Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 9818 |
| ensemblid | ENSG00000139496.18 |
| hgncid | 20261 |
| symbol | NUP58 |
| name | nucleoporin 58 |
| refseq_nuc | NM_014089.4 |
| refseq_prot | NP_054808.1 |
| ensembl_nuc | ENST00000381736.8 |
| ensembl_prot | ENSP00000371155.3 |
| mane_status | MANE Select |
| chr | chr13 |
| start | 25301625 |
| end | 25342421 |
| strand | + |
| ver | v1.2 |
| region | chr13:25301625-25342421 |
| region5000 | chr13:25296625-25347421 |
| regionname0 | NUP58_chr13_25301625_25342421 |
| regionname5000 | NUP58_chr13_25296625_25347421 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 599 | 223 | 71 | 39 | 79 | 11 | 22 | 67 | NUP58_chr13_25296625_25347421 | NUP58 | MSTGF others(594): Show |
chr13 | 25296625 | 25347421 |
| a0002 | 0/0 | 599 | 115 | 11 | 17 | 70 | 5 | 12 | 58 | NUP58_chr13_25296625_25347421 | NUP58 | MSTGF others(594): Show |
chr13 | 25296625 | 25347421 |
| a0003 | 0/0 | 599 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | MSTGF others(594): Show |
chr13 | 25296625 | 25347421 |
| a0004 | 0/1 | 599 | 2 | 0 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | MSTGF others(594): Show |
chr13 | 25296625 | 25347421 |
| a0005 | 0/0 | 599 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | MSTGF others(594): Show |
chr13 | 25296625 | 25347421 |
| a0006 | 0/0 | 599 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | MSTGF others(594): Show |
chr13 | 25296625 | 25347421 |
| a0007 | 0/0 | 595 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | MSTGF others(590): Show |
chr13 | 25296625 | 25347421 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1797 | 198 | 66 | 32 | 66 | 11 | 22 | NUP58_chr13_25296625_25347421 | NUP58 | ATGTC others(1792): Show |
chr13 | 25296625 | 25347421 | ||
| a0001c0003 | 0/0 | 1797 | 14 | 0 | 1 | 13 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | ATGTC others(1792): Show |
chr13 | 25296625 | 25347421 | ||
| a0001c0005 | 0/0 | 1797 | 4 | 4 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | ATGTC others(1792): Show |
chr13 | 25296625 | 25347421 | ||
| a0001c0006 | 0/0 | 1797 | 4 | 0 | 4 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | ATGTC others(1792): Show |
chr13 | 25296625 | 25347421 | ||
| a0001c0008 | 0/0 | 1797 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | ATGTC others(1792): Show |
chr13 | 25296625 | 25347421 | ||
| a0001c0010 | 0/0 | 1797 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | ATGTC others(1792): Show |
chr13 | 25296625 | 25347421 | ||
| a0001c0012 | 0/0 | 1797 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | ATGTC others(1792): Show |
chr13 | 25296625 | 25347421 | ||
| a0002c0002 | 0/0 | 1797 | 115 | 11 | 17 | 70 | 5 | 12 | NUP58_chr13_25296625_25347421 | NUP58 | ATGTC others(1792): Show |
chr13 | 25296625 | 25347421 | ||
| a0003c0004 | 0/0 | 1797 | 7 | 7 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | ATGTC others(1792): Show |
chr13 | 25296625 | 25347421 | ||
| a0004c0007 | 0/1 | 1797 | 2 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | ATGTC others(1792): Show |
chr13 | 25296625 | 25347421 | ||
| a0005c0009 | 0/0 | 1797 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | ATGTC others(1792): Show |
chr13 | 25296625 | 25347421 | ||
| a0006c0013 | 0/0 | 1797 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | ATGTC others(1792): Show |
chr13 | 25296625 | 25347421 | ||
| a0007c0011 | 0/0 | 1785 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | ATGTC others(1780): Show |
chr13 | 25296625 | 25347421 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 4236 | 88 | 37 | 8 | 33 | 0 | 9 | NUP58_chr13_25296625_25347421 | NUP58 | AGCCT others(4231): Show |
chr13 | 25296625 | 25347421 |
| a0001c0001t0002 | 0/0 | 4236 | 46 | 0 | 8 | 33 | 0 | 5 | NUP58_chr13_25296625_25347421 | NUP58 | AGCCT others(4231): Show |
chr13 | 25296625 | 25347421 |
| a0001c0001t0003 | 0/0 | 4236 | 32 | 12 | 10 | 0 | 7 | 3 | NUP58_chr13_25296625_25347421 | NUP58 | AGCCT others(4231): Show |
chr13 | 25296625 | 25347421 |
| a0001c0001t0005 | 0/0 | 4236 | 7 | 0 | 3 | 0 | 3 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | AGCCT others(4231): Show |
chr13 | 25296625 | 25347421 |
| a0001c0001t0006 | 0/0 | 4236 | 6 | 6 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | AGCCT others(4231): Show |
chr13 | 25296625 | 25347421 |
| a0001c0001t0007 | 0/0 | 4232 | 4 | 3 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | AGCCT others(4227): Show |
chr13 | 25296625 | 25347421 |
| a0001c0001t0009 | 0/0 | 4236 | 2 | 0 | 1 | 0 | 1 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | AGCCT others(4231): Show |
chr13 | 25296625 | 25347421 |
| a0001c0001t0010 | 0/0 | 4236 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | AGCCT others(4231): Show |
chr13 | 25296625 | 25347421 |
| a0001c0001t0011 | 0/0 | 4236 | 2 | 0 | 0 | 0 | 0 | 2 | NUP58_chr13_25296625_25347421 | NUP58 | AGCCT others(4231): Show |
chr13 | 25296625 | 25347421 |
| a0001c0001t0012 | 0/0 | 4236 | 2 | 2 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | AGCCT others(4231): Show |
chr13 | 25296625 | 25347421 |
| a0001c0001t0013 | 0/0 | 4236 | 2 | 2 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | AGCCT others(4231): Show |
chr13 | 25296625 | 25347421 |
| a0001c0001t0014 | 0/0 | 4236 | 2 | 2 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | AGCCT others(4231): Show |
chr13 | 25296625 | 25347421 |
| a0001c0001t0015 | 0/0 | 4236 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | AGCCT others(4231): Show |
chr13 | 25296625 | 25347421 |
| a0001c0001t0017 | 0/0 | 4236 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | AGCCT others(4231): Show |
chr13 | 25296625 | 25347421 |
| a0001c0001t0018 | 0/0 | 4236 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | AGCCT others(4231): Show |
chr13 | 25296625 | 25347421 |
| a0001c0001t0019 | 0/0 | 4236 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | AGCCT others(4231): Show |
chr13 | 25296625 | 25347421 |
| a0001c0003t0004 | 0/0 | 4236 | 13 | 0 | 0 | 13 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | AGCCT others(4231): Show |
chr13 | 25296625 | 25347421 |
| a0001c0003t0020 | 0/0 | 4236 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | AGCCT others(4231): Show |
chr13 | 25296625 | 25347421 |
| a0001c0005t0001 | 0/0 | 4236 | 4 | 4 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | AGCCT others(4231): Show |
chr13 | 25296625 | 25347421 |
| a0001c0006t0001 | 0/0 | 4236 | 4 | 0 | 4 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | AGCCT others(4231): Show |
chr13 | 25296625 | 25347421 |
| a0001c0008t0001 | 0/0 | 4236 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | AGCCT others(4231): Show |
chr13 | 25296625 | 25347421 |
| a0001c0010t0001 | 0/0 | 4236 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | AGCCT others(4231): Show |
chr13 | 25296625 | 25347421 |
| a0001c0012t0001 | 0/0 | 4236 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | AGCCT others(4231): Show |
chr13 | 25296625 | 25347421 |
| a0002c0002t0001 | 0/0 | 4236 | 110 | 11 | 16 | 67 | 5 | 11 | NUP58_chr13_25296625_25347421 | NUP58 | AGCCT others(4231): Show |
chr13 | 25296625 | 25347421 |
| a0002c0002t0003 | 0/0 | 4236 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | AGCCT others(4231): Show |
chr13 | 25296625 | 25347421 |
| a0002c0002t0008 | 0/0 | 4236 | 2 | 0 | 0 | 2 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | AGCCT others(4231): Show |
chr13 | 25296625 | 25347421 |
| a0002c0002t0016 | 0/0 | 4236 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | AGCCT others(4231): Show |
chr13 | 25296625 | 25347421 |
| a0002c0002t0021 | 0/0 | 4236 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | AGCCT others(4231): Show |
chr13 | 25296625 | 25347421 |
| a0003c0004t0001 | 0/0 | 4236 | 7 | 7 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | AGCCT others(4231): Show |
chr13 | 25296625 | 25347421 |
| a0004c0007t0003 | 0/1 | 4236 | 2 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | AGCCT others(4231): Show |
chr13 | 25296625 | 25347421 |
| a0005c0009t0001 | 0/0 | 4236 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | AGCCT others(4231): Show |
chr13 | 25296625 | 25347421 |
| a0006c0013t0010 | 0/0 | 4236 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | AGCCT others(4231): Show |
chr13 | 25296625 | 25347421 |
| a0007c0011t0004 | 0/0 | 4224 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | AGCCT others(4219): Show |
chr13 | 25296625 | 25347421 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 10 | 0 | 0 | 7 | 0 | 3 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0001g0007 | 0/0 | 5 | 3 | 2 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0001g0025 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0001g0028 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0002g0003 | 0/0 | 10 | 0 | 3 | 7 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0002g0006 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0002g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0003g0005 | 0/0 | 5 | 0 | 1 | 0 | 4 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0003g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0003g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0003g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0003g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0003g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0003g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0003g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0003g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0003g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0003g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0003g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0003g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0005g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0005g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0005g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0005g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0005g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0005g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0005g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0006g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0006g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0006g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0006g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0006g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0007g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0007g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0007g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0007g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0009g0005 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0010g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0011g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0011g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0012g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0012g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0013g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0013g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0014g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0015g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0017g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0018g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0001t0019g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0003t0004g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0003t0004g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0003t0004g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0003t0004g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0003t0004g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0003t0004g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0003t0004g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0003t0004g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0003t0004g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0003t0004g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0003t0004g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0003t0004g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0003t0004g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0003t0020g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0005t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0005t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0005t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0006t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0006t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0006t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0008t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0010t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0001c0012t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0002c0002t0001g0001 | 0/0 | 16 | 1 | 3 | 9 | 1 | 2 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0002c0002t0001g0004 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0002c0002t0001g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0002c0002t0001g0010 | 0/0 | 3 | 1 | 0 | 0 | 1 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0002c0002t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0002c0002t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0002c0002t0001g0014 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0002c0002t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0002c0002t0001g0016 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0002c0002t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0002c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0002c0002t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0002c0002t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0002c0002t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0002c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0002c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0002c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0002c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0002c0002t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0002c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0002c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0002c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0002c0002t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0002c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0002c0002t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0002c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0002c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0002c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0002c0002t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0002c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0002c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0002c0002t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0002c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0002c0002t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0002c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0002c0002t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0002c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0002c0002t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0002c0002t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0002c0002t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0002c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0002c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0002c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0002c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0002c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0002c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0002c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0002c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0002c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0002c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0002c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0002c0002t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0002c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0002c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0002c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0002c0002t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0002c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0002c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0002c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0002c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0002c0002t0003g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0002c0002t0008g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0002c0002t0008g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0002c0002t0016g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0002c0002t0021g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0003c0004t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0003c0004t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0003c0004t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0003c0004t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0003c0004t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0003c0004t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0003c0004t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0004c0007t0003g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0004c0007t0003g0170 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0005c0009t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0006c0013t0010g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| a0007c0011t0004g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0084 | EUR | GBR | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG00099 | hp2 | a0002 | c0002 | t0001 | g0001 | EUR | GBR | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG00140 | hp1 | a0002 | c0002 | t0001 | g0092 | EUR | GBR | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG00140 | hp2 | a0001 | c0001 | t0009 | g0005 | EUR | GBR | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0005 | EUR | FIN | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0026 | EUR | FIN | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG00323 | hp1 | a0002 | c0002 | t0001 | g0010 | EUR | FIN | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG00323 | hp2 | a0001 | c0001 | t0005 | g0087 | EUR | FIN | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | CHS | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG00423 | hp2 | a0002 | c0002 | t0001 | g0080 | EAS | CHS | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG00438 | hp1 | a0002 | c0002 | t0021 | g0001 | EAS | CHS | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | CHS | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG00558 | hp1 | a0002 | c0002 | t0001 | g0072 | EAS | CHS | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | CHS | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | CHS | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG00609 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | CHS | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0110 | AMR | PUR | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG00642 | hp1 | a0002 | c0002 | t0001 | g0074 | AMR | PUR | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG00733 | hp1 | a0002 | c0002 | t0001 | g0100 | AMR | PUR | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG00735 | hp1 | a0002 | c0002 | t0001 | g0014 | AMR | PUR | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG00738 | hp2 | a0001 | c0008 | t0001 | g0195 | AMR | PUR | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG00741 | hp1 | a0002 | c0002 | t0001 | g0060 | AMR | PUR | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG00741 | hp2 | a0002 | c0002 | t0001 | g0040 | AMR | PUR | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG01069 | hp1 | a0002 | c0002 | t0001 | g0091 | AMR | PUR | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0243 | AMR | PUR | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG01070 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG01070 | hp2 | a0001 | c0001 | t0003 | g0111 | AMR | PUR | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG01074 | hp1 | a0001 | c0006 | t0001 | g0219 | AMR | PUR | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG01074 | hp2 | a0001 | c0001 | t0015 | g0168 | AMR | PUR | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG01099 | hp1 | a0005 | c0009 | t0001 | g0061 | AMR | PUR | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG01099 | hp2 | a0001 | c0001 | t0005 | g0098 | AMR | PUR | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG01106 | hp1 | a0002 | c0002 | t0001 | g0051 | AMR | PUR | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG01109 | hp2 | a0002 | c0002 | t0001 | g0102 | AMR | PUR | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0039 | AMR | PUR | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG01243 | hp2 | a0001 | c0012 | t0001 | g0152 | AMR | PUR | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG01255 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | CLM | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG01256 | hp1 | a0001 | c0001 | t0009 | g0005 | AMR | CLM | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | CLM | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0070 | AMR | CLM | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0052 | AMR | CLM | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG01261 | hp2 | a0001 | c0001 | t0005 | g0053 | AMR | CLM | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG01346 | hp1 | a0004 | c0007 | t0003 | g0090 | AMR | CLM | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG01346 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG01358 | hp1 | a0002 | c0002 | t0001 | g0101 | AMR | CLM | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG01358 | hp2 | a0001 | c0001 | t0003 | g0105 | AMR | CLM | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0058 | AMR | CLM | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0031 | AMR | CLM | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG01496 | hp1 | a0001 | c0003 | t0020 | g0189 | AMR | CLM | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG01496 | hp2 | a0001 | c0001 | t0007 | g0149 | AMR | CLM | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0005 | EUR | IBS | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG01515 | hp2 | a0002 | c0002 | t0001 | g0043 | EUR | IBS | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG01516 | hp1 | a0001 | c0001 | t0005 | g0258 | EUR | IBS | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0005 | EUR | IBS | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG01517 | hp1 | a0001 | c0001 | t0005 | g0259 | EUR | IBS | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0005 | EUR | IBS | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | ACB | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | ACB | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG01891 | hp2 | a0001 | c0001 | t0006 | g0173 | AFR | ACB | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG01928 | hp1 | a0002 | c0002 | t0001 | g0016 | AMR | PEL | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG01928 | hp2 | a0001 | c0006 | t0001 | g0198 | AMR | PEL | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG01934 | hp1 | a0001 | c0006 | t0001 | g0020 | AMR | PEL | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0206 | AMR | PEL | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0121 | AMR | PEL | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0251 | AMR | PEL | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG01981 | hp1 | a0001 | c0001 | t0003 | g0005 | AMR | PEL | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG01981 | hp2 | a0002 | c0002 | t0003 | g0068 | AMR | PEL | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG02015 | hp1 | a0001 | c0003 | t0004 | g0182 | EAS | KHV | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG02015 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | KHV | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG02055 | hp1 | a0003 | c0004 | t0001 | g0271 | AFR | ACB | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | ACB | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0199 | EAS | KHV | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG02074 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG02129 | hp2 | a0002 | c0002 | t0001 | g0116 | EAS | KHV | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG02132 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG02132 | hp2 | a0001 | c0003 | t0004 | g0186 | EAS | KHV | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG02135 | hp1 | a0002 | c0002 | t0001 | g0114 | EAS | KHV | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | KHV | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | ACB | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | ACB | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG02148 | hp1 | a0002 | c0002 | t0001 | g0094 | AMR | PEL | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG02155 | hp1 | a0002 | c0002 | t0001 | g0125 | EAS | CDX | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG02155 | hp2 | a0001 | c0003 | t0004 | g0260 | EAS | CDX | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0238 | EAS | CDX | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG02165 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | CDX | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG02257 | hp1 | a0001 | c0005 | t0001 | g0024 | AFR | ACB | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0023 | AFR | ACB | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG02258 | hp1 | a0001 | c0001 | t0007 | g0150 | AFR | ACB | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG02258 | hp2 | a0001 | c0001 | t0010 | g0164 | AFR | ACB | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG02280 | hp1 | a0001 | c0005 | t0001 | g0166 | AFR | ACB | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | ACB | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG02293 | hp1 | a0001 | c0006 | t0001 | g0020 | AMR | PEL | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG02293 | hp2 | a0002 | c0002 | t0001 | g0176 | AMR | PEL | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG02451 | hp2 | a0006 | c0013 | t0010 | g0159 | AFR | ACB | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG02572 | hp1 | a0002 | c0002 | t0001 | g0046 | AFR | GWD | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG02615 | hp1 | a0003 | c0004 | t0001 | g0266 | AFR | GWD | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0086 | AFR | GWD | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG02622 | hp1 | a0003 | c0004 | t0001 | g0270 | AFR | GWD | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG02622 | hp2 | a0002 | c0002 | t0001 | g0008 | AFR | GWD | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0032 | AFR | GWD | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG02630 | hp2 | a0002 | c0002 | t0001 | g0088 | AFR | GWD | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG02683 | hp1 | a0001 | c0001 | t0003 | g0064 | SAS | PJL | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG02683 | hp2 | a0002 | c0002 | t0001 | g0014 | SAS | PJL | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0063 | SAS | PJL | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG02717 | hp2 | a0003 | c0004 | t0001 | g0268 | AFR | GWD | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0262 | SAS | PJL | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG02738 | hp1 | a0002 | c0002 | t0001 | g0119 | SAS | PJL | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0034 | SAS | PJL | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG02809 | hp2 | a0002 | c0002 | t0001 | g0044 | AFR | GWD | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0130 | AFR | GWD | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG02886 | hp1 | a0001 | c0010 | t0001 | g0165 | AFR | GWD | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG02886 | hp2 | a0003 | c0004 | t0001 | g0265 | AFR | GWD | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | GWD | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG02922 | hp1 | a0001 | c0001 | t0014 | g0011 | AFR | ESN | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG02922 | hp2 | a0001 | c0001 | t0013 | g0193 | AFR | ESN | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG02965 | hp1 | a0001 | c0001 | t0012 | g0161 | AFR | ESN | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG02965 | hp2 | a0001 | c0001 | t0006 | g0174 | AFR | ESN | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG02970 | hp1 | a0001 | c0005 | t0001 | g0024 | AFR | ESN | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG02970 | hp2 | a0001 | c0001 | t0006 | g0019 | AFR | ESN | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG02976 | hp1 | a0002 | c0002 | t0001 | g0008 | AFR | ESN | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | ESN | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG03098 | hp1 | a0001 | c0001 | t0006 | g0172 | AFR | MSL | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG03098 | hp2 | a0002 | c0002 | t0001 | g0045 | AFR | MSL | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG03130 | hp1 | a0001 | c0001 | t0006 | g0019 | AFR | ESN | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | ESN | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | ESN | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | ESN | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG03209 | hp1 | a0001 | c0001 | t0007 | g0151 | AFR | MSL | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0255 | AFR | MSL | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | MSL | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG03453 | hp2 | a0001 | c0001 | t0007 | g0148 | AFR | MSL | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | MSL | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | MSL | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG03490 | hp2 | a0002 | c0002 | t0001 | g0095 | SAS | PJL | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG03491 | hp1 | a0001 | c0001 | t0018 | g0264 | SAS | PJL | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG03491 | hp2 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG03492 | hp2 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG03516 | hp2 | a0001 | c0001 | t0006 | g0175 | AFR | ESN | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0033 | AFR | GWD | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG03654 | hp1 | a0001 | c0001 | t0003 | g0099 | SAS | PJL | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG03654 | hp2 | a0001 | c0001 | t0019 | g0188 | SAS | PJL | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0261 | SAS | STU | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0205 | SAS | STU | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG03704 | hp1 | a0002 | c0002 | t0001 | g0109 | SAS | PJL | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG03704 | hp2 | a0001 | c0001 | t0011 | g0227 | SAS | PJL | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG03710 | hp1 | a0002 | c0002 | t0016 | g0055 | SAS | PJL | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0213 | SAS | PJL | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG03831 | hp1 | a0002 | c0002 | t0001 | g0082 | SAS | BEB | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG03831 | hp2 | a0001 | c0001 | t0011 | g0234 | SAS | BEB | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0233 | SAS | BEB | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0059 | SAS | BEB | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0228 | SAS | STU | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG04115 | hp2 | a0002 | c0002 | t0001 | g0056 | SAS | STU | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG04184 | hp1 | a0002 | c0002 | t0001 | g0050 | SAS | BEB | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0208 | SAS | BEB | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0200 | SAS | STU | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0253 | SAS | STU | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG04228 | hp1 | a0002 | c0002 | t0001 | g0010 | SAS | STU | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG04228 | hp2 | a0001 | c0001 | t0005 | g0104 | SAS | STU | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0083 | AFR | YRI | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA18522 | hp2 | a0002 | c0002 | t0001 | g0008 | AFR | YRI | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CHB | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA18612 | hp2 | a0002 | c0002 | t0001 | g0097 | EAS | CHB | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | YRI | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0131 | AFR | YRI | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA18939 | hp1 | a0001 | c0003 | t0004 | g0187 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA18940 | hp1 | a0002 | c0002 | t0001 | g0079 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA18942 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA18944 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA18945 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA18946 | hp2 | a0002 | c0002 | t0001 | g0171 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA18950 | hp2 | a0002 | c0002 | t0001 | g0073 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA18952 | hp1 | a0002 | c0002 | t0001 | g0048 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA18952 | hp2 | a0001 | c0003 | t0004 | g0179 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA18953 | hp2 | a0002 | c0002 | t0001 | g0196 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA18956 | hp1 | a0002 | c0002 | t0001 | g0129 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA18962 | hp1 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA18963 | hp2 | a0001 | c0003 | t0004 | g0178 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA18964 | hp1 | a0002 | c0002 | t0001 | g0128 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA18965 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA18966 | hp2 | a0002 | c0002 | t0001 | g0107 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA18968 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA18970 | hp1 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA18971 | hp2 | a0002 | c0002 | t0001 | g0078 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA18973 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA18975 | hp1 | a0002 | c0002 | t0001 | g0117 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA18975 | hp2 | a0001 | c0003 | t0004 | g0185 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA18977 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA18977 | hp2 | a0002 | c0002 | t0001 | g0069 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA18978 | hp2 | a0002 | c0002 | t0001 | g0257 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA18979 | hp2 | a0001 | c0003 | t0004 | g0183 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA18980 | hp1 | a0002 | c0002 | t0001 | g0124 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA18981 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA18982 | hp1 | a0002 | c0002 | t0001 | g0263 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA18984 | hp1 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA18986 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA18987 | hp1 | a0001 | c0003 | t0004 | g0191 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA18987 | hp2 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA18990 | hp1 | a0002 | c0002 | t0008 | g0077 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA18990 | hp2 | a0002 | c0002 | t0001 | g0256 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA18992 | hp2 | a0002 | c0002 | t0001 | g0049 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA18993 | hp2 | a0002 | c0002 | t0001 | g0054 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA18994 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA19001 | hp1 | a0002 | c0002 | t0001 | g0112 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA19003 | hp1 | a0002 | c0002 | t0001 | g0071 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA19004 | hp2 | a0002 | c0002 | t0001 | g0075 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA19006 | hp1 | a0002 | c0002 | t0001 | g0120 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA19011 | hp2 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA19012 | hp1 | a0002 | c0002 | t0001 | g0108 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA19012 | hp2 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0035 | AFR | LWK | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0042 | AFR | LWK | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA19054 | hp2 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA19055 | hp1 | a0002 | c0002 | t0001 | g0066 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA19055 | hp2 | a0001 | c0003 | t0004 | g0180 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA19057 | hp2 | a0001 | c0003 | t0004 | g0177 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA19058 | hp1 | a0002 | c0002 | t0001 | g0169 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA19063 | hp1 | a0002 | c0002 | t0001 | g0067 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA19063 | hp2 | a0001 | c0003 | t0004 | g0181 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA19065 | hp1 | a0002 | c0002 | t0001 | g0123 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA19067 | hp1 | a0002 | c0002 | t0001 | g0103 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA19068 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA19070 | hp2 | a0002 | c0002 | t0001 | g0093 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA19072 | hp1 | a0007 | c0011 | t0004 | g0190 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA19072 | hp2 | a0002 | c0002 | t0001 | g0062 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA19075 | hp1 | a0002 | c0002 | t0001 | g0106 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA19076 | hp1 | a0002 | c0002 | t0001 | g0126 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA19077 | hp2 | a0002 | c0002 | t0001 | g0096 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA19078 | hp1 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA19079 | hp1 | a0002 | c0002 | t0008 | g0004 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA19082 | hp1 | a0002 | c0002 | t0001 | g0115 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA19083 | hp1 | a0002 | c0002 | t0001 | g0113 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA19084 | hp1 | a0001 | c0003 | t0004 | g0184 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA19084 | hp2 | a0002 | c0002 | t0001 | g0076 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA19086 | hp1 | a0002 | c0002 | t0001 | g0047 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA19090 | hp1 | a0002 | c0002 | t0001 | g0057 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA19091 | hp2 | a0002 | c0002 | t0001 | g0081 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA19240 | hp1 | a0001 | c0001 | t0014 | g0011 | AFR | YRI | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | YRI | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA20129 | hp1 | a0002 | c0002 | t0001 | g0010 | AFR | ASW | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0023 | AFR | ASW | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0085 | EUR | TSI | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA20805 | hp2 | a0002 | c0002 | t0001 | g0089 | EUR | TSI | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG01123 | hp1 | a0001 | c0001 | t0005 | g0118 | AMR | CLM | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG01123 | hp2 | a0002 | c0002 | t0001 | g0127 | AMR | CLM | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG02109 | hp1 | a0001 | c0005 | t0001 | g0167 | AFR | ACB | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0254 | AFR | ACB | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG02486 | hp1 | a0003 | c0004 | t0001 | g0269 | AFR | ACB | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG02559 | hp1 | a0001 | c0001 | t0013 | g0192 | AFR | ACB | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG02559 | hp2 | a0002 | c0002 | t0001 | g0008 | AFR | ACB | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | MSL | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | MSL | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG06807 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | USA | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| HG06807 | hp2 | a0001 | c0001 | t0017 | g0153 | AFR | USA | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA20300 | hp1 | a0001 | c0001 | t0012 | g0154 | AFR | USA | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA20300 | hp2 | a0003 | c0004 | t0001 | g0267 | AFR | USA | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA21309 | hp1 | a0002 | c0002 | t0001 | g0065 | AFR | LWK | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | LWK | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| homoSapiens | chm13v2 | a0004 | c0007 | t0003 | g0170 | REF | REF | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0028 | REF | REF | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:25301868 | C | T | 1 | a0006 | 1 | HG02451.hp2 | missense_variant | MODERATE | c.95C>T | p.Thr32Met | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/16 | 244/4236 | 95/1800 | 32/599 | chr13 | 25301868 | |||
| chr13:25301873 | G | A | 2 | a0002 a0005 |
116 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(113): Show |
missense_variant | MODERATE | c.100G>A | p.Ala34Thr | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/16 | 249/4236 | 100/1800 | 34/599 | chr13 | 25301873 | |||
| chr13:25312934 | A | G | 1 | a0003 | 7 | HG02055.hp1 HG02486.hp1 HG02615.hp1 others(4): Show |
missense_variant | MODERATE | c.338A>G | p.Asn113Ser | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 4/16 | 487/4236 | 338/1800 | 113/599 | chr13 | 25312934 | |||
| chr13:25313673 | T | C | 1 | a0005 | 1 | HG01099.hp1 | missense_variant | MODERATE | c.496T>C | p.Ser166Pro | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 5/16 | 645/4236 | 496/1800 | 166/599 | chr13 | 25313673 | |||
| chr13:25315357 | G | A | 1 | a0004 | 1 | HG01346.hp1 | missense_variant&splice_region_variant | MODERATE | c.575G>A | p.Gly192Glu | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/16 | 724/4236 | 575/1800 | 192/599 | chr13 | 25315357 | |||
| chr13:25319334 | ACGGGAAC others(5): Show |
A | 1 | a0007 | 1 | NA19072.hp1 | disruptive_inframe_deletion | MODERATE | c.696_707delGGGAACAA others(4): Show |
p.Gly233_Pro236del | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 7/16 | 845/4236 | 696/1800 | 232/599 | INFO_REALIGN_3_PRIME | chr13 | 25319334 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:25301869 | G | C | 1 | a0001c0008 | 1 | HG00738.hp2 | synonymous_variant | LOW | c.96G>C | p.Thr32Thr | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/16 | 245/4236 | 96/1800 | 32/599 | chr13 | 25301869 | |||
| chr13:25313640 | T | C | 2 | a0001c0005 a0001c0010 |
5 | HG02109.hp1 HG02257.hp1 HG02280.hp1 others(2): Show |
synonymous_variant | LOW | c.463T>C | p.Leu155Leu | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 5/16 | 612/4236 | 463/1800 | 155/599 | chr13 | 25313640 | |||
| chr13:25313684 | C | T | 1 | a0001c0010 | 1 | HG02886.hp1 | synonymous_variant | LOW | c.507C>T | p.Leu169Leu | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 5/16 | 656/4236 | 507/1800 | 169/599 | chr13 | 25313684 | |||
| chr13:25326994 | T | C | 1 | a0001c0012 | 1 | HG01243.hp2 | synonymous_variant | LOW | c.1110T>C | p.His370His | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 11/16 | 1259/4236 | 1110/1800 | 370/599 | chr13 | 25326994 | |||
| chr13:25327027 | C | G | 1 | a0001c0006 | 4 | HG01074.hp1 HG01928.hp2 HG01934.hp1 others(1): Show |
synonymous_variant | LOW | c.1143C>G | p.Thr381Thr | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 11/16 | 1292/4236 | 1143/1800 | 381/599 | chr13 | 25327027 | |||
| chr13:25340083 | A | G | 2 | a0001c0003 a0007c0011 |
15 | HG01496.hp1 HG02015.hp1 HG02132.hp2 others(12): Show |
synonymous_variant | LOW | c.1749A>G | p.Gln583Gln | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 16/16 | 1898/4236 | 1749/1800 | 583/599 | chr13 | 25340083 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:25301639 | C | G | 1 | a0001c0001t0014 | 2 | HG02922.hp1 NA19240.hp1 |
5_prime_UTR_variant | MODIFIER | c.-135C>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/16 | 135 | chr13 | 25301639 | ||||||
| chr13:25301706 | G | T | 1 | a0002c0002t0021 | 1 | HG00438.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-68G>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/16 | chr13 | 25301706 | |||||||
| chr13:25301741 | C | T | 4 | a0001c0001t0019 a0001c0003t0004 a0001c0003t0020 others(1): Show |
16 | HG01496.hp1 HG02015.hp1 HG02132.hp2 others(13): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-33C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/16 | chr13 | 25301741 | |||||||
| chr13:25301772 | A | C | 1 | a0001c0001t0007 | 4 | HG01496.hp2 HG02258.hp1 HG03209.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-2A>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/16 | 2 | chr13 | 25301772 | ||||||
| chr13:25340272 | C | T | 1 | a0001c0001t0014 | 2 | HG02922.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*138C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 16/16 | 138 | chr13 | 25340272 | ||||||
| chr13:25340328 | C | T | 6 | a0001c0001t0006 a0001c0001t0014 a0001c0001t0018 others(3): Show |
24 | HG01496.hp1 HG01891.hp2 HG02015.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*194C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 16/16 | 194 | chr13 | 25340328 | ||||||
| chr13:25340687 | C | T | 1 | a0001c0001t0017 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*553C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 16/16 | 553 | chr13 | 25340687 | ||||||
| chr13:25340713 | G | A | 1 | a0001c0001t0002 | 46 | HG00438.hp2 HG00733.hp2 HG01069.hp2 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*579G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 16/16 | 579 | chr13 | 25340713 | ||||||
| chr13:25340767 | A | G | 1 | a0001c0001t0013 | 2 | HG02559.hp1 HG02922.hp2 |
3_prime_UTR_variant | MODIFIER | c.*633A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 16/16 | 633 | chr13 | 25340767 | ||||||
| chr13:25340843 | G | A | 1 | a0001c0003t0020 | 1 | HG01496.hp1 | 3_prime_UTR_variant | MODIFIER | c.*709G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 16/16 | 709 | chr13 | 25340843 | ||||||
| chr13:25340876 | C | T | 3 | a0001c0003t0004 a0001c0003t0020 a0007c0011t0004 |
15 | HG01496.hp1 HG02015.hp1 HG02132.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*742C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 16/16 | 742 | chr13 | 25340876 | ||||||
| chr13:25341004 | G | C | 1 | a0002c0002t0008 | 2 | NA18990.hp1 NA19079.hp1 |
3_prime_UTR_variant | MODIFIER | c.*870G>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 16/16 | 870 | chr13 | 25341004 | ||||||
| chr13:25341235 | C | A | 1 | a0001c0001t0014 | 2 | HG02922.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1101C>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 16/16 | 1101 | chr13 | 25341235 | ||||||
| chr13:25341389 | A | G | 1 | a0001c0001t0012 | 2 | HG02965.hp1 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1255A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 16/16 | 1255 | chr13 | 25341389 | ||||||
| chr13:25341654 | A | C | 2 | a0001c0001t0006 a0001c0001t0012 |
8 | HG01891.hp2 HG02965.hp1 HG02965.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1520A>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 16/16 | 1520 | chr13 | 25341654 | ||||||
| chr13:25341749 | A | G | 1 | a0001c0001t0005 | 7 | HG00323.hp2 HG01099.hp2 HG01123.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1615A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 16/16 | 1615 | chr13 | 25341749 | ||||||
| chr13:25341810 | A | G | 1 | a0002c0002t0016 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1676A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 16/16 | 1676 | chr13 | 25341810 | ||||||
| chr13:25341835 | G | T | 2 | a0001c0001t0006 a0001c0001t0012 |
8 | HG01891.hp2 HG02965.hp1 HG02965.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1701G>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 16/16 | 1701 | chr13 | 25341835 | ||||||
| chr13:25341885 | A | G | 1 | a0001c0001t0011 | 2 | HG03704.hp2 HG03831.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1751A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 16/16 | 1751 | chr13 | 25341885 | ||||||
| chr13:25341921 | T | C | 5 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0009 others(2): Show |
43 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*1787T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 16/16 | 1787 | chr13 | 25341921 | ||||||
| chr13:25341985 | A | G | 1 | a0001c0001t0009 | 2 | HG00140.hp2 HG01256.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1851A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 16/16 | 1851 | chr13 | 25341985 | ||||||
| chr13:25342055 | ATTAT | A | 1 | a0001c0001t0007 | 4 | HG01496.hp2 HG02258.hp1 HG03209.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1926_*1929delTTAT | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 16/16 | 1926 | INFO_REALIGN_3_PRIME | chr13 | 25342055 | |||||
| chr13:25342090 | T | C | 2 | a0001c0001t0010 a0006c0013t0010 |
2 | HG02258.hp2 HG02451.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1956T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 16/16 | 1956 | chr13 | 25342090 | ||||||
| chr13:25342205 | T | A | 1 | a0001c0001t0014 | 2 | HG02922.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2071T>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 16/16 | 2071 | chr13 | 25342205 | ||||||
| chr13:25342305 | G | A | 1 | a0001c0001t0015 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2171G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 16/16 | 2171 | chr13 | 25342305 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:25301894 | C | T | 7 | a0003c0004t0001g0265 a0003c0004t0001g0266 a0003c0004t0001g0267 others(4): Show |
7 | HG02055.hp1 HG02486.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.107+14C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25301894 | |||||||
| chr13:25301909 | C | A | 1 | a0001c0001t0003g0026 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.107+29C>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25301909 | |||||||
| chr13:25301983 | C | T | 1 | a0001c0001t0001g0025 | 2 | HG01243.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.107+103C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25301983 | |||||||
| chr13:25302135 | A | G | 270 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0017 others(267): Show |
346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.107+255A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25302135 | |||||||
| chr13:25302232 | A | G | 1 | a0001c0001t0018g0264 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.107+352A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25302232 | |||||||
| chr13:25302317 | C | T | 1 | a0002c0002t0001g0263 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.107+437C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25302317 | |||||||
| chr13:25302537 | T | G | 1 | a0001c0001t0001g0030 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.107+657T>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25302537 | |||||||
| chr13:25302587 | T | A | 3 | a0001c0001t0003g0031 a0001c0001t0003g0032 a0001c0001t0003g0033 |
3 | HG01361.hp2 HG02630.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.107+707T>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25302587 | |||||||
| chr13:25302647 | A | G | 2 | a0001c0001t0002g0261 a0001c0001t0002g0262 |
2 | HG02735.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.107+767A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25302647 | |||||||
| chr13:25302773 | G | A | 1 | a0001c0001t0002g0034 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.107+893G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25302773 | |||||||
| chr13:25302784 | A | C | 1 | a0001c0001t0003g0033 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.107+904A>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25302784 | |||||||
| chr13:25302942 | T | C | 2 | a0001c0001t0014g0011 a0001c0001t0018g0264 |
3 | HG02922.hp1 HG03491.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.107+1062T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25302942 | |||||||
| chr13:25303088 | C | T | 1 | a0001c0003t0004g0260 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.107+1208C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25303088 | |||||||
| chr13:25303117 | A | G | 2 | a0001c0001t0005g0258 a0001c0001t0005g0259 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.107+1237A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25303117 | |||||||
| chr13:25303128 | C | T | 1 | a0001c0001t0018g0264 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.107+1248C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25303128 | |||||||
| chr13:25303202 | C | T | 2 | a0002c0002t0001g0256 a0002c0002t0001g0257 |
2 | NA18978.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.107+1322C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25303202 | |||||||
| chr13:25303297 | G | C | 1 | a0001c0001t0003g0035 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.107+1417G>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25303297 | |||||||
| chr13:25303348 | A | G | 5 | a0001c0001t0003g0023 a0001c0001t0003g0035 a0001c0001t0003g0254 others(2): Show |
7 | HG02109.hp2 HG02257.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.107+1468A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25303348 | |||||||
| chr13:25303377 | TAACTG | T | 4 | a0001c0001t0001g0007 a0001c0001t0001g0036 a0001c0001t0001g0037 others(1): Show |
8 | HG00738.hp1 HG01109.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.107+1500_107+1504d others(7): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25303377 | ||||||
| chr13:25303444 | C | CT | 73 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0022 others(70): Show |
103 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.107+1575dupT | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25303444 | ||||||
| chr13:25303502 | G | T | 1 | a0001c0001t0014g0011 | 2 | HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.107+1622G>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25303502 | |||||||
| chr13:25303755 | T | C | 1 | a0001c0001t0001g0194 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.107+1875T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25303755 | |||||||
| chr13:25303911 | C | T | 4 | a0003c0004t0001g0268 a0003c0004t0001g0269 a0003c0004t0001g0270 others(1): Show |
4 | HG02055.hp1 HG02486.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.107+2031C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25303911 | |||||||
| chr13:25303913 | A | G | 1 | a0001c0001t0001g0253 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.107+2033A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25303913 | |||||||
| chr13:25303957 | C | T | 2 | a0001c0001t0013g0192 a0001c0001t0013g0193 |
2 | HG02559.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.107+2077C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25303957 | |||||||
| chr13:25303991 | C | T | 1 | a0001c0001t0014g0011 | 2 | HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.107+2111C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25303991 | |||||||
| chr13:25304282 | A | G | 16 | a0001c0001t0019g0188 a0001c0003t0004g0177 a0001c0003t0004g0178 others(13): Show |
16 | HG01496.hp1 HG02015.hp1 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.107+2402A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25304282 | |||||||
| chr13:25304305 | G | C | 2 | a0001c0001t0003g0031 a0001c0001t0003g0039 |
2 | HG01175.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.107+2425G>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25304305 | |||||||
| chr13:25304336 | G | A | 1 | a0001c0001t0014g0011 | 2 | HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.107+2456G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25304336 | |||||||
| chr13:25304463 | G | T | 1 | a0002c0002t0001g0176 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.107+2583G>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25304463 | |||||||
| chr13:25304473 | C | G | 5 | a0001c0001t0006g0019 a0001c0001t0006g0172 a0001c0001t0006g0173 others(2): Show |
6 | HG01891.hp2 HG02965.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.107+2593C>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25304473 | |||||||
| chr13:25304478 | T | TTA | 17 | a0001c0001t0001g0007 a0001c0001t0001g0145 a0001c0001t0001g0156 others(14): Show |
22 | HG00438.hp1 HG00609.hp2 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.107+2636_107+2637d others(4): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25304478 | ||||||
| chr13:25304478 | T | TTATA | 23 | a0001c0001t0001g0007 a0001c0001t0001g0036 a0001c0001t0001g0037 others(20): Show |
25 | HG00558.hp1 HG00738.hp1 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.107+2634_107+2637d others(6): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25304478 | ||||||
| chr13:25304478 | T | TTATATA | 9 | a0001c0001t0001g0007 a0002c0002t0001g0004 a0002c0002t0001g0013 others(6): Show |
9 | HG02572.hp1 HG03098.hp2 HG03579.hp1 others(6): Show |
intron_variant | MODIFIER | c.107+2632_107+2637d others(8): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25304478 | ||||||
| chr13:25304478 | T | TTATATAT others(1): Show |
8 | a0002c0002t0001g0004 a0002c0002t0001g0008 a0002c0002t0001g0012 others(5): Show |
10 | HG02015.hp2 HG02622.hp2 HG02683.hp2 others(7): Show |
intron_variant | MODIFIER | c.107+2630_107+2637d others(10): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25304478 | ||||||
| chr13:25304478 | T | TTATATAT others(3): Show |
2 | a0001c0001t0007g0149 a0002c0002t0001g0080 |
2 | HG00423.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.107+2628_107+2637d others(12): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25304478 | ||||||
| chr13:25304478 | TTA | T | 34 | a0001c0001t0001g0018 a0001c0001t0001g0027 a0001c0001t0001g0138 others(31): Show |
38 | HG00323.hp1 HG00735.hp1 HG01099.hp1 others(35): Show |
intron_variant | MODIFIER | c.107+2636_107+2637d others(4): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25304478 | ||||||
| chr13:25304478 | TTATA | T | 14 | a0001c0001t0001g0155 a0001c0001t0001g0157 a0001c0001t0002g0006 others(11): Show |
16 | HG01123.hp2 HG01256.hp2 HG01346.hp2 others(13): Show |
intron_variant | MODIFIER | c.107+2634_107+2637d others(6): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25304478 | ||||||
| chr13:25304478 | TTATATA | T | 16 | a0001c0001t0001g0018 a0001c0001t0001g0041 a0001c0001t0001g0139 others(13): Show |
19 | HG00639.hp1 HG00642.hp2 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.107+2632_107+2637d others(8): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25304478 | ||||||
| chr13:25304478 | TTATATAT others(1): Show |
T | 38 | a0001c0001t0001g0002 a0001c0001t0001g0022 a0001c0001t0001g0140 others(35): Show |
52 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.107+2630_107+2637d others(10): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25304478 | ||||||
| chr13:25304478 | TTATATAT others(3): Show |
T | 32 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0021 others(29): Show |
42 | HG00558.hp2 HG00609.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.107+2628_107+2637d others(12): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25304478 | ||||||
| chr13:25304478 | TTATATAT others(7): Show |
T | 1 | a0002c0002t0001g0063 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.107+2624_107+2637d others(16): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25304478 | ||||||
| chr13:25304478 | TTATATAT others(9): Show |
T | 4 | a0001c0001t0001g0232 a0001c0001t0007g0151 a0002c0002t0008g0004 others(1): Show |
4 | HG03209.hp1 NA18982.hp2 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.107+2622_107+2637d others(18): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25304478 | ||||||
| chr13:25304478 | TTATATAT others(11): Show |
T | 1 | a0002c0002t0001g0004 | 2 | NA18942.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.107+2620_107+2637d others(20): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25304478 | ||||||
| chr13:25304478 | TTATATAT others(15): Show |
T | 1 | a0001c0001t0018g0264 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.107+2616_107+2637d others(24): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25304478 | ||||||
| chr13:25304478 | TTATATAT others(17): Show |
T | 11 | a0002c0002t0001g0001 a0002c0002t0001g0091 a0002c0002t0001g0094 others(8): Show |
12 | HG01069.hp1 HG01358.hp1 HG02074.hp2 others(9): Show |
intron_variant | MODIFIER | c.107+2614_107+2637d others(26): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25304478 | ||||||
| chr13:25304494 | A | G | 1 | a0002c0002t0001g0171 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.107+2614A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25304494 | |||||||
| chr13:25304496 | ATATATAT others(18): Show |
A | 1 | a0002c0002t0001g0171 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.107+2618_107+2642d others(27): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25304496 | ||||||
| chr13:25304500 | A | G | 10 | a0001c0001t0003g0005 a0001c0001t0003g0026 a0001c0001t0003g0052 others(7): Show |
15 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(12): Show |
intron_variant | MODIFIER | c.107+2620A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25304500 | |||||||
| chr13:25304502 | A | G | 1 | a0001c0001t0001g0137 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.107+2622A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25304502 | |||||||
| chr13:25304502 | ATATATAT others(12): Show |
A | 10 | a0001c0001t0003g0005 a0001c0001t0003g0026 a0001c0001t0003g0052 others(7): Show |
15 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(12): Show |
intron_variant | MODIFIER | c.107+2624_107+2642d others(21): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25304502 | ||||||
| chr13:25304504 | A | G | 1 | a0001c0003t0004g0185 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.107+2624A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25304504 | |||||||
| chr13:25304504 | ATATATAT others(10): Show |
A | 1 | a0001c0001t0001g0137 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.107+2626_107+2642d others(19): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25304504 | ||||||
| chr13:25304506 | A | G | 1 | a0001c0001t0014g0011 | 2 | HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.107+2626A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25304506 | |||||||
| chr13:25304506 | ATATATAT others(8): Show |
A | 1 | a0001c0003t0004g0185 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.107+2628_107+2642d others(17): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25304506 | ||||||
| chr13:25304508 | A | G | 2 | a0001c0003t0004g0179 a0003c0004t0001g0266 |
2 | HG02615.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.107+2628A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25304508 | |||||||
| chr13:25304508 | ATATATAT others(7): Show |
A | 1 | a0001c0001t0014g0011 | 2 | HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.107+2630_107+2643d others(16): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25304508 | ||||||
| chr13:25304510 | A | G | 5 | a0001c0001t0001g0122 a0001c0001t0002g0206 a0001c0001t0002g0250 others(2): Show |
5 | HG00323.hp2 HG01934.hp1 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.107+2630A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25304510 | |||||||
| chr13:25304510 | ATATATAT others(4): Show |
A | 2 | a0001c0003t0004g0179 a0003c0004t0001g0266 |
2 | HG02615.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.107+2632_107+2642d others(13): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25304510 | ||||||
| chr13:25304512 | A | G | 11 | a0001c0001t0001g0122 a0001c0001t0001g0142 a0001c0001t0003g0042 others(8): Show |
11 | HG01099.hp2 HG01123.hp1 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.107+2632A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25304512 | |||||||
| chr13:25304513 | TATATGTA | T | 3 | a0001c0001t0002g0206 a0001c0001t0002g0250 a0001c0006t0001g0020 |
3 | HG01934.hp1 HG01934.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.107+2634_107+2640d others(9): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25304513 | |||||||
| chr13:25304514 | A | G | 8 | a0001c0001t0001g0025 a0001c0001t0003g0031 a0001c0001t0003g0039 others(5): Show |
8 | HG00639.hp2 HG01070.hp2 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.107+2634A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25304514 | |||||||
| chr13:25304514 | ATATGTAT | A | 11 | a0001c0001t0001g0122 a0001c0001t0001g0142 a0001c0001t0003g0042 others(8): Show |
11 | HG01099.hp2 HG01123.hp1 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.107+2636_107+2642d others(9): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25304514 | ||||||
| chr13:25304516 | A | G | 1 | a0001c0001t0001g0143 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.107+2636A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25304516 | |||||||
| chr13:25304516 | ATGTAT | A | 8 | a0001c0001t0001g0025 a0001c0001t0003g0031 a0001c0001t0003g0039 others(5): Show |
8 | HG00639.hp2 HG01070.hp2 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.107+2638_107+2642d others(7): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25304516 | ||||||
| chr13:25304518 | G | A | 25 | a0001c0001t0001g0025 a0001c0001t0001g0134 a0001c0001t0003g0083 others(22): Show |
25 | HG01070.hp1 HG01496.hp1 HG02015.hp1 others(22): Show |
intron_variant | MODIFIER | c.107+2638G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25304518 | |||||||
| chr13:25304520 | A | ATATATAT others(6): Show |
1 | a0002c0002t0001g0012 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.107+2641_107+2642i others(15): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25304520 | ||||||
| chr13:25304520 | A | G | 7 | a0001c0001t0001g0025 a0001c0001t0001g0134 a0001c0005t0001g0166 others(4): Show |
7 | HG01070.hp1 HG02109.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.107+2640A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25304520 | |||||||
| chr13:25304520 | AT | A | 15 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0138 others(12): Show |
15 | HG01257.hp1 HG01361.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.107+2655delT | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25304520 | ||||||
| chr13:25304521 | T | TA | 4 | a0001c0001t0001g0025 a0001c0001t0001g0134 a0002c0002t0001g0001 others(1): Show |
4 | HG01070.hp1 HG03139.hp1 NA19078.hp1 others(1): Show |
intron_variant | MODIFIER | c.107+2641_107+2642i others(3): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25304521 | |||||||
| chr13:25304521 | T | TATATGTA | 9 | a0001c0001t0013g0193 a0001c0003t0004g0178 a0001c0003t0004g0181 others(6): Show |
9 | HG01496.hp1 HG02155.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.107+2641_107+2642i others(9): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25304521 | |||||||
| chr13:25304521 | T | TATGTA | 4 | a0001c0003t0004g0177 a0001c0003t0004g0180 a0001c0003t0004g0186 others(1): Show |
4 | HG02132.hp2 HG02717.hp2 NA19055.hp2 others(1): Show |
intron_variant | MODIFIER | c.107+2641_107+2642i others(7): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25304521 | |||||||
| chr13:25304521 | T | TGTA | 6 | a0001c0001t0003g0083 a0001c0001t0019g0188 a0001c0003t0004g0182 others(3): Show |
6 | HG02015.hp1 HG03490.hp2 HG03654.hp2 others(3): Show |
intron_variant | MODIFIER | c.107+2641_107+2642i others(5): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25304521 | |||||||
| chr13:25304578 | G | A | 1 | a0002c0002t0001g0040 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.107+2698G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25304578 | |||||||
| chr13:25304790 | A | C | 1 | a0002c0002t0001g0169 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.107+2910A>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25304790 | |||||||
| chr13:25304871 | A | G | 1 | a0001c0001t0015g0168 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.108-2935A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25304871 | |||||||
| chr13:25305025 | G | A | 1 | a0001c0001t0001g0041 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.108-2781G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25305025 | |||||||
| chr13:25305047 | G | A | 1 | a0001c0003t0004g0177 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.108-2759G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25305047 | |||||||
| chr13:25305057 | T | C | 1 | a0001c0008t0001g0195 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.108-2749T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25305057 | |||||||
| chr13:25305130 | G | GT | 11 | a0001c0001t0001g0029 a0001c0001t0001g0155 a0001c0001t0001g0156 others(8): Show |
11 | HG01175.hp2 HG01243.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.108-2645dupT | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25305130 | ||||||
| chr13:25305130 | G | GTT | 8 | a0001c0001t0001g0018 a0001c0001t0001g0041 a0001c0001t0001g0160 others(5): Show |
9 | HG02055.hp2 HG02145.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.108-2646_108-2645d others(4): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25305130 | ||||||
| chr13:25305130 | G | GTTT | 10 | a0001c0001t0006g0174 a0001c0001t0006g0175 a0001c0001t0019g0188 others(7): Show |
10 | HG01496.hp1 HG02132.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.108-2647_108-2645d others(5): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25305130 | ||||||
| chr13:25305130 | G | GTTTTTTT others(4): Show |
1 | a0001c0010t0001g0165 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.108-2655_108-2645d others(13): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25305130 | ||||||
| chr13:25305130 | G | GTTTTTTT others(10): Show |
1 | a0001c0005t0001g0166 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.108-2661_108-2645d others(19): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25305130 | ||||||
| chr13:25305130 | G | GTTTTTTT others(12): Show |
1 | a0001c0005t0001g0167 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.108-2663_108-2645d others(21): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25305130 | ||||||
| chr13:25305130 | GTTTTTTT others(3): Show |
G | 1 | a0001c0001t0006g0172 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.108-2654_108-2645d others(12): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25305130 | ||||||
| chr13:25305130 | GTTTTTTT others(4): Show |
G | 4 | a0003c0004t0001g0265 a0003c0004t0001g0266 a0003c0004t0001g0267 others(1): Show |
4 | HG02055.hp1 HG02615.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.108-2655_108-2645d others(13): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25305130 | ||||||
| chr13:25305130 | GTTTTTTT others(5): Show |
G | 4 | a0001c0003t0004g0178 a0003c0004t0001g0268 a0003c0004t0001g0269 others(1): Show |
4 | HG02486.hp1 HG02622.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.108-2656_108-2645d others(14): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25305130 | ||||||
| chr13:25305130 | GTTTTTTT others(6): Show |
G | 4 | a0001c0001t0001g0007 a0001c0001t0001g0036 a0001c0001t0001g0037 others(1): Show |
8 | HG00738.hp1 HG01109.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.108-2657_108-2645d others(15): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25305130 | ||||||
| chr13:25305139 | T | G | 1 | a0001c0001t0003g0042 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.108-2667T>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25305139 | |||||||
| chr13:25305139 | T | TTTGTTTG | 116 | a0001c0001t0001g0030 a0001c0001t0001g0122 a0001c0001t0003g0005 others(113): Show |
154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.108-2665_108-2664i others(9): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25305139 | ||||||
| chr13:25305139 | T | TTTTGTTT others(1): Show |
8 | a0001c0001t0001g0132 a0001c0001t0001g0197 a0001c0001t0001g0200 others(5): Show |
8 | HG00735.hp2 HG01928.hp2 HG02074.hp1 others(5): Show |
intron_variant | MODIFIER | c.108-2664_108-2663i others(10): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25305139 | ||||||
| chr13:25305142 | T | G | 5 | a0002c0002t0001g0126 a0002c0002t0001g0127 a0002c0002t0001g0128 others(2): Show |
5 | HG01123.hp2 NA18956.hp1 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.108-2664T>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25305142 | |||||||
| chr13:25305143 | T | G | 125 | a0001c0001t0001g0030 a0001c0001t0001g0122 a0001c0001t0001g0132 others(122): Show |
163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.108-2663T>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25305143 | |||||||
| chr13:25305143 | T | TTTTGTTT others(1): Show |
60 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0021 others(57): Show |
90 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.108-2660_108-2659i others(10): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25305143 | ||||||
| chr13:25305144 | T | G | 1 | a0001c0001t0014g0011 | 2 | HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.108-2662T>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25305144 | |||||||
| chr13:25305146 | T | G | 8 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0135 others(5): Show |
8 | HG01123.hp2 HG01884.hp1 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.108-2660T>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25305146 | |||||||
| chr13:25305146 | T | TTGTTTGT others(3): Show |
1 | a0001c0001t0002g0251 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.108-2659_108-2658i others(12): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25305146 | ||||||
| chr13:25305147 | T | G | 194 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0021 others(191): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.108-2659T>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25305147 | |||||||
| chr13:25305147 | T | TGTTTGTT others(2): Show |
4 | a0001c0001t0001g0247 a0001c0001t0001g0248 a0001c0001t0001g0249 others(1): Show |
4 | NA18979.hp1 NA18984.hp2 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.108-2659_108-2658i others(11): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25305147 | |||||||
| chr13:25305148 | T | G | 1 | a0001c0001t0014g0011 | 2 | HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.108-2658T>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25305148 | |||||||
| chr13:25305151 | T | G | 2 | a0002c0002t0001g0043 a0002c0002t0001g0044 |
2 | HG01515.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.108-2655T>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25305151 | |||||||
| chr13:25305152 | T | G | 1 | a0001c0001t0014g0011 | 2 | HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.108-2654T>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25305152 | |||||||
| chr13:25305253 | T | A | 3 | a0002c0002t0001g0008 a0002c0002t0001g0045 a0002c0002t0001g0046 |
6 | HG02559.hp2 HG02572.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.108-2553T>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25305253 | |||||||
| chr13:25305279 | G | C | 1 | a0001c0001t0002g0201 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.108-2527G>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25305279 | |||||||
| chr13:25305352 | G | A | 1 | a0001c0001t0018g0264 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.108-2454G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25305352 | |||||||
| chr13:25305460 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.108-2346C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25305460 | |||||||
| chr13:25305504 | C | T | 1 | a0001c0001t0014g0011 | 2 | HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.108-2302C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25305504 | |||||||
| chr13:25305872 | C | T | 1 | a0001c0001t0018g0264 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.108-1934C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25305872 | |||||||
| chr13:25305918 | T | C | 1 | a0001c0001t0001g0202 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.108-1888T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25305918 | |||||||
| chr13:25305995 | C | A | 1 | a0001c0012t0001g0152 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.108-1811C>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25305995 | |||||||
| chr13:25306133 | C | T | 4 | a0001c0001t0007g0148 a0001c0001t0007g0149 a0001c0001t0007g0150 others(1): Show |
4 | HG01496.hp2 HG02258.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.108-1673C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25306133 | |||||||
| chr13:25306150 | A | C | 3 | a0002c0002t0001g0123 a0002c0002t0001g0124 a0002c0002t0001g0125 |
3 | HG02155.hp1 NA18980.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.108-1656A>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25306150 | |||||||
| chr13:25306154 | C | T | 1 | a0001c0001t0001g0030 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.108-1652C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25306154 | |||||||
| chr13:25306368 | T | C | 1 | a0001c0001t0014g0011 | 2 | HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.108-1438T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25306368 | |||||||
| chr13:25306388 | C | T | 1 | a0001c0001t0018g0264 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.108-1418C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25306388 | |||||||
| chr13:25306393 | C | CA | 59 | a0001c0001t0001g0018 a0001c0001t0001g0030 a0001c0001t0001g0133 others(56): Show |
63 | HG00438.hp2 HG01106.hp1 HG01261.hp1 others(60): Show |
intron_variant | MODIFIER | c.108-1391dupA | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25306393 | ||||||
| chr13:25306393 | C | CAA | 8 | a0001c0001t0001g0041 a0001c0001t0007g0148 a0001c0001t0007g0149 others(5): Show |
8 | HG01496.hp2 HG02145.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.108-1392_108-1391d others(4): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25306393 | ||||||
| chr13:25306486 | G | A | 2 | a0001c0001t0012g0154 a0001c0001t0012g0161 |
2 | HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.108-1320G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25306486 | |||||||
| chr13:25306544 | G | A | 1 | a0002c0002t0001g0060 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.108-1262G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25306544 | |||||||
| chr13:25306595 | A | T | 1 | a0001c0001t0001g0253 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.108-1211A>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25306595 | |||||||
| chr13:25306601 | T | C | 1 | a0001c0001t0018g0264 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.108-1205T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25306601 | |||||||
| chr13:25306695 | A | G | 1 | a0001c0001t0006g0175 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.108-1111A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25306695 | |||||||
| chr13:25306749 | C | A | 1 | a0001c0001t0002g0213 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.108-1057C>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25306749 | |||||||
| chr13:25306807 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.108-999G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25306807 | |||||||
| chr13:25306939 | A | G | 75 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0021 others(72): Show |
105 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.108-867A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25306939 | |||||||
| chr13:25306968 | T | A | 2 | a0001c0001t0005g0258 a0001c0001t0005g0259 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.108-838T>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25306968 | |||||||
| chr13:25307050 | G | C | 1 | a0005c0009t0001g0061 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.108-756G>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25307050 | |||||||
| chr13:25307196 | G | A | 4 | a0001c0001t0001g0007 a0001c0001t0001g0036 a0001c0001t0001g0037 others(1): Show |
8 | HG00738.hp1 HG01109.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.108-610G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25307196 | |||||||
| chr13:25307211 | A | AT | 24 | a0001c0001t0001g0030 a0001c0001t0001g0139 a0001c0001t0001g0140 others(21): Show |
26 | HG01243.hp2 HG01496.hp2 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.108-574dupT | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25307211 | ||||||
| chr13:25307211 | A | ATT | 23 | a0001c0001t0001g0025 a0001c0001t0001g0133 a0001c0001t0001g0134 others(20): Show |
26 | HG00735.hp1 HG01243.hp1 HG01257.hp1 others(23): Show |
intron_variant | MODIFIER | c.108-575_108-574dup others(2): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25307211 | ||||||
| chr13:25307211 | A | ATTT | 140 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0021 others(137): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.108-576_108-574dup others(3): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25307211 | ||||||
| chr13:25307211 | A | ATTTT | 37 | a0001c0001t0001g0122 a0001c0001t0001g0143 a0001c0001t0001g0247 others(34): Show |
51 | HG00733.hp2 HG01069.hp2 HG01123.hp1 others(48): Show |
intron_variant | MODIFIER | c.108-577_108-574dup others(4): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25307211 | ||||||
| chr13:25307211 | A | ATTTTT | 8 | a0001c0001t0001g0211 a0001c0001t0002g0009 a0001c0001t0002g0034 others(5): Show |
11 | HG00438.hp2 HG02738.hp2 NA18940.hp2 others(8): Show |
intron_variant | MODIFIER | c.108-578_108-574dup others(5): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25307211 | ||||||
| chr13:25307211 | AT | A | 15 | a0001c0001t0019g0188 a0001c0003t0004g0177 a0001c0003t0004g0178 others(12): Show |
15 | HG01496.hp1 HG02015.hp1 HG02132.hp2 others(12): Show |
intron_variant | MODIFIER | c.108-574delT | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25307211 | ||||||
| chr13:25307348 | A | G | 5 | a0001c0003t0004g0177 a0001c0003t0004g0180 a0001c0003t0004g0182 others(2): Show |
5 | HG02015.hp1 NA18979.hp2 NA18987.hp1 others(2): Show |
intron_variant | MODIFIER | c.108-458A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25307348 | |||||||
| chr13:25307465 | C | T | 1 | a0001c0006t0001g0198 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.108-341C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25307465 | |||||||
| chr13:25307555 | G | A | 4 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(1): Show |
4 | HG02280.hp2 HG02818.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.108-251G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25307555 | |||||||
| chr13:25308151 | C | T | 76 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0021 others(73): Show |
106 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.250+203C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 2/15 | chr13 | 25308151 | |||||||
| chr13:25308241 | A | G | 1 | a0001c0001t0018g0264 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.250+293A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 2/15 | chr13 | 25308241 | |||||||
| chr13:25308355 | C | T | 2 | a0001c0005t0001g0166 a0001c0005t0001g0167 |
2 | HG02109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.250+407C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 2/15 | chr13 | 25308355 | |||||||
| chr13:25308465 | G | A | 1 | a0001c0008t0001g0195 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.250+517G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 2/15 | chr13 | 25308465 | |||||||
| chr13:25308469 | A | AT | 8 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0205 others(5): Show |
8 | HG02486.hp2 HG02723.hp2 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.250+540dupT | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr13 | 25308469 | ||||||
| chr13:25308469 | AT | A | 147 | a0001c0001t0001g0017 a0001c0001t0001g0025 a0001c0001t0001g0030 others(144): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.250+540delT | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr13 | 25308469 | ||||||
| chr13:25308492 | T | G | 20 | a0002c0002t0001g0004 a0002c0002t0001g0012 a0002c0002t0001g0071 others(17): Show |
27 | HG00423.hp2 HG00558.hp1 HG00609.hp2 others(24): Show |
intron_variant | MODIFIER | c.250+544T>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 2/15 | chr13 | 25308492 | |||||||
| chr13:25308586 | T | C | 1 | a0001c0001t0014g0011 | 2 | HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.250+638T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 2/15 | chr13 | 25308586 | |||||||
| chr13:25308653 | T | C | 3 | a0002c0002t0001g0008 a0002c0002t0001g0045 a0002c0002t0001g0046 |
6 | HG02559.hp2 HG02572.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.251-594T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 2/15 | chr13 | 25308653 | |||||||
| chr13:25308864 | A | G | 3 | a0001c0001t0007g0148 a0001c0001t0007g0149 a0001c0001t0007g0150 |
3 | HG01496.hp2 HG02258.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.251-383A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 2/15 | chr13 | 25308864 | |||||||
| chr13:25309082 | A | G | 2 | a0001c0001t0013g0192 a0001c0001t0013g0193 |
2 | HG02559.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.251-165A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 2/15 | chr13 | 25309082 | |||||||
| chr13:25309174 | C | T | 4 | a0001c0001t0003g0058 a0001c0001t0003g0110 a0001c0001t0003g0111 others(1): Show |
4 | HG00639.hp2 HG01070.hp2 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.251-73C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 2/15 | chr13 | 25309174 | |||||||
| chr13:25309425 | C | T | 2 | a0001c0001t0001g0122 a0001c0001t0001g0143 |
2 | HG02145.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.286+143C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | chr13 | 25309425 | |||||||
| chr13:25309583 | C | A | 1 | a0001c0001t0014g0011 | 2 | HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.286+301C>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | chr13 | 25309583 | |||||||
| chr13:25309619 | T | A | 1 | a0001c0001t0002g0238 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.286+337T>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | chr13 | 25309619 | |||||||
| chr13:25309666 | T | C | 3 | a0002c0002t0001g0016 a0002c0002t0001g0049 a0002c0002t0001g0081 |
4 | HG01928.hp1 NA18992.hp2 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.286+384T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | chr13 | 25309666 | |||||||
| chr13:25309726 | C | T | 4 | a0001c0001t0007g0148 a0001c0001t0007g0149 a0001c0001t0007g0150 others(1): Show |
4 | HG01496.hp2 HG02258.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.286+444C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | chr13 | 25309726 | |||||||
| chr13:25309792 | GAAAGGAA others(52): Show |
G | 1 | a0001c0001t0015g0168 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.286+560_286+618del others(59): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr13 | 25309792 | ||||||
| chr13:25309842 | A | G | 4 | a0001c0001t0007g0148 a0001c0001t0007g0149 a0001c0001t0007g0150 others(1): Show |
4 | HG01496.hp2 HG02258.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.286+560A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | chr13 | 25309842 | |||||||
| chr13:25309860 | GGAAAA | G | 29 | a0001c0001t0001g0211 a0001c0001t0002g0003 a0001c0001t0002g0006 others(26): Show |
46 | HG00438.hp2 HG00733.hp2 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.286+580_286+584del others(5): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr13 | 25309860 | ||||||
| chr13:25309963 | A | G | 20 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0135 others(17): Show |
21 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.286+681A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | chr13 | 25309963 | |||||||
| chr13:25310009 | A | G | 4 | a0001c0001t0007g0148 a0001c0001t0007g0149 a0001c0001t0007g0150 others(1): Show |
4 | HG01496.hp2 HG02258.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.286+727A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | chr13 | 25310009 | |||||||
| chr13:25310029 | C | A | 1 | a0001c0001t0018g0264 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.286+747C>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | chr13 | 25310029 | |||||||
| chr13:25310102 | G | A | 2 | a0002c0002t0001g0050 a0002c0002t0001g0082 |
2 | HG03831.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.286+820G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | chr13 | 25310102 | |||||||
| chr13:25310142 | A | G | 4 | a0002c0002t0001g0067 a0002c0002t0001g0107 a0002c0002t0001g0108 others(1): Show |
4 | NA18966.hp2 NA19006.hp1 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.286+860A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | chr13 | 25310142 | |||||||
| chr13:25310206 | A | AT | 24 | a0001c0001t0001g0029 a0001c0001t0001g0041 a0001c0001t0001g0147 others(21): Show |
24 | HG01175.hp2 HG01496.hp1 HG02015.hp1 others(21): Show |
intron_variant | MODIFIER | c.286+954dupT | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr13 | 25310206 | ||||||
| chr13:25310206 | AT | A | 62 | a0001c0001t0001g0132 a0001c0001t0001g0143 a0001c0001t0001g0217 others(59): Show |
81 | HG00558.hp1 HG00609.hp2 HG00642.hp1 others(78): Show |
intron_variant | MODIFIER | c.286+954delT | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr13 | 25310206 | ||||||
| chr13:25310206 | ATT | A | 86 | a0001c0001t0001g0017 a0001c0001t0001g0030 a0001c0001t0001g0122 others(83): Show |
118 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(115): Show |
intron_variant | MODIFIER | c.286+953_286+954del others(2): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr13 | 25310206 | ||||||
| chr13:25310206 | ATTTT | A | 6 | a0001c0001t0006g0019 a0001c0001t0006g0172 a0001c0001t0006g0174 others(3): Show |
8 | HG02486.hp1 HG02922.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.286+951_286+954del others(4): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr13 | 25310206 | ||||||
| chr13:25310206 | ATTTTT | A | 13 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0135 others(10): Show |
13 | HG01884.hp1 HG02055.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.286+950_286+954del others(5): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr13 | 25310206 | ||||||
| chr13:25310206 | ATTTTTTT others(3): Show |
A | 3 | a0001c0001t0007g0148 a0001c0001t0007g0149 a0001c0001t0007g0150 |
3 | HG01496.hp2 HG02258.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.286+945_286+954del others(10): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr13 | 25310206 | ||||||
| chr13:25310206 | ATTTTTTT others(5): Show |
A | 1 | a0001c0001t0001g0216 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.286+943_286+954del others(12): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr13 | 25310206 | ||||||
| chr13:25310206 | ATTTTTTT others(6): Show |
A | 1 | a0001c0012t0001g0152 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.286+942_286+954del others(13): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr13 | 25310206 | ||||||
| chr13:25310206 | ATTTTTTT others(7): Show |
A | 2 | a0001c0001t0002g0207 a0001c0001t0002g0239 |
2 | NA18978.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.286+941_286+954del others(14): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr13 | 25310206 | ||||||
| chr13:25310236 | T | A | 2 | a0001c0001t0014g0011 a0001c0001t0018g0264 |
3 | HG02922.hp1 HG03491.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.286+954T>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | chr13 | 25310236 | |||||||
| chr13:25310278 | T | C | 1 | a0001c0001t0001g0220 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.286+996T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | chr13 | 25310278 | |||||||
| chr13:25310283 | C | T | 20 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0135 others(17): Show |
21 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.286+1001C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | chr13 | 25310283 | |||||||
| chr13:25310307 | G | A | 2 | a0001c0001t0001g0139 a0001c0001t0001g0140 |
2 | HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.286+1025G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | chr13 | 25310307 | |||||||
| chr13:25310374 | C | T | 2 | a0001c0001t0005g0098 a0001c0001t0005g0104 |
2 | HG01099.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.286+1092C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | chr13 | 25310374 | |||||||
| chr13:25310440 | G | A | 7 | a0003c0004t0001g0265 a0003c0004t0001g0266 a0003c0004t0001g0267 others(4): Show |
7 | HG02055.hp1 HG02486.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.286+1158G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | chr13 | 25310440 | |||||||
| chr13:25310479 | C | T | 1 | a0001c0005t0001g0166 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.286+1197C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | chr13 | 25310479 | |||||||
| chr13:25310480 | G | A | 1 | a0002c0002t0001g0051 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.286+1198G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | chr13 | 25310480 | |||||||
| chr13:25310519 | C | CT | 159 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0021 others(156): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.286+1260dupT | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr13 | 25310519 | ||||||
| chr13:25310519 | C | CTT | 55 | a0001c0001t0001g0022 a0001c0001t0001g0194 a0001c0001t0001g0211 others(52): Show |
74 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.286+1259_286+1260d others(4): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr13 | 25310519 | ||||||
| chr13:25310519 | C | CTTT | 11 | a0001c0001t0001g0204 a0001c0001t0002g0034 a0001c0001t0002g0212 others(8): Show |
11 | HG01069.hp2 HG01361.hp1 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.286+1258_286+1260d others(5): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr13 | 25310519 | ||||||
| chr13:25310519 | CT | C | 19 | a0001c0001t0001g0018 a0001c0001t0001g0041 a0001c0001t0001g0144 others(16): Show |
21 | HG01891.hp1 HG01891.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.286+1260delT | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr13 | 25310519 | ||||||
| chr13:25310712 | C | T | 2 | a0001c0001t0003g0032 a0001c0001t0003g0033 |
2 | HG02630.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.286+1430C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | chr13 | 25310712 | |||||||
| chr13:25310801 | C | T | 1 | a0001c0001t0002g0243 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.286+1519C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | chr13 | 25310801 | |||||||
| chr13:25310955 | T | A | 1 | a0002c0002t0001g0063 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.286+1673T>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | chr13 | 25310955 | |||||||
| chr13:25311028 | G | C | 1 | a0001c0012t0001g0152 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.286+1746G>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | chr13 | 25311028 | |||||||
| chr13:25311109 | C | T | 2 | a0001c0001t0014g0011 a0001c0001t0018g0264 |
3 | HG02922.hp1 HG03491.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.287-1774C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | chr13 | 25311109 | |||||||
| chr13:25311138 | G | A | 1 | a0001c0001t0001g0027 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.287-1745G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | chr13 | 25311138 | |||||||
| chr13:25311174 | T | C | 1 | a0001c0001t0001g0221 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.287-1709T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | chr13 | 25311174 | |||||||
| chr13:25311191 | A | G | 3 | a0003c0004t0001g0265 a0003c0004t0001g0266 a0003c0004t0001g0267 |
3 | HG02615.hp1 HG02886.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.287-1692A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | chr13 | 25311191 | |||||||
| chr13:25311454 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.287-1429C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | chr13 | 25311454 | |||||||
| chr13:25311501 | G | A | 1 | a0002c0002t0001g0125 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.287-1382G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | chr13 | 25311501 | |||||||
| chr13:25311664 | G | T | 1 | a0001c0001t0018g0264 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.287-1219G>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | chr13 | 25311664 | |||||||
| chr13:25311673 | CT | C | 114 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0030 others(111): Show |
156 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.287-1189delT | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr13 | 25311673 | ||||||
| chr13:25311673 | CTT | C | 21 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0135 others(18): Show |
21 | HG00099.hp1 HG01884.hp1 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.287-1190_287-1189d others(4): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr13 | 25311673 | ||||||
| chr13:25311673 | CTTT | C | 14 | a0001c0001t0012g0161 a0001c0001t0019g0188 a0001c0003t0004g0177 others(11): Show |
14 | HG01496.hp1 HG02015.hp1 HG02132.hp2 others(11): Show |
intron_variant | MODIFIER | c.287-1191_287-1189d others(5): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr13 | 25311673 | ||||||
| chr13:25311693 | T | G | 1 | a0002c0002t0001g0044 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.287-1190T>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | chr13 | 25311693 | |||||||
| chr13:25311812 | G | A | 1 | a0001c0001t0014g0011 | 2 | HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.287-1071G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | chr13 | 25311812 | |||||||
| chr13:25312046 | C | A | 1 | a0001c0001t0014g0011 | 2 | HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.287-837C>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | chr13 | 25312046 | |||||||
| chr13:25312224 | A | G | 1 | a0001c0001t0014g0011 | 2 | HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.287-659A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | chr13 | 25312224 | |||||||
| chr13:25312524 | C | T | 1 | a0001c0012t0001g0152 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.287-359C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | chr13 | 25312524 | |||||||
| chr13:25312568 | G | A | 2 | a0001c0001t0014g0011 a0001c0001t0018g0264 |
3 | HG02922.hp1 HG03491.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.287-315G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | chr13 | 25312568 | |||||||
| chr13:25312607 | A | G | 1 | a0001c0001t0014g0011 | 2 | HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.287-276A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | chr13 | 25312607 | |||||||
| chr13:25312648 | G | T | 1 | a0001c0001t0001g0197 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.287-235G>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | chr13 | 25312648 | |||||||
| chr13:25312723 | C | T | 4 | a0001c0001t0001g0025 a0001c0001t0001g0139 a0001c0001t0001g0140 others(1): Show |
5 | HG01243.hp1 HG01884.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.287-160C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | chr13 | 25312723 | |||||||
| chr13:25312769 | C | T | 1 | a0003c0004t0001g0271 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.287-114C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | chr13 | 25312769 | |||||||
| chr13:25312794 | A | G | 252 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0017 others(249): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.287-89A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | chr13 | 25312794 | |||||||
| chr13:25313087 | G | A | 1 | a0001c0001t0018g0264 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.436+55G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 4/15 | chr13 | 25313087 | |||||||
| chr13:25313451 | T | C | 1 | a0001c0001t0002g0239 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.437-163T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 4/15 | chr13 | 25313451 | |||||||
| chr13:25313544 | G | A | 1 | a0002c0002t0001g0089 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.437-70G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 4/15 | chr13 | 25313544 | |||||||
| chr13:25313600 | C | T | 1 | a0005c0009t0001g0061 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.437-14C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 4/15 | chr13 | 25313600 | |||||||
| chr13:25313890 | G | C | 1 | a0002c0002t0001g0072 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.574+139G>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 5/15 | chr13 | 25313890 | |||||||
| chr13:25313956 | T | C | 4 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0162 others(1): Show |
4 | HG02055.hp2 HG02897.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.574+205T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 5/15 | chr13 | 25313956 | |||||||
| chr13:25314099 | T | A | 121 | a0001c0001t0003g0005 a0001c0001t0003g0023 a0001c0001t0003g0026 others(118): Show |
158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.574+348T>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 5/15 | chr13 | 25314099 | |||||||
| chr13:25314170 | T | A | 1 | a0002c0002t0001g0054 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.574+419T>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 5/15 | chr13 | 25314170 | |||||||
| chr13:25314176 | G | A | 4 | a0001c0001t0007g0148 a0001c0001t0007g0149 a0001c0001t0007g0150 others(1): Show |
4 | HG01496.hp2 HG02258.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.574+425G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 5/15 | chr13 | 25314176 | |||||||
| chr13:25314296 | C | G | 217 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0021 others(214): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.574+545C>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 5/15 | chr13 | 25314296 | |||||||
| chr13:25314310 | T | TTTAAGGA others(10): Show |
2 | a0001c0001t0012g0154 a0001c0001t0012g0161 |
2 | HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.574+561_574+577dup others(17): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr13 | 25314310 | ||||||
| chr13:25314314 | A | C | 1 | a0001c0001t0018g0264 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.574+563A>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 5/15 | chr13 | 25314314 | |||||||
| chr13:25314380 | T | G | 2 | a0001c0001t0014g0011 a0001c0001t0018g0264 |
3 | HG02922.hp1 HG03491.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.574+629T>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 5/15 | chr13 | 25314380 | |||||||
| chr13:25314417 | T | C | 1 | a0001c0001t0018g0264 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.574+666T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 5/15 | chr13 | 25314417 | |||||||
| chr13:25314423 | C | T | 85 | a0002c0002t0001g0001 a0002c0002t0001g0004 a0002c0002t0001g0008 others(82): Show |
116 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.574+672C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 5/15 | chr13 | 25314423 | |||||||
| chr13:25314607 | A | G | 1 | a0001c0001t0001g0141 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.575-750A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 5/15 | chr13 | 25314607 | |||||||
| chr13:25314610 | A | G | 1 | a0001c0001t0001g0036 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.575-747A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 5/15 | chr13 | 25314610 | |||||||
| chr13:25314665 | A | C | 2 | a0001c0001t0001g0226 a0001c0001t0001g0252 |
2 | NA19004.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.575-692A>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 5/15 | chr13 | 25314665 | |||||||
| chr13:25314682 | C | T | 4 | a0001c0001t0003g0023 a0001c0001t0003g0035 a0001c0001t0003g0254 others(1): Show |
5 | HG02109.hp2 HG02257.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.575-675C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 5/15 | chr13 | 25314682 | |||||||
| chr13:25314746 | G | T | 1 | a0001c0001t0014g0011 | 2 | HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.575-611G>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 5/15 | chr13 | 25314746 | |||||||
| chr13:25314850 | G | A | 247 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0021 others(244): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.575-507G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 5/15 | chr13 | 25314850 | |||||||
| chr13:25315062 | G | C | 85 | a0002c0002t0001g0001 a0002c0002t0001g0004 a0002c0002t0001g0008 others(82): Show |
116 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.575-295G>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 5/15 | chr13 | 25315062 | |||||||
| chr13:25315141 | GA | G | 4 | a0001c0005t0001g0024 a0001c0005t0001g0166 a0001c0005t0001g0167 others(1): Show |
5 | HG02109.hp1 HG02257.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.575-211delA | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr13 | 25315141 | ||||||
| chr13:25315232 | G | A | 2 | a0001c0001t0014g0011 a0001c0001t0018g0264 |
3 | HG02922.hp1 HG03491.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.575-125G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 5/15 | chr13 | 25315232 | |||||||
| chr13:25315531 | A | G | 2 | a0001c0001t0014g0011 a0001c0001t0018g0264 |
3 | HG02922.hp1 HG03491.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.685+64A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | chr13 | 25315531 | |||||||
| chr13:25315567 | TTAG | T | 4 | a0001c0001t0003g0023 a0001c0001t0003g0035 a0001c0001t0003g0254 others(1): Show |
5 | HG02109.hp2 HG02257.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.685+106_685+108del others(3): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr13 | 25315567 | ||||||
| chr13:25315682 | TTGTC | T | 199 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0021 others(196): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.685+220_685+223del others(4): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr13 | 25315682 | ||||||
| chr13:25315699 | T | C | 3 | a0003c0004t0001g0265 a0003c0004t0001g0266 a0003c0004t0001g0267 |
3 | HG02615.hp1 HG02886.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.685+232T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | chr13 | 25315699 | |||||||
| chr13:25315794 | T | A | 1 | a0001c0001t0001g0200 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.685+327T>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | chr13 | 25315794 | |||||||
| chr13:25315948 | G | A | 1 | a0001c0001t0003g0085 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.685+481G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | chr13 | 25315948 | |||||||
| chr13:25315952 | T | C | 1 | a0001c0001t0001g0030 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.685+485T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | chr13 | 25315952 | |||||||
| chr13:25316125 | A | C | 16 | a0001c0001t0019g0188 a0001c0003t0004g0177 a0001c0003t0004g0178 others(13): Show |
16 | HG01496.hp1 HG02015.hp1 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.685+658A>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | chr13 | 25316125 | |||||||
| chr13:25316413 | G | A | 1 | a0001c0001t0003g0070 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.685+946G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | chr13 | 25316413 | |||||||
| chr13:25316447 | CT | C | 230 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0021 others(227): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.685+989delT | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr13 | 25316447 | ||||||
| chr13:25316457 | A | T | 2 | a0001c0001t0013g0192 a0001c0001t0013g0193 |
2 | HG02559.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.685+990A>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | chr13 | 25316457 | |||||||
| chr13:25316560 | C | G | 3 | a0003c0004t0001g0265 a0003c0004t0001g0266 a0003c0004t0001g0267 |
3 | HG02615.hp1 HG02886.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.685+1093C>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | chr13 | 25316560 | |||||||
| chr13:25316568 | G | A | 247 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0021 others(244): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.685+1101G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | chr13 | 25316568 | |||||||
| chr13:25316580 | A | T | 7 | a0003c0004t0001g0265 a0003c0004t0001g0266 a0003c0004t0001g0267 others(4): Show |
7 | HG02055.hp1 HG02486.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.685+1113A>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | chr13 | 25316580 | |||||||
| chr13:25316690 | A | G | 1 | a0002c0002t0001g0040 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.685+1223A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | chr13 | 25316690 | |||||||
| chr13:25316694 | C | T | 254 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0017 others(251): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.685+1227C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | chr13 | 25316694 | |||||||
| chr13:25317032 | C | CT | 6 | a0001c0001t0002g0261 a0001c0001t0003g0023 a0001c0001t0003g0035 others(3): Show |
8 | HG02109.hp2 HG02257.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.685+1574dupT | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr13 | 25317032 | ||||||
| chr13:25317066 | A | G | 4 | a0003c0004t0001g0268 a0003c0004t0001g0269 a0003c0004t0001g0270 others(1): Show |
4 | HG02055.hp1 HG02486.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.685+1599A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | chr13 | 25317066 | |||||||
| chr13:25317073 | G | A | 4 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0247 others(1): Show |
6 | HG00423.hp1 HG00558.hp2 HG00609.hp1 others(3): Show |
intron_variant | MODIFIER | c.685+1606G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | chr13 | 25317073 | |||||||
| chr13:25317125 | G | A | 29 | a0001c0001t0002g0003 a0001c0001t0002g0006 a0001c0001t0002g0009 others(26): Show |
46 | HG00438.hp2 HG00733.hp2 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.685+1658G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | chr13 | 25317125 | |||||||
| chr13:25317137 | A | G | 76 | a0002c0002t0001g0001 a0002c0002t0001g0004 a0002c0002t0001g0010 others(73): Show |
102 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.685+1670A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | chr13 | 25317137 | |||||||
| chr13:25317267 | TCCTTATT others(2): Show |
T | 7 | a0001c0001t0006g0019 a0001c0001t0006g0172 a0001c0001t0006g0173 others(4): Show |
8 | HG01891.hp2 HG02965.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.685+1803_685+1811d others(11): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr13 | 25317267 | ||||||
| chr13:25317401 | A | G | 1 | a0001c0001t0003g0111 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.686-1925A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | chr13 | 25317401 | |||||||
| chr13:25317557 | TGTAA | T | 4 | a0003c0004t0001g0268 a0003c0004t0001g0269 a0003c0004t0001g0270 others(1): Show |
4 | HG02055.hp1 HG02486.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.686-1765_686-1762d others(6): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr13 | 25317557 | ||||||
| chr13:25317586 | T | C | 3 | a0003c0004t0001g0265 a0003c0004t0001g0266 a0003c0004t0001g0267 |
3 | HG02615.hp1 HG02886.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.686-1740T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | chr13 | 25317586 | |||||||
| chr13:25317694 | G | A | 270 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0017 others(267): Show |
346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.686-1632G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | chr13 | 25317694 | |||||||
| chr13:25317739 | GA | G | 3 | a0001c0001t0001g0025 a0001c0001t0001g0142 a0001c0001t0014g0011 |
5 | HG01243.hp1 HG01884.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.686-1580delA | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr13 | 25317739 | ||||||
| chr13:25317814 | C | G | 14 | a0001c0001t0006g0019 a0001c0001t0006g0172 a0001c0001t0006g0173 others(11): Show |
15 | HG01891.hp2 HG02055.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.686-1512C>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | chr13 | 25317814 | |||||||
| chr13:25317858 | A | AT | 168 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0022 others(165): Show |
228 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.686-1447dupT | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr13 | 25317858 | ||||||
| chr13:25317858 | A | ATT | 21 | a0001c0001t0001g0017 a0001c0001t0001g0132 a0001c0001t0001g0133 others(18): Show |
23 | HG00735.hp2 HG01074.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.686-1448_686-1447d others(4): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr13 | 25317858 | ||||||
| chr13:25317882 | GA | G | 3 | a0001c0005t0001g0166 a0001c0005t0001g0167 a0001c0010t0001g0165 |
3 | HG02109.hp1 HG02280.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.686-1443delA | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | chr13 | 25317882 | |||||||
| chr13:25317893 | T | G | 215 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0021 others(212): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.686-1433T>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | chr13 | 25317893 | |||||||
| chr13:25317915 | A | C | 1 | a0001c0001t0001g0224 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.686-1411A>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | chr13 | 25317915 | |||||||
| chr13:25317940 | T | C | 1 | a0001c0001t0005g0098 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.686-1386T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | chr13 | 25317940 | |||||||
| chr13:25317942 | C | T | 5 | a0001c0001t0003g0023 a0001c0001t0003g0035 a0001c0001t0003g0254 others(2): Show |
7 | HG02109.hp2 HG02257.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.686-1384C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | chr13 | 25317942 | |||||||
| chr13:25317977 | C | T | 1 | a0002c0002t0001g0095 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.686-1349C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | chr13 | 25317977 | |||||||
| chr13:25318010 | C | T | 1 | a0001c0001t0001g0218 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.686-1316C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | chr13 | 25318010 | |||||||
| chr13:25318032 | T | C | 1 | a0001c0001t0001g0030 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.686-1294T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | chr13 | 25318032 | |||||||
| chr13:25318067 | C | T | 4 | a0003c0004t0001g0268 a0003c0004t0001g0269 a0003c0004t0001g0270 others(1): Show |
4 | HG02055.hp1 HG02486.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.686-1259C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | chr13 | 25318067 | |||||||
| chr13:25318074 | A | T | 1 | a0001c0001t0014g0011 | 2 | HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.686-1252A>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | chr13 | 25318074 | |||||||
| chr13:25318195 | G | T | 3 | a0003c0004t0001g0265 a0003c0004t0001g0266 a0003c0004t0001g0267 |
3 | HG02615.hp1 HG02886.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.686-1131G>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | chr13 | 25318195 | |||||||
| chr13:25318322 | C | T | 7 | a0003c0004t0001g0265 a0003c0004t0001g0266 a0003c0004t0001g0267 others(4): Show |
7 | HG02055.hp1 HG02486.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.686-1004C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | chr13 | 25318322 | |||||||
| chr13:25318365 | C | T | 1 | a0001c0001t0001g0038 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.686-961C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | chr13 | 25318365 | |||||||
| chr13:25318699 | G | A | 1 | a0001c0001t0003g0084 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.686-627G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | chr13 | 25318699 | |||||||
| chr13:25318801 | T | C | 2 | a0001c0001t0012g0154 a0001c0001t0012g0161 |
2 | HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.686-525T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | chr13 | 25318801 | |||||||
| chr13:25318866 | G | C | 1 | a0001c0001t0011g0227 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.686-460G>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | chr13 | 25318866 | |||||||
| chr13:25318885 | G | A | 1 | a0003c0004t0001g0268 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.686-441G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | chr13 | 25318885 | |||||||
| chr13:25318924 | A | C | 1 | a0002c0002t0001g0114 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.686-402A>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | chr13 | 25318924 | |||||||
| chr13:25319083 | T | A | 117 | a0001c0001t0003g0005 a0001c0001t0003g0026 a0001c0001t0003g0031 others(114): Show |
153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.686-243T>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | chr13 | 25319083 | |||||||
| chr13:25319165 | G | A | 3 | a0003c0004t0001g0265 a0003c0004t0001g0266 a0003c0004t0001g0267 |
3 | HG02615.hp1 HG02886.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.686-161G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | chr13 | 25319165 | |||||||
| chr13:25319189 | A | G | 3 | a0001c0005t0001g0166 a0001c0005t0001g0167 a0001c0010t0001g0165 |
3 | HG02109.hp1 HG02280.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.686-137A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | chr13 | 25319189 | |||||||
| chr13:25319225 | GTTTATA | G | 195 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0021 others(192): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.686-94_686-89delTT others(4): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr13 | 25319225 | ||||||
| chr13:25319402 | T | C | 17 | a0001c0001t0014g0011 a0001c0001t0019g0188 a0001c0003t0004g0177 others(14): Show |
18 | HG01496.hp1 HG02015.hp1 HG02132.hp2 others(15): Show |
intron_variant | MODIFIER | c.710+52T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 7/15 | chr13 | 25319402 | |||||||
| chr13:25319466 | T | C | 16 | a0001c0001t0019g0188 a0001c0003t0004g0177 a0001c0003t0004g0178 others(13): Show |
16 | HG01496.hp1 HG02015.hp1 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.710+116T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 7/15 | chr13 | 25319466 | |||||||
| chr13:25319468 | T | C | 3 | a0001c0001t0001g0022 a0001c0001t0001g0247 a0001c0001t0001g0249 |
4 | HG00423.hp1 NA19001.hp2 NA19075.hp2 others(1): Show |
intron_variant | MODIFIER | c.710+118T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 7/15 | chr13 | 25319468 | |||||||
| chr13:25319595 | CTAATA | C | 7 | a0003c0004t0001g0265 a0003c0004t0001g0266 a0003c0004t0001g0267 others(4): Show |
7 | HG02055.hp1 HG02486.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.710+249_710+253del others(5): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr13 | 25319595 | ||||||
| chr13:25319631 | T | C | 1 | a0002c0002t0001g0100 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.710+281T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 7/15 | chr13 | 25319631 | |||||||
| chr13:25319707 | A | T | 1 | a0003c0004t0001g0267 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.710+357A>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 7/15 | chr13 | 25319707 | |||||||
| chr13:25319766 | A | G | 16 | a0001c0001t0019g0188 a0001c0003t0004g0177 a0001c0003t0004g0178 others(13): Show |
16 | HG01496.hp1 HG02015.hp1 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.710+416A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 7/15 | chr13 | 25319766 | |||||||
| chr13:25319796 | A | G | 7 | a0003c0004t0001g0265 a0003c0004t0001g0266 a0003c0004t0001g0267 others(4): Show |
7 | HG02055.hp1 HG02486.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.710+446A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 7/15 | chr13 | 25319796 | |||||||
| chr13:25319802 | T | A | 16 | a0001c0001t0019g0188 a0001c0003t0004g0177 a0001c0003t0004g0178 others(13): Show |
16 | HG01496.hp1 HG02015.hp1 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.710+452T>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 7/15 | chr13 | 25319802 | |||||||
| chr13:25319886 | A | G | 1 | a0001c0001t0001g0140 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.710+536A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 7/15 | chr13 | 25319886 | |||||||
| chr13:25319923 | A | G | 5 | a0001c0001t0006g0019 a0001c0001t0006g0172 a0001c0001t0006g0173 others(2): Show |
6 | HG01891.hp2 HG02965.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.710+573A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 7/15 | chr13 | 25319923 | |||||||
| chr13:25319959 | C | G | 1 | a0001c0001t0018g0264 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.711-571C>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 7/15 | chr13 | 25319959 | |||||||
| chr13:25319976 | A | T | 16 | a0001c0001t0019g0188 a0001c0003t0004g0177 a0001c0003t0004g0178 others(13): Show |
16 | HG01496.hp1 HG02015.hp1 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.711-554A>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 7/15 | chr13 | 25319976 | |||||||
| chr13:25320091 | C | G | 3 | a0001c0001t0001g0223 a0001c0001t0001g0229 a0001c0001t0003g0042 |
3 | HG00639.hp1 HG00642.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.711-439C>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 7/15 | chr13 | 25320091 | |||||||
| chr13:25320151 | T | C | 2 | a0001c0001t0001g0025 a0001c0001t0001g0142 |
3 | HG01243.hp1 HG01884.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.711-379T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 7/15 | chr13 | 25320151 | |||||||
| chr13:25320247 | T | C | 1 | a0002c0002t0001g0073 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.711-283T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 7/15 | chr13 | 25320247 | |||||||
| chr13:25320332 | A | G | 3 | a0002c0002t0001g0008 a0002c0002t0001g0045 a0002c0002t0001g0046 |
6 | HG02559.hp2 HG02572.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.711-198A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 7/15 | chr13 | 25320332 | |||||||
| chr13:25320409 | A | C | 3 | a0003c0004t0001g0268 a0003c0004t0001g0269 a0003c0004t0001g0270 |
3 | HG02486.hp1 HG02622.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.711-121A>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 7/15 | chr13 | 25320409 | |||||||
| chr13:25320525 | C | A | 2 | a0001c0005t0001g0166 a0001c0005t0001g0167 |
2 | HG02109.hp1 HG02280.hp1 |
splice_region_variant&intron_variant | LOW | c.711-5C>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 7/15 | chr13 | 25320525 | |||||||
| chr13:25320689 | A | T | 1 | a0002c0002t0001g0078 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.776+94A>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 8/15 | chr13 | 25320689 | |||||||
| chr13:25321238 | T | C | 1 | a0001c0001t0003g0084 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.951+145T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 9/15 | chr13 | 25321238 | |||||||
| chr13:25321368 | A | G | 1 | a0001c0001t0018g0264 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.951+275A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 9/15 | chr13 | 25321368 | |||||||
| chr13:25321447 | C | T | 4 | a0001c0005t0001g0024 a0001c0005t0001g0166 a0001c0005t0001g0167 others(1): Show |
5 | HG02109.hp1 HG02257.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.951+354C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 9/15 | chr13 | 25321447 | |||||||
| chr13:25321565 | A | G | 75 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0021 others(72): Show |
105 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.951+472A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 9/15 | chr13 | 25321565 | |||||||
| chr13:25321745 | C | T | 3 | a0001c0001t0005g0258 a0001c0001t0005g0259 a0001c0012t0001g0152 |
3 | HG01243.hp2 HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.951+652C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 9/15 | chr13 | 25321745 | |||||||
| chr13:25321746 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.951+653G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 9/15 | chr13 | 25321746 | |||||||
| chr13:25321854 | T | G | 1 | a0007c0011t0004g0190 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.951+761T>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 9/15 | chr13 | 25321854 | |||||||
| chr13:25322029 | G | A | 1 | a0001c0001t0014g0011 | 2 | HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.951+936G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 9/15 | chr13 | 25322029 | |||||||
| chr13:25322228 | G | A | 5 | a0001c0001t0006g0019 a0001c0001t0006g0172 a0001c0001t0006g0173 others(2): Show |
6 | HG01891.hp2 HG02965.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.951+1135G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 9/15 | chr13 | 25322228 | |||||||
| chr13:25322232 | T | G | 1 | a0007c0011t0004g0190 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.951+1139T>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 9/15 | chr13 | 25322232 | |||||||
| chr13:25322355 | C | T | 1 | a0006c0013t0010g0159 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.951+1262C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 9/15 | chr13 | 25322355 | |||||||
| chr13:25322459 | C | G | 1 | a0001c0001t0018g0264 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.951+1366C>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 9/15 | chr13 | 25322459 | |||||||
| chr13:25322936 | T | A | 16 | a0001c0001t0019g0188 a0001c0003t0004g0177 a0001c0003t0004g0178 others(13): Show |
16 | HG01496.hp1 HG02015.hp1 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.951+1843T>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 9/15 | chr13 | 25322936 | |||||||
| chr13:25323023 | C | T | 8 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0135 others(5): Show |
8 | HG01884.hp1 HG02723.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.951+1930C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 9/15 | chr13 | 25323023 | |||||||
| chr13:25323140 | T | A | 1 | a0001c0001t0002g0262 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.952-1849T>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 9/15 | chr13 | 25323140 | |||||||
| chr13:25323368 | T | C | 1 | a0002c0002t0001g0176 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.952-1621T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 9/15 | chr13 | 25323368 | |||||||
| chr13:25323377 | AT | A | 116 | a0001c0001t0003g0005 a0001c0001t0003g0026 a0001c0001t0003g0031 others(113): Show |
152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.952-1610delT | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr13 | 25323377 | ||||||
| chr13:25323379 | T | TA | 16 | a0001c0001t0019g0188 a0001c0003t0004g0177 a0001c0003t0004g0178 others(13): Show |
16 | HG01496.hp1 HG02015.hp1 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.952-1599dupA | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr13 | 25323379 | ||||||
| chr13:25323379 | TA | T | 100 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0021 others(97): Show |
133 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(130): Show |
intron_variant | MODIFIER | c.952-1599delA | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr13 | 25323379 | ||||||
| chr13:25323462 | A | G | 1 | a0001c0001t0013g0193 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.952-1527A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 9/15 | chr13 | 25323462 | |||||||
| chr13:25323502 | A | C | 1 | a0001c0001t0018g0264 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.952-1487A>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 9/15 | chr13 | 25323502 | |||||||
| chr13:25323592 | C | T | 193 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0021 others(190): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.952-1397C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 9/15 | chr13 | 25323592 | |||||||
| chr13:25323714 | GTTTAAA | G | 193 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0021 others(190): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.952-1272_952-1267d others(8): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr13 | 25323714 | ||||||
| chr13:25323733 | G | A | 1 | a0003c0004t0001g0267 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.952-1256G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 9/15 | chr13 | 25323733 | |||||||
| chr13:25323962 | A | G | 193 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0021 others(190): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.952-1027A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 9/15 | chr13 | 25323962 | |||||||
| chr13:25324024 | C | T | 1 | a0001c0001t0018g0264 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.952-965C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 9/15 | chr13 | 25324024 | |||||||
| chr13:25324282 | T | C | 6 | a0001c0001t0003g0026 a0001c0001t0003g0052 a0001c0001t0003g0064 others(3): Show |
6 | HG00280.hp2 HG01261.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.952-707T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 9/15 | chr13 | 25324282 | |||||||
| chr13:25324386 | G | T | 6 | a0001c0001t0006g0019 a0001c0001t0006g0172 a0001c0001t0006g0173 others(3): Show |
7 | HG01891.hp2 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.952-603G>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 9/15 | chr13 | 25324386 | |||||||
| chr13:25324397 | A | T | 2 | a0001c0005t0001g0166 a0001c0005t0001g0167 |
2 | HG02109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.952-592A>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 9/15 | chr13 | 25324397 | |||||||
| chr13:25324420 | T | G | 1 | a0001c0001t0014g0011 | 2 | HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.952-569T>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 9/15 | chr13 | 25324420 | |||||||
| chr13:25324907 | T | C | 1 | a0001c0001t0003g0052 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.952-82T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 9/15 | chr13 | 25324907 | |||||||
| chr13:25324936 | A | G | 1 | a0001c0001t0002g0206 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.952-53A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 9/15 | chr13 | 25324936 | |||||||
| chr13:25324953 | C | CT | 79 | a0001c0001t0001g0030 a0002c0002t0001g0001 a0002c0002t0001g0004 others(76): Show |
107 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.952-20dupT | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr13 | 25324953 | ||||||
| chr13:25325079 | G | A | 1 | a0001c0001t0018g0264 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1031+11G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 10/15 | chr13 | 25325079 | |||||||
| chr13:25325086 | TA | T | 2 | a0001c0001t0001g0017 a0001c0001t0001g0132 |
3 | HG00735.hp2 HG03195.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1031+23delA | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr13 | 25325086 | ||||||
| chr13:25325195 | G | T | 5 | a0001c0001t0006g0019 a0001c0001t0006g0172 a0001c0001t0006g0173 others(2): Show |
6 | HG01891.hp2 HG02965.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1031+127G>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 10/15 | chr13 | 25325195 | |||||||
| chr13:25325340 | A | G | 4 | a0001c0001t0003g0058 a0001c0001t0003g0110 a0001c0001t0003g0111 others(1): Show |
4 | HG00639.hp2 HG01070.hp2 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.1031+272A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 10/15 | chr13 | 25325340 | |||||||
| chr13:25325392 | G | A | 2 | a0001c0001t0012g0154 a0001c0001t0012g0161 |
2 | HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1031+324G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 10/15 | chr13 | 25325392 | |||||||
| chr13:25325489 | C | T | 1 | a0003c0004t0001g0266 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1031+421C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 10/15 | chr13 | 25325489 | |||||||
| chr13:25325546 | A | G | 9 | a0001c0001t0003g0023 a0001c0001t0003g0035 a0001c0001t0003g0254 others(6): Show |
11 | HG01496.hp2 HG02109.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1031+478A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 10/15 | chr13 | 25325546 | |||||||
| chr13:25325698 | G | A | 1 | a0001c0001t0003g0042 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1031+630G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 10/15 | chr13 | 25325698 | |||||||
| chr13:25325804 | C | T | 1 | a0001c0012t0001g0152 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1031+736C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 10/15 | chr13 | 25325804 | |||||||
| chr13:25325856 | G | C | 1 | a0001c0001t0015g0168 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1031+788G>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 10/15 | chr13 | 25325856 | |||||||
| chr13:25325886 | T | C | 1 | a0002c0002t0001g0196 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1031+818T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 10/15 | chr13 | 25325886 | |||||||
| chr13:25326077 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1032-839C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 10/15 | chr13 | 25326077 | |||||||
| chr13:25326161 | C | T | 1 | a0002c0002t0001g0106 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1032-755C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 10/15 | chr13 | 25326161 | |||||||
| chr13:25326174 | T | C | 5 | a0001c0001t0006g0019 a0001c0001t0006g0172 a0001c0001t0006g0173 others(2): Show |
6 | HG01891.hp2 HG02965.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1032-742T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 10/15 | chr13 | 25326174 | |||||||
| chr13:25326294 | G | GA | 5 | a0001c0001t0006g0019 a0001c0001t0006g0172 a0001c0001t0006g0173 others(2): Show |
6 | HG01891.hp2 HG02965.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1032-619dupA | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr13 | 25326294 | ||||||
| chr13:25326302 | T | C | 9 | a0001c0001t0003g0023 a0001c0001t0003g0035 a0001c0001t0003g0254 others(6): Show |
11 | HG01496.hp2 HG02109.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1032-614T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 10/15 | chr13 | 25326302 | |||||||
| chr13:25326336 | C | CT | 29 | a0001c0001t0001g0157 a0001c0001t0001g0162 a0001c0001t0001g0163 others(26): Show |
33 | HG01243.hp2 HG01361.hp2 HG01496.hp2 others(30): Show |
intron_variant | MODIFIER | c.1032-567dupT | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr13 | 25326336 | ||||||
| chr13:25326337 | T | C | 1 | a0001c0001t0018g0264 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1032-579T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 10/15 | chr13 | 25326337 | |||||||
| chr13:25326700 | C | T | 117 | a0001c0001t0003g0005 a0001c0001t0003g0026 a0001c0001t0003g0031 others(114): Show |
153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.1032-216C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 10/15 | chr13 | 25326700 | |||||||
| chr13:25327115 | A | C | 1 | a0002c0002t0001g0089 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1150+81A>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 11/15 | chr13 | 25327115 | |||||||
| chr13:25327135 | A | C | 1 | a0001c0001t0002g0241 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1150+101A>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 11/15 | chr13 | 25327135 | |||||||
| chr13:25327250 | A | C | 1 | a0002c0002t0001g0040 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1151-180A>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 11/15 | chr13 | 25327250 | |||||||
| chr13:25327276 | G | A | 5 | a0001c0001t0006g0019 a0001c0001t0006g0172 a0001c0001t0006g0173 others(2): Show |
6 | HG01891.hp2 HG02965.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1151-154G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 11/15 | chr13 | 25327276 | |||||||
| chr13:25327317 | T | C | 1 | a0001c0001t0014g0011 | 2 | HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1151-113T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 11/15 | chr13 | 25327317 | |||||||
| chr13:25327346 | A | G | 2 | a0001c0001t0013g0192 a0001c0001t0013g0193 |
2 | HG02559.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1151-84A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 11/15 | chr13 | 25327346 | |||||||
| chr13:25327389 | A | G | 1 | a0001c0001t0018g0264 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1151-41A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 11/15 | chr13 | 25327389 | |||||||
| chr13:25327643 | A | C | 248 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0021 others(245): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.1233+131A>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 12/15 | chr13 | 25327643 | |||||||
| chr13:25327671 | A | G | 1 | a0001c0001t0006g0173 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1233+159A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 12/15 | chr13 | 25327671 | |||||||
| chr13:25327708 | C | T | 1 | a0002c0002t0001g0114 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1233+196C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 12/15 | chr13 | 25327708 | |||||||
| chr13:25327709 | G | A | 2 | a0001c0001t0012g0154 a0001c0001t0012g0161 |
2 | HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1233+197G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 12/15 | chr13 | 25327709 | |||||||
| chr13:25327729 | CT | C | 4 | a0002c0002t0001g0071 a0002c0002t0001g0073 a0002c0002t0001g0075 others(1): Show |
4 | NA18950.hp2 NA18956.hp1 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.1233+225delT | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr13 | 25327729 | ||||||
| chr13:25327833 | A | G | 2 | a0001c0001t0012g0154 a0001c0001t0012g0161 |
2 | HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1233+321A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 12/15 | chr13 | 25327833 | |||||||
| chr13:25327918 | TAGTC | T | 4 | a0001c0001t0001g0007 a0001c0001t0001g0036 a0001c0001t0001g0037 others(1): Show |
8 | HG00738.hp1 HG01109.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1233+409_1233+412d others(6): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr13 | 25327918 | ||||||
| chr13:25327966 | C | T | 1 | a0002c0002t0001g0088 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1233+454C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 12/15 | chr13 | 25327966 | |||||||
| chr13:25327981 | A | G | 1 | a0001c0001t0014g0011 | 2 | HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1233+469A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 12/15 | chr13 | 25327981 | |||||||
| chr13:25328026 | C | G | 2 | a0001c0001t0001g0025 a0001c0001t0001g0142 |
3 | HG01243.hp1 HG01884.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1233+514C>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 12/15 | chr13 | 25328026 | |||||||
| chr13:25328032 | C | G | 5 | a0001c0001t0006g0019 a0001c0001t0006g0172 a0001c0001t0006g0173 others(2): Show |
6 | HG01891.hp2 HG02965.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1233+520C>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 12/15 | chr13 | 25328032 | |||||||
| chr13:25328055 | C | T | 2 | a0001c0001t0001g0025 a0001c0001t0001g0142 |
3 | HG01243.hp1 HG01884.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1233+543C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 12/15 | chr13 | 25328055 | |||||||
| chr13:25328114 | G | A | 4 | a0002c0002t0001g0067 a0002c0002t0001g0107 a0002c0002t0001g0108 others(1): Show |
4 | NA18966.hp2 NA19006.hp1 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.1233+602G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 12/15 | chr13 | 25328114 | |||||||
| chr13:25328140 | A | G | 9 | a0001c0001t0003g0023 a0001c0001t0003g0035 a0001c0001t0003g0254 others(6): Show |
11 | HG01496.hp2 HG02109.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1233+628A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 12/15 | chr13 | 25328140 | |||||||
| chr13:25328200 | A | G | 7 | a0003c0004t0001g0265 a0003c0004t0001g0266 a0003c0004t0001g0267 others(4): Show |
7 | HG02055.hp1 HG02486.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1233+688A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 12/15 | chr13 | 25328200 | |||||||
| chr13:25328246 | C | T | 1 | a0002c0002t0001g0094 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1233+734C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 12/15 | chr13 | 25328246 | |||||||
| chr13:25328340 | T | G | 1 | a0001c0001t0018g0264 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1233+828T>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 12/15 | chr13 | 25328340 | |||||||
| chr13:25328395 | CT | C | 212 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0017 others(209): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.1233+901delT | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr13 | 25328395 | ||||||
| chr13:25328420 | G | A | 1 | a0001c0001t0018g0264 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1233+908G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 12/15 | chr13 | 25328420 | |||||||
| chr13:25328438 | C | T | 1 | a0001c0001t0001g0030 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1233+926C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 12/15 | chr13 | 25328438 | |||||||
| chr13:25328512 | C | T | 15 | a0001c0003t0004g0177 a0001c0003t0004g0178 a0001c0003t0004g0179 others(12): Show |
15 | HG01496.hp1 HG02015.hp1 HG02132.hp2 others(12): Show |
intron_variant | MODIFIER | c.1233+1000C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 12/15 | chr13 | 25328512 | |||||||
| chr13:25328523 | A | C | 194 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0021 others(191): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.1233+1011A>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 12/15 | chr13 | 25328523 | |||||||
| chr13:25328646 | C | G | 1 | a0001c0001t0005g0087 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1233+1134C>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 12/15 | chr13 | 25328646 | |||||||
| chr13:25328694 | A | G | 9 | a0001c0001t0003g0023 a0001c0001t0003g0035 a0001c0001t0003g0254 others(6): Show |
11 | HG01496.hp2 HG02109.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1233+1182A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 12/15 | chr13 | 25328694 | |||||||
| chr13:25328852 | A | G | 2 | a0001c0001t0014g0011 a0001c0001t0018g0264 |
3 | HG02922.hp1 HG03491.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1233+1340A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 12/15 | chr13 | 25328852 | |||||||
| chr13:25328855 | G | A | 3 | a0001c0005t0001g0166 a0001c0005t0001g0167 a0001c0010t0001g0165 |
3 | HG02109.hp1 HG02280.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1233+1343G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 12/15 | chr13 | 25328855 | |||||||
| chr13:25328953 | G | A | 31 | a0001c0001t0003g0023 a0001c0001t0003g0035 a0001c0001t0003g0254 others(28): Show |
35 | HG01496.hp1 HG01496.hp2 HG01891.hp2 others(32): Show |
intron_variant | MODIFIER | c.1233+1441G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 12/15 | chr13 | 25328953 | |||||||
| chr13:25329230 | C | T | 1 | a0002c0002t0001g0060 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1233+1718C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 12/15 | chr13 | 25329230 | |||||||
| chr13:25329303 | A | G | 1 | a0002c0002t0001g0076 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1233+1791A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 12/15 | chr13 | 25329303 | |||||||
| chr13:25329320 | CT | C | 3 | a0002c0002t0001g0016 a0002c0002t0001g0049 a0002c0002t0001g0081 |
4 | HG01928.hp1 NA18992.hp2 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.1233+1815delT | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr13 | 25329320 | ||||||
| chr13:25329329 | C | G | 4 | a0001c0005t0001g0024 a0001c0005t0001g0166 a0001c0005t0001g0167 others(1): Show |
5 | HG02109.hp1 HG02257.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.1233+1817C>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 12/15 | chr13 | 25329329 | |||||||
| chr13:25329537 | G | A | 2 | a0002c0002t0001g0091 a0002c0002t0001g0094 |
2 | HG01069.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.1234-1820G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 12/15 | chr13 | 25329537 | |||||||
| chr13:25329614 | T | C | 15 | a0001c0003t0004g0177 a0001c0003t0004g0178 a0001c0003t0004g0179 others(12): Show |
15 | HG01496.hp1 HG02015.hp1 HG02132.hp2 others(12): Show |
intron_variant | MODIFIER | c.1234-1743T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 12/15 | chr13 | 25329614 | |||||||
| chr13:25329705 | G | A | 1 | a0002c0002t0001g0169 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1234-1652G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 12/15 | chr13 | 25329705 | |||||||
| chr13:25329768 | A | C | 1 | a0001c0001t0003g0130 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1234-1589A>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 12/15 | chr13 | 25329768 | |||||||
| chr13:25329935 | G | A | 1 | a0002c0002t0001g0116 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1234-1422G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 12/15 | chr13 | 25329935 | |||||||
| chr13:25330261 | C | T | 1 | a0003c0004t0001g0271 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1234-1096C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 12/15 | chr13 | 25330261 | |||||||
| chr13:25330659 | T | C | 82 | a0002c0002t0001g0001 a0002c0002t0001g0004 a0002c0002t0001g0010 others(79): Show |
110 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.1234-698T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 12/15 | chr13 | 25330659 | |||||||
| chr13:25330766 | A | G | 122 | a0001c0001t0003g0005 a0001c0001t0003g0023 a0001c0001t0003g0026 others(119): Show |
160 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(157): Show |
intron_variant | MODIFIER | c.1234-591A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 12/15 | chr13 | 25330766 | |||||||
| chr13:25330849 | C | T | 1 | a0001c0001t0018g0264 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1234-508C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 12/15 | chr13 | 25330849 | |||||||
| chr13:25331169 | A | G | 7 | a0003c0004t0001g0265 a0003c0004t0001g0266 a0003c0004t0001g0267 others(4): Show |
7 | HG02055.hp1 HG02486.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1234-188A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 12/15 | chr13 | 25331169 | |||||||
| chr13:25331253 | A | G | 5 | a0001c0001t0006g0019 a0001c0001t0006g0172 a0001c0001t0006g0173 others(2): Show |
6 | HG01891.hp2 HG02965.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1234-104A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 12/15 | chr13 | 25331253 | |||||||
| chr13:25331278 | T | C | 258 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0017 others(255): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.1234-79T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 12/15 | chr13 | 25331278 | |||||||
| chr13:25331344 | A | ATTTT | 39 | a0001c0001t0003g0023 a0001c0001t0003g0035 a0001c0001t0003g0254 others(36): Show |
43 | HG01496.hp1 HG01496.hp2 HG01891.hp2 others(40): Show |
intron_variant | MODIFIER | c.1234-11_1234-10ins others(4): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr13 | 25331344 | ||||||
| chr13:25331566 | C | T | 1 | a0002c0002t0001g0119 | 1 | HG02738.hp1 | splice_region_variant&intron_variant | LOW | c.1435+8C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | chr13 | 25331566 | |||||||
| chr13:25331804 | A | T | 7 | a0001c0001t0006g0019 a0001c0001t0006g0172 a0001c0001t0006g0173 others(4): Show |
9 | HG01891.hp2 HG02922.hp1 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.1435+246A>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | chr13 | 25331804 | |||||||
| chr13:25331819 | T | G | 2 | a0001c0001t0014g0011 a0001c0001t0018g0264 |
3 | HG02922.hp1 HG03491.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1435+261T>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | chr13 | 25331819 | |||||||
| chr13:25331868 | AT | A | 7 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(4): Show |
7 | HG01891.hp1 HG02258.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1435+312delT | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr13 | 25331868 | ||||||
| chr13:25331883 | C | T | 7 | a0001c0001t0006g0019 a0001c0001t0006g0172 a0001c0001t0006g0173 others(4): Show |
9 | HG01891.hp2 HG02922.hp1 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.1435+325C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | chr13 | 25331883 | |||||||
| chr13:25331946 | A | T | 7 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0135 others(4): Show |
7 | HG01884.hp1 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.1435+388A>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | chr13 | 25331946 | |||||||
| chr13:25332052 | A | G | 2 | a0001c0001t0001g0037 a0001c0001t0018g0264 |
2 | HG02723.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.1435+494A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | chr13 | 25332052 | |||||||
| chr13:25332153 | C | G | 1 | a0001c0001t0018g0264 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1435+595C>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | chr13 | 25332153 | |||||||
| chr13:25332231 | A | G | 2 | a0001c0001t0003g0130 a0001c0001t0003g0131 |
2 | HG02818.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1435+673A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | chr13 | 25332231 | |||||||
| chr13:25332537 | C | A | 1 | a0001c0012t0001g0152 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1435+979C>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | chr13 | 25332537 | |||||||
| chr13:25332537 | CAAAA | C | 116 | a0001c0001t0003g0005 a0001c0001t0003g0026 a0001c0001t0003g0031 others(113): Show |
152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.1435+983_1435+986d others(6): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr13 | 25332537 | ||||||
| chr13:25332565 | A | G | 1 | a0002c0002t0001g0074 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1435+1007A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | chr13 | 25332565 | |||||||
| chr13:25332582 | T | C | 1 | a0001c0001t0002g0207 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1435+1024T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | chr13 | 25332582 | |||||||
| chr13:25332583 | A | T | 1 | a0001c0001t0002g0207 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1435+1025A>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | chr13 | 25332583 | |||||||
| chr13:25332607 | T | C | 1 | a0002c0002t0001g0069 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1435+1049T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | chr13 | 25332607 | |||||||
| chr13:25332709 | C | T | 1 | a0002c0002t0001g0128 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1435+1151C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | chr13 | 25332709 | |||||||
| chr13:25332713 | G | A | 2 | a0003c0004t0001g0269 a0003c0004t0001g0270 |
2 | HG02486.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1435+1155G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | chr13 | 25332713 | |||||||
| chr13:25332787 | A | G | 194 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0021 others(191): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.1435+1229A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | chr13 | 25332787 | |||||||
| chr13:25332854 | A | G | 2 | a0001c0001t0012g0154 a0001c0001t0012g0161 |
2 | HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1435+1296A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | chr13 | 25332854 | |||||||
| chr13:25332906 | A | G | 7 | a0001c0001t0003g0023 a0001c0001t0003g0035 a0001c0001t0003g0254 others(4): Show |
10 | HG02109.hp2 HG02257.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1435+1348A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | chr13 | 25332906 | |||||||
| chr13:25333061 | G | T | 1 | a0001c0001t0002g0244 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1435+1503G>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | chr13 | 25333061 | |||||||
| chr13:25333162 | T | C | 2 | a0001c0001t0014g0011 a0001c0001t0018g0264 |
3 | HG02922.hp1 HG03491.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1435+1604T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | chr13 | 25333162 | |||||||
| chr13:25333196 | T | C | 3 | a0001c0001t0003g0110 a0001c0001t0003g0111 a0001c0001t0003g0121 |
3 | HG00639.hp2 HG01070.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.1435+1638T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | chr13 | 25333196 | |||||||
| chr13:25333209 | T | C | 22 | a0001c0001t0006g0019 a0001c0001t0006g0172 a0001c0001t0006g0173 others(19): Show |
24 | HG01496.hp1 HG01891.hp2 HG02015.hp1 others(21): Show |
intron_variant | MODIFIER | c.1435+1651T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | chr13 | 25333209 | |||||||
| chr13:25333643 | G | A | 4 | a0001c0001t0007g0148 a0001c0001t0007g0149 a0001c0001t0007g0150 others(1): Show |
4 | HG01496.hp2 HG02258.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1435+2085G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | chr13 | 25333643 | |||||||
| chr13:25333700 | A | G | 2 | a0001c0001t0012g0154 a0001c0001t0012g0161 |
2 | HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1435+2142A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | chr13 | 25333700 | |||||||
| chr13:25333816 | A | T | 1 | a0001c0001t0014g0011 | 2 | HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1435+2258A>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | chr13 | 25333816 | |||||||
| chr13:25333840 | TTGTTTTT others(9): Show |
T | 1 | a0003c0004t0001g0271 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1435+2287_1435+230 others(20): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr13 | 25333840 | ||||||
| chr13:25333910 | A | G | 1 | a0001c0001t0003g0105 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1435+2352A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | chr13 | 25333910 | |||||||
| chr13:25334142 | G | T | 1 | a0001c0001t0001g0232 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1435+2584G>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | chr13 | 25334142 | |||||||
| chr13:25334214 | A | T | 2 | a0001c0001t0005g0258 a0001c0001t0005g0259 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1435+2656A>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | chr13 | 25334214 | |||||||
| chr13:25334400 | G | A | 5 | a0001c0001t0001g0202 a0001c0001t0001g0204 a0001c0001t0001g0211 others(2): Show |
5 | NA18945.hp2 NA18950.hp1 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.1436-2536G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | chr13 | 25334400 | |||||||
| chr13:25334609 | T | G | 2 | a0001c0001t0012g0154 a0001c0001t0012g0161 |
2 | HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1436-2327T>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | chr13 | 25334609 | |||||||
| chr13:25334650 | A | G | 2 | a0001c0001t0007g0149 a0001c0001t0007g0150 |
2 | HG01496.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1436-2286A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | chr13 | 25334650 | |||||||
| chr13:25334850 | A | G | 1 | a0002c0002t0001g0196 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1436-2086A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | chr13 | 25334850 | |||||||
| chr13:25335021 | A | T | 3 | a0001c0005t0001g0166 a0001c0005t0001g0167 a0001c0010t0001g0165 |
3 | HG02109.hp1 HG02280.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1436-1915A>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | chr13 | 25335021 | |||||||
| chr13:25335064 | A | G | 2 | a0001c0001t0002g0261 a0001c0001t0002g0262 |
2 | HG02735.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.1436-1872A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | chr13 | 25335064 | |||||||
| chr13:25335203 | T | C | 1 | a0001c0001t0001g0222 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1436-1733T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | chr13 | 25335203 | |||||||
| chr13:25335394 | C | G | 1 | a0001c0001t0003g0255 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1436-1542C>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | chr13 | 25335394 | |||||||
| chr13:25335506 | A | G | 2 | a0001c0001t0002g0241 a0001c0001t0002g0242 |
2 | NA18981.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.1436-1430A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | chr13 | 25335506 | |||||||
| chr13:25335816 | G | A | 76 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0021 others(73): Show |
106 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.1436-1120G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | chr13 | 25335816 | |||||||
| chr13:25335975 | T | A | 5 | a0001c0001t0003g0130 a0001c0001t0003g0131 a0001c0001t0006g0172 others(2): Show |
5 | HG02818.hp1 HG03098.hp1 HG03710.hp1 others(2): Show |
intron_variant | MODIFIER | c.1436-961T>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | chr13 | 25335975 | |||||||
| chr13:25335976 | A | T | 1 | a0002c0002t0001g0092 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1436-960A>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | chr13 | 25335976 | |||||||
| chr13:25336501 | A | G | 7 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0135 others(4): Show |
7 | HG01884.hp1 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.1436-435A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | chr13 | 25336501 | |||||||
| chr13:25336609 | G | A | 1 | a0001c0001t0014g0011 | 2 | HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1436-327G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | chr13 | 25336609 | |||||||
| chr13:25336912 | A | AT | 12 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0141 others(9): Show |
12 | HG02055.hp1 HG02486.hp1 HG02615.hp1 others(9): Show |
splice_region_variant&intron_variant | LOW | c.1436-8dupT | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr13 | 25336912 | ||||||
| chr13:25336912 | AT | A | 6 | a0001c0001t0006g0019 a0001c0001t0006g0172 a0001c0001t0006g0173 others(3): Show |
7 | HG01358.hp1 HG01891.hp2 HG02965.hp2 others(4): Show |
splice_region_variant&intron_variant | LOW | c.1436-8delT | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr13 | 25336912 | ||||||
| chr13:25337169 | A | G | 1 | a0001c0010t0001g0165 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1534+135A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 14/15 | chr13 | 25337169 | |||||||
| chr13:25337736 | C | T | 1 | a0001c0001t0002g0240 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1534+702C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 14/15 | chr13 | 25337736 | |||||||
| chr13:25337750 | A | G | 1 | a0002c0002t0001g0051 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1534+716A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 14/15 | chr13 | 25337750 | |||||||
| chr13:25337897 | A | G | 158 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0017 others(155): Show |
201 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(198): Show |
intron_variant | MODIFIER | c.1535-739A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 14/15 | chr13 | 25337897 | |||||||
| chr13:25337944 | G | A | 1 | a0001c0010t0001g0165 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1535-692G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 14/15 | chr13 | 25337944 | |||||||
| chr13:25337991 | T | A | 1 | a0001c0001t0018g0264 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1535-645T>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 14/15 | chr13 | 25337991 | |||||||
| chr13:25338235 | T | C | 2 | a0001c0001t0001g0017 a0001c0001t0001g0132 |
3 | HG00735.hp2 HG03195.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1535-401T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 14/15 | chr13 | 25338235 | |||||||
| chr13:25338530 | A | G | 1 | a0001c0001t0002g0238 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1535-106A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 14/15 | chr13 | 25338530 | |||||||
| chr13:25338562 | C | T | 1 | a0001c0001t0017g0153 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1535-74C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 14/15 | chr13 | 25338562 | |||||||
| chr13:25338988 | C | G | 1 | a0001c0001t0007g0149 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1630+257C>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 15/15 | chr13 | 25338988 | |||||||
| chr13:25339038 | TAC | T | 18 | a0001c0001t0001g0018 a0001c0001t0001g0027 a0001c0001t0001g0029 others(15): Show |
19 | HG01175.hp2 HG01891.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.1630+309_1630+310d others(4): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr13 | 25339038 | ||||||
| chr13:25339055 | C | G | 1 | a0001c0001t0001g0222 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1630+324C>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 15/15 | chr13 | 25339055 | |||||||
| chr13:25339068 | T | A | 1 | a0001c0001t0001g0222 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1630+337T>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 15/15 | chr13 | 25339068 | |||||||
| chr13:25339136 | C | T | 1 | a0001c0008t0001g0195 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1630+405C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 15/15 | chr13 | 25339136 | |||||||
| chr13:25339246 | A | G | 4 | a0001c0001t0002g0009 a0001c0001t0002g0210 a0001c0001t0002g0245 others(1): Show |
7 | NA18963.hp1 NA18964.hp2 NA18971.hp1 others(4): Show |
intron_variant | MODIFIER | c.1630+515A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 15/15 | chr13 | 25339246 | |||||||
| chr13:25339380 | C | T | 1 | a0001c0001t0001g0197 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1631-585C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 15/15 | chr13 | 25339380 | |||||||
| chr13:25339527 | G | A | 15 | a0001c0003t0004g0177 a0001c0003t0004g0178 a0001c0003t0004g0179 others(12): Show |
15 | HG01496.hp1 HG02015.hp1 HG02132.hp2 others(12): Show |
intron_variant | MODIFIER | c.1631-438G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 15/15 | chr13 | 25339527 | |||||||
| chr13:25339533 | T | G | 1 | a0001c0001t0014g0011 | 2 | HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1631-432T>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 15/15 | chr13 | 25339533 | |||||||
| chr13:25339593 | G | A | 1 | a0002c0002t0001g0092 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1631-372G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 15/15 | chr13 | 25339593 | |||||||
| chr13:25339620 | A | G | 2 | a0001c0001t0014g0011 a0001c0001t0018g0264 |
3 | HG02922.hp1 HG03491.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1631-345A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 15/15 | chr13 | 25339620 | |||||||
| chr13:25339660 | G | A | 117 | a0001c0001t0003g0005 a0001c0001t0003g0026 a0001c0001t0003g0031 others(114): Show |
153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.1631-305G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 15/15 | chr13 | 25339660 |