Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 53371 |
| ensemblid | ENSG00000138750.16 |
| hgncid | 17359 |
| symbol | NUP54 |
| name | nucleoporin 54 |
| refseq_nuc | NM_017426.4 |
| refseq_prot | NP_059122.2 |
| ensembl_nuc | ENST00000264883.8 |
| ensembl_prot | ENSP00000264883.3 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 76114664 |
| end | 76148397 |
| strand | - |
| ver | v1.2 |
| region | chr4:76114664-76148397 |
| region5000 | chr4:76109664-76153397 |
| regionname0 | NUP54_chr4_76114664_76148397 |
| regionname5000 | NUP54_chr4_76109664_76153397 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 507 | 240 | 57 | 43 | 103 | 12 | 23 | 80 | NUP54_chr4_76109664_76153397 | NUP54 | MAFNF others(502): Show |
chr4 | 76109664 | 76153397 |
| a0002 | 0/0 | 508 | 85 | 5 | 12 | 61 | 1 | 6 | 46 | NUP54_chr4_76109664_76153397 | NUP54 | MAFNF others(503): Show |
chr4 | 76109664 | 76153397 |
| a0003 | 0/0 | 507 | 43 | 22 | 13 | 3 | 3 | 2 | 3 | NUP54_chr4_76109664_76153397 | NUP54 | MAFNF others(502): Show |
chr4 | 76109664 | 76153397 |
| a0004 | 0/0 | 508 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | MAFNF others(503): Show |
chr4 | 76109664 | 76153397 |
| a0005 | 0/0 | 508 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | MAFNF others(503): Show |
chr4 | 76109664 | 76153397 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1521 | 214 | 45 | 43 | 89 | 12 | 23 | NUP54_chr4_76109664_76153397 | NUP54 | ATGGC others(1516): Show |
chr4 | 76109664 | 76153397 | ||
| a0001c0004 | 0/0 | 1521 | 25 | 11 | 0 | 14 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | ATGGC others(1516): Show |
chr4 | 76109664 | 76153397 | ||
| a0001c0008 | 0/0 | 1521 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | ATGGC others(1516): Show |
chr4 | 76109664 | 76153397 | ||
| a0002c0002 | 0/0 | 1524 | 85 | 5 | 12 | 61 | 1 | 6 | NUP54_chr4_76109664_76153397 | NUP54 | ATGGC others(1519): Show |
chr4 | 76109664 | 76153397 | ||
| a0003c0003 | 0/0 | 1521 | 39 | 18 | 13 | 3 | 3 | 2 | NUP54_chr4_76109664_76153397 | NUP54 | ATGGC others(1516): Show |
chr4 | 76109664 | 76153397 | ||
| a0003c0005 | 0/0 | 1521 | 4 | 4 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | ATGGC others(1516): Show |
chr4 | 76109664 | 76153397 | ||
| a0004c0007 | 0/0 | 1524 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | ATGGC others(1519): Show |
chr4 | 76109664 | 76153397 | ||
| a0005c0006 | 0/0 | 1524 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | ATGGC others(1519): Show |
chr4 | 76109664 | 76153397 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2249 | 37 | 1 | 14 | 6 | 7 | 7 | NUP54_chr4_76109664_76153397 | NUP54 | ACTTG others(2244): Show |
chr4 | 76109664 | 76153397 |
| a0001c0001t0002 | 0/0 | 2249 | 98 | 37 | 15 | 33 | 4 | 9 | NUP54_chr4_76109664_76153397 | NUP54 | ACTTG others(2244): Show |
chr4 | 76109664 | 76153397 |
| a0001c0001t0004 | 0/0 | 2245 | 70 | 0 | 13 | 50 | 1 | 6 | NUP54_chr4_76109664_76153397 | NUP54 | ACTTG others(2240): Show |
chr4 | 76109664 | 76153397 |
| a0001c0001t0005 | 0/0 | 2249 | 6 | 5 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | ACTTG others(2244): Show |
chr4 | 76109664 | 76153397 |
| a0001c0001t0006 | 0/0 | 2249 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | ACTTG others(2244): Show |
chr4 | 76109664 | 76153397 |
| a0001c0001t0007 | 0/0 | 2249 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | ACTTG others(2244): Show |
chr4 | 76109664 | 76153397 |
| a0001c0001t0008 | 0/0 | 2249 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | ACTTG others(2244): Show |
chr4 | 76109664 | 76153397 |
| a0001c0004t0001 | 0/0 | 2249 | 18 | 4 | 0 | 14 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | ACTTG others(2244): Show |
chr4 | 76109664 | 76153397 |
| a0001c0004t0004 | 0/0 | 2245 | 7 | 7 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | ACTTG others(2240): Show |
chr4 | 76109664 | 76153397 |
| a0001c0008t0005 | 0/0 | 2249 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | ACTTG others(2244): Show |
chr4 | 76109664 | 76153397 |
| a0002c0002t0003 | 0/0 | 2252 | 85 | 5 | 12 | 61 | 1 | 6 | NUP54_chr4_76109664_76153397 | NUP54 | ACTTG others(2247): Show |
chr4 | 76109664 | 76153397 |
| a0003c0003t0001 | 0/0 | 2249 | 39 | 18 | 13 | 3 | 3 | 2 | NUP54_chr4_76109664_76153397 | NUP54 | ACTTG others(2244): Show |
chr4 | 76109664 | 76153397 |
| a0003c0005t0001 | 0/0 | 2249 | 4 | 4 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | ACTTG others(2244): Show |
chr4 | 76109664 | 76153397 |
| a0004c0007t0003 | 0/0 | 2252 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | ACTTG others(2247): Show |
chr4 | 76109664 | 76153397 |
| a0005c0006t0003 | 0/0 | 2252 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | ACTTG others(2247): Show |
chr4 | 76109664 | 76153397 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0010 | 1/0 | 3 | 0 | 1 | 0 | 1 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0001g0237 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0002g0004 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0002g0005 | 0/0 | 4 | 2 | 0 | 2 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0002g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0002g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0002g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0002g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0002g0020 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0004g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0004g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0004g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0004g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0004g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0004g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0004g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0004g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0004g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0004g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0004g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0004g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0004g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0004g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0004g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0004g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0004g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0004g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0004g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0004g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0004g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0004g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0004g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0004g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0004g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0004g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0004g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0004g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0004g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0004g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0004g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0004g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0004g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0004g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0004g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0004g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0004g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0004g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0004g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0004g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0004g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0004g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0004g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0004g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0004g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0004g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0004g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0004g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0004g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0004g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0004g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0004g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0004g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0004g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0004g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0004g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0004g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0004g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0004g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0004g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0004g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0004g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0004g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0004g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0004g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0005g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0005g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0005g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0005g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0005g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0005g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0006g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0007g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0001t0008g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0004t0001g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0004t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0004t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0004t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0004t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0004t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0004t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0004t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0004t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0004t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0004t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0004t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0004t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0004t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0004t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0004t0004g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0004t0004g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0004t0004g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0004t0004g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0004t0004g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0004t0004g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0004t0004g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0001c0008t0005g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0002c0002t0003g0001 | 0/0 | 10 | 0 | 2 | 8 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0002c0002t0003g0002 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0002c0002t0003g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0002c0002t0003g0007 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0002c0002t0003g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0002c0002t0003g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0002c0002t0003g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0002c0002t0003g0013 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0002c0002t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0002c0002t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0002c0002t0003g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0002c0002t0003g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0002c0002t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0002c0002t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0002c0002t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0002c0002t0003g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0002c0002t0003g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0002c0002t0003g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0002c0002t0003g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0002c0002t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0002c0002t0003g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0002c0002t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0002c0002t0003g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0002c0002t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0002c0002t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0002c0002t0003g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0002c0002t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0002c0002t0003g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0002c0002t0003g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0002c0002t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0002c0002t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0002c0002t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0002c0002t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0002c0002t0003g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0002c0002t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0002c0002t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0002c0002t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0002c0002t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0002c0002t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0002c0002t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0002c0002t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0002c0002t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0002c0002t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0002c0002t0003g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0002c0002t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0002c0002t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0002c0002t0003g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0002c0002t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0002c0002t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0002c0002t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0002c0002t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0002c0002t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0002c0002t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0002c0002t0003g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0002c0002t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0002c0002t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0002c0002t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0002c0002t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0002c0002t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0002c0002t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0003c0003t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0003c0003t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0003c0003t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0003c0003t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0003c0003t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0003c0003t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0003c0003t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0003c0003t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0003c0003t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0003c0003t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0003c0003t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0003c0003t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0003c0003t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0003c0003t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0003c0003t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0003c0003t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0003c0003t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0003c0003t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0003c0003t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0003c0003t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0003c0003t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0003c0003t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0003c0003t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0003c0003t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0003c0003t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0003c0003t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0003c0003t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0003c0003t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0003c0003t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0003c0003t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0003c0003t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0003c0003t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0003c0003t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0003c0003t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0003c0003t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0003c0003t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0003c0003t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0003c0003t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0003c0003t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0003c0005t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0003c0005t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0003c0005t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0003c0005t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0004c0007t0003g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| a0005c0006t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0004 | g0223 | EUR | GBR | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0010 | EUR | GBR | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG00140 | hp1 | a0003 | c0003 | t0001 | g0268 | EUR | GBR | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0252 | EUR | GBR | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0251 | EUR | FIN | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0295 | EUR | FIN | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0224 | EUR | FIN | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0086 | EUR | FIN | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG00423 | hp1 | a0002 | c0002 | t0003 | g0070 | EAS | CHS | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0215 | EAS | CHS | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG00438 | hp1 | a0001 | c0001 | t0004 | g0111 | EAS | CHS | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | CHS | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG00544 | hp1 | a0001 | c0001 | t0004 | g0116 | EAS | CHS | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0186 | EAS | CHS | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG00558 | hp1 | a0001 | c0001 | t0004 | g0131 | EAS | CHS | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG00558 | hp2 | a0002 | c0002 | t0003 | g0062 | EAS | CHS | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG00597 | hp1 | a0001 | c0001 | t0004 | g0110 | EAS | CHS | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG00597 | hp2 | a0002 | c0002 | t0003 | g0007 | EAS | CHS | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG00609 | hp1 | a0002 | c0002 | t0003 | g0077 | EAS | CHS | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG00609 | hp2 | a0001 | c0001 | t0004 | g0093 | EAS | CHS | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG00621 | hp1 | a0001 | c0001 | t0004 | g0118 | EAS | CHS | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | CHS | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG00639 | hp1 | a0001 | c0001 | t0004 | g0124 | AMR | PUR | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG00639 | hp2 | a0001 | c0001 | t0004 | g0138 | AMR | PUR | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG00642 | hp2 | a0001 | c0001 | t0004 | g0103 | AMR | PUR | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG00673 | hp1 | a0001 | c0004 | t0001 | g0320 | EAS | CHS | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG00673 | hp2 | a0002 | c0002 | t0003 | g0008 | EAS | CHS | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG00738 | hp2 | a0003 | c0003 | t0001 | g0264 | AMR | PUR | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG01069 | hp1 | a0002 | c0002 | t0003 | g0002 | AMR | PUR | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG01069 | hp2 | a0003 | c0003 | t0001 | g0274 | AMR | PUR | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG01071 | hp2 | a0003 | c0003 | t0001 | g0269 | AMR | PUR | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG01081 | hp1 | a0001 | c0001 | t0004 | g0104 | AMR | PUR | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG01099 | hp1 | a0001 | c0001 | t0004 | g0021 | AMR | PUR | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG01099 | hp2 | a0002 | c0002 | t0003 | g0033 | AMR | PUR | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG01106 | hp1 | a0002 | c0002 | t0003 | g0002 | AMR | PUR | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG01106 | hp2 | a0001 | c0001 | t0004 | g0101 | AMR | PUR | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0152 | AMR | PUR | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0018 | AMR | PUR | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG01168 | hp2 | a0003 | c0003 | t0001 | g0272 | AMR | PUR | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0253 | AMR | PUR | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0018 | AMR | PUR | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG01175 | hp1 | a0001 | c0001 | t0004 | g0097 | AMR | PUR | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG01175 | hp2 | a0001 | c0001 | t0005 | g0082 | AMR | PUR | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG01192 | hp1 | a0001 | c0001 | t0004 | g0096 | AMR | PUR | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG01192 | hp2 | a0002 | c0002 | t0003 | g0061 | AMR | PUR | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG01243 | hp1 | a0001 | c0001 | t0004 | g0250 | AMR | PUR | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG01243 | hp2 | a0002 | c0002 | t0003 | g0046 | AMR | PUR | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG01255 | hp1 | a0003 | c0003 | t0001 | g0259 | AMR | CLM | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG01255 | hp2 | a0003 | c0003 | t0001 | g0285 | AMR | CLM | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0019 | AMR | CLM | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | CLM | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0238 | AMR | CLM | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0192 | AMR | CLM | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG01261 | hp1 | a0002 | c0002 | t0003 | g0028 | AMR | CLM | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG01261 | hp2 | a0001 | c0001 | t0004 | g0021 | AMR | CLM | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0205 | AMR | CLM | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG01346 | hp2 | a0002 | c0002 | t0003 | g0013 | AMR | CLM | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0207 | AMR | CLM | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0246 | AMR | CLM | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG01361 | hp1 | a0003 | c0003 | t0001 | g0291 | AMR | CLM | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0242 | AMR | CLM | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | CLM | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG01496 | hp1 | a0003 | c0003 | t0001 | g0236 | AMR | CLM | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG01496 | hp2 | a0003 | c0003 | t0001 | g0288 | AMR | CLM | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0226 | EUR | IBS | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0184 | EUR | IBS | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG01516 | hp1 | a0003 | c0003 | t0001 | g0267 | EUR | IBS | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0022 | EUR | IBS | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0022 | EUR | IBS | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0020 | EUR | IBS | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG01884 | hp1 | a0003 | c0005 | t0001 | g0306 | AFR | ACB | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0149 | AFR | ACB | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0175 | AFR | ACB | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0145 | AFR | ACB | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0179 | AMR | PEL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG01928 | hp2 | a0002 | c0002 | t0003 | g0038 | AMR | PEL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0198 | AMR | PEL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG01934 | hp2 | a0002 | c0002 | t0003 | g0043 | AMR | PEL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG01975 | hp1 | a0002 | c0002 | t0003 | g0001 | AMR | PEL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG01975 | hp2 | a0001 | c0001 | t0004 | g0100 | AMR | PEL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG01978 | hp1 | a0002 | c0002 | t0003 | g0045 | AMR | PEL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0210 | AMR | PEL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG01981 | hp1 | a0001 | c0001 | t0004 | g0099 | AMR | PEL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0200 | AMR | PEL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG01993 | hp1 | a0003 | c0003 | t0001 | g0287 | AMR | PEL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0019 | AMR | PEL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG02004 | hp1 | a0003 | c0003 | t0001 | g0292 | AMR | PEL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG02004 | hp2 | a0002 | c0002 | t0003 | g0001 | AMR | PEL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG02015 | hp1 | a0002 | c0002 | t0003 | g0012 | EAS | KHV | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG02015 | hp2 | a0001 | c0001 | t0004 | g0128 | EAS | KHV | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG02027 | hp1 | a0002 | c0002 | t0003 | g0066 | EAS | KHV | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG02027 | hp2 | a0001 | c0001 | t0004 | g0092 | EAS | KHV | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | KHV | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG02040 | hp2 | a0002 | c0002 | t0003 | g0052 | EAS | KHV | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG02055 | hp1 | a0002 | c0002 | t0003 | g0007 | AFR | ACB | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG02055 | hp2 | a0002 | c0002 | t0003 | g0026 | AFR | ACB | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG02071 | hp1 | a0002 | c0002 | t0003 | g0042 | EAS | KHV | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG02071 | hp2 | a0001 | c0001 | t0004 | g0141 | EAS | KHV | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG02080 | hp1 | a0002 | c0002 | t0003 | g0060 | EAS | KHV | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG02080 | hp2 | a0001 | c0001 | t0004 | g0009 | EAS | KHV | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG02083 | hp1 | a0001 | c0004 | t0001 | g0006 | EAS | KHV | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG02083 | hp2 | a0001 | c0001 | t0004 | g0136 | EAS | KHV | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG02129 | hp1 | a0002 | c0002 | t0003 | g0073 | EAS | KHV | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG02129 | hp2 | a0002 | c0002 | t0003 | g0067 | EAS | KHV | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0148 | AFR | ACB | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG02145 | hp2 | a0003 | c0005 | t0001 | g0304 | AFR | ACB | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG02148 | hp1 | a0003 | c0003 | t0001 | g0282 | AMR | PEL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG02148 | hp2 | a0003 | c0003 | t0001 | g0290 | AMR | PEL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG02155 | hp1 | a0001 | c0001 | t0004 | g0108 | EAS | CDX | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG02155 | hp2 | a0002 | c0002 | t0003 | g0008 | EAS | CDX | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG02165 | hp1 | a0001 | c0001 | t0004 | g0135 | EAS | CDX | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG02165 | hp2 | a0001 | c0001 | t0004 | g0142 | EAS | CDX | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0164 | AFR | ACB | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG02258 | hp2 | a0003 | c0003 | t0001 | g0262 | AFR | ACB | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0206 | AMR | PEL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG02273 | hp2 | a0001 | c0001 | t0004 | g0098 | AMR | PEL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG02280 | hp1 | a0001 | c0004 | t0004 | g0300 | AFR | ACB | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG02280 | hp2 | a0003 | c0003 | t0001 | g0271 | AFR | ACB | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG02572 | hp1 | a0003 | c0003 | t0001 | g0273 | AFR | GWD | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0166 | AFR | GWD | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG02602 | hp1 | a0001 | c0001 | t0004 | g0102 | SAS | PJL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG02602 | hp2 | a0003 | c0003 | t0001 | g0284 | SAS | PJL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0165 | AFR | GWD | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0143 | AFR | GWD | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | GWD | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG02622 | hp2 | a0003 | c0003 | t0001 | g0232 | AFR | GWD | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0158 | AFR | GWD | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG02630 | hp2 | a0003 | c0003 | t0001 | g0266 | AFR | GWD | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG02647 | hp1 | a0003 | c0003 | t0001 | g0270 | AFR | GWD | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG02717 | hp1 | a0003 | c0003 | t0001 | g0277 | AFR | GWD | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | GWD | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0161 | AFR | GWD | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG02723 | hp2 | a0003 | c0003 | t0001 | g0235 | AFR | GWD | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG02735 | hp1 | a0002 | c0002 | t0003 | g0035 | SAS | PJL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0257 | SAS | PJL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0217 | SAS | PJL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG02809 | hp1 | a0001 | c0001 | t0005 | g0088 | AFR | GWD | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0168 | AFR | GWD | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG02818 | hp1 | a0001 | c0008 | t0005 | g0298 | AFR | GWD | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG02818 | hp2 | a0003 | c0003 | t0001 | g0260 | AFR | GWD | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0159 | AFR | GWD | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG02886 | hp2 | a0003 | c0003 | t0001 | g0233 | AFR | GWD | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG02895 | hp1 | a0003 | c0005 | t0001 | g0305 | AFR | GWD | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0146 | AFR | GWD | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG02897 | hp1 | a0003 | c0003 | t0001 | g0225 | AFR | GWD | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0147 | AFR | GWD | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0174 | AFR | ESN | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG02922 | hp2 | a0002 | c0002 | t0003 | g0064 | AFR | ESN | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG02970 | hp1 | a0003 | c0003 | t0001 | g0234 | AFR | ESN | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0154 | AFR | ESN | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG02976 | hp1 | a0003 | c0003 | t0001 | g0275 | AFR | ESN | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0155 | AFR | ESN | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG03041 | hp1 | a0001 | c0004 | t0001 | g0311 | AFR | GWD | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG03041 | hp2 | a0003 | c0005 | t0001 | g0307 | AFR | GWD | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG03098 | hp1 | a0001 | c0001 | t0005 | g0087 | AFR | MSL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0172 | AFR | MSL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG03130 | hp1 | a0001 | c0004 | t0004 | g0299 | AFR | ESN | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG03130 | hp2 | a0003 | c0003 | t0001 | g0276 | AFR | ESN | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0151 | AFR | ESN | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG03139 | hp2 | a0001 | c0001 | t0005 | g0083 | AFR | ESN | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0187 | AFR | ESN | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG03195 | hp2 | a0001 | c0004 | t0004 | g0302 | AFR | ESN | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG03225 | hp1 | a0001 | c0001 | t0005 | g0081 | AFR | MSL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | MSL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0254 | SAS | PJL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG03239 | hp2 | a0001 | c0001 | t0004 | g0106 | SAS | PJL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | MSL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG03453 | hp2 | a0002 | c0002 | t0003 | g0025 | AFR | MSL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0167 | AFR | MSL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0160 | AFR | MSL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0180 | SAS | PJL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0080 | SAS | PJL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0202 | SAS | PJL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0181 | SAS | PJL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG03516 | hp1 | a0001 | c0001 | t0005 | g0084 | AFR | ESN | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG03516 | hp2 | a0003 | c0003 | t0001 | g0231 | AFR | ESN | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG03540 | hp1 | a0001 | c0004 | t0004 | g0296 | AFR | GWD | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0176 | AFR | GWD | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG03579 | hp1 | a0003 | c0003 | t0001 | g0261 | AFR | MSL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG03579 | hp2 | a0001 | c0001 | t0008 | g0150 | AFR | MSL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG03654 | hp1 | a0001 | c0001 | t0004 | g0107 | SAS | PJL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0079 | SAS | PJL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0256 | SAS | PJL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG03669 | hp2 | a0001 | c0001 | t0004 | g0140 | SAS | PJL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0085 | SAS | PJL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG03710 | hp2 | a0002 | c0002 | t0003 | g0040 | SAS | PJL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0228 | SAS | BEB | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG03831 | hp2 | a0002 | c0002 | t0003 | g0065 | SAS | BEB | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG03834 | hp1 | a0002 | c0002 | t0003 | g0036 | SAS | BEB | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG03834 | hp2 | a0003 | c0003 | t0001 | g0289 | SAS | BEB | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG03927 | hp1 | a0001 | c0001 | t0004 | g0095 | SAS | BEB | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG03927 | hp2 | a0002 | c0002 | t0003 | g0034 | SAS | BEB | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0293 | SAS | STU | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0249 | SAS | STU | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG04184 | hp1 | a0004 | c0007 | t0003 | g0063 | SAS | BEB | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0178 | SAS | BEB | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0229 | SAS | STU | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG04199 | hp2 | a0002 | c0002 | t0003 | g0072 | SAS | STU | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG04204 | hp1 | a0001 | c0001 | t0004 | g0105 | SAS | STU | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG04204 | hp2 | a0001 | c0001 | t0006 | g0278 | SAS | STU | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0213 | AFR | YRI | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18522 | hp2 | a0001 | c0004 | t0004 | g0297 | AFR | YRI | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18612 | hp1 | a0002 | c0002 | t0003 | g0002 | EAS | CHB | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0169 | EAS | CHB | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | CHB | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18747 | hp2 | a0002 | c0002 | t0003 | g0055 | EAS | CHB | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0153 | AFR | YRI | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18906 | hp2 | a0001 | c0004 | t0001 | g0309 | AFR | YRI | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18939 | hp1 | a0002 | c0002 | t0003 | g0003 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18939 | hp2 | a0003 | c0003 | t0001 | g0281 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18940 | hp2 | a0002 | c0002 | t0003 | g0071 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18941 | hp2 | a0002 | c0002 | t0003 | g0003 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18942 | hp2 | a0002 | c0002 | t0003 | g0001 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18943 | hp1 | a0002 | c0002 | t0003 | g0003 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18944 | hp1 | a0001 | c0001 | t0004 | g0123 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18944 | hp2 | a0003 | c0003 | t0001 | g0286 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18945 | hp1 | a0002 | c0002 | t0003 | g0076 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18945 | hp2 | a0001 | c0001 | t0004 | g0120 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18946 | hp1 | a0002 | c0002 | t0003 | g0001 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18947 | hp1 | a0002 | c0002 | t0003 | g0012 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18947 | hp2 | a0001 | c0001 | t0004 | g0119 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18948 | hp1 | a0001 | c0004 | t0001 | g0313 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18948 | hp2 | a0001 | c0001 | t0004 | g0015 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18949 | hp2 | a0001 | c0001 | t0004 | g0137 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18953 | hp1 | a0002 | c0002 | t0003 | g0075 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18957 | hp1 | a0002 | c0002 | t0003 | g0059 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18957 | hp2 | a0001 | c0001 | t0004 | g0115 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18960 | hp1 | a0002 | c0002 | t0003 | g0029 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18960 | hp2 | a0002 | c0002 | t0003 | g0001 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18962 | hp2 | a0001 | c0004 | t0001 | g0314 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18963 | hp2 | a0002 | c0002 | t0003 | g0069 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18964 | hp1 | a0001 | c0001 | t0004 | g0222 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18964 | hp2 | a0002 | c0002 | t0003 | g0003 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18965 | hp2 | a0002 | c0002 | t0003 | g0011 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18966 | hp1 | a0002 | c0002 | t0003 | g0013 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18966 | hp2 | a0001 | c0004 | t0001 | g0315 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18968 | hp1 | a0002 | c0002 | t0003 | g0058 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18968 | hp2 | a0001 | c0001 | t0004 | g0127 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18969 | hp1 | a0002 | c0002 | t0003 | g0049 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18969 | hp2 | a0001 | c0001 | t0004 | g0121 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18970 | hp1 | a0001 | c0001 | t0004 | g0129 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18970 | hp2 | a0001 | c0004 | t0001 | g0006 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18971 | hp1 | a0001 | c0001 | t0004 | g0220 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18971 | hp2 | a0001 | c0001 | t0004 | g0122 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18972 | hp1 | a0002 | c0002 | t0003 | g0078 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18973 | hp2 | a0002 | c0002 | t0003 | g0039 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18974 | hp1 | a0002 | c0002 | t0003 | g0027 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18974 | hp2 | a0001 | c0004 | t0001 | g0319 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18977 | hp2 | a0002 | c0002 | t0003 | g0074 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18978 | hp1 | a0001 | c0001 | t0004 | g0091 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18979 | hp1 | a0005 | c0006 | t0003 | g0032 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18980 | hp2 | a0002 | c0002 | t0003 | g0008 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18981 | hp1 | a0002 | c0002 | t0003 | g0002 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18981 | hp2 | a0001 | c0001 | t0004 | g0130 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18984 | hp1 | a0001 | c0001 | t0004 | g0113 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18984 | hp2 | a0002 | c0002 | t0003 | g0030 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18986 | hp1 | a0002 | c0002 | t0003 | g0050 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18986 | hp2 | a0001 | c0001 | t0004 | g0219 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18988 | hp2 | a0001 | c0001 | t0004 | g0094 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18989 | hp2 | a0002 | c0002 | t0003 | g0044 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18990 | hp1 | a0002 | c0002 | t0003 | g0054 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18991 | hp1 | a0001 | c0004 | t0001 | g0310 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18991 | hp2 | a0002 | c0002 | t0003 | g0048 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18992 | hp1 | a0001 | c0001 | t0004 | g0133 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18992 | hp2 | a0002 | c0002 | t0003 | g0001 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18993 | hp1 | a0001 | c0001 | t0004 | g0112 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18994 | hp1 | a0001 | c0004 | t0001 | g0308 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18994 | hp2 | a0002 | c0002 | t0003 | g0053 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA18999 | hp2 | a0001 | c0004 | t0001 | g0312 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA19000 | hp2 | a0003 | c0003 | t0001 | g0283 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA19003 | hp1 | a0001 | c0001 | t0004 | g0139 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA19003 | hp2 | a0002 | c0002 | t0003 | g0068 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA19004 | hp1 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA19004 | hp2 | a0002 | c0002 | t0003 | g0003 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA19009 | hp2 | a0002 | c0002 | t0003 | g0001 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA19010 | hp1 | a0001 | c0001 | t0004 | g0015 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA19010 | hp2 | a0001 | c0004 | t0001 | g0321 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA19011 | hp1 | a0002 | c0002 | t0003 | g0011 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA19012 | hp2 | a0001 | c0001 | t0004 | g0014 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA19030 | hp1 | a0001 | c0004 | t0001 | g0318 | AFR | LWK | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0171 | AFR | LWK | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA19043 | hp1 | a0001 | c0004 | t0004 | g0301 | AFR | LWK | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0162 | AFR | LWK | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA19054 | hp1 | a0001 | c0001 | t0004 | g0134 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA19057 | hp2 | a0001 | c0001 | t0004 | g0090 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA19058 | hp1 | a0001 | c0001 | t0004 | g0221 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA19058 | hp2 | a0002 | c0002 | t0003 | g0056 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA19060 | hp1 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA19060 | hp2 | a0002 | c0002 | t0003 | g0007 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA19062 | hp1 | a0002 | c0002 | t0003 | g0002 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA19062 | hp2 | a0001 | c0001 | t0004 | g0109 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA19064 | hp1 | a0001 | c0001 | t0004 | g0114 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA19064 | hp2 | a0001 | c0004 | t0001 | g0006 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA19065 | hp1 | a0001 | c0001 | t0004 | g0117 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA19065 | hp2 | a0002 | c0002 | t0003 | g0001 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA19068 | hp1 | a0002 | c0002 | t0003 | g0002 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA19068 | hp2 | a0001 | c0001 | t0004 | g0218 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA19074 | hp1 | a0002 | c0002 | t0003 | g0001 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA19076 | hp1 | a0001 | c0001 | t0004 | g0294 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA19076 | hp2 | a0002 | c0002 | t0003 | g0031 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA19077 | hp1 | a0002 | c0002 | t0003 | g0037 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA19077 | hp2 | a0001 | c0004 | t0001 | g0006 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA19078 | hp2 | a0001 | c0004 | t0001 | g0317 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA19080 | hp1 | a0001 | c0001 | t0004 | g0125 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA19080 | hp2 | a0002 | c0002 | t0003 | g0001 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA19081 | hp1 | a0002 | c0002 | t0003 | g0057 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA19081 | hp2 | a0001 | c0001 | t0004 | g0126 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA19084 | hp1 | a0001 | c0001 | t0004 | g0014 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA19084 | hp2 | a0002 | c0002 | t0003 | g0047 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA19088 | hp1 | a0001 | c0001 | t0004 | g0132 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA20129 | hp1 | a0001 | c0004 | t0001 | g0316 | AFR | ASW | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0157 | AFR | ASW | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA20752 | hp1 | a0002 | c0002 | t0003 | g0051 | EUR | TSI | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA20752 | hp2 | a0003 | c0003 | t0001 | g0230 | EUR | TSI | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG02109 | hp1 | a0003 | c0003 | t0001 | g0280 | AFR | ACB | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG02109 | hp2 | a0002 | c0002 | t0003 | g0041 | AFR | ACB | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0163 | AFR | MSL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG03471 | hp2 | a0003 | c0003 | t0001 | g0265 | AFR | MSL | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0017 | AFR | USA | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| HG06807 | hp2 | a0001 | c0001 | t0007 | g0156 | AFR | USA | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0144 | AFR | USA | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | USA | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA21309 | hp1 | a0001 | c0004 | t0004 | g0303 | AFR | LWK | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0212 | AFR | LWK | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0237 | REF | REF | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0010 | REF | REF | NUP54_chr4_76109664_76153397 | NUP54 | chr4 | 76109664 | 76153397 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:76132681 | T | C | 1 | a0003 | 43 | HG00140.hp1 HG00738.hp2 HG01069.hp2 others(40): Show |
missense_variant | MODERATE | c.749A>G | p.Asn250Ser | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 6/12 | 772/2249 | 749/1524 | 250/507 | chr4 | 76132681 | |||
| chr4:76144165 | C | CTGT | 3 | a0002 a0004 a0005 |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
disruptive_inframe_insertion | MODERATE | c.276_278dupACA | p.Gln93dup | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/12 | 301/2249 | 278/1524 | 93/507 | chr4 | 76144165 | |||
| chr4:76144239 | T | G | 1 | a0004 | 1 | HG04184.hp1 | missense_variant | MODERATE | c.205A>C | p.Thr69Pro | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/12 | 228/2249 | 205/1524 | 69/507 | chr4 | 76144239 | |||
| chr4:76144473 | C | G | 1 | a0005 | 1 | NA18979.hp1 | missense_variant&splice_region_variant | MODERATE | c.68G>C | p.Gly23Ala | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 2/12 | 91/2249 | 68/1524 | 23/507 | chr4 | 76144473 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:76132650 | C | T | 1 | a0001c0008 | 1 | HG02818.hp1 | synonymous_variant | LOW | c.780G>A | p.Thr260Thr | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 6/12 | 803/2249 | 780/1524 | 260/507 | chr4 | 76132650 | |||
| chr4:76134321 | A | G | 3 | a0002c0002 a0004c0007 a0005c0006 |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
synonymous_variant | LOW | c.564T>C | p.Asp188Asp | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 5/12 | 587/2249 | 564/1524 | 188/507 | chr4 | 76134321 | |||
| chr4:76136348 | A | G | 3 | a0002c0002 a0004c0007 a0005c0006 |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
synonymous_variant | LOW | c.360T>C | p.Thr120Thr | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 4/12 | 383/2249 | 360/1524 | 120/507 | chr4 | 76136348 | |||
| chr4:76144427 | T | C | 3 | a0002c0002 a0004c0007 a0005c0006 |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
synonymous_variant | LOW | c.114A>G | p.Ala38Ala | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 2/12 | 137/2249 | 114/1524 | 38/507 | chr4 | 76144427 | |||
| chr4:76148321 | G | A | 3 | a0001c0004 a0001c0008 a0003c0005 |
30 | HG00673.hp1 HG01884.hp1 HG02083.hp1 others(27): Show |
synonymous_variant | LOW | c.54C>T | p.Thr18Thr | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/12 | 77/2249 | 54/1524 | 18/507 | chr4 | 76148321 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:76114729 | A | T | 1 | a0001c0001t0008 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*637T>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 12/12 | 637 | chr4 | 76114729 | ||||||
| chr4:76114742 | T | A | 3 | a0002c0002t0003 a0004c0007t0003 a0005c0006t0003 |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*624A>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 12/12 | 624 | chr4 | 76114742 | ||||||
| chr4:76114754 | TTAAG | T | 2 | a0001c0001t0004 a0001c0004t0004 |
77 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*608_*611delCTTA | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 12/12 | 608 | chr4 | 76114754 | ||||||
| chr4:76114761 | G | A | 3 | a0002c0002t0003 a0004c0007t0003 a0005c0006t0003 |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*605C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 12/12 | 605 | chr4 | 76114761 | ||||||
| chr4:76114892 | C | T | 1 | a0001c0001t0006 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*474G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 12/12 | 474 | chr4 | 76114892 | ||||||
| chr4:76114929 | A | C | 1 | a0001c0001t0007 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*437T>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 12/12 | 437 | chr4 | 76114929 | ||||||
| chr4:76114969 | T | C | 3 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0008 |
100 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*397A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 12/12 | 397 | chr4 | 76114969 | ||||||
| chr4:76114975 | G | C | 10 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(7): Show |
271 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(268): Show |
3_prime_UTR_variant | MODIFIER | c.*391C>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 12/12 | 391 | chr4 | 76114975 | ||||||
| chr4:76115216 | G | A | 3 | a0002c0002t0003 a0004c0007t0003 a0005c0006t0003 |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*150C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 12/12 | 150 | chr4 | 76115216 | ||||||
| chr4:76115253 | T | G | 3 | a0002c0002t0003 a0004c0007t0003 a0005c0006t0003 |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*113A>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 12/12 | 113 | chr4 | 76115253 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:76115526 | T | A | 6 | a0001c0001t0002g0161 a0001c0001t0002g0162 a0001c0001t0002g0163 others(3): Show |
6 | HG02258.hp1 HG02572.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1396-32A>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 11/11 | chr4 | 76115526 | |||||||
| chr4:76115591 | C | G | 1 | a0001c0001t0004g0221 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1396-97G>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 11/11 | chr4 | 76115591 | |||||||
| chr4:76115683 | T | A | 3 | a0003c0003t0001g0231 a0003c0003t0001g0265 a0003c0003t0001g0276 |
3 | HG03130.hp2 HG03471.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1396-189A>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 11/11 | chr4 | 76115683 | |||||||
| chr4:76115858 | T | G | 91 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0016 others(88): Show |
102 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.1396-364A>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 11/11 | chr4 | 76115858 | |||||||
| chr4:76115878 | G | A | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1396-384C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 11/11 | chr4 | 76115878 | |||||||
| chr4:76115892 | T | C | 91 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0016 others(88): Show |
102 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.1396-398A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 11/11 | chr4 | 76115892 | |||||||
| chr4:76116125 | A | T | 1 | a0002c0002t0003g0054 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1396-631T>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 11/11 | chr4 | 76116125 | |||||||
| chr4:76116372 | T | C | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1396-878A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 11/11 | chr4 | 76116372 | |||||||
| chr4:76116476 | T | C | 1 | a0002c0002t0003g0046 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1396-982A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 11/11 | chr4 | 76116476 | |||||||
| chr4:76116629 | A | G | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1395+1035T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 11/11 | chr4 | 76116629 | |||||||
| chr4:76116693 | C | T | 1 | a0003c0003t0001g0234 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1395+971G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 11/11 | chr4 | 76116693 | |||||||
| chr4:76116807 | G | T | 3 | a0001c0001t0001g0022 a0001c0001t0001g0242 a0001c0001t0001g0243 |
4 | HG00738.hp1 HG01361.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1395+857C>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 11/11 | chr4 | 76116807 | |||||||
| chr4:76117016 | C | T | 1 | a0001c0001t0001g0253 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1395+648G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 11/11 | chr4 | 76117016 | |||||||
| chr4:76117022 | C | G | 1 | a0001c0001t0001g0253 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1395+642G>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 11/11 | chr4 | 76117022 | |||||||
| chr4:76117023 | C | G | 1 | a0001c0001t0001g0253 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1395+641G>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 11/11 | chr4 | 76117023 | |||||||
| chr4:76117027 | T | A | 1 | a0001c0001t0001g0253 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1395+637A>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 11/11 | chr4 | 76117027 | |||||||
| chr4:76117030 | T | G | 1 | a0001c0001t0001g0253 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1395+634A>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 11/11 | chr4 | 76117030 | |||||||
| chr4:76117031 | T | C | 1 | a0001c0001t0001g0253 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1395+633A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 11/11 | chr4 | 76117031 | |||||||
| chr4:76117033 | A | G | 1 | a0001c0001t0001g0253 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1395+631T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 11/11 | chr4 | 76117033 | |||||||
| chr4:76117040 | T | A | 1 | a0001c0001t0001g0253 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1395+624A>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 11/11 | chr4 | 76117040 | |||||||
| chr4:76117292 | C | A | 225 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0016 others(222): Show |
266 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(263): Show |
intron_variant | MODIFIER | c.1395+372G>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 11/11 | chr4 | 76117292 | |||||||
| chr4:76117320 | T | C | 134 | a0001c0001t0004g0009 a0001c0001t0004g0014 a0001c0001t0004g0015 others(131): Show |
164 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(161): Show |
intron_variant | MODIFIER | c.1395+344A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 11/11 | chr4 | 76117320 | |||||||
| chr4:76117417 | C | T | 163 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0016 others(160): Show |
179 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.1395+247G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 11/11 | chr4 | 76117417 | |||||||
| chr4:76117421 | C | G | 2 | a0003c0003t0001g0231 a0003c0003t0001g0276 |
2 | HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1395+243G>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 11/11 | chr4 | 76117421 | |||||||
| chr4:76117445 | C | G | 3 | a0002c0002t0003g0033 a0002c0002t0003g0040 a0002c0002t0003g0041 |
3 | HG01099.hp2 HG02109.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.1395+219G>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 11/11 | chr4 | 76117445 | |||||||
| chr4:76117446 | C | T | 3 | a0002c0002t0003g0033 a0002c0002t0003g0040 a0002c0002t0003g0041 |
3 | HG01099.hp2 HG02109.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.1395+218G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 11/11 | chr4 | 76117446 | |||||||
| chr4:76117448 | G | A | 1 | a0002c0002t0003g0046 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1395+216C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 11/11 | chr4 | 76117448 | |||||||
| chr4:76117454 | T | C | 1 | a0001c0008t0005g0298 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1395+210A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 11/11 | chr4 | 76117454 | |||||||
| chr4:76117490 | C | T | 72 | a0001c0001t0004g0009 a0001c0001t0004g0014 a0001c0001t0004g0015 others(69): Show |
77 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.1395+174G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 11/11 | chr4 | 76117490 | |||||||
| chr4:76117509 | G | C | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1395+155C>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 11/11 | chr4 | 76117509 | |||||||
| chr4:76117541 | G | A | 1 | a0001c0008t0005g0298 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1395+123C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 11/11 | chr4 | 76117541 | |||||||
| chr4:76117567 | TCTCA | T | 3 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0004t0004g0301 |
3 | HG01081.hp2 HG01258.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1395+93_1395+96del others(4): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 11/11 | chr4 | 76117567 | |||||||
| chr4:76117654 | C | T | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1395+10G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 11/11 | chr4 | 76117654 | |||||||
| chr4:76117821 | T | A | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1285-47A>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 10/11 | chr4 | 76117821 | |||||||
| chr4:76117903 | C | T | 4 | a0001c0004t0004g0296 a0001c0004t0004g0299 a0001c0004t0004g0300 others(1): Show |
4 | HG02280.hp1 HG03130.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1285-129G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 10/11 | chr4 | 76117903 | |||||||
| chr4:76118021 | G | C | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1284+54C>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 10/11 | chr4 | 76118021 | |||||||
| chr4:76118028 | G | T | 1 | a0002c0002t0003g0064 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1284+47C>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 10/11 | chr4 | 76118028 | |||||||
| chr4:76118040 | A | T | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1284+35T>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 10/11 | chr4 | 76118040 | |||||||
| chr4:76118198 | T | C | 1 | a0003c0003t0001g0234 | 1 | HG02970.hp1 | splice_region_variant&intron_variant | LOW | c.1165-4A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76118198 | |||||||
| chr4:76118199 | A | G | 71 | a0001c0001t0004g0009 a0001c0001t0004g0014 a0001c0001t0004g0015 others(68): Show |
76 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(73): Show |
splice_region_variant&intron_variant | LOW | c.1165-5T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76118199 | |||||||
| chr4:76118368 | T | C | 225 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0016 others(222): Show |
266 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(263): Show |
intron_variant | MODIFIER | c.1165-174A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76118368 | |||||||
| chr4:76118378 | A | C | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1165-184T>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76118378 | |||||||
| chr4:76118384 | T | G | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1165-190A>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76118384 | |||||||
| chr4:76118568 | C | CGGGGGTG others(6): Show |
1 | a0001c0001t0002g0293 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1165-375_1165-374i others(15): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76118568 | |||||||
| chr4:76118568 | C | T | 1 | a0001c0008t0005g0298 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1165-374G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76118568 | |||||||
| chr4:76118569 | G | GGGGGTGG others(3): Show |
1 | a0001c0001t0004g0130 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1165-376_1165-375i others(12): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76118569 | |||||||
| chr4:76118573 | T | G | 2 | a0001c0001t0002g0293 a0001c0001t0004g0130 |
2 | HG04115.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.1165-379A>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76118573 | |||||||
| chr4:76118573 | T | TG | 26 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0245 others(23): Show |
26 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(23): Show |
intron_variant | MODIFIER | c.1165-380dupC | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76118573 | |||||||
| chr4:76118573 | T | TGGGGCGG others(2): Show |
34 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0079 others(31): Show |
41 | HG00423.hp2 HG01070.hp1 HG01071.hp2 others(38): Show |
intron_variant | MODIFIER | c.1165-380_1165-379i others(11): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76118573 | |||||||
| chr4:76118573 | T | TGGGGCGG others(3): Show |
41 | a0001c0001t0001g0248 a0001c0001t0002g0018 a0001c0001t0002g0019 others(38): Show |
44 | HG00280.hp2 HG00544.hp2 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.1165-380_1165-379i others(12): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76118573 | |||||||
| chr4:76118573 | T | TGGGGCGG others(4): Show |
23 | a0001c0001t0002g0145 a0001c0001t0002g0147 a0001c0001t0002g0153 others(20): Show |
25 | HG00558.hp1 HG00639.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.1165-380_1165-379i others(13): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76118573 | |||||||
| chr4:76118573 | T | TGGGGCGG others(5): Show |
16 | a0001c0001t0002g0143 a0001c0001t0002g0144 a0001c0001t0002g0146 others(13): Show |
16 | HG00438.hp1 HG00544.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.1165-380_1165-379i others(14): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76118573 | |||||||
| chr4:76118573 | T | TGGGGCGG others(6): Show |
6 | a0001c0001t0002g0159 a0001c0001t0002g0193 a0001c0001t0004g0119 others(3): Show |
6 | HG02165.hp2 HG02886.hp1 NA18947.hp2 others(3): Show |
intron_variant | MODIFIER | c.1165-380_1165-379i others(15): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76118573 | |||||||
| chr4:76118573 | T | TGGGGCGG others(7): Show |
2 | a0001c0001t0002g0217 a0001c0001t0004g0108 |
2 | HG02155.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.1165-380_1165-379i others(16): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76118573 | |||||||
| chr4:76118573 | TG | T | 69 | a0001c0001t0001g0224 a0001c0001t0004g0014 a0001c0001t0004g0112 others(66): Show |
95 | HG00323.hp1 HG00423.hp1 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.1165-380delC | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76118573 | |||||||
| chr4:76118577 | G | GCGGGGGG others(3): Show |
1 | a0001c0001t0004g0110 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1165-384_1165-383i others(12): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76118577 | |||||||
| chr4:76118579 | G | C | 2 | a0001c0001t0004g0112 a0001c0001t0004g0115 |
2 | NA18957.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.1165-385C>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76118579 | |||||||
| chr4:76118583 | G | T | 85 | a0001c0001t0002g0143 a0001c0001t0002g0144 a0001c0001t0002g0145 others(82): Show |
111 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.1165-389C>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76118583 | |||||||
| chr4:76118641 | T | C | 66 | a0001c0001t0005g0081 a0001c0001t0005g0082 a0001c0001t0005g0083 others(63): Show |
91 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.1165-447A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76118641 | |||||||
| chr4:76118727 | G | A | 4 | a0001c0004t0004g0296 a0001c0004t0004g0299 a0001c0004t0004g0300 others(1): Show |
4 | HG02280.hp1 HG03130.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1165-533C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76118727 | |||||||
| chr4:76118734 | G | A | 1 | a0001c0001t0004g0250 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1165-540C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76118734 | |||||||
| chr4:76118747 | G | A | 2 | a0001c0001t0004g0090 a0001c0001t0004g0132 |
2 | NA19057.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.1165-553C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76118747 | |||||||
| chr4:76118820 | T | C | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1165-626A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76118820 | |||||||
| chr4:76118880 | C | T | 1 | a0001c0001t0002g0179 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1165-686G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76118880 | |||||||
| chr4:76118931 | G | A | 1 | a0001c0001t0002g0202 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1165-737C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76118931 | |||||||
| chr4:76118962 | C | T | 4 | a0001c0004t0004g0296 a0001c0004t0004g0299 a0001c0004t0004g0300 others(1): Show |
4 | HG02280.hp1 HG03130.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1165-768G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76118962 | |||||||
| chr4:76119022 | A | T | 72 | a0001c0001t0004g0009 a0001c0001t0004g0014 a0001c0001t0004g0015 others(69): Show |
77 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.1165-828T>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76119022 | |||||||
| chr4:76119258 | G | A | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1165-1064C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76119258 | |||||||
| chr4:76119271 | T | C | 224 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0016 others(221): Show |
265 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(262): Show |
intron_variant | MODIFIER | c.1165-1077A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76119271 | |||||||
| chr4:76119294 | G | A | 71 | a0001c0001t0004g0009 a0001c0001t0004g0014 a0001c0001t0004g0015 others(68): Show |
76 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.1165-1100C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76119294 | |||||||
| chr4:76119334 | T | C | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1165-1140A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76119334 | |||||||
| chr4:76119542 | C | T | 1 | a0001c0001t0002g0193 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1165-1348G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76119542 | |||||||
| chr4:76119542 | CT | C | 174 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0016 others(171): Show |
193 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.1165-1349delA | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76119542 | |||||||
| chr4:76119542 | CTT | C | 63 | a0001c0001t0002g0079 a0001c0001t0004g0130 a0002c0002t0003g0001 others(60): Show |
88 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.1165-1350_1165-134 others(6): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76119542 | |||||||
| chr4:76119543 | T | C | 1 | a0001c0001t0002g0193 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1165-1349A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76119543 | |||||||
| chr4:76119658 | G | A | 4 | a0002c0002t0003g0030 a0002c0002t0003g0055 a0002c0002t0003g0066 others(1): Show |
4 | HG02027.hp1 HG02129.hp2 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.1165-1464C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76119658 | |||||||
| chr4:76119677 | T | C | 225 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0016 others(222): Show |
266 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(263): Show |
intron_variant | MODIFIER | c.1165-1483A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76119677 | |||||||
| chr4:76119710 | G | A | 4 | a0001c0004t0004g0296 a0001c0004t0004g0299 a0001c0004t0004g0300 others(1): Show |
4 | HG02280.hp1 HG03130.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1165-1516C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76119710 | |||||||
| chr4:76119773 | G | A | 3 | a0002c0002t0003g0029 a0002c0002t0003g0036 a0002c0002t0003g0056 |
3 | HG03834.hp1 NA18960.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.1165-1579C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76119773 | |||||||
| chr4:76119842 | T | G | 1 | a0001c0004t0001g0311 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1165-1648A>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76119842 | |||||||
| chr4:76119855 | C | T | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1165-1661G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76119855 | |||||||
| chr4:76119893 | T | A | 1 | a0001c0001t0001g0249 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1165-1699A>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76119893 | |||||||
| chr4:76119910 | A | T | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1165-1716T>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76119910 | |||||||
| chr4:76120083 | A | G | 3 | a0001c0001t0005g0081 a0001c0001t0005g0082 a0001c0001t0005g0083 |
3 | HG01175.hp2 HG03139.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1165-1889T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76120083 | |||||||
| chr4:76120099 | C | T | 163 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0016 others(160): Show |
179 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.1165-1905G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76120099 | |||||||
| chr4:76120101 | C | T | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1165-1907G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76120101 | |||||||
| chr4:76120271 | C | G | 1 | a0001c0001t0004g0124 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1165-2077G>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76120271 | |||||||
| chr4:76120297 | T | C | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1165-2103A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76120297 | |||||||
| chr4:76120304 | T | G | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1165-2110A>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76120304 | |||||||
| chr4:76120381 | G | T | 225 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0016 others(222): Show |
266 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(263): Show |
intron_variant | MODIFIER | c.1165-2187C>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76120381 | |||||||
| chr4:76120401 | G | A | 3 | a0001c0001t0005g0081 a0001c0001t0005g0082 a0001c0001t0005g0083 |
3 | HG01175.hp2 HG03139.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1165-2207C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76120401 | |||||||
| chr4:76120421 | CT | C | 48 | a0001c0001t0001g0239 a0001c0004t0001g0006 a0001c0004t0001g0308 others(45): Show |
51 | HG00140.hp1 HG00673.hp1 HG01069.hp2 others(48): Show |
intron_variant | MODIFIER | c.1165-2228delA | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76120421 | |||||||
| chr4:76120421 | CTTT | C | 9 | a0001c0001t0002g0178 a0001c0001t0002g0194 a0001c0001t0002g0195 others(6): Show |
9 | HG00438.hp1 HG00597.hp1 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.1165-2230_1165-222 others(7): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76120421 | |||||||
| chr4:76120421 | CTTTT | C | 148 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0016 others(145): Show |
164 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.1165-2231_1165-222 others(8): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76120421 | |||||||
| chr4:76120421 | CTTTTT | C | 6 | a0001c0001t0002g0184 a0001c0004t0004g0296 a0001c0004t0004g0299 others(3): Show |
6 | HG01515.hp2 HG02280.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1165-2232_1165-222 others(9): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76120421 | |||||||
| chr4:76120427 | T | C | 2 | a0001c0001t0005g0087 a0001c0001t0005g0088 |
2 | HG02809.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1165-2233A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76120427 | |||||||
| chr4:76120443 | T | C | 59 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(56): Show |
84 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.1165-2249A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76120443 | |||||||
| chr4:76120443 | T | TC | 3 | a0002c0002t0003g0045 a0002c0002t0003g0048 a0002c0002t0003g0066 |
3 | HG01978.hp1 HG02027.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.1165-2250_1165-224 others(5): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76120443 | |||||||
| chr4:76120444 | T | C | 1 | a0001c0001t0002g0173 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1165-2250A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76120444 | |||||||
| chr4:76120459 | G | T | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1165-2265C>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76120459 | |||||||
| chr4:76120465 | T | C | 2 | a0003c0003t0001g0235 a0003c0003t0001g0236 |
2 | HG01496.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1165-2271A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76120465 | |||||||
| chr4:76120485 | A | C | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1165-2291T>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76120485 | |||||||
| chr4:76120491 | G | A | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1165-2297C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76120491 | |||||||
| chr4:76120515 | C | T | 5 | a0001c0001t0002g0183 a0001c0001t0002g0185 a0001c0001t0002g0189 others(2): Show |
5 | HG02040.hp1 NA18940.hp1 NA18946.hp2 others(2): Show |
intron_variant | MODIFIER | c.1165-2321G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76120515 | |||||||
| chr4:76120574 | A | G | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1165-2380T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76120574 | |||||||
| chr4:76120618 | G | A | 64 | a0001c0001t0004g0009 a0001c0001t0004g0014 a0001c0001t0004g0015 others(61): Show |
69 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.1165-2424C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76120618 | |||||||
| chr4:76120635 | G | A | 4 | a0001c0004t0004g0296 a0001c0004t0004g0299 a0001c0004t0004g0300 others(1): Show |
4 | HG02280.hp1 HG03130.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1165-2441C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76120635 | |||||||
| chr4:76120674 | G | A | 71 | a0001c0001t0004g0009 a0001c0001t0004g0014 a0001c0001t0004g0015 others(68): Show |
76 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.1165-2480C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76120674 | |||||||
| chr4:76120678 | C | T | 3 | a0001c0004t0004g0297 a0001c0004t0004g0301 a0001c0004t0004g0302 |
3 | HG03195.hp2 NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1165-2484G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76120678 | |||||||
| chr4:76121370 | G | T | 1 | a0001c0001t0004g0134 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1165-3176C>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76121370 | |||||||
| chr4:76121628 | G | A | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1164+3021C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76121628 | |||||||
| chr4:76121636 | T | A | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1164+3013A>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76121636 | |||||||
| chr4:76121659 | T | C | 1 | a0001c0001t0002g0158 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1164+2990A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76121659 | |||||||
| chr4:76121938 | TG | T | 4 | a0001c0001t0004g0092 a0001c0001t0004g0116 a0001c0001t0004g0126 others(1): Show |
4 | HG00544.hp1 HG02027.hp2 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.1164+2710delC | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76121938 | |||||||
| chr4:76121939 | G | T | 1 | a0001c0001t0004g0130 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1164+2710C>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76121939 | |||||||
| chr4:76122004 | T | C | 1 | a0001c0001t0002g0160 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1164+2645A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76122004 | |||||||
| chr4:76122005 | A | G | 1 | a0001c0004t0004g0303 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1164+2644T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76122005 | |||||||
| chr4:76122060 | G | T | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1164+2589C>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76122060 | |||||||
| chr4:76122199 | G | A | 2 | a0001c0001t0002g0174 a0001c0001t0002g0175 |
2 | HG01891.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1164+2450C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76122199 | |||||||
| chr4:76122297 | T | C | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1164+2352A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76122297 | |||||||
| chr4:76122361 | C | T | 6 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0149 others(3): Show |
8 | HG01884.hp2 HG02622.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1164+2288G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76122361 | |||||||
| chr4:76122362 | AC | A | 4 | a0001c0004t0004g0296 a0001c0004t0004g0299 a0001c0004t0004g0300 others(1): Show |
4 | HG02280.hp1 HG03130.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1164+2286delG | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76122362 | |||||||
| chr4:76122401 | A | G | 1 | a0001c0001t0002g0295 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1164+2248T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76122401 | |||||||
| chr4:76122450 | C | A | 3 | a0001c0004t0004g0297 a0001c0004t0004g0301 a0001c0004t0004g0302 |
3 | HG03195.hp2 NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1164+2199G>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76122450 | |||||||
| chr4:76122650 | T | C | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1164+1999A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76122650 | |||||||
| chr4:76122676 | C | T | 1 | a0001c0001t0004g0140 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1164+1973G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76122676 | |||||||
| chr4:76122708 | T | C | 1 | a0002c0002t0003g0046 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1164+1941A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76122708 | |||||||
| chr4:76122781 | T | C | 91 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0016 others(88): Show |
102 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.1164+1868A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76122781 | |||||||
| chr4:76122789 | A | G | 67 | a0001c0001t0004g0009 a0001c0001t0004g0014 a0001c0001t0004g0015 others(64): Show |
72 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.1164+1860T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76122789 | |||||||
| chr4:76122792 | G | T | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1164+1857C>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76122792 | |||||||
| chr4:76122794 | G | GAACCACC others(3): Show |
1 | a0002c0002t0003g0031 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1164+1845_1164+185 others(14): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76122794 | |||||||
| chr4:76122808 | T | C | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1164+1841A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76122808 | |||||||
| chr4:76122826 | T | C | 72 | a0001c0001t0004g0009 a0001c0001t0004g0014 a0001c0001t0004g0015 others(69): Show |
77 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.1164+1823A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76122826 | |||||||
| chr4:76122971 | G | A | 4 | a0001c0004t0004g0296 a0001c0004t0004g0299 a0001c0004t0004g0300 others(1): Show |
4 | HG02280.hp1 HG03130.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1164+1678C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76122971 | |||||||
| chr4:76123084 | C | T | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1164+1565G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76123084 | |||||||
| chr4:76123105 | C | T | 243 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0016 others(240): Show |
287 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(284): Show |
intron_variant | MODIFIER | c.1164+1544G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76123105 | |||||||
| chr4:76123238 | C | T | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1164+1411G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76123238 | |||||||
| chr4:76123281 | C | T | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1164+1368G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76123281 | |||||||
| chr4:76123350 | C | G | 1 | a0001c0001t0004g0021 | 2 | HG01099.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.1164+1299G>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76123350 | |||||||
| chr4:76123365 | A | G | 64 | a0001c0001t0004g0009 a0001c0001t0004g0014 a0001c0001t0004g0015 others(61): Show |
69 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.1164+1284T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76123365 | |||||||
| chr4:76123387 | T | C | 2 | a0001c0001t0004g0091 a0001c0001t0004g0117 |
2 | NA18978.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.1164+1262A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76123387 | |||||||
| chr4:76123450 | C | T | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1164+1199G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76123450 | |||||||
| chr4:76123653 | C | T | 1 | a0001c0008t0005g0298 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1164+996G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76123653 | |||||||
| chr4:76123658 | A | G | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1164+991T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76123658 | |||||||
| chr4:76123803 | T | C | 133 | a0001c0001t0004g0009 a0001c0001t0004g0014 a0001c0001t0004g0015 others(130): Show |
163 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(160): Show |
intron_variant | MODIFIER | c.1164+846A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76123803 | |||||||
| chr4:76123851 | G | A | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1164+798C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76123851 | |||||||
| chr4:76124016 | T | C | 1 | a0001c0001t0002g0187 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1164+633A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76124016 | |||||||
| chr4:76124037 | T | C | 1 | a0001c0001t0004g0133 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1164+612A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76124037 | |||||||
| chr4:76124441 | C | T | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1164+208G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76124441 | |||||||
| chr4:76124575 | A | T | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1164+74T>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76124575 | |||||||
| chr4:76124583 | ATATT | A | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1164+62_1164+65del others(4): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76124583 | |||||||
| chr4:76124609 | T | G | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1164+40A>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76124609 | |||||||
| chr4:76124624 | TGG | T | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1164+23_1164+24del others(2): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76124624 | |||||||
| chr4:76124629 | G | C | 4 | a0001c0004t0004g0296 a0001c0004t0004g0299 a0001c0004t0004g0300 others(1): Show |
4 | HG02280.hp1 HG03130.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1164+20C>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 9/11 | chr4 | 76124629 | |||||||
| chr4:76124783 | A | G | 1 | a0001c0001t0004g0130 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1057-27T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76124783 | |||||||
| chr4:76124784 | G | A | 1 | a0001c0001t0004g0130 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1057-28C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76124784 | |||||||
| chr4:76124832 | TTCTAA | T | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1057-81_1057-77del others(5): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76124832 | |||||||
| chr4:76124948 | T | C | 1 | a0002c0002t0003g0052 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1057-192A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76124948 | |||||||
| chr4:76124999 | GA | G | 5 | a0001c0004t0004g0296 a0001c0004t0004g0299 a0001c0004t0004g0300 others(2): Show |
5 | HG02280.hp1 HG02280.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1057-244delT | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76124999 | |||||||
| chr4:76125061 | A | G | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1057-305T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125061 | |||||||
| chr4:76125139 | G | GA | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1057-384dupT | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125139 | |||||||
| chr4:76125258 | CAACAGAG others(33): Show |
C | 12 | a0002c0002t0003g0003 a0002c0002t0003g0008 a0002c0002t0003g0031 others(9): Show |
18 | HG00558.hp2 HG00673.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.1057-542_1057-503d others(42): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125258 | |||||||
| chr4:76125269 | A | G | 50 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0007 others(47): Show |
69 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.1057-513T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125269 | |||||||
| chr4:76125276 | TCTCACAG others(37): Show |
T | 2 | a0002c0002t0003g0025 a0002c0002t0003g0026 |
2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1057-564_1057-521d others(46): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125276 | |||||||
| chr4:76125276 | TCTCACAG others(43): Show |
T | 1 | a0002c0002t0003g0064 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1057-570_1057-521d others(52): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125276 | |||||||
| chr4:76125278 | T | A | 47 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0007 others(44): Show |
66 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.1057-522A>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125278 | |||||||
| chr4:76125280 | ACAGAAAC others(29): Show |
A | 4 | a0002c0002t0003g0002 a0002c0002t0003g0040 a0002c0002t0003g0041 others(1): Show |
6 | HG01069.hp1 HG01192.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.1057-560_1057-525d others(38): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125280 | |||||||
| chr4:76125282 | AGAAACAA others(27): Show |
A | 30 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0007 others(27): Show |
34 | HG00423.hp1 HG00609.hp1 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.1057-560_1057-527d others(36): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125282 | |||||||
| chr4:76125283 | G | C | 17 | a0002c0002t0003g0001 a0002c0002t0003g0007 a0002c0002t0003g0012 others(14): Show |
26 | HG00597.hp2 HG01099.hp2 HG01934.hp2 others(23): Show |
intron_variant | MODIFIER | c.1057-527C>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125283 | |||||||
| chr4:76125283 | GAAACAAA | G | 15 | a0001c0004t0001g0006 a0001c0004t0001g0308 a0001c0004t0001g0309 others(12): Show |
18 | HG00673.hp1 HG02083.hp1 HG03041.hp1 others(15): Show |
intron_variant | MODIFIER | c.1057-534_1057-528d others(9): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125283 | |||||||
| chr4:76125284 | AAACAAAA others(25): Show |
A | 15 | a0002c0002t0003g0001 a0002c0002t0003g0007 a0002c0002t0003g0012 others(12): Show |
24 | HG00597.hp2 HG01099.hp2 HG01934.hp2 others(21): Show |
intron_variant | MODIFIER | c.1057-560_1057-529d others(34): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125284 | |||||||
| chr4:76125285 | A | C | 2 | a0002c0002t0003g0044 a0002c0002t0003g0072 |
2 | HG04199.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.1057-529T>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125285 | |||||||
| chr4:76125286 | ACAAAAAA others(23): Show |
A | 2 | a0002c0002t0003g0044 a0002c0002t0003g0072 |
2 | HG04199.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.1057-560_1057-531d others(32): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125286 | |||||||
| chr4:76125316 | T | TCA | 34 | a0001c0001t0001g0249 a0001c0001t0002g0016 a0001c0001t0002g0017 others(31): Show |
36 | HG00544.hp1 HG00639.hp1 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.1057-562_1057-561d others(4): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125316 | |||||||
| chr4:76125316 | T | TCACA | 10 | a0001c0001t0002g0149 a0001c0001t0002g0160 a0001c0001t0002g0212 others(7): Show |
10 | HG01884.hp1 HG01884.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1057-564_1057-561d others(6): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125316 | |||||||
| chr4:76125316 | T | TCACACAC others(3): Show |
3 | a0001c0004t0004g0297 a0001c0004t0004g0301 a0001c0004t0004g0302 |
3 | HG03195.hp2 NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1057-570_1057-561d others(12): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125316 | |||||||
| chr4:76125316 | TCA | T | 84 | a0001c0001t0001g0022 a0001c0001t0001g0228 a0001c0001t0001g0242 others(81): Show |
91 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.1057-562_1057-561d others(4): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125316 | |||||||
| chr4:76125316 | TCACA | T | 14 | a0001c0001t0005g0087 a0001c0004t0001g0006 a0001c0004t0001g0308 others(11): Show |
17 | HG00673.hp1 HG02083.hp1 HG03098.hp1 others(14): Show |
intron_variant | MODIFIER | c.1057-564_1057-561d others(6): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125316 | |||||||
| chr4:76125316 | TCACACAC others(3): Show |
T | 1 | a0001c0001t0004g0103 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1057-570_1057-561d others(12): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125316 | |||||||
| chr4:76125330 | A | G | 1 | a0002c0002t0003g0046 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1057-574T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125330 | |||||||
| chr4:76125331 | C | T | 1 | a0002c0002t0003g0046 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1057-575G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125331 | |||||||
| chr4:76125332 | A | G | 3 | a0002c0002t0003g0046 a0002c0002t0003g0069 a0002c0002t0003g0072 |
3 | HG01243.hp2 HG04199.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.1057-576T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125332 | |||||||
| chr4:76125334 | A | G | 23 | a0002c0002t0003g0001 a0002c0002t0003g0007 a0002c0002t0003g0012 others(20): Show |
35 | HG00597.hp2 HG01099.hp2 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.1057-578T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125334 | |||||||
| chr4:76125335 | C | T | 3 | a0002c0002t0003g0048 a0002c0002t0003g0053 a0002c0002t0003g0074 |
3 | NA18977.hp2 NA18991.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.1057-579G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125335 | |||||||
| chr4:76125336 | A | G | 47 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0007 others(44): Show |
66 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.1057-580T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125336 | |||||||
| chr4:76125338 | A | ACGTG | 5 | a0002c0002t0003g0008 a0002c0002t0003g0042 a0002c0002t0003g0062 others(2): Show |
7 | HG00558.hp2 HG00673.hp2 HG02071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1057-583_1057-582i others(6): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125338 | |||||||
| chr4:76125338 | A | G | 47 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0007 others(44): Show |
66 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.1057-582T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125338 | |||||||
| chr4:76125340 | A | ACGCGCGC | 2 | a0002c0002t0003g0003 a0004c0007t0003g0063 |
6 | HG04184.hp1 NA18939.hp1 NA18941.hp2 others(3): Show |
intron_variant | MODIFIER | c.1057-585_1057-584i others(9): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125340 | |||||||
| chr4:76125340 | A | G | 54 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0007 others(51): Show |
75 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.1057-584T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125340 | |||||||
| chr4:76125342 | A | G | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1057-586T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125342 | |||||||
| chr4:76125343 | C | T | 1 | a0002c0002t0003g0046 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1057-587G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125343 | |||||||
| chr4:76125344 | A | G | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1057-588T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125344 | |||||||
| chr4:76125345 | C | CGCGCGCT | 3 | a0002c0002t0003g0047 a0002c0002t0003g0051 a0002c0002t0003g0052 |
3 | HG02040.hp2 NA19084.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1057-590_1057-589i others(9): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125345 | |||||||
| chr4:76125346 | A | G | 60 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(57): Show |
85 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.1057-590T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125346 | |||||||
| chr4:76125348 | A | G | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1057-592T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125348 | |||||||
| chr4:76125350 | A | G | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1057-594T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125350 | |||||||
| chr4:76125359 | C | A | 72 | a0001c0001t0004g0009 a0001c0001t0004g0014 a0001c0001t0004g0015 others(69): Show |
77 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.1057-603G>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125359 | |||||||
| chr4:76125619 | G | GGAGAGGG others(1): Show |
51 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(48): Show |
76 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.1057-871_1057-864d others(10): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125619 | |||||||
| chr4:76125619 | G | GGAGGGGG others(1): Show |
21 | a0001c0001t0004g0092 a0001c0001t0004g0094 a0001c0001t0004g0095 others(18): Show |
21 | HG01106.hp2 HG01175.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.1057-864_1057-863i others(10): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125619 | |||||||
| chr4:76125619 | G | GGAGGGGG others(9): Show |
32 | a0001c0001t0004g0009 a0001c0001t0004g0014 a0001c0001t0004g0021 others(29): Show |
36 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(33): Show |
intron_variant | MODIFIER | c.1057-864_1057-863i others(18): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125619 | |||||||
| chr4:76125619 | G | GGAGGGGG others(17): Show |
6 | a0001c0001t0004g0015 a0001c0001t0004g0120 a0001c0001t0004g0124 others(3): Show |
7 | HG00558.hp1 HG00639.hp1 HG00639.hp2 others(4): Show |
intron_variant | MODIFIER | c.1057-864_1057-863i others(26): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125619 | |||||||
| chr4:76125619 | G | GGAGGGGG others(25): Show |
1 | a0001c0001t0004g0132 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1057-864_1057-863i others(34): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125619 | |||||||
| chr4:76125619 | G | GGAGGGGG others(10): Show |
1 | a0001c0001t0004g0140 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1057-864_1057-863i others(19): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125619 | |||||||
| chr4:76125619 | G | GGAGGGGG others(9): Show |
1 | a0001c0001t0004g0142 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1057-864_1057-863i others(18): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125619 | |||||||
| chr4:76125619 | GGAGAGGG others(1): Show |
G | 4 | a0001c0004t0004g0296 a0001c0004t0004g0299 a0001c0004t0004g0300 others(1): Show |
4 | HG02280.hp1 HG03130.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1057-871_1057-864d others(10): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125619 | |||||||
| chr4:76125623 | A | AGGGAGAG others(1): Show |
8 | a0001c0001t0002g0148 a0001c0001t0002g0152 a0001c0001t0002g0153 others(5): Show |
8 | HG01109.hp2 HG02145.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1057-875_1057-868d others(10): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125623 | |||||||
| chr4:76125623 | A | AGGGAGAG others(9): Show |
2 | a0001c0001t0002g0157 a0001c0001t0002g0159 |
2 | HG02886.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1057-883_1057-868d others(18): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125623 | |||||||
| chr4:76125623 | A | G | 66 | a0001c0001t0004g0009 a0001c0001t0004g0014 a0001c0001t0004g0015 others(63): Show |
71 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.1057-867T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125623 | |||||||
| chr4:76125630 | GGGGGAGA others(8): Show |
G | 1 | a0001c0001t0002g0184 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1057-889_1057-875d others(17): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125630 | |||||||
| chr4:76125631 | G | A | 12 | a0001c0008t0005g0298 a0002c0002t0003g0025 a0002c0002t0003g0026 others(9): Show |
12 | HG02055.hp2 HG02818.hp1 HG02922.hp2 others(9): Show |
intron_variant | MODIFIER | c.1057-875C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125631 | |||||||
| chr4:76125637 | A | AGGGGGAG others(10): Show |
1 | a0001c0001t0004g0110 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1057-898_1057-882d others(19): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125637 | |||||||
| chr4:76125642 | GAGAGGGG others(8): Show |
G | 5 | a0001c0001t0002g0005 a0002c0002t0003g0034 a0002c0002t0003g0050 others(2): Show |
5 | HG02647.hp2 HG03831.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.1057-901_1057-887d others(17): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125642 | |||||||
| chr4:76125643 | AGAGGGG | A | 50 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(47): Show |
75 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.1057-893_1057-888d others(8): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125643 | |||||||
| chr4:76125646 | GGGGGAGA others(8): Show |
G | 1 | a0001c0001t0002g0215 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1057-905_1057-891d others(17): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125646 | |||||||
| chr4:76125649 | GGAGAGGG others(1): Show |
G | 5 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0149 others(2): Show |
6 | HG01884.hp2 HG02717.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1057-901_1057-894d others(10): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125649 | |||||||
| chr4:76125655 | G | A | 7 | a0002c0002t0003g0025 a0002c0002t0003g0026 a0002c0002t0003g0031 others(4): Show |
7 | HG02055.hp2 HG02922.hp2 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.1057-899C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125655 | |||||||
| chr4:76125655 | GGAGAGAG others(9): Show |
G | 54 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0018 others(51): Show |
62 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.1057-915_1057-900d others(18): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125655 | |||||||
| chr4:76125655 | GGAGAGAG others(17): Show |
G | 9 | a0001c0001t0002g0016 a0001c0001t0002g0161 a0001c0001t0002g0162 others(6): Show |
9 | HG02258.hp1 HG02572.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1057-923_1057-900d others(26): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125655 | |||||||
| chr4:76125656 | GAGAGAGG others(8): Show |
G | 1 | a0001c0001t0002g0208 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1057-915_1057-901d others(17): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125656 | |||||||
| chr4:76125657 | A | G | 102 | a0001c0001t0002g0143 a0001c0001t0002g0144 a0001c0001t0002g0145 others(99): Show |
107 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.1057-901T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125657 | |||||||
| chr4:76125661 | A | AGGGGGAG others(10): Show |
1 | a0001c0001t0004g0105 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1057-906_1057-905i others(19): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125661 | |||||||
| chr4:76125663 | G | A | 8 | a0002c0002t0003g0025 a0002c0002t0003g0026 a0002c0002t0003g0031 others(5): Show |
8 | HG01243.hp2 HG02055.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.1057-907C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125663 | |||||||
| chr4:76125665 | G | A | 50 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(47): Show |
75 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.1057-909C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125665 | |||||||
| chr4:76125667 | A | T | 1 | a0001c0001t0004g0134 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1057-911T>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125667 | |||||||
| chr4:76125667 | AGAGAGGG others(2): Show |
A | 50 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(47): Show |
75 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.1057-920_1057-912d others(11): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125667 | |||||||
| chr4:76125669 | AGAGGGAG | A | 7 | a0002c0002t0003g0025 a0002c0002t0003g0026 a0002c0002t0003g0031 others(4): Show |
7 | HG02055.hp2 HG02922.hp2 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.1057-920_1057-914d others(9): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125669 | |||||||
| chr4:76125671 | A | G | 27 | a0001c0001t0002g0005 a0001c0001t0002g0016 a0001c0001t0002g0017 others(24): Show |
28 | HG00423.hp2 HG01109.hp2 HG01515.hp2 others(25): Show |
intron_variant | MODIFIER | c.1057-915T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125671 | |||||||
| chr4:76125673 | G | GGGGGAGA others(40): Show |
1 | a0001c0001t0004g0134 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1057-918_1057-917i others(49): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125673 | |||||||
| chr4:76125677 | A | G | 1 | a0001c0001t0004g0134 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1057-921T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125677 | |||||||
| chr4:76125678 | GAGGGAGA others(8): Show |
G | 1 | a0001c0001t0002g0210 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1057-937_1057-923d others(17): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125678 | |||||||
| chr4:76125679 | A | G | 62 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0016 others(59): Show |
72 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.1057-923T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125679 | |||||||
| chr4:76125681 | G | GGAGAGGG others(11): Show |
1 | a0001c0008t0005g0298 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1057-926_1057-925i others(20): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125681 | |||||||
| chr4:76125682 | G | GAGA | 4 | a0002c0002t0003g0034 a0002c0002t0003g0050 a0002c0002t0003g0065 others(1): Show |
4 | HG03831.hp2 HG03927.hp2 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.1057-929_1057-927d others(5): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125682 | |||||||
| chr4:76125685 | AGGGAG | A | 58 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(55): Show |
83 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.1057-934_1057-930d others(7): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125685 | |||||||
| chr4:76125689 | A | G | 67 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0016 others(64): Show |
78 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.1057-933T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125689 | |||||||
| chr4:76125690 | G | GA | 4 | a0002c0002t0003g0034 a0002c0002t0003g0050 a0002c0002t0003g0065 others(1): Show |
4 | HG03831.hp2 HG03927.hp2 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.1057-935dupT | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125690 | |||||||
| chr4:76125693 | AGGGAGAA others(3): Show |
A | 1 | a0001c0001t0002g0203 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1057-947_1057-938d others(12): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125693 | |||||||
| chr4:76125723 | G | GAGAAGAG others(5): Show |
1 | a0001c0001t0004g0134 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1057-968_1057-967i others(14): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125723 | |||||||
| chr4:76125735 | A | T | 1 | a0001c0001t0004g0134 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1057-979T>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125735 | |||||||
| chr4:76125737 | AAGAGGGA others(9): Show |
A | 14 | a0001c0004t0001g0006 a0001c0004t0001g0308 a0001c0004t0001g0309 others(11): Show |
17 | HG00673.hp1 HG02083.hp1 HG03041.hp1 others(14): Show |
intron_variant | MODIFIER | c.1057-997_1057-982d others(18): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125737 | |||||||
| chr4:76125744 | A | AGAGAGGG others(9): Show |
1 | a0001c0001t0001g0255 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1057-1004_1057-989 others(19): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125744 | |||||||
| chr4:76125744 | A | C | 1 | a0001c0001t0004g0134 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1057-988T>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125744 | |||||||
| chr4:76125744 | AGAGAGGG others(1): Show |
A | 45 | a0001c0001t0001g0254 a0001c0001t0002g0158 a0001c0001t0002g0176 others(42): Show |
45 | HG00140.hp1 HG00738.hp2 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.1057-996_1057-989d others(10): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125744 | |||||||
| chr4:76125752 | G | GGAGAGAG others(37): Show |
1 | a0003c0003t0001g0232 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1057-997_1057-996i others(46): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125752 | |||||||
| chr4:76125752 | G | GGAGAGGG others(11): Show |
59 | a0001c0001t0004g0009 a0001c0001t0004g0014 a0001c0001t0004g0015 others(56): Show |
64 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.1057-997_1057-996i others(20): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125752 | |||||||
| chr4:76125752 | G | GGAGAGGG others(74): Show |
2 | a0001c0004t0004g0299 a0001c0004t0004g0303 |
2 | HG03130.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1057-997_1057-996i others(83): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125752 | |||||||
| chr4:76125752 | G | GGAGAGGG others(75): Show |
1 | a0001c0004t0004g0296 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1057-997_1057-996i others(84): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125752 | |||||||
| chr4:76125752 | G | GGAGAGGG others(37): Show |
1 | a0001c0001t0004g0118 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1057-997_1057-996i others(46): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125752 | |||||||
| chr4:76125752 | G | GGGAGAGG others(4): Show |
2 | a0001c0001t0002g0188 a0001c0001t0002g0210 |
2 | HG01978.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.1057-997_1057-996i others(13): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125752 | |||||||
| chr4:76125752 | G | GGGAGAGG others(13): Show |
1 | a0001c0001t0004g0221 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1057-997_1057-996i others(22): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125752 | |||||||
| chr4:76125756 | A | AGGGGGAG others(13): Show |
1 | a0001c0001t0004g0091 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1057-1001_1057-100 others(24): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125756 | |||||||
| chr4:76125758 | G | A | 63 | a0001c0001t0004g0134 a0002c0002t0003g0001 a0002c0002t0003g0002 others(60): Show |
88 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.1057-1002C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125758 | |||||||
| chr4:76125760 | G | A | 3 | a0001c0001t0002g0188 a0001c0001t0002g0210 a0003c0003t0001g0232 |
3 | HG01978.hp2 HG02622.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.1057-1004C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125760 | |||||||
| chr4:76125760 | G | GGAGAGAG others(3): Show |
86 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0016 others(83): Show |
97 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.1057-1005_1057-100 others(14): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125760 | |||||||
| chr4:76125760 | G | GGGAGAGA others(4): Show |
1 | a0001c0001t0002g0152 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1057-1005_1057-100 others(15): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125760 | |||||||
| chr4:76125762 | A | G | 1 | a0001c0001t0004g0134 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1057-1006T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125762 | |||||||
| chr4:76125764 | A | AGAGGGAG others(12): Show |
1 | a0001c0001t0004g0125 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1057-1009_1057-100 others(23): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125764 | |||||||
| chr4:76125764 | A | AGAGGGAG others(75): Show |
1 | a0001c0004t0004g0300 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1057-1009_1057-100 others(86): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125764 | |||||||
| chr4:76125766 | G | A | 67 | a0001c0001t0002g0176 a0001c0001t0004g0099 a0001c0001t0004g0109 others(64): Show |
92 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(89): Show |
intron_variant | MODIFIER | c.1057-1010C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125766 | |||||||
| chr4:76125768 | GGA | G | 58 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(55): Show |
83 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.1057-1014_1057-101 others(6): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125768 | |||||||
| chr4:76125770 | A | G | 1 | a0001c0001t0004g0134 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1057-1014T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125770 | |||||||
| chr4:76125774 | A | G | 4 | a0002c0002t0003g0044 a0002c0002t0003g0057 a0002c0002t0003g0058 others(1): Show |
4 | HG03831.hp2 NA18968.hp1 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.1057-1018T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125774 | |||||||
| chr4:76125774 | AGGGAGAG others(3): Show |
A | 1 | a0001c0008t0005g0298 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1057-1028_1057-101 others(14): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125774 | |||||||
| chr4:76125776 | G | A | 4 | a0002c0002t0003g0044 a0002c0002t0003g0057 a0002c0002t0003g0058 others(1): Show |
4 | HG03831.hp2 NA18968.hp1 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.1057-1020C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125776 | |||||||
| chr4:76125778 | A | G | 4 | a0001c0001t0002g0176 a0001c0001t0004g0099 a0001c0001t0004g0109 others(1): Show |
4 | HG01981.hp1 HG03540.hp2 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.1057-1022T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125778 | |||||||
| chr4:76125784 | G | A | 59 | a0001c0001t0002g0176 a0002c0002t0003g0001 a0002c0002t0003g0002 others(56): Show |
84 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.1057-1028C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125784 | |||||||
| chr4:76125784 | G | GGGGAGAG others(1): Show |
90 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0016 others(87): Show |
101 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.1057-1036_1057-102 others(12): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125784 | |||||||
| chr4:76125784 | G | GGGGAGAG others(9): Show |
1 | a0001c0001t0002g0158 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1057-1029_1057-102 others(20): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125784 | |||||||
| chr4:76125784 | G | GGGGGAGA others(26): Show |
1 | a0001c0001t0004g0133 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1057-1029_1057-102 others(37): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125784 | |||||||
| chr4:76125786 | G | A | 4 | a0002c0002t0003g0044 a0002c0002t0003g0057 a0002c0002t0003g0058 others(1): Show |
4 | HG03831.hp2 NA18968.hp1 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.1057-1030C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125786 | |||||||
| chr4:76125788 | AG | A | 4 | a0002c0002t0003g0044 a0002c0002t0003g0057 a0002c0002t0003g0058 others(1): Show |
4 | HG03831.hp2 NA18968.hp1 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.1057-1033delC | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125788 | |||||||
| chr4:76125789 | G | GAGAGGGA others(13): Show |
1 | a0001c0001t0004g0134 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1057-1034_1057-103 others(24): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125789 | |||||||
| chr4:76125790 | AGAGGG | A | 58 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(55): Show |
83 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.1057-1039_1057-103 others(9): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125790 | |||||||
| chr4:76125791 | G | GAGGGAGA others(19): Show |
2 | a0001c0001t0004g0099 a0001c0001t0004g0109 |
2 | HG01981.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.1057-1036_1057-103 others(30): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125791 | |||||||
| chr4:76125791 | G | GAGGGAGA others(1): Show |
63 | a0001c0001t0004g0009 a0001c0001t0004g0014 a0001c0001t0004g0015 others(60): Show |
68 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.1057-1036_1057-103 others(12): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125791 | |||||||
| chr4:76125791 | G | T | 1 | a0001c0001t0004g0133 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1057-1035C>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125791 | |||||||
| chr4:76125792 | AGGGAGAG others(28): Show |
A | 3 | a0001c0001t0002g0085 a0001c0001t0002g0086 a0001c0001t0002g0202 |
3 | HG00323.hp2 HG03492.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1057-1071_1057-103 others(39): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125792 | |||||||
| chr4:76125797 | G | GAA | 3 | a0002c0002t0003g0044 a0002c0002t0003g0057 a0002c0002t0003g0058 |
3 | NA18968.hp1 NA18989.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.1057-1042_1057-104 others(6): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125797 | |||||||
| chr4:76125802 | A | G | 3 | a0002c0002t0003g0044 a0002c0002t0003g0057 a0002c0002t0003g0058 |
3 | NA18968.hp1 NA18989.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.1057-1046T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125802 | |||||||
| chr4:76125805 | G | A | 59 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(56): Show |
84 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.1057-1049C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125805 | |||||||
| chr4:76125807 | G | T | 1 | a0001c0001t0004g0134 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1057-1051C>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125807 | |||||||
| chr4:76125808 | A | G | 59 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(56): Show |
84 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.1057-1052T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125808 | |||||||
| chr4:76125813 | GA | G | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1057-1058delT | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125813 | |||||||
| chr4:76125822 | GAA | G | 61 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(58): Show |
86 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.1057-1068_1057-106 others(6): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125822 | |||||||
| chr4:76125824 | A | G | 1 | a0002c0002t0003g0068 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1057-1068T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125824 | |||||||
| chr4:76125827 | G | A | 61 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(58): Show |
86 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.1057-1071C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125827 | |||||||
| chr4:76125827 | G | GGGGAGAG others(18): Show |
1 | a0001c0001t0004g0112 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1057-1072_1057-107 others(29): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125827 | |||||||
| chr4:76125827 | GGGGAGAG others(1): Show |
G | 14 | a0001c0004t0001g0006 a0001c0004t0001g0308 a0001c0004t0001g0309 others(11): Show |
17 | HG00673.hp1 HG02083.hp1 HG03041.hp1 others(14): Show |
intron_variant | MODIFIER | c.1057-1079_1057-107 others(12): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125827 | |||||||
| chr4:76125828 | G | T | 1 | a0001c0001t0004g0134 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1057-1072C>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125828 | |||||||
| chr4:76125829 | G | A | 1 | a0002c0002t0003g0068 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1057-1073C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125829 | |||||||
| chr4:76125837 | G | A | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1057-1081C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125837 | |||||||
| chr4:76125847 | A | G | 3 | a0001c0001t0002g0085 a0001c0001t0002g0086 a0001c0001t0002g0202 |
3 | HG00323.hp2 HG03492.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1057-1091T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125847 | |||||||
| chr4:76125851 | A | G | 3 | a0001c0001t0002g0085 a0001c0001t0002g0086 a0001c0001t0002g0202 |
3 | HG00323.hp2 HG03492.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1057-1095T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125851 | |||||||
| chr4:76125855 | G | A | 3 | a0001c0001t0002g0085 a0001c0001t0002g0086 a0001c0001t0002g0202 |
3 | HG00323.hp2 HG03492.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1057-1099C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125855 | |||||||
| chr4:76125857 | A | G | 3 | a0001c0001t0002g0085 a0001c0001t0002g0086 a0001c0001t0002g0202 |
3 | HG00323.hp2 HG03492.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1057-1101T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125857 | |||||||
| chr4:76125859 | G | A | 3 | a0001c0001t0002g0085 a0001c0001t0002g0086 a0001c0001t0002g0202 |
3 | HG00323.hp2 HG03492.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1057-1103C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125859 | |||||||
| chr4:76125859 | G | GGA | 60 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(57): Show |
85 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.1057-1104_1057-110 others(6): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125859 | |||||||
| chr4:76125861 | G | A | 63 | a0001c0001t0002g0085 a0001c0001t0002g0086 a0001c0001t0002g0202 others(60): Show |
88 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.1057-1105C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125861 | |||||||
| chr4:76125865 | G | A | 64 | a0001c0001t0002g0085 a0001c0001t0002g0086 a0001c0001t0002g0202 others(61): Show |
89 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.1057-1109C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125865 | |||||||
| chr4:76125865 | G | GGAGAGA | 69 | a0001c0001t0004g0009 a0001c0001t0004g0014 a0001c0001t0004g0015 others(66): Show |
74 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.1057-1115_1057-111 others(10): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125865 | |||||||
| chr4:76125865 | G | GGAGAGAG others(1): Show |
90 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0016 others(87): Show |
101 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.1057-1117_1057-111 others(12): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125865 | |||||||
| chr4:76125865 | G | GGAGAGAG others(3): Show |
1 | a0001c0001t0002g0164 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1057-1119_1057-111 others(14): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125865 | |||||||
| chr4:76125922 | C | G | 1 | a0001c0001t0004g0112 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1057-1166G>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125922 | |||||||
| chr4:76125936 | ATAAT | A | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1057-1184_1057-118 others(8): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125936 | |||||||
| chr4:76125964 | A | T | 1 | a0001c0001t0004g0112 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1057-1208T>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125964 | |||||||
| chr4:76125965 | T | G | 1 | a0001c0001t0004g0112 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1057-1209A>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125965 | |||||||
| chr4:76125968 | A | T | 1 | a0001c0001t0004g0112 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1057-1212T>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125968 | |||||||
| chr4:76125974 | C | G | 1 | a0001c0001t0004g0112 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1057-1218G>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125974 | |||||||
| chr4:76125975 | A | T | 1 | a0001c0001t0004g0112 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1057-1219T>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125975 | |||||||
| chr4:76125977 | C | A | 1 | a0001c0001t0004g0112 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1057-1221G>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125977 | |||||||
| chr4:76125982 | T | A | 1 | a0001c0001t0004g0112 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1057-1226A>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125982 | |||||||
| chr4:76125984 | T | G | 1 | a0001c0001t0004g0112 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1057-1228A>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125984 | |||||||
| chr4:76125985 | G | T | 1 | a0001c0001t0004g0112 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1057-1229C>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125985 | |||||||
| chr4:76125989 | G | T | 1 | a0001c0001t0004g0112 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1057-1233C>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125989 | |||||||
| chr4:76125991 | A | AAAAAGGT others(6): Show |
1 | a0001c0001t0004g0112 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1057-1236_1057-123 others(17): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125991 | |||||||
| chr4:76125998 | T | G | 1 | a0001c0001t0004g0112 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1057-1242A>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76125998 | |||||||
| chr4:76126066 | G | T | 91 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0016 others(88): Show |
102 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.1057-1310C>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76126066 | |||||||
| chr4:76126115 | G | A | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1057-1359C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76126115 | |||||||
| chr4:76126351 | T | A | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1057-1595A>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76126351 | |||||||
| chr4:76126425 | C | A | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1057-1669G>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76126425 | |||||||
| chr4:76126468 | G | C | 1 | a0002c0002t0003g0064 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1057-1712C>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76126468 | |||||||
| chr4:76126634 | ACCATCTA others(18): Show |
A | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1057-1903_1057-187 others(29): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76126634 | |||||||
| chr4:76126692 | G | A | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1057-1936C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76126692 | |||||||
| chr4:76126743 | G | A | 225 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0016 others(222): Show |
266 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(263): Show |
intron_variant | MODIFIER | c.1057-1987C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76126743 | |||||||
| chr4:76126761 | T | C | 71 | a0001c0001t0004g0009 a0001c0001t0004g0014 a0001c0001t0004g0015 others(68): Show |
76 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.1057-2005A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76126761 | |||||||
| chr4:76126934 | G | A | 1 | a0001c0008t0005g0298 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1057-2178C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76126934 | |||||||
| chr4:76127046 | A | G | 91 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0016 others(88): Show |
102 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.1057-2290T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76127046 | |||||||
| chr4:76127154 | T | C | 244 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0016 others(241): Show |
288 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(285): Show |
intron_variant | MODIFIER | c.1057-2398A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76127154 | |||||||
| chr4:76127171 | G | A | 1 | a0003c0003t0001g0264 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1057-2415C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76127171 | |||||||
| chr4:76127204 | G | A | 60 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(57): Show |
85 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.1057-2448C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76127204 | |||||||
| chr4:76127348 | C | T | 1 | a0001c0008t0005g0298 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1057-2592G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76127348 | |||||||
| chr4:76127381 | G | A | 1 | a0001c0004t0001g0319 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1057-2625C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76127381 | |||||||
| chr4:76127385 | T | C | 67 | a0001c0001t0004g0009 a0001c0001t0004g0014 a0001c0001t0004g0015 others(64): Show |
72 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.1057-2629A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76127385 | |||||||
| chr4:76127389 | G | A | 60 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(57): Show |
85 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.1057-2633C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76127389 | |||||||
| chr4:76127411 | G | A | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1057-2655C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76127411 | |||||||
| chr4:76127415 | G | A | 1 | a0001c0001t0004g0090 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1057-2659C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76127415 | |||||||
| chr4:76127432 | C | CA | 12 | a0001c0001t0001g0240 a0001c0001t0001g0245 a0001c0001t0001g0249 others(9): Show |
12 | HG00597.hp1 HG01109.hp1 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.1057-2677dupT | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76127432 | |||||||
| chr4:76127432 | C | CAAA | 48 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(45): Show |
73 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.1057-2679_1057-267 others(7): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76127432 | |||||||
| chr4:76127432 | C | CAAAA | 10 | a0002c0002t0003g0027 a0002c0002t0003g0034 a0002c0002t0003g0045 others(7): Show |
10 | HG00609.hp1 HG01243.hp2 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.1057-2680_1057-267 others(8): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76127432 | |||||||
| chr4:76127432 | C | CAAAAA | 6 | a0001c0001t0002g0155 a0001c0001t0002g0177 a0001c0001t0002g0183 others(3): Show |
6 | HG02976.hp2 NA18946.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1057-2681_1057-267 others(9): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76127432 | |||||||
| chr4:76127432 | C | CAAAAAA | 58 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0018 others(55): Show |
67 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.1057-2682_1057-267 others(10): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76127432 | |||||||
| chr4:76127432 | C | CAAAAAAA | 25 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0143 others(22): Show |
27 | HG00423.hp2 HG01258.hp2 HG01346.hp1 others(24): Show |
intron_variant | MODIFIER | c.1057-2683_1057-267 others(11): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76127432 | |||||||
| chr4:76127432 | CA | C | 13 | a0001c0001t0001g0251 a0001c0001t0004g0095 a0001c0001t0004g0100 others(10): Show |
13 | HG00280.hp1 HG00639.hp1 HG01975.hp2 others(10): Show |
intron_variant | MODIFIER | c.1057-2677delT | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76127432 | |||||||
| chr4:76127532 | C | A | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1057-2776G>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76127532 | |||||||
| chr4:76127545 | C | T | 244 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0016 others(241): Show |
288 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(285): Show |
intron_variant | MODIFIER | c.1057-2789G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76127545 | |||||||
| chr4:76127706 | G | A | 2 | a0003c0003t0001g0283 a0003c0003t0001g0286 |
2 | NA18944.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.1056+2950C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76127706 | |||||||
| chr4:76127750 | G | A | 1 | a0001c0001t0005g0084 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1056+2906C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76127750 | |||||||
| chr4:76127824 | A | C | 1 | a0001c0001t0002g0176 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1056+2832T>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76127824 | |||||||
| chr4:76127859 | G | A | 71 | a0001c0001t0004g0009 a0001c0001t0004g0014 a0001c0001t0004g0015 others(68): Show |
76 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.1056+2797C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76127859 | |||||||
| chr4:76127862 | C | T | 4 | a0001c0001t0005g0081 a0001c0001t0005g0082 a0001c0001t0005g0083 others(1): Show |
4 | HG01175.hp2 HG03139.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1056+2794G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76127862 | |||||||
| chr4:76128112 | T | C | 1 | a0001c0008t0005g0298 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1056+2544A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76128112 | |||||||
| chr4:76128117 | A | C | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1056+2539T>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76128117 | |||||||
| chr4:76128134 | A | G | 4 | a0001c0001t0005g0081 a0001c0001t0005g0082 a0001c0001t0005g0083 others(1): Show |
4 | HG01175.hp2 HG03139.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1056+2522T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76128134 | |||||||
| chr4:76128367 | C | T | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1056+2289G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76128367 | |||||||
| chr4:76128396 | G | GA | 10 | a0001c0001t0001g0240 a0001c0001t0002g0143 a0001c0001t0002g0144 others(7): Show |
10 | HG01243.hp2 HG01891.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1056+2259dupT | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76128396 | |||||||
| chr4:76128396 | G | GAA | 156 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0016 others(153): Show |
172 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.1056+2258_1056+225 others(6): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76128396 | |||||||
| chr4:76128531 | G | A | 91 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0016 others(88): Show |
102 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.1056+2125C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76128531 | |||||||
| chr4:76128650 | T | A | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1056+2006A>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76128650 | |||||||
| chr4:76128947 | G | A | 91 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0016 others(88): Show |
102 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.1056+1709C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76128947 | |||||||
| chr4:76128985 | C | G | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1056+1671G>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76128985 | |||||||
| chr4:76129024 | T | C | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1056+1632A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76129024 | |||||||
| chr4:76129071 | G | T | 2 | a0001c0001t0002g0154 a0001c0001t0002g0155 |
2 | HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1056+1585C>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76129071 | |||||||
| chr4:76129088 | A | G | 1 | a0001c0001t0004g0122 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1056+1568T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76129088 | |||||||
| chr4:76129140 | T | C | 91 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0016 others(88): Show |
102 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.1056+1516A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76129140 | |||||||
| chr4:76129155 | A | G | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1056+1501T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76129155 | |||||||
| chr4:76129208 | C | T | 4 | a0003c0003t0001g0266 a0003c0003t0001g0271 a0003c0003t0001g0273 others(1): Show |
4 | HG02280.hp2 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1056+1448G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76129208 | |||||||
| chr4:76129209 | G | C | 2 | a0001c0001t0005g0082 a0001c0001t0005g0083 |
2 | HG01175.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1056+1447C>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76129209 | |||||||
| chr4:76129221 | TAAAAG | T | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1056+1430_1056+143 others(9): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76129221 | |||||||
| chr4:76129470 | G | A | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1056+1186C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76129470 | |||||||
| chr4:76129518 | A | C | 1 | a0002c0002t0003g0025 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1056+1138T>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76129518 | |||||||
| chr4:76129614 | T | C | 1 | a0003c0003t0001g0277 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1056+1042A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76129614 | |||||||
| chr4:76129781 | C | T | 1 | a0001c0001t0002g0167 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1056+875G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76129781 | |||||||
| chr4:76129820 | G | A | 4 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0001g0241 others(1): Show |
4 | HG01081.hp2 HG01243.hp1 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.1056+836C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76129820 | |||||||
| chr4:76129843 | C | T | 3 | a0001c0001t0002g0143 a0001c0001t0002g0144 a0001c0001t0002g0145 |
3 | HG01891.hp2 HG02615.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1056+813G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76129843 | |||||||
| chr4:76129863 | C | CA | 39 | a0001c0001t0001g0024 a0001c0001t0001g0226 a0001c0001t0001g0228 others(36): Show |
41 | HG00438.hp1 HG00438.hp2 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.1056+792dupT | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76129863 | |||||||
| chr4:76129863 | CA | C | 24 | a0001c0001t0002g0170 a0001c0001t0002g0175 a0001c0001t0002g0178 others(21): Show |
24 | HG01358.hp1 HG01891.hp1 HG01928.hp1 others(21): Show |
intron_variant | MODIFIER | c.1056+792delT | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76129863 | |||||||
| chr4:76129863 | CAA | C | 44 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0018 others(41): Show |
53 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.1056+791_1056+792d others(4): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76129863 | |||||||
| chr4:76129863 | CAAA | C | 30 | a0001c0001t0002g0144 a0001c0001t0002g0145 a0001c0001t0002g0152 others(27): Show |
30 | HG01069.hp2 HG01109.hp2 HG01361.hp1 others(27): Show |
intron_variant | MODIFIER | c.1056+790_1056+792d others(5): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76129863 | |||||||
| chr4:76129863 | CAAAA | C | 63 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0143 others(60): Show |
68 | HG00140.hp1 HG00673.hp1 HG00738.hp2 others(65): Show |
intron_variant | MODIFIER | c.1056+789_1056+792d others(6): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76129863 | |||||||
| chr4:76129882 | A | C | 2 | a0001c0001t0001g0238 a0001c0001t0001g0239 |
2 | HG01081.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1056+774T>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76129882 | |||||||
| chr4:76129883 | AAAAAACC others(5): Show |
A | 51 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(48): Show |
74 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.1056+761_1056+772d others(14): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76129883 | |||||||
| chr4:76129884 | AAAAACCT others(4): Show |
A | 9 | a0002c0002t0003g0012 a0002c0002t0003g0013 a0002c0002t0003g0037 others(6): Show |
11 | HG01346.hp2 HG02015.hp1 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.1056+761_1056+771d others(13): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76129884 | |||||||
| chr4:76129885 | AAAACCTT others(3): Show |
A | 2 | a0002c0002t0003g0025 a0002c0002t0003g0026 |
2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1056+761_1056+770d others(12): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76129885 | |||||||
| chr4:76129966 | G | GT | 15 | a0001c0001t0001g0226 a0001c0001t0001g0242 a0001c0001t0001g0243 others(12): Show |
15 | HG00438.hp2 HG00621.hp2 HG00642.hp1 others(12): Show |
intron_variant | MODIFIER | c.1056+689dupA | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76129966 | |||||||
| chr4:76129966 | G | GTT | 11 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0227 others(8): Show |
13 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.1056+688_1056+689d others(4): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76129966 | |||||||
| chr4:76129966 | GT | G | 23 | a0003c0003t0001g0231 a0003c0003t0001g0232 a0003c0003t0001g0233 others(20): Show |
23 | HG00140.hp1 HG00738.hp2 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.1056+689delA | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76129966 | |||||||
| chr4:76129966 | GTT | G | 13 | a0003c0003t0001g0225 a0003c0003t0001g0235 a0003c0003t0001g0236 others(10): Show |
13 | HG01069.hp2 HG01168.hp2 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.1056+688_1056+689d others(4): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76129966 | |||||||
| chr4:76129966 | GTTT | G | 7 | a0001c0004t0001g0308 a0001c0004t0001g0309 a0001c0004t0001g0310 others(4): Show |
7 | HG02976.hp1 NA18906.hp2 NA18974.hp2 others(4): Show |
intron_variant | MODIFIER | c.1056+687_1056+689d others(5): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76129966 | |||||||
| chr4:76129966 | GTTTT | G | 7 | a0001c0001t0002g0079 a0001c0001t0002g0173 a0001c0004t0001g0006 others(4): Show |
10 | HG00673.hp1 HG02083.hp1 HG03041.hp1 others(7): Show |
intron_variant | MODIFIER | c.1056+686_1056+689d others(6): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76129966 | |||||||
| chr4:76129966 | GTTTTT | G | 34 | a0001c0001t0002g0004 a0001c0001t0002g0019 a0001c0001t0002g0080 others(31): Show |
38 | HG00544.hp2 HG01070.hp1 HG01257.hp1 others(35): Show |
intron_variant | MODIFIER | c.1056+685_1056+689d others(7): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76129966 | |||||||
| chr4:76129966 | GTTTTTT | G | 27 | a0001c0001t0002g0005 a0001c0001t0002g0018 a0001c0001t0002g0020 others(24): Show |
32 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(29): Show |
intron_variant | MODIFIER | c.1056+684_1056+689d others(8): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76129966 | |||||||
| chr4:76129966 | GTTTTTTT others(1): Show |
G | 13 | a0001c0001t0002g0016 a0001c0001t0002g0143 a0001c0001t0002g0144 others(10): Show |
14 | HG01884.hp2 HG01891.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.1056+682_1056+689d others(10): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76129966 | |||||||
| chr4:76129966 | GTTTTTTT others(2): Show |
G | 20 | a0001c0001t0002g0017 a0001c0001t0002g0146 a0001c0001t0002g0147 others(17): Show |
21 | HG02258.hp1 HG02615.hp1 HG02630.hp1 others(18): Show |
intron_variant | MODIFIER | c.1056+681_1056+689d others(11): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76129966 | |||||||
| chr4:76129966 | GTTTTTTT others(3): Show |
G | 19 | a0001c0001t0004g0112 a0001c0004t0004g0300 a0001c0004t0004g0303 others(16): Show |
21 | HG00597.hp2 HG01243.hp2 HG01934.hp2 others(18): Show |
intron_variant | MODIFIER | c.1056+680_1056+689d others(12): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76129966 | |||||||
| chr4:76129966 | GTTTTTTT others(4): Show |
G | 68 | a0001c0001t0004g0091 a0001c0001t0004g0092 a0001c0001t0004g0094 others(65): Show |
91 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.1056+679_1056+689d others(13): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76129966 | |||||||
| chr4:76129966 | GTTTTTTT others(5): Show |
G | 44 | a0001c0001t0004g0009 a0001c0001t0004g0014 a0001c0001t0004g0015 others(41): Show |
49 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.1056+678_1056+689d others(14): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76129966 | |||||||
| chr4:76129966 | GTTTTTTT others(6): Show |
G | 1 | a0001c0004t0004g0302 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1056+677_1056+689d others(15): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76129966 | |||||||
| chr4:76129966 | GTTTTTTT others(14): Show |
G | 1 | a0001c0001t0005g0082 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1056+669_1056+689d others(23): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76129966 | |||||||
| chr4:76129980 | T | G | 3 | a0001c0001t0004g0105 a0001c0001t0004g0106 a0001c0001t0004g0107 |
3 | HG03239.hp2 HG03654.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1056+676A>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76129980 | |||||||
| chr4:76130011 | C | A | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1056+645G>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76130011 | |||||||
| chr4:76130036 | A | G | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1056+620T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76130036 | |||||||
| chr4:76130040 | G | T | 1 | a0001c0001t0004g0218 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1056+616C>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76130040 | |||||||
| chr4:76130044 | G | A | 1 | a0001c0001t0004g0138 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1056+612C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76130044 | |||||||
| chr4:76130115 | G | A | 1 | a0001c0004t0004g0302 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1056+541C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76130115 | |||||||
| chr4:76130183 | A | T | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1056+473T>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76130183 | |||||||
| chr4:76130496 | T | A | 33 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0143 others(30): Show |
35 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(32): Show |
intron_variant | MODIFIER | c.1056+160A>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76130496 | |||||||
| chr4:76130509 | G | T | 31 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0143 others(28): Show |
33 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.1056+147C>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76130509 | |||||||
| chr4:76130550 | G | T | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1056+106C>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 8/11 | chr4 | 76130550 | |||||||
| chr4:76130825 | C | T | 2 | a0001c0001t0002g0180 a0001c0001t0002g0181 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.963-76G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 7/11 | chr4 | 76130825 | |||||||
| chr4:76130878 | A | G | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.963-129T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 7/11 | chr4 | 76130878 | |||||||
| chr4:76130915 | A | G | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.963-166T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 7/11 | chr4 | 76130915 | |||||||
| chr4:76131031 | C | A | 1 | a0002c0002t0003g0026 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.962+199G>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 7/11 | chr4 | 76131031 | |||||||
| chr4:76131038 | C | CT | 60 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(57): Show |
85 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.962+191dupA | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 7/11 | chr4 | 76131038 | |||||||
| chr4:76131135 | T | C | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.962+95A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 7/11 | chr4 | 76131135 | |||||||
| chr4:76131377 | T | C | 225 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0016 others(222): Show |
266 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(263): Show |
intron_variant | MODIFIER | c.908-93A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 6/11 | chr4 | 76131377 | |||||||
| chr4:76131499 | T | C | 1 | a0002c0002t0003g0072 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.908-215A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 6/11 | chr4 | 76131499 | |||||||
| chr4:76131567 | T | C | 1 | a0002c0002t0003g0060 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.908-283A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 6/11 | chr4 | 76131567 | |||||||
| chr4:76131675 | GA | G | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.908-392delT | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 6/11 | chr4 | 76131675 | |||||||
| chr4:76131696 | T | C | 70 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0016 others(67): Show |
81 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.908-412A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 6/11 | chr4 | 76131696 | |||||||
| chr4:76131971 | T | C | 3 | a0001c0001t0005g0081 a0001c0001t0005g0082 a0001c0001t0005g0083 |
3 | HG01175.hp2 HG03139.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.907+552A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 6/11 | chr4 | 76131971 | |||||||
| chr4:76131975 | G | A | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.907+548C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 6/11 | chr4 | 76131975 | |||||||
| chr4:76132036 | T | C | 1 | a0001c0001t0004g0139 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.907+487A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 6/11 | chr4 | 76132036 | |||||||
| chr4:76132049 | A | G | 91 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0016 others(88): Show |
102 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.907+474T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 6/11 | chr4 | 76132049 | |||||||
| chr4:76132118 | G | A | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.907+405C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 6/11 | chr4 | 76132118 | |||||||
| chr4:76132335 | C | T | 91 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0016 others(88): Show |
102 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.907+188G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 6/11 | chr4 | 76132335 | |||||||
| chr4:76132380 | A | T | 1 | a0003c0003t0001g0284 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.907+143T>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 6/11 | chr4 | 76132380 | |||||||
| chr4:76132405 | A | G | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.907+118T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 6/11 | chr4 | 76132405 | |||||||
| chr4:76132409 | C | T | 283 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0016 others(280): Show |
327 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(324): Show |
intron_variant | MODIFIER | c.907+114G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 6/11 | chr4 | 76132409 | |||||||
| chr4:76132489 | T | C | 1 | a0002c0002t0003g0051 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.907+34A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 6/11 | chr4 | 76132489 | |||||||
| chr4:76132746 | A | G | 1 | a0001c0004t0004g0303 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.711-27T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 5/11 | chr4 | 76132746 | |||||||
| chr4:76132826 | A | T | 1 | a0001c0001t0002g0179 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.711-107T>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 5/11 | chr4 | 76132826 | |||||||
| chr4:76132829 | T | C | 1 | a0001c0001t0001g0257 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.711-110A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 5/11 | chr4 | 76132829 | |||||||
| chr4:76132860 | C | CT | 9 | a0001c0001t0002g0165 a0001c0001t0004g0092 a0001c0001t0004g0094 others(6): Show |
9 | HG00438.hp1 HG00597.hp1 HG02027.hp2 others(6): Show |
intron_variant | MODIFIER | c.711-142dupA | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 5/11 | chr4 | 76132860 | |||||||
| chr4:76132860 | CT | C | 8 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0149 others(5): Show |
10 | HG01884.hp2 HG02622.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.711-142delA | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 5/11 | chr4 | 76132860 | |||||||
| chr4:76132879 | C | A | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.711-160G>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 5/11 | chr4 | 76132879 | |||||||
| chr4:76132991 | C | T | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.711-272G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 5/11 | chr4 | 76132991 | |||||||
| chr4:76133001 | G | A | 58 | a0001c0004t0001g0006 a0001c0004t0001g0308 a0001c0004t0001g0309 others(55): Show |
61 | HG00140.hp1 HG00673.hp1 HG00738.hp2 others(58): Show |
intron_variant | MODIFIER | c.711-282C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 5/11 | chr4 | 76133001 | |||||||
| chr4:76133016 | CAT | C | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.711-299_711-298del others(2): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 5/11 | chr4 | 76133016 | |||||||
| chr4:76133021 | A | G | 225 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0016 others(222): Show |
266 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(263): Show |
intron_variant | MODIFIER | c.711-302T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 5/11 | chr4 | 76133021 | |||||||
| chr4:76133029 | C | G | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.711-310G>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 5/11 | chr4 | 76133029 | |||||||
| chr4:76133047 | GAT | G | 151 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0016 others(148): Show |
187 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.711-330_711-329del others(2): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 5/11 | chr4 | 76133047 | |||||||
| chr4:76133051 | T | G | 60 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(57): Show |
85 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.711-332A>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 5/11 | chr4 | 76133051 | |||||||
| chr4:76133057 | T | C | 64 | a0001c0001t0004g0009 a0001c0001t0004g0014 a0001c0001t0004g0015 others(61): Show |
69 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.711-338A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 5/11 | chr4 | 76133057 | |||||||
| chr4:76133062 | A | T | 1 | a0001c0001t0002g0187 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.711-343T>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 5/11 | chr4 | 76133062 | |||||||
| chr4:76133063 | T | C | 1 | a0001c0008t0005g0298 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.711-344A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 5/11 | chr4 | 76133063 | |||||||
| chr4:76133064 | A | T | 91 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0016 others(88): Show |
102 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.711-345T>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 5/11 | chr4 | 76133064 | |||||||
| chr4:76133144 | C | T | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.711-425G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 5/11 | chr4 | 76133144 | |||||||
| chr4:76133146 | C | A | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.711-427G>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 5/11 | chr4 | 76133146 | |||||||
| chr4:76133152 | C | T | 4 | a0001c0001t0005g0081 a0001c0001t0005g0082 a0001c0001t0005g0083 others(1): Show |
4 | HG01175.hp2 HG03139.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.711-433G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 5/11 | chr4 | 76133152 | |||||||
| chr4:76133272 | T | C | 2 | a0001c0004t0004g0299 a0001c0004t0004g0300 |
2 | HG02280.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.711-553A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 5/11 | chr4 | 76133272 | |||||||
| chr4:76133312 | G | GT | 93 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0016 others(90): Show |
104 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.711-594dupA | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 5/11 | chr4 | 76133312 | |||||||
| chr4:76133312 | GT | G | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.711-594delA | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 5/11 | chr4 | 76133312 | |||||||
| chr4:76133367 | T | G | 225 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0016 others(222): Show |
266 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(263): Show |
intron_variant | MODIFIER | c.711-648A>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 5/11 | chr4 | 76133367 | |||||||
| chr4:76133398 | T | C | 66 | a0001c0004t0004g0296 a0001c0004t0004g0299 a0001c0004t0004g0300 others(63): Show |
91 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.711-679A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 5/11 | chr4 | 76133398 | |||||||
| chr4:76133462 | C | T | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.710+713G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 5/11 | chr4 | 76133462 | |||||||
| chr4:76133469 | C | A | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.710+706G>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 5/11 | chr4 | 76133469 | |||||||
| chr4:76133553 | C | T | 67 | a0001c0001t0004g0009 a0001c0001t0004g0014 a0001c0001t0004g0015 others(64): Show |
72 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.710+622G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 5/11 | chr4 | 76133553 | |||||||
| chr4:76133697 | C | T | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.710+478G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 5/11 | chr4 | 76133697 | |||||||
| chr4:76133706 | T | C | 4 | a0001c0004t0004g0296 a0001c0004t0004g0299 a0001c0004t0004g0300 others(1): Show |
4 | HG02280.hp1 HG03130.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.710+469A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 5/11 | chr4 | 76133706 | |||||||
| chr4:76133732 | G | GA | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.710+442_710+443ins others(1): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 5/11 | chr4 | 76133732 | |||||||
| chr4:76133741 | T | C | 1 | a0001c0004t0001g0316 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.710+434A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 5/11 | chr4 | 76133741 | |||||||
| chr4:76133911 | A | G | 1 | a0001c0001t0004g0109 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.710+264T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 5/11 | chr4 | 76133911 | |||||||
| chr4:76133917 | A | G | 1 | a0001c0008t0005g0298 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.710+258T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 5/11 | chr4 | 76133917 | |||||||
| chr4:76134038 | C | G | 1 | a0002c0002t0003g0026 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.710+137G>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 5/11 | chr4 | 76134038 | |||||||
| chr4:76134425 | A | G | 1 | a0001c0001t0001g0224 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.523-63T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 4/11 | chr4 | 76134425 | |||||||
| chr4:76134473 | G | A | 3 | a0001c0001t0002g0161 a0001c0001t0002g0165 a0001c0001t0002g0166 |
3 | HG02572.hp2 HG02615.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.523-111C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 4/11 | chr4 | 76134473 | |||||||
| chr4:76134511 | C | T | 3 | a0002c0002t0003g0033 a0002c0002t0003g0040 a0002c0002t0003g0041 |
3 | HG01099.hp2 HG02109.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.523-149G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 4/11 | chr4 | 76134511 | |||||||
| chr4:76134593 | CTT | C | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.523-233_523-232del others(2): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 4/11 | chr4 | 76134593 | |||||||
| chr4:76134734 | A | ATTG | 225 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0016 others(222): Show |
266 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(263): Show |
intron_variant | MODIFIER | c.523-373_523-372ins others(3): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 4/11 | chr4 | 76134734 | |||||||
| chr4:76134760 | T | C | 1 | a0001c0001t0002g0160 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.523-398A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 4/11 | chr4 | 76134760 | |||||||
| chr4:76134770 | G | A | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.523-408C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 4/11 | chr4 | 76134770 | |||||||
| chr4:76134909 | T | A | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.523-547A>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 4/11 | chr4 | 76134909 | |||||||
| chr4:76135020 | A | C | 64 | a0001c0001t0004g0009 a0001c0001t0004g0014 a0001c0001t0004g0015 others(61): Show |
69 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.523-658T>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 4/11 | chr4 | 76135020 | |||||||
| chr4:76135028 | CATA | C | 3 | a0001c0001t0002g0174 a0001c0001t0002g0175 a0001c0001t0002g0176 |
3 | HG01891.hp1 HG02922.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.523-669_523-667del others(3): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 4/11 | chr4 | 76135028 | |||||||
| chr4:76135139 | G | T | 12 | a0003c0003t0001g0230 a0003c0003t0001g0264 a0003c0003t0001g0266 others(9): Show |
12 | HG00140.hp1 HG00738.hp2 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.523-777C>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 4/11 | chr4 | 76135139 | |||||||
| chr4:76135306 | A | C | 1 | a0001c0001t0002g0161 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.522+880T>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 4/11 | chr4 | 76135306 | |||||||
| chr4:76135311 | C | T | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.522+875G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 4/11 | chr4 | 76135311 | |||||||
| chr4:76135345 | G | A | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.522+841C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 4/11 | chr4 | 76135345 | |||||||
| chr4:76135373 | A | G | 2 | a0001c0001t0005g0087 a0001c0001t0005g0088 |
2 | HG02809.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.522+813T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 4/11 | chr4 | 76135373 | |||||||
| chr4:76135578 | A | G | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.522+608T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 4/11 | chr4 | 76135578 | |||||||
| chr4:76135585 | T | C | 1 | a0003c0003t0001g0289 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.522+601A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 4/11 | chr4 | 76135585 | |||||||
| chr4:76135596 | A | T | 1 | a0001c0001t0004g0108 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.522+590T>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 4/11 | chr4 | 76135596 | |||||||
| chr4:76135655 | G | A | 225 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0016 others(222): Show |
266 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(263): Show |
intron_variant | MODIFIER | c.522+531C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 4/11 | chr4 | 76135655 | |||||||
| chr4:76135734 | A | G | 2 | a0001c0001t0005g0082 a0001c0001t0005g0083 |
2 | HG01175.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.522+452T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 4/11 | chr4 | 76135734 | |||||||
| chr4:76135751 | G | A | 71 | a0001c0001t0004g0009 a0001c0001t0004g0014 a0001c0001t0004g0015 others(68): Show |
76 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.522+435C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 4/11 | chr4 | 76135751 | |||||||
| chr4:76135828 | T | C | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.522+358A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 4/11 | chr4 | 76135828 | |||||||
| chr4:76135870 | T | C | 1 | a0001c0001t0004g0140 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.522+316A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 4/11 | chr4 | 76135870 | |||||||
| chr4:76136595 | C | T | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.296-183G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76136595 | |||||||
| chr4:76136669 | C | A | 283 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0016 others(280): Show |
327 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(324): Show |
intron_variant | MODIFIER | c.296-257G>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76136669 | |||||||
| chr4:76136731 | G | A | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.296-319C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76136731 | |||||||
| chr4:76136752 | G | T | 58 | a0001c0004t0001g0006 a0001c0004t0001g0308 a0001c0004t0001g0309 others(55): Show |
61 | HG00140.hp1 HG00673.hp1 HG00738.hp2 others(58): Show |
intron_variant | MODIFIER | c.296-340C>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76136752 | |||||||
| chr4:76136783 | G | A | 1 | a0003c0003t0001g0290 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.296-371C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76136783 | |||||||
| chr4:76136904 | T | G | 2 | a0002c0002t0003g0073 a0002c0002t0003g0074 |
2 | HG02129.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.296-492A>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76136904 | |||||||
| chr4:76136981 | A | G | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.296-569T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76136981 | |||||||
| chr4:76136988 | TTTTCTAA others(40): Show |
T | 1 | a0002c0002t0003g0064 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.296-623_296-577del others(47): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76136988 | |||||||
| chr4:76137096 | A | C | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.296-684T>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76137096 | |||||||
| chr4:76137098 | C | T | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.296-686G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76137098 | |||||||
| chr4:76137165 | A | T | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.296-753T>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76137165 | |||||||
| chr4:76137258 | A | G | 6 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0149 others(3): Show |
8 | HG01884.hp2 HG02622.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.296-846T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76137258 | |||||||
| chr4:76137365 | C | T | 67 | a0001c0001t0004g0009 a0001c0001t0004g0014 a0001c0001t0004g0015 others(64): Show |
72 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.296-953G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76137365 | |||||||
| chr4:76137617 | G | C | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.296-1205C>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76137617 | |||||||
| chr4:76137635 | G | C | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.296-1223C>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76137635 | |||||||
| chr4:76137642 | C | CACTT | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.296-1231_296-1230i others(6): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76137642 | |||||||
| chr4:76137676 | AG | A | 91 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0016 others(88): Show |
102 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.296-1265delC | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76137676 | |||||||
| chr4:76137830 | T | C | 42 | a0001c0001t0004g0009 a0001c0001t0004g0014 a0001c0001t0004g0015 others(39): Show |
46 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.296-1418A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76137830 | |||||||
| chr4:76137850 | G | C | 1 | a0003c0003t0001g0291 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.296-1438C>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76137850 | |||||||
| chr4:76137877 | T | C | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.296-1465A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76137877 | |||||||
| chr4:76137877 | TAGC | T | 3 | a0001c0004t0004g0297 a0001c0004t0004g0301 a0001c0004t0004g0302 |
3 | HG03195.hp2 NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.296-1468_296-1466d others(5): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76137877 | |||||||
| chr4:76137911 | T | C | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.296-1499A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76137911 | |||||||
| chr4:76137944 | A | G | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.296-1532T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76137944 | |||||||
| chr4:76137966 | G | C | 2 | a0001c0001t0005g0082 a0001c0001t0005g0083 |
2 | HG01175.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.296-1554C>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76137966 | |||||||
| chr4:76137977 | G | A | 229 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0016 others(226): Show |
270 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(267): Show |
intron_variant | MODIFIER | c.296-1565C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76137977 | |||||||
| chr4:76138022 | G | A | 1 | a0001c0001t0001g0258 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.296-1610C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76138022 | |||||||
| chr4:76138268 | C | A | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.296-1856G>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76138268 | |||||||
| chr4:76138329 | TG | T | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.296-1918delC | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76138329 | |||||||
| chr4:76138361 | C | T | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.296-1949G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76138361 | |||||||
| chr4:76138654 | G | T | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.296-2242C>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76138654 | |||||||
| chr4:76138696 | G | GCACTTCA others(39): Show |
1 | a0002c0002t0003g0064 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.296-2285_296-2284i others(48): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76138696 | |||||||
| chr4:76138817 | A | T | 4 | a0001c0001t0005g0081 a0001c0001t0005g0082 a0001c0001t0005g0083 others(1): Show |
4 | HG01175.hp2 HG03139.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.296-2405T>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76138817 | |||||||
| chr4:76138959 | AT | A | 4 | a0001c0004t0004g0296 a0001c0004t0004g0299 a0001c0004t0004g0300 others(1): Show |
4 | HG02280.hp1 HG03130.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.296-2548delA | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76138959 | |||||||
| chr4:76139007 | C | T | 1 | a0001c0001t0002g0173 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.296-2595G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76139007 | |||||||
| chr4:76139260 | G | A | 4 | a0001c0004t0004g0296 a0001c0004t0004g0299 a0001c0004t0004g0300 others(1): Show |
4 | HG02280.hp1 HG03130.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.296-2848C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76139260 | |||||||
| chr4:76139311 | T | C | 2 | a0001c0001t0002g0169 a0001c0001t0002g0170 |
2 | NA18612.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.296-2899A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76139311 | |||||||
| chr4:76139322 | C | T | 63 | a0001c0008t0005g0298 a0002c0002t0003g0001 a0002c0002t0003g0002 others(60): Show |
88 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.296-2910G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76139322 | |||||||
| chr4:76139350 | A | G | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.296-2938T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76139350 | |||||||
| chr4:76139426 | T | TA | 58 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0018 others(55): Show |
67 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.296-3015dupT | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76139426 | |||||||
| chr4:76139452 | C | CAGA | 71 | a0001c0001t0004g0009 a0001c0001t0004g0014 a0001c0001t0004g0015 others(68): Show |
76 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.296-3043_296-3041d others(5): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76139452 | |||||||
| chr4:76139493 | T | C | 2 | a0001c0001t0005g0087 a0001c0001t0005g0088 |
2 | HG02809.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.296-3081A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76139493 | |||||||
| chr4:76139716 | G | C | 91 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0016 others(88): Show |
102 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.296-3304C>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76139716 | |||||||
| chr4:76139750 | C | T | 63 | a0001c0008t0005g0298 a0002c0002t0003g0001 a0002c0002t0003g0002 others(60): Show |
88 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.296-3338G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76139750 | |||||||
| chr4:76139917 | T | G | 2 | a0001c0001t0005g0087 a0001c0001t0005g0088 |
2 | HG02809.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.296-3505A>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76139917 | |||||||
| chr4:76139972 | T | C | 1 | a0002c0002t0003g0064 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.296-3560A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76139972 | |||||||
| chr4:76139977 | G | A | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.296-3565C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76139977 | |||||||
| chr4:76140113 | G | A | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.296-3701C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76140113 | |||||||
| chr4:76140285 | G | GT | 66 | a0001c0001t0001g0227 a0001c0001t0001g0228 a0001c0001t0001g0229 others(63): Show |
90 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.295+3863dupA | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76140285 | |||||||
| chr4:76140285 | G | GTT | 7 | a0002c0002t0003g0011 a0002c0002t0003g0025 a0002c0002t0003g0037 others(4): Show |
8 | HG01928.hp2 HG03453.hp2 NA18953.hp1 others(5): Show |
intron_variant | MODIFIER | c.295+3862_295+3863d others(4): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76140285 | |||||||
| chr4:76140285 | GT | G | 68 | a0001c0001t0004g0009 a0001c0001t0004g0014 a0001c0001t0004g0015 others(65): Show |
73 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.295+3863delA | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76140285 | |||||||
| chr4:76140363 | G | A | 4 | a0001c0004t0004g0296 a0001c0004t0004g0299 a0001c0004t0004g0300 others(1): Show |
4 | HG02280.hp1 HG03130.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.295+3786C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76140363 | |||||||
| chr4:76140387 | G | A | 3 | a0001c0004t0004g0297 a0001c0004t0004g0301 a0001c0004t0004g0302 |
3 | HG03195.hp2 NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.295+3762C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76140387 | |||||||
| chr4:76140447 | A | G | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.295+3702T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76140447 | |||||||
| chr4:76140682 | C | T | 2 | a0002c0002t0003g0029 a0002c0002t0003g0036 |
2 | HG03834.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.295+3467G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76140682 | |||||||
| chr4:76140683 | A | G | 225 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0016 others(222): Show |
266 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(263): Show |
intron_variant | MODIFIER | c.295+3466T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76140683 | |||||||
| chr4:76140687 | G | A | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.295+3462C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76140687 | |||||||
| chr4:76140694 | T | C | 4 | a0003c0005t0001g0304 a0003c0005t0001g0305 a0003c0005t0001g0306 others(1): Show |
4 | HG01884.hp1 HG02145.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.295+3455A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76140694 | |||||||
| chr4:76140741 | G | A | 1 | a0001c0001t0004g0141 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.295+3408C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76140741 | |||||||
| chr4:76140837 | G | C | 1 | a0002c0002t0003g0027 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.295+3312C>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76140837 | |||||||
| chr4:76140942 | T | C | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.295+3207A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76140942 | |||||||
| chr4:76141015 | G | A | 163 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0016 others(160): Show |
179 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.295+3134C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76141015 | |||||||
| chr4:76141037 | A | G | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.295+3112T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76141037 | |||||||
| chr4:76141059 | C | G | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.295+3090G>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76141059 | |||||||
| chr4:76141149 | T | A | 163 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0016 others(160): Show |
179 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.295+3000A>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76141149 | |||||||
| chr4:76141154 | A | AATACATG others(1): Show |
91 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0016 others(88): Show |
102 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.295+2987_295+2994d others(10): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76141154 | |||||||
| chr4:76141247 | G | A | 1 | a0001c0001t0004g0142 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.295+2902C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76141247 | |||||||
| chr4:76141251 | A | G | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.295+2898T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76141251 | |||||||
| chr4:76141252 | T | C | 3 | a0001c0004t0004g0299 a0001c0004t0004g0300 a0001c0004t0004g0303 |
3 | HG02280.hp1 HG03130.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.295+2897A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76141252 | |||||||
| chr4:76141397 | T | C | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.295+2752A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76141397 | |||||||
| chr4:76141509 | C | T | 1 | a0003c0003t0001g0281 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.295+2640G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76141509 | |||||||
| chr4:76141656 | G | T | 1 | a0001c0001t0001g0226 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.295+2493C>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76141656 | |||||||
| chr4:76141711 | GT | G | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.295+2437delA | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76141711 | |||||||
| chr4:76141758 | A | AG | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.295+2390_295+2391i others(3): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76141758 | |||||||
| chr4:76141810 | C | T | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.295+2339G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76141810 | |||||||
| chr4:76141821 | C | T | 2 | a0001c0001t0002g0169 a0001c0001t0002g0170 |
2 | NA18612.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.295+2328G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76141821 | |||||||
| chr4:76141861 | T | C | 225 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0016 others(222): Show |
266 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(263): Show |
intron_variant | MODIFIER | c.295+2288A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76141861 | |||||||
| chr4:76141887 | T | TA | 61 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(58): Show |
86 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.295+2261dupT | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76141887 | |||||||
| chr4:76141895 | C | A | 1 | a0001c0001t0002g0211 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.295+2254G>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76141895 | |||||||
| chr4:76142090 | C | T | 1 | a0001c0001t0004g0091 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.295+2059G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76142090 | |||||||
| chr4:76142137 | C | A | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.295+2012G>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76142137 | |||||||
| chr4:76142162 | G | A | 2 | a0001c0001t0002g0167 a0001c0001t0002g0168 |
2 | HG02809.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.295+1987C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76142162 | |||||||
| chr4:76142259 | A | G | 1 | a0001c0008t0005g0298 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.295+1890T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76142259 | |||||||
| chr4:76142275 | C | T | 1 | a0001c0004t0004g0296 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.295+1874G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76142275 | |||||||
| chr4:76142344 | C | T | 3 | a0001c0001t0002g0167 a0001c0001t0002g0168 a0001c0001t0002g0212 |
3 | HG02809.hp2 HG03486.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.295+1805G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76142344 | |||||||
| chr4:76142388 | G | A | 244 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0016 others(241): Show |
288 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(285): Show |
intron_variant | MODIFIER | c.295+1761C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76142388 | |||||||
| chr4:76142396 | G | A | 3 | a0003c0003t0001g0259 a0003c0003t0001g0260 a0003c0003t0001g0280 |
3 | HG01255.hp1 HG02109.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.295+1753C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76142396 | |||||||
| chr4:76142510 | G | A | 225 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0016 others(222): Show |
266 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(263): Show |
intron_variant | MODIFIER | c.295+1639C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76142510 | |||||||
| chr4:76142513 | T | A | 6 | a0001c0001t0002g0161 a0001c0001t0002g0162 a0001c0001t0002g0163 others(3): Show |
6 | HG02258.hp1 HG02572.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.295+1636A>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76142513 | |||||||
| chr4:76142741 | G | A | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.295+1408C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76142741 | |||||||
| chr4:76142867 | T | C | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.295+1282A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76142867 | |||||||
| chr4:76142963 | C | T | 3 | a0001c0001t0005g0081 a0001c0001t0005g0082 a0001c0001t0005g0083 |
3 | HG01175.hp2 HG03139.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.295+1186G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76142963 | |||||||
| chr4:76143017 | T | C | 4 | a0001c0004t0004g0296 a0001c0004t0004g0299 a0001c0004t0004g0300 others(1): Show |
4 | HG02280.hp1 HG03130.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.295+1132A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76143017 | |||||||
| chr4:76143073 | T | A | 163 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0016 others(160): Show |
179 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.295+1076A>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76143073 | |||||||
| chr4:76143118 | G | A | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.295+1031C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76143118 | |||||||
| chr4:76143172 | C | T | 3 | a0002c0002t0003g0034 a0002c0002t0003g0035 a0002c0002t0003g0065 |
3 | HG02735.hp1 HG03831.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.295+977G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76143172 | |||||||
| chr4:76143212 | A | C | 91 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0016 others(88): Show |
102 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.295+937T>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76143212 | |||||||
| chr4:76143332 | G | A | 1 | a0001c0008t0005g0298 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.295+817C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76143332 | |||||||
| chr4:76143340 | G | A | 1 | a0001c0008t0005g0298 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.295+809C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76143340 | |||||||
| chr4:76143344 | A | G | 61 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(58): Show |
86 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.295+805T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76143344 | |||||||
| chr4:76143387 | C | T | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.295+762G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76143387 | |||||||
| chr4:76143406 | C | A | 3 | a0001c0004t0004g0297 a0001c0004t0004g0301 a0001c0004t0004g0302 |
3 | HG03195.hp2 NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.295+743G>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76143406 | |||||||
| chr4:76143426 | A | G | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.295+723T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76143426 | |||||||
| chr4:76143433 | G | A | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.295+716C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76143433 | |||||||
| chr4:76143436 | T | C | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.295+713A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76143436 | |||||||
| chr4:76143476 | C | A | 1 | a0001c0001t0002g0212 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.295+673G>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76143476 | |||||||
| chr4:76143534 | G | A | 91 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0016 others(88): Show |
102 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.295+615C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76143534 | |||||||
| chr4:76143553 | G | A | 3 | a0003c0003t0001g0225 a0003c0003t0001g0261 a0003c0003t0001g0262 |
3 | HG02258.hp2 HG02897.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.295+596C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76143553 | |||||||
| chr4:76143599 | G | A | 1 | a0002c0002t0003g0062 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.295+550C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76143599 | |||||||
| chr4:76143690 | T | G | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.295+459A>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76143690 | |||||||
| chr4:76143786 | C | T | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.295+363G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76143786 | |||||||
| chr4:76143989 | C | T | 91 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0016 others(88): Show |
102 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.295+160G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76143989 | |||||||
| chr4:76144070 | A | G | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.295+79T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76144070 | |||||||
| chr4:76144111 | C | T | 225 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0016 others(222): Show |
266 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(263): Show |
intron_variant | MODIFIER | c.295+38G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76144111 | |||||||
| chr4:76144135 | A | C | 1 | a0002c0002t0003g0033 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.295+14T>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 3/11 | chr4 | 76144135 | |||||||
| chr4:76144323 | T | TA | 12 | a0003c0003t0001g0281 a0003c0003t0001g0282 a0003c0003t0001g0283 others(9): Show |
12 | HG01255.hp2 HG01361.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.152-32dupT | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 2/11 | chr4 | 76144323 | |||||||
| chr4:76144323 | TAA | T | 164 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0016 others(161): Show |
180 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(177): Show |
intron_variant | MODIFIER | c.152-33_152-32delTT | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 2/11 | chr4 | 76144323 | |||||||
| chr4:76144323 | TAAA | T | 61 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(58): Show |
86 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.152-34_152-32delTT others(1): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 2/11 | chr4 | 76144323 | |||||||
| chr4:76144365 | T | C | 222 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0016 others(219): Show |
263 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(260): Show |
intron_variant | MODIFIER | c.151+25A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 2/11 | chr4 | 76144365 | |||||||
| chr4:76144978 | T | G | 1 | a0001c0001t0001g0263 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.68-505A>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76144978 | |||||||
| chr4:76144993 | G | C | 61 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(58): Show |
86 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.68-520C>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76144993 | |||||||
| chr4:76144994 | A | C | 1 | a0002c0002t0003g0027 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.68-521T>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76144994 | |||||||
| chr4:76145084 | C | T | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.68-611G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76145084 | |||||||
| chr4:76145089 | G | C | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.68-616C>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76145089 | |||||||
| chr4:76145090 | G | A | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.68-617C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76145090 | |||||||
| chr4:76145104 | G | A | 1 | a0002c0002t0003g0064 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.68-631C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76145104 | |||||||
| chr4:76145119 | C | A | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.68-646G>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76145119 | |||||||
| chr4:76145122 | T | C | 1 | a0001c0001t0002g0086 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.68-649A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76145122 | |||||||
| chr4:76145148 | G | C | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.68-675C>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76145148 | |||||||
| chr4:76145149 | T | C | 1 | a0001c0001t0002g0213 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.68-676A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76145149 | |||||||
| chr4:76145175 | G | A | 61 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(58): Show |
86 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.68-702C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76145175 | |||||||
| chr4:76145177 | G | C | 1 | a0002c0002t0003g0027 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.68-704C>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76145177 | |||||||
| chr4:76145178 | C | T | 163 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0016 others(160): Show |
179 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.68-705G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76145178 | |||||||
| chr4:76145183 | C | T | 225 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0016 others(222): Show |
266 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(263): Show |
intron_variant | MODIFIER | c.68-710G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76145183 | |||||||
| chr4:76145190 | C | T | 2 | a0001c0004t0004g0299 a0001c0004t0004g0300 |
2 | HG02280.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.68-717G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76145190 | |||||||
| chr4:76145191 | G | A | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.68-718C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76145191 | |||||||
| chr4:76145234 | C | T | 163 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0016 others(160): Show |
179 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.68-761G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76145234 | |||||||
| chr4:76145290 | C | T | 5 | a0001c0001t0002g0143 a0001c0001t0002g0144 a0001c0001t0002g0145 others(2): Show |
5 | HG01891.hp2 HG02615.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.68-817G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76145290 | |||||||
| chr4:76145292 | C | T | 244 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0016 others(241): Show |
288 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(285): Show |
intron_variant | MODIFIER | c.68-819G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76145292 | |||||||
| chr4:76145317 | C | CA | 29 | a0001c0001t0001g0279 a0001c0001t0005g0084 a0001c0001t0005g0088 others(26): Show |
29 | HG00140.hp1 HG00673.hp1 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.68-845dupT | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76145317 | |||||||
| chr4:76145317 | CA | C | 55 | a0001c0001t0001g0224 a0001c0001t0002g0214 a0001c0001t0002g0215 others(52): Show |
80 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.68-845delT | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76145317 | |||||||
| chr4:76145317 | CAA | C | 62 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0019 others(59): Show |
70 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.68-846_68-845delTT | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76145317 | |||||||
| chr4:76145317 | CAAA | C | 93 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0018 others(90): Show |
101 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.68-847_68-845delTT others(1): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76145317 | |||||||
| chr4:76145317 | CAAAA | C | 6 | a0001c0001t0004g0090 a0001c0004t0004g0296 a0001c0004t0004g0299 others(3): Show |
6 | HG02280.hp1 HG02818.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.68-848_68-845delTT others(2): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76145317 | |||||||
| chr4:76145370 | C | CT | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.68-898dupA | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76145370 | |||||||
| chr4:76145425 | T | C | 4 | a0002c0002t0003g0075 a0002c0002t0003g0076 a0002c0002t0003g0077 others(1): Show |
4 | HG00609.hp1 NA18945.hp1 NA18953.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-952A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76145425 | |||||||
| chr4:76145434 | T | C | 163 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0016 others(160): Show |
179 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.68-961A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76145434 | |||||||
| chr4:76145675 | A | G | 1 | a0001c0008t0005g0298 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.68-1202T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76145675 | |||||||
| chr4:76145734 | G | T | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.68-1261C>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76145734 | |||||||
| chr4:76145761 | C | G | 3 | a0001c0004t0004g0297 a0001c0004t0004g0301 a0001c0004t0004g0302 |
3 | HG03195.hp2 NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.68-1288G>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76145761 | |||||||
| chr4:76145980 | C | T | 225 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0016 others(222): Show |
266 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(263): Show |
intron_variant | MODIFIER | c.68-1507G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76145980 | |||||||
| chr4:76145982 | C | A | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.68-1509G>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76145982 | |||||||
| chr4:76146012 | A | G | 1 | a0002c0002t0003g0029 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.68-1539T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76146012 | |||||||
| chr4:76146177 | T | C | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.68-1704A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76146177 | |||||||
| chr4:76146182 | G | A | 4 | a0001c0004t0004g0296 a0001c0004t0004g0299 a0001c0004t0004g0300 others(1): Show |
4 | HG02280.hp1 HG03130.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-1709C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76146182 | |||||||
| chr4:76146215 | A | G | 225 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0016 others(222): Show |
266 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(263): Show |
intron_variant | MODIFIER | c.68-1742T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76146215 | |||||||
| chr4:76146236 | A | G | 64 | a0001c0001t0004g0009 a0001c0001t0004g0014 a0001c0001t0004g0015 others(61): Show |
69 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.68-1763T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76146236 | |||||||
| chr4:76146246 | G | T | 1 | a0001c0001t0002g0089 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.68-1773C>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76146246 | |||||||
| chr4:76146272 | A | G | 1 | a0001c0001t0001g0022 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.68-1799T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76146272 | |||||||
| chr4:76146281 | C | T | 163 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0016 others(160): Show |
179 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.68-1808G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76146281 | |||||||
| chr4:76146295 | ATTG | A | 6 | a0001c0001t0004g0218 a0001c0001t0004g0219 a0001c0001t0004g0220 others(3): Show |
6 | NA18964.hp1 NA18971.hp1 NA18986.hp2 others(3): Show |
intron_variant | MODIFIER | c.68-1825_68-1823del others(3): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76146295 | |||||||
| chr4:76146296 | T | C | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.68-1823A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76146296 | |||||||
| chr4:76146330 | A | G | 61 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(58): Show |
86 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.68-1857T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76146330 | |||||||
| chr4:76146347 | A | G | 2 | a0001c0001t0005g0087 a0001c0001t0005g0088 |
2 | HG02809.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.68-1874T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76146347 | |||||||
| chr4:76146489 | G | C | 2 | a0001c0004t0004g0301 a0001c0004t0004g0302 |
2 | HG03195.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.67+1819C>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76146489 | |||||||
| chr4:76146529 | G | T | 2 | a0001c0001t0002g0085 a0001c0001t0002g0086 |
2 | HG00323.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.67+1779C>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76146529 | |||||||
| chr4:76146582 | GTAAA | G | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.67+1722_67+1725del others(4): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76146582 | |||||||
| chr4:76146638 | A | G | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.67+1670T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76146638 | |||||||
| chr4:76146715 | C | A | 225 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0016 others(222): Show |
266 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(263): Show |
intron_variant | MODIFIER | c.67+1593G>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76146715 | |||||||
| chr4:76146837 | T | A | 1 | a0001c0004t0004g0303 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.67+1471A>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76146837 | |||||||
| chr4:76146863 | C | G | 225 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0016 others(222): Show |
266 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(263): Show |
intron_variant | MODIFIER | c.67+1445G>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76146863 | |||||||
| chr4:76147195 | C | T | 225 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0016 others(222): Show |
266 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(263): Show |
intron_variant | MODIFIER | c.67+1113G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76147195 | |||||||
| chr4:76147214 | A | ATATAT | 62 | a0002c0002t0003g0001 a0002c0002t0003g0002 a0002c0002t0003g0003 others(59): Show |
87 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.67+1093_67+1094ins others(5): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76147214 | |||||||
| chr4:76147229 | T | C | 12 | a0003c0003t0001g0281 a0003c0003t0001g0282 a0003c0003t0001g0283 others(9): Show |
12 | HG01255.hp2 HG01361.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.67+1079A>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76147229 | |||||||
| chr4:76147281 | C | T | 223 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0016 others(220): Show |
263 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(260): Show |
intron_variant | MODIFIER | c.67+1027G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76147281 | |||||||
| chr4:76147409 | C | T | 1 | a0002c0002t0003g0028 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.67+899G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76147409 | |||||||
| chr4:76147500 | C | CAAAATTG others(7): Show |
1 | a0002c0002t0003g0027 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.67+794_67+807dupCT others(12): Show |
NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76147500 | |||||||
| chr4:76147733 | A | G | 2 | a0002c0002t0003g0025 a0002c0002t0003g0026 |
2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.67+575T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76147733 | |||||||
| chr4:76147755 | C | A | 1 | a0001c0001t0002g0293 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.67+553G>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76147755 | |||||||
| chr4:76147786 | A | G | 1 | a0001c0004t0004g0296 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.67+522T>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76147786 | |||||||
| chr4:76147828 | T | TA | 15 | a0001c0004t0001g0006 a0001c0004t0001g0308 a0001c0004t0001g0309 others(12): Show |
18 | HG00673.hp1 HG02083.hp1 HG03041.hp1 others(15): Show |
intron_variant | MODIFIER | c.67+479dupT | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76147828 | |||||||
| chr4:76147889 | G | C | 1 | a0001c0001t0004g0294 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.67+419C>G | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76147889 | |||||||
| chr4:76147911 | C | T | 4 | a0001c0001t0005g0081 a0001c0001t0005g0082 a0001c0001t0005g0083 others(1): Show |
4 | HG01175.hp2 HG03139.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+397G>A | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76147911 | |||||||
| chr4:76147943 | G | A | 64 | a0001c0001t0002g0079 a0001c0001t0002g0080 a0002c0002t0003g0001 others(61): Show |
89 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.67+365C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76147943 | |||||||
| chr4:76148060 | C | G | 64 | a0001c0001t0002g0079 a0001c0001t0002g0080 a0002c0002t0003g0001 others(61): Show |
89 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.67+248G>C | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76148060 | |||||||
| chr4:76148101 | G | A | 1 | a0001c0001t0002g0295 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.67+207C>T | NUP54 | ENSG00000138750.16 | transcript | ENST00000264883.8 | protein_coding | 1/11 | chr4 | 76148101 |