Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 4927 |
| ensemblid | ENSG00000108559.13 |
| hgncid | 8067 |
| symbol | NUP88 |
| name | nucleoporin 88 |
| refseq_nuc | NM_002532.6 |
| refseq_prot | NP_002523.2 |
| ensembl_nuc | ENST00000573584.6 |
| ensembl_prot | ENSP00000458954.1 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 5384833 |
| end | 5419662 |
| strand | - |
| ver | v1.2 |
| region | chr17:5384833-5419662 |
| region5000 | chr17:5379833-5424662 |
| regionname0 | NUP88_chr17_5384833_5419662 |
| regionname5000 | NUP88_chr17_5379833_5424662 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 741 | 359 | 85 | 66 | 148 | 16 | 42 | 112 | NUP88_chr17_5379833_5424662 | NUP88 | MAAAE others(736): Show |
chr17 | 5379833 | 5424662 |
| a0002 | 0/0 | 741 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | MAAAE others(736): Show |
chr17 | 5379833 | 5424662 |
| a0003 | 0/0 | 741 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | MAAAE others(736): Show |
chr17 | 5379833 | 5424662 |
| a0004 | 0/0 | 741 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | MAAAE others(736): Show |
chr17 | 5379833 | 5424662 |
| a0005 | 0/0 | 741 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | MAAAE others(736): Show |
chr17 | 5379833 | 5424662 |
| a0006 | 0/0 | 741 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | MAAAE others(736): Show |
chr17 | 5379833 | 5424662 |
| a0007 | 0/0 | 741 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NUP88_chr17_5379833_5424662 | NUP88 | MAAAE others(736): Show |
chr17 | 5379833 | 5424662 |
| a0008 | 0/0 | 741 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NUP88_chr17_5379833_5424662 | NUP88 | MAAAE others(736): Show |
chr17 | 5379833 | 5424662 |
| a0009 | 0/0 | 741 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | MAAAE others(736): Show |
chr17 | 5379833 | 5424662 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2223 | 141 | 42 | 39 | 33 | 10 | 15 | NUP88_chr17_5379833_5424662 | NUP88 | ATGGC others(2218): Show |
chr17 | 5379833 | 5424662 | ||
| a0001c0002 | 0/0 | 2223 | 109 | 33 | 9 | 55 | 1 | 11 | NUP88_chr17_5379833_5424662 | NUP88 | ATGGC others(2218): Show |
chr17 | 5379833 | 5424662 | ||
| a0001c0003 | 0/0 | 2223 | 97 | 1 | 17 | 59 | 5 | 15 | NUP88_chr17_5379833_5424662 | NUP88 | ATGGC others(2218): Show |
chr17 | 5379833 | 5424662 | ||
| a0001c0004 | 0/0 | 2223 | 6 | 6 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | ATGGC others(2218): Show |
chr17 | 5379833 | 5424662 | ||
| a0001c0007 | 0/0 | 2223 | 2 | 2 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | ATGGC others(2218): Show |
chr17 | 5379833 | 5424662 | ||
| a0001c0009 | 0/0 | 2223 | 1 | 0 | 1 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | ATGGC others(2218): Show |
chr17 | 5379833 | 5424662 | ||
| a0001c0010 | 0/0 | 2223 | 1 | 1 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | ATGGC others(2218): Show |
chr17 | 5379833 | 5424662 | ||
| a0001c0011 | 0/0 | 2223 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | ATGGC others(2218): Show |
chr17 | 5379833 | 5424662 | ||
| a0001c0013 | 0/0 | 2223 | 1 | 0 | 0 | 0 | 0 | 1 | NUP88_chr17_5379833_5424662 | NUP88 | ATGGC others(2218): Show |
chr17 | 5379833 | 5424662 | ||
| a0002c0005 | 0/0 | 2223 | 3 | 0 | 3 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | ATGGC others(2218): Show |
chr17 | 5379833 | 5424662 | ||
| a0003c0006 | 0/0 | 2223 | 2 | 0 | 2 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | ATGGC others(2218): Show |
chr17 | 5379833 | 5424662 | ||
| a0004c0012 | 0/0 | 2223 | 1 | 0 | 1 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | ATGGC others(2218): Show |
chr17 | 5379833 | 5424662 | ||
| a0005c0008 | 0/0 | 2223 | 1 | 1 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | ATGGC others(2218): Show |
chr17 | 5379833 | 5424662 | ||
| a0006c0014 | 0/0 | 2223 | 1 | 0 | 0 | 0 | 0 | 1 | NUP88_chr17_5379833_5424662 | NUP88 | ATGGC others(2218): Show |
chr17 | 5379833 | 5424662 | ||
| a0007c0015 | 0/0 | 2223 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | ATGGC others(2218): Show |
chr17 | 5379833 | 5424662 | ||
| a0008c0017 | 0/0 | 2223 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | ATGGC others(2218): Show |
chr17 | 5379833 | 5424662 | ||
| a0009c0016 | 0/0 | 2223 | 1 | 0 | 0 | 0 | 0 | 1 | NUP88_chr17_5379833_5424662 | NUP88 | ATGGC others(2218): Show |
chr17 | 5379833 | 5424662 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002 | 1/0 | 3611 | 92 | 30 | 34 | 6 | 8 | 13 | NUP88_chr17_5379833_5424662 | NUP88 | AGTTG others(3606): Show |
chr17 | 5379833 | 5424662 |
| a0001c0001t0003 | 0/0 | 3611 | 46 | 12 | 5 | 26 | 1 | 2 | NUP88_chr17_5379833_5424662 | NUP88 | AGTTG others(3606): Show |
chr17 | 5379833 | 5424662 |
| a0001c0001t0013 | 0/0 | 3611 | 1 | 0 | 0 | 0 | 1 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | AGTTG others(3606): Show |
chr17 | 5379833 | 5424662 |
| a0001c0001t0014 | 0/0 | 3611 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | AGTTG others(3606): Show |
chr17 | 5379833 | 5424662 |
| a0001c0001t0015 | 0/1 | 3609 | 1 | 0 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | AGTTG others(3604): Show |
chr17 | 5379833 | 5424662 |
| a0001c0002t0001 | 0/0 | 3606 | 20 | 11 | 5 | 1 | 0 | 3 | NUP88_chr17_5379833_5424662 | NUP88 | AGTTG others(3601): Show |
chr17 | 5379833 | 5424662 |
| a0001c0002t0004 | 0/0 | 3607 | 44 | 0 | 0 | 38 | 0 | 6 | NUP88_chr17_5379833_5424662 | NUP88 | AGTTG others(3602): Show |
chr17 | 5379833 | 5424662 |
| a0001c0002t0005 | 0/0 | 3606 | 32 | 11 | 4 | 15 | 0 | 2 | NUP88_chr17_5379833_5424662 | NUP88 | AGTTG others(3601): Show |
chr17 | 5379833 | 5424662 |
| a0001c0002t0007 | 0/0 | 3606 | 4 | 3 | 0 | 0 | 1 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | AGTTG others(3601): Show |
chr17 | 5379833 | 5424662 |
| a0001c0002t0008 | 0/0 | 3606 | 4 | 4 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | AGTTG others(3601): Show |
chr17 | 5379833 | 5424662 |
| a0001c0002t0009 | 0/0 | 3606 | 3 | 3 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | AGTTG others(3601): Show |
chr17 | 5379833 | 5424662 |
| a0001c0002t0011 | 0/0 | 3606 | 1 | 1 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | AGTTG others(3601): Show |
chr17 | 5379833 | 5424662 |
| a0001c0002t0017 | 0/0 | 3606 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | AGTTG others(3601): Show |
chr17 | 5379833 | 5424662 |
| a0001c0003t0001 | 0/0 | 3606 | 93 | 1 | 16 | 57 | 5 | 14 | NUP88_chr17_5379833_5424662 | NUP88 | AGTTG others(3601): Show |
chr17 | 5379833 | 5424662 |
| a0001c0003t0012 | 0/0 | 3606 | 1 | 0 | 0 | 0 | 0 | 1 | NUP88_chr17_5379833_5424662 | NUP88 | AGTTG others(3601): Show |
chr17 | 5379833 | 5424662 |
| a0001c0003t0016 | 0/0 | 3606 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | AGTTG others(3601): Show |
chr17 | 5379833 | 5424662 |
| a0001c0003t0018 | 0/0 | 3606 | 1 | 0 | 1 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | AGTTG others(3601): Show |
chr17 | 5379833 | 5424662 |
| a0001c0003t0019 | 0/0 | 3606 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | AGTTG others(3601): Show |
chr17 | 5379833 | 5424662 |
| a0001c0004t0002 | 0/0 | 3611 | 1 | 1 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | AGTTG others(3606): Show |
chr17 | 5379833 | 5424662 |
| a0001c0004t0006 | 0/0 | 3611 | 5 | 5 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | AGTTG others(3606): Show |
chr17 | 5379833 | 5424662 |
| a0001c0007t0007 | 0/0 | 3606 | 2 | 2 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | AGTTG others(3601): Show |
chr17 | 5379833 | 5424662 |
| a0001c0009t0006 | 0/0 | 3611 | 1 | 0 | 1 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | AGTTG others(3606): Show |
chr17 | 5379833 | 5424662 |
| a0001c0010t0001 | 0/0 | 3606 | 1 | 1 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | AGTTG others(3601): Show |
chr17 | 5379833 | 5424662 |
| a0001c0011t0003 | 0/0 | 3611 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | AGTTG others(3606): Show |
chr17 | 5379833 | 5424662 |
| a0001c0013t0005 | 0/0 | 3606 | 1 | 0 | 0 | 0 | 0 | 1 | NUP88_chr17_5379833_5424662 | NUP88 | AGTTG others(3601): Show |
chr17 | 5379833 | 5424662 |
| a0002c0005t0001 | 0/0 | 3606 | 3 | 0 | 3 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | AGTTG others(3601): Show |
chr17 | 5379833 | 5424662 |
| a0003c0006t0010 | 0/0 | 3611 | 2 | 0 | 2 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | AGTTG others(3606): Show |
chr17 | 5379833 | 5424662 |
| a0004c0012t0002 | 0/0 | 3611 | 1 | 0 | 1 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | AGTTG others(3606): Show |
chr17 | 5379833 | 5424662 |
| a0005c0008t0001 | 0/0 | 3606 | 1 | 1 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | AGTTG others(3601): Show |
chr17 | 5379833 | 5424662 |
| a0006c0014t0005 | 0/0 | 3606 | 1 | 0 | 0 | 0 | 0 | 1 | NUP88_chr17_5379833_5424662 | NUP88 | AGTTG others(3601): Show |
chr17 | 5379833 | 5424662 |
| a0007c0015t0005 | 0/0 | 3606 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | AGTTG others(3601): Show |
chr17 | 5379833 | 5424662 |
| a0008c0017t0008 | 0/0 | 3606 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | AGTTG others(3601): Show |
chr17 | 5379833 | 5424662 |
| a0009c0016t0002 | 0/0 | 3611 | 1 | 0 | 0 | 0 | 0 | 1 | NUP88_chr17_5379833_5424662 | NUP88 | AGTTG others(3606): Show |
chr17 | 5379833 | 5424662 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002g0001 | 0/0 | 15 | 0 | 10 | 0 | 3 | 2 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0002g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0002g0013 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0002g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0002g0022 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0002g0024 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0002g0025 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0002g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0002g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0002g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0002g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0002g0245 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0002g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0002g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0003g0005 | 0/0 | 7 | 0 | 1 | 6 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0003g0012 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0003g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0003g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0003g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0003g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0003g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0003g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0003g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0003g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0003g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0003g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0003g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0003g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0003g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0003g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0013g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0014g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0001t0015g0222 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0004g0004 | 0/0 | 8 | 0 | 0 | 6 | 0 | 2 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0004g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0004g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0004g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0004g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0004g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0004g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0004g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0004g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0004g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0004g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0004g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0004g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0004g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0004g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0004g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0004g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0004g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0004g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0004g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0004g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0004g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0004g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0004g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0004g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0004g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0004g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0004g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0004g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0004g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0004g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0005g0009 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0005g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0005g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0005g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0005g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0005g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0005g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0005g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0005g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0005g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0005g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0005g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0005g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0005g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0005g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0005g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0005g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0005g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0005g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0005g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0005g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0005g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0005g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0005g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0005g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0005g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0005g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0005g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0005g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0007g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0007g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0007g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0007g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0008g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0008g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0008g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0008g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0009g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0009g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0009g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0011g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0002t0017g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0003t0001g0002 | 0/0 | 14 | 0 | 4 | 8 | 1 | 1 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0003t0001g0003 | 0/0 | 8 | 0 | 1 | 5 | 0 | 2 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0003t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0003t0001g0008 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0003t0001g0015 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0003t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0003t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0003t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0003t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0003t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0003t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0003t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0003t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0003t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0003t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0003t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0003t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0003t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0003t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0003t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0003t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0003t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0003t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0003t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0003t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0003t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0003t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0003t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0003t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0003t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0003t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0003t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0003t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0003t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0003t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0003t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0003t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0003t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0003t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0003t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0003t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0003t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0003t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0003t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0003t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0003t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0003t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0003t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0003t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0003t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0003t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0003t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0003t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0003t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0003t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0003t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0003t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0003t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0003t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0003t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0003t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0003t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0003t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0003t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0003t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0003t0012g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0003t0016g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0003t0018g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0003t0019g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0004t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0004t0006g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0004t0006g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0004t0006g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0004t0006g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0004t0006g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0007t0007g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0007t0007g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0009t0006g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0010t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0011t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0001c0013t0005g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0002c0005t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0002c0005t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0002c0005t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0003c0006t0010g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0004c0012t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0005c0008t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0006c0014t0005g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0007c0015t0005g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0008c0017t0008g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| a0009c0016t0002g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0199 | EUR | GBR | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG00099 | hp2 | a0001 | c0003 | t0001 | g0002 | EUR | GBR | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0001 | EUR | GBR | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0256 | EUR | GBR | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG00280 | hp1 | a0001 | c0003 | t0001 | g0094 | EUR | FIN | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG00280 | hp2 | a0001 | c0002 | t0007 | g0116 | EUR | FIN | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG00408 | hp1 | a0001 | c0003 | t0001 | g0018 | EAS | CHS | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | CHS | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG00438 | hp1 | a0001 | c0003 | t0001 | g0076 | EAS | CHS | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG00438 | hp2 | a0001 | c0002 | t0004 | g0150 | EAS | CHS | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG00544 | hp1 | a0001 | c0003 | t0001 | g0093 | EAS | CHS | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG00544 | hp2 | a0001 | c0002 | t0005 | g0159 | EAS | CHS | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG00558 | hp1 | a0001 | c0003 | t0001 | g0101 | EAS | CHS | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG00558 | hp2 | a0001 | c0003 | t0001 | g0084 | EAS | CHS | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG00609 | hp1 | a0001 | c0003 | t0001 | g0102 | EAS | CHS | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG00609 | hp2 | a0001 | c0002 | t0004 | g0035 | EAS | CHS | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0266 | EAS | CHS | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG00621 | hp2 | a0001 | c0002 | t0005 | g0118 | EAS | CHS | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0171 | AMR | PUR | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0005 | AMR | PUR | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0235 | EAS | CHS | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG00673 | hp2 | a0001 | c0002 | t0005 | g0158 | EAS | CHS | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG00733 | hp2 | a0002 | c0005 | t0001 | g0057 | AMR | PUR | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG00735 | hp1 | a0004 | c0012 | t0002 | g0204 | AMR | PUR | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0248 | AMR | PUR | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG00738 | hp1 | a0001 | c0003 | t0001 | g0043 | AMR | PUR | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0205 | AMR | PUR | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG00741 | hp1 | a0001 | c0002 | t0001 | g0105 | AMR | PUR | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0259 | AMR | PUR | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG01071 | hp2 | a0001 | c0002 | t0005 | g0117 | AMR | PUR | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG01074 | hp1 | a0001 | c0002 | t0005 | g0009 | AMR | PUR | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0244 | AMR | PUR | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0223 | AMR | PUR | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG01081 | hp2 | a0001 | c0003 | t0001 | g0179 | AMR | PUR | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0029 | AMR | PUR | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0022 | AMR | PUR | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG01167 | hp1 | a0003 | c0006 | t0010 | g0014 | AMR | PUR | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0225 | AMR | PUR | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0263 | AMR | PUR | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0262 | AMR | PUR | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0264 | AMR | PUR | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG01169 | hp2 | a0003 | c0006 | t0010 | g0014 | AMR | PUR | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0221 | AMR | PUR | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0271 | AMR | PUR | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG01192 | hp1 | a0001 | c0003 | t0001 | g0045 | AMR | PUR | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG01192 | hp2 | a0001 | c0003 | t0001 | g0177 | AMR | PUR | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG01243 | hp1 | a0001 | c0009 | t0006 | g0186 | AMR | PUR | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0206 | AMR | PUR | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG01255 | hp1 | a0001 | c0003 | t0001 | g0002 | AMR | CLM | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0224 | AMR | CLM | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0253 | AMR | CLM | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0250 | AMR | CLM | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG01261 | hp2 | a0001 | c0003 | t0001 | g0097 | AMR | CLM | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG01346 | hp1 | a0001 | c0003 | t0001 | g0092 | AMR | CLM | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0034 | AMR | CLM | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG01358 | hp1 | a0001 | c0002 | t0005 | g0009 | AMR | CLM | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG01358 | hp2 | a0001 | c0003 | t0001 | g0176 | AMR | CLM | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0249 | AMR | CLM | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0012 | AMR | CLM | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0103 | AMR | CLM | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0247 | AMR | CLM | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG01496 | hp1 | a0001 | c0003 | t0001 | g0099 | AMR | CLM | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0025 | EUR | IBS | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0024 | EUR | IBS | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0001 | EUR | IBS | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG01516 | hp2 | a0001 | c0003 | t0001 | g0015 | EUR | IBS | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0025 | EUR | IBS | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG01517 | hp2 | a0001 | c0003 | t0001 | g0015 | EUR | IBS | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0026 | AFR | ACB | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG01884 | hp2 | a0001 | c0002 | t0007 | g0196 | AFR | ACB | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0023 | AFR | ACB | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG01891 | hp2 | a0001 | c0002 | t0005 | g0167 | AFR | ACB | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG01928 | hp1 | a0001 | c0001 | t0003 | g0228 | AMR | PEL | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG01928 | hp2 | a0001 | c0003 | t0001 | g0002 | AMR | PEL | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0029 | AMR | PEL | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG01934 | hp2 | a0002 | c0005 | t0001 | g0058 | AMR | PEL | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG01943 | hp1 | a0001 | c0001 | t0003 | g0231 | AMR | PEL | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG01952 | hp1 | a0001 | c0002 | t0001 | g0106 | AMR | PEL | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG01952 | hp2 | a0001 | c0003 | t0001 | g0047 | AMR | PEL | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG01975 | hp1 | a0001 | c0002 | t0005 | g0131 | AMR | PEL | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG01975 | hp2 | a0002 | c0005 | t0001 | g0059 | AMR | PEL | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG01978 | hp1 | a0001 | c0003 | t0001 | g0002 | AMR | PEL | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG01981 | hp1 | a0001 | c0003 | t0001 | g0003 | AMR | PEL | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0268 | AMR | PEL | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG01993 | hp2 | a0001 | c0003 | t0001 | g0002 | AMR | PEL | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG02015 | hp1 | a0001 | c0003 | t0001 | g0002 | EAS | KHV | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG02015 | hp2 | a0001 | c0001 | t0003 | g0030 | EAS | KHV | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG02027 | hp1 | a0001 | c0003 | t0001 | g0016 | EAS | KHV | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG02027 | hp2 | a0001 | c0002 | t0004 | g0010 | EAS | KHV | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG02040 | hp1 | a0001 | c0002 | t0004 | g0004 | EAS | KHV | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG02040 | hp2 | a0001 | c0003 | t0001 | g0003 | EAS | KHV | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG02071 | hp1 | a0001 | c0003 | t0019 | g0073 | EAS | KHV | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG02071 | hp2 | a0001 | c0002 | t0004 | g0004 | EAS | KHV | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG02074 | hp1 | a0001 | c0003 | t0001 | g0065 | EAS | KHV | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG02074 | hp2 | a0001 | c0001 | t0003 | g0229 | EAS | KHV | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG02080 | hp1 | a0001 | c0002 | t0004 | g0010 | EAS | KHV | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG02080 | hp2 | a0001 | c0003 | t0001 | g0074 | EAS | KHV | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG02132 | hp1 | a0001 | c0003 | t0001 | g0002 | EAS | KHV | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG02132 | hp2 | a0001 | c0002 | t0004 | g0140 | EAS | KHV | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0254 | AFR | ACB | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0273 | AFR | ACB | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG02165 | hp1 | a0001 | c0002 | t0004 | g0004 | EAS | CDX | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG02165 | hp2 | a0001 | c0003 | t0001 | g0003 | EAS | CDX | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0280 | AFR | ACB | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG02257 | hp2 | a0001 | c0002 | t0001 | g0111 | AFR | ACB | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | ACB | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0219 | AFR | ACB | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG02273 | hp2 | a0001 | c0003 | t0018 | g0064 | AMR | PEL | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG02280 | hp1 | a0001 | c0002 | t0005 | g0185 | AFR | ACB | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG02280 | hp2 | a0001 | c0002 | t0009 | g0193 | AFR | ACB | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG02293 | hp2 | a0001 | c0003 | t0001 | g0046 | AMR | PEL | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0269 | AMR | PEL | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG02300 | hp2 | a0001 | c0003 | t0001 | g0096 | AMR | PEL | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG02451 | hp1 | a0001 | c0002 | t0001 | g0110 | AFR | ACB | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG02451 | hp2 | a0001 | c0002 | t0009 | g0191 | AFR | ACB | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG02523 | hp1 | a0001 | c0003 | t0001 | g0083 | EAS | KHV | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0257 | EAS | KHV | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0037 | AFR | GWD | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG02572 | hp2 | a0001 | c0002 | t0007 | g0284 | AFR | GWD | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG02602 | hp1 | a0001 | c0002 | t0004 | g0145 | SAS | PJL | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG02602 | hp2 | a0001 | c0003 | t0001 | g0003 | SAS | PJL | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG02615 | hp1 | a0001 | c0002 | t0008 | g0162 | AFR | GWD | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0218 | AFR | GWD | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0026 | AFR | GWD | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0213 | AFR | GWD | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | GWD | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0277 | AFR | GWD | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG02683 | hp1 | a0001 | c0003 | t0001 | g0095 | SAS | PJL | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG02683 | hp2 | a0001 | c0003 | t0001 | g0050 | SAS | PJL | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0024 | SAS | PJL | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0207 | AFR | GWD | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG02717 | hp2 | a0005 | c0008 | t0001 | g0032 | AFR | GWD | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0220 | AFR | GWD | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0174 | AFR | GWD | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG02735 | hp1 | a0001 | c0002 | t0004 | g0004 | SAS | PJL | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG02735 | hp2 | a0001 | c0003 | t0001 | g0098 | SAS | PJL | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0175 | SAS | PJL | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0270 | SAS | PJL | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG02809 | hp1 | a0001 | c0002 | t0005 | g0120 | AFR | GWD | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | GWD | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0031 | AFR | GWD | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG02818 | hp2 | a0001 | c0002 | t0005 | g0019 | AFR | GWD | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0211 | AFR | GWD | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG02886 | hp2 | a0001 | c0004 | t0006 | g0187 | AFR | GWD | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG02896 | hp1 | a0001 | c0007 | t0007 | g0194 | AFR | GWD | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0275 | AFR | GWD | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG02897 | hp1 | a0001 | c0007 | t0007 | g0195 | AFR | GWD | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0033 | AFR | GWD | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG02922 | hp1 | a0001 | c0002 | t0005 | g0009 | AFR | ESN | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG02922 | hp2 | a0001 | c0004 | t0006 | g0188 | AFR | ESN | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG02965 | hp1 | a0001 | c0004 | t0006 | g0189 | AFR | ESN | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0274 | AFR | ESN | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG02970 | hp1 | a0001 | c0002 | t0009 | g0192 | AFR | ESN | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG02970 | hp2 | a0001 | c0002 | t0001 | g0108 | AFR | ESN | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG02976 | hp1 | a0001 | c0002 | t0001 | g0173 | AFR | ESN | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0282 | AFR | ESN | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0242 | SAS | PJL | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG03017 | hp2 | a0001 | c0002 | t0004 | g0147 | SAS | PJL | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0209 | AFR | GWD | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG03041 | hp2 | a0001 | c0004 | t0006 | g0190 | AFR | GWD | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG03098 | hp1 | a0001 | c0002 | t0001 | g0182 | AFR | MSL | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0281 | AFR | MSL | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0278 | AFR | ESN | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG03130 | hp2 | a0001 | c0002 | t0001 | g0115 | AFR | ESN | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG03139 | hp1 | a0001 | c0002 | t0005 | g0019 | AFR | ESN | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0023 | AFR | ESN | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0031 | AFR | ESN | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0028 | AFR | ESN | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG03209 | hp1 | a0001 | c0002 | t0005 | g0168 | AFR | MSL | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG03209 | hp2 | a0001 | c0002 | t0008 | g0163 | AFR | MSL | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG03225 | hp1 | a0001 | c0002 | t0005 | g0121 | AFR | MSL | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0201 | AFR | MSL | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0241 | SAS | PJL | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0240 | SAS | PJL | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG03453 | hp1 | a0001 | c0004 | t0002 | g0212 | AFR | MSL | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG03453 | hp2 | a0001 | c0002 | t0008 | g0161 | AFR | MSL | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG03486 | hp1 | a0001 | c0002 | t0005 | g0040 | AFR | MSL | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0286 | AFR | MSL | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG03490 | hp1 | a0006 | c0014 | t0005 | g0133 | SAS | PJL | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0272 | SAS | PJL | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG03492 | hp1 | a0001 | c0002 | t0004 | g0004 | SAS | PJL | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0258 | SAS | PJL | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0021 | AFR | GWD | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG03540 | hp2 | a0001 | c0002 | t0001 | g0113 | AFR | GWD | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0022 | AFR | MSL | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0215 | AFR | MSL | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG03654 | hp1 | a0001 | c0002 | t0004 | g0143 | SAS | PJL | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0012 | SAS | PJL | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0104 | SAS | PJL | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0169 | SAS | PJL | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG03704 | hp1 | a0001 | c0003 | t0001 | g0002 | SAS | PJL | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG03704 | hp2 | a0001 | c0003 | t0012 | g0181 | SAS | PJL | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG03710 | hp1 | a0001 | c0003 | t0001 | g0085 | SAS | PJL | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG03710 | hp2 | a0001 | c0002 | t0005 | g0119 | SAS | PJL | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | BEB | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG03834 | hp2 | a0001 | c0003 | t0001 | g0068 | SAS | BEB | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG03927 | hp1 | a0001 | c0003 | t0001 | g0008 | SAS | BEB | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0243 | SAS | BEB | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG03942 | hp1 | a0001 | c0002 | t0005 | g0125 | SAS | BEB | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0246 | SAS | BEB | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG04115 | hp1 | a0001 | c0013 | t0005 | g0130 | SAS | STU | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG04115 | hp2 | a0001 | c0003 | t0001 | g0069 | SAS | STU | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0232 | SAS | BEB | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG04184 | hp2 | a0001 | c0002 | t0004 | g0148 | SAS | BEB | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG04199 | hp1 | a0001 | c0003 | t0001 | g0100 | SAS | STU | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0252 | SAS | STU | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG04204 | hp1 | a0001 | c0003 | t0001 | g0003 | SAS | STU | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0261 | SAS | STU | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG04228 | hp1 | a0001 | c0003 | t0001 | g0078 | SAS | STU | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG04228 | hp2 | a0001 | c0003 | t0001 | g0044 | SAS | STU | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA18522 | hp1 | a0001 | c0002 | t0008 | g0157 | AFR | YRI | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | YRI | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA18612 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | CHB | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA18612 | hp2 | a0001 | c0002 | t0004 | g0146 | EAS | CHB | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA18747 | hp1 | a0001 | c0002 | t0004 | g0151 | EAS | CHB | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA18747 | hp2 | a0001 | c0003 | t0001 | g0086 | EAS | CHB | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA18906 | hp1 | a0001 | c0002 | t0011 | g0039 | AFR | YRI | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0027 | AFR | YRI | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA18939 | hp1 | a0001 | c0003 | t0001 | g0077 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA18939 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA18940 | hp1 | a0001 | c0002 | t0004 | g0165 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA18940 | hp2 | a0001 | c0003 | t0001 | g0075 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0226 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA18942 | hp2 | a0001 | c0002 | t0004 | g0006 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA18944 | hp1 | a0001 | c0002 | t0004 | g0149 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA18944 | hp2 | a0001 | c0003 | t0001 | g0008 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA18945 | hp1 | a0001 | c0003 | t0001 | g0007 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA18945 | hp2 | a0001 | c0002 | t0005 | g0107 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA18947 | hp1 | a0001 | c0001 | t0003 | g0227 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA18947 | hp2 | a0001 | c0003 | t0001 | g0088 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA18948 | hp1 | a0001 | c0002 | t0004 | g0006 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA18948 | hp2 | a0001 | c0003 | t0016 | g0079 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA18950 | hp1 | a0001 | c0002 | t0004 | g0164 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA18950 | hp2 | a0001 | c0001 | t0003 | g0238 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA18951 | hp1 | a0001 | c0003 | t0001 | g0063 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA18951 | hp2 | a0001 | c0002 | t0004 | g0139 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA18952 | hp1 | a0001 | c0003 | t0001 | g0066 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA18952 | hp2 | a0001 | c0002 | t0005 | g0128 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA18953 | hp1 | a0001 | c0003 | t0001 | g0060 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA18953 | hp2 | a0001 | c0002 | t0004 | g0160 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA18954 | hp1 | a0001 | c0002 | t0005 | g0127 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA18954 | hp2 | a0001 | c0001 | t0003 | g0265 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA18956 | hp1 | a0001 | c0003 | t0001 | g0042 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA18956 | hp2 | a0001 | c0002 | t0004 | g0154 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA18957 | hp1 | a0001 | c0003 | t0001 | g0002 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA18957 | hp2 | a0001 | c0002 | t0004 | g0138 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA18959 | hp1 | a0001 | c0003 | t0001 | g0007 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA18959 | hp2 | a0001 | c0002 | t0004 | g0036 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA18960 | hp1 | a0001 | c0002 | t0005 | g0054 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA18960 | hp2 | a0001 | c0003 | t0001 | g0002 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA18964 | hp1 | a0001 | c0002 | t0004 | g0010 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA18964 | hp2 | a0001 | c0003 | t0001 | g0002 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA18965 | hp2 | a0001 | c0002 | t0004 | g0136 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA18966 | hp1 | a0001 | c0003 | t0001 | g0007 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA18971 | hp1 | a0001 | c0002 | t0004 | g0006 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA18971 | hp2 | a0001 | c0003 | t0001 | g0002 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA18973 | hp1 | a0001 | c0003 | t0001 | g0062 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA18973 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA18975 | hp1 | a0001 | c0003 | t0001 | g0089 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA18975 | hp2 | a0001 | c0002 | t0001 | g0170 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA18977 | hp1 | a0001 | c0001 | t0003 | g0233 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA18977 | hp2 | a0001 | c0002 | t0005 | g0055 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA18980 | hp1 | a0007 | c0015 | t0005 | g0132 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA18980 | hp2 | a0001 | c0003 | t0001 | g0090 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA18981 | hp1 | a0001 | c0002 | t0004 | g0152 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA18981 | hp2 | a0001 | c0003 | t0001 | g0002 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA18983 | hp1 | a0001 | c0003 | t0001 | g0003 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA18987 | hp1 | a0001 | c0002 | t0005 | g0122 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA18987 | hp2 | a0001 | c0001 | t0003 | g0236 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA18988 | hp1 | a0001 | c0002 | t0005 | g0129 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA18988 | hp2 | a0001 | c0003 | t0001 | g0017 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA18989 | hp1 | a0001 | c0002 | t0004 | g0006 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA18991 | hp1 | a0001 | c0001 | t0003 | g0237 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA18991 | hp2 | a0001 | c0002 | t0004 | g0141 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA18994 | hp1 | a0001 | c0003 | t0001 | g0067 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA18994 | hp2 | a0001 | c0002 | t0004 | g0135 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA18995 | hp1 | a0001 | c0002 | t0004 | g0142 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA18995 | hp2 | a0001 | c0002 | t0004 | g0156 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA18998 | hp1 | a0001 | c0002 | t0004 | g0155 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA18999 | hp1 | a0001 | c0003 | t0001 | g0008 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA18999 | hp2 | a0001 | c0002 | t0004 | g0004 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA19001 | hp1 | a0001 | c0001 | t0003 | g0267 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA19002 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA19002 | hp2 | a0001 | c0002 | t0004 | g0004 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA19003 | hp1 | a0001 | c0003 | t0001 | g0002 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA19003 | hp2 | a0001 | c0002 | t0004 | g0006 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA19004 | hp1 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA19004 | hp2 | a0001 | c0003 | t0001 | g0283 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA19005 | hp1 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA19005 | hp2 | a0001 | c0003 | t0001 | g0053 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA19007 | hp1 | a0001 | c0002 | t0005 | g0126 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA19007 | hp2 | a0001 | c0003 | t0001 | g0091 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA19010 | hp2 | a0001 | c0003 | t0001 | g0048 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA19011 | hp1 | a0001 | c0001 | t0003 | g0239 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA19011 | hp2 | a0001 | c0003 | t0001 | g0003 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0279 | AFR | LWK | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA19043 | hp2 | a0001 | c0010 | t0001 | g0114 | AFR | LWK | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA19054 | hp1 | a0001 | c0003 | t0001 | g0072 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA19054 | hp2 | a0001 | c0002 | t0004 | g0134 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA19055 | hp1 | a0008 | c0017 | t0008 | g0287 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA19055 | hp2 | a0001 | c0003 | t0001 | g0070 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA19056 | hp1 | a0001 | c0001 | t0003 | g0230 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA19056 | hp2 | a0001 | c0002 | t0005 | g0056 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA19057 | hp1 | a0001 | c0003 | t0001 | g0003 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA19057 | hp2 | a0001 | c0002 | t0004 | g0137 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA19058 | hp1 | a0001 | c0002 | t0004 | g0144 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA19058 | hp2 | a0001 | c0003 | t0001 | g0184 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA19060 | hp1 | a0001 | c0003 | t0001 | g0080 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA19060 | hp2 | a0001 | c0003 | t0001 | g0061 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA19065 | hp1 | a0001 | c0002 | t0004 | g0004 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA19065 | hp2 | a0001 | c0001 | t0014 | g0216 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA19072 | hp1 | a0001 | c0003 | t0001 | g0081 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA19072 | hp2 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA19075 | hp1 | a0001 | c0001 | t0003 | g0234 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA19075 | hp2 | a0001 | c0003 | t0001 | g0049 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA19078 | hp1 | a0001 | c0003 | t0001 | g0017 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA19078 | hp2 | a0001 | c0001 | t0003 | g0203 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA19079 | hp1 | a0001 | c0002 | t0017 | g0051 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA19079 | hp2 | a0001 | c0002 | t0005 | g0123 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA19083 | hp1 | a0001 | c0003 | t0001 | g0180 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA19083 | hp2 | a0001 | c0003 | t0001 | g0016 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA19085 | hp1 | a0001 | c0003 | t0001 | g0018 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA19085 | hp2 | a0001 | c0002 | t0005 | g0124 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA19086 | hp1 | a0001 | c0002 | t0004 | g0082 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA19086 | hp2 | a0001 | c0002 | t0005 | g0153 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA19089 | hp1 | a0001 | c0011 | t0003 | g0200 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA19089 | hp2 | a0001 | c0003 | t0001 | g0178 | EAS | JPT | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA20752 | hp1 | a0001 | c0001 | t0013 | g0255 | EUR | TSI | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0038 | EUR | TSI | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0001 | EUR | TSI | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA20805 | hp2 | a0001 | c0003 | t0001 | g0071 | EUR | TSI | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA20905 | hp1 | a0009 | c0016 | t0002 | g0251 | SAS | GIH | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA20905 | hp2 | a0001 | c0003 | t0001 | g0052 | SAS | GIH | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0172 | AMR | CLM | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0021 | AFR | ACB | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0260 | AFR | ACB | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0109 | AFR | ACB | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0202 | AFR | ACB | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0027 | AFR | ACB | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0112 | AFR | ACB | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0214 | AFR | MSL | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG03471 | hp2 | a0001 | c0002 | t0001 | g0183 | AFR | MSL | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0028 | AFR | USA | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| HG06807 | hp2 | a0001 | c0002 | t0007 | g0197 | AFR | USA | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA20300 | hp1 | a0001 | c0002 | t0005 | g0166 | AFR | USA | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA20300 | hp2 | a0001 | c0003 | t0001 | g0087 | AFR | USA | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA21309 | hp1 | a0001 | c0002 | t0005 | g0041 | AFR | LWK | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| NA21309 | hp2 | a0001 | c0004 | t0006 | g0285 | AFR | LWK | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0015 | g0222 | REF | REF | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0245 | REF | REF | NUP88_chr17_5379833_5424662 | NUP88 | chr17 | 5379833 | 5424662 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:5386234 | T | C | 1 | a0004 | 1 | HG00735.hp1 | missense_variant | MODERATE | c.2198A>G | p.Asn733Ser | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 17/17 | 2210/3611 | 2198/2226 | 733/741 | chr17 | 5386234 | |||
| chr17:5387806 | T | C | 1 | a0006 | 1 | HG03490.hp1 | missense_variant | MODERATE | c.1742A>G | p.Asp581Gly | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 12/17 | 1754/3611 | 1742/2226 | 581/741 | chr17 | 5387806 | |||
| chr17:5405059 | T | C | 1 | a0007 | 1 | NA18980.hp1 | missense_variant&splice_region_variant | MODERATE | c.1042A>G | p.Thr348Ala | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 6/17 | 1054/3611 | 1042/2226 | 348/741 | chr17 | 5405059 | |||
| chr17:5405091 | A | G | 1 | a0002 | 3 | HG00733.hp2 HG01934.hp2 HG01975.hp2 |
missense_variant | MODERATE | c.1010T>C | p.Val337Ala | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 6/17 | 1022/3611 | 1010/2226 | 337/741 | chr17 | 5405091 | |||
| chr17:5405169 | G | A | 1 | a0009 | 1 | NA20905.hp1 | missense_variant | MODERATE | c.932C>T | p.Ala311Val | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 6/17 | 944/3611 | 932/2226 | 311/741 | chr17 | 5405169 | |||
| chr17:5419472 | A | G | 1 | a0005 | 1 | HG02717.hp2 | missense_variant | MODERATE | c.179T>C | p.Val60Ala | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 1/17 | 191/3611 | 179/2226 | 60/741 | chr17 | 5419472 | |||
| chr17:5419626 | C | A | 1 | a0008 | 1 | NA19055.hp1 | missense_variant | MODERATE | c.25G>T | p.Gly9Cys | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 1/17 | 37/3611 | 25/2226 | 9/741 | chr17 | 5419626 | |||
| chr17:5419635 | C | T | 1 | a0003 | 2 | HG01167.hp1 HG01169.hp2 |
missense_variant | MODERATE | c.16G>A | p.Gly6Arg | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 1/17 | 28/3611 | 16/2226 | 6/741 | chr17 | 5419635 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:5386260 | A | G | 12 | a0001c0002 a0001c0003 a0001c0004 others(9): Show |
225 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(222): Show |
synonymous_variant | LOW | c.2172T>C | p.His724His | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 17/17 | 2184/3611 | 2172/2226 | 724/741 | chr17 | 5386260 | |||
| chr17:5386713 | T | C | 10 | a0001c0002 a0001c0003 a0001c0007 others(7): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
synonymous_variant | LOW | c.2157A>G | p.Lys719Lys | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 16/17 | 2169/3611 | 2157/2226 | 719/741 | chr17 | 5386713 | |||
| chr17:5387643 | C | T | 1 | a0001c0011 | 1 | NA19089.hp1 | synonymous_variant | LOW | c.1797G>A | p.Lys599Lys | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 13/17 | 1809/3611 | 1797/2226 | 599/741 | chr17 | 5387643 | |||
| chr17:5388942 | C | T | 2 | a0001c0013 a0006c0014 |
2 | HG03490.hp1 HG04115.hp1 |
synonymous_variant | LOW | c.1503G>A | p.Ala501Ala | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 11/17 | 1515/3611 | 1503/2226 | 501/741 | chr17 | 5388942 | |||
| chr17:5391656 | T | A | 10 | a0001c0002 a0001c0003 a0001c0007 others(7): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
synonymous_variant | LOW | c.1389A>T | p.Pro463Pro | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 10/17 | 1401/3611 | 1389/2226 | 463/741 | chr17 | 5391656 | |||
| chr17:5405057 | C | T | 3 | a0001c0003 a0001c0010 a0002c0005 |
101 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(98): Show |
splice_region_variant&synonymous_variant | LOW | c.1044G>A | p.Thr348Thr | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 6/17 | 1056/3611 | 1044/2226 | 348/741 | chr17 | 5405057 | |||
| chr17:5405090 | G | A | 1 | a0001c0007 | 2 | HG02896.hp1 HG02897.hp1 |
synonymous_variant | LOW | c.1011C>T | p.Val337Val | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 6/17 | 1023/3611 | 1011/2226 | 337/741 | chr17 | 5405090 | |||
| chr17:5408903 | C | T | 1 | a0001c0009 | 1 | HG01243.hp1 | synonymous_variant | LOW | c.687G>A | p.Ala229Ala | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 5/17 | 699/3611 | 687/2226 | 229/741 | chr17 | 5408903 | |||
| chr17:5414017 | G | A | 1 | a0003c0006 | 2 | HG01167.hp1 HG01169.hp2 |
synonymous_variant | LOW | c.585C>T | p.Asn195Asn | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 3/17 | 597/3611 | 585/2226 | 195/741 | chr17 | 5414017 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:5384859 | A | T | 11 | a0001c0002t0001 a0001c0002t0007 a0001c0003t0001 others(8): Show |
128 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(125): Show |
3_prime_UTR_variant | MODIFIER | c.*1347T>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 17/17 | 1347 | chr17 | 5384859 | ||||||
| chr17:5384869 | A | G | 1 | a0001c0001t0014 | 1 | NA19065.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1337T>C | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 17/17 | 1337 | chr17 | 5384869 | ||||||
| chr17:5384883 | C | T | 21 | a0001c0002t0001 a0001c0002t0004 a0001c0002t0005 others(18): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
3_prime_UTR_variant | MODIFIER | c.*1323G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 17/17 | 1323 | chr17 | 5384883 | ||||||
| chr17:5384920 | C | T | 1 | a0001c0002t0017 | 1 | NA19079.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1286G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 17/17 | 1286 | chr17 | 5384920 | ||||||
| chr17:5385059 | G | C | 2 | a0001c0002t0008 a0008c0017t0008 |
5 | HG02615.hp1 HG03209.hp2 HG03453.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1147C>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 17/17 | 1147 | chr17 | 5385059 | ||||||
| chr17:5385170 | T | A | 1 | a0001c0003t0019 | 1 | HG02071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1036A>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 17/17 | 1036 | chr17 | 5385170 | ||||||
| chr17:5385172 | T | C | 2 | a0001c0002t0007 a0001c0007t0007 |
6 | HG00280.hp2 HG01884.hp2 HG02572.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1034A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 17/17 | 1034 | chr17 | 5385172 | ||||||
| chr17:5385190 | T | C | 1 | a0001c0003t0018 | 1 | HG02273.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1016A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 17/17 | 1016 | chr17 | 5385190 | ||||||
| chr17:5385334 | C | T | 1 | a0001c0003t0016 | 1 | NA18948.hp2 | 3_prime_UTR_variant | MODIFIER | c.*872G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 17/17 | 872 | chr17 | 5385334 | ||||||
| chr17:5385440 | A | G | 23 | a0001c0002t0001 a0001c0002t0005 a0001c0002t0007 others(20): Show |
181 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(178): Show |
3_prime_UTR_variant | MODIFIER | c.*766T>C | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 17/17 | 766 | chr17 | 5385440 | ||||||
| chr17:5385449 | CA | C | 20 | a0001c0002t0001 a0001c0002t0005 a0001c0002t0007 others(17): Show |
173 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(170): Show |
3_prime_UTR_variant | MODIFIER | c.*756delT | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 17/17 | 756 | chr17 | 5385449 | ||||||
| chr17:5385458 | C | G | 1 | a0001c0002t0009 | 3 | HG02280.hp2 HG02451.hp2 HG02970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*748G>C | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 17/17 | 748 | chr17 | 5385458 | ||||||
| chr17:5385474 | G | C | 20 | a0001c0002t0001 a0001c0002t0005 a0001c0002t0007 others(17): Show |
173 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(170): Show |
3_prime_UTR_variant | MODIFIER | c.*732C>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 17/17 | 732 | chr17 | 5385474 | ||||||
| chr17:5385488 | T | C | 1 | a0003c0006t0010 | 2 | HG01167.hp1 HG01169.hp2 |
3_prime_UTR_variant | MODIFIER | c.*718A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 17/17 | 718 | chr17 | 5385488 | ||||||
| chr17:5385558 | A | G | 1 | a0001c0001t0013 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*648T>C | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 17/17 | 648 | chr17 | 5385558 | ||||||
| chr17:5385663 | T | C | 26 | a0001c0001t0003 a0001c0002t0001 a0001c0002t0004 others(23): Show |
272 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(269): Show |
3_prime_UTR_variant | MODIFIER | c.*543A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 17/17 | 543 | chr17 | 5385663 | ||||||
| chr17:5385699 | G | C | 1 | a0001c0003t0019 | 1 | HG02071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*507C>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 17/17 | 507 | chr17 | 5385699 | ||||||
| chr17:5385708 | G | A | 20 | a0001c0002t0001 a0001c0002t0005 a0001c0002t0007 others(17): Show |
173 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(170): Show |
3_prime_UTR_variant | MODIFIER | c.*498C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 17/17 | 498 | chr17 | 5385708 | ||||||
| chr17:5385903 | ATAAC | A | 21 | a0001c0002t0001 a0001c0002t0004 a0001c0002t0005 others(18): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
3_prime_UTR_variant | MODIFIER | c.*299_*302delGTTA | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 17/17 | 299 | chr17 | 5385903 | ||||||
| chr17:5386029 | C | T | 1 | a0001c0003t0012 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*177G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 17/17 | 177 | chr17 | 5386029 | ||||||
| chr17:5386122 | A | G | 1 | a0001c0002t0011 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*84T>C | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 17/17 | 84 | chr17 | 5386122 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:5386356 | C | T | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.2163-87G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 16/16 | chr17 | 5386356 | |||||||
| chr17:5386393 | G | C | 1 | a0001c0002t0005g0041 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2163-124C>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 16/16 | chr17 | 5386393 | |||||||
| chr17:5386442 | G | A | 1 | a0001c0003t0001g0283 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.2163-173C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 16/16 | chr17 | 5386442 | |||||||
| chr17:5386514 | A | T | 1 | a0001c0001t0003g0234 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2162+194T>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 16/16 | chr17 | 5386514 | |||||||
| chr17:5386545 | CAT | C | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.2162+161_2162+162d others(4): Show |
NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 16/16 | chr17 | 5386545 | |||||||
| chr17:5386568 | T | A | 1 | a0001c0001t0003g0234 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2162+140A>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 16/16 | chr17 | 5386568 | |||||||
| chr17:5386642 | T | A | 1 | a0001c0001t0003g0265 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.2162+66A>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 16/16 | chr17 | 5386642 | |||||||
| chr17:5386679 | A | G | 3 | a0001c0001t0002g0011 a0001c0001t0002g0022 a0001c0001t0002g0213 |
6 | HG01109.hp2 HG02258.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.2162+29T>C | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 16/16 | chr17 | 5386679 | |||||||
| chr17:5387279 | G | A | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1916+107C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 14/16 | chr17 | 5387279 | |||||||
| chr17:5387336 | A | G | 1 | a0001c0002t0005g0123 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1916+50T>C | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 14/16 | chr17 | 5387336 | |||||||
| chr17:5387338 | C | T | 2 | a0001c0001t0002g0210 a0001c0002t0007g0116 |
2 | HG00280.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.1916+48G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 14/16 | chr17 | 5387338 | |||||||
| chr17:5387350 | C | T | 3 | a0001c0003t0001g0016 a0001c0003t0001g0042 a0001c0003t0001g0072 |
4 | HG02027.hp1 NA18956.hp1 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.1916+36G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 14/16 | chr17 | 5387350 | |||||||
| chr17:5387361 | A | C | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1916+25T>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 14/16 | chr17 | 5387361 | |||||||
| chr17:5387372 | T | C | 7 | a0001c0004t0006g0187 a0001c0004t0006g0188 a0001c0004t0006g0189 others(4): Show |
8 | HG01167.hp1 HG01169.hp2 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.1916+14A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 14/16 | chr17 | 5387372 | |||||||
| chr17:5387383 | G | A | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
splice_region_variant&intron_variant | LOW | c.1916+3C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 14/16 | chr17 | 5387383 | |||||||
| chr17:5387504 | C | A | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1836-38G>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 13/16 | chr17 | 5387504 | |||||||
| chr17:5387537 | C | T | 1 | a0001c0001t0003g0227 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1835+68G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 13/16 | chr17 | 5387537 | |||||||
| chr17:5387750 | C | T | 1 | a0001c0001t0002g0240 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1769+29G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 12/16 | chr17 | 5387750 | |||||||
| chr17:5387940 | C | T | 1 | a0001c0001t0002g0027 | 2 | HG02559.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1644-36G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 11/16 | chr17 | 5387940 | |||||||
| chr17:5387956 | AAAAT | A | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1644-56_1644-53del others(4): Show |
NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 11/16 | chr17 | 5387956 | |||||||
| chr17:5387964 | T | C | 2 | a0001c0004t0006g0285 a0001c0009t0006g0186 |
2 | HG01243.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1644-60A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 11/16 | chr17 | 5387964 | |||||||
| chr17:5388057 | T | A | 180 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(177): Show |
225 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.1644-153A>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 11/16 | chr17 | 5388057 | |||||||
| chr17:5388234 | T | C | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1644-330A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 11/16 | chr17 | 5388234 | |||||||
| chr17:5388268 | T | C | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1644-364A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 11/16 | chr17 | 5388268 | |||||||
| chr17:5388281 | G | A | 1 | a0001c0002t0004g0136 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1644-377C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 11/16 | chr17 | 5388281 | |||||||
| chr17:5388319 | A | ACT | 180 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(177): Show |
225 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.1644-417_1644-416d others(4): Show |
NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 11/16 | chr17 | 5388319 | |||||||
| chr17:5388325 | G | A | 1 | a0001c0002t0004g0137 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1644-421C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 11/16 | chr17 | 5388325 | |||||||
| chr17:5388390 | G | A | 180 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(177): Show |
225 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.1643+412C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 11/16 | chr17 | 5388390 | |||||||
| chr17:5388452 | A | AT | 109 | a0001c0001t0002g0270 a0001c0002t0001g0103 a0001c0002t0001g0104 others(106): Show |
137 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.1643+349dupA | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 11/16 | chr17 | 5388452 | |||||||
| chr17:5388524 | G | A | 2 | a0001c0004t0006g0285 a0001c0009t0006g0186 |
2 | HG01243.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1643+278C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 11/16 | chr17 | 5388524 | |||||||
| chr17:5388532 | C | T | 1 | a0001c0001t0002g0263 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1643+270G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 11/16 | chr17 | 5388532 | |||||||
| chr17:5388542 | T | C | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1643+260A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 11/16 | chr17 | 5388542 | |||||||
| chr17:5388577 | C | T | 1 | a0001c0002t0005g0054 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1643+225G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 11/16 | chr17 | 5388577 | |||||||
| chr17:5388713 | T | A | 1 | a0001c0002t0007g0116 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1643+89A>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 11/16 | chr17 | 5388713 | |||||||
| chr17:5388728 | C | T | 2 | a0001c0001t0002g0258 a0001c0001t0002g0272 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1643+74G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 11/16 | chr17 | 5388728 | |||||||
| chr17:5388735 | G | A | 4 | a0001c0004t0006g0187 a0001c0004t0006g0188 a0001c0004t0006g0189 others(1): Show |
4 | HG02886.hp2 HG02922.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1643+67C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 11/16 | chr17 | 5388735 | |||||||
| chr17:5388735 | G | T | 1 | a0001c0011t0003g0200 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1643+67C>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 11/16 | chr17 | 5388735 | |||||||
| chr17:5388777 | A | C | 5 | a0001c0001t0002g0033 a0001c0001t0003g0279 a0001c0001t0003g0280 others(2): Show |
5 | HG02257.hp1 HG02897.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1643+25T>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 11/16 | chr17 | 5388777 | |||||||
| chr17:5389127 | C | T | 1 | a0001c0002t0001g0110 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1485-167G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 10/16 | chr17 | 5389127 | |||||||
| chr17:5389362 | T | C | 1 | a0001c0003t0001g0283 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1485-402A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 10/16 | chr17 | 5389362 | |||||||
| chr17:5389442 | C | T | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1485-482G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 10/16 | chr17 | 5389442 | |||||||
| chr17:5389544 | G | A | 3 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 |
3 | HG02257.hp1 HG02976.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1485-584C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 10/16 | chr17 | 5389544 | |||||||
| chr17:5389635 | G | A | 2 | a0001c0001t0002g0224 a0001c0001t0002g0225 |
2 | HG01167.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.1485-675C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 10/16 | chr17 | 5389635 | |||||||
| chr17:5389760 | A | C | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1485-800T>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 10/16 | chr17 | 5389760 | |||||||
| chr17:5389775 | C | CA | 70 | a0001c0001t0002g0033 a0001c0001t0003g0026 a0001c0001t0003g0199 others(67): Show |
87 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.1485-816dupT | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 10/16 | chr17 | 5389775 | |||||||
| chr17:5389775 | C | CAA | 26 | a0001c0002t0001g0108 a0001c0002t0001g0109 a0001c0002t0001g0110 others(23): Show |
26 | HG00642.hp1 HG01123.hp1 HG01934.hp2 others(23): Show |
intron_variant | MODIFIER | c.1485-817_1485-816d others(4): Show |
NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 10/16 | chr17 | 5389775 | |||||||
| chr17:5389775 | C | CAAA | 80 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(77): Show |
108 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.1485-818_1485-816d others(5): Show |
NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 10/16 | chr17 | 5389775 | |||||||
| chr17:5389775 | C | CAAAA | 6 | a0001c0002t0009g0191 a0001c0002t0009g0192 a0001c0002t0009g0193 others(3): Show |
6 | HG02074.hp1 HG02280.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1485-819_1485-816d others(6): Show |
NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 10/16 | chr17 | 5389775 | |||||||
| chr17:5389775 | CAA | C | 6 | a0001c0004t0006g0187 a0001c0004t0006g0188 a0001c0004t0006g0189 others(3): Show |
7 | HG01167.hp1 HG01169.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1485-817_1485-816d others(4): Show |
NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 10/16 | chr17 | 5389775 | |||||||
| chr17:5389888 | T | C | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1485-928A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 10/16 | chr17 | 5389888 | |||||||
| chr17:5389893 | C | T | 4 | a0001c0004t0006g0187 a0001c0004t0006g0188 a0001c0004t0006g0189 others(1): Show |
4 | HG02886.hp2 HG02922.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1485-933G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 10/16 | chr17 | 5389893 | |||||||
| chr17:5389932 | G | A | 1 | a0001c0003t0001g0091 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1485-972C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 10/16 | chr17 | 5389932 | |||||||
| chr17:5390120 | G | A | 2 | a0001c0004t0006g0285 a0001c0009t0006g0186 |
2 | HG01243.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1485-1160C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 10/16 | chr17 | 5390120 | |||||||
| chr17:5390128 | G | A | 1 | a0001c0003t0001g0093 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1485-1168C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 10/16 | chr17 | 5390128 | |||||||
| chr17:5390143 | C | T | 2 | a0001c0002t0001g0182 a0001c0002t0001g0183 |
2 | HG03098.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1485-1183G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 10/16 | chr17 | 5390143 | |||||||
| chr17:5390163 | C | CA | 15 | a0001c0001t0002g0037 a0001c0001t0002g0202 a0001c0001t0002g0206 others(12): Show |
15 | HG00738.hp1 HG01081.hp2 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.1485-1204dupT | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 10/16 | chr17 | 5390163 | |||||||
| chr17:5390163 | C | CAA | 69 | a0001c0001t0003g0279 a0001c0001t0003g0280 a0001c0001t0003g0282 others(66): Show |
97 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.1485-1205_1485-120 others(6): Show |
NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 10/16 | chr17 | 5390163 | |||||||
| chr17:5390163 | CA | C | 28 | a0001c0001t0002g0210 a0001c0001t0002g0225 a0001c0001t0002g0276 others(25): Show |
40 | HG00621.hp1 HG00642.hp2 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.1485-1204delT | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 10/16 | chr17 | 5390163 | |||||||
| chr17:5390181 | A | AAAAAT | 7 | a0001c0002t0008g0157 a0001c0002t0008g0161 a0001c0002t0008g0162 others(4): Show |
7 | HG02451.hp2 HG02615.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1485-1222_1485-122 others(9): Show |
NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 10/16 | chr17 | 5390181 | |||||||
| chr17:5390181 | A | AAAAT | 9 | a0001c0002t0001g0105 a0001c0002t0004g0036 a0001c0002t0004g0141 others(6): Show |
9 | HG00280.hp2 HG00741.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1485-1222_1485-122 others(8): Show |
NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 10/16 | chr17 | 5390181 | |||||||
| chr17:5390181 | A | AAAT | 75 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0106 others(72): Show |
91 | HG00438.hp2 HG00544.hp2 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.1485-1222_1485-122 others(7): Show |
NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 10/16 | chr17 | 5390181 | |||||||
| chr17:5390181 | AT | A | 3 | a0001c0001t0002g0198 a0001c0001t0002g0258 a0001c0001t0002g0272 |
3 | HG03490.hp2 HG03492.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.1485-1222delA | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 10/16 | chr17 | 5390181 | |||||||
| chr17:5390182 | T | A | 1 | a0001c0003t0001g0078 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1485-1222A>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 10/16 | chr17 | 5390182 | |||||||
| chr17:5390307 | T | G | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1484+1254A>C | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 10/16 | chr17 | 5390307 | |||||||
| chr17:5390561 | C | T | 7 | a0001c0004t0006g0187 a0001c0004t0006g0188 a0001c0004t0006g0189 others(4): Show |
8 | HG01167.hp1 HG01169.hp2 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.1484+1000G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 10/16 | chr17 | 5390561 | |||||||
| chr17:5390634 | A | G | 1 | a0001c0001t0002g0209 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1484+927T>C | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 10/16 | chr17 | 5390634 | |||||||
| chr17:5390642 | T | C | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1484+919A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 10/16 | chr17 | 5390642 | |||||||
| chr17:5390706 | GT | G | 177 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(174): Show |
222 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.1484+854delA | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 10/16 | chr17 | 5390706 | |||||||
| chr17:5390726 | C | G | 1 | a0001c0001t0003g0231 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1484+835G>C | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 10/16 | chr17 | 5390726 | |||||||
| chr17:5390753 | T | G | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1484+808A>C | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 10/16 | chr17 | 5390753 | |||||||
| chr17:5390857 | G | A | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1484+704C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 10/16 | chr17 | 5390857 | |||||||
| chr17:5391130 | C | T | 109 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(106): Show |
137 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.1484+431G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 10/16 | chr17 | 5391130 | |||||||
| chr17:5391213 | G | A | 2 | a0001c0002t0004g0150 a0001c0002t0004g0151 |
2 | HG00438.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.1484+348C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 10/16 | chr17 | 5391213 | |||||||
| chr17:5391354 | T | G | 1 | a0003c0006t0010g0014 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1484+207A>C | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 10/16 | chr17 | 5391354 | |||||||
| chr17:5391375 | T | C | 2 | a0001c0002t0004g0147 a0001c0002t0004g0148 |
2 | HG03017.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.1484+186A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 10/16 | chr17 | 5391375 | |||||||
| chr17:5391467 | T | G | 7 | a0001c0002t0001g0169 a0001c0002t0001g0170 a0001c0002t0001g0171 others(4): Show |
7 | HG00642.hp1 HG01123.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1484+94A>C | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 10/16 | chr17 | 5391467 | |||||||
| chr17:5391670 | AAC | A | 4 | a0001c0001t0003g0279 a0001c0001t0003g0280 a0001c0001t0003g0281 others(1): Show |
4 | HG02257.hp1 HG02976.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1383-10_1383-9delG others(1): Show |
NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 9/16 | chr17 | 5391670 | |||||||
| chr17:5391678 | C | T | 1 | a0001c0001t0002g0033 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1383-16G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 9/16 | chr17 | 5391678 | |||||||
| chr17:5391681 | A | G | 82 | a0001c0002t0001g0108 a0001c0002t0001g0109 a0001c0002t0001g0110 others(79): Show |
110 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.1383-19T>C | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 9/16 | chr17 | 5391681 | |||||||
| chr17:5391887 | G | A | 1 | a0001c0001t0002g0248 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1383-225C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 9/16 | chr17 | 5391887 | |||||||
| chr17:5391923 | A | T | 1 | a0001c0001t0002g0208 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1383-261T>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 9/16 | chr17 | 5391923 | |||||||
| chr17:5391929 | G | GATCT | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1383-271_1383-268d others(6): Show |
NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 9/16 | chr17 | 5391929 | |||||||
| chr17:5391982 | G | GT | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1383-321_1383-320i others(3): Show |
NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 9/16 | chr17 | 5391982 | |||||||
| chr17:5392009 | T | C | 2 | a0001c0003t0001g0177 a0001c0003t0001g0179 |
2 | HG01081.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.1383-347A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 9/16 | chr17 | 5392009 | |||||||
| chr17:5392034 | C | A | 2 | a0001c0002t0004g0143 a0001c0002t0004g0145 |
2 | HG02602.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.1383-372G>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 9/16 | chr17 | 5392034 | |||||||
| chr17:5392037 | T | C | 6 | a0001c0002t0001g0169 a0001c0002t0001g0170 a0001c0002t0001g0171 others(3): Show |
6 | HG00642.hp1 HG01123.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1383-375A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 9/16 | chr17 | 5392037 | |||||||
| chr17:5392051 | T | C | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1383-389A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 9/16 | chr17 | 5392051 | |||||||
| chr17:5392052 | G | A | 1 | a0001c0003t0001g0066 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1383-390C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 9/16 | chr17 | 5392052 | |||||||
| chr17:5392079 | C | T | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1383-417G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 9/16 | chr17 | 5392079 | |||||||
| chr17:5392181 | G | C | 2 | a0001c0002t0001g0108 a0001c0002t0001g0110 |
2 | HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1383-519C>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 9/16 | chr17 | 5392181 | |||||||
| chr17:5392182 | C | T | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1383-520G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 9/16 | chr17 | 5392182 | |||||||
| chr17:5392208 | T | C | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1383-546A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 9/16 | chr17 | 5392208 | |||||||
| chr17:5392236 | G | T | 1 | a0001c0001t0003g0026 | 2 | HG01884.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1383-574C>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 9/16 | chr17 | 5392236 | |||||||
| chr17:5392560 | G | A | 2 | a0001c0007t0007g0194 a0001c0007t0007g0195 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1383-898C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 9/16 | chr17 | 5392560 | |||||||
| chr17:5392633 | C | A | 63 | a0001c0002t0004g0004 a0001c0002t0004g0006 a0001c0002t0004g0010 others(60): Show |
79 | HG00438.hp2 HG00544.hp2 HG00609.hp2 others(76): Show |
intron_variant | MODIFIER | c.1383-971G>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 9/16 | chr17 | 5392633 | |||||||
| chr17:5392739 | C | T | 215 | a0001c0001t0002g0033 a0001c0001t0002g0210 a0001c0001t0003g0005 others(212): Show |
271 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.1383-1077G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 9/16 | chr17 | 5392739 | |||||||
| chr17:5393040 | C | T | 1 | a0001c0002t0004g0156 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1383-1378G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 9/16 | chr17 | 5393040 | |||||||
| chr17:5393119 | AT | A | 180 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(177): Show |
225 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.1383-1458delA | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 9/16 | chr17 | 5393119 | |||||||
| chr17:5393141 | G | C | 1 | a0001c0001t0002g0249 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1383-1479C>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 9/16 | chr17 | 5393141 | |||||||
| chr17:5393230 | C | T | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1383-1568G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 9/16 | chr17 | 5393230 | |||||||
| chr17:5393259 | C | T | 63 | a0001c0002t0004g0004 a0001c0002t0004g0006 a0001c0002t0004g0010 others(60): Show |
79 | HG00438.hp2 HG00544.hp2 HG00609.hp2 others(76): Show |
intron_variant | MODIFIER | c.1383-1597G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 9/16 | chr17 | 5393259 | |||||||
| chr17:5393263 | C | G | 1 | a0001c0003t0001g0043 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1383-1601G>C | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 9/16 | chr17 | 5393263 | |||||||
| chr17:5393367 | A | T | 2 | a0001c0001t0003g0020 a0001c0011t0003g0200 |
3 | NA19004.hp1 NA19005.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.1382+1524T>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 9/16 | chr17 | 5393367 | |||||||
| chr17:5393399 | A | G | 2 | a0001c0002t0001g0182 a0001c0002t0001g0183 |
2 | HG03098.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1382+1492T>C | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 9/16 | chr17 | 5393399 | |||||||
| chr17:5393435 | C | CT | 13 | a0001c0001t0002g0246 a0001c0002t0004g0135 a0001c0002t0004g0141 others(10): Show |
13 | HG00621.hp2 HG00733.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.1382+1455dupA | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 9/16 | chr17 | 5393435 | |||||||
| chr17:5393435 | CT | C | 14 | a0001c0001t0002g0252 a0001c0002t0001g0103 a0001c0002t0001g0104 others(11): Show |
14 | HG00642.hp1 HG00741.hp1 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.1382+1455delA | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 9/16 | chr17 | 5393435 | |||||||
| chr17:5393435 | CTTT | C | 8 | a0001c0002t0004g0006 a0001c0002t0004g0082 a0001c0002t0004g0154 others(5): Show |
12 | NA18940.hp1 NA18942.hp2 NA18948.hp1 others(9): Show |
intron_variant | MODIFIER | c.1382+1453_1382+145 others(7): Show |
NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 9/16 | chr17 | 5393435 | |||||||
| chr17:5393440 | T | C | 1 | a0001c0003t0001g0100 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1382+1451A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 9/16 | chr17 | 5393440 | |||||||
| chr17:5393476 | A | G | 180 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(177): Show |
225 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.1382+1415T>C | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 9/16 | chr17 | 5393476 | |||||||
| chr17:5393521 | G | C | 64 | a0001c0002t0004g0004 a0001c0002t0004g0006 a0001c0002t0004g0010 others(61): Show |
80 | HG00438.hp2 HG00544.hp2 HG00609.hp2 others(77): Show |
intron_variant | MODIFIER | c.1382+1370C>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 9/16 | chr17 | 5393521 | |||||||
| chr17:5393635 | A | G | 64 | a0001c0002t0004g0004 a0001c0002t0004g0006 a0001c0002t0004g0010 others(61): Show |
80 | HG00438.hp2 HG00544.hp2 HG00609.hp2 others(77): Show |
intron_variant | MODIFIER | c.1382+1256T>C | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 9/16 | chr17 | 5393635 | |||||||
| chr17:5393689 | A | G | 185 | a0001c0001t0002g0033 a0001c0001t0003g0279 a0001c0001t0003g0280 others(182): Show |
230 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.1382+1202T>C | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 9/16 | chr17 | 5393689 | |||||||
| chr17:5393718 | A | G | 110 | a0001c0001t0003g0275 a0001c0002t0001g0103 a0001c0002t0001g0104 others(107): Show |
138 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.1382+1173T>C | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 9/16 | chr17 | 5393718 | |||||||
| chr17:5393829 | T | C | 178 | a0001c0001t0002g0202 a0001c0001t0002g0208 a0001c0001t0002g0217 others(175): Show |
222 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.1382+1062A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 9/16 | chr17 | 5393829 | |||||||
| chr17:5393914 | T | C | 1 | a0003c0006t0010g0014 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1382+977A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 9/16 | chr17 | 5393914 | |||||||
| chr17:5394018 | G | T | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1382+873C>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 9/16 | chr17 | 5394018 | |||||||
| chr17:5394030 | A | G | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1382+861T>C | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 9/16 | chr17 | 5394030 | |||||||
| chr17:5394118 | G | A | 1 | a0001c0002t0007g0197 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1382+773C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 9/16 | chr17 | 5394118 | |||||||
| chr17:5394137 | T | C | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1382+754A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 9/16 | chr17 | 5394137 | |||||||
| chr17:5394152 | C | T | 1 | a0001c0002t0005g0117 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1382+739G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 9/16 | chr17 | 5394152 | |||||||
| chr17:5394193 | C | T | 1 | a0001c0001t0003g0229 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1382+698G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 9/16 | chr17 | 5394193 | |||||||
| chr17:5394231 | A | G | 172 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(169): Show |
216 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.1382+660T>C | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 9/16 | chr17 | 5394231 | |||||||
| chr17:5394243 | G | T | 1 | a0001c0001t0002g0033 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1382+648C>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 9/16 | chr17 | 5394243 | |||||||
| chr17:5394258 | A | G | 2 | a0001c0004t0006g0285 a0001c0009t0006g0186 |
2 | HG01243.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1382+633T>C | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 9/16 | chr17 | 5394258 | |||||||
| chr17:5394412 | C | A | 4 | a0001c0001t0003g0279 a0001c0001t0003g0280 a0001c0001t0003g0281 others(1): Show |
4 | HG02257.hp1 HG02976.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1382+479G>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 9/16 | chr17 | 5394412 | |||||||
| chr17:5394422 | C | T | 174 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(171): Show |
218 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.1382+469G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 9/16 | chr17 | 5394422 | |||||||
| chr17:5394441 | A | G | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1382+450T>C | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 9/16 | chr17 | 5394441 | |||||||
| chr17:5394446 | C | G | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1382+445G>C | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 9/16 | chr17 | 5394446 | |||||||
| chr17:5394470 | T | C | 7 | a0001c0004t0006g0187 a0001c0004t0006g0188 a0001c0004t0006g0189 others(4): Show |
8 | HG01167.hp1 HG01169.hp2 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.1382+421A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 9/16 | chr17 | 5394470 | |||||||
| chr17:5394477 | C | T | 7 | a0001c0004t0006g0187 a0001c0004t0006g0188 a0001c0004t0006g0189 others(4): Show |
8 | HG01167.hp1 HG01169.hp2 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.1382+414G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 9/16 | chr17 | 5394477 | |||||||
| chr17:5394519 | T | G | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1382+372A>C | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 9/16 | chr17 | 5394519 | |||||||
| chr17:5394609 | G | A | 1 | a0001c0002t0005g0126 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1382+282C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 9/16 | chr17 | 5394609 | |||||||
| chr17:5394652 | C | A | 4 | a0001c0001t0002g0031 a0001c0001t0002g0277 a0001c0001t0002g0278 others(1): Show |
5 | HG02647.hp2 HG02818.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1382+239G>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 9/16 | chr17 | 5394652 | |||||||
| chr17:5394676 | A | C | 6 | a0001c0001t0002g0256 a0001c0001t0002g0257 a0001c0001t0002g0258 others(3): Show |
6 | HG00140.hp2 HG00741.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.1382+215T>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 9/16 | chr17 | 5394676 | |||||||
| chr17:5394768 | G | A | 1 | a0001c0003t0001g0046 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1382+123C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 9/16 | chr17 | 5394768 | |||||||
| chr17:5394866 | T | C | 1 | a0001c0001t0003g0267 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1382+25A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 9/16 | chr17 | 5394866 | |||||||
| chr17:5395000 | C | T | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1292-19G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5395000 | |||||||
| chr17:5395076 | G | A | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1292-95C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5395076 | |||||||
| chr17:5395170 | T | C | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1292-189A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5395170 | |||||||
| chr17:5395321 | C | T | 14 | a0001c0002t0007g0116 a0001c0002t0007g0196 a0001c0002t0007g0197 others(11): Show |
14 | HG00280.hp2 HG01884.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.1292-340G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5395321 | |||||||
| chr17:5395324 | AT | A | 214 | a0001c0001t0002g0033 a0001c0001t0002g0210 a0001c0001t0003g0005 others(211): Show |
270 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.1292-344delA | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5395324 | |||||||
| chr17:5395398 | C | G | 4 | a0001c0001t0002g0031 a0001c0001t0002g0277 a0001c0001t0002g0278 others(1): Show |
5 | HG02647.hp2 HG02818.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1292-417G>C | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5395398 | |||||||
| chr17:5395425 | G | A | 1 | a0001c0003t0001g0086 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1292-444C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5395425 | |||||||
| chr17:5395472 | T | C | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1292-491A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5395472 | |||||||
| chr17:5395475 | A | G | 1 | a0001c0003t0001g0078 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1292-494T>C | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5395475 | |||||||
| chr17:5395525 | T | G | 7 | a0001c0002t0001g0108 a0001c0002t0001g0109 a0001c0002t0001g0110 others(4): Show |
7 | HG02257.hp2 HG02451.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1292-544A>C | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5395525 | |||||||
| chr17:5395534 | C | CT | 167 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(164): Show |
211 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.1292-554dupA | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5395534 | |||||||
| chr17:5395534 | C | CTT | 6 | a0001c0002t0004g0154 a0001c0002t0005g0054 a0001c0002t0007g0196 others(3): Show |
6 | HG01884.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1292-555_1292-554d others(4): Show |
NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5395534 | |||||||
| chr17:5395538 | A | T | 180 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(177): Show |
225 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.1292-557T>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5395538 | |||||||
| chr17:5395604 | A | G | 1 | a0001c0001t0002g0208 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1292-623T>C | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5395604 | |||||||
| chr17:5395614 | C | T | 4 | a0001c0001t0002g0031 a0001c0001t0002g0277 a0001c0001t0002g0278 others(1): Show |
5 | HG02647.hp2 HG02818.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1292-633G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5395614 | |||||||
| chr17:5395685 | C | A | 1 | a0001c0003t0001g0283 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1292-704G>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5395685 | |||||||
| chr17:5395738 | G | A | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1292-757C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5395738 | |||||||
| chr17:5395773 | C | T | 1 | a0001c0003t0001g0068 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1292-792G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5395773 | |||||||
| chr17:5395993 | C | A | 1 | a0001c0003t0001g0095 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1292-1012G>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5395993 | |||||||
| chr17:5396028 | T | C | 1 | a0001c0001t0002g0033 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1292-1047A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5396028 | |||||||
| chr17:5396036 | C | T | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1292-1055G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5396036 | |||||||
| chr17:5396039 | C | T | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1292-1058G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5396039 | |||||||
| chr17:5396063 | T | C | 2 | a0001c0007t0007g0194 a0001c0007t0007g0195 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1292-1082A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5396063 | |||||||
| chr17:5396125 | C | T | 63 | a0001c0002t0004g0004 a0001c0002t0004g0006 a0001c0002t0004g0010 others(60): Show |
79 | HG00438.hp2 HG00544.hp2 HG00609.hp2 others(76): Show |
intron_variant | MODIFIER | c.1292-1144G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5396125 | |||||||
| chr17:5396207 | G | A | 175 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(172): Show |
219 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.1292-1226C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5396207 | |||||||
| chr17:5396354 | C | G | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1292-1373G>C | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5396354 | |||||||
| chr17:5396392 | C | T | 1 | a0001c0009t0006g0186 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1292-1411G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5396392 | |||||||
| chr17:5396471 | C | A | 1 | a0001c0002t0017g0051 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1292-1490G>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5396471 | |||||||
| chr17:5396620 | C | T | 1 | a0001c0001t0002g0033 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1292-1639G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5396620 | |||||||
| chr17:5396630 | T | C | 109 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(106): Show |
137 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.1292-1649A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5396630 | |||||||
| chr17:5396767 | T | A | 2 | a0001c0001t0003g0234 a0001c0001t0003g0236 |
2 | NA18987.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.1292-1786A>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5396767 | |||||||
| chr17:5396863 | T | C | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1292-1882A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5396863 | |||||||
| chr17:5396885 | A | G | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1292-1904T>C | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5396885 | |||||||
| chr17:5396942 | G | A | 3 | a0001c0002t0009g0191 a0001c0002t0009g0192 a0001c0002t0009g0193 |
3 | HG02280.hp2 HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1292-1961C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5396942 | |||||||
| chr17:5397163 | A | G | 1 | a0001c0004t0006g0188 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1292-2182T>C | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5397163 | |||||||
| chr17:5397180 | A | G | 4 | a0001c0004t0006g0187 a0001c0004t0006g0188 a0001c0004t0006g0189 others(1): Show |
4 | HG02886.hp2 HG02922.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1292-2199T>C | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5397180 | |||||||
| chr17:5397350 | AT | A | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1291+2201delA | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5397350 | |||||||
| chr17:5397370 | G | A | 5 | a0001c0001t0002g0033 a0001c0001t0003g0279 a0001c0001t0003g0280 others(2): Show |
5 | HG02257.hp1 HG02897.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1291+2182C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5397370 | |||||||
| chr17:5397516 | T | C | 1 | a0003c0006t0010g0014 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1291+2036A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5397516 | |||||||
| chr17:5397523 | G | C | 3 | a0001c0001t0003g0273 a0001c0001t0003g0274 a0001c0001t0003g0275 |
3 | HG02145.hp2 HG02896.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1291+2029C>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5397523 | |||||||
| chr17:5397635 | A | G | 1 | a0001c0003t0001g0180 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1291+1917T>C | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5397635 | |||||||
| chr17:5397646 | A | T | 1 | a0001c0001t0002g0243 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1291+1906T>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5397646 | |||||||
| chr17:5397651 | G | T | 1 | a0001c0001t0002g0243 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1291+1901C>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5397651 | |||||||
| chr17:5397680 | G | A | 5 | a0001c0003t0001g0074 a0001c0003t0001g0081 a0001c0003t0001g0085 others(2): Show |
5 | HG01346.hp1 HG02080.hp2 HG03710.hp1 others(2): Show |
intron_variant | MODIFIER | c.1291+1872C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5397680 | |||||||
| chr17:5397722 | CTT | C | 42 | a0001c0002t0004g0004 a0001c0002t0004g0006 a0001c0002t0004g0010 others(39): Show |
55 | HG00438.hp2 HG00609.hp2 HG01071.hp2 others(52): Show |
intron_variant | MODIFIER | c.1291+1828_1291+182 others(6): Show |
NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5397722 | |||||||
| chr17:5397750 | C | G | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1291+1802G>C | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5397750 | |||||||
| chr17:5397844 | A | AT | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1291+1707dupA | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5397844 | |||||||
| chr17:5397954 | G | C | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1291+1598C>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5397954 | |||||||
| chr17:5397977 | GA | G | 184 | a0001c0001t0003g0279 a0001c0001t0003g0280 a0001c0001t0003g0281 others(181): Show |
229 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.1291+1574delT | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5397977 | |||||||
| chr17:5398042 | G | T | 4 | a0001c0003t0001g0015 a0001c0003t0001g0045 a0001c0003t0001g0046 others(1): Show |
5 | HG01192.hp1 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1291+1510C>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5398042 | |||||||
| chr17:5398136 | G | C | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1291+1416C>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5398136 | |||||||
| chr17:5398145 | TCAAGTG | T | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1291+1401_1291+140 others(10): Show |
NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5398145 | |||||||
| chr17:5398153 | C | T | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1291+1399G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5398153 | |||||||
| chr17:5398211 | T | C | 1 | a0001c0003t0001g0088 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1291+1341A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5398211 | |||||||
| chr17:5398374 | C | T | 1 | a0001c0009t0006g0186 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1291+1178G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5398374 | |||||||
| chr17:5398375 | G | A | 1 | a0001c0002t0004g0152 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1291+1177C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5398375 | |||||||
| chr17:5398391 | C | T | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1291+1161G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5398391 | |||||||
| chr17:5398434 | G | A | 1 | a0001c0003t0001g0180 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1291+1118C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5398434 | |||||||
| chr17:5398486 | G | A | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1291+1066C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5398486 | |||||||
| chr17:5398498 | A | G | 1 | a0001c0001t0002g0218 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1291+1054T>C | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5398498 | |||||||
| chr17:5398504 | T | A | 3 | a0001c0001t0003g0273 a0001c0001t0003g0274 a0001c0001t0003g0275 |
3 | HG02145.hp2 HG02896.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1291+1048A>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5398504 | |||||||
| chr17:5398608 | T | C | 171 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(168): Show |
215 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.1291+944A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5398608 | |||||||
| chr17:5398692 | G | A | 1 | a0001c0001t0002g0033 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1291+860C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5398692 | |||||||
| chr17:5398819 | T | C | 1 | a0001c0001t0003g0274 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1291+733A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5398819 | |||||||
| chr17:5398860 | G | C | 1 | a0001c0003t0001g0084 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1291+692C>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5398860 | |||||||
| chr17:5398863 | T | C | 1 | a0001c0003t0001g0084 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1291+689A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5398863 | |||||||
| chr17:5398866 | A | C | 1 | a0001c0003t0001g0084 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1291+686T>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5398866 | |||||||
| chr17:5398871 | A | G | 1 | a0001c0003t0001g0084 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1291+681T>C | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5398871 | |||||||
| chr17:5398880 | T | C | 172 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(169): Show |
216 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.1291+672A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5398880 | |||||||
| chr17:5398883 | A | G | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1291+669T>C | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5398883 | |||||||
| chr17:5398890 | C | CT | 104 | a0001c0001t0002g0246 a0001c0001t0002g0256 a0001c0001t0003g0203 others(101): Show |
132 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.1291+661dupA | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5398890 | |||||||
| chr17:5398890 | C | CTT | 14 | a0001c0002t0001g0182 a0001c0002t0007g0116 a0001c0002t0007g0196 others(11): Show |
14 | HG00280.hp2 HG00558.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.1291+660_1291+661d others(4): Show |
NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5398890 | |||||||
| chr17:5398907 | G | C | 1 | a0001c0002t0004g0152 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1291+645C>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5398907 | |||||||
| chr17:5398912 | G | A | 2 | a0001c0004t0006g0285 a0001c0009t0006g0186 |
2 | HG01243.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1291+640C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5398912 | |||||||
| chr17:5399008 | T | C | 2 | a0001c0002t0001g0111 a0001c0002t0001g0112 |
2 | HG02257.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.1291+544A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5399008 | |||||||
| chr17:5399050 | G | A | 1 | a0001c0001t0002g0260 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1291+502C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5399050 | |||||||
| chr17:5399093 | A | G | 1 | a0001c0003t0001g0085 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1291+459T>C | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5399093 | |||||||
| chr17:5399128 | T | C | 2 | a0001c0001t0002g0223 a0001c0001t0002g0244 |
2 | HG01074.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.1291+424A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5399128 | |||||||
| chr17:5399134 | A | G | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1291+418T>C | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5399134 | |||||||
| chr17:5399171 | G | A | 5 | a0001c0001t0002g0033 a0001c0001t0003g0279 a0001c0001t0003g0280 others(2): Show |
5 | HG02257.hp1 HG02897.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1291+381C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5399171 | |||||||
| chr17:5399187 | G | A | 2 | a0001c0001t0003g0023 a0001c0001t0003g0214 |
3 | HG01891.hp1 HG03139.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1291+365C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5399187 | |||||||
| chr17:5399190 | CT | C | 15 | a0001c0001t0002g0033 a0001c0001t0002g0209 a0001c0001t0002g0272 others(12): Show |
17 | HG00673.hp1 HG01167.hp1 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.1291+361delA | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5399190 | |||||||
| chr17:5399190 | CTT | C | 62 | a0001c0002t0004g0004 a0001c0002t0004g0006 a0001c0002t0004g0010 others(59): Show |
77 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.1291+360_1291+361d others(4): Show |
NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5399190 | |||||||
| chr17:5399190 | CTTT | C | 113 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(110): Show |
142 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.1291+359_1291+361d others(5): Show |
NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5399190 | |||||||
| chr17:5399231 | C | T | 4 | a0001c0004t0006g0187 a0001c0004t0006g0188 a0001c0004t0006g0189 others(1): Show |
4 | HG02886.hp2 HG02922.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1291+321G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5399231 | |||||||
| chr17:5399252 | G | GT | 110 | a0001c0001t0002g0001 a0001c0001t0002g0011 a0001c0001t0002g0013 others(107): Show |
149 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.1291+299dupA | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5399252 | |||||||
| chr17:5399252 | GT | G | 80 | a0001c0002t0001g0108 a0001c0002t0001g0109 a0001c0002t0001g0110 others(77): Show |
108 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.1291+299delA | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5399252 | |||||||
| chr17:5399325 | T | C | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1291+227A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5399325 | |||||||
| chr17:5399458 | T | C | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1291+94A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 8/16 | chr17 | 5399458 | |||||||
| chr17:5399743 | A | G | 1 | a0001c0002t0004g0149 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1193-93T>C | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 7/16 | chr17 | 5399743 | |||||||
| chr17:5399745 | C | T | 1 | a0001c0001t0002g0207 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1193-95G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 7/16 | chr17 | 5399745 | |||||||
| chr17:5399746 | G | A | 6 | a0001c0002t0007g0116 a0001c0002t0007g0196 a0001c0002t0007g0197 others(3): Show |
6 | HG00280.hp2 HG01884.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1193-96C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 7/16 | chr17 | 5399746 | |||||||
| chr17:5399895 | G | A | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1193-245C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 7/16 | chr17 | 5399895 | |||||||
| chr17:5400026 | A | G | 1 | a0001c0001t0003g0026 | 2 | HG01884.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1193-376T>C | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 7/16 | chr17 | 5400026 | |||||||
| chr17:5400053 | A | G | 1 | a0001c0001t0002g0210 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1193-403T>C | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 7/16 | chr17 | 5400053 | |||||||
| chr17:5400066 | G | A | 1 | a0001c0002t0004g0140 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1193-416C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 7/16 | chr17 | 5400066 | |||||||
| chr17:5400070 | C | CAGTG | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1193-421_1193-420i others(6): Show |
NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 7/16 | chr17 | 5400070 | |||||||
| chr17:5400092 | G | C | 2 | a0001c0002t0001g0182 a0001c0002t0001g0183 |
2 | HG03098.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1193-442C>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 7/16 | chr17 | 5400092 | |||||||
| chr17:5400117 | G | A | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1193-467C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 7/16 | chr17 | 5400117 | |||||||
| chr17:5400139 | T | TAAAAAAA others(3): Show |
1 | a0001c0003t0001g0081 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1193-490_1193-489i others(12): Show |
NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 7/16 | chr17 | 5400139 | |||||||
| chr17:5400139 | T | TAAAAAAA others(4): Show |
52 | a0001c0002t0001g0108 a0001c0002t0001g0113 a0001c0002t0001g0115 others(49): Show |
70 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.1193-490_1193-489i others(13): Show |
NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 7/16 | chr17 | 5400139 | |||||||
| chr17:5400139 | T | TAAAAAAA others(5): Show |
78 | a0001c0002t0001g0105 a0001c0002t0001g0109 a0001c0002t0001g0110 others(75): Show |
95 | HG00438.hp2 HG00544.hp2 HG00609.hp1 others(92): Show |
intron_variant | MODIFIER | c.1193-490_1193-489i others(14): Show |
NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 7/16 | chr17 | 5400139 | |||||||
| chr17:5400139 | T | TAAAAAAA others(6): Show |
30 | a0001c0002t0001g0111 a0001c0002t0001g0171 a0001c0002t0001g0172 others(27): Show |
39 | HG00544.hp1 HG00642.hp1 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.1193-490_1193-489i others(15): Show |
NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 7/16 | chr17 | 5400139 | |||||||
| chr17:5400139 | T | TAAAAAAA others(7): Show |
9 | a0001c0002t0001g0104 a0001c0002t0001g0175 a0001c0002t0001g0183 others(6): Show |
9 | HG00438.hp1 HG01891.hp2 HG01975.hp1 others(6): Show |
intron_variant | MODIFIER | c.1193-490_1193-489i others(16): Show |
NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 7/16 | chr17 | 5400139 | |||||||
| chr17:5400139 | T | TAAAAAAA others(8): Show |
1 | a0001c0002t0001g0106 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1193-490_1193-489i others(17): Show |
NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 7/16 | chr17 | 5400139 | |||||||
| chr17:5400139 | T | TAAAAAAA others(10): Show |
1 | a0001c0002t0001g0103 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1193-490_1193-489i others(19): Show |
NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 7/16 | chr17 | 5400139 | |||||||
| chr17:5400140 | T | A | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1193-490A>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 7/16 | chr17 | 5400140 | |||||||
| chr17:5400140 | T | TA | 8 | a0001c0001t0002g0033 a0001c0001t0002g0206 a0001c0001t0002g0217 others(5): Show |
8 | HG01175.hp1 HG01243.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1193-491dupT | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 7/16 | chr17 | 5400140 | |||||||
| chr17:5400140 | TA | T | 9 | a0001c0001t0002g0021 a0001c0001t0003g0023 a0001c0001t0003g0214 others(6): Show |
12 | HG00621.hp1 HG01167.hp1 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.1193-491delT | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 7/16 | chr17 | 5400140 | |||||||
| chr17:5400173 | A | G | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1193-523T>C | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 7/16 | chr17 | 5400173 | |||||||
| chr17:5400352 | T | C | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1193-702A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 7/16 | chr17 | 5400352 | |||||||
| chr17:5400421 | G | A | 1 | a0001c0002t0007g0284 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1193-771C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 7/16 | chr17 | 5400421 | |||||||
| chr17:5400427 | T | C | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1193-777A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 7/16 | chr17 | 5400427 | |||||||
| chr17:5400453 | G | A | 24 | a0001c0001t0003g0005 a0001c0001t0003g0012 a0001c0001t0003g0020 others(21): Show |
34 | HG00621.hp1 HG00642.hp2 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.1193-803C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 7/16 | chr17 | 5400453 | |||||||
| chr17:5400489 | G | A | 1 | a0001c0003t0001g0077 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1193-839C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 7/16 | chr17 | 5400489 | |||||||
| chr17:5400493 | C | CA | 45 | a0001c0001t0002g0013 a0001c0001t0002g0022 a0001c0001t0002g0037 others(42): Show |
51 | HG00099.hp1 HG00621.hp1 HG00733.hp1 others(48): Show |
intron_variant | MODIFIER | c.1193-844dupT | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 7/16 | chr17 | 5400493 | |||||||
| chr17:5400498 | A | AC | 169 | a0001c0002t0001g0105 a0001c0002t0001g0108 a0001c0002t0001g0109 others(166): Show |
213 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.1193-849_1193-848i others(3): Show |
NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 7/16 | chr17 | 5400498 | |||||||
| chr17:5400498 | A | ACAAAAC | 3 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0106 |
3 | HG01433.hp1 HG01952.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.1193-849_1193-848i others(8): Show |
NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 7/16 | chr17 | 5400498 | |||||||
| chr17:5400503 | A | C | 172 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(169): Show |
216 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.1193-853T>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 7/16 | chr17 | 5400503 | |||||||
| chr17:5400508 | A | C | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1193-858T>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 7/16 | chr17 | 5400508 | |||||||
| chr17:5400513 | A | C | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1193-863T>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 7/16 | chr17 | 5400513 | |||||||
| chr17:5400642 | G | A | 2 | a0001c0007t0007g0194 a0001c0007t0007g0195 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1193-992C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 7/16 | chr17 | 5400642 | |||||||
| chr17:5400686 | C | T | 1 | a0001c0001t0003g0199 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1193-1036G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 7/16 | chr17 | 5400686 | |||||||
| chr17:5400922 | T | C | 2 | a0001c0001t0002g0037 a0001c0004t0002g0212 |
2 | HG02572.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1193-1272A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 7/16 | chr17 | 5400922 | |||||||
| chr17:5400990 | A | G | 1 | a0001c0001t0003g0199 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1193-1340T>C | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 7/16 | chr17 | 5400990 | |||||||
| chr17:5401104 | C | A | 1 | a0001c0002t0001g0171 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1193-1454G>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 7/16 | chr17 | 5401104 | |||||||
| chr17:5401121 | C | T | 1 | a0001c0002t0005g0167 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1193-1471G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 7/16 | chr17 | 5401121 | |||||||
| chr17:5401255 | T | C | 180 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(177): Show |
225 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.1193-1605A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 7/16 | chr17 | 5401255 | |||||||
| chr17:5401370 | G | A | 1 | a0005c0008t0001g0032 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1193-1720C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 7/16 | chr17 | 5401370 | |||||||
| chr17:5401391 | AC | A | 172 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(169): Show |
216 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.1193-1742delG | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 7/16 | chr17 | 5401391 | |||||||
| chr17:5401392 | C | A | 1 | a0001c0002t0005g0122 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1193-1742G>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 7/16 | chr17 | 5401392 | |||||||
| chr17:5401407 | T | G | 1 | a0001c0001t0003g0026 | 2 | HG01884.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1193-1757A>C | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 7/16 | chr17 | 5401407 | |||||||
| chr17:5401439 | T | C | 1 | a0001c0001t0002g0033 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1193-1789A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 7/16 | chr17 | 5401439 | |||||||
| chr17:5401443 | T | C | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1193-1793A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 7/16 | chr17 | 5401443 | |||||||
| chr17:5401472 | C | A | 7 | a0001c0004t0006g0187 a0001c0004t0006g0188 a0001c0004t0006g0189 others(4): Show |
8 | HG01167.hp1 HG01169.hp2 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.1193-1822G>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 7/16 | chr17 | 5401472 | |||||||
| chr17:5401601 | A | G | 1 | a0001c0001t0002g0223 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1193-1951T>C | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 7/16 | chr17 | 5401601 | |||||||
| chr17:5401707 | G | C | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1193-2057C>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 7/16 | chr17 | 5401707 | |||||||
| chr17:5401757 | T | C | 1 | a0005c0008t0001g0032 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1193-2107A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 7/16 | chr17 | 5401757 | |||||||
| chr17:5401806 | A | G | 25 | a0001c0001t0002g0210 a0001c0001t0003g0005 a0001c0001t0003g0012 others(22): Show |
35 | HG00621.hp1 HG00642.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.1193-2156T>C | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 7/16 | chr17 | 5401806 | |||||||
| chr17:5402050 | T | C | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1192+2049A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 7/16 | chr17 | 5402050 | |||||||
| chr17:5402094 | A | T | 1 | a0005c0008t0001g0032 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1192+2005T>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 7/16 | chr17 | 5402094 | |||||||
| chr17:5402269 | T | C | 1 | a0001c0003t0001g0098 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1192+1830A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 7/16 | chr17 | 5402269 | |||||||
| chr17:5402307 | CAAA | C | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1192+1789_1192+179 others(7): Show |
NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 7/16 | chr17 | 5402307 | |||||||
| chr17:5402395 | G | C | 1 | a0001c0004t0006g0190 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1192+1704C>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 7/16 | chr17 | 5402395 | |||||||
| chr17:5402567 | C | G | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1192+1532G>C | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 7/16 | chr17 | 5402567 | |||||||
| chr17:5402604 | G | A | 180 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(177): Show |
225 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.1192+1495C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 7/16 | chr17 | 5402604 | |||||||
| chr17:5402701 | T | C | 1 | a0001c0001t0002g0218 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1192+1398A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 7/16 | chr17 | 5402701 | |||||||
| chr17:5402719 | T | C | 1 | a0001c0001t0002g0250 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1192+1380A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 7/16 | chr17 | 5402719 | |||||||
| chr17:5402727 | G | C | 7 | a0001c0002t0001g0169 a0001c0002t0001g0170 a0001c0002t0001g0171 others(4): Show |
7 | HG00642.hp1 HG01123.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1192+1372C>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 7/16 | chr17 | 5402727 | |||||||
| chr17:5403044 | T | A | 1 | a0001c0003t0001g0043 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1192+1055A>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 7/16 | chr17 | 5403044 | |||||||
| chr17:5403061 | C | T | 1 | a0001c0004t0006g0188 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1192+1038G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 7/16 | chr17 | 5403061 | |||||||
| chr17:5403069 | G | A | 1 | a0003c0006t0010g0014 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1192+1030C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 7/16 | chr17 | 5403069 | |||||||
| chr17:5403070 | C | T | 1 | a0005c0008t0001g0032 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1192+1029G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 7/16 | chr17 | 5403070 | |||||||
| chr17:5403144 | G | A | 172 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(169): Show |
216 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.1192+955C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 7/16 | chr17 | 5403144 | |||||||
| chr17:5403149 | G | C | 1 | a0001c0003t0001g0078 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1192+950C>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 7/16 | chr17 | 5403149 | |||||||
| chr17:5403216 | G | T | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1192+883C>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 7/16 | chr17 | 5403216 | |||||||
| chr17:5403351 | C | T | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1192+748G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 7/16 | chr17 | 5403351 | |||||||
| chr17:5403643 | G | C | 3 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 |
3 | HG02257.hp1 HG02976.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1192+456C>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 7/16 | chr17 | 5403643 | |||||||
| chr17:5403658 | T | TCAACAA | 168 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(165): Show |
212 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.1192+435_1192+440d others(8): Show |
NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 7/16 | chr17 | 5403658 | |||||||
| chr17:5403658 | TCAA | T | 8 | a0001c0003t0001g0060 a0001c0003t0001g0061 a0001c0003t0001g0062 others(5): Show |
9 | HG01167.hp1 HG01169.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.1192+438_1192+440d others(5): Show |
NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 7/16 | chr17 | 5403658 | |||||||
| chr17:5403696 | T | G | 1 | a0001c0003t0001g0097 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1192+403A>C | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 7/16 | chr17 | 5403696 | |||||||
| chr17:5403764 | T | C | 215 | a0001c0001t0002g0033 a0001c0001t0002g0210 a0001c0001t0003g0005 others(212): Show |
271 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.1192+335A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 7/16 | chr17 | 5403764 | |||||||
| chr17:5403803 | A | G | 1 | a0001c0001t0003g0228 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1192+296T>C | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 7/16 | chr17 | 5403803 | |||||||
| chr17:5403869 | C | A | 6 | a0001c0002t0007g0116 a0001c0002t0007g0196 a0001c0002t0007g0197 others(3): Show |
6 | HG00280.hp2 HG01884.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1192+230G>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 7/16 | chr17 | 5403869 | |||||||
| chr17:5404324 | G | A | 1 | a0001c0001t0002g0213 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1045-78C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 6/16 | chr17 | 5404324 | |||||||
| chr17:5404399 | G | A | 3 | a0001c0001t0002g0224 a0001c0001t0002g0225 a0001c0002t0005g0041 |
3 | HG01167.hp2 HG01255.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1045-153C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 6/16 | chr17 | 5404399 | |||||||
| chr17:5404411 | G | A | 1 | a0001c0003t0001g0098 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1045-165C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 6/16 | chr17 | 5404411 | |||||||
| chr17:5404432 | C | T | 2 | a0001c0002t0005g0120 a0001c0002t0005g0121 |
2 | HG02809.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1045-186G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 6/16 | chr17 | 5404432 | |||||||
| chr17:5404461 | G | A | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1045-215C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 6/16 | chr17 | 5404461 | |||||||
| chr17:5404477 | G | A | 2 | a0001c0001t0003g0023 a0001c0001t0003g0214 |
3 | HG01891.hp1 HG03139.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1045-231C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 6/16 | chr17 | 5404477 | |||||||
| chr17:5404512 | G | A | 63 | a0001c0002t0004g0004 a0001c0002t0004g0006 a0001c0002t0004g0010 others(60): Show |
79 | HG00438.hp2 HG00544.hp2 HG00609.hp2 others(76): Show |
intron_variant | MODIFIER | c.1045-266C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 6/16 | chr17 | 5404512 | |||||||
| chr17:5404517 | C | T | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1045-271G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 6/16 | chr17 | 5404517 | |||||||
| chr17:5404529 | G | A | 5 | a0001c0001t0002g0033 a0001c0001t0003g0279 a0001c0001t0003g0280 others(2): Show |
5 | HG02257.hp1 HG02897.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1045-283C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 6/16 | chr17 | 5404529 | |||||||
| chr17:5404671 | G | A | 2 | a0001c0007t0007g0194 a0001c0007t0007g0195 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1044+386C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 6/16 | chr17 | 5404671 | |||||||
| chr17:5404734 | G | A | 24 | a0001c0001t0003g0005 a0001c0001t0003g0012 a0001c0001t0003g0020 others(21): Show |
34 | HG00621.hp1 HG00642.hp2 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.1044+323C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 6/16 | chr17 | 5404734 | |||||||
| chr17:5404841 | G | A | 2 | a0001c0001t0002g0218 a0001c0001t0002g0220 |
2 | HG02615.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1044+216C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 6/16 | chr17 | 5404841 | |||||||
| chr17:5404959 | G | A | 180 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(177): Show |
225 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.1044+98C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 6/16 | chr17 | 5404959 | |||||||
| chr17:5404988 | G | A | 6 | a0001c0001t0002g0013 a0001c0001t0002g0027 a0001c0001t0002g0028 others(3): Show |
10 | HG00733.hp1 HG01106.hp2 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.1044+69C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 6/16 | chr17 | 5404988 | |||||||
| chr17:5405023 | G | C | 1 | a0001c0002t0001g0106 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1044+34C>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 6/16 | chr17 | 5405023 | |||||||
| chr17:5405049 | G | T | 4 | a0001c0004t0006g0187 a0001c0004t0006g0188 a0001c0004t0006g0189 others(1): Show |
4 | HG02886.hp2 HG02922.hp2 HG02965.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.1044+8C>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 6/16 | chr17 | 5405049 | |||||||
| chr17:5405283 | G | A | 238 | a0001c0001t0002g0011 a0001c0001t0002g0021 a0001c0001t0002g0022 others(235): Show |
301 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.858-40C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 5/16 | chr17 | 5405283 | |||||||
| chr17:5405409 | CTG | C | 3 | a0001c0002t0009g0191 a0001c0002t0009g0192 a0001c0002t0009g0193 |
3 | HG02280.hp2 HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.858-168_858-167del others(2): Show |
NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 5/16 | chr17 | 5405409 | |||||||
| chr17:5405444 | G | A | 1 | a0001c0003t0016g0079 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.858-201C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 5/16 | chr17 | 5405444 | |||||||
| chr17:5405566 | C | T | 1 | a0001c0001t0003g0199 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.858-323G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 5/16 | chr17 | 5405566 | |||||||
| chr17:5405865 | G | A | 1 | a0001c0001t0003g0026 | 2 | HG01884.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.858-622C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 5/16 | chr17 | 5405865 | |||||||
| chr17:5406370 | G | C | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.858-1127C>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 5/16 | chr17 | 5406370 | |||||||
| chr17:5406391 | T | C | 109 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(106): Show |
137 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.858-1148A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 5/16 | chr17 | 5406391 | |||||||
| chr17:5406597 | C | CAGACAGA others(9): Show |
3 | a0001c0003t0001g0045 a0001c0003t0001g0046 a0001c0003t0001g0047 |
3 | HG01192.hp1 HG01952.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.858-1355_858-1354i others(18): Show |
NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 5/16 | chr17 | 5406597 | |||||||
| chr17:5406599 | G | C | 1 | a0001c0001t0002g0252 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.858-1356C>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 5/16 | chr17 | 5406599 | |||||||
| chr17:5406604 | A | ATGGTGAA others(9): Show |
170 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(167): Show |
214 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.858-1362_858-1361i others(18): Show |
NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 5/16 | chr17 | 5406604 | |||||||
| chr17:5406604 | A | G | 3 | a0001c0003t0001g0045 a0001c0003t0001g0046 a0001c0003t0001g0047 |
3 | HG01192.hp1 HG01952.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.858-1361T>C | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 5/16 | chr17 | 5406604 | |||||||
| chr17:5406713 | C | A | 1 | a0001c0003t0001g0080 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.858-1470G>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 5/16 | chr17 | 5406713 | |||||||
| chr17:5406713 | C | G | 172 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(169): Show |
216 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.858-1470G>C | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 5/16 | chr17 | 5406713 | |||||||
| chr17:5406769 | AAAAAG | A | 172 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(169): Show |
216 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.858-1531_858-1527d others(7): Show |
NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 5/16 | chr17 | 5406769 | |||||||
| chr17:5406801 | A | C | 180 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(177): Show |
225 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.858-1558T>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 5/16 | chr17 | 5406801 | |||||||
| chr17:5406808 | T | C | 1 | a0001c0001t0002g0262 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.858-1565A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 5/16 | chr17 | 5406808 | |||||||
| chr17:5406835 | T | C | 1 | a0001c0001t0002g0253 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.858-1592A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 5/16 | chr17 | 5406835 | |||||||
| chr17:5406868 | G | A | 4 | a0001c0004t0006g0187 a0001c0004t0006g0188 a0001c0004t0006g0189 others(1): Show |
4 | HG02886.hp2 HG02922.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.858-1625C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 5/16 | chr17 | 5406868 | |||||||
| chr17:5406875 | G | A | 7 | a0001c0002t0001g0108 a0001c0002t0001g0109 a0001c0002t0001g0110 others(4): Show |
7 | HG02257.hp2 HG02451.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.858-1632C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 5/16 | chr17 | 5406875 | |||||||
| chr17:5406988 | G | C | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.857+1745C>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 5/16 | chr17 | 5406988 | |||||||
| chr17:5407089 | T | C | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.857+1644A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 5/16 | chr17 | 5407089 | |||||||
| chr17:5407091 | T | G | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.857+1642A>C | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 5/16 | chr17 | 5407091 | |||||||
| chr17:5407136 | G | T | 2 | a0001c0002t0005g0120 a0001c0002t0005g0121 |
2 | HG02809.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.857+1597C>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 5/16 | chr17 | 5407136 | |||||||
| chr17:5407164 | G | A | 3 | a0001c0002t0009g0191 a0001c0002t0009g0192 a0001c0002t0009g0193 |
3 | HG02280.hp2 HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.857+1569C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 5/16 | chr17 | 5407164 | |||||||
| chr17:5407259 | A | G | 1 | a0001c0003t0001g0083 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.857+1474T>C | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 5/16 | chr17 | 5407259 | |||||||
| chr17:5407492 | C | T | 1 | a0001c0001t0002g0269 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.857+1241G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 5/16 | chr17 | 5407492 | |||||||
| chr17:5407823 | T | C | 172 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(169): Show |
216 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.857+910A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 5/16 | chr17 | 5407823 | |||||||
| chr17:5408018 | CT | C | 214 | a0001c0001t0002g0033 a0001c0001t0003g0005 a0001c0001t0003g0012 others(211): Show |
270 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.857+714delA | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 5/16 | chr17 | 5408018 | |||||||
| chr17:5408045 | C | T | 1 | a0001c0002t0005g0166 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.857+688G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 5/16 | chr17 | 5408045 | |||||||
| chr17:5408093 | A | C | 1 | a0001c0001t0002g0206 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.857+640T>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 5/16 | chr17 | 5408093 | |||||||
| chr17:5408130 | A | G | 1 | a0001c0002t0008g0162 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.857+603T>C | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 5/16 | chr17 | 5408130 | |||||||
| chr17:5408169 | C | T | 1 | a0001c0001t0003g0267 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.857+564G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 5/16 | chr17 | 5408169 | |||||||
| chr17:5408228 | T | C | 1 | a0001c0001t0003g0026 | 2 | HG01884.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.857+505A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 5/16 | chr17 | 5408228 | |||||||
| chr17:5408271 | C | A | 1 | a0003c0006t0010g0014 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.857+462G>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 5/16 | chr17 | 5408271 | |||||||
| chr17:5408318 | C | T | 2 | a0001c0004t0006g0285 a0001c0009t0006g0186 |
2 | HG01243.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.857+415G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 5/16 | chr17 | 5408318 | |||||||
| chr17:5408377 | T | C | 1 | a0001c0001t0013g0255 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.857+356A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 5/16 | chr17 | 5408377 | |||||||
| chr17:5408422 | C | T | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.857+311G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 5/16 | chr17 | 5408422 | |||||||
| chr17:5408429 | G | A | 1 | a0001c0001t0002g0215 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.857+304C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 5/16 | chr17 | 5408429 | |||||||
| chr17:5408473 | A | T | 1 | a0005c0008t0001g0032 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.857+260T>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 5/16 | chr17 | 5408473 | |||||||
| chr17:5408509 | A | G | 2 | a0001c0004t0006g0285 a0001c0009t0006g0186 |
2 | HG01243.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.857+224T>C | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 5/16 | chr17 | 5408509 | |||||||
| chr17:5408588 | C | A | 7 | a0001c0004t0006g0187 a0001c0004t0006g0188 a0001c0004t0006g0189 others(4): Show |
8 | HG01167.hp1 HG01169.hp2 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.857+145G>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 5/16 | chr17 | 5408588 | |||||||
| chr17:5408951 | A | G | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.681-42T>C | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 4/16 | chr17 | 5408951 | |||||||
| chr17:5409048 | A | C | 1 | a0001c0002t0005g0119 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.681-139T>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 4/16 | chr17 | 5409048 | |||||||
| chr17:5409238 | G | C | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.681-329C>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 4/16 | chr17 | 5409238 | |||||||
| chr17:5409339 | A | G | 4 | a0001c0002t0001g0108 a0001c0002t0001g0109 a0001c0002t0001g0110 others(1): Show |
4 | HG02451.hp1 HG02486.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.681-430T>C | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 4/16 | chr17 | 5409339 | |||||||
| chr17:5409352 | C | T | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.681-443G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 4/16 | chr17 | 5409352 | |||||||
| chr17:5409369 | C | T | 2 | a0001c0003t0001g0017 a0001c0003t0001g0053 |
3 | NA18988.hp2 NA19005.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.681-460G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 4/16 | chr17 | 5409369 | |||||||
| chr17:5409374 | C | CA | 11 | a0001c0001t0002g0029 a0001c0001t0002g0217 a0001c0001t0002g0218 others(8): Show |
12 | HG00621.hp1 HG00673.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.681-466dupT | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 4/16 | chr17 | 5409374 | |||||||
| chr17:5409374 | CA | C | 10 | a0001c0001t0002g0242 a0001c0001t0002g0263 a0001c0001t0002g0268 others(7): Show |
11 | HG01167.hp1 HG01168.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.681-466delT | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 4/16 | chr17 | 5409374 | |||||||
| chr17:5409374 | CAAA | C | 8 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(5): Show |
8 | HG00741.hp1 HG01433.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.681-468_681-466del others(3): Show |
NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 4/16 | chr17 | 5409374 | |||||||
| chr17:5409374 | CAAAA | C | 161 | a0001c0002t0001g0108 a0001c0002t0001g0109 a0001c0002t0001g0110 others(158): Show |
205 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.681-469_681-466del others(4): Show |
NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 4/16 | chr17 | 5409374 | |||||||
| chr17:5409387 | A | G | 1 | a0001c0003t0001g0047 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.681-478T>C | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 4/16 | chr17 | 5409387 | |||||||
| chr17:5409425 | G | T | 1 | a0001c0002t0005g0041 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.681-516C>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 4/16 | chr17 | 5409425 | |||||||
| chr17:5409446 | A | C | 1 | a0001c0001t0002g0261 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.681-537T>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 4/16 | chr17 | 5409446 | |||||||
| chr17:5409490 | A | G | 5 | a0001c0002t0008g0157 a0001c0002t0008g0161 a0001c0002t0008g0162 others(2): Show |
5 | HG02615.hp1 HG03209.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.681-581T>C | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 4/16 | chr17 | 5409490 | |||||||
| chr17:5409572 | A | G | 177 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(174): Show |
221 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.681-663T>C | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 4/16 | chr17 | 5409572 | |||||||
| chr17:5409640 | G | A | 1 | a0001c0001t0003g0199 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.681-731C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 4/16 | chr17 | 5409640 | |||||||
| chr17:5409766 | T | C | 7 | a0001c0002t0001g0169 a0001c0002t0001g0170 a0001c0002t0001g0171 others(4): Show |
7 | HG00642.hp1 HG01123.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.681-857A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 4/16 | chr17 | 5409766 | |||||||
| chr17:5409832 | T | A | 177 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(174): Show |
221 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.680+871A>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 4/16 | chr17 | 5409832 | |||||||
| chr17:5409842 | G | A | 3 | a0001c0002t0009g0191 a0001c0002t0009g0192 a0001c0002t0009g0193 |
3 | HG02280.hp2 HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.680+861C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 4/16 | chr17 | 5409842 | |||||||
| chr17:5409899 | G | C | 1 | a0001c0001t0003g0026 | 2 | HG01884.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.680+804C>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 4/16 | chr17 | 5409899 | |||||||
| chr17:5410067 | A | G | 1 | a0001c0001t0002g0033 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.680+636T>C | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 4/16 | chr17 | 5410067 | |||||||
| chr17:5410202 | C | T | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.680+501G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 4/16 | chr17 | 5410202 | |||||||
| chr17:5410437 | A | G | 1 | a0001c0003t0001g0045 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.680+266T>C | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 4/16 | chr17 | 5410437 | |||||||
| chr17:5410487 | TG | T | 245 | a0001c0001t0002g0011 a0001c0001t0002g0021 a0001c0001t0002g0022 others(242): Show |
308 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.680+215delC | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 4/16 | chr17 | 5410487 | |||||||
| chr17:5410519 | C | T | 4 | a0001c0001t0003g0279 a0001c0001t0003g0280 a0001c0001t0003g0281 others(1): Show |
4 | HG02257.hp1 HG02976.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.680+184G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 4/16 | chr17 | 5410519 | |||||||
| chr17:5410633 | T | C | 1 | a0001c0002t0004g0156 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.680+70A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 4/16 | chr17 | 5410633 | |||||||
| chr17:5410668 | T | C | 1 | a0001c0002t0001g0172 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.680+35A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 4/16 | chr17 | 5410668 | |||||||
| chr17:5410809 | A | T | 1 | a0001c0001t0003g0238 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.594-20T>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 3/16 | chr17 | 5410809 | |||||||
| chr17:5410868 | G | A | 31 | a0001c0002t0004g0004 a0001c0002t0004g0006 a0001c0002t0004g0010 others(28): Show |
44 | HG00438.hp2 HG00609.hp2 HG02027.hp2 others(41): Show |
intron_variant | MODIFIER | c.594-79C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 3/16 | chr17 | 5410868 | |||||||
| chr17:5410877 | T | C | 1 | a0001c0001t0002g0220 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.594-88A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 3/16 | chr17 | 5410877 | |||||||
| chr17:5410940 | C | G | 7 | a0001c0004t0006g0187 a0001c0004t0006g0188 a0001c0004t0006g0189 others(4): Show |
8 | HG01167.hp1 HG01169.hp2 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.594-151G>C | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 3/16 | chr17 | 5410940 | |||||||
| chr17:5410943 | G | C | 214 | a0001c0001t0002g0033 a0001c0001t0003g0005 a0001c0001t0003g0012 others(211): Show |
270 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.594-154C>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 3/16 | chr17 | 5410943 | |||||||
| chr17:5410978 | T | C | 1 | a0001c0002t0004g0143 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.594-189A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 3/16 | chr17 | 5410978 | |||||||
| chr17:5411037 | A | C | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.594-248T>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 3/16 | chr17 | 5411037 | |||||||
| chr17:5411081 | C | T | 1 | a0001c0001t0003g0228 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.594-292G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 3/16 | chr17 | 5411081 | |||||||
| chr17:5411157 | T | C | 6 | a0001c0002t0007g0116 a0001c0002t0007g0196 a0001c0002t0007g0197 others(3): Show |
6 | HG00280.hp2 HG01884.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.594-368A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 3/16 | chr17 | 5411157 | |||||||
| chr17:5411191 | T | A | 2 | a0001c0004t0006g0285 a0001c0009t0006g0186 |
2 | HG01243.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.594-402A>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 3/16 | chr17 | 5411191 | |||||||
| chr17:5411253 | A | C | 1 | a0001c0003t0001g0052 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.594-464T>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 3/16 | chr17 | 5411253 | |||||||
| chr17:5411313 | T | C | 4 | a0001c0004t0006g0187 a0001c0004t0006g0188 a0001c0004t0006g0189 others(1): Show |
4 | HG02886.hp2 HG02922.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.594-524A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 3/16 | chr17 | 5411313 | |||||||
| chr17:5411361 | C | T | 1 | a0001c0002t0005g0118 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.594-572G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 3/16 | chr17 | 5411361 | |||||||
| chr17:5411392 | C | T | 2 | a0001c0001t0003g0026 a0001c0001t0003g0199 |
3 | HG00099.hp1 HG01884.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.594-603G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 3/16 | chr17 | 5411392 | |||||||
| chr17:5411459 | G | A | 1 | a0001c0001t0013g0255 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.594-670C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 3/16 | chr17 | 5411459 | |||||||
| chr17:5411479 | A | G | 180 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(177): Show |
225 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.594-690T>C | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 3/16 | chr17 | 5411479 | |||||||
| chr17:5411504 | C | T | 2 | a0001c0004t0006g0285 a0001c0009t0006g0186 |
2 | HG01243.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.594-715G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 3/16 | chr17 | 5411504 | |||||||
| chr17:5411580 | C | A | 6 | a0001c0001t0002g0256 a0001c0001t0002g0257 a0001c0001t0002g0258 others(3): Show |
6 | HG00140.hp2 HG00741.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.594-791G>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 3/16 | chr17 | 5411580 | |||||||
| chr17:5411580 | C | CA | 11 | a0001c0001t0002g0261 a0001c0001t0003g0026 a0001c0001t0003g0238 others(8): Show |
13 | HG01167.hp1 HG01169.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.594-792dupT | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 3/16 | chr17 | 5411580 | |||||||
| chr17:5411580 | CA | C | 153 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(150): Show |
195 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.594-792delT | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 3/16 | chr17 | 5411580 | |||||||
| chr17:5411597 | A | C | 4 | a0001c0001t0003g0279 a0001c0001t0003g0280 a0001c0001t0003g0281 others(1): Show |
4 | HG02257.hp1 HG02976.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.594-808T>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 3/16 | chr17 | 5411597 | |||||||
| chr17:5411636 | C | T | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.594-847G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 3/16 | chr17 | 5411636 | |||||||
| chr17:5411657 | AT | A | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.594-869delA | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 3/16 | chr17 | 5411657 | |||||||
| chr17:5411667 | C | T | 8 | a0001c0002t0008g0157 a0001c0002t0008g0161 a0001c0002t0008g0162 others(5): Show |
8 | HG02280.hp2 HG02451.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.594-878G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 3/16 | chr17 | 5411667 | |||||||
| chr17:5411769 | G | A | 180 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(177): Show |
225 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.594-980C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 3/16 | chr17 | 5411769 | |||||||
| chr17:5411789 | T | C | 1 | a0001c0001t0003g0275 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.594-1000A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 3/16 | chr17 | 5411789 | |||||||
| chr17:5411868 | T | C | 2 | a0001c0001t0003g0239 a0001c0001t0003g0267 |
2 | NA19001.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.594-1079A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 3/16 | chr17 | 5411868 | |||||||
| chr17:5411933 | G | A | 1 | a0001c0002t0005g0041 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.594-1144C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 3/16 | chr17 | 5411933 | |||||||
| chr17:5411979 | C | T | 180 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(177): Show |
225 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.594-1190G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 3/16 | chr17 | 5411979 | |||||||
| chr17:5412121 | T | C | 1 | a0001c0002t0001g0173 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.594-1332A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 3/16 | chr17 | 5412121 | |||||||
| chr17:5412182 | C | T | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.594-1393G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 3/16 | chr17 | 5412182 | |||||||
| chr17:5412341 | A | G | 1 | a0001c0001t0002g0033 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.594-1552T>C | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 3/16 | chr17 | 5412341 | |||||||
| chr17:5412371 | G | A | 2 | a0001c0002t0004g0147 a0001c0002t0004g0148 |
2 | HG03017.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.594-1582C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 3/16 | chr17 | 5412371 | |||||||
| chr17:5412483 | G | A | 1 | a0001c0001t0002g0262 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.593+1526C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 3/16 | chr17 | 5412483 | |||||||
| chr17:5412487 | C | T | 1 | a0001c0002t0007g0284 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.593+1522G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 3/16 | chr17 | 5412487 | |||||||
| chr17:5412499 | G | C | 1 | a0001c0001t0002g0220 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.593+1510C>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 3/16 | chr17 | 5412499 | |||||||
| chr17:5412504 | G | T | 1 | a0001c0002t0005g0041 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.593+1505C>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 3/16 | chr17 | 5412504 | |||||||
| chr17:5412667 | T | C | 4 | a0001c0004t0006g0187 a0001c0004t0006g0188 a0001c0004t0006g0189 others(1): Show |
4 | HG02886.hp2 HG02922.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.593+1342A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 3/16 | chr17 | 5412667 | |||||||
| chr17:5412761 | A | G | 1 | a0001c0002t0001g0115 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.593+1248T>C | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 3/16 | chr17 | 5412761 | |||||||
| chr17:5412875 | C | T | 2 | a0001c0001t0002g0205 a0004c0012t0002g0204 |
2 | HG00735.hp1 HG00738.hp2 |
intron_variant | MODIFIER | c.593+1134G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 3/16 | chr17 | 5412875 | |||||||
| chr17:5413139 | A | G | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.593+870T>C | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 3/16 | chr17 | 5413139 | |||||||
| chr17:5413177 | GC | G | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.593+831delG | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 3/16 | chr17 | 5413177 | |||||||
| chr17:5413191 | C | T | 1 | a0001c0002t0005g0041 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.593+818G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 3/16 | chr17 | 5413191 | |||||||
| chr17:5413318 | C | T | 1 | a0001c0002t0005g0041 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.593+691G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 3/16 | chr17 | 5413318 | |||||||
| chr17:5413360 | G | A | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.593+649C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 3/16 | chr17 | 5413360 | |||||||
| chr17:5413422 | T | C | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.593+587A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 3/16 | chr17 | 5413422 | |||||||
| chr17:5413445 | C | T | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.593+564G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 3/16 | chr17 | 5413445 | |||||||
| chr17:5413449 | T | C | 210 | a0001c0001t0002g0033 a0001c0001t0003g0005 a0001c0001t0003g0012 others(207): Show |
266 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.593+560A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 3/16 | chr17 | 5413449 | |||||||
| chr17:5413619 | C | T | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.593+390G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 3/16 | chr17 | 5413619 | |||||||
| chr17:5413688 | A | C | 211 | a0001c0001t0002g0033 a0001c0001t0003g0005 a0001c0001t0003g0012 others(208): Show |
267 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.593+321T>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 3/16 | chr17 | 5413688 | |||||||
| chr17:5413879 | T | C | 3 | a0001c0001t0002g0038 a0001c0001t0002g0263 a0001c0001t0002g0264 |
3 | HG01168.hp1 HG01169.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.593+130A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 3/16 | chr17 | 5413879 | |||||||
| chr17:5413976 | C | T | 24 | a0001c0001t0003g0005 a0001c0001t0003g0012 a0001c0001t0003g0020 others(21): Show |
34 | HG00621.hp1 HG00642.hp2 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.593+33G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 3/16 | chr17 | 5413976 | |||||||
| chr17:5414172 | C | A | 110 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(107): Show |
138 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.468-38G>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 2/16 | chr17 | 5414172 | |||||||
| chr17:5414215 | G | T | 7 | a0001c0004t0006g0187 a0001c0004t0006g0188 a0001c0004t0006g0189 others(4): Show |
8 | HG01167.hp1 HG01169.hp2 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.468-81C>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 2/16 | chr17 | 5414215 | |||||||
| chr17:5414290 | G | C | 111 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(108): Show |
139 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.468-156C>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 2/16 | chr17 | 5414290 | |||||||
| chr17:5414349 | C | T | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.468-215G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 2/16 | chr17 | 5414349 | |||||||
| chr17:5414353 | G | A | 2 | a0001c0001t0003g0030 a0001c0001t0003g0265 |
3 | HG02015.hp2 NA18954.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.468-219C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 2/16 | chr17 | 5414353 | |||||||
| chr17:5414486 | C | T | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.468-352G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 2/16 | chr17 | 5414486 | |||||||
| chr17:5414605 | T | C | 2 | a0001c0002t0007g0196 a0001c0002t0007g0197 |
2 | HG01884.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.468-471A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 2/16 | chr17 | 5414605 | |||||||
| chr17:5414655 | C | T | 1 | a0001c0003t0001g0050 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.468-521G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 2/16 | chr17 | 5414655 | |||||||
| chr17:5414659 | C | T | 6 | a0001c0004t0006g0187 a0001c0004t0006g0188 a0001c0004t0006g0189 others(3): Show |
6 | HG01243.hp1 HG02886.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.468-525G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 2/16 | chr17 | 5414659 | |||||||
| chr17:5414802 | C | CCA | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.468-669_468-668ins others(2): Show |
NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 2/16 | chr17 | 5414802 | |||||||
| chr17:5414802 | C | CCT | 7 | a0001c0004t0006g0187 a0001c0004t0006g0188 a0001c0004t0006g0189 others(4): Show |
8 | HG01167.hp1 HG01169.hp2 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.468-669_468-668ins others(2): Show |
NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 2/16 | chr17 | 5414802 | |||||||
| chr17:5414848 | T | C | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.468-714A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 2/16 | chr17 | 5414848 | |||||||
| chr17:5415001 | T | C | 1 | a0001c0001t0002g0201 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.468-867A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 2/16 | chr17 | 5415001 | |||||||
| chr17:5415035 | T | C | 2 | a0001c0004t0006g0285 a0001c0009t0006g0186 |
2 | HG01243.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.468-901A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 2/16 | chr17 | 5415035 | |||||||
| chr17:5415108 | C | T | 1 | a0001c0001t0003g0199 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.468-974G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 2/16 | chr17 | 5415108 | |||||||
| chr17:5415182 | A | G | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.468-1048T>C | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 2/16 | chr17 | 5415182 | |||||||
| chr17:5415183 | C | G | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.468-1049G>C | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 2/16 | chr17 | 5415183 | |||||||
| chr17:5415289 | G | A | 12 | a0001c0002t0004g0006 a0001c0002t0004g0149 a0001c0002t0004g0150 others(9): Show |
16 | HG00438.hp2 NA18747.hp1 NA18940.hp1 others(13): Show |
intron_variant | MODIFIER | c.468-1155C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 2/16 | chr17 | 5415289 | |||||||
| chr17:5415330 | G | T | 4 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(1): Show |
4 | HG00741.hp1 HG01433.hp1 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.467+1183C>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 2/16 | chr17 | 5415330 | |||||||
| chr17:5415494 | G | T | 1 | a0001c0001t0002g0202 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.467+1019C>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 2/16 | chr17 | 5415494 | |||||||
| chr17:5415537 | T | C | 3 | a0001c0001t0003g0273 a0001c0001t0003g0274 a0001c0001t0003g0275 |
3 | HG02145.hp2 HG02896.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.467+976A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 2/16 | chr17 | 5415537 | |||||||
| chr17:5415640 | G | C | 1 | a0001c0002t0005g0041 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.467+873C>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 2/16 | chr17 | 5415640 | |||||||
| chr17:5415658 | C | T | 2 | a0001c0001t0003g0226 a0001c0001t0003g0227 |
2 | NA18942.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.467+855G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 2/16 | chr17 | 5415658 | |||||||
| chr17:5415683 | G | A | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.467+830C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 2/16 | chr17 | 5415683 | |||||||
| chr17:5415692 | T | C | 3 | a0001c0002t0009g0191 a0001c0002t0009g0192 a0001c0002t0009g0193 |
3 | HG02280.hp2 HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.467+821A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 2/16 | chr17 | 5415692 | |||||||
| chr17:5415701 | G | A | 1 | a0005c0008t0001g0032 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.467+812C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 2/16 | chr17 | 5415701 | |||||||
| chr17:5415733 | C | G | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.467+780G>C | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 2/16 | chr17 | 5415733 | |||||||
| chr17:5415768 | A | G | 2 | a0001c0004t0006g0187 a0001c0004t0006g0188 |
2 | HG02886.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.467+745T>C | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 2/16 | chr17 | 5415768 | |||||||
| chr17:5415770 | C | T | 1 | a0001c0003t0001g0184 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.467+743G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 2/16 | chr17 | 5415770 | |||||||
| chr17:5415780 | G | A | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.467+733C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 2/16 | chr17 | 5415780 | |||||||
| chr17:5415894 | C | T | 174 | a0001c0001t0002g0201 a0001c0002t0001g0103 a0001c0002t0001g0104 others(171): Show |
218 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.467+619G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 2/16 | chr17 | 5415894 | |||||||
| chr17:5415919 | T | G | 2 | a0001c0007t0007g0194 a0001c0007t0007g0195 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.467+594A>C | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 2/16 | chr17 | 5415919 | |||||||
| chr17:5415974 | G | A | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.467+539C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 2/16 | chr17 | 5415974 | |||||||
| chr17:5416078 | G | GAGC | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.467+432_467+434dup others(3): Show |
NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 2/16 | chr17 | 5416078 | |||||||
| chr17:5416144 | C | CA | 10 | a0001c0001t0002g0033 a0001c0001t0002g0268 a0001c0001t0002g0269 others(7): Show |
10 | HG00621.hp1 HG01175.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.467+368dupT | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 2/16 | chr17 | 5416144 | |||||||
| chr17:5416144 | CA | C | 9 | a0001c0001t0002g0037 a0001c0001t0002g0223 a0001c0001t0002g0224 others(6): Show |
9 | HG01081.hp1 HG01167.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.467+368delT | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 2/16 | chr17 | 5416144 | |||||||
| chr17:5416144 | CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0003g0273 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.467+356_467+368del others(13): Show |
NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 2/16 | chr17 | 5416144 | |||||||
| chr17:5416156 | A | AAGTATAT others(4): Show |
1 | a0001c0002t0001g0103 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.467+356_467+357ins others(11): Show |
NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 2/16 | chr17 | 5416156 | |||||||
| chr17:5416158 | A | AAGTATAT others(4): Show |
2 | a0001c0002t0007g0116 a0001c0002t0007g0284 |
2 | HG00280.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.467+354_467+355ins others(11): Show |
NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 2/16 | chr17 | 5416158 | |||||||
| chr17:5416158 | A | AGTATAT | 12 | a0001c0002t0001g0108 a0001c0002t0001g0109 a0001c0002t0001g0169 others(9): Show |
14 | HG00642.hp1 HG01123.hp1 HG01261.hp2 others(11): Show |
intron_variant | MODIFIER | c.467+354_467+355ins others(6): Show |
NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 2/16 | chr17 | 5416158 | |||||||
| chr17:5416158 | A | AGTATATA others(1): Show |
54 | a0001c0002t0001g0110 a0001c0002t0001g0111 a0001c0002t0001g0174 others(51): Show |
79 | HG00099.hp2 HG00438.hp1 HG00609.hp1 others(76): Show |
intron_variant | MODIFIER | c.467+354_467+355ins others(8): Show |
NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 2/16 | chr17 | 5416158 | |||||||
| chr17:5416158 | A | AGTATATA others(3): Show |
17 | a0001c0002t0001g0112 a0001c0002t0001g0115 a0001c0003t0001g0018 others(14): Show |
18 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(15): Show |
intron_variant | MODIFIER | c.467+354_467+355ins others(10): Show |
NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 2/16 | chr17 | 5416158 | |||||||
| chr17:5416158 | A | AGTATATA others(5): Show |
1 | a0001c0003t0001g0094 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.467+354_467+355ins others(12): Show |
NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 2/16 | chr17 | 5416158 | |||||||
| chr17:5416158 | A | AGTATATA others(7): Show |
1 | a0001c0002t0005g0041 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.467+354_467+355ins others(14): Show |
NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 2/16 | chr17 | 5416158 | |||||||
| chr17:5416158 | A | T | 4 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(1): Show |
4 | HG00741.hp1 HG01433.hp1 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.467+355T>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 2/16 | chr17 | 5416158 | |||||||
| chr17:5416159 | A | G | 78 | a0001c0002t0001g0182 a0001c0002t0001g0183 a0001c0002t0004g0004 others(75): Show |
94 | HG00438.hp2 HG00544.hp2 HG00609.hp2 others(91): Show |
intron_variant | MODIFIER | c.467+354T>C | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 2/16 | chr17 | 5416159 | |||||||
| chr17:5416160 | A | T | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.467+353T>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 2/16 | chr17 | 5416160 | |||||||
| chr17:5416162 | A | T | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.467+351T>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 2/16 | chr17 | 5416162 | |||||||
| chr17:5416164 | A | T | 170 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(167): Show |
214 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.467+349T>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 2/16 | chr17 | 5416164 | |||||||
| chr17:5416165 | AAG | A | 57 | a0001c0002t0001g0182 a0001c0002t0001g0183 a0001c0002t0004g0004 others(54): Show |
71 | HG00438.hp2 HG00544.hp2 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.467+346_467+347del others(2): Show |
NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 2/16 | chr17 | 5416165 | |||||||
| chr17:5416166 | A | T | 114 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(111): Show |
143 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.467+347T>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 2/16 | chr17 | 5416166 | |||||||
| chr17:5416167 | G | A | 114 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(111): Show |
143 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.467+346C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 2/16 | chr17 | 5416167 | |||||||
| chr17:5416176 | T | TACACACA others(3): Show |
2 | a0001c0002t0004g0164 a0001c0002t0004g0165 |
2 | NA18940.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.467+336_467+337ins others(10): Show |
NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 2/16 | chr17 | 5416176 | |||||||
| chr17:5416178 | T | C | 4 | a0001c0002t0004g0164 a0001c0002t0004g0165 a0001c0002t0005g0107 others(1): Show |
4 | HG01071.hp2 NA18940.hp1 NA18945.hp2 others(1): Show |
intron_variant | MODIFIER | c.467+335A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 2/16 | chr17 | 5416178 | |||||||
| chr17:5416178 | T | TATATATA others(15): Show |
1 | a0005c0008t0001g0032 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.467+334_467+335ins others(22): Show |
NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 2/16 | chr17 | 5416178 | |||||||
| chr17:5416178 | T | TATATATA others(17): Show |
1 | a0001c0010t0001g0114 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.467+334_467+335ins others(24): Show |
NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 2/16 | chr17 | 5416178 | |||||||
| chr17:5416180 | T | C | 60 | a0001c0002t0001g0182 a0001c0002t0001g0183 a0001c0002t0004g0004 others(57): Show |
76 | HG00438.hp2 HG00544.hp2 HG00609.hp2 others(73): Show |
intron_variant | MODIFIER | c.467+333A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 2/16 | chr17 | 5416180 | |||||||
| chr17:5416180 | T | TACACACA others(3): Show |
1 | a0003c0006t0010g0014 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.467+332_467+333ins others(10): Show |
NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 2/16 | chr17 | 5416180 | |||||||
| chr17:5416180 | T | TATATATA others(17): Show |
3 | a0001c0007t0007g0194 a0001c0007t0007g0195 a0008c0017t0008g0287 |
3 | HG02896.hp1 HG02897.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.467+332_467+333ins others(24): Show |
NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 2/16 | chr17 | 5416180 | |||||||
| chr17:5416180 | T | TATATATA others(23): Show |
1 | a0001c0002t0008g0163 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.467+332_467+333ins others(30): Show |
NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 2/16 | chr17 | 5416180 | |||||||
| chr17:5416180 | T | TATATATA others(19): Show |
3 | a0001c0002t0007g0196 a0001c0002t0007g0197 a0001c0002t0008g0157 |
3 | HG01884.hp2 HG06807.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.467+332_467+333ins others(26): Show |
NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 2/16 | chr17 | 5416180 | |||||||
| chr17:5416180 | T | TATATATA others(19): Show |
3 | a0001c0002t0009g0191 a0001c0002t0009g0192 a0001c0002t0009g0193 |
3 | HG02280.hp2 HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.467+332_467+333ins others(26): Show |
NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 2/16 | chr17 | 5416180 | |||||||
| chr17:5416180 | T | TATATATA others(23): Show |
1 | a0001c0002t0008g0161 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.467+332_467+333ins others(30): Show |
NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 2/16 | chr17 | 5416180 | |||||||
| chr17:5416180 | T | TATATATA others(25): Show |
1 | a0001c0002t0008g0162 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.467+332_467+333ins others(32): Show |
NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 2/16 | chr17 | 5416180 | |||||||
| chr17:5416188 | T | C | 22 | a0001c0002t0004g0164 a0001c0002t0004g0165 a0001c0002t0005g0041 others(19): Show |
23 | HG01071.hp2 HG01167.hp1 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.467+325A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 2/16 | chr17 | 5416188 | |||||||
| chr17:5416188 | T | TACACAC | 75 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(72): Show |
103 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.467+319_467+324dup others(6): Show |
NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 2/16 | chr17 | 5416188 | |||||||
| chr17:5416188 | T | TACACACA others(1): Show |
16 | a0001c0002t0001g0108 a0001c0002t0001g0109 a0001c0002t0001g0110 others(13): Show |
16 | HG00642.hp1 HG01123.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.467+317_467+324dup others(8): Show |
NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 2/16 | chr17 | 5416188 | |||||||
| chr17:5416188 | T | TACACACA others(3): Show |
3 | a0001c0002t0001g0115 a0001c0002t0007g0116 a0001c0004t0006g0187 |
3 | HG00280.hp2 HG02886.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.467+315_467+324dup others(10): Show |
NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 2/16 | chr17 | 5416188 | |||||||
| chr17:5416188 | T | TACACACA others(5): Show |
58 | a0001c0002t0001g0182 a0001c0002t0001g0183 a0001c0002t0004g0004 others(55): Show |
74 | HG00438.hp2 HG00609.hp2 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.467+313_467+324dup others(12): Show |
NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 2/16 | chr17 | 5416188 | |||||||
| chr17:5416188 | T | TACACACA others(7): Show |
3 | a0001c0002t0004g0160 a0001c0002t0005g0158 a0001c0002t0005g0159 |
3 | HG00544.hp2 HG00673.hp2 NA18953.hp2 |
intron_variant | MODIFIER | c.467+311_467+324dup others(14): Show |
NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 2/16 | chr17 | 5416188 | |||||||
| chr17:5416208 | T | C | 1 | a0001c0003t0001g0101 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.467+305A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 2/16 | chr17 | 5416208 | |||||||
| chr17:5416215 | C | T | 1 | a0001c0003t0001g0043 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.467+298G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 2/16 | chr17 | 5416215 | |||||||
| chr17:5416240 | T | C | 1 | a0001c0003t0001g0102 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.467+273A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 2/16 | chr17 | 5416240 | |||||||
| chr17:5416282 | G | A | 5 | a0001c0002t0005g0019 a0001c0002t0005g0040 a0001c0002t0005g0166 others(2): Show |
6 | HG01891.hp2 HG02818.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.467+231C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 2/16 | chr17 | 5416282 | |||||||
| chr17:5416300 | C | A | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.467+213G>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 2/16 | chr17 | 5416300 | |||||||
| chr17:5416428 | A | C | 77 | a0001c0002t0004g0082 a0001c0002t0005g0054 a0001c0002t0005g0055 others(74): Show |
105 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.467+85T>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 2/16 | chr17 | 5416428 | |||||||
| chr17:5416488 | T | C | 1 | a0001c0001t0002g0025 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.467+25A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 2/16 | chr17 | 5416488 | |||||||
| chr17:5416712 | G | T | 1 | a0001c0001t0002g0037 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.298-30C>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 1/16 | chr17 | 5416712 | |||||||
| chr17:5416724 | T | A | 180 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(177): Show |
225 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.298-42A>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 1/16 | chr17 | 5416724 | |||||||
| chr17:5416762 | C | CT | 185 | a0001c0001t0002g0033 a0001c0001t0003g0279 a0001c0001t0003g0280 others(182): Show |
230 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.298-81dupA | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 1/16 | chr17 | 5416762 | |||||||
| chr17:5416832 | A | AT | 212 | a0001c0001t0002g0011 a0001c0001t0002g0021 a0001c0001t0002g0022 others(209): Show |
264 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(261): Show |
intron_variant | MODIFIER | c.298-151dupA | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 1/16 | chr17 | 5416832 | |||||||
| chr17:5416997 | GT | G | 172 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(169): Show |
216 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.298-316delA | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 1/16 | chr17 | 5416997 | |||||||
| chr17:5417058 | C | T | 2 | a0001c0001t0003g0020 a0001c0011t0003g0200 |
3 | NA19004.hp1 NA19005.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.298-376G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 1/16 | chr17 | 5417058 | |||||||
| chr17:5417118 | A | G | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.298-436T>C | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 1/16 | chr17 | 5417118 | |||||||
| chr17:5417327 | C | T | 77 | a0001c0002t0004g0082 a0001c0002t0005g0054 a0001c0002t0005g0055 others(74): Show |
105 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.298-645G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 1/16 | chr17 | 5417327 | |||||||
| chr17:5417341 | C | T | 1 | a0001c0002t0005g0041 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.298-659G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 1/16 | chr17 | 5417341 | |||||||
| chr17:5417365 | C | G | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.298-683G>C | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 1/16 | chr17 | 5417365 | |||||||
| chr17:5417403 | G | C | 7 | a0001c0002t0001g0169 a0001c0002t0001g0170 a0001c0002t0001g0171 others(4): Show |
7 | HG00642.hp1 HG01123.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.298-721C>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 1/16 | chr17 | 5417403 | |||||||
| chr17:5417488 | G | A | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.298-806C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 1/16 | chr17 | 5417488 | |||||||
| chr17:5417518 | C | A | 3 | a0001c0001t0003g0273 a0001c0001t0003g0274 a0001c0001t0003g0275 |
3 | HG02145.hp2 HG02896.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.298-836G>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 1/16 | chr17 | 5417518 | |||||||
| chr17:5417908 | A | G | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.298-1226T>C | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 1/16 | chr17 | 5417908 | |||||||
| chr17:5417968 | C | T | 2 | a0001c0004t0006g0285 a0001c0009t0006g0186 |
2 | HG01243.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.298-1286G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 1/16 | chr17 | 5417968 | |||||||
| chr17:5418035 | G | C | 173 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(170): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.297+1319C>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 1/16 | chr17 | 5418035 | |||||||
| chr17:5418037 | G | C | 2 | a0001c0001t0002g0198 a0001c0001t0002g0276 |
2 | NA18965.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.297+1317C>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 1/16 | chr17 | 5418037 | |||||||
| chr17:5418041 | G | C | 1 | a0001c0001t0003g0199 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.297+1313C>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 1/16 | chr17 | 5418041 | |||||||
| chr17:5418093 | G | A | 3 | a0001c0003t0001g0176 a0001c0003t0001g0177 a0001c0003t0001g0179 |
3 | HG01081.hp2 HG01192.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.297+1261C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 1/16 | chr17 | 5418093 | |||||||
| chr17:5418138 | C | T | 1 | a0001c0001t0003g0199 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.297+1216G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 1/16 | chr17 | 5418138 | |||||||
| chr17:5418144 | CA | C | 177 | a0001c0001t0002g0198 a0001c0002t0001g0103 a0001c0002t0001g0104 others(174): Show |
222 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.297+1209delT | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 1/16 | chr17 | 5418144 | |||||||
| chr17:5418178 | T | C | 1 | a0001c0003t0001g0180 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.297+1176A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 1/16 | chr17 | 5418178 | |||||||
| chr17:5418197 | T | C | 4 | a0001c0001t0002g0031 a0001c0001t0002g0277 a0001c0001t0002g0278 others(1): Show |
5 | HG02647.hp2 HG02818.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.297+1157A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 1/16 | chr17 | 5418197 | |||||||
| chr17:5418265 | A | C | 1 | a0001c0002t0005g0040 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.297+1089T>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 1/16 | chr17 | 5418265 | |||||||
| chr17:5418302 | G | A | 3 | a0001c0002t0001g0182 a0001c0002t0001g0183 a0001c0003t0012g0181 |
3 | HG03098.hp1 HG03471.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.297+1052C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 1/16 | chr17 | 5418302 | |||||||
| chr17:5418553 | T | C | 4 | a0001c0001t0003g0279 a0001c0001t0003g0280 a0001c0001t0003g0281 others(1): Show |
4 | HG02257.hp1 HG02976.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.297+801A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 1/16 | chr17 | 5418553 | |||||||
| chr17:5418630 | T | C | 1 | a0001c0001t0002g0033 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.297+724A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 1/16 | chr17 | 5418630 | |||||||
| chr17:5418662 | T | G | 1 | a0001c0001t0002g0037 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.297+692A>C | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 1/16 | chr17 | 5418662 | |||||||
| chr17:5418665 | G | A | 1 | a0001c0003t0001g0184 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.297+689C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 1/16 | chr17 | 5418665 | |||||||
| chr17:5418775 | C | G | 2 | a0001c0002t0005g0185 a0001c0002t0011g0039 |
2 | HG02280.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.297+579G>C | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 1/16 | chr17 | 5418775 | |||||||
| chr17:5418784 | G | A | 1 | a0001c0002t0005g0185 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.297+570C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 1/16 | chr17 | 5418784 | |||||||
| chr17:5418786 | C | T | 165 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(162): Show |
209 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.297+568G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 1/16 | chr17 | 5418786 | |||||||
| chr17:5418818 | A | G | 1 | a0001c0001t0002g0038 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.297+536T>C | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 1/16 | chr17 | 5418818 | |||||||
| chr17:5418948 | G | T | 1 | a0001c0001t0002g0037 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.297+406C>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 1/16 | chr17 | 5418948 | |||||||
| chr17:5418968 | A | G | 2 | a0001c0002t0004g0035 a0001c0002t0004g0036 |
2 | HG00609.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.297+386T>C | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 1/16 | chr17 | 5418968 | |||||||
| chr17:5419011 | C | T | 1 | a0001c0001t0002g0034 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.297+343G>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 1/16 | chr17 | 5419011 | |||||||
| chr17:5419013 | T | C | 1 | a0001c0003t0001g0283 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.297+341A>G | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 1/16 | chr17 | 5419013 | |||||||
| chr17:5419021 | G | A | 1 | a0001c0002t0007g0284 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.297+333C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 1/16 | chr17 | 5419021 | |||||||
| chr17:5419200 | G | T | 1 | a0001c0001t0002g0033 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.297+154C>A | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 1/16 | chr17 | 5419200 | |||||||
| chr17:5419293 | G | A | 1 | a0001c0004t0006g0285 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.297+61C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 1/16 | chr17 | 5419293 | |||||||
| chr17:5419303 | G | A | 1 | a0001c0001t0002g0286 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.297+51C>T | NUP88 | ENSG00000108559.13 | transcript | ENST00000573584.6 | protein_coding | 1/16 | chr17 | 5419303 |