9:131196025 | T | TCCCTCCC others(3): Show |
5 | a0001c0001t0001g0052 a0001c0001t0001g0065 a0001c0001t0001g0230 others(2): Show |
5 | HG01168.hp1 HG01516.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.3721+734_3721+735i others(12): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr9 | 131196025 | ||||||
| chr9:131196025 | T | TCCCTCCC others(4): Show |
6 | a0001c0001t0001g0027 a0001c0001t0001g0073 a0001c0001t0001g0189 others(3): Show |
6 | HG00642.hp2 HG02293.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.3721+734_3721+735i others(13): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr9 | 131196025 | ||||||
| chr9:131196025 | T | TCCCTCCC others(5): Show |
7 | a0001c0001t0001g0004 a0001c0001t0001g0050 a0001c0001t0001g0058 others(4): Show |
7 | HG02523.hp1 HG03017.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.3721+734_3721+735i others(14): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr9 | 131196025 | ||||||
| chr9:131196025 | T | TCCCTCCC others(6): Show |
7 | a0001c0001t0001g0051 a0001c0001t0001g0066 a0001c0001t0001g0082 others(4): Show |
7 | HG02135.hp1 HG02897.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.3721+734_3721+735i others(15): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr9 | 131196025 | ||||||
| chr9:131196025 | T | TCCCTCCC others(7): Show |
6 | a0001c0001t0001g0061 a0001c0001t0001g0176 a0001c0007t0001g0086 others(3): Show |
6 | HG01433.hp1 HG02109.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.3721+734_3721+735i others(16): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr9 | 131196025 | ||||||
| chr9:131196025 | T | TCCCTCCC others(8): Show |
6 | a0001c0001t0001g0008 a0001c0001t0001g0053 a0001c0001t0001g0059 others(3): Show |
6 | HG00642.hp1 HG01081.hp2 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.3721+734_3721+735i others(17): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr9 | 131196025 | ||||||
| chr9:131196025 | T | TCCCTCCC others(9): Show |
2 | a0001c0001t0001g0014 a0001c0001t0001g0114 |
2 | HG04199.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.3721+734_3721+735i others(18): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr9 | 131196025 | ||||||
| chr9:131196025 | T | TCCCTCCC others(12): Show |
2 | a0001c0001t0001g0087 a0006c0008t0001g0109 |
2 | HG01943.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.3721+734_3721+735i others(21): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr9 | 131196025 | ||||||
| chr9:131196025 | T | TCCCTCCC others(19): Show |
1 | a0001c0001t0001g0015 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.3721+734_3721+735i others(28): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr9 | 131196025 | ||||||
| chr9:131196025 | T | TCCCTCCC others(6): Show |
1 | a0001c0001t0001g0089 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3721+734_3721+735i others(15): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr9 | 131196025 | ||||||
| chr9:131196025 | T | TCCCTCTC others(3): Show |
2 | a0001c0001t0001g0038 a0014c0014t0001g0099 |
2 | HG03492.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.3721+734_3721+735i others(12): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr9 | 131196025 | ||||||
| chr9:131196025 | T | TCCCTCTC others(4): Show |
3 | a0001c0001t0001g0028 a0001c0026t0001g0055 a0004c0009t0001g0031 |
3 | HG03130.hp2 NA19055.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.3721+734_3721+735i others(13): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr9 | 131196025 | ||||||
| chr9:131196025 | T | TCCCTCTC others(5): Show |
5 | a0001c0001t0001g0020 a0001c0001t0001g0079 a0001c0001t0001g0110 others(2): Show |
5 | HG00408.hp1 HG00597.hp2 NA18945.hp2 others(2): Show |
intron_variant | MODIFIER | c.3721+734_3721+735i others(14): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr9 | 131196025 | ||||||
| chr9:131196025 | T | TCCCTCTC others(6): Show |
4 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0007g0042 others(1): Show |
4 | HG01928.hp1 NA18983.hp1 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.3721+734_3721+735i others(15): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr9 | 131196025 | ||||||
| chr9:131196025 | T | TCCCTCTC others(7): Show |
6 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0009g0072 others(3): Show |
6 | HG00609.hp1 HG03942.hp2 HG04184.hp1 others(3): Show |
intron_variant | MODIFIER | c.3721+734_3721+735i others(16): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr9 | 131196025 | ||||||
| chr9:131196025 | T | TCCCTCTC others(8): Show |
4 | a0001c0001t0001g0010 a0001c0001t0001g0092 a0001c0027t0001g0085 others(1): Show |
4 | HG00639.hp1 HG00741.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.3721+734_3721+735i others(17): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr9 | 131196025 | ||||||
| chr9:131196025 | T | TCCCTCTC others(9): Show |
1 | a0003c0013t0001g0070 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3721+734_3721+735i others(18): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr9 | 131196025 | ||||||
| chr9:131196025 | T | TCCCTCTC others(10): Show |
8 | a0001c0001t0001g0036 a0001c0001t0001g0047 a0001c0001t0001g0048 others(5): Show |
8 | HG00423.hp1 HG00544.hp2 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.3721+734_3721+735i others(19): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr9 | 131196025 | ||||||
| chr9:131196025 | T | TCCCTCTC others(11): Show |
2 | a0001c0001t0001g0033 a0001c0001t0001g0034 |
2 | HG02132.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.3721+734_3721+735i others(20): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr9 | 131196025 | ||||||
| chr9:131196025 | T | TCCCTCTC others(13): Show |
1 | a0001c0001t0001g0094 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.3721+734_3721+735i others(22): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr9 | 131196025 | ||||||
| chr9:131196025 | T | TCCCTCTC others(14): Show |
1 | a0001c0001t0001g0017 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.3721+734_3721+735i others(23): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr9 | 131196025 | ||||||
| chr9:131196025 | T | TCCCTCTC others(15): Show |
1 | a0001c0001t0001g0024 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.3721+734_3721+735i others(24): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr9 | 131196025 | ||||||
| chr9:131196025 | T | TCCCTCTC others(18): Show |
1 | a0002c0003t0001g0045 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3721+734_3721+735i others(27): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr9 | 131196025 | ||||||
| chr9:131196025 | T | TCCGTCCC | 17 | a0001c0004t0001g0138 a0001c0004t0001g0140 a0002c0002t0001g0067 others(14): Show |
17 | HG00609.hp2 HG00741.hp2 HG02056.hp1 others(14): Show |
intron_variant | MODIFIER | c.3721+733_3721+734i others(9): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr9 | 131196025 | ||||||
| chr9:131196025 | T | TCCGTCCC others(1): Show |
15 | a0001c0001t0001g0090 a0001c0004t0001g0209 a0002c0002t0001g0009 others(12): Show |
15 | HG00558.hp2 HG00639.hp2 HG00733.hp1 others(12): Show |
intron_variant | MODIFIER | c.3721+733_3721+734i others(10): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr9 | 131196025 | ||||||
| chr9:131196025 | T | TCCGTCCC others(2): Show |
18 | a0001c0004t0001g0131 a0001c0004t0001g0137 a0001c0004t0001g0198 others(15): Show |
18 | HG00099.hp2 HG01243.hp1 HG01361.hp1 others(15): Show |
intron_variant | MODIFIER | c.3721+733_3721+734i others(11): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr9 | 131196025 | ||||||
| chr9:131196025 | T | TCCGTCCC others(3): Show |
7 | a0001c0001t0001g0022 a0001c0004t0001g0227 a0002c0002t0001g0142 others(4): Show |
7 | HG01433.hp2 HG01928.hp2 HG01993.hp1 others(4): Show |
intron_variant | MODIFIER | c.3721+733_3721+734i others(12): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr9 | 131196025 | ||||||
| chr9:131196025 | T | TCCGTCCC others(4): Show |
7 | a0002c0002t0001g0130 a0002c0002t0001g0143 a0002c0002t0001g0163 others(4): Show |
7 | HG01175.hp1 HG01361.hp2 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.3721+733_3721+734i others(13): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr9 | 131196025 | ||||||
| chr9:131196025 | T | TCCGTCCC others(5): Show |
5 | a0001c0006t0001g0179 a0002c0002t0001g0134 a0002c0002t0001g0192 others(2): Show |
5 | HG01884.hp2 HG02135.hp2 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.3721+733_3721+734i others(14): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr9 | 131196025 | ||||||
| chr9:131196025 | T | TCCGTCCC others(6): Show |
8 | a0001c0004t0001g0162 a0001c0006t0001g0168 a0001c0006t0001g0169 others(5): Show |
8 | HG00408.hp2 HG00544.hp1 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.3721+733_3721+734i others(15): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr9 | 131196025 | ||||||
| chr9:131196025 | T | TCCGTCCC others(7): Show |
3 | a0001c0004t0001g0197 a0002c0002t0001g0193 a0002c0002t0001g0224 |
3 | HG00423.hp2 HG01943.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.3721+733_3721+734i others(16): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr9 | 131196025 | ||||||
| chr9:131196025 | T | TCCGTCCC others(8): Show |
1 | a0001c0004t0001g0196 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.3721+733_3721+734i others(17): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr9 | 131196025 | ||||||
| chr9:131196025 | T | TCCGTCCC others(9): Show |
1 | a0002c0002t0001g0152 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.3721+733_3721+734i others(18): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr9 | 131196025 | ||||||
| chr9:131196025 | T | TCCGTCCC others(10): Show |
2 | a0002c0002t0001g0185 a0002c0002t0001g0187 |
2 | HG02523.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.3721+733_3721+734i others(19): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr9 | 131196025 | ||||||
| chr9:131196025 | T | TCCGTCCC others(13): Show |
2 | a0002c0002t0001g0150 a0002c0002t0008g0148 |
2 | HG00597.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.3721+733_3721+734i others(22): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr9 | 131196025 | ||||||
| chr9:131196025 | T | TCGTCCCC others(3): Show |
1 | a0002c0002t0001g0221 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3721+732_3721+733i others(12): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr9 | 131196025 | ||||||
| chr9:131196028 | C | T | 1 | a0002c0002t0001g0154 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.3721+734C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | chr9 | 131196028 | |||||||
| chr9:131196029 | C | T | 2 | a0001c0001t0006g0075 a0001c0001t0010g0234 |
2 | HG00438.hp1 HG00438.hp2 |
intron_variant | MODIFIER | c.3721+735C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | chr9 | 131196029 | |||||||
| chr9:131196032 | C | G | 1 | a0002c0018t0002g0107 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.3721+738C>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | chr9 | 131196032 | |||||||
| chr9:131196039 | C | CCCGCCCC others(3): Show |
2 | a0001c0010t0003g0214 a0001c0010t0003g0228 |
2 | HG01109.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.3721+745_3721+746i others(12): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | chr9 | 131196039 | |||||||
| chr9:131196039 | C | G | 1 | a0001c0010t0003g0229 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3721+745C>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | chr9 | 131196039 | |||||||
| chr9:131196040 | G | C | 214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(211): Show |
214 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(211): Show |
intron_variant | MODIFIER | c.3721+746G>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | chr9 | 131196040 | |||||||
| chr9:131196042 | G | C | 1 | a0001c0001t0001g0024 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.3721+748G>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | chr9 | 131196042 | |||||||
| chr9:131196139 | G | A | 1 | a0001c0001t0001g0029 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.3721+845G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | chr9 | 131196139 | |||||||
| chr9:131196377 | G | C | 7 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0212 others(4): Show |
7 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.3722-839G>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | chr9 | 131196377 | |||||||
| chr9:131196396 | C | T | 50 | a0001c0004t0001g0131 a0001c0004t0001g0137 a0001c0004t0001g0138 others(47): Show |
50 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(47): Show |
intron_variant | MODIFIER | c.3722-820C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | chr9 | 131196396 | |||||||
| chr9:131196450 | C | T | 1 | a0001c0001t0001g0001 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3722-766C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | chr9 | 131196450 | |||||||
| chr9:131196506 | A | G | 1 | a0001c0001t0001g0002 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.3722-710A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | chr9 | 131196506 | |||||||
| chr9:131196836 | A | G | 1 | a0002c0020t0012g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3722-380A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | chr9 | 131196836 | |||||||
| chr9:131196856 | T | A | 1 | a0001c0001t0001g0027 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.3722-360T>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 28/35 | chr9 | 131196856 | |||||||
| chr9:131199126 | A | G | 1 | a0001c0001t0001g0020 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.5521+111A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 29/35 | chr9 | 131199126 | |||||||
| chr9:131199369 | TTA | T | 2 | a0005c0012t0001g0006 a0005c0012t0001g0007 |
2 | HG01106.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.5521+357_5521+358d others(4): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 29/35 | INFO_REALIGN_3_PRIME | chr9 | 131199369 | ||||||
| chr9:131199522 | C | T | 7 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0212 others(4): Show |
7 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.5521+507C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 29/35 | chr9 | 131199522 | |||||||
| chr9:131199782 | G | T | 2 | a0002c0002t0001g0077 a0002c0002t0001g0078 |
2 | HG00642.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.5521+767G>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 29/35 | chr9 | 131199782 | |||||||
| chr9:131199912 | A | C | 2 | a0001c0005t0002g0205 a0001c0005t0002g0206 |
2 | HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.5521+897A>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 29/35 | chr9 | 131199912 | |||||||
| chr9:131199922 | G | A | 2 | a0001c0005t0002g0213 a0008c0028t0004g0207 |
2 | HG01496.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.5521+907G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 29/35 | chr9 | 131199922 | |||||||
| chr9:131199933 | GAC | G | 7 | a0001c0001t0001g0014 a0001c0001t0001g0068 a0001c0001t0001g0082 others(4): Show |
7 | HG00642.hp1 HG02135.hp1 HG04228.hp1 others(4): Show |
intron_variant | MODIFIER | c.5521+920_5521+921d others(4): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 29/35 | INFO_REALIGN_3_PRIME | chr9 | 131199933 | ||||||
| chr9:131199985 | T | C | 11 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0212 others(8): Show |
11 | HG01109.hp1 HG01496.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.5521+970T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 29/35 | chr9 | 131199985 | |||||||
| chr9:131200090 | C | T | 1 | a0001c0005t0002g0212 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.5521+1075C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 29/35 | chr9 | 131200090 | |||||||
| chr9:131200254 | T | C | 1 | a0002c0002t0001g0210 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.5521+1239T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 29/35 | chr9 | 131200254 | |||||||
| chr9:131200314 | G | A | 7 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0212 others(4): Show |
7 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.5521+1299G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 29/35 | chr9 | 131200314 | |||||||
| chr9:131200686 | G | A | 1 | a0012c0023t0005g0003 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.5522-961G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 29/35 | chr9 | 131200686 | |||||||
| chr9:131200694 | G | A | 1 | a0001c0001t0001g0216 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.5522-953G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 29/35 | chr9 | 131200694 | |||||||
| chr9:131201068 | C | A | 1 | a0002c0002t0001g0181 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.5522-579C>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 29/35 | chr9 | 131201068 | |||||||
| chr9:131201360 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.5522-287C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 29/35 | chr9 | 131201360 | |||||||
| chr9:131201362 | C | T | 1 | a0008c0028t0004g0207 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.5522-285C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 29/35 | chr9 | 131201362 | |||||||
| chr9:131201523 | C | T | 1 | a0002c0002t0001g0158 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.5522-124C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 29/35 | chr9 | 131201523 | |||||||
| chr9:131201563 | C | CA | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(126): Show |
129 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.5522-72dupA | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 29/35 | INFO_REALIGN_3_PRIME | chr9 | 131201563 | ||||||
| chr9:131201576 | C | A | 2 | a0002c0003t0001g0071 a0002c0003t0001g0074 |
2 | HG02723.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.5522-71C>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 29/35 | chr9 | 131201576 | |||||||
| chr9:131201617 | T | C | 1 | a0001c0005t0002g0213 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.5522-30T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 29/35 | chr9 | 131201617 | |||||||
| chr9:131201889 | T | C | 11 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0212 others(8): Show |
11 | HG01109.hp1 HG01496.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.5592+172T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131201889 | |||||||
| chr9:131201992 | C | G | 1 | a0008c0028t0004g0207 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.5592+275C>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131201992 | |||||||
| chr9:131202116 | A | G | 3 | a0001c0010t0003g0214 a0001c0010t0003g0228 a0001c0010t0003g0229 |
3 | HG01109.hp1 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.5592+399A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131202116 | |||||||
| chr9:131202173 | G | A | 1 | a0002c0003t0001g0124 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.5592+456G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131202173 | |||||||
| chr9:131202219 | C | T | 4 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0003g0211 others(1): Show |
4 | HG01891.hp2 HG02451.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.5592+502C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131202219 | |||||||
| chr9:131202377 | A | G | 1 | a0001c0001t0001g0053 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.5592+660A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131202377 | |||||||
| chr9:131202386 | T | TACAC | 2 | a0001c0001t0001g0004 a0002c0020t0012g0132 |
2 | HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.5592+683_5592+686d others(6): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | INFO_REALIGN_3_PRIME | chr9 | 131202386 | ||||||
| chr9:131202404 | T | C | 1 | a0002c0020t0012g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.5592+687T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131202404 | |||||||
| chr9:131202459 | T | G | 1 | a0001c0005t0002g0212 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.5592+742T>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131202459 | |||||||
| chr9:131202577 | C | T | 1 | a0001c0005t0002g0206 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.5592+860C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131202577 | |||||||
| chr9:131202580 | C | G | 1 | a0002c0002t0001g0021 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.5592+863C>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131202580 | |||||||
| chr9:131202905 | T | A | 1 | a0001c0001t0001g0014 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.5592+1188T>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131202905 | |||||||
| chr9:131203092 | C | T | 1 | a0001c0005t0002g0213 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.5592+1375C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131203092 | |||||||
| chr9:131203167 | G | C | 1 | a0001c0001t0001g0232 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.5592+1450G>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131203167 | |||||||
| chr9:131203237 | A | G | 11 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0212 others(8): Show |
11 | HG01109.hp1 HG01496.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.5592+1520A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131203237 | |||||||
| chr9:131203383 | G | A | 11 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0212 others(8): Show |
11 | HG01109.hp1 HG01496.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.5592+1666G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131203383 | |||||||
| chr9:131203388 | C | T | 1 | a0001c0004t0001g0198 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.5592+1671C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131203388 | |||||||
| chr9:131203456 | A | T | 14 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(11): Show |
14 | HG00099.hp1 HG00733.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.5592+1739A>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131203456 | |||||||
| chr9:131203579 | C | T | 1 | a0001c0001t0001g0216 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.5592+1862C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131203579 | |||||||
| chr9:131203849 | T | C | 3 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0217 |
3 | HG02109.hp1 HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.5592+2132T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131203849 | |||||||
| chr9:131203993 | A | G | 1 | a0001c0005t0002g0213 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.5592+2276A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131203993 | |||||||
| chr9:131204030 | C | T | 1 | a0002c0020t0012g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.5592+2313C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131204030 | |||||||
| chr9:131204039 | C | CG | 4 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0003g0211 others(1): Show |
4 | HG01891.hp2 HG02451.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.5592+2323dupG | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | INFO_REALIGN_3_PRIME | chr9 | 131204039 | ||||||
| chr9:131204188 | C | T | 1 | a0002c0020t0012g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.5592+2471C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131204188 | |||||||
| chr9:131204500 | C | T | 1 | a0001c0001t0001g0103 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.5592+2783C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131204500 | |||||||
| chr9:131204731 | AAGAG | A | 2 | a0001c0001t0001g0079 a0001c0006t0001g0169 |
2 | HG00408.hp1 HG00408.hp2 |
intron_variant | MODIFIER | c.5592+3018_5592+302 others(8): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | INFO_REALIGN_3_PRIME | chr9 | 131204731 | ||||||
| chr9:131204763 | C | A | 1 | a0002c0003t0001g0063 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.5592+3046C>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131204763 | |||||||
| chr9:131204808 | G | A | 2 | a0001c0010t0003g0228 a0001c0010t0003g0229 |
2 | HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.5592+3091G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131204808 | |||||||
| chr9:131204933 | T | A | 3 | a0001c0004t0001g0219 a0002c0002t0001g0225 a0002c0002t0001g0226 |
3 | HG01884.hp2 HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.5592+3216T>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131204933 | |||||||
| chr9:131205641 | T | A | 1 | a0002c0003t0001g0124 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.5592+3924T>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131205641 | |||||||
| chr9:131205717 | C | T | 1 | a0002c0020t0012g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.5592+4000C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131205717 | |||||||
| chr9:131206015 | A | G | 3 | a0001c0001t0001g0008 a0001c0001t0001g0114 a0002c0002t0001g0104 |
3 | HG03688.hp2 HG03942.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.5592+4298A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131206015 | |||||||
| chr9:131206148 | C | CTTTTTTC others(13): Show |
1 | a0001c0007t0001g0086 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.5592+4437_5592+443 others(24): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | INFO_REALIGN_3_PRIME | chr9 | 131206148 | ||||||
| chr9:131206148 | C | CTTTTTTT others(5): Show |
1 | a0002c0002t0001g0175 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.5592+4434_5592+444 others(16): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | INFO_REALIGN_3_PRIME | chr9 | 131206148 | ||||||
| chr9:131206148 | C | CTTTTTTT others(6): Show |
2 | a0001c0001t0001g0053 a0001c0005t0002g0206 |
2 | HG02451.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.5592+4433_5592+444 others(17): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | INFO_REALIGN_3_PRIME | chr9 | 131206148 | ||||||
| chr9:131206148 | C | CTTTTTTT others(7): Show |
6 | a0001c0005t0002g0205 a0001c0005t0002g0213 a0001c0005t0003g0211 others(3): Show |
6 | HG01496.hp2 HG01891.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.5592+4432_5592+444 others(18): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | INFO_REALIGN_3_PRIME | chr9 | 131206148 | ||||||
| chr9:131206148 | C | CTTTTTTT others(8): Show |
4 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0217 others(1): Show |
4 | HG02109.hp1 HG02818.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.5592+4445_5592+444 others(19): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | INFO_REALIGN_3_PRIME | chr9 | 131206148 | ||||||
| chr9:131206148 | C | CTTTTTTT others(9): Show |
3 | a0001c0001t0001g0048 a0001c0010t0003g0214 a0016c0022t0001g0112 |
3 | HG01109.hp1 HG02922.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.5592+4445_5592+444 others(20): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | INFO_REALIGN_3_PRIME | chr9 | 131206148 | ||||||
| chr9:131206148 | C | CTTTTTTT others(10): Show |
18 | a0001c0001t0001g0011 a0001c0001t0001g0058 a0001c0001t0001g0065 others(15): Show |
18 | HG00642.hp1 HG00642.hp2 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.5592+4445_5592+444 others(21): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | INFO_REALIGN_3_PRIME | chr9 | 131206148 | ||||||
| chr9:131206148 | C | CTTTTTTT others(11): Show |
66 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(63): Show |
66 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.5592+4445_5592+444 others(22): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | INFO_REALIGN_3_PRIME | chr9 | 131206148 | ||||||
| chr9:131206148 | C | CTTTTTTT others(12): Show |
48 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0022 others(45): Show |
48 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.5592+4445_5592+444 others(23): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | INFO_REALIGN_3_PRIME | chr9 | 131206148 | ||||||
| chr9:131206148 | C | CTTTTTTT others(13): Show |
23 | a0001c0001t0001g0014 a0001c0001t0001g0018 a0001c0001t0001g0038 others(20): Show |
23 | HG00423.hp2 HG00741.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.5592+4445_5592+444 others(24): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | INFO_REALIGN_3_PRIME | chr9 | 131206148 | ||||||
| chr9:131206148 | C | CTTTTTTT others(14): Show |
11 | a0001c0001t0001g0079 a0001c0001t0001g0170 a0001c0001t0001g0189 others(8): Show |
11 | HG00408.hp1 HG00408.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.5592+4445_5592+444 others(25): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | INFO_REALIGN_3_PRIME | chr9 | 131206148 | ||||||
| chr9:131206148 | C | CTTTTTTT others(15): Show |
2 | a0001c0004t0001g0219 a0002c0002t0001g0163 |
2 | HG02055.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.5592+4445_5592+444 others(26): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | INFO_REALIGN_3_PRIME | chr9 | 131206148 | ||||||
| chr9:131206148 | CTT | C | 24 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(21): Show |
24 | HG00099.hp1 HG01074.hp1 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.5592+4444_5592+444 others(6): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | INFO_REALIGN_3_PRIME | chr9 | 131206148 | ||||||
| chr9:131206168 | A | G | 7 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0212 others(4): Show |
7 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.5592+4451A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131206168 | |||||||
| chr9:131206289 | G | A | 1 | a0001c0001t0001g0068 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.5592+4572G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131206289 | |||||||
| chr9:131206643 | G | A | 1 | a0001c0005t0002g0213 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.5592+4926G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131206643 | |||||||
| chr9:131206647 | T | G | 1 | a0001c0001t0001g0081 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.5592+4930T>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131206647 | |||||||
| chr9:131206793 | A | G | 7 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0212 others(4): Show |
7 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.5592+5076A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131206793 | |||||||
| chr9:131207104 | G | A | 1 | a0001c0001t0001g0059 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.5592+5387G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131207104 | |||||||
| chr9:131207166 | T | C | 1 | a0002c0002t0001g0163 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.5592+5449T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131207166 | |||||||
| chr9:131207171 | G | A | 11 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0212 others(8): Show |
11 | HG01109.hp1 HG01496.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.5592+5454G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131207171 | |||||||
| chr9:131207403 | G | T | 2 | a0002c0002t0001g0177 a0002c0002t0001g0184 |
2 | HG01175.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.5592+5686G>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131207403 | |||||||
| chr9:131207853 | A | G | 7 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0212 others(4): Show |
7 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.5592+6136A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131207853 | |||||||
| chr9:131207919 | G | T | 2 | a0002c0002t0001g0157 a0002c0002t0001g0167 |
2 | NA18968.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.5592+6202G>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131207919 | |||||||
| chr9:131208049 | A | G | 1 | a0002c0020t0012g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.5592+6332A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131208049 | |||||||
| chr9:131208480 | G | A | 7 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0212 others(4): Show |
7 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.5593-6732G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131208480 | |||||||
| chr9:131208590 | G | A | 1 | a0002c0020t0012g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.5593-6622G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131208590 | |||||||
| chr9:131208671 | T | G | 1 | a0002c0018t0002g0107 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.5593-6541T>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131208671 | |||||||
| chr9:131208885 | C | T | 1 | a0001c0005t0002g0213 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.5593-6327C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131208885 | |||||||
| chr9:131209268 | C | T | 1 | a0001c0005t0002g0212 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.5593-5944C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131209268 | |||||||
| chr9:131209413 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.5593-5799C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131209413 | |||||||
| chr9:131209435 | T | C | 11 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0212 others(8): Show |
11 | HG01109.hp1 HG01496.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.5593-5777T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131209435 | |||||||
| chr9:131209639 | C | T | 1 | a0002c0002t0001g0175 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.5593-5573C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131209639 | |||||||
| chr9:131209724 | T | C | 1 | a0001c0001t0001g0054 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.5593-5488T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131209724 | |||||||
| chr9:131209791 | C | T | 1 | a0010c0017t0001g0108 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.5593-5421C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131209791 | |||||||
| chr9:131209890 | C | G | 7 | a0001c0001t0001g0050 a0001c0001t0001g0052 a0001c0001t0001g0095 others(4): Show |
7 | HG01168.hp1 HG01169.hp2 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.5593-5322C>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131209890 | |||||||
| chr9:131210181 | A | G | 1 | a0006c0008t0001g0109 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.5593-5031A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131210181 | |||||||
| chr9:131210296 | T | C | 3 | a0001c0010t0003g0214 a0001c0010t0003g0228 a0001c0010t0003g0229 |
3 | HG01109.hp1 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.5593-4916T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131210296 | |||||||
| chr9:131210394 | C | T | 1 | a0001c0001t0001g0002 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.5593-4818C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131210394 | |||||||
| chr9:131210497 | C | T | 1 | a0001c0004t0001g0227 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.5593-4715C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131210497 | |||||||
| chr9:131210626 | C | CA | 9 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0024 others(6): Show |
9 | HG01109.hp1 HG02630.hp2 HG03486.hp1 others(6): Show |
intron_variant | MODIFIER | c.5593-4575dupA | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | INFO_REALIGN_3_PRIME | chr9 | 131210626 | ||||||
| chr9:131210638 | C | A | 11 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0212 others(8): Show |
11 | HG01109.hp1 HG01496.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.5593-4574C>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131210638 | |||||||
| chr9:131210802 | G | C | 3 | a0005c0012t0001g0005 a0005c0012t0001g0006 a0005c0012t0001g0007 |
3 | HG01106.hp2 HG02723.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.5593-4410G>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131210802 | |||||||
| chr9:131211009 | C | T | 1 | a0002c0020t0012g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.5593-4203C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131211009 | |||||||
| chr9:131211577 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.5593-3635G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131211577 | |||||||
| chr9:131211773 | C | T | 11 | a0001c0001t0001g0110 a0001c0010t0003g0214 a0001c0010t0003g0228 others(8): Show |
11 | HG00597.hp1 HG01109.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.5593-3439C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131211773 | |||||||
| chr9:131211821 | G | A | 1 | a0002c0018t0002g0107 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.5593-3391G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131211821 | |||||||
| chr9:131211885 | A | G | 1 | a0001c0001t0001g0065 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.5593-3327A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131211885 | |||||||
| chr9:131211923 | A | G | 3 | a0005c0012t0001g0005 a0005c0012t0001g0006 a0005c0012t0001g0007 |
3 | HG01106.hp2 HG02723.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.5593-3289A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131211923 | |||||||
| chr9:131212040 | C | T | 1 | a0002c0020t0012g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.5593-3172C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131212040 | |||||||
| chr9:131212195 | TAGTC | T | 2 | a0001c0005t0002g0205 a0001c0005t0002g0206 |
2 | HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.5593-3014_5593-301 others(8): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | INFO_REALIGN_3_PRIME | chr9 | 131212195 | ||||||
| chr9:131212286 | G | T | 1 | a0008c0028t0004g0207 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.5593-2926G>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131212286 | |||||||
| chr9:131212454 | G | A | 1 | a0001c0005t0002g0213 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.5593-2758G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131212454 | |||||||
| chr9:131212964 | TTTTTGTA others(19): Show |
T | 4 | a0001c0010t0003g0214 a0001c0010t0003g0228 a0001c0010t0003g0229 others(1): Show |
4 | HG01109.hp1 HG02818.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.5593-2217_5593-219 others(30): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | INFO_REALIGN_3_PRIME | chr9 | 131212964 | ||||||
| chr9:131213178 | C | CT | 5 | a0001c0001t0001g0051 a0001c0005t0002g0205 a0001c0005t0002g0206 others(2): Show |
5 | HG01109.hp1 HG02451.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.5593-2018dupT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | INFO_REALIGN_3_PRIME | chr9 | 131213178 | ||||||
| chr9:131213220 | G | T | 7 | a0001c0001t0001g0050 a0001c0001t0001g0052 a0001c0001t0001g0095 others(4): Show |
7 | HG01168.hp1 HG01169.hp2 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.5593-1992G>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131213220 | |||||||
| chr9:131213270 | G | A | 1 | a0002c0002t0001g0139 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.5593-1942G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131213270 | |||||||
| chr9:131213632 | G | A | 1 | a0001c0005t0002g0213 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.5593-1580G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131213632 | |||||||
| chr9:131213751 | C | CTGT | 80 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0019 others(77): Show |
80 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.5593-1426_5593-142 others(7): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | INFO_REALIGN_3_PRIME | chr9 | 131213751 | ||||||
| chr9:131213751 | C | CTGTTGT | 67 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0018 others(64): Show |
67 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.5593-1429_5593-142 others(10): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | INFO_REALIGN_3_PRIME | chr9 | 131213751 | ||||||
| chr9:131213751 | C | CTGTTGTT others(2): Show |
48 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(45): Show |
48 | HG00438.hp1 HG00642.hp2 HG00733.hp1 others(45): Show |
intron_variant | MODIFIER | c.5593-1432_5593-142 others(13): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | INFO_REALIGN_3_PRIME | chr9 | 131213751 | ||||||
| chr9:131213751 | C | CTGTTGTT others(5): Show |
5 | a0001c0001t0001g0053 a0001c0001t0001g0058 a0001c0001t0001g0102 others(2): Show |
5 | HG03017.hp1 HG03491.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.5593-1435_5593-142 others(16): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | INFO_REALIGN_3_PRIME | chr9 | 131213751 | ||||||
| chr9:131213751 | CTGT | C | 4 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0217 others(1): Show |
4 | HG02109.hp1 HG02976.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.5593-1426_5593-142 others(7): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | INFO_REALIGN_3_PRIME | chr9 | 131213751 | ||||||
| chr9:131213751 | CTGTTGTT others(5): Show |
C | 1 | a0001c0005t0002g0212 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.5593-1435_5593-142 others(16): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | INFO_REALIGN_3_PRIME | chr9 | 131213751 | ||||||
| chr9:131213805 | G | GA | 209 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(206): Show |
209 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.5593-1399dupA | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | INFO_REALIGN_3_PRIME | chr9 | 131213805 | ||||||
| chr9:131213805 | G | GAA | 10 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0212 others(7): Show |
10 | HG01109.hp1 HG01496.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.5593-1400_5593-139 others(6): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | INFO_REALIGN_3_PRIME | chr9 | 131213805 | ||||||
| chr9:131213841 | A | G | 11 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0212 others(8): Show |
11 | HG01109.hp1 HG01496.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.5593-1371A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131213841 | |||||||
| chr9:131213870 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.5593-1342T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131213870 | |||||||
| chr9:131213910 | G | A | 1 | a0002c0003t0001g0063 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.5593-1302G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131213910 | |||||||
| chr9:131213988 | G | A | 1 | a0002c0002t0001g0208 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.5593-1224G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131213988 | |||||||
| chr9:131214063 | C | G | 1 | a0012c0023t0005g0003 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.5593-1149C>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131214063 | |||||||
| chr9:131214368 | G | A | 11 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0212 others(8): Show |
11 | HG01109.hp1 HG01496.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.5593-844G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131214368 | |||||||
| chr9:131214403 | T | C | 1 | a0003c0011t0001g0191 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.5593-809T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131214403 | |||||||
| chr9:131214466 | C | T | 11 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0212 others(8): Show |
11 | HG01109.hp1 HG01496.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.5593-746C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131214466 | |||||||
| chr9:131214540 | A | G | 2 | a0001c0001t0001g0052 a0001c0001t0001g0095 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.5593-672A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131214540 | |||||||
| chr9:131214695 | A | T | 1 | a0003c0013t0001g0041 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.5593-517A>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131214695 | |||||||
| chr9:131215059 | A | G | 10 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0212 others(7): Show |
10 | HG01109.hp1 HG01496.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.5593-153A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131215059 | |||||||
| chr9:131215063 | T | G | 7 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0212 others(4): Show |
7 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.5593-149T>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131215063 | |||||||
| chr9:131215068 | T | G | 1 | a0001c0001t0001g0050 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.5593-144T>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131215068 | |||||||
| chr9:131215101 | C | A | 1 | a0001c0001t0001g0089 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.5593-111C>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 30/35 | chr9 | 131215101 | |||||||
| chr9:131215386 | T | C | 1 | a0002c0002t0001g0147 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.5749+18T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131215386 | |||||||
| chr9:131215537 | T | C | 3 | a0005c0012t0001g0005 a0005c0012t0001g0006 a0005c0012t0001g0007 |
3 | HG01106.hp2 HG02723.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.5749+169T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131215537 | |||||||
| chr9:131215583 | GC | G | 106 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(103): Show |
106 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.5749+216delC | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131215583 | |||||||
| chr9:131215616 | C | T | 3 | a0002c0002t0001g0180 a0002c0002t0001g0192 a0002c0002t0001g0194 |
3 | HG01928.hp2 HG01993.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.5749+248C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131215616 | |||||||
| chr9:131215705 | G | A | 1 | a0001c0005t0002g0212 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.5749+337G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131215705 | |||||||
| chr9:131215744 | C | A | 1 | a0008c0028t0004g0207 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.5749+376C>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131215744 | |||||||
| chr9:131215897 | A | AT | 25 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(22): Show |
25 | HG00099.hp1 HG01106.hp2 HG01175.hp2 others(22): Show |
intron_variant | MODIFIER | c.5749+551dupT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | INFO_REALIGN_3_PRIME | chr9 | 131215897 | ||||||
| chr9:131215897 | AT | A | 15 | a0001c0001t0001g0004 a0001c0001t0001g0095 a0001c0001t0001g0102 others(12): Show |
15 | HG00558.hp2 HG00609.hp1 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.5749+551delT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | INFO_REALIGN_3_PRIME | chr9 | 131215897 | ||||||
| chr9:131215924 | CAG | C | 7 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0212 others(4): Show |
7 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.5749+559_5749+560d others(4): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | INFO_REALIGN_3_PRIME | chr9 | 131215924 | ||||||
| chr9:131216180 | A | G | 3 | a0001c0010t0003g0214 a0001c0010t0003g0228 a0001c0010t0003g0229 |
3 | HG01109.hp1 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.5749+812A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131216180 | |||||||
| chr9:131216213 | CT | C | 15 | a0001c0001t0001g0014 a0001c0005t0002g0205 a0001c0005t0002g0206 others(12): Show |
15 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.5749+861delT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | INFO_REALIGN_3_PRIME | chr9 | 131216213 | ||||||
| chr9:131216286 | G | A | 7 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0212 others(4): Show |
7 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.5749+918G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131216286 | |||||||
| chr9:131216312 | C | T | 3 | a0001c0001t0001g0052 a0001c0001t0001g0095 a0002c0002t0001g0161 |
3 | HG01168.hp1 HG01169.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.5749+944C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131216312 | |||||||
| chr9:131216385 | C | T | 1 | a0001c0005t0003g0211 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.5749+1017C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131216385 | |||||||
| chr9:131216525 | C | CT | 123 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(120): Show |
123 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.5749+1172dupT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | INFO_REALIGN_3_PRIME | chr9 | 131216525 | ||||||
| chr9:131216525 | C | CTT | 15 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0049 others(12): Show |
15 | HG00438.hp1 HG01109.hp2 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.5749+1171_5749+117 others(6): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | INFO_REALIGN_3_PRIME | chr9 | 131216525 | ||||||
| chr9:131216557 | G | A | 1 | a0012c0023t0005g0003 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.5749+1189G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131216557 | |||||||
| chr9:131216601 | C | T | 1 | a0013c0021t0001g0173 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.5749+1233C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131216601 | |||||||
| chr9:131216797 | G | T | 1 | a0002c0002t0001g0143 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.5749+1429G>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131216797 | |||||||
| chr9:131216824 | G | A | 1 | a0001c0001t0006g0075 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.5749+1456G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131216824 | |||||||
| chr9:131217026 | T | C | 3 | a0001c0010t0003g0214 a0001c0010t0003g0228 a0001c0010t0003g0229 |
3 | HG01109.hp1 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.5749+1658T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131217026 | |||||||
| chr9:131217134 | T | C | 1 | a0001c0001t0001g0176 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.5749+1766T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131217134 | |||||||
| chr9:131217178 | T | C | 1 | a0001c0001t0001g0036 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.5749+1810T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131217178 | |||||||
| chr9:131217189 | A | G | 3 | a0001c0004t0001g0137 a0002c0002t0001g0136 a0002c0002t0001g0208 |
3 | HG00733.hp1 HG01243.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.5749+1821A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131217189 | |||||||
| chr9:131217450 | G | A | 1 | a0002c0018t0002g0107 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.5749+2082G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131217450 | |||||||
| chr9:131217452 | A | G | 1 | a0001c0005t0003g0211 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.5749+2084A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131217452 | |||||||
| chr9:131217705 | G | C | 5 | a0001c0010t0003g0214 a0001c0010t0003g0228 a0001c0010t0003g0229 others(2): Show |
5 | HG01109.hp1 HG02818.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.5749+2337G>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131217705 | |||||||
| chr9:131217919 | T | A | 110 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(107): Show |
110 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.5749+2551T>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131217919 | |||||||
| chr9:131217926 | A | G | 1 | a0002c0020t0012g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.5749+2558A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131217926 | |||||||
| chr9:131217928 | C | T | 2 | a0001c0001t0001g0058 a0001c0001t0001g0170 |
2 | HG03017.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.5749+2560C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131217928 | |||||||
| chr9:131218055 | A | C | 1 | a0008c0028t0004g0207 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.5749+2687A>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131218055 | |||||||
| chr9:131218123 | A | G | 1 | a0002c0020t0012g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.5749+2755A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131218123 | |||||||
| chr9:131218262 | A | G | 2 | a0001c0004t0001g0196 a0001c0004t0001g0198 |
2 | HG02165.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.5749+2894A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131218262 | |||||||
| chr9:131218579 | C | T | 1 | a0012c0023t0005g0003 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.5749+3211C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131218579 | |||||||
| chr9:131219142 | G | A | 1 | a0001c0005t0003g0211 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.5750-3636G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131219142 | |||||||
| chr9:131219415 | C | T | 4 | a0001c0001t0001g0050 a0001c0001t0001g0052 a0001c0001t0001g0095 others(1): Show |
4 | HG01168.hp1 HG01169.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.5750-3363C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131219415 | |||||||
| chr9:131219416 | G | A | 1 | a0001c0001t0001g0231 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.5750-3362G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131219416 | |||||||
| chr9:131219584 | A | G | 1 | a0001c0005t0002g0213 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.5750-3194A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131219584 | |||||||
| chr9:131219601 | T | G | 7 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0212 others(4): Show |
7 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.5750-3177T>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131219601 | |||||||
| chr9:131219704 | A | G | 3 | a0001c0010t0003g0214 a0001c0010t0003g0228 a0001c0010t0003g0229 |
3 | HG01109.hp1 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.5750-3074A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131219704 | |||||||
| chr9:131219804 | C | T | 1 | a0012c0023t0005g0003 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.5750-2974C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131219804 | |||||||
| chr9:131219816 | G | A | 2 | a0001c0001t0001g0026 a0001c0001t0001g0080 |
2 | HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.5750-2962G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131219816 | |||||||
| chr9:131219826 | A | C | 1 | a0016c0022t0001g0112 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.5750-2952A>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131219826 | |||||||
| chr9:131220176 | G | A | 1 | a0002c0020t0012g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.5750-2602G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131220176 | |||||||
| chr9:131220254 | A | G | 1 | a0002c0020t0012g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.5750-2524A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131220254 | |||||||
| chr9:131220272 | A | G | 1 | a0002c0002t0001g0078 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.5750-2506A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131220272 | |||||||
| chr9:131220376 | A | C | 1 | a0008c0028t0004g0207 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.5750-2402A>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131220376 | |||||||
| chr9:131220628 | C | T | 91 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0001g0043 others(88): Show |
91 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.5750-2150C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131220628 | |||||||
| chr9:131220722 | G | C | 7 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0212 others(4): Show |
7 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.5750-2056G>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131220722 | |||||||
| chr9:131220759 | G | C | 1 | a0001c0001t0001g0048 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.5750-2019G>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131220759 | |||||||
| chr9:131220921 | T | A | 1 | a0008c0028t0004g0207 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.5750-1857T>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131220921 | |||||||
| chr9:131221464 | G | A | 1 | a0002c0002t0001g0193 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.5750-1314G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131221464 | |||||||
| chr9:131221841 | C | T | 1 | a0012c0023t0005g0003 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.5750-937C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131221841 | |||||||
| chr9:131221842 | G | A | 1 | a0001c0005t0002g0213 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.5750-936G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131221842 | |||||||
| chr9:131221854 | C | CA | 34 | a0001c0001t0001g0023 a0001c0001t0001g0073 a0001c0001t0001g0110 others(31): Show |
34 | HG00597.hp1 HG01175.hp1 HG02027.hp2 others(31): Show |
intron_variant | MODIFIER | c.5750-917dupA | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | INFO_REALIGN_3_PRIME | chr9 | 131221854 | ||||||
| chr9:131222075 | T | A | 2 | a0001c0005t0002g0205 a0001c0005t0002g0206 |
2 | HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.5750-703T>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131222075 | |||||||
| chr9:131222138 | C | G | 3 | a0001c0001t0001g0052 a0001c0001t0001g0095 a0002c0002t0001g0161 |
3 | HG01168.hp1 HG01169.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.5750-640C>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131222138 | |||||||
| chr9:131222146 | C | A | 7 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0212 others(4): Show |
7 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.5750-632C>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131222146 | |||||||
| chr9:131222304 | T | A | 222 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(219): Show |
222 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(219): Show |
intron_variant | MODIFIER | c.5750-474T>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131222304 | |||||||
| chr9:131222511 | C | T | 2 | a0001c0001t0001g0037 a0001c0001t0001g0038 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.5750-267C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131222511 | |||||||
| chr9:131222665 | C | T | 4 | a0002c0002t0001g0159 a0002c0002t0001g0160 a0002c0002t0001g0172 others(1): Show |
4 | NA18945.hp1 NA19009.hp1 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.5750-113C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131222665 | |||||||
| chr9:131222712 | G | C | 11 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0212 others(8): Show |
11 | HG01109.hp1 HG01496.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.5750-66G>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131222712 | |||||||
| chr9:131222764 | C | G | 1 | a0001c0001t0001g0092 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.5750-14C>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 31/35 | chr9 | 131222764 | |||||||
| chr9:131222970 | G | T | 1 | a0001c0005t0002g0212 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.5902+40G>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131222970 | |||||||
| chr9:131223061 | C | T | 4 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0003g0211 others(1): Show |
4 | HG01891.hp2 HG02451.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.5902+131C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131223061 | |||||||
| chr9:131223162 | A | AT | 11 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0212 others(8): Show |
11 | HG01109.hp1 HG01496.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.5902+241dupT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223162 | ||||||
| chr9:131223454 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.5902+524C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131223454 | |||||||
| chr9:131223671 | A | G | 4 | a0001c0010t0003g0214 a0001c0010t0003g0228 a0001c0010t0003g0229 others(1): Show |
4 | HG01109.hp1 HG02818.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.5902+741A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131223671 | |||||||
| chr9:131223699 | CT | C | 33 | a0001c0001t0001g0023 a0001c0001t0001g0073 a0001c0001t0001g0110 others(30): Show |
33 | HG00597.hp1 HG01175.hp1 HG02027.hp2 others(30): Show |
intron_variant | MODIFIER | c.5902+778delT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223699 | ||||||
| chr9:131223708 | T | A | 1 | a0006c0008t0001g0109 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.5902+778T>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131223708 | |||||||
| chr9:131223723 | A | ATTTATTT others(13): Show |
1 | a0001c0010t0003g0228 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.5902+808_5902+809i others(22): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223723 | ||||||
| chr9:131223723 | A | ATTTTTTT others(15): Show |
1 | a0001c0001t0001g0215 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.5902+796_5902+797i others(24): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223723 | ||||||
| chr9:131223723 | A | ATTTTTTT others(16): Show |
2 | a0001c0001t0001g0216 a0002c0002t0001g0177 |
2 | HG02109.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.5902+796_5902+797i others(25): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223723 | ||||||
| chr9:131223727 | A | ATTTATTT others(3): Show |
1 | a0002c0002t0001g0226 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.5902+800_5902+801i others(12): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | ||||||
| chr9:131223727 | A | ATTTATTT others(21): Show |
1 | a0001c0004t0001g0138 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.5902+800_5902+801i others(30): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | ||||||
| chr9:131223727 | A | ATTTATTT others(14): Show |
1 | a0002c0003t0001g0063 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.5902+800_5902+801i others(23): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | ||||||
| chr9:131223727 | A | ATTTATTT others(18): Show |
1 | a0002c0002t0001g0077 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.5902+800_5902+801i others(27): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | ||||||
| chr9:131223727 | A | ATTTATTT others(19): Show |
4 | a0001c0001t0001g0020 a0001c0001t0001g0033 a0002c0002t0001g0152 others(1): Show |
4 | HG02132.hp2 NA18960.hp2 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.5902+800_5902+801i others(28): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | ||||||
| chr9:131223727 | A | ATTTATTT others(20): Show |
1 | a0001c0001t0001g0024 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.5902+800_5902+801i others(29): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | ||||||
| chr9:131223727 | A | ATTTATTT others(19): Show |
6 | a0001c0001t0001g0018 a0001c0001t0001g0066 a0001c0001t0001g0176 others(3): Show |
6 | HG02015.hp2 HG02451.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.5902+800_5902+801i others(28): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | ||||||
| chr9:131223727 | A | ATTTATTT others(20): Show |
4 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0006t0001g0169 others(1): Show |
4 | HG00408.hp2 HG00544.hp2 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.5902+800_5902+801i others(29): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | ||||||
| chr9:131223727 | A | ATTTATTT others(21): Show |
2 | a0001c0001t0001g0081 a0002c0002t0001g0183 |
2 | HG00423.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.5902+800_5902+801i others(30): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | ||||||
| chr9:131223727 | A | ATTTATTT others(22): Show |
2 | a0001c0001t0001g0094 a0002c0003t0001g0045 |
2 | HG01243.hp2 HG02027.hp1 |
intron_variant | MODIFIER | c.5902+800_5902+801i others(31): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | ||||||
| chr9:131223727 | A | ATTTATTT others(16): Show |
1 | a0001c0001t0001g0001 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.5902+800_5902+801i others(25): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | ||||||
| chr9:131223727 | A | ATTTATTT others(17): Show |
1 | a0001c0001t0001g0053 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.5902+800_5902+801i others(26): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | ||||||
| chr9:131223727 | A | ATTTATTT others(18): Show |
1 | a0001c0001t0001g0054 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.5902+800_5902+801i others(27): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | ||||||
| chr9:131223727 | A | ATTTATTT others(19): Show |
1 | a0001c0001t0001g0098 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.5902+800_5902+801i others(28): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | ||||||
| chr9:131223727 | A | ATTTATTT others(14): Show |
1 | a0012c0023t0005g0003 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.5902+800_5902+801i others(23): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | ||||||
| chr9:131223727 | A | ATTTATTT others(15): Show |
1 | a0001c0001t0001g0002 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.5902+800_5902+801i others(24): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | ||||||
| chr9:131223727 | A | ATTTATTT others(16): Show |
2 | a0001c0001t0001g0051 a0001c0001t0010g0234 |
2 | HG00438.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.5902+800_5902+801i others(25): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | ||||||
| chr9:131223727 | A | ATTTATTT others(17): Show |
2 | a0002c0002t0001g0164 a0002c0002t0001g0184 |
2 | HG01175.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.5902+800_5902+801i others(26): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | ||||||
| chr9:131223727 | A | ATTTATTT others(18): Show |
2 | a0002c0002t0001g0078 a0004c0009t0001g0030 |
2 | HG00597.hp2 HG00642.hp1 |
intron_variant | MODIFIER | c.5902+800_5902+801i others(27): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | ||||||
| chr9:131223727 | A | ATTTATTT others(19): Show |
8 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0019 others(5): Show |
8 | HG00558.hp1 HG00639.hp1 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.5902+800_5902+801i others(28): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | ||||||
| chr9:131223727 | A | ATTTATTT others(20): Show |
4 | a0001c0001t0001g0047 a0001c0001t0001g0111 a0002c0003t0001g0083 others(1): Show |
4 | HG01106.hp1 HG03209.hp1 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.5902+800_5902+801i others(29): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | ||||||
| chr9:131223727 | A | ATTTATTT others(21): Show |
3 | a0002c0002t0001g0118 a0002c0003t0001g0044 a0003c0011t0001g0186 |
3 | HG01074.hp2 NA18952.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.5902+800_5902+801i others(30): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | ||||||
| chr9:131223727 | A | ATTTATTT others(25): Show |
1 | a0001c0001t0001g0043 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.5902+800_5902+801i others(34): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | ||||||
| chr9:131223727 | A | ATTTATTT others(18): Show |
1 | a0003c0013t0001g0041 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.5902+800_5902+801i others(27): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | ||||||
| chr9:131223727 | A | ATTTATTT others(13): Show |
1 | a0001c0010t0003g0214 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.5902+800_5902+801i others(22): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | ||||||
| chr9:131223727 | A | ATTTATTT others(15): Show |
1 | a0002c0002t0001g0146 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.5902+800_5902+801i others(24): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | ||||||
| chr9:131223727 | A | ATTTATTT others(16): Show |
8 | a0001c0001t0001g0065 a0001c0001t0001g0231 a0001c0007t0001g0064 others(5): Show |
8 | HG00733.hp1 HG01496.hp1 HG02083.hp2 others(5): Show |
intron_variant | MODIFIER | c.5902+800_5902+801i others(25): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | ||||||
| chr9:131223727 | A | ATTTATTT others(17): Show |
10 | a0001c0001t0001g0025 a0001c0001t0001g0233 a0001c0004t0001g0140 others(7): Show |
10 | HG00609.hp2 HG02015.hp1 HG03831.hp2 others(7): Show |
intron_variant | MODIFIER | c.5902+800_5902+801i others(26): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | ||||||
| chr9:131223727 | A | ATTTATTT others(18): Show |
6 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0076 others(3): Show |
6 | HG01515.hp1 HG01981.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.5902+800_5902+801i others(27): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | ||||||
| chr9:131223727 | A | ATTTATTT others(19): Show |
2 | a0002c0002t0001g0194 a0004c0009t0001g0031 |
2 | HG01928.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.5902+800_5902+801i others(28): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | ||||||
| chr9:131223727 | A | ATTTATTT others(20): Show |
2 | a0001c0001t0001g0037 a0001c0007t0001g0086 |
2 | HG02145.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.5902+800_5902+801i others(29): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | ||||||
| chr9:131223727 | A | ATTTATTT others(21): Show |
5 | a0001c0001t0001g0038 a0001c0001t0001g0048 a0001c0001t0001g0089 others(2): Show |
5 | HG00609.hp1 HG01891.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.5902+800_5902+801i others(30): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | ||||||
| chr9:131223727 | A | ATTTATTT others(22): Show |
1 | a0006c0008t0001g0032 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.5902+800_5902+801i others(31): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | ||||||
| chr9:131223727 | A | ATTTATTT others(39): Show |
1 | a0002c0002t0001g0067 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.5902+800_5902+801i others(48): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | ||||||
| chr9:131223727 | A | ATTTATTT others(7): Show |
3 | a0001c0001t0001g0057 a0001c0005t0003g0211 a0001c0026t0001g0055 |
3 | HG00099.hp1 HG01891.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.5902+800_5902+801i others(16): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | ||||||
| chr9:131223727 | A | ATTTATTT others(15): Show |
1 | a0013c0021t0001g0173 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.5902+800_5902+801i others(24): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | ||||||
| chr9:131223727 | A | ATTTATTT others(16): Show |
7 | a0001c0001t0001g0027 a0001c0001t0001g0114 a0001c0001t0001g0230 others(4): Show |
7 | HG00423.hp2 HG01169.hp1 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.5902+800_5902+801i others(25): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | ||||||
| chr9:131223727 | A | ATTTATTT others(17): Show |
10 | a0001c0001t0001g0014 a0001c0001t0001g0068 a0001c0001t0001g0189 others(7): Show |
10 | HG00642.hp2 HG03490.hp2 HG03927.hp1 others(7): Show |
intron_variant | MODIFIER | c.5902+800_5902+801i others(26): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | ||||||
| chr9:131223727 | A | ATTTATTT others(18): Show |
6 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0082 others(3): Show |
6 | HG01081.hp2 HG01433.hp1 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.5902+800_5902+801i others(27): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | ||||||
| chr9:131223727 | A | ATTTATTT others(19): Show |
2 | a0001c0001t0001g0103 a0009c0029t0001g0062 |
2 | HG02523.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.5902+800_5902+801i others(28): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | ||||||
| chr9:131223727 | A | ATTTATTT others(20): Show |
1 | a0001c0001t0009g0072 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.5902+800_5902+801i others(29): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | ||||||
| chr9:131223727 | A | ATTTATTT others(21): Show |
2 | a0001c0001t0001g0049 a0006c0008t0001g0040 |
2 | HG01109.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.5902+800_5902+801i others(30): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | ||||||
| chr9:131223727 | A | ATTTATTT others(23): Show |
2 | a0001c0004t0001g0196 a0001c0004t0001g0198 |
2 | HG02165.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.5902+800_5902+801i others(32): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | ||||||
| chr9:131223727 | A | ATTTATTT others(29): Show |
1 | a0002c0002t0001g0210 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.5902+800_5902+801i others(38): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | ||||||
| chr9:131223727 | A | ATTTATTT others(30): Show |
1 | a0002c0002t0001g0113 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.5902+800_5902+801i others(39): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | ||||||
| chr9:131223727 | A | ATTTATTT others(4): Show |
2 | a0001c0001t0001g0087 a0002c0002t0001g0175 |
2 | HG01943.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.5902+800_5902+801i others(13): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | ||||||
| chr9:131223727 | A | ATTTATTT others(5): Show |
1 | a0001c0005t0002g0212 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.5902+800_5902+801i others(14): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | ||||||
| chr9:131223727 | A | ATTTATTT others(7): Show |
2 | a0002c0003t0001g0074 a0002c0020t0012g0132 |
2 | HG02723.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.5902+800_5902+801i others(16): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | ||||||
| chr9:131223727 | A | ATTTATTT others(8): Show |
4 | a0001c0004t0001g0131 a0001c0024t0001g0056 a0001c0027t0001g0085 others(1): Show |
4 | HG00741.hp2 HG01361.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.5902+800_5902+801i others(17): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | ||||||
| chr9:131223727 | A | ATTTATTT others(16): Show |
8 | a0001c0001t0001g0008 a0001c0001t0001g0073 a0001c0001t0001g0170 others(5): Show |
8 | HG00558.hp2 HG02027.hp2 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.5902+800_5902+801i others(25): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | ||||||
| chr9:131223727 | A | ATTTATTT others(17): Show |
10 | a0001c0001t0001g0110 a0001c0006t0001g0174 a0002c0002t0001g0116 others(7): Show |
10 | HG00099.hp2 HG01243.hp1 HG02735.hp2 others(7): Show |
intron_variant | MODIFIER | c.5902+800_5902+801i others(26): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | ||||||
| chr9:131223727 | A | ATTTATTT others(18): Show |
5 | a0001c0004t0001g0201 a0002c0002t0001g0115 a0002c0002t0001g0133 others(2): Show |
5 | HG01516.hp2 HG01993.hp1 HG02056.hp1 others(2): Show |
intron_variant | MODIFIER | c.5902+800_5902+801i others(27): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | ||||||
| chr9:131223727 | A | ATTTATTT others(19): Show |
1 | a0005c0012t0001g0006 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.5902+800_5902+801i others(28): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | ||||||
| chr9:131223727 | A | ATTTATTT others(21): Show |
4 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0026 others(1): Show |
4 | HG00733.hp2 HG01074.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.5902+800_5902+801i others(30): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | ||||||
| chr9:131223727 | A | ATTTATTT others(23): Show |
2 | a0001c0001t0001g0013 a0001c0001t0001g0023 |
2 | HG01175.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.5902+800_5902+801i others(32): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | ||||||
| chr9:131223727 | A | ATTTATTT others(32): Show |
1 | a0002c0002t0001g0225 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.5902+800_5902+801i others(41): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | ||||||
| chr9:131223727 | A | ATTTATTT others(36): Show |
1 | a0002c0002t0001g0021 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.5902+800_5902+801i others(45): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | ||||||
| chr9:131223727 | A | ATTTATTT others(38): Show |
1 | a0002c0002t0001g0009 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.5902+800_5902+801i others(47): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | ||||||
| chr9:131223727 | A | ATTTTTAT others(38): Show |
1 | a0002c0002t0001g0163 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.5902+802_5902+803i others(47): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | ||||||
| chr9:131223727 | A | ATTTTTTT others(18): Show |
1 | a0002c0002t0001g0200 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.5902+804_5902+805i others(27): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | ||||||
| chr9:131223727 | A | ATTTTTTT others(4): Show |
2 | a0002c0002t0001g0104 a0002c0018t0002g0107 |
2 | HG03942.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.5902+812_5902+822d others(13): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | ||||||
| chr9:131223727 | A | ATTTTTTT others(5): Show |
1 | a0008c0028t0004g0207 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.5902+811_5902+822d others(14): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | ||||||
| chr9:131223727 | A | ATTTTTTT others(8): Show |
1 | a0001c0004t0001g0219 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.5902+808_5902+822d others(17): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | ||||||
| chr9:131223727 | A | ATTTTTTT others(10): Show |
1 | a0002c0003t0001g0071 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.5902+806_5902+822d others(19): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | ||||||
| chr9:131223727 | A | ATTTTTTT others(15): Show |
2 | a0001c0001t0001g0058 a0001c0010t0003g0229 |
2 | HG02818.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.5902+801_5902+822d others(24): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | ||||||
| chr9:131223727 | A | ATTTTTTT others(16): Show |
4 | a0001c0001t0001g0217 a0002c0002t0001g0151 a0002c0002t0001g0181 others(1): Show |
4 | HG02132.hp1 HG03195.hp2 NA18948.hp2 others(1): Show |
intron_variant | MODIFIER | c.5902+800_5902+822d others(25): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | ||||||
| chr9:131223727 | A | ATTTTTTT others(17): Show |
8 | a0001c0001t0001g0079 a0001c0004t0001g0204 a0001c0006t0001g0168 others(5): Show |
8 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(5): Show |
intron_variant | MODIFIER | c.5902+799_5902+822d others(26): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | ||||||
| chr9:131223727 | A | ATTTTTTT others(18): Show |
1 | a0001c0001t0001g0059 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.5902+798_5902+822d others(27): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | ||||||
| chr9:131223727 | A | ATTTTTTT others(19): Show |
2 | a0002c0002t0001g0156 a0005c0012t0001g0007 |
2 | HG01106.hp2 NA18949.hp2 |
intron_variant | MODIFIER | c.5902+822_5902+823i others(28): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | ||||||
| chr9:131223727 | A | ATTTTTTT others(20): Show |
2 | a0001c0001t0001g0015 a0005c0012t0001g0005 |
2 | HG01981.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.5902+822_5902+823i others(29): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | ||||||
| chr9:131223727 | A | ATTTTTTT others(22): Show |
1 | a0002c0002t0001g0135 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.5902+822_5902+823i others(31): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | ||||||
| chr9:131223727 | A | ATTTTTTT others(25): Show |
1 | a0001c0001t0001g0080 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.5902+822_5902+823i others(34): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223727 | ||||||
| chr9:131223727 | A | T | 4 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0002c0002t0001g0177 others(1): Show |
4 | HG02109.hp1 HG02698.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.5902+797A>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131223727 | |||||||
| chr9:131223729 | T | TTATTTAT others(3): Show |
2 | a0001c0005t0002g0205 a0001c0005t0002g0206 |
2 | HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.5902+800_5902+801i others(12): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223729 | ||||||
| chr9:131223729 | T | TTATTTAT others(19): Show |
1 | a0001c0001t0001g0022 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.5902+800_5902+801i others(28): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131223729 | ||||||
| chr9:131223730 | T | TATTTTA | 2 | a0001c0001t0001g0050 a0002c0002t0001g0161 |
2 | HG01515.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.5902+800_5902+801i others(8): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131223730 | |||||||
| chr9:131223731 | T | A | 1 | a0002c0020t0012g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.5902+801T>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131223731 | |||||||
| chr9:131223732 | T | A | 3 | a0002c0002t0001g0143 a0002c0002t0001g0154 a0002c0002t0001g0155 |
3 | HG02738.hp2 HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.5902+802T>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131223732 | |||||||
| chr9:131223733 | T | A | 1 | a0001c0005t0002g0206 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.5902+803T>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131223733 | |||||||
| chr9:131223736 | T | A | 1 | a0002c0002t0001g0143 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.5902+806T>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131223736 | |||||||
| chr9:131223737 | T | A | 1 | a0001c0005t0002g0206 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.5902+807T>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131223737 | |||||||
| chr9:131223849 | G | A | 3 | a0005c0012t0001g0005 a0005c0012t0001g0006 a0005c0012t0001g0007 |
3 | HG01106.hp2 HG02723.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.5902+919G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131223849 | |||||||
| chr9:131223892 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.5902+962G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131223892 | |||||||
| chr9:131223906 | T | C | 7 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0212 others(4): Show |
7 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.5902+976T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131223906 | |||||||
| chr9:131223966 | C | T | 4 | a0001c0007t0001g0064 a0001c0007t0001g0086 a0001c0007t0001g0088 others(1): Show |
4 | HG02145.hp2 HG02897.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.5902+1036C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131223966 | |||||||
| chr9:131223996 | C | A | 219 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(216): Show |
219 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.5902+1066C>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131223996 | |||||||
| chr9:131224060 | G | A | 1 | a0001c0004t0001g0219 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.5902+1130G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131224060 | |||||||
| chr9:131224241 | A | G | 1 | a0002c0002t0001g0226 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.5902+1311A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131224241 | |||||||
| chr9:131224284 | A | G | 2 | a0010c0017t0001g0108 a0016c0022t0001g0112 |
2 | HG02886.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.5902+1354A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131224284 | |||||||
| chr9:131224300 | T | A | 7 | a0001c0001t0001g0110 a0002c0002t0001g0135 a0002c0002t0001g0150 others(4): Show |
7 | HG00597.hp1 NA18948.hp2 NA18949.hp2 others(4): Show |
intron_variant | MODIFIER | c.5902+1370T>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131224300 | |||||||
| chr9:131224325 | GTC | G | 6 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0213 others(3): Show |
6 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.5902+1399_5902+140 others(6): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131224325 | ||||||
| chr9:131224569 | G | A | 2 | a0001c0001t0001g0008 a0001c0001t0001g0114 |
2 | HG03688.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.5902+1639G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131224569 | |||||||
| chr9:131224674 | G | A | 1 | a0001c0001t0001g0073 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.5902+1744G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131224674 | |||||||
| chr9:131224777 | G | C | 7 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0212 others(4): Show |
7 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.5902+1847G>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131224777 | |||||||
| chr9:131224870 | A | G | 1 | a0001c0004t0001g0137 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.5902+1940A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131224870 | |||||||
| chr9:131224927 | G | A | 206 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(203): Show |
206 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(203): Show |
intron_variant | MODIFIER | c.5902+1997G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131224927 | |||||||
| chr9:131225241 | C | T | 1 | a0012c0023t0005g0003 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.5902+2311C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131225241 | |||||||
| chr9:131225312 | G | A | 1 | a0003c0013t0001g0070 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.5902+2382G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131225312 | |||||||
| chr9:131225488 | A | G | 1 | a0001c0001t0001g0028 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.5902+2558A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131225488 | |||||||
| chr9:131225716 | C | T | 3 | a0005c0012t0001g0005 a0005c0012t0001g0006 a0005c0012t0001g0007 |
3 | HG01106.hp2 HG02723.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.5903-2444C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131225716 | |||||||
| chr9:131225717 | G | A | 2 | a0001c0005t0002g0213 a0008c0028t0004g0207 |
2 | HG01496.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.5903-2443G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131225717 | |||||||
| chr9:131226385 | C | T | 2 | a0002c0002t0001g0195 a0002c0002t0001g0203 |
2 | HG01169.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.5903-1775C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131226385 | |||||||
| chr9:131226624 | C | CT | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(214): Show |
217 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.5903-1526dupT | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131226624 | ||||||
| chr9:131226836 | A | C | 1 | a0001c0007t0001g0088 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.5903-1324A>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131226836 | |||||||
| chr9:131226850 | A | T | 3 | a0001c0001t0001g0025 a0001c0004t0001g0140 a0002c0002t0001g0139 |
3 | HG00609.hp2 HG03927.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.5903-1310A>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131226850 | |||||||
| chr9:131227040 | C | T | 1 | a0002c0002t0001g0146 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.5903-1120C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131227040 | |||||||
| chr9:131227171 | C | T | 1 | a0001c0007t0001g0088 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.5903-989C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131227171 | |||||||
| chr9:131227530 | A | T | 2 | a0001c0005t0002g0205 a0001c0005t0002g0206 |
2 | HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.5903-630A>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131227530 | |||||||
| chr9:131227539 | G | A | 7 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0212 others(4): Show |
7 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.5903-621G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131227539 | |||||||
| chr9:131227584 | C | T | 2 | a0002c0002t0001g0159 a0002c0002t0001g0160 |
2 | NA18945.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.5903-576C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131227584 | |||||||
| chr9:131227597 | G | A | 2 | a0001c0005t0002g0213 a0008c0028t0004g0207 |
2 | HG01496.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.5903-563G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131227597 | |||||||
| chr9:131227741 | A | G | 13 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0212 others(10): Show |
13 | HG01109.hp1 HG01496.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.5903-419A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131227741 | |||||||
| chr9:131227838 | T | C | 1 | a0008c0028t0004g0207 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.5903-322T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131227838 | |||||||
| chr9:131227842 | C | T | 4 | a0001c0001t0001g0047 a0001c0001t0001g0094 a0001c0004t0001g0138 others(1): Show |
4 | HG02027.hp1 HG02083.hp1 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.5903-318C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131227842 | |||||||
| chr9:131227879 | G | A | 3 | a0001c0010t0003g0214 a0001c0010t0003g0228 a0001c0010t0003g0229 |
3 | HG01109.hp1 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.5903-281G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131227879 | |||||||
| chr9:131227922 | G | A | 7 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0212 others(4): Show |
7 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.5903-238G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131227922 | |||||||
| chr9:131227976 | A | G | 10 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0212 others(7): Show |
10 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.5903-184A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131227976 | |||||||
| chr9:131227985 | C | T | 1 | a0001c0004t0001g0227 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.5903-175C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131227985 | |||||||
| chr9:131227988 | G | T | 1 | a0001c0001t0007g0042 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.5903-172G>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131227988 | |||||||
| chr9:131228087 | GCTCAATG others(4): Show |
G | 2 | a0001c0007t0001g0064 a0001c0007t0001g0088 |
2 | HG02897.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.5903-69_5903-59del others(11): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr9 | 131228087 | ||||||
| chr9:131228111 | C | T | 1 | a0001c0001t0001g0050 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.5903-49C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 32/35 | chr9 | 131228111 | |||||||
| chr9:131228372 | G | A | 48 | a0001c0001t0001g0025 a0001c0001t0001g0043 a0001c0001t0001g0068 others(45): Show |
48 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(45): Show |
intron_variant | MODIFIER | c.6074+41G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 33/35 | chr9 | 131228372 | |||||||
| chr9:131228399 | T | C | 2 | a0010c0017t0001g0108 a0016c0022t0001g0112 |
2 | HG02886.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.6074+68T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 33/35 | chr9 | 131228399 | |||||||
| chr9:131228422 | A | G | 1 | a0012c0023t0005g0003 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.6074+91A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 33/35 | chr9 | 131228422 | |||||||
| chr9:131228656 | G | A | 10 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0212 others(7): Show |
10 | HG01109.hp1 HG01496.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.6074+325G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 33/35 | chr9 | 131228656 | |||||||
| chr9:131228679 | G | A | 1 | a0002c0002t0001g0220 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.6074+348G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 33/35 | chr9 | 131228679 | |||||||
| chr9:131228689 | A | G | 1 | a0001c0001t0001g0023 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.6074+358A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 33/35 | chr9 | 131228689 | |||||||
| chr9:131228742 | C | T | 1 | a0001c0005t0002g0212 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.6074+411C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 33/35 | chr9 | 131228742 | |||||||
| chr9:131228789 | C | G | 7 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0212 others(4): Show |
7 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.6074+458C>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 33/35 | chr9 | 131228789 | |||||||
| chr9:131228840 | G | T | 2 | a0002c0003t0001g0044 a0002c0003t0001g0045 |
2 | HG01074.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.6074+509G>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 33/35 | chr9 | 131228840 | |||||||
| chr9:131229006 | A | G | 1 | a0002c0002t0001g0078 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.6074+675A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 33/35 | chr9 | 131229006 | |||||||
| chr9:131229406 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.6074+1075G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 33/35 | chr9 | 131229406 | |||||||
| chr9:131229465 | A | G | 9 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0212 others(6): Show |
9 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.6074+1134A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 33/35 | chr9 | 131229465 | |||||||
| chr9:131229476 | G | C | 1 | a0001c0005t0003g0211 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.6074+1145G>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 33/35 | chr9 | 131229476 | |||||||
| chr9:131229661 | A | G | 9 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0212 others(6): Show |
9 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.6075-969A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 33/35 | chr9 | 131229661 | |||||||
| chr9:131229773 | G | A | 1 | a0001c0005t0003g0211 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.6075-857G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 33/35 | chr9 | 131229773 | |||||||
| chr9:131229817 | C | A | 1 | a0002c0020t0012g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.6075-813C>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 33/35 | chr9 | 131229817 | |||||||
| chr9:131229848 | A | G | 9 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0212 others(6): Show |
9 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.6075-782A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 33/35 | chr9 | 131229848 | |||||||
| chr9:131229852 | T | G | 7 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0212 others(4): Show |
7 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.6075-778T>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 33/35 | chr9 | 131229852 | |||||||
| chr9:131229863 | T | G | 7 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0212 others(4): Show |
7 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.6075-767T>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 33/35 | chr9 | 131229863 | |||||||
| chr9:131229955 | C | A | 3 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0217 |
3 | HG02109.hp1 HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.6075-675C>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 33/35 | chr9 | 131229955 | |||||||
| chr9:131229979 | C | G | 1 | a0001c0005t0002g0212 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.6075-651C>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 33/35 | chr9 | 131229979 | |||||||
| chr9:131229979 | C | T | 4 | a0001c0010t0003g0214 a0001c0010t0003g0228 a0001c0010t0003g0229 others(1): Show |
4 | HG01109.hp1 HG02818.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.6075-651C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 33/35 | chr9 | 131229979 | |||||||
| chr9:131230057 | G | T | 1 | a0001c0001t0001g0076 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.6075-573G>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 33/35 | chr9 | 131230057 | |||||||
| chr9:131230319 | G | T | 3 | a0001c0010t0003g0214 a0001c0010t0003g0228 a0001c0010t0003g0229 |
3 | HG01109.hp1 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.6075-311G>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 33/35 | chr9 | 131230319 | |||||||
| chr9:131230552 | A | G | 219 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(216): Show |
219 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.6075-78A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 33/35 | chr9 | 131230552 | |||||||
| chr9:131230784 | G | A | 3 | a0001c0010t0003g0214 a0001c0010t0003g0228 a0001c0010t0003g0229 |
3 | HG01109.hp1 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.6214+15G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 34/35 | chr9 | 131230784 | |||||||
| chr9:131230976 | C | T | 1 | a0002c0002t0001g0185 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.6214+207C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 34/35 | chr9 | 131230976 | |||||||
| chr9:131231085 | G | A | 1 | a0002c0002t0001g0200 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.6214+316G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 34/35 | chr9 | 131231085 | |||||||
| chr9:131231087 | T | C | 1 | a0002c0002t0001g0225 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.6214+318T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 34/35 | chr9 | 131231087 | |||||||
| chr9:131231186 | A | C | 7 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0212 others(4): Show |
7 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.6214+417A>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 34/35 | chr9 | 131231186 | |||||||
| chr9:131231188 | C | CATAT | 3 | a0002c0002t0001g0067 a0008c0028t0004g0207 a0012c0023t0005g0003 |
3 | HG02145.hp1 HG03579.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.6214+434_6214+437d others(6): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 34/35 | INFO_REALIGN_3_PRIME | chr9 | 131231188 | ||||||
| chr9:131231188 | CAT | C | 4 | a0001c0010t0003g0214 a0001c0010t0003g0228 a0001c0010t0003g0229 others(1): Show |
4 | HG01109.hp1 HG02818.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.6214+436_6214+437d others(4): Show |
NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 34/35 | INFO_REALIGN_3_PRIME | chr9 | 131231188 | ||||||
| chr9:131231205 | A | T | 4 | a0001c0010t0003g0214 a0001c0010t0003g0228 a0001c0010t0003g0229 others(1): Show |
4 | HG01109.hp1 HG02818.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.6214+436A>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 34/35 | chr9 | 131231205 | |||||||
| chr9:131231410 | C | T | 1 | a0001c0024t0001g0056 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.6214+641C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 34/35 | chr9 | 131231410 | |||||||
| chr9:131231779 | C | T | 1 | a0001c0001t0001g0053 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.6215-505C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 34/35 | chr9 | 131231779 | |||||||
| chr9:131231818 | C | T | 1 | a0002c0003t0001g0069 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.6215-466C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 34/35 | chr9 | 131231818 | |||||||
| chr9:131231829 | A | T | 3 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0217 |
3 | HG02109.hp1 HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.6215-455A>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 34/35 | chr9 | 131231829 | |||||||
| chr9:131231912 | C | CA | 24 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(21): Show |
24 | HG00558.hp1 HG00642.hp1 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.6215-350dupA | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 34/35 | INFO_REALIGN_3_PRIME | chr9 | 131231912 | ||||||
| chr9:131231912 | CA | C | 6 | a0001c0001t0001g0111 a0001c0005t0002g0205 a0001c0005t0002g0206 others(3): Show |
6 | HG01106.hp1 HG01496.hp2 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.6215-350delA | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 34/35 | INFO_REALIGN_3_PRIME | chr9 | 131231912 | ||||||
| chr9:131232015 | G | A | 1 | a0010c0017t0001g0108 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.6215-269G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 34/35 | chr9 | 131232015 | |||||||
| chr9:131232212 | A | G | 3 | a0001c0010t0003g0214 a0001c0010t0003g0228 a0001c0010t0003g0229 |
3 | HG01109.hp1 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.6215-72A>G | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 34/35 | chr9 | 131232212 | |||||||
| chr9:131232246 | G | A | 3 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0217 |
3 | HG02109.hp1 HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.6215-38G>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 34/35 | chr9 | 131232246 | |||||||
| chr9:131232333 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.6239+25C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 35/35 | chr9 | 131232333 | |||||||
| chr9:131232429 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.6239+121C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 35/35 | chr9 | 131232429 | |||||||
| chr9:131232682 | C | T | 1 | a0002c0002t0001g0147 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.6239+374C>T | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 35/35 | chr9 | 131232682 | |||||||
| chr9:131232934 | T | C | 4 | a0001c0010t0003g0214 a0001c0010t0003g0228 a0001c0010t0003g0229 others(1): Show |
4 | HG01109.hp1 HG02818.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.6240-520T>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 35/35 | chr9 | 131232934 | |||||||
| chr9:131233020 | T | A | 215 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(212): Show |
215 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(212): Show |
intron_variant | MODIFIER | c.6240-434T>A | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 35/35 | chr9 | 131233020 | |||||||
| chr9:131233178 | A | C | 13 | a0001c0005t0002g0205 a0001c0005t0002g0206 a0001c0005t0002g0212 others(10): Show |
13 | HG01109.hp1 HG01496.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.6240-276A>C | NUP214 | ENSG00000126883.19 | transcript | ENST00000359428.10 | protein_coding | 35/35 | chr9 | 131233178 |