Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 3843 |
| ensemblid | ENSG00000065150.21 |
| hgncid | 6402 |
| symbol | IPO5 |
| name | importin 5 |
| refseq_nuc | NM_002271.6 |
| refseq_prot | NP_002262.4 |
| ensembl_nuc | ENST00000651721.2 |
| ensembl_prot | ENSP00000499125.1 |
| mane_status | MANE Select |
| chr | chr13 |
| start | 97953675 |
| end | 98024296 |
| strand | + |
| ver | v1.2 |
| region | chr13:97953675-98024296 |
| region5000 | chr13:97948675-98029296 |
| regionname0 | IPO5_chr13_97953675_98024296 |
| regionname5000 | IPO5_chr13_97948675_98029296 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1097 | 375 | 92 | 67 | 166 | 6 | 42 | 128 | IPO5_chr13_97948675_98029296 | IPO5 | MAAAA others(1092): Show |
chr13 | 97948675 | 98029296 |
| a0002 | 0/0 | 1097 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | MAAAA others(1092): Show |
chr13 | 97948675 | 98029296 |
| a0003 | 0/0 | 1097 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | MAAAA others(1092): Show |
chr13 | 97948675 | 98029296 |
| a0004 | 0/0 | 1097 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | MAAAA others(1092): Show |
chr13 | 97948675 | 98029296 |
| a0005 | 0/0 | 1097 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | IPO5_chr13_97948675_98029296 | IPO5 | MAAAA others(1092): Show |
chr13 | 97948675 | 98029296 |
| a0006 | 0/0 | 1097 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | IPO5_chr13_97948675_98029296 | IPO5 | MAAAA others(1092): Show |
chr13 | 97948675 | 98029296 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 3291 | 273 | 84 | 61 | 86 | 6 | 34 | IPO5_chr13_97948675_98029296 | IPO5 | ATGGC others(3286): Show |
chr13 | 97948675 | 98029296 | ||
| a0001c0002 | 0/0 | 3291 | 63 | 0 | 3 | 53 | 0 | 7 | IPO5_chr13_97948675_98029296 | IPO5 | ATGGC others(3286): Show |
chr13 | 97948675 | 98029296 | ||
| a0001c0003 | 0/0 | 3291 | 14 | 0 | 0 | 14 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | ATGGC others(3286): Show |
chr13 | 97948675 | 98029296 | ||
| a0001c0004 | 0/0 | 3291 | 9 | 0 | 0 | 9 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | ATGGC others(3286): Show |
chr13 | 97948675 | 98029296 | ||
| a0001c0005 | 0/0 | 3291 | 7 | 6 | 1 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | ATGGC others(3286): Show |
chr13 | 97948675 | 98029296 | ||
| a0001c0007 | 0/0 | 3291 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | ATGGC others(3286): Show |
chr13 | 97948675 | 98029296 | ||
| a0001c0008 | 0/0 | 3291 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | ATGGC others(3286): Show |
chr13 | 97948675 | 98029296 | ||
| a0001c0009 | 0/0 | 3291 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | ATGGC others(3286): Show |
chr13 | 97948675 | 98029296 | ||
| a0001c0010 | 0/0 | 3291 | 1 | 0 | 1 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | ATGGC others(3286): Show |
chr13 | 97948675 | 98029296 | ||
| a0001c0012 | 0/0 | 3291 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | ATGGC others(3286): Show |
chr13 | 97948675 | 98029296 | ||
| a0001c0013 | 0/0 | 3291 | 1 | 0 | 1 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | ATGGC others(3286): Show |
chr13 | 97948675 | 98029296 | ||
| a0001c0014 | 0/0 | 3291 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | ATGGC others(3286): Show |
chr13 | 97948675 | 98029296 | ||
| a0001c0015 | 0/0 | 3291 | 1 | 0 | 0 | 0 | 0 | 1 | IPO5_chr13_97948675_98029296 | IPO5 | ATGGC others(3286): Show |
chr13 | 97948675 | 98029296 | ||
| a0001c0018 | 0/0 | 3291 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | ATGGC others(3286): Show |
chr13 | 97948675 | 98029296 | ||
| a0002c0011 | 0/0 | 3291 | 1 | 0 | 1 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | ATGGC others(3286): Show |
chr13 | 97948675 | 98029296 | ||
| a0003c0017 | 0/0 | 3291 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | ATGGC others(3286): Show |
chr13 | 97948675 | 98029296 | ||
| a0004c0019 | 0/0 | 3291 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | ATGGC others(3286): Show |
chr13 | 97948675 | 98029296 | ||
| a0005c0006 | 0/0 | 3291 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | ATGGC others(3286): Show |
chr13 | 97948675 | 98029296 | ||
| a0006c0016 | 0/0 | 3291 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | ATGGC others(3286): Show |
chr13 | 97948675 | 98029296 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 6002 | 202 | 64 | 35 | 77 | 4 | 21 | IPO5_chr13_97948675_98029296 | IPO5 | GACCT others(5997): Show |
chr13 | 97948675 | 98029296 |
| a0001c0001t0002 | 0/1 | 6002 | 50 | 10 | 21 | 4 | 2 | 12 | IPO5_chr13_97948675_98029296 | IPO5 | GACCT others(5997): Show |
chr13 | 97948675 | 98029296 |
| a0001c0001t0006 | 0/0 | 6002 | 5 | 4 | 1 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | GACCT others(5997): Show |
chr13 | 97948675 | 98029296 |
| a0001c0001t0007 | 0/0 | 6002 | 2 | 0 | 0 | 2 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | GACCT others(5997): Show |
chr13 | 97948675 | 98029296 |
| a0001c0001t0008 | 0/0 | 6002 | 2 | 0 | 1 | 0 | 0 | 1 | IPO5_chr13_97948675_98029296 | IPO5 | GACCT others(5997): Show |
chr13 | 97948675 | 98029296 |
| a0001c0001t0009 | 0/0 | 6002 | 1 | 0 | 1 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | GACCT others(5997): Show |
chr13 | 97948675 | 98029296 |
| a0001c0001t0010 | 0/0 | 6002 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | GACCT others(5997): Show |
chr13 | 97948675 | 98029296 |
| a0001c0001t0011 | 0/0 | 6002 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | GACCT others(5997): Show |
chr13 | 97948675 | 98029296 |
| a0001c0001t0012 | 0/0 | 6002 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | GACCT others(5997): Show |
chr13 | 97948675 | 98029296 |
| a0001c0001t0013 | 0/0 | 6002 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | GACCT others(5997): Show |
chr13 | 97948675 | 98029296 |
| a0001c0001t0014 | 0/0 | 6002 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | GACCT others(5997): Show |
chr13 | 97948675 | 98029296 |
| a0001c0001t0016 | 0/0 | 6002 | 1 | 0 | 1 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | GACCT others(5997): Show |
chr13 | 97948675 | 98029296 |
| a0001c0001t0017 | 0/0 | 6002 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | GACCT others(5997): Show |
chr13 | 97948675 | 98029296 |
| a0001c0001t0018 | 0/0 | 6002 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | GACCT others(5997): Show |
chr13 | 97948675 | 98029296 |
| a0001c0001t0020 | 0/0 | 6002 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | GACCT others(5997): Show |
chr13 | 97948675 | 98029296 |
| a0001c0001t0021 | 0/0 | 6002 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | GACCT others(5997): Show |
chr13 | 97948675 | 98029296 |
| a0001c0001t0023 | 0/0 | 6002 | 1 | 0 | 1 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | GACCT others(5997): Show |
chr13 | 97948675 | 98029296 |
| a0001c0002t0001 | 0/0 | 6002 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | GACCT others(5997): Show |
chr13 | 97948675 | 98029296 |
| a0001c0002t0003 | 0/0 | 6002 | 48 | 0 | 2 | 39 | 0 | 7 | IPO5_chr13_97948675_98029296 | IPO5 | GACCT others(5997): Show |
chr13 | 97948675 | 98029296 |
| a0001c0002t0004 | 0/0 | 6002 | 13 | 0 | 0 | 13 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | GACCT others(5997): Show |
chr13 | 97948675 | 98029296 |
| a0001c0002t0015 | 0/0 | 6002 | 1 | 0 | 1 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | GACCT others(5997): Show |
chr13 | 97948675 | 98029296 |
| a0001c0003t0001 | 0/0 | 6002 | 14 | 0 | 0 | 14 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | GACCT others(5997): Show |
chr13 | 97948675 | 98029296 |
| a0001c0004t0005 | 0/0 | 6002 | 8 | 0 | 0 | 8 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | GACCT others(5997): Show |
chr13 | 97948675 | 98029296 |
| a0001c0004t0022 | 0/0 | 6002 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | GACCT others(5997): Show |
chr13 | 97948675 | 98029296 |
| a0001c0005t0001 | 0/0 | 6002 | 6 | 5 | 1 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | GACCT others(5997): Show |
chr13 | 97948675 | 98029296 |
| a0001c0005t0019 | 0/0 | 6002 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | GACCT others(5997): Show |
chr13 | 97948675 | 98029296 |
| a0001c0007t0001 | 0/0 | 6002 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | GACCT others(5997): Show |
chr13 | 97948675 | 98029296 |
| a0001c0008t0001 | 0/0 | 6002 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | GACCT others(5997): Show |
chr13 | 97948675 | 98029296 |
| a0001c0009t0001 | 0/0 | 6002 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | GACCT others(5997): Show |
chr13 | 97948675 | 98029296 |
| a0001c0010t0002 | 0/0 | 6002 | 1 | 0 | 1 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | GACCT others(5997): Show |
chr13 | 97948675 | 98029296 |
| a0001c0012t0001 | 0/0 | 6002 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | GACCT others(5997): Show |
chr13 | 97948675 | 98029296 |
| a0001c0013t0001 | 0/0 | 6002 | 1 | 0 | 1 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | GACCT others(5997): Show |
chr13 | 97948675 | 98029296 |
| a0001c0014t0001 | 0/0 | 6002 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | GACCT others(5997): Show |
chr13 | 97948675 | 98029296 |
| a0001c0015t0001 | 0/0 | 6002 | 1 | 0 | 0 | 0 | 0 | 1 | IPO5_chr13_97948675_98029296 | IPO5 | GACCT others(5997): Show |
chr13 | 97948675 | 98029296 |
| a0001c0018t0001 | 0/0 | 6002 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | GACCT others(5997): Show |
chr13 | 97948675 | 98029296 |
| a0002c0011t0001 | 0/0 | 6002 | 1 | 0 | 1 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | GACCT others(5997): Show |
chr13 | 97948675 | 98029296 |
| a0003c0017t0003 | 0/0 | 6002 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | GACCT others(5997): Show |
chr13 | 97948675 | 98029296 |
| a0004c0019t0001 | 0/0 | 6002 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | GACCT others(5997): Show |
chr13 | 97948675 | 98029296 |
| a0005c0006t0004 | 0/0 | 6002 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | GACCT others(5997): Show |
chr13 | 97948675 | 98029296 |
| a0006c0016t0003 | 0/0 | 6002 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | GACCT others(5997): Show |
chr13 | 97948675 | 98029296 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0263 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0001g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0002g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0002g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0002g0150 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0002g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0002g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0006g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0006g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0006g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0006g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0007g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0008g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0008g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0009g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0010g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0011g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0012g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0013g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0014g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0016g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0017g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0018g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0020g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0021g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0001t0023g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0002t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0002t0003g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0002t0003g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0002t0003g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0002t0003g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0002t0003g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0002t0003g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0002t0003g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0002t0003g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0002t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0002t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0002t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0002t0003g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0002t0003g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0002t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0002t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0002t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0002t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0002t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0002t0003g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0002t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0002t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0002t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0002t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0002t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0002t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0002t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0002t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0002t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0002t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0002t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0002t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0002t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0002t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0002t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0002t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0002t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0002t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0002t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0002t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0002t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0002t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0002t0003g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0002t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0002t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0002t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0002t0003g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0002t0003g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0002t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0002t0004g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0002t0004g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0002t0004g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0002t0004g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0002t0004g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0002t0004g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0002t0004g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0002t0004g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0002t0004g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0002t0004g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0002t0004g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0002t0015g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0003t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0003t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0003t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0003t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0003t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0003t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0003t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0003t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0003t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0003t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0003t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0003t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0003t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0003t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0004t0005g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0004t0005g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0004t0005g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0004t0005g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0004t0005g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0004t0005g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0004t0005g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0004t0005g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0004t0022g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0005t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0005t0001g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0005t0001g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0005t0001g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0005t0001g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0005t0001g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0005t0019g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0007t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0008t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0009t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0010t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0012t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0013t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0014t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0015t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0001c0018t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0002c0011t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0003c0017t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0004c0019t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0005c0006t0004g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| a0006c0016t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0130 | EUR | GBR | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0270 | EUR | GBR | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG00423 | hp1 | a0001 | c0002 | t0003 | g0029 | EAS | CHS | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG00423 | hp2 | a0001 | c0002 | t0003 | g0025 | EAS | CHS | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | CHS | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | CHS | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG00544 | hp1 | a0001 | c0002 | t0003 | g0015 | EAS | CHS | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | CHS | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG00558 | hp1 | a0001 | c0002 | t0003 | g0061 | EAS | CHS | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | CHS | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | CHS | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG00597 | hp2 | a0001 | c0002 | t0003 | g0062 | EAS | CHS | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | CHS | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | CHS | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG00621 | hp1 | a0001 | c0012 | t0001 | g0219 | EAS | CHS | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG00621 | hp2 | a0001 | c0002 | t0004 | g0044 | EAS | CHS | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG00639 | hp2 | a0001 | c0002 | t0015 | g0017 | AMR | PUR | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0164 | AMR | PUR | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG00735 | hp1 | a0001 | c0010 | t0002 | g0180 | AMR | PUR | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0304 | AMR | PUR | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0159 | AMR | PUR | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG01069 | hp2 | a0001 | c0002 | t0003 | g0018 | AMR | PUR | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0246 | AMR | PUR | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0166 | AMR | PUR | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0136 | AMR | PUR | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG01099 | hp1 | a0001 | c0001 | t0016 | g0260 | AMR | PUR | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG01099 | hp2 | a0001 | c0001 | t0008 | g0167 | AMR | PUR | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0284 | AMR | PUR | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG01106 | hp2 | a0002 | c0011 | t0001 | g0251 | AMR | PUR | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0367 | AMR | PUR | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0135 | AMR | PUR | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0285 | AMR | PUR | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | PUR | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0161 | AMR | PUR | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0297 | AMR | PUR | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0160 | AMR | PUR | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0153 | AMR | PUR | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | PUR | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0125 | AMR | PUR | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG01192 | hp2 | a0001 | c0005 | t0001 | g0344 | AMR | PUR | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG01243 | hp1 | a0001 | c0001 | t0006 | g0333 | AMR | PUR | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0127 | AMR | PUR | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | CLM | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0172 | AMR | CLM | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0300 | AMR | CLM | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG01261 | hp2 | a0001 | c0001 | t0009 | g0320 | AMR | CLM | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0262 | AMR | CLM | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0163 | AMR | CLM | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | CLM | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0131 | AMR | CLM | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | CLM | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0119 | EUR | IBS | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0268 | EUR | IBS | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | ACB | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | ACB | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG01891 | hp1 | a0001 | c0005 | t0001 | g0349 | AFR | ACB | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | ACB | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0179 | AMR | PEL | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0317 | AMR | PEL | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG01934 | hp1 | a0001 | c0013 | t0001 | g0293 | AMR | PEL | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0272 | AMR | PEL | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG01952 | hp1 | a0001 | c0002 | t0003 | g0020 | AMR | PEL | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0176 | AMR | PEL | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0157 | AMR | PEL | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0339 | AMR | PEL | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0308 | AMR | PEL | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0170 | AMR | PEL | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PEL | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG01981 | hp2 | a0001 | c0001 | t0023 | g0174 | AMR | PEL | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0299 | AMR | PEL | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0178 | AMR | PEL | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | KHV | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG02015 | hp2 | a0001 | c0002 | t0003 | g0060 | EAS | KHV | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG02027 | hp1 | a0001 | c0008 | t0001 | g0286 | EAS | KHV | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG02027 | hp2 | a0001 | c0002 | t0003 | g0030 | EAS | KHV | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | KHV | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG02040 | hp2 | a0001 | c0002 | t0003 | g0055 | EAS | KHV | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | ACB | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0128 | AFR | ACB | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | KHV | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0321 | EAS | KHV | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | KHV | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | KHV | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG02129 | hp2 | a0001 | c0002 | t0003 | g0073 | EAS | KHV | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | KHV | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG02132 | hp2 | a0001 | c0002 | t0003 | g0024 | EAS | KHV | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG02135 | hp1 | a0001 | c0002 | t0003 | g0035 | EAS | KHV | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG02135 | hp2 | a0001 | c0001 | t0013 | g0278 | EAS | KHV | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0292 | AMR | PEL | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0181 | AMR | PEL | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG02155 | hp1 | a0001 | c0002 | t0003 | g0028 | EAS | CDX | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | CDX | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | CDX | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0186 | EAS | CDX | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0364 | AFR | ACB | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG02257 | hp2 | a0001 | c0001 | t0018 | g0190 | AFR | ACB | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0261 | AFR | ACB | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | ACB | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | ACB | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | ACB | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0291 | AMR | PEL | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0155 | AMR | PEL | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0369 | AFR | ACB | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | KHV | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG02523 | hp2 | a0001 | c0002 | t0003 | g0063 | EAS | KHV | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0258 | AFR | GWD | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0365 | AFR | GWD | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0168 | SAS | PJL | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0350 | AFR | GWD | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0370 | AFR | GWD | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG02647 | hp1 | a0001 | c0001 | t0014 | g0169 | AFR | GWD | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0336 | AFR | GWD | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0183 | SAS | PJL | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG02683 | hp2 | a0001 | c0002 | t0003 | g0022 | SAS | PJL | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0162 | SAS | PJL | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG02717 | hp1 | a0003 | c0017 | t0003 | g0021 | AFR | GWD | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0325 | AFR | GWD | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0248 | SAS | PJL | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0152 | SAS | PJL | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0177 | SAS | PJL | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0129 | AFR | GWD | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0337 | AFR | GWD | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0368 | AFR | GWD | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG02886 | hp1 | a0001 | c0005 | t0001 | g0348 | AFR | GWD | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | GWD | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | GWD | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG02896 | hp1 | a0001 | c0001 | t0006 | g0009 | AFR | GWD | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG02896 | hp2 | a0001 | c0001 | t0021 | g0338 | AFR | GWD | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG02897 | hp2 | a0001 | c0001 | t0006 | g0009 | AFR | GWD | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0112 | AFR | ESN | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0328 | AFR | ESN | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | ESN | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0361 | AFR | ESN | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | ESN | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0126 | AFR | GWD | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0326 | AFR | MSL | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG03098 | hp2 | a0001 | c0005 | t0001 | g0347 | AFR | MSL | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | ESN | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG03130 | hp2 | a0001 | c0014 | t0001 | g0110 | AFR | ESN | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG03195 | hp1 | a0001 | c0001 | t0006 | g0332 | AFR | ESN | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG03195 | hp2 | a0001 | c0005 | t0001 | g0185 | AFR | ESN | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | MSL | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | MSL | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | MSL | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0335 | AFR | MSL | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG03239 | hp1 | a0001 | c0001 | t0008 | g0173 | SAS | PJL | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG03453 | hp1 | a0001 | c0001 | t0012 | g0359 | AFR | MSL | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0351 | AFR | MSL | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG03486 | hp1 | a0001 | c0005 | t0001 | g0345 | AFR | MSL | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG03486 | hp2 | a0001 | c0001 | t0017 | g0116 | AFR | MSL | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0156 | SAS | PJL | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0305 | SAS | PJL | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0306 | SAS | PJL | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0165 | SAS | PJL | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | ESN | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG03516 | hp2 | a0001 | c0001 | t0010 | g0255 | AFR | ESN | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | GWD | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG03579 | hp1 | a0004 | c0019 | t0001 | g0340 | AFR | MSL | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | MSL | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG03654 | hp2 | a0001 | c0002 | t0003 | g0072 | SAS | PJL | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0175 | SAS | STU | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | STU | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0301 | SAS | PJL | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG03704 | hp2 | a0001 | c0002 | t0003 | g0023 | SAS | PJL | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG03710 | hp1 | a0001 | c0015 | t0001 | g0147 | SAS | PJL | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0151 | SAS | PJL | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0247 | SAS | BEB | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG03831 | hp2 | a0001 | c0002 | t0003 | g0066 | SAS | BEB | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0154 | SAS | BEB | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | BEB | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0316 | SAS | BEB | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0205 | SAS | BEB | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0271 | SAS | BEB | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | BEB | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0237 | SAS | STU | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0330 | SAS | STU | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | BEB | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | BEB | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG04199 | hp1 | a0001 | c0002 | t0003 | g0014 | SAS | STU | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0334 | SAS | STU | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0303 | SAS | STU | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0105 | SAS | STU | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | YRI | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | YRI | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | CHB | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA18612 | hp2 | a0001 | c0002 | t0003 | g0036 | EAS | CHB | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | YRI | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | YRI | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA18940 | hp2 | a0001 | c0002 | t0003 | g0041 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA18944 | hp2 | a0001 | c0009 | t0001 | g0309 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA18946 | hp1 | a0001 | c0002 | t0001 | g0327 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA18946 | hp2 | a0001 | c0007 | t0001 | g0198 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA18947 | hp2 | a0001 | c0002 | t0003 | g0059 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA18949 | hp1 | a0001 | c0002 | t0003 | g0052 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA18950 | hp1 | a0001 | c0002 | t0003 | g0016 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA18950 | hp2 | a0001 | c0004 | t0022 | g0010 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA18952 | hp1 | a0001 | c0002 | t0003 | g0051 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA18957 | hp1 | a0001 | c0003 | t0001 | g0197 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA18959 | hp1 | a0001 | c0002 | t0004 | g0042 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA18959 | hp2 | a0001 | c0002 | t0003 | g0037 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA18960 | hp1 | a0001 | c0003 | t0001 | g0240 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA18960 | hp2 | a0001 | c0002 | t0003 | g0043 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA18961 | hp1 | a0001 | c0003 | t0001 | g0218 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA18964 | hp1 | a0001 | c0002 | t0003 | g0065 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA18966 | hp1 | a0001 | c0004 | t0005 | g0354 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA18971 | hp1 | a0001 | c0001 | t0007 | g0005 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA18971 | hp2 | a0005 | c0006 | t0004 | g0013 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA18980 | hp1 | a0001 | c0002 | t0003 | g0058 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA18981 | hp1 | a0001 | c0002 | t0003 | g0026 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA18982 | hp1 | a0001 | c0004 | t0005 | g0010 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA18983 | hp1 | a0001 | c0001 | t0007 | g0005 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA18983 | hp2 | a0001 | c0002 | t0003 | g0056 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA18984 | hp2 | a0001 | c0003 | t0001 | g0342 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA18986 | hp1 | a0006 | c0016 | t0003 | g0047 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA18994 | hp2 | a0001 | c0002 | t0004 | g0002 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA18995 | hp1 | a0001 | c0004 | t0005 | g0353 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA18998 | hp1 | a0001 | c0003 | t0001 | g0122 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA18998 | hp2 | a0001 | c0002 | t0003 | g0053 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA18999 | hp2 | a0001 | c0003 | t0001 | g0196 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA19000 | hp1 | a0001 | c0004 | t0005 | g0357 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA19002 | hp1 | a0001 | c0002 | t0003 | g0032 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA19004 | hp1 | a0001 | c0003 | t0001 | g0123 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA19007 | hp1 | a0001 | c0002 | t0003 | g0027 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA19007 | hp2 | a0001 | c0002 | t0004 | g0001 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA19009 | hp1 | a0001 | c0001 | t0011 | g0319 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA19009 | hp2 | a0001 | c0002 | t0003 | g0038 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA19010 | hp2 | a0001 | c0002 | t0004 | g0314 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | LWK | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0124 | AFR | LWK | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | LWK | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | LWK | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA19054 | hp2 | a0001 | c0002 | t0004 | g0031 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA19055 | hp2 | a0001 | c0004 | t0005 | g0358 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA19056 | hp1 | a0001 | c0003 | t0001 | g0343 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA19056 | hp2 | a0001 | c0003 | t0001 | g0201 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA19057 | hp1 | a0001 | c0002 | t0003 | g0049 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA19058 | hp1 | a0001 | c0002 | t0004 | g0050 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA19063 | hp1 | a0001 | c0002 | t0003 | g0034 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA19066 | hp1 | a0001 | c0002 | t0003 | g0040 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA19068 | hp2 | a0001 | c0004 | t0005 | g0352 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA19070 | hp1 | a0001 | c0002 | t0003 | g0033 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA19070 | hp2 | a0001 | c0004 | t0005 | g0355 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA19074 | hp1 | a0001 | c0003 | t0001 | g0200 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA19074 | hp2 | a0001 | c0001 | t0020 | g0341 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA19077 | hp1 | a0001 | c0002 | t0003 | g0064 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA19079 | hp1 | a0001 | c0003 | t0001 | g0217 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA19079 | hp2 | a0001 | c0002 | t0003 | g0054 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA19082 | hp1 | a0001 | c0002 | t0004 | g0045 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA19082 | hp2 | a0001 | c0003 | t0001 | g0203 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA19083 | hp1 | a0001 | c0002 | t0004 | g0048 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA19083 | hp2 | a0001 | c0003 | t0001 | g0215 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA19084 | hp2 | a0001 | c0002 | t0004 | g0046 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA19085 | hp1 | a0001 | c0002 | t0003 | g0057 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA19086 | hp2 | a0001 | c0002 | t0004 | g0069 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA19087 | hp1 | a0001 | c0003 | t0001 | g0207 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA19087 | hp2 | a0001 | c0002 | t0003 | g0070 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA19088 | hp1 | a0001 | c0002 | t0004 | g0001 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA19088 | hp2 | a0001 | c0004 | t0005 | g0356 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA19090 | hp2 | a0001 | c0002 | t0003 | g0067 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA19091 | hp1 | a0001 | c0002 | t0004 | g0002 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA19091 | hp2 | a0001 | c0002 | t0003 | g0068 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0329 | AFR | YRI | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA19240 | hp2 | a0001 | c0018 | t0001 | g0191 | AFR | YRI | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | ASW | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0362 | AFR | ASW | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0253 | EUR | TSI | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0158 | EUR | TSI | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA20905 | hp1 | a0001 | c0002 | t0003 | g0071 | SAS | GIH | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA20905 | hp2 | a0001 | c0002 | t0003 | g0019 | SAS | GIH | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0363 | AMR | CLM | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0171 | AMR | CLM | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0184 | AFR | ACB | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG02109 | hp2 | a0001 | c0005 | t0019 | g0346 | AFR | ACB | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | ACB | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | ACB | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0366 | AFR | ACB | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG02559 | hp2 | a0001 | c0001 | t0006 | g0331 | AFR | ACB | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | MSL | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0360 | AFR | USA | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | USA | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | LWK | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | LWK | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0150 | REF | REF | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0263 | REF | REF | IPO5_chr13_97948675_98029296 | IPO5 | chr13 | 97948675 | 98029296 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:97985479 | T | C | 1 | a0005 | 1 | NA18971.hp2 | missense_variant | MODERATE | c.230T>C | p.Val77Ala | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 6/29 | 464/6002 | 230/3294 | 77/1097 | chr13 | 97985479 | |||
| chr13:97990524 | C | T | 1 | a0004 | 1 | HG03579.hp1 | missense_variant | MODERATE | c.656C>T | p.Pro219Leu | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 9/29 | 890/6002 | 656/3294 | 219/1097 | chr13 | 97990524 | |||
| chr13:97993162 | G | A | 1 | a0006 | 1 | NA18986.hp1 | missense_variant | MODERATE | c.850G>A | p.Val284Ile | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 11/29 | 1084/6002 | 850/3294 | 284/1097 | chr13 | 97993162 | |||
| chr13:98000610 | T | C | 1 | a0003 | 1 | HG02717.hp1 | missense_variant | MODERATE | c.1073T>C | p.Met358Thr | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 13/29 | 1307/6002 | 1073/3294 | 358/1097 | chr13 | 98000610 | |||
| chr13:98019629 | C | T | 1 | a0002 | 1 | HG01106.hp2 | missense_variant | MODERATE | c.2885C>T | p.Thr962Ile | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 27/29 | 3119/6002 | 2885/3294 | 962/1097 | chr13 | 98019629 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:97990132 | T | C | 1 | a0001c0007 | 1 | NA18946.hp2 | synonymous_variant | LOW | c.474T>C | p.Phe158Phe | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 8/29 | 708/6002 | 474/3294 | 158/1097 | chr13 | 97990132 | |||
| chr13:97992942 | C | T | 1 | a0001c0018 | 1 | NA19240.hp2 | synonymous_variant | LOW | c.720C>T | p.Leu240Leu | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 10/29 | 954/6002 | 720/3294 | 240/1097 | chr13 | 97992942 | |||
| chr13:97992999 | A | G | 5 | a0001c0002 a0001c0005 a0003c0017 others(2): Show |
73 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(70): Show |
synonymous_variant | LOW | c.777A>G | p.Leu259Leu | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 10/29 | 1011/6002 | 777/3294 | 259/1097 | chr13 | 97992999 | |||
| chr13:97997544 | A | G | 1 | a0001c0015 | 1 | HG03710.hp1 | synonymous_variant | LOW | c.927A>G | p.Leu309Leu | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 12/29 | 1161/6002 | 927/3294 | 309/1097 | chr13 | 97997544 | |||
| chr13:98000581 | C | T | 1 | a0001c0014 | 1 | HG03130.hp2 | synonymous_variant | LOW | c.1044C>T | p.Cys348Cys | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 13/29 | 1278/6002 | 1044/3294 | 348/1097 | chr13 | 98000581 | |||
| chr13:98006192 | C | T | 1 | a0001c0013 | 1 | HG01934.hp1 | synonymous_variant | LOW | c.1560C>T | p.Ala520Ala | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 17/29 | 1794/6002 | 1560/3294 | 520/1097 | chr13 | 98006192 | |||
| chr13:98008103 | C | A | 1 | a0001c0008 | 1 | HG02027.hp1 | synonymous_variant | LOW | c.1761C>A | p.Thr587Thr | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 18/29 | 1995/6002 | 1761/3294 | 587/1097 | chr13 | 98008103 | |||
| chr13:98009979 | G | A | 1 | a0001c0009 | 1 | NA18944.hp2 | synonymous_variant | LOW | c.1899G>A | p.Thr633Thr | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 19/29 | 2133/6002 | 1899/3294 | 633/1097 | chr13 | 98009979 | |||
| chr13:98014061 | G | A | 1 | a0001c0010 | 1 | HG00735.hp1 | synonymous_variant | LOW | c.2172G>A | p.Ala724Ala | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 22/29 | 2406/6002 | 2172/3294 | 724/1097 | chr13 | 98014061 | |||
| chr13:98018574 | C | T | 1 | a0001c0004 | 9 | NA18950.hp2 NA18966.hp1 NA18982.hp1 others(6): Show |
synonymous_variant | LOW | c.2706C>T | p.Tyr902Tyr | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 26/29 | 2940/6002 | 2706/3294 | 902/1097 | chr13 | 98018574 | |||
| chr13:98018577 | A | C | 1 | a0001c0003 | 14 | NA18957.hp1 NA18960.hp1 NA18961.hp1 others(11): Show |
synonymous_variant | LOW | c.2709A>C | p.Ala903Ala | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 26/29 | 2943/6002 | 2709/3294 | 903/1097 | chr13 | 98018577 | |||
| chr13:98018634 | G | A | 1 | a0001c0005 | 7 | HG01192.hp2 HG01891.hp1 HG02109.hp2 others(4): Show |
synonymous_variant | LOW | c.2766G>A | p.Arg922Arg | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 26/29 | 3000/6002 | 2766/3294 | 922/1097 | chr13 | 98018634 | |||
| chr13:98018673 | C | T | 1 | a0001c0012 | 1 | HG00621.hp1 | synonymous_variant | LOW | c.2805C>T | p.Tyr935Tyr | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 26/29 | 3039/6002 | 2805/3294 | 935/1097 | chr13 | 98018673 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:97953697 | C | G | 1 | a0001c0001t0023 | 1 | HG01981.hp2 | 5_prime_UTR_variant | MODIFIER | c.-212C>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 1/29 | 23000 | chr13 | 97953697 | ||||||
| chr13:97969746 | A | C | 2 | a0001c0004t0005 a0001c0004t0022 |
9 | NA18950.hp2 NA18966.hp1 NA18982.hp1 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-89A>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/29 | 6951 | chr13 | 97969746 | ||||||
| chr13:98021899 | T | C | 1 | a0001c0001t0009 | 1 | HG01261.hp2 | 3_prime_UTR_variant | MODIFIER | c.*77T>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 29/29 | 77 | chr13 | 98021899 | ||||||
| chr13:98021974 | G | A | 1 | a0001c0001t0010 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*152G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 29/29 | 152 | chr13 | 98021974 | ||||||
| chr13:98022088 | G | A | 1 | a0001c0001t0011 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*266G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 29/29 | 266 | chr13 | 98022088 | ||||||
| chr13:98022128 | A | G | 1 | a0001c0001t0021 | 1 | HG02896.hp2 | 3_prime_UTR_variant | MODIFIER | c.*306A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 29/29 | 306 | chr13 | 98022128 | ||||||
| chr13:98022173 | G | A | 2 | a0001c0001t0007 a0001c0001t0012 |
3 | HG03453.hp1 NA18971.hp1 NA18983.hp1 |
3_prime_UTR_variant | MODIFIER | c.*351G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 29/29 | 351 | chr13 | 98022173 | ||||||
| chr13:98022675 | G | A | 1 | a0001c0001t0013 | 1 | HG02135.hp2 | 3_prime_UTR_variant | MODIFIER | c.*853G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 29/29 | 853 | chr13 | 98022675 | ||||||
| chr13:98022719 | A | G | 2 | a0001c0002t0004 a0005c0006t0004 |
14 | HG00621.hp2 NA18959.hp1 NA18971.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*897A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 29/29 | 897 | chr13 | 98022719 | ||||||
| chr13:98022838 | T | C | 1 | a0001c0001t0014 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1016T>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 29/29 | 1016 | chr13 | 98022838 | ||||||
| chr13:98023035 | T | G | 1 | a0001c0004t0022 | 1 | NA18950.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1213T>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 29/29 | 1213 | chr13 | 98023035 | ||||||
| chr13:98023065 | G | T | 1 | a0001c0001t0012 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1243G>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 29/29 | 1243 | chr13 | 98023065 | ||||||
| chr13:98023153 | C | T | 1 | a0001c0001t0020 | 1 | NA19074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1331C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 29/29 | 1331 | chr13 | 98023153 | ||||||
| chr13:98023185 | C | T | 1 | a0001c0005t0019 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1363C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 29/29 | 1363 | chr13 | 98023185 | ||||||
| chr13:98023349 | A | G | 1 | a0001c0001t0018 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1527A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 29/29 | 1527 | chr13 | 98023349 | ||||||
| chr13:98023387 | C | A | 6 | a0001c0002t0003 a0001c0002t0004 a0001c0002t0015 others(3): Show |
65 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*1565C>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 29/29 | 1565 | chr13 | 98023387 | ||||||
| chr13:98023421 | G | A | 1 | a0001c0002t0015 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1599G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 29/29 | 1599 | chr13 | 98023421 | ||||||
| chr13:98023484 | A | C | 1 | a0001c0001t0017 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1662A>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 29/29 | 1662 | chr13 | 98023484 | ||||||
| chr13:98023665 | T | G | 1 | a0001c0001t0006 | 5 | HG01243.hp1 HG02559.hp2 HG02896.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1843T>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 29/29 | 1843 | chr13 | 98023665 | ||||||
| chr13:98023697 | A | G | 5 | a0001c0001t0002 a0001c0001t0008 a0001c0001t0014 others(2): Show |
54 | HG00099.hp1 HG00642.hp1 HG00735.hp1 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*1875A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 29/29 | 1875 | chr13 | 98023697 | ||||||
| chr13:98023710 | G | A | 1 | a0001c0001t0016 | 1 | HG01099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1888G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 29/29 | 1888 | chr13 | 98023710 | ||||||
| chr13:98024127 | T | G | 1 | a0001c0001t0008 | 2 | HG01099.hp2 HG03239.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2305T>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 29/29 | 2305 | chr13 | 98024127 | ||||||
| chr13:98024140 | A | G | 1 | a0001c0001t0008 | 2 | HG01099.hp2 HG03239.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2318A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 29/29 | 2318 | chr13 | 98024140 | ||||||
| chr13:98024222 | C | T | 2 | a0001c0004t0005 a0001c0004t0022 |
9 | NA18950.hp2 NA18966.hp1 NA18982.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2400C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 29/29 | 2400 | chr13 | 98024222 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:97953771 | C | A | 1 | a0001c0001t0001g0011 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-193+55C>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 1/28 | chr13 | 97953771 | |||||||
| chr13:97953943 | G | A | 1 | a0001c0001t0001g0012 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-192-176G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 1/28 | chr13 | 97953943 | |||||||
| chr13:97954348 | G | A | 64 | a0001c0001t0001g0012 a0001c0001t0002g0039 a0001c0002t0003g0014 others(61): Show |
66 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.-113+150G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97954348 | |||||||
| chr13:97954489 | C | A | 1 | a0005c0006t0004g0013 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-113+291C>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97954489 | |||||||
| chr13:97954502 | T | C | 41 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0074 others(38): Show |
44 | HG01109.hp1 HG01361.hp1 HG01884.hp1 others(41): Show |
intron_variant | MODIFIER | c.-113+304T>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97954502 | |||||||
| chr13:97954504 | G | A | 1 | a0001c0001t0002g0112 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-113+306G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97954504 | |||||||
| chr13:97954526 | G | A | 10 | a0001c0001t0001g0011 a0001c0001t0001g0113 a0001c0001t0001g0114 others(7): Show |
10 | HG00639.hp1 HG01517.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.-113+328G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97954526 | |||||||
| chr13:97954650 | C | T | 3 | a0001c0001t0001g0368 a0001c0001t0001g0369 a0001c0001t0001g0370 |
3 | HG02451.hp2 HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.-113+452C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97954650 | |||||||
| chr13:97954786 | C | A | 1 | a0001c0002t0003g0014 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-113+588C>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97954786 | |||||||
| chr13:97954813 | G | A | 5 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0115 others(2): Show |
5 | HG01884.hp2 HG03209.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-113+615G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97954813 | |||||||
| chr13:97954824 | G | C | 2 | a0001c0003t0001g0122 a0001c0003t0001g0123 |
2 | NA18998.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.-113+626G>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97954824 | |||||||
| chr13:97954852 | T | A | 9 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0112 others(6): Show |
11 | HG01192.hp1 HG01243.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.-113+654T>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97954852 | |||||||
| chr13:97954872 | T | C | 2 | a0001c0001t0002g0130 a0001c0001t0002g0131 |
2 | HG00099.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.-113+674T>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97954872 | |||||||
| chr13:97954938 | A | C | 1 | a0001c0001t0012g0359 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-113+740A>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97954938 | |||||||
| chr13:97954938 | A | G | 8 | a0001c0001t0001g0360 a0001c0001t0001g0361 a0001c0001t0001g0362 others(5): Show |
8 | HG01109.hp2 HG01123.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.-113+740A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97954938 | |||||||
| chr13:97954945 | C | T | 1 | a0001c0001t0012g0359 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-113+747C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97954945 | |||||||
| chr13:97955042 | A | T | 9 | a0001c0004t0005g0010 a0001c0004t0005g0352 a0001c0004t0005g0353 others(6): Show |
9 | NA18950.hp2 NA18966.hp1 NA18982.hp1 others(6): Show |
intron_variant | MODIFIER | c.-113+844A>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97955042 | |||||||
| chr13:97955229 | G | GA | 22 | a0001c0001t0001g0003 a0001c0001t0001g0074 a0001c0001t0001g0075 others(19): Show |
23 | HG01109.hp1 HG01361.hp1 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.-113+1043dupA | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr13 | 97955229 | ||||||
| chr13:97956081 | A | G | 1 | a0001c0001t0012g0359 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-113+1883A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97956081 | |||||||
| chr13:97956128 | T | C | 1 | a0001c0001t0001g0132 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-113+1930T>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97956128 | |||||||
| chr13:97956131 | C | CA | 57 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0139 others(54): Show |
57 | HG00099.hp1 HG00544.hp1 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.-113+1946dupA | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr13 | 97956131 | ||||||
| chr13:97956146 | G | A | 1 | a0001c0001t0012g0359 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-113+1948G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97956146 | |||||||
| chr13:97956196 | G | A | 2 | a0001c0001t0002g0133 a0001c0001t0002g0134 |
2 | NA18952.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.-113+1998G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97956196 | |||||||
| chr13:97956210 | G | A | 1 | a0001c0001t0002g0135 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-113+2012G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97956210 | |||||||
| chr13:97956518 | G | A | 1 | a0001c0001t0002g0136 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-113+2320G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97956518 | |||||||
| chr13:97956856 | G | A | 4 | a0001c0001t0001g0004 a0001c0001t0001g0095 a0001c0001t0001g0096 others(1): Show |
5 | HG02615.hp1 HG03471.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-113+2658G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97956856 | |||||||
| chr13:97956880 | T | G | 1 | a0001c0001t0001g0187 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-113+2682T>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97956880 | |||||||
| chr13:97956993 | G | A | 2 | a0001c0001t0001g0074 a0001c0001t0001g0188 |
2 | HG01891.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.-113+2795G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97956993 | |||||||
| chr13:97957090 | T | C | 3 | a0001c0001t0001g0189 a0001c0001t0018g0190 a0001c0018t0001g0191 |
3 | HG02257.hp2 HG02723.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-113+2892T>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97957090 | |||||||
| chr13:97957221 | T | G | 1 | a0001c0001t0012g0359 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-113+3023T>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97957221 | |||||||
| chr13:97957562 | T | C | 2 | a0001c0001t0001g0075 a0001c0001t0001g0076 |
2 | HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-113+3364T>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97957562 | |||||||
| chr13:97957846 | A | G | 1 | a0001c0001t0002g0186 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-113+3648A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97957846 | |||||||
| chr13:97958049 | A | T | 1 | a0001c0001t0001g0188 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-113+3851A>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97958049 | |||||||
| chr13:97958132 | A | C | 1 | a0001c0018t0001g0191 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-113+3934A>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97958132 | |||||||
| chr13:97958246 | C | T | 9 | a0001c0001t0001g0350 a0001c0001t0001g0351 a0001c0005t0001g0185 others(6): Show |
9 | HG01192.hp2 HG01891.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.-113+4048C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97958246 | |||||||
| chr13:97958305 | A | G | 4 | a0001c0001t0001g0004 a0001c0001t0001g0095 a0001c0001t0001g0096 others(1): Show |
5 | HG02615.hp1 HG03471.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-113+4107A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97958305 | |||||||
| chr13:97958423 | C | T | 3 | a0001c0001t0020g0341 a0001c0003t0001g0342 a0001c0003t0001g0343 |
3 | NA18984.hp2 NA19056.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.-113+4225C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97958423 | |||||||
| chr13:97958424 | G | A | 9 | a0001c0004t0005g0010 a0001c0004t0005g0352 a0001c0004t0005g0353 others(6): Show |
9 | NA18950.hp2 NA18966.hp1 NA18982.hp1 others(6): Show |
intron_variant | MODIFIER | c.-113+4226G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97958424 | |||||||
| chr13:97958578 | T | C | 39 | a0001c0001t0001g0132 a0001c0001t0001g0137 a0001c0001t0001g0187 others(36): Show |
39 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.-113+4380T>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97958578 | |||||||
| chr13:97958607 | C | T | 38 | a0001c0001t0001g0132 a0001c0001t0001g0137 a0001c0001t0001g0187 others(35): Show |
38 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.-113+4409C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97958607 | |||||||
| chr13:97958667 | A | G | 1 | a0001c0001t0001g0221 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-113+4469A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97958667 | |||||||
| chr13:97958852 | A | G | 252 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(249): Show |
260 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(257): Show |
intron_variant | MODIFIER | c.-113+4654A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97958852 | |||||||
| chr13:97958877 | T | C | 1 | a0001c0002t0003g0016 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-113+4679T>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97958877 | |||||||
| chr13:97958899 | C | T | 1 | a0001c0001t0001g0325 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-113+4701C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97958899 | |||||||
| chr13:97958900 | G | A | 11 | a0001c0001t0001g0138 a0001c0001t0001g0222 a0001c0001t0001g0223 others(8): Show |
11 | HG00438.hp2 HG00558.hp2 HG02155.hp2 others(8): Show |
intron_variant | MODIFIER | c.-113+4702G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97958900 | |||||||
| chr13:97958950 | T | C | 9 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(6): Show |
10 | HG02523.hp1 HG02965.hp2 HG03239.hp2 others(7): Show |
intron_variant | MODIFIER | c.-113+4752T>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97958950 | |||||||
| chr13:97959032 | C | T | 1 | a0001c0002t0003g0073 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-113+4834C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97959032 | |||||||
| chr13:97959041 | G | A | 1 | a0001c0001t0001g0326 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-113+4843G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97959041 | |||||||
| chr13:97959180 | A | G | 3 | a0001c0002t0003g0014 a0001c0002t0003g0071 a0001c0002t0003g0072 |
3 | HG03654.hp2 HG04199.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.-113+4982A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97959180 | |||||||
| chr13:97959472 | A | G | 2 | a0001c0001t0001g0011 a0001c0001t0001g0121 |
2 | HG02976.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-113+5274A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97959472 | |||||||
| chr13:97959526 | A | C | 2 | a0001c0001t0001g0323 a0001c0001t0001g0324 |
2 | NA18974.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.-113+5328A>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97959526 | |||||||
| chr13:97959697 | G | A | 5 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0001g0234 others(2): Show |
5 | HG00733.hp1 HG00741.hp1 HG01070.hp1 others(2): Show |
intron_variant | MODIFIER | c.-113+5499G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97959697 | |||||||
| chr13:97959722 | G | T | 6 | a0001c0001t0001g0335 a0001c0001t0001g0336 a0001c0001t0001g0337 others(3): Show |
6 | HG01975.hp2 HG02647.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.-113+5524G>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97959722 | |||||||
| chr13:97959773 | T | A | 119 | a0001c0001t0001g0012 a0001c0001t0001g0132 a0001c0001t0001g0137 others(116): Show |
121 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.-113+5575T>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97959773 | |||||||
| chr13:97959909 | G | A | 7 | a0001c0005t0001g0185 a0001c0005t0001g0344 a0001c0005t0001g0345 others(4): Show |
7 | HG01192.hp2 HG01891.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.-113+5711G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97959909 | |||||||
| chr13:97960236 | G | A | 9 | a0001c0002t0003g0018 a0001c0002t0003g0019 a0001c0002t0003g0020 others(6): Show |
9 | HG00423.hp2 HG00639.hp2 HG01069.hp2 others(6): Show |
intron_variant | MODIFIER | c.-113+6038G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97960236 | |||||||
| chr13:97960429 | G | A | 119 | a0001c0001t0001g0012 a0001c0001t0001g0132 a0001c0001t0001g0137 others(116): Show |
121 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.-113+6231G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97960429 | |||||||
| chr13:97960495 | T | C | 4 | a0001c0001t0001g0004 a0001c0001t0001g0095 a0001c0001t0001g0096 others(1): Show |
5 | HG02615.hp1 HG03471.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-113+6297T>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97960495 | |||||||
| chr13:97960541 | C | CT | 248 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(245): Show |
256 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(253): Show |
intron_variant | MODIFIER | c.-113+6348dupT | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr13 | 97960541 | ||||||
| chr13:97960561 | G | GT | 25 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0098 others(22): Show |
25 | HG00438.hp2 HG00558.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.-113+6377dupT | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr13 | 97960561 | ||||||
| chr13:97960561 | GT | G | 108 | a0001c0001t0001g0012 a0001c0001t0001g0132 a0001c0001t0001g0137 others(105): Show |
110 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(107): Show |
intron_variant | MODIFIER | c.-113+6377delT | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr13 | 97960561 | ||||||
| chr13:97960628 | G | A | 11 | a0001c0001t0001g0350 a0001c0001t0001g0351 a0001c0004t0005g0010 others(8): Show |
11 | HG02622.hp2 HG03453.hp2 NA18950.hp2 others(8): Show |
intron_variant | MODIFIER | c.-113+6430G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97960628 | |||||||
| chr13:97960706 | G | A | 4 | a0001c0001t0002g0006 a0001c0001t0002g0112 a0001c0001t0002g0124 others(1): Show |
5 | HG01192.hp1 HG02280.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-113+6508G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97960706 | |||||||
| chr13:97960806 | G | A | 8 | a0001c0001t0001g0360 a0001c0001t0001g0361 a0001c0001t0001g0362 others(5): Show |
8 | HG01109.hp2 HG01123.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.-113+6608G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97960806 | |||||||
| chr13:97960822 | G | T | 1 | a0001c0001t0001g0092 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-113+6624G>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97960822 | |||||||
| chr13:97960902 | T | C | 65 | a0001c0001t0001g0012 a0001c0001t0002g0039 a0001c0002t0001g0327 others(62): Show |
67 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.-113+6704T>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97960902 | |||||||
| chr13:97961071 | C | CA | 20 | a0001c0001t0001g0138 a0001c0001t0001g0222 a0001c0001t0001g0223 others(17): Show |
20 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.-113+6880dupA | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr13 | 97961071 | ||||||
| chr13:97961107 | A | C | 8 | a0001c0001t0001g0360 a0001c0001t0001g0361 a0001c0001t0001g0362 others(5): Show |
8 | HG01109.hp2 HG01123.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.-113+6909A>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97961107 | |||||||
| chr13:97961401 | G | A | 39 | a0001c0001t0001g0132 a0001c0001t0001g0137 a0001c0001t0001g0187 others(36): Show |
39 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.-113+7203G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97961401 | |||||||
| chr13:97961413 | C | A | 6 | a0001c0001t0001g0012 a0001c0002t0003g0027 a0001c0002t0003g0028 others(3): Show |
6 | HG00423.hp1 HG02027.hp2 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.-113+7215C>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97961413 | |||||||
| chr13:97961571 | C | T | 3 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0120 |
3 | HG00639.hp1 HG01517.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.-113+7373C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97961571 | |||||||
| chr13:97961625 | T | C | 1 | a0001c0001t0001g0316 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-113+7427T>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97961625 | |||||||
| chr13:97961674 | T | A | 39 | a0001c0001t0001g0132 a0001c0001t0001g0137 a0001c0001t0001g0187 others(36): Show |
39 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.-113+7476T>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97961674 | |||||||
| chr13:97961893 | C | G | 1 | a0001c0001t0001g0326 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-113+7695C>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97961893 | |||||||
| chr13:97961998 | G | A | 8 | a0001c0001t0001g0328 a0001c0001t0001g0335 a0001c0001t0001g0336 others(5): Show |
8 | HG01975.hp2 HG02647.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.-112-7725G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97961998 | |||||||
| chr13:97962049 | A | C | 7 | a0001c0001t0001g0310 a0001c0001t0001g0311 a0001c0001t0001g0312 others(4): Show |
7 | HG00438.hp1 NA18944.hp2 NA18949.hp2 others(4): Show |
intron_variant | MODIFIER | c.-112-7674A>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97962049 | |||||||
| chr13:97962050 | A | T | 7 | a0001c0001t0001g0335 a0001c0001t0001g0336 a0001c0001t0001g0337 others(4): Show |
7 | HG01975.hp2 HG02647.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.-112-7673A>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97962050 | |||||||
| chr13:97962197 | GTCCTTAA others(14): Show |
G | 2 | a0001c0001t0002g0154 a0001c0001t0002g0155 |
2 | HG02300.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.-112-7524_-112-750 others(25): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr13 | 97962197 | ||||||
| chr13:97962219 | T | A | 2 | a0001c0001t0002g0154 a0001c0001t0002g0155 |
2 | HG02300.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.-112-7504T>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97962219 | |||||||
| chr13:97962356 | G | C | 1 | a0001c0002t0003g0025 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-112-7367G>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97962356 | |||||||
| chr13:97962429 | C | T | 1 | a0001c0001t0001g0216 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-112-7294C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97962429 | |||||||
| chr13:97962683 | G | T | 1 | a0001c0001t0001g0098 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-112-7040G>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97962683 | |||||||
| chr13:97962696 | G | A | 2 | a0001c0001t0001g0326 a0001c0001t0001g0329 |
2 | HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-112-7027G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97962696 | |||||||
| chr13:97962761 | G | A | 3 | a0001c0001t0001g0241 a0001c0001t0001g0242 a0001c0001t0001g0243 |
3 | HG00738.hp2 HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.-112-6962G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97962761 | |||||||
| chr13:97962816 | CA | C | 8 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(5): Show |
8 | HG01109.hp1 HG02055.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.-112-6893delA | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr13 | 97962816 | ||||||
| chr13:97962859 | T | C | 1 | a0001c0018t0001g0191 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-112-6864T>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97962859 | |||||||
| chr13:97963018 | T | C | 1 | a0001c0001t0002g0156 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-112-6705T>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97963018 | |||||||
| chr13:97963248 | C | G | 1 | a0001c0002t0001g0327 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-112-6475C>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97963248 | |||||||
| chr13:97963372 | C | CT | 25 | a0001c0001t0001g0074 a0001c0001t0001g0149 a0001c0001t0001g0304 others(22): Show |
25 | HG00738.hp1 HG01109.hp2 HG01978.hp1 others(22): Show |
intron_variant | MODIFIER | c.-112-6335dupT | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr13 | 97963372 | ||||||
| chr13:97963372 | CT | C | 9 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0002g0130 others(6): Show |
9 | HG00099.hp1 HG01361.hp2 HG01975.hp1 others(6): Show |
intron_variant | MODIFIER | c.-112-6335delT | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr13 | 97963372 | ||||||
| chr13:97963402 | G | A | 64 | a0001c0001t0002g0039 a0001c0002t0001g0327 a0001c0002t0003g0014 others(61): Show |
66 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.-112-6321G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97963402 | |||||||
| chr13:97963451 | T | C | 251 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(248): Show |
259 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(256): Show |
intron_variant | MODIFIER | c.-112-6272T>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97963451 | |||||||
| chr13:97963526 | C | T | 1 | a0001c0001t0001g0303 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-112-6197C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97963526 | |||||||
| chr13:97963556 | G | A | 1 | a0001c0001t0001g0335 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-112-6167G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97963556 | |||||||
| chr13:97963615 | G | A | 2 | a0001c0001t0001g0192 a0001c0001t0001g0193 |
2 | HG02071.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.-112-6108G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97963615 | |||||||
| chr13:97963663 | C | T | 4 | a0001c0001t0006g0009 a0001c0001t0006g0331 a0001c0001t0006g0332 others(1): Show |
5 | HG01243.hp1 HG02559.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-112-6060C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97963663 | |||||||
| chr13:97963845 | C | G | 1 | a0001c0002t0003g0030 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-112-5878C>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97963845 | |||||||
| chr13:97964041 | G | A | 7 | a0001c0001t0001g0011 a0001c0001t0001g0113 a0001c0001t0001g0114 others(4): Show |
7 | HG01884.hp2 HG02976.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.-112-5682G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97964041 | |||||||
| chr13:97964443 | C | CT | 22 | a0001c0001t0001g0074 a0001c0001t0001g0111 a0001c0001t0001g0117 others(19): Show |
22 | HG00597.hp1 HG01175.hp1 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.-112-5259dupT | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr13 | 97964443 | ||||||
| chr13:97964443 | CT | C | 43 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0222 others(40): Show |
43 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(40): Show |
intron_variant | MODIFIER | c.-112-5259delT | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr13 | 97964443 | ||||||
| chr13:97964443 | CTTTTTTT others(5): Show |
C | 4 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0077 others(1): Show |
4 | HG02486.hp2 HG02809.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-112-5270_-112-525 others(16): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr13 | 97964443 | ||||||
| chr13:97964509 | G | T | 64 | a0001c0001t0002g0039 a0001c0002t0001g0327 a0001c0002t0003g0014 others(61): Show |
66 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.-112-5214G>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97964509 | |||||||
| chr13:97964604 | A | C | 1 | a0001c0010t0002g0180 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-112-5119A>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97964604 | |||||||
| chr13:97964640 | G | A | 2 | a0001c0001t0001g0305 a0001c0001t0001g0306 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-112-5083G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97964640 | |||||||
| chr13:97964651 | G | A | 53 | a0001c0001t0001g0328 a0001c0001t0001g0350 a0001c0001t0001g0351 others(50): Show |
55 | HG00099.hp1 HG00642.hp1 HG00741.hp2 others(52): Show |
intron_variant | MODIFIER | c.-112-5072G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97964651 | |||||||
| chr13:97964729 | G | A | 4 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0092 others(1): Show |
4 | HG02280.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-112-4994G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97964729 | |||||||
| chr13:97964778 | T | C | 6 | a0001c0001t0002g0039 a0001c0002t0003g0026 a0001c0002t0003g0036 others(3): Show |
6 | NA18612.hp2 NA18959.hp2 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.-112-4945T>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97964778 | |||||||
| chr13:97964783 | C | T | 1 | a0001c0002t0003g0064 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-112-4940C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97964783 | |||||||
| chr13:97964849 | C | T | 9 | a0001c0004t0005g0010 a0001c0004t0005g0352 a0001c0004t0005g0353 others(6): Show |
9 | NA18950.hp2 NA18966.hp1 NA18982.hp1 others(6): Show |
intron_variant | MODIFIER | c.-112-4874C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97964849 | |||||||
| chr13:97965189 | G | T | 4 | a0001c0001t0001g0004 a0001c0001t0001g0095 a0001c0001t0001g0096 others(1): Show |
5 | HG02615.hp1 HG03471.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-112-4534G>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97965189 | |||||||
| chr13:97965191 | G | C | 1 | a0001c0001t0001g0326 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-112-4532G>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97965191 | |||||||
| chr13:97965223 | G | A | 1 | a0001c0001t0001g0350 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-112-4500G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97965223 | |||||||
| chr13:97965304 | C | G | 43 | a0001c0001t0002g0039 a0001c0001t0002g0130 a0001c0001t0002g0131 others(40): Show |
43 | HG00099.hp1 HG00642.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.-112-4419C>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97965304 | |||||||
| chr13:97965332 | A | G | 2 | a0001c0001t0001g0080 a0001c0001t0001g0093 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-112-4391A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97965332 | |||||||
| chr13:97965497 | T | C | 12 | a0001c0001t0001g0074 a0001c0001t0001g0118 a0001c0001t0001g0119 others(9): Show |
13 | HG00639.hp1 HG01243.hp1 HG01517.hp1 others(10): Show |
intron_variant | MODIFIER | c.-112-4226T>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97965497 | |||||||
| chr13:97965549 | TCAGCATA others(9): Show |
T | 1 | a0001c0002t0003g0026 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-112-4170_-112-415 others(20): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr13 | 97965549 | ||||||
| chr13:97965563 | C | T | 1 | a0001c0001t0001g0365 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-112-4160C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97965563 | |||||||
| chr13:97965711 | G | A | 1 | a0001c0001t0001g0300 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-112-4012G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97965711 | |||||||
| chr13:97965752 | AGTTTGT | A | 3 | a0001c0001t0001g0003 a0001c0001t0001g0081 a0001c0001t0001g0082 |
4 | HG01884.hp1 HG02486.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-112-3968_-112-396 others(10): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr13 | 97965752 | ||||||
| chr13:97965755 | T | TTG | 10 | a0001c0001t0001g0256 a0001c0001t0001g0274 a0001c0001t0001g0275 others(7): Show |
10 | HG00609.hp2 HG01099.hp1 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.-112-3937_-112-393 others(6): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr13 | 97965755 | ||||||
| chr13:97965755 | TTG | T | 158 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0076 others(155): Show |
163 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(160): Show |
intron_variant | MODIFIER | c.-112-3937_-112-393 others(6): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr13 | 97965755 | ||||||
| chr13:97965755 | TTGTG | T | 69 | a0001c0001t0001g0075 a0001c0001t0001g0087 a0001c0001t0001g0094 others(66): Show |
70 | HG00423.hp2 HG00558.hp1 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.-112-3939_-112-393 others(8): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr13 | 97965755 | ||||||
| chr13:97965755 | TTGTGTGT others(3): Show |
T | 1 | a0001c0001t0001g0366 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-112-3945_-112-393 others(14): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr13 | 97965755 | ||||||
| chr13:97965772 | T | C | 1 | a0001c0002t0003g0040 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-112-3951T>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97965772 | |||||||
| chr13:97965877 | G | T | 1 | a0001c0001t0001g0328 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-112-3846G>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97965877 | |||||||
| chr13:97965901 | C | T | 8 | a0001c0001t0001g0132 a0001c0001t0001g0208 a0001c0001t0001g0209 others(5): Show |
8 | HG00597.hp1 HG02015.hp1 NA18969.hp1 others(5): Show |
intron_variant | MODIFIER | c.-112-3822C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97965901 | |||||||
| chr13:97966057 | C | G | 51 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0112 others(48): Show |
53 | HG00099.hp1 HG00642.hp1 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.-112-3666C>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97966057 | |||||||
| chr13:97966133 | C | CA | 31 | a0001c0001t0001g0074 a0001c0001t0001g0094 a0001c0001t0001g0099 others(28): Show |
31 | HG00741.hp2 HG01175.hp1 HG01884.hp2 others(28): Show |
intron_variant | MODIFIER | c.-112-3568dupA | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr13 | 97966133 | ||||||
| chr13:97966133 | CA | C | 117 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(114): Show |
119 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.-112-3568delA | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr13 | 97966133 | ||||||
| chr13:97966133 | CAA | C | 34 | a0001c0001t0001g0241 a0001c0001t0001g0295 a0001c0001t0001g0296 others(31): Show |
36 | HG00423.hp2 HG00621.hp2 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.-112-3569_-112-356 others(6): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr13 | 97966133 | ||||||
| chr13:97966133 | CAAA | C | 30 | a0001c0002t0003g0015 a0001c0002t0003g0016 a0001c0002t0003g0026 others(27): Show |
30 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(27): Show |
intron_variant | MODIFIER | c.-112-3570_-112-356 others(7): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr13 | 97966133 | ||||||
| chr13:97966261 | T | A | 9 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0112 others(6): Show |
11 | HG01192.hp1 HG01243.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.-112-3462T>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97966261 | |||||||
| chr13:97966282 | T | G | 2 | a0001c0001t0001g0143 a0001c0001t0001g0264 |
2 | HG00735.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.-112-3441T>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97966282 | |||||||
| chr13:97966328 | G | A | 1 | a0001c0001t0001g0301 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-112-3395G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97966328 | |||||||
| chr13:97966355 | C | A | 2 | a0001c0001t0002g0154 a0001c0001t0002g0155 |
2 | HG02300.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.-112-3368C>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97966355 | |||||||
| chr13:97966404 | G | A | 6 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0001g0252 others(3): Show |
6 | HG00642.hp2 HG00733.hp2 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.-112-3319G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97966404 | |||||||
| chr13:97966573 | T | C | 1 | a0001c0001t0001g0329 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-112-3150T>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97966573 | |||||||
| chr13:97966852 | A | G | 1 | a0001c0001t0001g0329 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-112-2871A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97966852 | |||||||
| chr13:97966925 | A | T | 1 | a0001c0001t0018g0190 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-112-2798A>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97966925 | |||||||
| chr13:97966992 | C | T | 62 | a0001c0002t0003g0014 a0001c0002t0003g0015 a0001c0002t0003g0016 others(59): Show |
64 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.-112-2731C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97966992 | |||||||
| chr13:97967122 | A | G | 1 | a0004c0019t0001g0340 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-112-2601A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97967122 | |||||||
| chr13:97967490 | A | G | 1 | a0001c0001t0001g0109 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-112-2233A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97967490 | |||||||
| chr13:97967630 | C | CTGTT | 8 | a0001c0001t0001g0189 a0001c0001t0001g0291 a0001c0001t0001g0292 others(5): Show |
8 | HG01261.hp1 HG01934.hp1 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.-112-2070_-112-206 others(8): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr13 | 97967630 | ||||||
| chr13:97967630 | CTGTT | C | 3 | a0001c0001t0001g0074 a0001c0001t0001g0188 a0001c0001t0001g0339 |
3 | HG01891.hp2 HG01975.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.-112-2070_-112-206 others(8): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr13 | 97967630 | ||||||
| chr13:97967761 | A | G | 9 | a0001c0004t0005g0010 a0001c0004t0005g0352 a0001c0004t0005g0353 others(6): Show |
9 | NA18950.hp2 NA18966.hp1 NA18982.hp1 others(6): Show |
intron_variant | MODIFIER | c.-112-1962A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97967761 | |||||||
| chr13:97967831 | C | A | 1 | a0001c0002t0003g0049 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-112-1892C>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97967831 | |||||||
| chr13:97967875 | C | T | 7 | a0001c0001t0001g0011 a0001c0001t0001g0113 a0001c0001t0001g0114 others(4): Show |
7 | HG01884.hp2 HG02976.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.-112-1848C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97967875 | |||||||
| chr13:97967921 | G | A | 63 | a0001c0001t0002g0039 a0001c0002t0003g0014 a0001c0002t0003g0015 others(60): Show |
65 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.-112-1802G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97967921 | |||||||
| chr13:97967926 | C | T | 39 | a0001c0001t0001g0132 a0001c0001t0001g0137 a0001c0001t0001g0187 others(36): Show |
39 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.-112-1797C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97967926 | |||||||
| chr13:97968020 | C | T | 1 | a0001c0001t0001g0248 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-112-1703C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97968020 | |||||||
| chr13:97968519 | ATTCTGTC others(4): Show |
A | 2 | a0001c0002t0003g0024 a0001c0002t0003g0025 |
2 | HG00423.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.-112-1201_-112-119 others(15): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr13 | 97968519 | ||||||
| chr13:97968520 | T | C | 8 | a0001c0001t0020g0341 a0001c0003t0001g0122 a0001c0003t0001g0123 others(5): Show |
8 | NA18957.hp1 NA18984.hp2 NA18998.hp1 others(5): Show |
intron_variant | MODIFIER | c.-112-1203T>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97968520 | |||||||
| chr13:97968554 | G | A | 5 | a0001c0001t0002g0135 a0001c0001t0002g0158 a0001c0001t0002g0160 others(2): Show |
5 | HG01167.hp1 HG01168.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.-112-1169G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97968554 | |||||||
| chr13:97968705 | T | C | 9 | a0001c0004t0005g0010 a0001c0004t0005g0352 a0001c0004t0005g0353 others(6): Show |
9 | NA18950.hp2 NA18966.hp1 NA18982.hp1 others(6): Show |
intron_variant | MODIFIER | c.-112-1018T>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97968705 | |||||||
| chr13:97968723 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-112-1000C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97968723 | |||||||
| chr13:97968798 | C | A | 62 | a0001c0002t0003g0014 a0001c0002t0003g0015 a0001c0002t0003g0016 others(59): Show |
64 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.-112-925C>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97968798 | |||||||
| chr13:97969013 | G | A | 1 | a0001c0001t0001g0195 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-112-710G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97969013 | |||||||
| chr13:97969153 | G | GTA | 22 | a0001c0001t0001g0003 a0001c0001t0001g0075 a0001c0001t0001g0076 others(19): Show |
23 | HG00733.hp1 HG00735.hp2 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.-112-548_-112-547d others(4): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr13 | 97969153 | ||||||
| chr13:97969153 | G | GTATA | 5 | a0001c0001t0010g0255 a0001c0003t0001g0122 a0001c0003t0001g0123 others(2): Show |
5 | HG03516.hp2 NA18957.hp1 NA18998.hp1 others(2): Show |
intron_variant | MODIFIER | c.-112-550_-112-547d others(6): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr13 | 97969153 | ||||||
| chr13:97969153 | G | GTATATAT others(3): Show |
4 | a0001c0001t0002g0164 a0001c0001t0002g0165 a0001c0001t0002g0168 others(1): Show |
4 | HG00642.hp1 HG02602.hp2 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.-112-556_-112-547d others(12): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr13 | 97969153 | ||||||
| chr13:97969153 | G | GTATATAT others(5): Show |
6 | a0001c0001t0002g0136 a0001c0001t0002g0159 a0001c0001t0002g0161 others(3): Show |
6 | HG00735.hp1 HG00741.hp2 HG01081.hp1 others(3): Show |
intron_variant | MODIFIER | c.-112-558_-112-547d others(14): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr13 | 97969153 | ||||||
| chr13:97969153 | G | GTATATAT others(7): Show |
1 | a0001c0001t0002g0154 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-112-560_-112-547d others(16): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr13 | 97969153 | ||||||
| chr13:97969153 | G | GTATATAT others(9): Show |
1 | a0001c0001t0002g0163 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-112-562_-112-547d others(18): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr13 | 97969153 | ||||||
| chr13:97969171 | A | ATTT | 3 | a0001c0001t0001g0188 a0001c0001t0001g0195 a0001c0001t0018g0190 |
3 | HG01891.hp2 HG02165.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.-112-551_-112-550i others(5): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr13 | 97969171 | ||||||
| chr13:97969173 | A | AT | 9 | a0001c0001t0001g0261 a0001c0001t0001g0329 a0001c0001t0001g0360 others(6): Show |
9 | HG02258.hp1 HG02896.hp1 NA18950.hp2 others(6): Show |
intron_variant | MODIFIER | c.-112-549dupT | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr13 | 97969173 | ||||||
| chr13:97969173 | A | ATT | 9 | a0001c0001t0001g0087 a0001c0001t0001g0094 a0001c0001t0001g0212 others(6): Show |
9 | HG01109.hp1 HG02055.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.-112-549_-112-548i others(4): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr13 | 97969173 | ||||||
| chr13:97969173 | A | ATTT | 5 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0208 others(2): Show |
5 | HG02071.hp1 HG02080.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-112-549_-112-548i others(5): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr13 | 97969173 | ||||||
| chr13:97969173 | A | ATTTT | 6 | a0001c0001t0001g0074 a0001c0001t0001g0206 a0001c0001t0001g0213 others(3): Show |
6 | HG01192.hp2 HG01243.hp2 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.-112-549_-112-548i others(6): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr13 | 97969173 | ||||||
| chr13:97969173 | A | T | 12 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0115 others(9): Show |
12 | HG01243.hp1 HG01884.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.-112-550A>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97969173 | |||||||
| chr13:97969173 | ATATTTTT others(7): Show |
A | 4 | a0001c0001t0001g0004 a0001c0001t0001g0095 a0001c0001t0001g0096 others(1): Show |
4 | HG02615.hp1 HG03540.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.-112-548_-112-535d others(16): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr13 | 97969173 | ||||||
| chr13:97969175 | A | AT | 14 | a0001c0001t0001g0078 a0001c0001t0001g0104 a0001c0001t0001g0106 others(11): Show |
15 | HG00738.hp1 HG02451.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.-112-524dupT | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr13 | 97969175 | ||||||
| chr13:97969175 | A | ATAT | 15 | a0001c0001t0001g0088 a0001c0001t0001g0090 a0001c0001t0001g0091 others(12): Show |
15 | HG02630.hp2 HG02886.hp2 HG02965.hp2 others(12): Show |
intron_variant | MODIFIER | c.-112-547_-112-546i others(5): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr13 | 97969175 | ||||||
| chr13:97969175 | A | ATATATAT others(4): Show |
2 | a0001c0001t0002g0151 a0001c0001t0002g0184 |
2 | HG02109.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.-112-547_-112-546i others(13): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr13 | 97969175 | ||||||
| chr13:97969175 | A | ATATATAT others(6): Show |
1 | a0001c0001t0002g0133 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-112-547_-112-546i others(15): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr13 | 97969175 | ||||||
| chr13:97969175 | A | ATATATAT others(7): Show |
1 | a0001c0001t0002g0175 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-112-547_-112-546i others(16): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr13 | 97969175 | ||||||
| chr13:97969175 | A | ATATATAT others(5): Show |
3 | a0001c0001t0002g0153 a0001c0001t0002g0162 a0001c0001t0002g0181 |
3 | HG01175.hp1 HG02148.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.-112-547_-112-546i others(14): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr13 | 97969175 | ||||||
| chr13:97969175 | A | ATATATAT others(6): Show |
1 | a0001c0001t0002g0134 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-112-547_-112-546i others(15): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr13 | 97969175 | ||||||
| chr13:97969175 | A | ATATATAT others(3): Show |
6 | a0001c0001t0002g0171 a0001c0001t0002g0176 a0001c0001t0002g0179 others(3): Show |
6 | HG01123.hp2 HG01928.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.-112-547_-112-546i others(12): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr13 | 97969175 | ||||||
| chr13:97969175 | A | ATATATAT others(4): Show |
2 | a0001c0001t0002g0177 a0001c0001t0008g0173 |
2 | HG02738.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.-112-547_-112-546i others(13): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr13 | 97969175 | ||||||
| chr13:97969175 | A | ATATATAT others(5): Show |
1 | a0001c0001t0002g0131 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-112-547_-112-546i others(14): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr13 | 97969175 | ||||||
| chr13:97969175 | A | ATATATAT others(8): Show |
1 | a0001c0002t0003g0056 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-112-547_-112-546i others(17): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr13 | 97969175 | ||||||
| chr13:97969175 | A | ATATATAT others(3): Show |
1 | a0001c0001t0002g0152 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-112-547_-112-546i others(12): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr13 | 97969175 | ||||||
| chr13:97969175 | A | ATATATAT others(6): Show |
2 | a0001c0002t0003g0057 a0001c0002t0003g0058 |
2 | NA18980.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.-112-547_-112-546i others(15): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr13 | 97969175 | ||||||
| chr13:97969175 | A | ATATATTT others(3): Show |
15 | a0001c0001t0002g0130 a0001c0001t0002g0172 a0001c0002t0003g0019 others(12): Show |
17 | HG00099.hp1 HG01255.hp2 HG02027.hp2 others(14): Show |
intron_variant | MODIFIER | c.-112-547_-112-546i others(12): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr13 | 97969175 | ||||||
| chr13:97969175 | A | ATATATTT others(4): Show |
5 | a0001c0001t0001g0370 a0001c0002t0003g0034 a0001c0002t0003g0035 others(2): Show |
5 | HG02135.hp1 HG02630.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-112-547_-112-546i others(13): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr13 | 97969175 | ||||||
| chr13:97969175 | A | ATATATTT others(5): Show |
3 | a0001c0002t0003g0016 a0001c0002t0003g0067 a0001c0002t0003g0072 |
3 | HG03654.hp2 NA18950.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.-112-547_-112-546i others(14): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr13 | 97969175 | ||||||
| chr13:97969175 | A | ATATATTT others(6): Show |
1 | a0001c0002t0003g0014 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-112-547_-112-546i others(15): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr13 | 97969175 | ||||||
| chr13:97969175 | A | ATATTTTT others(2): Show |
7 | a0001c0001t0001g0369 a0001c0002t0003g0026 a0001c0002t0003g0053 others(4): Show |
7 | HG00558.hp1 HG02451.hp2 HG02523.hp2 others(4): Show |
intron_variant | MODIFIER | c.-112-547_-112-546i others(11): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr13 | 97969175 | ||||||
| chr13:97969175 | A | ATATTTTT others(3): Show |
14 | a0001c0001t0001g0326 a0001c0002t0001g0327 a0001c0002t0003g0022 others(11): Show |
14 | HG00423.hp2 HG00597.hp2 HG02132.hp2 others(11): Show |
intron_variant | MODIFIER | c.-112-547_-112-546i others(12): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr13 | 97969175 | ||||||
| chr13:97969175 | A | ATATTTTT others(4): Show |
5 | a0001c0002t0003g0018 a0001c0002t0003g0028 a0001c0002t0003g0041 others(2): Show |
5 | HG00639.hp2 HG01069.hp2 HG02015.hp2 others(2): Show |
intron_variant | MODIFIER | c.-112-547_-112-546i others(13): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr13 | 97969175 | ||||||
| chr13:97969175 | A | ATATTTTT others(5): Show |
1 | a0001c0002t0003g0059 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-112-547_-112-546i others(14): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr13 | 97969175 | ||||||
| chr13:97969175 | A | ATATTTTT others(6): Show |
1 | a0001c0002t0003g0066 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-112-547_-112-546i others(15): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr13 | 97969175 | ||||||
| chr13:97969175 | A | ATTT | 23 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0089 others(20): Show |
24 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.-112-526_-112-524d others(5): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr13 | 97969175 | ||||||
| chr13:97969175 | A | ATTTTTTT others(3): Show |
5 | a0001c0001t0002g0039 a0001c0002t0003g0029 a0001c0002t0003g0036 others(2): Show |
5 | HG00423.hp1 HG02040.hp2 NA18612.hp2 others(2): Show |
intron_variant | MODIFIER | c.-112-533_-112-524d others(12): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr13 | 97969175 | ||||||
| chr13:97969175 | A | ATTTTTTT others(4): Show |
2 | a0001c0001t0001g0121 a0001c0002t0003g0070 |
2 | NA19087.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-112-534_-112-524d others(13): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr13 | 97969175 | ||||||
| chr13:97969175 | A | T | 46 | a0001c0001t0001g0011 a0001c0001t0001g0074 a0001c0001t0001g0087 others(43): Show |
47 | HG00544.hp1 HG01109.hp1 HG01192.hp2 others(44): Show |
intron_variant | MODIFIER | c.-112-548A>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97969175 | |||||||
| chr13:97969175 | AT | A | 15 | a0001c0001t0001g0144 a0001c0001t0001g0241 a0001c0001t0001g0245 others(12): Show |
15 | HG00099.hp2 HG00642.hp2 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.-112-524delT | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr13 | 97969175 | ||||||
| chr13:97969175 | ATTTTTTT others(5): Show |
A | 1 | a0001c0001t0001g0004 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-112-535_-112-524d others(14): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr13 | 97969175 | ||||||
| chr13:97969175 | ATTTTTTT others(6): Show |
A | 1 | a0001c0001t0001g0108 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-112-536_-112-524d others(15): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr13 | 97969175 | ||||||
| chr13:97969176 | T | TA | 23 | a0001c0001t0001g0077 a0001c0001t0001g0081 a0001c0001t0001g0098 others(20): Show |
23 | HG00438.hp2 HG00558.hp2 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.-112-547_-112-546i others(3): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97969176 | |||||||
| chr13:97969176 | T | TATA | 6 | a0001c0001t0001g0080 a0001c0001t0001g0093 a0001c0001t0001g0103 others(3): Show |
6 | HG02523.hp1 HG02622.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-112-547_-112-546i others(5): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97969176 | |||||||
| chr13:97969176 | T | TATATA | 4 | a0001c0001t0001g0083 a0001c0001t0001g0109 a0001c0001t0001g0237 others(1): Show |
4 | HG01361.hp1 HG02080.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.-112-547_-112-546i others(7): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97969176 | |||||||
| chr13:97969176 | T | TATATATA others(4): Show |
2 | a0001c0001t0002g0156 a0001c0001t0002g0160 |
2 | HG01169.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.-112-547_-112-546i others(13): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97969176 | |||||||
| chr13:97969176 | T | TATATATA others(6): Show |
1 | a0001c0001t0002g0135 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-112-547_-112-546i others(15): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97969176 | |||||||
| chr13:97969177 | T | A | 28 | a0001c0001t0001g0075 a0001c0001t0001g0084 a0001c0001t0001g0140 others(25): Show |
28 | HG00642.hp1 HG00733.hp1 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.-112-546T>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97969177 | |||||||
| chr13:97969178 | T | A | 16 | a0001c0001t0001g0138 a0001c0001t0001g0222 a0001c0001t0001g0224 others(13): Show |
16 | HG00438.hp2 HG00558.hp2 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.-112-545T>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97969178 | |||||||
| chr13:97969179 | T | A | 8 | a0001c0001t0001g0223 a0001c0001t0001g0233 a0001c0001t0001g0234 others(5): Show |
8 | HG00642.hp1 HG00733.hp1 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.-112-544T>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97969179 | |||||||
| chr13:97969180 | T | A | 7 | a0001c0001t0001g0222 a0001c0001t0001g0225 a0001c0001t0001g0226 others(4): Show |
7 | HG00438.hp2 HG00558.hp2 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.-112-543T>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97969180 | |||||||
| chr13:97969182 | T | A | 1 | a0001c0001t0001g0226 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-112-541T>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97969182 | |||||||
| chr13:97969267 | T | C | 251 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(248): Show |
259 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(256): Show |
intron_variant | MODIFIER | c.-112-456T>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97969267 | |||||||
| chr13:97969314 | T | TG | 9 | a0001c0001t0002g0157 a0001c0001t0002g0165 a0001c0001t0002g0175 others(6): Show |
9 | HG00735.hp1 HG01928.hp1 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.-112-406dupG | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr13 | 97969314 | ||||||
| chr13:97969315 | G | A | 1 | a0001c0001t0002g0184 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-112-408G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97969315 | |||||||
| chr13:97969384 | G | A | 1 | a0001c0002t0003g0043 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-112-339G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97969384 | |||||||
| chr13:97969398 | G | A | 7 | a0001c0005t0001g0185 a0001c0005t0001g0344 a0001c0005t0001g0345 others(4): Show |
7 | HG01192.hp2 HG01891.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.-112-325G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97969398 | |||||||
| chr13:97969686 | C | T | 63 | a0001c0002t0003g0014 a0001c0002t0003g0015 a0001c0002t0003g0016 others(60): Show |
65 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.-112-37C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 2/28 | chr13 | 97969686 | |||||||
| chr13:97969836 | T | C | 1 | a0001c0001t0002g0168 | 1 | HG02602.hp2 | splice_region_variant&intron_variant | LOW | c.-5+6T>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | chr13 | 97969836 | |||||||
| chr13:97969933 | A | C | 52 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0039 others(49): Show |
54 | HG00099.hp1 HG00642.hp1 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.-5+103A>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | chr13 | 97969933 | |||||||
| chr13:97969979 | G | A | 2 | a0001c0001t0001g0074 a0001c0001t0001g0188 |
2 | HG01891.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.-5+149G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | chr13 | 97969979 | |||||||
| chr13:97970214 | T | C | 3 | a0001c0001t0001g0328 a0001c0001t0001g0350 a0001c0001t0001g0351 |
3 | HG02622.hp2 HG02922.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-5+384T>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | chr13 | 97970214 | |||||||
| chr13:97970352 | G | T | 1 | a0001c0001t0001g0091 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-5+522G>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | chr13 | 97970352 | |||||||
| chr13:97970448 | G | A | 63 | a0001c0002t0003g0014 a0001c0002t0003g0015 a0001c0002t0003g0016 others(60): Show |
65 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.-5+618G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | chr13 | 97970448 | |||||||
| chr13:97970506 | A | T | 1 | a0001c0002t0003g0026 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-5+676A>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | chr13 | 97970506 | |||||||
| chr13:97970619 | G | A | 4 | a0001c0001t0006g0009 a0001c0001t0006g0331 a0001c0001t0006g0332 others(1): Show |
5 | HG01243.hp1 HG02559.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-5+789G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | chr13 | 97970619 | |||||||
| chr13:97970754 | C | T | 63 | a0001c0002t0003g0014 a0001c0002t0003g0015 a0001c0002t0003g0016 others(60): Show |
65 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.-5+924C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | chr13 | 97970754 | |||||||
| chr13:97970895 | T | G | 4 | a0001c0001t0002g0163 a0001c0001t0002g0168 a0001c0001t0002g0183 others(1): Show |
4 | HG01346.hp2 HG02602.hp2 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.-5+1065T>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | chr13 | 97970895 | |||||||
| chr13:97970908 | T | C | 19 | a0001c0001t0001g0138 a0001c0001t0001g0222 a0001c0001t0001g0223 others(16): Show |
19 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.-5+1078T>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | chr13 | 97970908 | |||||||
| chr13:97970933 | T | C | 1 | a0001c0001t0001g0085 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-5+1103T>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | chr13 | 97970933 | |||||||
| chr13:97970955 | C | A | 46 | a0001c0001t0001g0011 a0001c0001t0001g0113 a0001c0001t0001g0114 others(43): Show |
46 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.-5+1125C>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | chr13 | 97970955 | |||||||
| chr13:97970982 | CAGT | C | 9 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0112 others(6): Show |
11 | HG01192.hp1 HG01243.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.-5+1157_-5+1159del others(3): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | INFO_REALIGN_3_PRIME | chr13 | 97970982 | ||||||
| chr13:97971063 | C | T | 1 | a0001c0013t0001g0293 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-5+1233C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | chr13 | 97971063 | |||||||
| chr13:97971109 | C | T | 5 | a0001c0002t0003g0027 a0001c0002t0003g0028 a0001c0002t0003g0029 others(2): Show |
5 | HG00423.hp1 HG02155.hp1 HG02523.hp2 others(2): Show |
intron_variant | MODIFIER | c.-5+1279C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | chr13 | 97971109 | |||||||
| chr13:97971129 | C | T | 1 | a0001c0010t0002g0180 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-5+1299C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | chr13 | 97971129 | |||||||
| chr13:97971421 | AT | A | 5 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0077 others(2): Show |
5 | HG02486.hp2 HG02809.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-5+1596delT | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | INFO_REALIGN_3_PRIME | chr13 | 97971421 | ||||||
| chr13:97971500 | C | A | 1 | a0001c0002t0003g0026 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-5+1670C>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | chr13 | 97971500 | |||||||
| chr13:97971532 | A | T | 1 | a0001c0002t0003g0026 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-5+1702A>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | chr13 | 97971532 | |||||||
| chr13:97971557 | T | A | 2 | a0001c0001t0001g0189 a0001c0001t0018g0190 |
2 | HG02257.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.-5+1727T>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | chr13 | 97971557 | |||||||
| chr13:97971674 | C | T | 1 | a0001c0001t0001g0245 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-5+1844C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | chr13 | 97971674 | |||||||
| chr13:97971684 | C | G | 7 | a0001c0005t0001g0185 a0001c0005t0001g0344 a0001c0005t0001g0345 others(4): Show |
7 | HG01192.hp2 HG01891.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.-5+1854C>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | chr13 | 97971684 | |||||||
| chr13:97971694 | A | G | 9 | a0001c0004t0005g0010 a0001c0004t0005g0352 a0001c0004t0005g0353 others(6): Show |
9 | NA18950.hp2 NA18966.hp1 NA18982.hp1 others(6): Show |
intron_variant | MODIFIER | c.-5+1864A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | chr13 | 97971694 | |||||||
| chr13:97972142 | A | G | 9 | a0001c0004t0005g0010 a0001c0004t0005g0352 a0001c0004t0005g0353 others(6): Show |
9 | NA18950.hp2 NA18966.hp1 NA18982.hp1 others(6): Show |
intron_variant | MODIFIER | c.-5+2312A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | chr13 | 97972142 | |||||||
| chr13:97972163 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-5+2333C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | chr13 | 97972163 | |||||||
| chr13:97972167 | A | G | 1 | a0001c0001t0001g0120 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-5+2337A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | chr13 | 97972167 | |||||||
| chr13:97972281 | G | C | 1 | a0001c0001t0001g0301 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-5+2451G>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | chr13 | 97972281 | |||||||
| chr13:97972355 | G | A | 1 | a0001c0001t0001g0329 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-5+2525G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | chr13 | 97972355 | |||||||
| chr13:97972431 | C | A | 1 | a0001c0001t0001g0209 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-5+2601C>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | chr13 | 97972431 | |||||||
| chr13:97972432 | A | T | 1 | a0001c0001t0001g0209 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-5+2602A>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | chr13 | 97972432 | |||||||
| chr13:97972869 | AC | A | 63 | a0001c0002t0003g0014 a0001c0002t0003g0015 a0001c0002t0003g0016 others(60): Show |
65 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.-5+3040delC | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | chr13 | 97972869 | |||||||
| chr13:97973038 | CT | C | 168 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0098 others(165): Show |
172 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(169): Show |
intron_variant | MODIFIER | c.-5+3230delT | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | INFO_REALIGN_3_PRIME | chr13 | 97973038 | ||||||
| chr13:97973038 | CTT | C | 175 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(172): Show |
180 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(177): Show |
intron_variant | MODIFIER | c.-5+3229_-5+3230del others(2): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | INFO_REALIGN_3_PRIME | chr13 | 97973038 | ||||||
| chr13:97973038 | CTTT | C | 15 | a0001c0001t0001g0210 a0001c0001t0001g0213 a0001c0001t0001g0223 others(12): Show |
15 | HG00099.hp1 HG01192.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.-5+3228_-5+3230del others(3): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | INFO_REALIGN_3_PRIME | chr13 | 97973038 | ||||||
| chr13:97973143 | A | G | 9 | a0001c0004t0005g0010 a0001c0004t0005g0352 a0001c0004t0005g0353 others(6): Show |
9 | NA18950.hp2 NA18966.hp1 NA18982.hp1 others(6): Show |
intron_variant | MODIFIER | c.-5+3313A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | chr13 | 97973143 | |||||||
| chr13:97973187 | C | T | 1 | a0001c0001t0012g0359 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-5+3357C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | chr13 | 97973187 | |||||||
| chr13:97973239 | G | C | 1 | a0001c0001t0001g0325 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-5+3409G>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | chr13 | 97973239 | |||||||
| chr13:97973345 | G | C | 1 | a0001c0001t0012g0359 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-4-3348G>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | chr13 | 97973345 | |||||||
| chr13:97973393 | C | T | 2 | a0001c0002t0003g0061 a0001c0002t0003g0062 |
2 | HG00558.hp1 HG00597.hp2 |
intron_variant | MODIFIER | c.-4-3300C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | chr13 | 97973393 | |||||||
| chr13:97973795 | T | C | 14 | a0001c0001t0001g0084 a0001c0001t0001g0099 a0001c0001t0001g0100 others(11): Show |
15 | HG02258.hp2 HG02451.hp1 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.-4-2898T>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | chr13 | 97973795 | |||||||
| chr13:97973825 | T | C | 2 | a0001c0001t0001g0350 a0001c0001t0001g0351 |
2 | HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-4-2868T>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | chr13 | 97973825 | |||||||
| chr13:97973828 | G | A | 1 | a0001c0001t0001g0365 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-4-2865G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | chr13 | 97973828 | |||||||
| chr13:97973857 | C | T | 1 | a0001c0001t0002g0168 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-4-2836C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | chr13 | 97973857 | |||||||
| chr13:97973858 | T | TCAGGAGT others(20): Show |
1 | a0001c0001t0001g0213 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-4-2834_-4-2808dup others(27): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | INFO_REALIGN_3_PRIME | chr13 | 97973858 | ||||||
| chr13:97974149 | A | C | 9 | a0001c0004t0005g0010 a0001c0004t0005g0352 a0001c0004t0005g0353 others(6): Show |
9 | NA18950.hp2 NA18966.hp1 NA18982.hp1 others(6): Show |
intron_variant | MODIFIER | c.-4-2544A>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | chr13 | 97974149 | |||||||
| chr13:97974166 | G | C | 1 | a0001c0001t0021g0338 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-4-2527G>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | chr13 | 97974166 | |||||||
| chr13:97974234 | T | C | 172 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(169): Show |
178 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(175): Show |
intron_variant | MODIFIER | c.-4-2459T>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | chr13 | 97974234 | |||||||
| chr13:97974309 | C | CT | 8 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0247 others(5): Show |
8 | HG01109.hp2 HG02109.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-4-2369dupT | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | INFO_REALIGN_3_PRIME | chr13 | 97974309 | ||||||
| chr13:97974376 | G | A | 1 | a0001c0005t0001g0347 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-4-2317G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | chr13 | 97974376 | |||||||
| chr13:97974433 | A | C | 1 | a0001c0001t0001g0329 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-4-2260A>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | chr13 | 97974433 | |||||||
| chr13:97974683 | C | CA | 245 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(242): Show |
253 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(250): Show |
intron_variant | MODIFIER | c.-4-1995dupA | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | INFO_REALIGN_3_PRIME | chr13 | 97974683 | ||||||
| chr13:97974683 | C | CAA | 9 | a0001c0001t0001g0086 a0001c0001t0001g0109 a0001c0001t0001g0326 others(6): Show |
9 | HG00735.hp1 HG02451.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.-4-1996_-4-1995dup others(2): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | INFO_REALIGN_3_PRIME | chr13 | 97974683 | ||||||
| chr13:97974740 | T | C | 3 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0120 |
3 | HG00639.hp1 HG01517.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.-4-1953T>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | chr13 | 97974740 | |||||||
| chr13:97974776 | A | G | 1 | a0001c0001t0001g0088 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-4-1917A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | chr13 | 97974776 | |||||||
| chr13:97974830 | C | T | 4 | a0001c0001t0006g0009 a0001c0001t0006g0331 a0001c0001t0006g0332 others(1): Show |
5 | HG01243.hp1 HG02559.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-4-1863C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | chr13 | 97974830 | |||||||
| chr13:97974960 | G | A | 9 | a0001c0004t0005g0010 a0001c0004t0005g0352 a0001c0004t0005g0353 others(6): Show |
9 | NA18950.hp2 NA18966.hp1 NA18982.hp1 others(6): Show |
intron_variant | MODIFIER | c.-4-1733G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | chr13 | 97974960 | |||||||
| chr13:97975032 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-4-1661G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | chr13 | 97975032 | |||||||
| chr13:97975165 | G | A | 2 | a0001c0001t0001g0305 a0001c0001t0001g0306 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-4-1528G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | chr13 | 97975165 | |||||||
| chr13:97975241 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-4-1452C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | chr13 | 97975241 | |||||||
| chr13:97975252 | C | CG | 25 | a0001c0001t0001g0109 a0001c0001t0001g0119 a0001c0001t0001g0206 others(22): Show |
25 | HG00597.hp2 HG01109.hp2 HG01123.hp1 others(22): Show |
intron_variant | MODIFIER | c.-4-1433dupG | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | INFO_REALIGN_3_PRIME | chr13 | 97975252 | ||||||
| chr13:97975253 | G | A | 1 | a0001c0002t0003g0019 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-4-1440G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | chr13 | 97975253 | |||||||
| chr13:97975259 | G | C | 4 | a0001c0001t0001g0004 a0001c0001t0001g0095 a0001c0001t0001g0096 others(1): Show |
5 | HG02615.hp1 HG03471.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4-1434G>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | chr13 | 97975259 | |||||||
| chr13:97975305 | T | C | 2 | a0001c0001t0002g0168 a0001c0001t0002g0334 |
2 | HG02602.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.-4-1388T>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | chr13 | 97975305 | |||||||
| chr13:97975308 | G | A | 1 | a0001c0001t0001g0270 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-4-1385G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | chr13 | 97975308 | |||||||
| chr13:97975309 | T | G | 1 | a0001c0001t0001g0270 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-4-1384T>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | chr13 | 97975309 | |||||||
| chr13:97975467 | G | A | 2 | a0001c0001t0002g0127 a0001c0001t0002g0128 |
2 | HG01243.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.-4-1226G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | chr13 | 97975467 | |||||||
| chr13:97975488 | C | T | 5 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0001g0234 others(2): Show |
5 | HG00733.hp1 HG00741.hp1 HG01070.hp1 others(2): Show |
intron_variant | MODIFIER | c.-4-1205C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | chr13 | 97975488 | |||||||
| chr13:97975819 | A | G | 1 | a0001c0001t0018g0190 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-4-874A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | chr13 | 97975819 | |||||||
| chr13:97975862 | C | G | 172 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(169): Show |
178 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(175): Show |
intron_variant | MODIFIER | c.-4-831C>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | chr13 | 97975862 | |||||||
| chr13:97975921 | G | C | 1 | a0001c0001t0014g0169 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-4-772G>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | chr13 | 97975921 | |||||||
| chr13:97975951 | C | G | 7 | a0001c0005t0001g0185 a0001c0005t0001g0344 a0001c0005t0001g0345 others(4): Show |
7 | HG01192.hp2 HG01891.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.-4-742C>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | chr13 | 97975951 | |||||||
| chr13:97976065 | C | G | 1 | a0001c0001t0001g0238 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-4-628C>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | chr13 | 97976065 | |||||||
| chr13:97976120 | C | A | 9 | a0001c0004t0005g0010 a0001c0004t0005g0352 a0001c0004t0005g0353 others(6): Show |
9 | NA18950.hp2 NA18966.hp1 NA18982.hp1 others(6): Show |
intron_variant | MODIFIER | c.-4-573C>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | chr13 | 97976120 | |||||||
| chr13:97976127 | A | G | 1 | a0001c0001t0001g0329 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-4-566A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | chr13 | 97976127 | |||||||
| chr13:97976132 | G | A | 1 | a0001c0002t0003g0035 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-4-561G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | chr13 | 97976132 | |||||||
| chr13:97976167 | C | T | 3 | a0001c0001t0001g0244 a0001c0001t0001g0288 a0001c0001t0001g0289 |
3 | NA18961.hp2 NA18994.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.-4-526C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | chr13 | 97976167 | |||||||
| chr13:97976297 | C | A | 5 | a0001c0001t0001g0244 a0001c0001t0001g0269 a0001c0001t0001g0288 others(2): Show |
5 | HG01928.hp2 NA18961.hp2 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4-396C>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | chr13 | 97976297 | |||||||
| chr13:97976352 | A | C | 1 | a0001c0001t0001g0194 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-4-341A>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | chr13 | 97976352 | |||||||
| chr13:97976360 | T | C | 71 | a0001c0002t0001g0327 a0001c0002t0003g0014 a0001c0002t0003g0015 others(68): Show |
73 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.-4-333T>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | chr13 | 97976360 | |||||||
| chr13:97976381 | C | T | 3 | a0001c0001t0001g0368 a0001c0001t0001g0369 a0001c0001t0001g0370 |
3 | HG02451.hp2 HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.-4-312C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | chr13 | 97976381 | |||||||
| chr13:97976424 | G | A | 9 | a0001c0004t0005g0010 a0001c0004t0005g0352 a0001c0004t0005g0353 others(6): Show |
9 | NA18950.hp2 NA18966.hp1 NA18982.hp1 others(6): Show |
intron_variant | MODIFIER | c.-4-269G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | chr13 | 97976424 | |||||||
| chr13:97976426 | CCCCCGAG others(18): Show |
C | 1 | a0001c0001t0001g0109 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-4-262_-4-238delGA others(23): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | INFO_REALIGN_3_PRIME | chr13 | 97976426 | ||||||
| chr13:97976453 | C | G | 1 | a0001c0001t0001g0109 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-4-240C>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | chr13 | 97976453 | |||||||
| chr13:97976456 | C | T | 1 | a0001c0001t0001g0109 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-4-237C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | chr13 | 97976456 | |||||||
| chr13:97976463 | C | A | 12 | a0001c0002t0004g0001 a0001c0002t0004g0002 a0001c0002t0004g0031 others(9): Show |
14 | HG00621.hp2 NA18959.hp1 NA18971.hp2 others(11): Show |
intron_variant | MODIFIER | c.-4-230C>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | chr13 | 97976463 | |||||||
| chr13:97976519 | C | T | 1 | a0001c0001t0001g0224 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-4-174C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | chr13 | 97976519 | |||||||
| chr13:97976531 | C | T | 2 | a0001c0001t0001g0323 a0001c0001t0001g0324 |
2 | NA18974.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.-4-162C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | chr13 | 97976531 | |||||||
| chr13:97976630 | C | T | 2 | a0001c0001t0001g0189 a0001c0001t0018g0190 |
2 | HG02257.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.-4-63C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | chr13 | 97976630 | |||||||
| chr13:97976634 | G | A | 5 | a0001c0001t0001g0310 a0001c0001t0001g0311 a0001c0001t0001g0312 others(2): Show |
5 | HG00438.hp1 NA18944.hp2 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.-4-59G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | chr13 | 97976634 | |||||||
| chr13:97976690 | T | G | 1 | a0001c0001t0023g0174 | 1 | HG01981.hp2 | splice_region_variant&intron_variant | LOW | c.-4-3T>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 3/28 | chr13 | 97976690 | |||||||
| chr13:97976824 | C | T | 1 | a0001c0001t0001g0224 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.90+38C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 4/28 | chr13 | 97976824 | |||||||
| chr13:97976827 | C | G | 1 | a0001c0002t0003g0023 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.90+41C>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 4/28 | chr13 | 97976827 | |||||||
| chr13:97976849 | C | G | 2 | a0001c0001t0008g0167 a0001c0001t0008g0173 |
2 | HG01099.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.90+63C>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 4/28 | chr13 | 97976849 | |||||||
| chr13:97976918 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.90+132G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 4/28 | chr13 | 97976918 | |||||||
| chr13:97976986 | C | T | 1 | a0001c0001t0001g0194 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.90+200C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 4/28 | chr13 | 97976986 | |||||||
| chr13:97977080 | G | C | 251 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(248): Show |
259 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(256): Show |
intron_variant | MODIFIER | c.90+294G>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 4/28 | chr13 | 97977080 | |||||||
| chr13:97977213 | C | A | 3 | a0001c0001t0001g0368 a0001c0001t0001g0369 a0001c0001t0001g0370 |
3 | HG02451.hp2 HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.90+427C>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 4/28 | chr13 | 97977213 | |||||||
| chr13:97977239 | C | T | 9 | a0001c0004t0005g0010 a0001c0004t0005g0352 a0001c0004t0005g0353 others(6): Show |
9 | NA18950.hp2 NA18966.hp1 NA18982.hp1 others(6): Show |
intron_variant | MODIFIER | c.90+453C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 4/28 | chr13 | 97977239 | |||||||
| chr13:97977533 | G | A | 3 | a0001c0001t0001g0368 a0001c0001t0001g0369 a0001c0001t0001g0370 |
3 | HG02451.hp2 HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.90+747G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 4/28 | chr13 | 97977533 | |||||||
| chr13:97977608 | A | C | 7 | a0001c0005t0001g0185 a0001c0005t0001g0344 a0001c0005t0001g0345 others(4): Show |
7 | HG01192.hp2 HG01891.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.90+822A>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 4/28 | chr13 | 97977608 | |||||||
| chr13:97977635 | T | C | 1 | a0001c0001t0001g0120 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.90+849T>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 4/28 | chr13 | 97977635 | |||||||
| chr13:97977679 | G | A | 39 | a0001c0001t0001g0132 a0001c0001t0001g0137 a0001c0001t0001g0187 others(36): Show |
39 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.90+893G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 4/28 | chr13 | 97977679 | |||||||
| chr13:97977737 | T | G | 171 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(168): Show |
177 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(174): Show |
intron_variant | MODIFIER | c.90+951T>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 4/28 | chr13 | 97977737 | |||||||
| chr13:97977740 | T | G | 1 | a0001c0001t0001g0271 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.90+954T>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 4/28 | chr13 | 97977740 | |||||||
| chr13:97977859 | G | A | 9 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0112 others(6): Show |
11 | HG01192.hp1 HG01243.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.90+1073G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 4/28 | chr13 | 97977859 | |||||||
| chr13:97978018 | G | A | 1 | a0001c0001t0002g0156 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.90+1232G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 4/28 | chr13 | 97978018 | |||||||
| chr13:97978301 | A | G | 5 | a0001c0001t0001g0004 a0001c0001t0001g0095 a0001c0001t0001g0096 others(2): Show |
6 | HG02615.hp1 HG03471.hp2 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.90+1515A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 4/28 | chr13 | 97978301 | |||||||
| chr13:97978317 | C | T | 3 | a0001c0001t0001g0248 a0001c0001t0001g0261 a0001c0001t0001g0304 |
3 | HG00738.hp1 HG02258.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.90+1531C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 4/28 | chr13 | 97978317 | |||||||
| chr13:97978653 | A | G | 2 | a0001c0001t0001g0075 a0001c0001t0001g0076 |
2 | HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.90+1867A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 4/28 | chr13 | 97978653 | |||||||
| chr13:97978744 | A | G | 1 | a0001c0001t0002g0155 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.90+1958A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 4/28 | chr13 | 97978744 | |||||||
| chr13:97978788 | C | T | 170 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(167): Show |
176 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(173): Show |
intron_variant | MODIFIER | c.90+2002C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 4/28 | chr13 | 97978788 | |||||||
| chr13:97978815 | A | G | 15 | a0001c0001t0001g0335 a0001c0001t0001g0336 a0001c0001t0001g0337 others(12): Show |
15 | HG01109.hp2 HG01123.hp1 HG01975.hp2 others(12): Show |
intron_variant | MODIFIER | c.90+2029A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 4/28 | chr13 | 97978815 | |||||||
| chr13:97978828 | G | A | 1 | a0001c0001t0001g0272 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.90+2042G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 4/28 | chr13 | 97978828 | |||||||
| chr13:97978882 | T | C | 64 | a0001c0002t0001g0327 a0001c0002t0003g0014 a0001c0002t0003g0015 others(61): Show |
66 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.90+2096T>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 4/28 | chr13 | 97978882 | |||||||
| chr13:97978943 | T | A | 1 | a0001c0001t0001g0144 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.90+2157T>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 4/28 | chr13 | 97978943 | |||||||
| chr13:97979189 | T | G | 3 | a0001c0001t0001g0368 a0001c0001t0001g0369 a0001c0001t0001g0370 |
3 | HG02451.hp2 HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.90+2403T>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 4/28 | chr13 | 97979189 | |||||||
| chr13:97979237 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.90+2451C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 4/28 | chr13 | 97979237 | |||||||
| chr13:97979375 | G | A | 4 | a0001c0001t0006g0009 a0001c0001t0006g0331 a0001c0001t0006g0332 others(1): Show |
5 | HG01243.hp1 HG02559.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.90+2589G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 4/28 | chr13 | 97979375 | |||||||
| chr13:97979574 | T | G | 1 | a0001c0001t0001g0079 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.90+2788T>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 4/28 | chr13 | 97979574 | |||||||
| chr13:97979724 | G | A | 71 | a0001c0002t0001g0327 a0001c0002t0003g0014 a0001c0002t0003g0015 others(68): Show |
73 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.91-2779G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 4/28 | chr13 | 97979724 | |||||||
| chr13:97979734 | G | A | 1 | a0001c0001t0021g0338 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.91-2769G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 4/28 | chr13 | 97979734 | |||||||
| chr13:97979807 | T | C | 1 | a0001c0001t0001g0211 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.91-2696T>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 4/28 | chr13 | 97979807 | |||||||
| chr13:97979808 | G | C | 1 | a0001c0001t0001g0211 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.91-2695G>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 4/28 | chr13 | 97979808 | |||||||
| chr13:97979814 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.91-2689C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 4/28 | chr13 | 97979814 | |||||||
| chr13:97979842 | A | G | 1 | a0001c0012t0001g0219 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.91-2661A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 4/28 | chr13 | 97979842 | |||||||
| chr13:97979858 | A | T | 1 | a0001c0001t0001g0079 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.91-2645A>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 4/28 | chr13 | 97979858 | |||||||
| chr13:97980095 | A | G | 250 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(247): Show |
258 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(255): Show |
intron_variant | MODIFIER | c.91-2408A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 4/28 | chr13 | 97980095 | |||||||
| chr13:97980217 | T | C | 15 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0099 others(12): Show |
16 | HG02258.hp2 HG02451.hp1 HG02523.hp1 others(13): Show |
intron_variant | MODIFIER | c.91-2286T>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 4/28 | chr13 | 97980217 | |||||||
| chr13:97980368 | C | T | 1 | a0001c0001t0006g0009 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.91-2135C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 4/28 | chr13 | 97980368 | |||||||
| chr13:97980494 | C | A | 9 | a0001c0004t0005g0010 a0001c0004t0005g0352 a0001c0004t0005g0353 others(6): Show |
9 | NA18950.hp2 NA18966.hp1 NA18982.hp1 others(6): Show |
intron_variant | MODIFIER | c.91-2009C>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 4/28 | chr13 | 97980494 | |||||||
| chr13:97980499 | G | A | 2 | a0001c0001t0001g0360 a0001c0001t0001g0365 |
2 | HG02572.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.91-2004G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 4/28 | chr13 | 97980499 | |||||||
| chr13:97980596 | G | A | 1 | a0001c0009t0001g0309 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.91-1907G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 4/28 | chr13 | 97980596 | |||||||
| chr13:97980826 | C | CA | 117 | a0001c0001t0001g0075 a0001c0001t0001g0093 a0001c0001t0001g0095 others(114): Show |
119 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.91-1659dupA | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr13 | 97980826 | ||||||
| chr13:97980826 | C | CAA | 24 | a0001c0001t0002g0039 a0001c0001t0002g0133 a0001c0001t0002g0134 others(21): Show |
24 | HG00558.hp1 HG00597.hp2 HG01978.hp2 others(21): Show |
intron_variant | MODIFIER | c.91-1660_91-1659dup others(2): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr13 | 97980826 | ||||||
| chr13:97980940 | T | C | 1 | a0001c0001t0001g0273 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.91-1563T>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 4/28 | chr13 | 97980940 | |||||||
| chr13:97981111 | C | T | 6 | a0001c0005t0001g0185 a0001c0005t0001g0344 a0001c0005t0001g0345 others(3): Show |
6 | HG01192.hp2 HG01891.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.91-1392C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 4/28 | chr13 | 97981111 | |||||||
| chr13:97981113 | C | G | 4 | a0001c0001t0002g0157 a0001c0001t0002g0178 a0001c0001t0002g0179 others(1): Show |
4 | HG01928.hp1 HG01975.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.91-1390C>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 4/28 | chr13 | 97981113 | |||||||
| chr13:97981391 | A | G | 1 | a0001c0001t0002g0170 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.91-1112A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 4/28 | chr13 | 97981391 | |||||||
| chr13:97981417 | T | C | 1 | a0001c0001t0001g0328 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.91-1086T>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 4/28 | chr13 | 97981417 | |||||||
| chr13:97981555 | G | A | 2 | a0001c0001t0001g0350 a0001c0001t0001g0351 |
2 | HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.91-948G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 4/28 | chr13 | 97981555 | |||||||
| chr13:97981831 | A | T | 3 | a0001c0001t0001g0137 a0001c0001t0001g0204 a0001c0001t0001g0205 |
3 | HG02602.hp1 HG03927.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.91-672A>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 4/28 | chr13 | 97981831 | |||||||
| chr13:97981939 | G | A | 9 | a0001c0004t0005g0010 a0001c0004t0005g0352 a0001c0004t0005g0353 others(6): Show |
9 | NA18950.hp2 NA18966.hp1 NA18982.hp1 others(6): Show |
intron_variant | MODIFIER | c.91-564G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 4/28 | chr13 | 97981939 | |||||||
| chr13:97982125 | C | T | 2 | a0001c0002t0003g0019 a0001c0002t0003g0022 |
2 | HG02683.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.91-378C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 4/28 | chr13 | 97982125 | |||||||
| chr13:97982318 | T | A | 52 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0039 others(49): Show |
54 | HG00099.hp1 HG00642.hp1 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.91-185T>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 4/28 | chr13 | 97982318 | |||||||
| chr13:97982387 | A | G | 1 | a0001c0001t0001g0324 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.91-116A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 4/28 | chr13 | 97982387 | |||||||
| chr13:97982454 | A | T | 6 | a0001c0001t0001g0310 a0001c0001t0001g0311 a0001c0001t0001g0312 others(3): Show |
6 | HG00438.hp1 NA18944.hp2 NA18949.hp2 others(3): Show |
intron_variant | MODIFIER | c.91-49A>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 4/28 | chr13 | 97982454 | |||||||
| chr13:97982738 | T | C | 2 | a0001c0001t0001g0292 a0001c0002t0003g0026 |
2 | HG02148.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.171+155T>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 5/28 | chr13 | 97982738 | |||||||
| chr13:97982745 | AT | A | 7 | a0001c0005t0001g0185 a0001c0005t0001g0344 a0001c0005t0001g0345 others(4): Show |
7 | HG01192.hp2 HG01891.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.171+168delT | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 5/28 | INFO_REALIGN_3_PRIME | chr13 | 97982745 | ||||||
| chr13:97982879 | A | G | 1 | a0001c0001t0012g0359 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.171+296A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 5/28 | chr13 | 97982879 | |||||||
| chr13:97983015 | C | T | 1 | a0001c0001t0001g0329 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.171+432C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 5/28 | chr13 | 97983015 | |||||||
| chr13:97983016 | G | A | 2 | a0001c0001t0001g0237 a0001c0001t0001g0238 |
2 | HG02080.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.171+433G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 5/28 | chr13 | 97983016 | |||||||
| chr13:97983279 | AT | A | 15 | a0001c0001t0001g0335 a0001c0001t0001g0336 a0001c0001t0001g0337 others(12): Show |
15 | HG01109.hp2 HG01123.hp1 HG01975.hp2 others(12): Show |
intron_variant | MODIFIER | c.171+703delT | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 5/28 | INFO_REALIGN_3_PRIME | chr13 | 97983279 | ||||||
| chr13:97983480 | A | AT | 9 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0112 others(6): Show |
11 | HG01192.hp1 HG01243.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.171+900dupT | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 5/28 | INFO_REALIGN_3_PRIME | chr13 | 97983480 | ||||||
| chr13:97983537 | A | AC | 25 | a0001c0001t0001g0144 a0001c0001t0001g0182 a0001c0001t0001g0241 others(22): Show |
25 | HG00099.hp2 HG00438.hp1 HG00544.hp2 others(22): Show |
intron_variant | MODIFIER | c.171+966dupC | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 5/28 | INFO_REALIGN_3_PRIME | chr13 | 97983537 | ||||||
| chr13:97983537 | AC | A | 44 | a0001c0001t0001g0106 a0001c0001t0001g0119 a0001c0001t0001g0139 others(41): Show |
44 | HG00558.hp2 HG00642.hp1 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.171+966delC | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 5/28 | INFO_REALIGN_3_PRIME | chr13 | 97983537 | ||||||
| chr13:97983537 | ACC | A | 115 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0074 others(112): Show |
120 | HG00099.hp1 HG00735.hp1 HG00741.hp2 others(117): Show |
intron_variant | MODIFIER | c.171+965_171+966del others(2): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 5/28 | INFO_REALIGN_3_PRIME | chr13 | 97983537 | ||||||
| chr13:97983537 | ACCC | A | 109 | a0001c0001t0001g0004 a0001c0001t0001g0095 a0001c0001t0001g0096 others(106): Show |
112 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.171+964_171+966del others(3): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 5/28 | INFO_REALIGN_3_PRIME | chr13 | 97983537 | ||||||
| chr13:97983541 | C | G | 1 | a0001c0001t0001g0103 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.171+958C>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 5/28 | chr13 | 97983541 | |||||||
| chr13:97983554 | T | TC | 7 | a0001c0001t0001g0192 a0001c0001t0001g0204 a0001c0001t0001g0205 others(4): Show |
7 | HG02080.hp1 HG02602.hp1 HG03927.hp2 others(4): Show |
intron_variant | MODIFIER | c.171+977dupC | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 5/28 | INFO_REALIGN_3_PRIME | chr13 | 97983554 | ||||||
| chr13:97983576 | T | G | 20 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0224 others(17): Show |
20 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.171+993T>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 5/28 | chr13 | 97983576 | |||||||
| chr13:97983692 | A | G | 1 | a0001c0014t0001g0110 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.171+1109A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 5/28 | chr13 | 97983692 | |||||||
| chr13:97983786 | CCAGT | C | 2 | a0001c0001t0001g0003 a0001c0001t0001g0081 |
3 | HG01884.hp1 HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.171+1212_171+1215d others(6): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 5/28 | INFO_REALIGN_3_PRIME | chr13 | 97983786 | ||||||
| chr13:97983857 | AT | A | 9 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0112 others(6): Show |
11 | HG01192.hp1 HG01243.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.171+1285delT | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 5/28 | INFO_REALIGN_3_PRIME | chr13 | 97983857 | ||||||
| chr13:97983943 | A | G | 1 | a0001c0001t0018g0190 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.171+1360A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 5/28 | chr13 | 97983943 | |||||||
| chr13:97983962 | CTTCTTTT others(10): Show |
C | 1 | a0001c0001t0001g0261 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.171+1382_171+1398d others(19): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 5/28 | INFO_REALIGN_3_PRIME | chr13 | 97983962 | ||||||
| chr13:97983965 | C | CT | 37 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0090 others(34): Show |
37 | HG00609.hp2 HG00735.hp2 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.171+1413dupT | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 5/28 | INFO_REALIGN_3_PRIME | chr13 | 97983965 | ||||||
| chr13:97983965 | C | CTT | 45 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0148 others(42): Show |
45 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.171+1412_171+1413d others(4): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 5/28 | INFO_REALIGN_3_PRIME | chr13 | 97983965 | ||||||
| chr13:97983965 | C | CTTT | 27 | a0001c0001t0001g0074 a0001c0001t0001g0142 a0001c0001t0001g0231 others(24): Show |
27 | HG00099.hp2 HG00544.hp2 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.171+1411_171+1413d others(5): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 5/28 | INFO_REALIGN_3_PRIME | chr13 | 97983965 | ||||||
| chr13:97983965 | C | CTTTT | 9 | a0001c0001t0001g0146 a0001c0001t0001g0182 a0001c0001t0001g0241 others(6): Show |
9 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.171+1410_171+1413d others(6): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 5/28 | INFO_REALIGN_3_PRIME | chr13 | 97983965 | ||||||
| chr13:97983965 | CT | C | 50 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0075 others(47): Show |
52 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.171+1413delT | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 5/28 | INFO_REALIGN_3_PRIME | chr13 | 97983965 | ||||||
| chr13:97983965 | CTT | C | 22 | a0001c0001t0001g0011 a0001c0001t0001g0329 a0001c0001t0001g0337 others(19): Show |
23 | HG01192.hp1 HG01243.hp1 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.171+1412_171+1413d others(4): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 5/28 | INFO_REALIGN_3_PRIME | chr13 | 97983965 | ||||||
| chr13:97983965 | CTTT | C | 23 | a0001c0001t0001g0117 a0001c0001t0001g0121 a0001c0001t0001g0137 others(20): Show |
23 | HG01109.hp2 HG01123.hp1 HG01192.hp2 others(20): Show |
intron_variant | MODIFIER | c.171+1411_171+1413d others(5): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 5/28 | INFO_REALIGN_3_PRIME | chr13 | 97983965 | ||||||
| chr13:97983965 | CTTTT | C | 47 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0115 others(44): Show |
47 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.171+1410_171+1413d others(6): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 5/28 | INFO_REALIGN_3_PRIME | chr13 | 97983965 | ||||||
| chr13:97983965 | CTTTTTTT others(3): Show |
C | 4 | a0001c0002t0003g0035 a0001c0002t0003g0066 a0001c0002t0004g0031 others(1): Show |
4 | HG00621.hp2 HG02135.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.171+1404_171+1413d others(12): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 5/28 | INFO_REALIGN_3_PRIME | chr13 | 97983965 | ||||||
| chr13:97983965 | CTTTTTTT others(4): Show |
C | 59 | a0001c0002t0001g0327 a0001c0002t0003g0014 a0001c0002t0003g0015 others(56): Show |
61 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.171+1403_171+1413d others(13): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 5/28 | INFO_REALIGN_3_PRIME | chr13 | 97983965 | ||||||
| chr13:97983965 | CTTTTTTT others(5): Show |
C | 1 | a0001c0002t0003g0063 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.171+1402_171+1413d others(14): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 5/28 | INFO_REALIGN_3_PRIME | chr13 | 97983965 | ||||||
| chr13:97983965 | CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0012g0359 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.171+1401_171+1413d others(15): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 5/28 | INFO_REALIGN_3_PRIME | chr13 | 97983965 | ||||||
| chr13:97983965 | CTTTTTTT others(8): Show |
C | 1 | a0001c0001t0001g0301 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.171+1399_171+1413d others(17): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 5/28 | INFO_REALIGN_3_PRIME | chr13 | 97983965 | ||||||
| chr13:97984002 | G | A | 2 | a0001c0001t0001g0189 a0001c0001t0018g0190 |
2 | HG02257.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.171+1419G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 5/28 | chr13 | 97984002 | |||||||
| chr13:97984017 | C | T | 2 | a0001c0001t0001g0350 a0001c0001t0001g0351 |
2 | HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.172-1404C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 5/28 | chr13 | 97984017 | |||||||
| chr13:97984065 | G | A | 1 | a0001c0001t0001g0329 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.172-1356G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 5/28 | chr13 | 97984065 | |||||||
| chr13:97984084 | T | G | 2 | a0001c0001t0001g0074 a0001c0001t0001g0188 |
2 | HG01891.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.172-1337T>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 5/28 | chr13 | 97984084 | |||||||
| chr13:97984128 | G | A | 1 | a0001c0001t0001g0248 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.172-1293G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 5/28 | chr13 | 97984128 | |||||||
| chr13:97984229 | C | T | 1 | a0001c0001t0017g0116 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.172-1192C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 5/28 | chr13 | 97984229 | |||||||
| chr13:97984258 | G | A | 1 | a0001c0002t0003g0027 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.172-1163G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 5/28 | chr13 | 97984258 | |||||||
| chr13:97984481 | G | A | 170 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(167): Show |
176 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(173): Show |
intron_variant | MODIFIER | c.172-940G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 5/28 | chr13 | 97984481 | |||||||
| chr13:97984556 | G | C | 1 | a0001c0001t0001g0329 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.172-865G>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 5/28 | chr13 | 97984556 | |||||||
| chr13:97984928 | TTAGGTAT others(10): Show |
T | 2 | a0001c0001t0001g0074 a0001c0001t0001g0188 |
2 | HG01891.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.172-490_172-474del others(17): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 5/28 | INFO_REALIGN_3_PRIME | chr13 | 97984928 | ||||||
| chr13:97984945 | G | A | 1 | a0001c0001t0001g0109 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.172-476G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 5/28 | chr13 | 97984945 | |||||||
| chr13:97984969 | G | A | 1 | a0001c0001t0001g0226 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.172-452G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 5/28 | chr13 | 97984969 | |||||||
| chr13:97984984 | T | C | 39 | a0001c0001t0001g0132 a0001c0001t0001g0137 a0001c0001t0001g0187 others(36): Show |
39 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.172-437T>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 5/28 | chr13 | 97984984 | |||||||
| chr13:97985035 | G | A | 1 | a0001c0001t0001g0329 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.172-386G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 5/28 | chr13 | 97985035 | |||||||
| chr13:97985045 | G | A | 1 | a0001c0015t0001g0147 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.172-376G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 5/28 | chr13 | 97985045 | |||||||
| chr13:97985282 | A | G | 2 | a0001c0001t0001g0189 a0001c0001t0018g0190 |
2 | HG02257.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.172-139A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 5/28 | chr13 | 97985282 | |||||||
| chr13:97985663 | CT | C | 166 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(163): Show |
171 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(168): Show |
intron_variant | MODIFIER | c.364+64delT | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 6/28 | INFO_REALIGN_3_PRIME | chr13 | 97985663 | ||||||
| chr13:97985677 | T | A | 42 | a0001c0001t0002g0039 a0001c0001t0002g0130 a0001c0001t0002g0131 others(39): Show |
42 | HG00099.hp1 HG00642.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.364+64T>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 6/28 | chr13 | 97985677 | |||||||
| chr13:97985908 | A | T | 1 | a0001c0002t0004g0042 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.364+295A>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 6/28 | chr13 | 97985908 | |||||||
| chr13:97986123 | G | GA | 39 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0075 others(36): Show |
42 | HG01106.hp2 HG01109.hp1 HG01361.hp1 others(39): Show |
intron_variant | MODIFIER | c.364+520dupA | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 6/28 | INFO_REALIGN_3_PRIME | chr13 | 97986123 | ||||||
| chr13:97986151 | T | G | 1 | a0001c0002t0003g0030 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.364+538T>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 6/28 | chr13 | 97986151 | |||||||
| chr13:97986269 | A | G | 1 | a0001c0002t0003g0060 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.364+656A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 6/28 | chr13 | 97986269 | |||||||
| chr13:97986358 | A | AT | 11 | a0001c0001t0002g0184 a0001c0001t0002g0330 a0001c0004t0005g0010 others(8): Show |
11 | HG02109.hp1 HG04115.hp2 NA18950.hp2 others(8): Show |
intron_variant | MODIFIER | c.364+746dupT | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 6/28 | INFO_REALIGN_3_PRIME | chr13 | 97986358 | ||||||
| chr13:97986359 | TA | T | 62 | a0001c0002t0003g0014 a0001c0002t0003g0015 a0001c0002t0003g0016 others(59): Show |
64 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.364+747delA | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 6/28 | chr13 | 97986359 | |||||||
| chr13:97986360 | A | T | 124 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0075 others(121): Show |
129 | HG00099.hp1 HG00639.hp1 HG00735.hp1 others(126): Show |
intron_variant | MODIFIER | c.364+747A>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 6/28 | chr13 | 97986360 | |||||||
| chr13:97986361 | T | TA | 4 | a0001c0001t0006g0009 a0001c0001t0006g0331 a0001c0001t0006g0332 others(1): Show |
5 | HG01243.hp1 HG02559.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.364+748_364+749ins others(1): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 6/28 | chr13 | 97986361 | |||||||
| chr13:97986362 | T | A | 16 | a0001c0001t0001g0113 a0001c0001t0001g0222 a0001c0001t0001g0223 others(13): Show |
16 | HG00438.hp2 HG00558.hp2 HG02080.hp2 others(13): Show |
intron_variant | MODIFIER | c.364+749T>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 6/28 | chr13 | 97986362 | |||||||
| chr13:97986381 | GT | G | 11 | a0001c0002t0003g0032 a0001c0002t0003g0033 a0001c0002t0003g0034 others(8): Show |
11 | HG00558.hp1 HG00597.hp2 HG02040.hp2 others(8): Show |
intron_variant | MODIFIER | c.364+771delT | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 6/28 | INFO_REALIGN_3_PRIME | chr13 | 97986381 | ||||||
| chr13:97986593 | G | C | 7 | a0001c0001t0001g0335 a0001c0001t0001g0336 a0001c0001t0001g0337 others(4): Show |
7 | HG01975.hp2 HG02647.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.364+980G>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 6/28 | chr13 | 97986593 | |||||||
| chr13:97986629 | C | A | 1 | a0001c0001t0001g0189 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.364+1016C>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 6/28 | chr13 | 97986629 | |||||||
| chr13:97986896 | C | T | 9 | a0001c0004t0005g0010 a0001c0004t0005g0352 a0001c0004t0005g0353 others(6): Show |
9 | NA18950.hp2 NA18966.hp1 NA18982.hp1 others(6): Show |
intron_variant | MODIFIER | c.364+1283C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 6/28 | chr13 | 97986896 | |||||||
| chr13:97987039 | C | G | 2 | a0001c0001t0001g0087 a0001c0001t0001g0094 |
2 | HG01109.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.364+1426C>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 6/28 | chr13 | 97987039 | |||||||
| chr13:97987244 | A | G | 250 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(247): Show |
258 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(255): Show |
intron_variant | MODIFIER | c.364+1631A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 6/28 | chr13 | 97987244 | |||||||
| chr13:97987252 | CT | C | 63 | a0001c0002t0001g0327 a0001c0002t0003g0014 a0001c0002t0003g0015 others(60): Show |
65 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.364+1654delT | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 6/28 | INFO_REALIGN_3_PRIME | chr13 | 97987252 | ||||||
| chr13:97987633 | C | G | 7 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0294 others(4): Show |
7 | HG01261.hp1 HG01934.hp1 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.365-1429C>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 6/28 | chr13 | 97987633 | |||||||
| chr13:97987705 | G | T | 1 | a0001c0001t0001g0361 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.365-1357G>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 6/28 | chr13 | 97987705 | |||||||
| chr13:97987788 | C | A | 1 | a0001c0001t0001g0339 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.365-1274C>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 6/28 | chr13 | 97987788 | |||||||
| chr13:97987950 | AT | A | 83 | a0001c0001t0002g0007 a0001c0001t0002g0126 a0001c0001t0002g0129 others(80): Show |
86 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.365-1100delT | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 6/28 | INFO_REALIGN_3_PRIME | chr13 | 97987950 | ||||||
| chr13:97987983 | C | G | 4 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0115 others(1): Show |
4 | HG01884.hp2 HG03209.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.365-1079C>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 6/28 | chr13 | 97987983 | |||||||
| chr13:97988040 | G | T | 1 | a0001c0001t0001g0335 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.365-1022G>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 6/28 | chr13 | 97988040 | |||||||
| chr13:97988064 | C | G | 71 | a0001c0002t0001g0327 a0001c0002t0003g0014 a0001c0002t0003g0015 others(68): Show |
73 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.365-998C>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 6/28 | chr13 | 97988064 | |||||||
| chr13:97988064 | C | T | 227 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(224): Show |
233 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(230): Show |
intron_variant | MODIFIER | c.365-998C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 6/28 | chr13 | 97988064 | |||||||
| chr13:97988071 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.365-991C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 6/28 | chr13 | 97988071 | |||||||
| chr13:97988132 | A | G | 250 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(247): Show |
258 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(255): Show |
intron_variant | MODIFIER | c.365-930A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 6/28 | chr13 | 97988132 | |||||||
| chr13:97988138 | T | C | 7 | a0001c0001t0001g0011 a0001c0001t0001g0113 a0001c0001t0001g0114 others(4): Show |
7 | HG01884.hp2 HG02976.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.365-924T>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 6/28 | chr13 | 97988138 | |||||||
| chr13:97988154 | A | C | 4 | a0001c0001t0006g0009 a0001c0001t0006g0331 a0001c0001t0006g0332 others(1): Show |
5 | HG01243.hp1 HG02559.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.365-908A>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 6/28 | chr13 | 97988154 | |||||||
| chr13:97988252 | C | G | 39 | a0001c0001t0001g0132 a0001c0001t0001g0137 a0001c0001t0001g0187 others(36): Show |
39 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.365-810C>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 6/28 | chr13 | 97988252 | |||||||
| chr13:97988267 | C | G | 1 | a0001c0001t0012g0359 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.365-795C>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 6/28 | chr13 | 97988267 | |||||||
| chr13:97988394 | T | C | 2 | a0001c0001t0001g0336 a0001c0001t0001g0337 |
2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.365-668T>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 6/28 | chr13 | 97988394 | |||||||
| chr13:97988680 | C | T | 5 | a0001c0001t0002g0157 a0001c0001t0002g0176 a0001c0001t0002g0178 others(2): Show |
5 | HG01928.hp1 HG01952.hp2 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.365-382C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 6/28 | chr13 | 97988680 | |||||||
| chr13:97988865 | CT | C | 16 | a0001c0004t0005g0010 a0001c0004t0005g0352 a0001c0004t0005g0353 others(13): Show |
16 | HG01192.hp2 HG01891.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.365-184delT | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 6/28 | INFO_REALIGN_3_PRIME | chr13 | 97988865 | ||||||
| chr13:97988865 | CTT | C | 64 | a0001c0002t0001g0327 a0001c0002t0003g0014 a0001c0002t0003g0015 others(61): Show |
66 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.365-185_365-184del others(2): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 6/28 | INFO_REALIGN_3_PRIME | chr13 | 97988865 | ||||||
| chr13:97988905 | G | A | 1 | a0001c0001t0002g0176 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.365-157G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 6/28 | chr13 | 97988905 | |||||||
| chr13:97988969 | G | GT | 80 | a0001c0002t0001g0327 a0001c0002t0003g0014 a0001c0002t0003g0015 others(77): Show |
82 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.365-90dupT | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 6/28 | INFO_REALIGN_3_PRIME | chr13 | 97988969 | ||||||
| chr13:97989169 | A | G | 9 | a0001c0004t0005g0010 a0001c0004t0005g0352 a0001c0004t0005g0353 others(6): Show |
9 | NA18950.hp2 NA18966.hp1 NA18982.hp1 others(6): Show |
splice_region_variant&intron_variant | LOW | c.467+5A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 7/28 | chr13 | 97989169 | |||||||
| chr13:97989292 | G | C | 1 | a0001c0001t0001g0104 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.467+128G>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 7/28 | chr13 | 97989292 | |||||||
| chr13:97989323 | A | T | 43 | a0001c0001t0002g0039 a0001c0001t0002g0130 a0001c0001t0002g0131 others(40): Show |
43 | HG00099.hp1 HG00642.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.467+159A>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 7/28 | chr13 | 97989323 | |||||||
| chr13:97989460 | A | G | 71 | a0001c0002t0001g0327 a0001c0002t0003g0014 a0001c0002t0003g0015 others(68): Show |
73 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.467+296A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 7/28 | chr13 | 97989460 | |||||||
| chr13:97989488 | A | G | 1 | a0001c0001t0001g0365 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.467+324A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 7/28 | chr13 | 97989488 | |||||||
| chr13:97989566 | A | G | 2 | a0001c0005t0001g0185 a0001c0005t0001g0349 |
2 | HG01891.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.467+402A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 7/28 | chr13 | 97989566 | |||||||
| chr13:97989604 | A | T | 2 | a0001c0001t0002g0130 a0001c0001t0002g0131 |
2 | HG00099.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.467+440A>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 7/28 | chr13 | 97989604 | |||||||
| chr13:97989653 | A | G | 1 | a0001c0001t0001g0299 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.468-473A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 7/28 | chr13 | 97989653 | |||||||
| chr13:97989736 | T | C | 1 | a0001c0001t0001g0329 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.468-390T>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 7/28 | chr13 | 97989736 | |||||||
| chr13:97989957 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.468-169C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 7/28 | chr13 | 97989957 | |||||||
| chr13:97990043 | C | G | 1 | a0001c0001t0001g0140 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.468-83C>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 7/28 | chr13 | 97990043 | |||||||
| chr13:97990385 | G | A | 4 | a0001c0002t0003g0049 a0001c0002t0003g0056 a0001c0002t0003g0057 others(1): Show |
4 | NA18983.hp2 NA19057.hp1 NA19085.hp1 others(1): Show |
intron_variant | MODIFIER | c.565-48G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 8/28 | chr13 | 97990385 | |||||||
| chr13:97991045 | C | G | 1 | a0001c0001t0001g0326 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.669+508C>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 9/28 | chr13 | 97991045 | |||||||
| chr13:97991053 | GA | G | 9 | a0001c0004t0005g0010 a0001c0004t0005g0352 a0001c0004t0005g0353 others(6): Show |
9 | NA18950.hp2 NA18966.hp1 NA18982.hp1 others(6): Show |
intron_variant | MODIFIER | c.669+523delA | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 9/28 | INFO_REALIGN_3_PRIME | chr13 | 97991053 | ||||||
| chr13:97991188 | A | G | 1 | a0001c0001t0001g0097 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.669+651A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 9/28 | chr13 | 97991188 | |||||||
| chr13:97991243 | C | G | 2 | a0001c0001t0001g0074 a0001c0001t0001g0188 |
2 | HG01891.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.669+706C>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 9/28 | chr13 | 97991243 | |||||||
| chr13:97991440 | G | A | 63 | a0001c0002t0003g0014 a0001c0002t0003g0015 a0001c0002t0003g0016 others(60): Show |
65 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.669+903G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 9/28 | chr13 | 97991440 | |||||||
| chr13:97991464 | G | A | 1 | a0001c0001t0014g0169 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.669+927G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 9/28 | chr13 | 97991464 | |||||||
| chr13:97991707 | A | G | 1 | a0001c0001t0002g0158 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.669+1170A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 9/28 | chr13 | 97991707 | |||||||
| chr13:97992085 | C | A | 250 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(247): Show |
258 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(255): Show |
intron_variant | MODIFIER | c.670-807C>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 9/28 | chr13 | 97992085 | |||||||
| chr13:97992193 | C | T | 1 | a0001c0002t0003g0057 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.670-699C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 9/28 | chr13 | 97992193 | |||||||
| chr13:97992394 | G | A | 249 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(246): Show |
257 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(254): Show |
intron_variant | MODIFIER | c.670-498G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 9/28 | chr13 | 97992394 | |||||||
| chr13:97992447 | A | G | 1 | a0001c0001t0001g0205 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.670-445A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 9/28 | chr13 | 97992447 | |||||||
| chr13:97992537 | C | T | 1 | a0001c0002t0003g0029 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.670-355C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 9/28 | chr13 | 97992537 | |||||||
| chr13:97992546 | G | A | 1 | a0001c0013t0001g0293 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.670-346G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 9/28 | chr13 | 97992546 | |||||||
| chr13:97992587 | A | G | 8 | a0001c0003t0001g0122 a0001c0003t0001g0123 a0001c0003t0001g0196 others(5): Show |
8 | NA18957.hp1 NA18984.hp2 NA18998.hp1 others(5): Show |
intron_variant | MODIFIER | c.670-305A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 9/28 | chr13 | 97992587 | |||||||
| chr13:97993037 | C | T | 2 | a0001c0001t0001g0250 a0001c0001t0001g0254 |
2 | HG00733.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.792+23C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 10/28 | chr13 | 97993037 | |||||||
| chr13:97993326 | G | A | 52 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0039 others(49): Show |
54 | HG00099.hp1 HG00642.hp1 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.913+101G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 11/28 | chr13 | 97993326 | |||||||
| chr13:97993448 | T | A | 1 | a0001c0001t0002g0170 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.913+223T>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 11/28 | chr13 | 97993448 | |||||||
| chr13:97993486 | T | C | 1 | a0001c0001t0014g0169 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.913+261T>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 11/28 | chr13 | 97993486 | |||||||
| chr13:97993562 | A | G | 7 | a0001c0005t0001g0185 a0001c0005t0001g0344 a0001c0005t0001g0345 others(4): Show |
7 | HG01192.hp2 HG01891.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.913+337A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 11/28 | chr13 | 97993562 | |||||||
| chr13:97993601 | A | G | 272 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(269): Show |
280 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(277): Show |
intron_variant | MODIFIER | c.913+376A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 11/28 | chr13 | 97993601 | |||||||
| chr13:97993619 | C | G | 15 | a0001c0001t0001g0335 a0001c0001t0001g0336 a0001c0001t0001g0337 others(12): Show |
15 | HG01109.hp2 HG01123.hp1 HG01975.hp2 others(12): Show |
intron_variant | MODIFIER | c.913+394C>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 11/28 | chr13 | 97993619 | |||||||
| chr13:97993798 | C | CT | 7 | a0001c0001t0001g0011 a0001c0001t0001g0113 a0001c0001t0001g0114 others(4): Show |
7 | HG01884.hp2 HG02976.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.913+574dupT | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr13 | 97993798 | ||||||
| chr13:97993852 | T | A | 44 | a0001c0001t0001g0104 a0001c0001t0002g0039 a0001c0001t0002g0130 others(41): Show |
44 | HG00099.hp1 HG00642.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.913+627T>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 11/28 | chr13 | 97993852 | |||||||
| chr13:97994167 | A | G | 80 | a0001c0002t0001g0327 a0001c0002t0003g0014 a0001c0002t0003g0015 others(77): Show |
82 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.913+942A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 11/28 | chr13 | 97994167 | |||||||
| chr13:97994183 | C | T | 43 | a0001c0001t0002g0039 a0001c0001t0002g0130 a0001c0001t0002g0131 others(40): Show |
43 | HG00099.hp1 HG00642.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.913+958C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 11/28 | chr13 | 97994183 | |||||||
| chr13:97994307 | C | CA | 70 | a0001c0002t0001g0327 a0001c0002t0003g0014 a0001c0002t0003g0015 others(67): Show |
72 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.913+1090dupA | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr13 | 97994307 | ||||||
| chr13:97994596 | A | G | 1 | a0001c0001t0012g0359 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.913+1371A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 11/28 | chr13 | 97994596 | |||||||
| chr13:97994729 | G | T | 39 | a0001c0001t0001g0132 a0001c0001t0001g0137 a0001c0001t0001g0187 others(36): Show |
39 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.913+1504G>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 11/28 | chr13 | 97994729 | |||||||
| chr13:97994858 | G | A | 42 | a0001c0001t0002g0039 a0001c0001t0002g0130 a0001c0001t0002g0131 others(39): Show |
42 | HG00099.hp1 HG00642.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.913+1633G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 11/28 | chr13 | 97994858 | |||||||
| chr13:97994880 | A | G | 2 | a0001c0003t0001g0207 a0001c0003t0001g0217 |
2 | NA19079.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.913+1655A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 11/28 | chr13 | 97994880 | |||||||
| chr13:97995012 | G | A | 7 | a0001c0005t0001g0185 a0001c0005t0001g0344 a0001c0005t0001g0345 others(4): Show |
7 | HG01192.hp2 HG01891.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.913+1787G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 11/28 | chr13 | 97995012 | |||||||
| chr13:97995057 | C | G | 1 | a0001c0001t0001g0326 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.913+1832C>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 11/28 | chr13 | 97995057 | |||||||
| chr13:97995124 | C | CA | 8 | a0001c0001t0001g0308 a0001c0001t0001g0323 a0001c0001t0001g0360 others(5): Show |
8 | HG01978.hp1 HG02027.hp2 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.913+1916dupA | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr13 | 97995124 | ||||||
| chr13:97995157 | T | G | 5 | a0001c0001t0001g0256 a0001c0001t0001g0262 a0001c0001t0001g0305 others(2): Show |
5 | HG01099.hp1 HG01255.hp1 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.913+1932T>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 11/28 | chr13 | 97995157 | |||||||
| chr13:97995179 | G | GT | 13 | a0001c0001t0001g0285 a0001c0001t0002g0006 a0001c0001t0002g0007 others(10): Show |
15 | HG00621.hp1 HG01167.hp2 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.913+1968dupT | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr13 | 97995179 | ||||||
| chr13:97995186 | T | G | 4 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0115 others(1): Show |
4 | HG01884.hp2 HG03209.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.913+1961T>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 11/28 | chr13 | 97995186 | |||||||
| chr13:97995190 | T | G | 41 | a0001c0001t0001g0011 a0001c0001t0001g0074 a0001c0001t0001g0104 others(38): Show |
41 | HG00544.hp2 HG01192.hp2 HG01884.hp2 others(38): Show |
intron_variant | MODIFIER | c.913+1965T>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 11/28 | chr13 | 97995190 | |||||||
| chr13:97995191 | T | G | 1 | a0001c0001t0002g0184 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.913+1966T>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 11/28 | chr13 | 97995191 | |||||||
| chr13:97995241 | T | C | 85 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(82): Show |
88 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(85): Show |
intron_variant | MODIFIER | c.913+2016T>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 11/28 | chr13 | 97995241 | |||||||
| chr13:97995347 | A | G | 1 | a0001c0001t0012g0359 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.913+2122A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 11/28 | chr13 | 97995347 | |||||||
| chr13:97995483 | C | T | 2 | a0001c0001t0001g0336 a0001c0001t0001g0337 |
2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.914-2048C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 11/28 | chr13 | 97995483 | |||||||
| chr13:97995484 | G | A | 4 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0299 others(1): Show |
4 | HG01261.hp1 HG01993.hp1 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.914-2047G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 11/28 | chr13 | 97995484 | |||||||
| chr13:97995549 | A | T | 9 | a0001c0004t0005g0010 a0001c0004t0005g0352 a0001c0004t0005g0353 others(6): Show |
9 | NA18950.hp2 NA18966.hp1 NA18982.hp1 others(6): Show |
intron_variant | MODIFIER | c.914-1982A>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 11/28 | chr13 | 97995549 | |||||||
| chr13:97995552 | A | G | 272 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(269): Show |
280 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(277): Show |
intron_variant | MODIFIER | c.914-1979A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 11/28 | chr13 | 97995552 | |||||||
| chr13:97995649 | G | A | 9 | a0001c0004t0005g0010 a0001c0004t0005g0352 a0001c0004t0005g0353 others(6): Show |
9 | NA18950.hp2 NA18966.hp1 NA18982.hp1 others(6): Show |
intron_variant | MODIFIER | c.914-1882G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 11/28 | chr13 | 97995649 | |||||||
| chr13:97995687 | A | G | 43 | a0001c0001t0001g0104 a0001c0001t0002g0039 a0001c0001t0002g0130 others(40): Show |
43 | HG00099.hp1 HG00642.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.914-1844A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 11/28 | chr13 | 97995687 | |||||||
| chr13:97995734 | A | G | 80 | a0001c0002t0001g0327 a0001c0002t0003g0014 a0001c0002t0003g0015 others(77): Show |
82 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.914-1797A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 11/28 | chr13 | 97995734 | |||||||
| chr13:97995817 | C | T | 1 | a0001c0001t0012g0359 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.914-1714C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 11/28 | chr13 | 97995817 | |||||||
| chr13:97995979 | A | G | 1 | a0001c0001t0001g0329 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.914-1552A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 11/28 | chr13 | 97995979 | |||||||
| chr13:97996040 | A | G | 4 | a0001c0001t0001g0003 a0001c0001t0001g0081 a0001c0001t0001g0082 others(1): Show |
5 | HG01361.hp1 HG01884.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.914-1491A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 11/28 | chr13 | 97996040 | |||||||
| chr13:97996530 | A | G | 2 | a0001c0001t0001g0360 a0001c0001t0001g0365 |
2 | HG02572.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.914-1001A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 11/28 | chr13 | 97996530 | |||||||
| chr13:97996641 | C | G | 5 | a0001c0001t0001g0074 a0001c0001t0001g0118 a0001c0001t0001g0119 others(2): Show |
5 | HG00639.hp1 HG01517.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.914-890C>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 11/28 | chr13 | 97996641 | |||||||
| chr13:97996698 | G | A | 1 | a0001c0001t0001g0339 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.914-833G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 11/28 | chr13 | 97996698 | |||||||
| chr13:97996751 | C | T | 1 | a0001c0001t0014g0169 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.914-780C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 11/28 | chr13 | 97996751 | |||||||
| chr13:97996795 | T | C | 1 | a0001c0001t0001g0084 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.914-736T>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 11/28 | chr13 | 97996795 | |||||||
| chr13:97996835 | G | A | 9 | a0001c0004t0005g0010 a0001c0004t0005g0352 a0001c0004t0005g0353 others(6): Show |
9 | NA18950.hp2 NA18966.hp1 NA18982.hp1 others(6): Show |
intron_variant | MODIFIER | c.914-696G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 11/28 | chr13 | 97996835 | |||||||
| chr13:97997024 | A | G | 1 | a0001c0001t0002g0181 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.914-507A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 11/28 | chr13 | 97997024 | |||||||
| chr13:97997337 | C | CTTCATTA others(3): Show |
13 | a0001c0002t0003g0037 a0001c0002t0004g0001 a0001c0002t0004g0002 others(10): Show |
15 | HG00621.hp2 NA18959.hp1 NA18959.hp2 others(12): Show |
intron_variant | MODIFIER | c.914-192_914-191ins others(10): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr13 | 97997337 | ||||||
| chr13:97997479 | A | G | 1 | a0001c0002t0003g0029 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.914-52A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 11/28 | chr13 | 97997479 | |||||||
| chr13:97997486 | A | C | 71 | a0001c0002t0001g0327 a0001c0002t0003g0014 a0001c0002t0003g0015 others(68): Show |
73 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.914-45A>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 11/28 | chr13 | 97997486 | |||||||
| chr13:97997496 | A | C | 3 | a0001c0001t0001g0085 a0001c0001t0001g0087 a0001c0001t0001g0094 |
3 | HG01109.hp1 HG02055.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.914-35A>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 11/28 | chr13 | 97997496 | |||||||
| chr13:97997675 | C | T | 1 | a0001c0001t0002g0176 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1001+57C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 12/28 | chr13 | 97997675 | |||||||
| chr13:97997770 | G | T | 249 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(246): Show |
257 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(254): Show |
intron_variant | MODIFIER | c.1001+152G>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 12/28 | chr13 | 97997770 | |||||||
| chr13:97997847 | A | G | 4 | a0001c0001t0001g0004 a0001c0001t0001g0095 a0001c0001t0001g0096 others(1): Show |
5 | HG02615.hp1 HG03471.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1001+229A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 12/28 | chr13 | 97997847 | |||||||
| chr13:97997945 | T | C | 71 | a0001c0002t0001g0327 a0001c0002t0003g0014 a0001c0002t0003g0015 others(68): Show |
73 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.1001+327T>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 12/28 | chr13 | 97997945 | |||||||
| chr13:97998015 | GC | G | 5 | a0001c0001t0001g0361 a0001c0001t0001g0362 a0001c0001t0001g0363 others(2): Show |
5 | HG01109.hp2 HG01123.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1001+400delC | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 12/28 | INFO_REALIGN_3_PRIME | chr13 | 97998015 | ||||||
| chr13:97998038 | C | G | 1 | a0001c0001t0001g0108 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1001+420C>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 12/28 | chr13 | 97998038 | |||||||
| chr13:97998045 | G | A | 1 | a0001c0001t0001g0194 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1001+427G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 12/28 | chr13 | 97998045 | |||||||
| chr13:97998175 | C | G | 3 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0120 |
3 | HG00639.hp1 HG01517.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1001+557C>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 12/28 | chr13 | 97998175 | |||||||
| chr13:97998212 | T | C | 1 | a0001c0004t0005g0353 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1001+594T>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 12/28 | chr13 | 97998212 | |||||||
| chr13:97998222 | G | A | 43 | a0001c0001t0002g0039 a0001c0001t0002g0130 a0001c0001t0002g0131 others(40): Show |
43 | HG00099.hp1 HG00642.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.1001+604G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 12/28 | chr13 | 97998222 | |||||||
| chr13:97998265 | G | A | 4 | a0001c0002t0003g0025 a0001c0002t0003g0027 a0001c0002t0003g0028 others(1): Show |
4 | HG00423.hp2 HG02155.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.1001+647G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 12/28 | chr13 | 97998265 | |||||||
| chr13:97998297 | C | T | 4 | a0001c0001t0001g0368 a0001c0001t0001g0369 a0001c0001t0001g0370 others(1): Show |
4 | HG02257.hp2 HG02451.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1001+679C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 12/28 | chr13 | 97998297 | |||||||
| chr13:97998298 | G | A | 1 | a0001c0001t0001g0248 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1001+680G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 12/28 | chr13 | 97998298 | |||||||
| chr13:97998336 | T | G | 1 | a0001c0001t0001g0208 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1001+718T>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 12/28 | chr13 | 97998336 | |||||||
| chr13:97998363 | A | G | 15 | a0001c0001t0001g0335 a0001c0001t0001g0336 a0001c0001t0001g0337 others(12): Show |
15 | HG01109.hp2 HG01123.hp1 HG01975.hp2 others(12): Show |
intron_variant | MODIFIER | c.1001+745A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 12/28 | chr13 | 97998363 | |||||||
| chr13:97998626 | G | A | 2 | a0001c0001t0001g0138 a0001c0001t0001g0145 |
2 | NA18975.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.1001+1008G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 12/28 | chr13 | 97998626 | |||||||
| chr13:97998836 | C | T | 1 | a0001c0001t0001g0301 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1001+1218C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 12/28 | chr13 | 97998836 | |||||||
| chr13:97999108 | G | A | 79 | a0001c0002t0003g0014 a0001c0002t0003g0015 a0001c0002t0003g0016 others(76): Show |
81 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.1002-1431G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 12/28 | chr13 | 97999108 | |||||||
| chr13:97999142 | CA | C | 15 | a0001c0001t0001g0335 a0001c0001t0001g0336 a0001c0001t0001g0337 others(12): Show |
15 | HG01109.hp2 HG01123.hp1 HG01975.hp2 others(12): Show |
intron_variant | MODIFIER | c.1002-1389delA | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 12/28 | INFO_REALIGN_3_PRIME | chr13 | 97999142 | ||||||
| chr13:97999281 | A | G | 63 | a0001c0002t0003g0014 a0001c0002t0003g0015 a0001c0002t0003g0016 others(60): Show |
65 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.1002-1258A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 12/28 | chr13 | 97999281 | |||||||
| chr13:97999370 | A | C | 2 | a0001c0001t0001g0257 a0001c0001t0001g0258 |
2 | HG02572.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1002-1169A>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 12/28 | chr13 | 97999370 | |||||||
| chr13:97999381 | G | A | 63 | a0001c0002t0003g0014 a0001c0002t0003g0015 a0001c0002t0003g0016 others(60): Show |
65 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.1002-1158G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 12/28 | chr13 | 97999381 | |||||||
| chr13:97999481 | T | G | 2 | a0001c0001t0001g0080 a0001c0001t0001g0093 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1002-1058T>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 12/28 | chr13 | 97999481 | |||||||
| chr13:97999575 | G | C | 1 | a0001c0001t0001g0325 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1002-964G>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 12/28 | chr13 | 97999575 | |||||||
| chr13:97999839 | A | G | 1 | a0001c0001t0001g0326 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1002-700A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 12/28 | chr13 | 97999839 | |||||||
| chr13:97999864 | A | C | 1 | a0001c0001t0012g0359 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1002-675A>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 12/28 | chr13 | 97999864 | |||||||
| chr13:97999924 | G | A | 9 | a0001c0004t0005g0010 a0001c0004t0005g0352 a0001c0004t0005g0353 others(6): Show |
9 | NA18950.hp2 NA18966.hp1 NA18982.hp1 others(6): Show |
intron_variant | MODIFIER | c.1002-615G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 12/28 | chr13 | 97999924 | |||||||
| chr13:97999974 | G | A | 1 | a0001c0001t0001g0362 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1002-565G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 12/28 | chr13 | 97999974 | |||||||
| chr13:97999985 | C | G | 2 | a0001c0001t0001g0084 a0001c0001t0001g0107 |
2 | HG02451.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1002-554C>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 12/28 | chr13 | 97999985 | |||||||
| chr13:98000049 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1002-490C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 12/28 | chr13 | 98000049 | |||||||
| chr13:98000059 | C | T | 63 | a0001c0002t0003g0014 a0001c0002t0003g0015 a0001c0002t0003g0016 others(60): Show |
65 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.1002-480C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 12/28 | chr13 | 98000059 | |||||||
| chr13:98000081 | A | G | 10 | a0001c0001t0018g0190 a0001c0004t0005g0010 a0001c0004t0005g0352 others(7): Show |
10 | HG02257.hp2 NA18950.hp2 NA18966.hp1 others(7): Show |
intron_variant | MODIFIER | c.1002-458A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 12/28 | chr13 | 98000081 | |||||||
| chr13:98000088 | T | C | 3 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0120 |
3 | HG00639.hp1 HG01517.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1002-451T>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 12/28 | chr13 | 98000088 | |||||||
| chr13:98000098 | C | T | 2 | a0001c0001t0002g0151 a0001c0001t0002g0153 |
2 | HG01175.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.1002-441C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 12/28 | chr13 | 98000098 | |||||||
| chr13:98000099 | A | G | 57 | a0001c0001t0001g0074 a0001c0001t0001g0188 a0001c0001t0001g0350 others(54): Show |
59 | HG00099.hp1 HG00642.hp1 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.1002-440A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 12/28 | chr13 | 98000099 | |||||||
| chr13:98000144 | G | T | 1 | a0001c0001t0012g0359 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1002-395G>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 12/28 | chr13 | 98000144 | |||||||
| chr13:98000224 | G | A | 1 | a0001c0001t0001g0329 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1002-315G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 12/28 | chr13 | 98000224 | |||||||
| chr13:98000227 | G | C | 3 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0120 |
3 | HG00639.hp1 HG01517.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1002-312G>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 12/28 | chr13 | 98000227 | |||||||
| chr13:98000234 | G | A | 1 | a0001c0001t0001g0216 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1002-305G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 12/28 | chr13 | 98000234 | |||||||
| chr13:98000240 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1002-299G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 12/28 | chr13 | 98000240 | |||||||
| chr13:98000271 | C | T | 1 | a0001c0002t0003g0023 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1002-268C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 12/28 | chr13 | 98000271 | |||||||
| chr13:98000329 | T | C | 9 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0112 others(6): Show |
11 | HG01192.hp1 HG01243.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1002-210T>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 12/28 | chr13 | 98000329 | |||||||
| chr13:98000390 | C | A | 1 | a0001c0001t0001g0231 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1002-149C>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 12/28 | chr13 | 98000390 | |||||||
| chr13:98000513 | G | A | 4 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0195 others(1): Show |
4 | HG02071.hp1 HG02080.hp1 HG02165.hp1 others(1): Show |
intron_variant | MODIFIER | c.1002-26G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 12/28 | chr13 | 98000513 | |||||||
| chr13:98000651 | C | T | 1 | a0001c0001t0001g0365 | 1 | HG02572.hp2 | splice_region_variant&intron_variant | LOW | c.1108+6C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 13/28 | chr13 | 98000651 | |||||||
| chr13:98000784 | G | A | 2 | a0001c0001t0001g0146 a0001c0001t0001g0279 |
2 | NA18966.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.1108+139G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 13/28 | chr13 | 98000784 | |||||||
| chr13:98001008 | C | T | 2 | a0001c0001t0001g0267 a0001c0001t0011g0319 |
2 | NA19009.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.1108+363C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 13/28 | chr13 | 98001008 | |||||||
| chr13:98001061 | A | C | 1 | a0001c0012t0001g0219 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1108+416A>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 13/28 | chr13 | 98001061 | |||||||
| chr13:98001096 | A | T | 4 | a0001c0004t0005g0010 a0001c0004t0005g0353 a0001c0004t0005g0357 others(1): Show |
4 | NA18950.hp2 NA18982.hp1 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.1108+451A>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 13/28 | chr13 | 98001096 | |||||||
| chr13:98001112 | A | G | 1 | a0001c0001t0002g0183 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1108+467A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 13/28 | chr13 | 98001112 | |||||||
| chr13:98001137 | G | A | 1 | a0001c0001t0001g0328 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1108+492G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 13/28 | chr13 | 98001137 | |||||||
| chr13:98001174 | A | G | 38 | a0001c0001t0001g0132 a0001c0001t0001g0137 a0001c0001t0001g0187 others(35): Show |
38 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.1108+529A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 13/28 | chr13 | 98001174 | |||||||
| chr13:98001377 | C | A | 1 | a0001c0001t0001g0231 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1108+732C>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 13/28 | chr13 | 98001377 | |||||||
| chr13:98001726 | C | G | 4 | a0001c0001t0001g0086 a0001c0001t0001g0088 a0001c0001t0001g0089 others(1): Show |
4 | HG02622.hp1 HG02630.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1109-741C>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 13/28 | chr13 | 98001726 | |||||||
| chr13:98001802 | C | T | 1 | a0001c0001t0001g0350 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1109-665C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 13/28 | chr13 | 98001802 | |||||||
| chr13:98001811 | G | A | 21 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0224 others(18): Show |
21 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.1109-656G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 13/28 | chr13 | 98001811 | |||||||
| chr13:98001881 | T | C | 64 | a0001c0002t0001g0327 a0001c0002t0003g0014 a0001c0002t0003g0015 others(61): Show |
66 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.1109-586T>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 13/28 | chr13 | 98001881 | |||||||
| chr13:98001888 | A | G | 1 | a0001c0002t0003g0071 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1109-579A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 13/28 | chr13 | 98001888 | |||||||
| chr13:98001944 | G | A | 2 | a0001c0001t0001g0257 a0001c0001t0001g0258 |
2 | HG02572.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1109-523G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 13/28 | chr13 | 98001944 | |||||||
| chr13:98001978 | A | G | 1 | a0001c0002t0003g0033 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1109-489A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 13/28 | chr13 | 98001978 | |||||||
| chr13:98002021 | G | GT | 24 | a0001c0001t0001g0138 a0001c0001t0001g0142 a0001c0001t0001g0145 others(21): Show |
24 | HG00544.hp2 HG01346.hp1 NA18950.hp2 others(21): Show |
intron_variant | MODIFIER | c.1109-436dupT | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 13/28 | INFO_REALIGN_3_PRIME | chr13 | 98002021 | ||||||
| chr13:98002080 | C | T | 1 | a0001c0001t0001g0328 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1109-387C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 13/28 | chr13 | 98002080 | |||||||
| chr13:98002205 | C | T | 3 | a0001c0001t0001g0268 a0001c0001t0001g0270 a0001c0001t0001g0284 |
3 | HG00099.hp2 HG01106.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1109-262C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 13/28 | chr13 | 98002205 | |||||||
| chr13:98002218 | C | T | 5 | a0001c0005t0001g0185 a0001c0005t0001g0344 a0001c0005t0001g0345 others(2): Show |
5 | HG01192.hp2 HG02886.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1109-249C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 13/28 | chr13 | 98002218 | |||||||
| chr13:98002294 | C | T | 1 | a0001c0001t0002g0128 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1109-173C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 13/28 | chr13 | 98002294 | |||||||
| chr13:98002301 | C | T | 39 | a0001c0001t0001g0132 a0001c0001t0001g0137 a0001c0001t0001g0187 others(36): Show |
39 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.1109-166C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 13/28 | chr13 | 98002301 | |||||||
| chr13:98002354 | T | C | 80 | a0001c0002t0001g0327 a0001c0002t0003g0014 a0001c0002t0003g0015 others(77): Show |
82 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.1109-113T>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 13/28 | chr13 | 98002354 | |||||||
| chr13:98002421 | G | A | 5 | a0001c0001t0001g0248 a0001c0001t0001g0256 a0001c0001t0001g0261 others(2): Show |
5 | HG00738.hp1 HG01099.hp1 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.1109-46G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 13/28 | chr13 | 98002421 | |||||||
| chr13:98002830 | T | A | 2 | a0001c0001t0001g0350 a0001c0001t0001g0351 |
2 | HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1324-34T>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 15/28 | chr13 | 98002830 | |||||||
| chr13:98003136 | TA | T | 7 | a0001c0005t0001g0185 a0001c0005t0001g0344 a0001c0005t0001g0345 others(4): Show |
7 | HG01192.hp2 HG01891.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1497+102delA | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 16/28 | INFO_REALIGN_3_PRIME | chr13 | 98003136 | ||||||
| chr13:98003169 | A | G | 1 | a0001c0001t0001g0109 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1497+132A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 16/28 | chr13 | 98003169 | |||||||
| chr13:98003174 | G | C | 15 | a0001c0001t0001g0335 a0001c0001t0001g0336 a0001c0001t0001g0337 others(12): Show |
15 | HG01109.hp2 HG01123.hp1 HG01975.hp2 others(12): Show |
intron_variant | MODIFIER | c.1497+137G>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 16/28 | chr13 | 98003174 | |||||||
| chr13:98003228 | A | C | 20 | a0001c0001t0001g0012 a0001c0001t0001g0144 a0001c0001t0001g0244 others(17): Show |
20 | HG00609.hp2 HG01928.hp2 HG02027.hp1 others(17): Show |
intron_variant | MODIFIER | c.1497+191A>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 16/28 | chr13 | 98003228 | |||||||
| chr13:98003266 | A | G | 9 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0112 others(6): Show |
11 | HG01192.hp1 HG01243.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1497+229A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 16/28 | chr13 | 98003266 | |||||||
| chr13:98003572 | C | T | 64 | a0001c0002t0001g0327 a0001c0002t0003g0014 a0001c0002t0003g0015 others(61): Show |
66 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.1497+535C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 16/28 | chr13 | 98003572 | |||||||
| chr13:98003664 | A | T | 1 | a0001c0001t0012g0359 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1497+627A>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 16/28 | chr13 | 98003664 | |||||||
| chr13:98003686 | C | T | 1 | a0001c0001t0001g0328 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1497+649C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 16/28 | chr13 | 98003686 | |||||||
| chr13:98004073 | T | C | 7 | a0001c0005t0001g0185 a0001c0005t0001g0344 a0001c0005t0001g0345 others(4): Show |
7 | HG01192.hp2 HG01891.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1497+1036T>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 16/28 | chr13 | 98004073 | |||||||
| chr13:98004158 | A | G | 1 | a0001c0014t0001g0110 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1497+1121A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 16/28 | chr13 | 98004158 | |||||||
| chr13:98004198 | C | T | 3 | a0001c0001t0001g0003 a0001c0001t0001g0081 a0001c0001t0001g0082 |
4 | HG01884.hp1 HG02486.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1497+1161C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 16/28 | chr13 | 98004198 | |||||||
| chr13:98004261 | C | G | 2 | a0001c0001t0001g0202 a0001c0001t0001g0214 |
2 | HG00609.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.1497+1224C>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 16/28 | chr13 | 98004261 | |||||||
| chr13:98004321 | G | A | 5 | a0001c0002t0003g0026 a0001c0002t0003g0036 a0001c0002t0003g0037 others(2): Show |
5 | NA18612.hp2 NA18959.hp2 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.1497+1284G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 16/28 | chr13 | 98004321 | |||||||
| chr13:98004330 | T | C | 6 | a0001c0001t0001g0329 a0001c0001t0002g0157 a0001c0001t0002g0176 others(3): Show |
6 | HG01928.hp1 HG01952.hp2 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.1497+1293T>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 16/28 | chr13 | 98004330 | |||||||
| chr13:98004370 | C | G | 2 | a0001c0001t0001g0138 a0001c0001t0001g0145 |
2 | NA18975.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.1497+1333C>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 16/28 | chr13 | 98004370 | |||||||
| chr13:98004488 | AGGTTTGG others(6): Show |
A | 2 | a0001c0001t0001g0087 a0001c0001t0001g0094 |
2 | HG01109.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.1497+1454_1497+146 others(17): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 16/28 | INFO_REALIGN_3_PRIME | chr13 | 98004488 | ||||||
| chr13:98004514 | A | T | 5 | a0001c0002t0003g0034 a0001c0002t0003g0051 a0001c0002t0003g0053 others(2): Show |
5 | HG00558.hp1 HG00597.hp2 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.1497+1477A>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 16/28 | chr13 | 98004514 | |||||||
| chr13:98004556 | A | G | 3 | a0001c0001t0001g0368 a0001c0001t0001g0369 a0001c0001t0001g0370 |
3 | HG02451.hp2 HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1497+1519A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 16/28 | chr13 | 98004556 | |||||||
| chr13:98004661 | G | A | 2 | a0001c0001t0001g0189 a0001c0001t0018g0190 |
2 | HG02257.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1498-1469G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 16/28 | chr13 | 98004661 | |||||||
| chr13:98004873 | ATATTT | A | 9 | a0001c0004t0005g0010 a0001c0004t0005g0352 a0001c0004t0005g0353 others(6): Show |
9 | NA18950.hp2 NA18966.hp1 NA18982.hp1 others(6): Show |
intron_variant | MODIFIER | c.1498-1236_1498-123 others(9): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 16/28 | INFO_REALIGN_3_PRIME | chr13 | 98004873 | ||||||
| chr13:98004891 | TTTTA | T | 15 | a0001c0001t0001g0335 a0001c0001t0001g0336 a0001c0001t0001g0337 others(12): Show |
15 | HG01109.hp2 HG01123.hp1 HG01975.hp2 others(12): Show |
intron_variant | MODIFIER | c.1498-1219_1498-121 others(8): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 16/28 | INFO_REALIGN_3_PRIME | chr13 | 98004891 | ||||||
| chr13:98004895 | A | AT | 3 | a0001c0001t0001g0139 a0001c0001t0001g0246 a0001c0001t0001g0247 |
3 | HG01070.hp2 HG03831.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1498-1232dupT | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 16/28 | INFO_REALIGN_3_PRIME | chr13 | 98004895 | ||||||
| chr13:98005020 | C | G | 11 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0224 others(8): Show |
11 | HG00438.hp2 HG00558.hp2 HG02155.hp2 others(8): Show |
intron_variant | MODIFIER | c.1498-1110C>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 16/28 | chr13 | 98005020 | |||||||
| chr13:98005101 | T | C | 4 | a0001c0001t0006g0009 a0001c0001t0006g0331 a0001c0001t0006g0332 others(1): Show |
5 | HG01243.hp1 HG02559.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1498-1029T>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 16/28 | chr13 | 98005101 | |||||||
| chr13:98005132 | A | G | 9 | a0001c0004t0005g0010 a0001c0004t0005g0352 a0001c0004t0005g0353 others(6): Show |
9 | NA18950.hp2 NA18966.hp1 NA18982.hp1 others(6): Show |
intron_variant | MODIFIER | c.1498-998A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 16/28 | chr13 | 98005132 | |||||||
| chr13:98005137 | T | A | 1 | a0001c0001t0001g0111 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1498-993T>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 16/28 | chr13 | 98005137 | |||||||
| chr13:98005158 | A | C | 7 | a0001c0001t0001g0335 a0001c0001t0001g0336 a0001c0001t0001g0337 others(4): Show |
7 | HG01975.hp2 HG02647.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1498-972A>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 16/28 | chr13 | 98005158 | |||||||
| chr13:98005173 | A | G | 170 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(167): Show |
176 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(173): Show |
intron_variant | MODIFIER | c.1498-957A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 16/28 | chr13 | 98005173 | |||||||
| chr13:98005180 | A | C | 1 | a0001c0001t0002g0166 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1498-950A>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 16/28 | chr13 | 98005180 | |||||||
| chr13:98005187 | G | A | 7 | a0001c0005t0001g0185 a0001c0005t0001g0344 a0001c0005t0001g0345 others(4): Show |
7 | HG01192.hp2 HG01891.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1498-943G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 16/28 | chr13 | 98005187 | |||||||
| chr13:98005211 | T | TC | 7 | a0001c0005t0001g0185 a0001c0005t0001g0344 a0001c0005t0001g0345 others(4): Show |
7 | HG01192.hp2 HG01891.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1498-915dupC | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 16/28 | INFO_REALIGN_3_PRIME | chr13 | 98005211 | ||||||
| chr13:98005258 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1498-872C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 16/28 | chr13 | 98005258 | |||||||
| chr13:98005305 | C | G | 2 | a0001c0001t0001g0257 a0001c0001t0001g0258 |
2 | HG02572.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1498-825C>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 16/28 | chr13 | 98005305 | |||||||
| chr13:98005338 | A | G | 2 | a0001c0001t0001g0257 a0001c0001t0001g0258 |
2 | HG02572.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1498-792A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 16/28 | chr13 | 98005338 | |||||||
| chr13:98005365 | T | TTTTA | 18 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0143 others(15): Show |
18 | HG00438.hp1 HG00735.hp2 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.1498-724_1498-721d others(6): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 16/28 | INFO_REALIGN_3_PRIME | chr13 | 98005365 | ||||||
| chr13:98005365 | TTTTA | T | 7 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0115 others(4): Show |
7 | HG01884.hp2 HG01928.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1498-724_1498-721d others(6): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 16/28 | INFO_REALIGN_3_PRIME | chr13 | 98005365 | ||||||
| chr13:98005365 | TTTTATTT others(1): Show |
T | 103 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(100): Show |
106 | HG00099.hp1 HG00642.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.1498-728_1498-721d others(10): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 16/28 | INFO_REALIGN_3_PRIME | chr13 | 98005365 | ||||||
| chr13:98005365 | TTTTATTT others(5): Show |
T | 23 | a0001c0001t0001g0074 a0001c0001t0001g0118 a0001c0001t0001g0119 others(20): Show |
26 | HG00639.hp1 HG01192.hp1 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.1498-732_1498-721d others(14): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 16/28 | INFO_REALIGN_3_PRIME | chr13 | 98005365 | ||||||
| chr13:98005365 | TTTTATTT others(9): Show |
T | 80 | a0001c0001t0001g0084 a0001c0001t0001g0109 a0001c0002t0003g0014 others(77): Show |
82 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.1498-736_1498-721d others(18): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 16/28 | INFO_REALIGN_3_PRIME | chr13 | 98005365 | ||||||
| chr13:98005550 | G | A | 2 | a0001c0001t0001g0208 a0001c0001t0001g0210 |
2 | NA18978.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.1498-580G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 16/28 | chr13 | 98005550 | |||||||
| chr13:98005594 | C | T | 20 | a0001c0001t0001g0003 a0001c0001t0001g0075 a0001c0001t0001g0076 others(17): Show |
21 | HG01109.hp1 HG01361.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.1498-536C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 16/28 | chr13 | 98005594 | |||||||
| chr13:98005674 | G | A | 1 | a0001c0001t0001g0328 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1498-456G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 16/28 | chr13 | 98005674 | |||||||
| chr13:98005762 | TATAATC | T | 9 | a0001c0004t0005g0010 a0001c0004t0005g0352 a0001c0004t0005g0353 others(6): Show |
9 | NA18950.hp2 NA18966.hp1 NA18982.hp1 others(6): Show |
intron_variant | MODIFIER | c.1498-363_1498-358d others(8): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 16/28 | INFO_REALIGN_3_PRIME | chr13 | 98005762 | ||||||
| chr13:98005899 | T | G | 1 | a0001c0002t0003g0060 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1498-231T>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 16/28 | chr13 | 98005899 | |||||||
| chr13:98006104 | G | A | 250 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(247): Show |
258 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(255): Show |
intron_variant | MODIFIER | c.1498-26G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 16/28 | chr13 | 98006104 | |||||||
| chr13:98006356 | A | AT | 48 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0113 others(45): Show |
49 | HG00099.hp2 HG00733.hp2 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.1716+44dupT | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 17/28 | INFO_REALIGN_3_PRIME | chr13 | 98006356 | ||||||
| chr13:98006356 | A | ATT | 22 | a0001c0001t0001g0083 a0001c0001t0001g0115 a0001c0001t0001g0246 others(19): Show |
22 | HG00438.hp1 HG01070.hp2 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.1716+43_1716+44dup others(2): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 17/28 | INFO_REALIGN_3_PRIME | chr13 | 98006356 | ||||||
| chr13:98006356 | A | ATTT | 24 | a0001c0001t0001g0074 a0001c0001t0001g0119 a0001c0001t0001g0120 others(21): Show |
25 | HG01192.hp1 HG01517.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.1716+42_1716+44dup others(3): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 17/28 | INFO_REALIGN_3_PRIME | chr13 | 98006356 | ||||||
| chr13:98006356 | A | ATTTT | 10 | a0001c0001t0001g0118 a0001c0001t0001g0121 a0001c0001t0001g0149 others(7): Show |
11 | HG00639.hp1 HG02055.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.1716+41_1716+44dup others(4): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 17/28 | INFO_REALIGN_3_PRIME | chr13 | 98006356 | ||||||
| chr13:98006356 | A | ATTTTTTT others(2): Show |
9 | a0001c0001t0001g0004 a0001c0001t0001g0096 a0001c0001t0001g0097 others(6): Show |
10 | HG02258.hp2 HG03239.hp2 HG03471.hp2 others(7): Show |
intron_variant | MODIFIER | c.1716+36_1716+44dup others(9): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 17/28 | INFO_REALIGN_3_PRIME | chr13 | 98006356 | ||||||
| chr13:98006356 | A | ATTTTTTT others(3): Show |
12 | a0001c0001t0001g0003 a0001c0001t0001g0100 a0001c0001t0001g0101 others(9): Show |
13 | HG00597.hp1 HG00621.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1716+35_1716+44dup others(10): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 17/28 | INFO_REALIGN_3_PRIME | chr13 | 98006356 | ||||||
| chr13:98006356 | A | ATTTTTTT others(4): Show |
15 | a0001c0001t0001g0081 a0001c0001t0001g0192 a0001c0001t0001g0194 others(12): Show |
15 | HG00609.hp1 HG01884.hp1 HG02040.hp1 others(12): Show |
intron_variant | MODIFIER | c.1716+34_1716+44dup others(11): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 17/28 | INFO_REALIGN_3_PRIME | chr13 | 98006356 | ||||||
| chr13:98006356 | A | ATTTTTTT others(5): Show |
9 | a0001c0001t0001g0082 a0001c0001t0001g0137 a0001c0001t0001g0193 others(6): Show |
9 | HG02071.hp1 HG02165.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1716+33_1716+44dup others(12): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 17/28 | INFO_REALIGN_3_PRIME | chr13 | 98006356 | ||||||
| chr13:98006356 | A | ATTTTTTT others(6): Show |
5 | a0001c0001t0001g0094 a0001c0001t0001g0103 a0001c0003t0001g0203 others(2): Show |
5 | HG02055.hp1 HG02523.hp1 NA18960.hp1 others(2): Show |
intron_variant | MODIFIER | c.1716+32_1716+44dup others(13): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 17/28 | INFO_REALIGN_3_PRIME | chr13 | 98006356 | ||||||
| chr13:98006356 | A | ATTTTTTT others(7): Show |
2 | a0001c0001t0001g0087 a0001c0001t0001g0108 |
2 | HG01109.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1716+31_1716+44dup others(14): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 17/28 | INFO_REALIGN_3_PRIME | chr13 | 98006356 | ||||||
| chr13:98006356 | A | ATTTTTTT others(8): Show |
2 | a0001c0001t0001g0105 a0001c0001t0001g0220 |
2 | HG04204.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.1716+30_1716+44dup others(15): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 17/28 | INFO_REALIGN_3_PRIME | chr13 | 98006356 | ||||||
| chr13:98006356 | A | ATTTTTTT others(10): Show |
1 | a0001c0001t0001g0205 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1716+28_1716+44dup others(17): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 17/28 | INFO_REALIGN_3_PRIME | chr13 | 98006356 | ||||||
| chr13:98006356 | A | ATTTTTTT others(11): Show |
2 | a0001c0001t0001g0085 a0001c0001t0001g0091 |
2 | HG02615.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1716+27_1716+44dup others(18): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 17/28 | INFO_REALIGN_3_PRIME | chr13 | 98006356 | ||||||
| chr13:98006356 | A | ATTTTTTT others(18): Show |
1 | a0001c0001t0001g0109 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1716+20_1716+44dup others(25): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 17/28 | INFO_REALIGN_3_PRIME | chr13 | 98006356 | ||||||
| chr13:98006356 | A | ATTTTTTT others(20): Show |
1 | a0001c0001t0001g0350 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1716+18_1716+44dup others(27): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 17/28 | INFO_REALIGN_3_PRIME | chr13 | 98006356 | ||||||
| chr13:98006356 | AT | A | 5 | a0001c0001t0001g0285 a0001c0001t0001g0298 a0001c0001t0006g0009 others(2): Show |
6 | HG01167.hp2 HG02027.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1716+44delT | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 17/28 | INFO_REALIGN_3_PRIME | chr13 | 98006356 | ||||||
| chr13:98006356 | ATTTTTTT others(2): Show |
A | 16 | a0001c0001t0001g0092 a0001c0001t0001g0361 a0001c0001t0001g0362 others(13): Show |
16 | HG00741.hp2 HG01099.hp2 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.1716+36_1716+44del others(9): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 17/28 | INFO_REALIGN_3_PRIME | chr13 | 98006356 | ||||||
| chr13:98006356 | ATTTTTTT others(3): Show |
A | 36 | a0001c0001t0001g0080 a0001c0001t0001g0093 a0001c0001t0002g0039 others(33): Show |
36 | HG00099.hp1 HG00642.hp1 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.1716+35_1716+44del others(10): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 17/28 | INFO_REALIGN_3_PRIME | chr13 | 98006356 | ||||||
| chr13:98006356 | ATTTTTTT others(4): Show |
A | 6 | a0001c0001t0001g0079 a0001c0001t0001g0235 a0001c0001t0001g0292 others(3): Show |
6 | HG00733.hp1 HG01261.hp1 HG02148.hp1 others(3): Show |
intron_variant | MODIFIER | c.1716+34_1716+44del others(11): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 17/28 | INFO_REALIGN_3_PRIME | chr13 | 98006356 | ||||||
| chr13:98006356 | ATTTTTTT others(5): Show |
A | 25 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0077 others(22): Show |
25 | HG00438.hp2 HG00558.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.1716+33_1716+44del others(12): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 17/28 | INFO_REALIGN_3_PRIME | chr13 | 98006356 | ||||||
| chr13:98006356 | ATTTTTTT others(6): Show |
A | 1 | a0001c0001t0001g0225 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1716+32_1716+44del others(13): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 17/28 | INFO_REALIGN_3_PRIME | chr13 | 98006356 | ||||||
| chr13:98006356 | ATTTTTTT others(7): Show |
A | 5 | a0001c0001t0001g0086 a0001c0001t0001g0088 a0001c0001t0001g0089 others(2): Show |
5 | HG02622.hp1 HG02630.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1716+31_1716+44del others(14): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 17/28 | INFO_REALIGN_3_PRIME | chr13 | 98006356 | ||||||
| chr13:98006356 | ATTTTTTT others(8): Show |
A | 3 | a0001c0002t0003g0016 a0001c0002t0003g0060 a0001c0002t0004g0048 |
3 | HG02015.hp2 NA18950.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.1716+30_1716+44del others(15): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 17/28 | INFO_REALIGN_3_PRIME | chr13 | 98006356 | ||||||
| chr13:98006356 | ATTTTTTT others(9): Show |
A | 58 | a0001c0002t0003g0014 a0001c0002t0003g0015 a0001c0002t0003g0018 others(55): Show |
60 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.1716+29_1716+44del others(16): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 17/28 | INFO_REALIGN_3_PRIME | chr13 | 98006356 | ||||||
| chr13:98006356 | ATTTTTTT others(10): Show |
A | 1 | a0001c0002t0004g0050 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1716+28_1716+44del others(17): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 17/28 | INFO_REALIGN_3_PRIME | chr13 | 98006356 | ||||||
| chr13:98006500 | G | A | 1 | a0001c0001t0001g0252 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1716+152G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 17/28 | chr13 | 98006500 | |||||||
| chr13:98006525 | C | T | 1 | a0001c0001t0001g0079 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1716+177C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 17/28 | chr13 | 98006525 | |||||||
| chr13:98006535 | C | T | 1 | a0001c0001t0001g0226 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1716+187C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 17/28 | chr13 | 98006535 | |||||||
| chr13:98006633 | C | G | 1 | a0001c0001t0001g0239 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1716+285C>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 17/28 | chr13 | 98006633 | |||||||
| chr13:98006674 | T | A | 269 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(266): Show |
277 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(274): Show |
intron_variant | MODIFIER | c.1716+326T>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 17/28 | chr13 | 98006674 | |||||||
| chr13:98006807 | C | T | 1 | a0001c0001t0001g0258 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1716+459C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 17/28 | chr13 | 98006807 | |||||||
| chr13:98006863 | G | C | 1 | a0001c0005t0019g0346 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1716+515G>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 17/28 | chr13 | 98006863 | |||||||
| chr13:98006866 | G | GT | 32 | a0001c0001t0001g0011 a0001c0001t0001g0105 a0001c0001t0001g0121 others(29): Show |
33 | HG00597.hp2 HG00733.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.1716+535dupT | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 17/28 | INFO_REALIGN_3_PRIME | chr13 | 98006866 | ||||||
| chr13:98006902 | A | G | 43 | a0001c0001t0001g0104 a0001c0001t0002g0039 a0001c0001t0002g0130 others(40): Show |
43 | HG00099.hp1 HG00642.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.1716+554A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 17/28 | chr13 | 98006902 | |||||||
| chr13:98006919 | G | A | 1 | a0001c0001t0001g0321 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1716+571G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 17/28 | chr13 | 98006919 | |||||||
| chr13:98006973 | C | A | 1 | a0001c0001t0001g0249 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1716+625C>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 17/28 | chr13 | 98006973 | |||||||
| chr13:98007040 | A | AT | 28 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0075 others(25): Show |
30 | HG00639.hp2 HG01109.hp1 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.1716+704dupT | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 17/28 | INFO_REALIGN_3_PRIME | chr13 | 98007040 | ||||||
| chr13:98007139 | C | T | 2 | a0001c0001t0001g0323 a0001c0001t0001g0324 |
2 | NA18974.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1716+791C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 17/28 | chr13 | 98007139 | |||||||
| chr13:98007268 | G | C | 15 | a0001c0001t0001g0335 a0001c0001t0001g0336 a0001c0001t0001g0337 others(12): Show |
15 | HG01109.hp2 HG01123.hp1 HG01975.hp2 others(12): Show |
intron_variant | MODIFIER | c.1717-791G>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 17/28 | chr13 | 98007268 | |||||||
| chr13:98007383 | A | C | 1 | a0001c0001t0001g0248 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1717-676A>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 17/28 | chr13 | 98007383 | |||||||
| chr13:98007505 | T | G | 1 | a0001c0001t0001g0328 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1717-554T>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 17/28 | chr13 | 98007505 | |||||||
| chr13:98007532 | A | G | 4 | a0001c0002t0003g0025 a0001c0002t0003g0027 a0001c0002t0003g0028 others(1): Show |
4 | HG00423.hp2 HG02155.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.1717-527A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 17/28 | chr13 | 98007532 | |||||||
| chr13:98007562 | G | C | 1 | a0001c0001t0001g0012 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1717-497G>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 17/28 | chr13 | 98007562 | |||||||
| chr13:98007630 | A | G | 14 | a0001c0001t0001g0084 a0001c0001t0001g0099 a0001c0001t0001g0100 others(11): Show |
15 | HG02258.hp2 HG02451.hp1 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.1717-429A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 17/28 | chr13 | 98007630 | |||||||
| chr13:98007646 | A | G | 64 | a0001c0002t0001g0327 a0001c0002t0003g0014 a0001c0002t0003g0015 others(61): Show |
66 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.1717-413A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 17/28 | chr13 | 98007646 | |||||||
| chr13:98007707 | G | C | 1 | a0001c0001t0001g0324 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1717-352G>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 17/28 | chr13 | 98007707 | |||||||
| chr13:98008173 | C | T | 4 | a0001c0001t0006g0009 a0001c0001t0006g0331 a0001c0001t0006g0332 others(1): Show |
5 | HG01243.hp1 HG02559.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1800+31C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 18/28 | chr13 | 98008173 | |||||||
| chr13:98008486 | T | C | 1 | a0001c0001t0010g0255 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1800+344T>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 18/28 | chr13 | 98008486 | |||||||
| chr13:98008596 | C | A | 1 | a0001c0004t0005g0358 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1800+454C>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 18/28 | chr13 | 98008596 | |||||||
| chr13:98008606 | C | T | 11 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(8): Show |
11 | HG01192.hp2 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1800+464C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 18/28 | chr13 | 98008606 | |||||||
| chr13:98008684 | A | G | 20 | a0001c0001t0001g0012 a0001c0001t0001g0144 a0001c0001t0001g0244 others(17): Show |
20 | HG00609.hp2 HG01928.hp2 HG02027.hp1 others(17): Show |
intron_variant | MODIFIER | c.1800+542A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 18/28 | chr13 | 98008684 | |||||||
| chr13:98009039 | C | A | 1 | a0001c0001t0001g0294 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1801-842C>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 18/28 | chr13 | 98009039 | |||||||
| chr13:98009059 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1801-822C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 18/28 | chr13 | 98009059 | |||||||
| chr13:98009094 | G | A | 12 | a0001c0002t0004g0001 a0001c0002t0004g0002 a0001c0002t0004g0031 others(9): Show |
14 | HG00621.hp2 NA18959.hp1 NA18971.hp2 others(11): Show |
intron_variant | MODIFIER | c.1801-787G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 18/28 | chr13 | 98009094 | |||||||
| chr13:98009405 | T | C | 65 | a0001c0001t0001g0084 a0001c0002t0001g0327 a0001c0002t0003g0014 others(62): Show |
67 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.1801-476T>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 18/28 | chr13 | 98009405 | |||||||
| chr13:98009671 | T | C | 6 | a0001c0001t0001g0361 a0001c0001t0001g0362 a0001c0001t0001g0363 others(3): Show |
6 | HG01109.hp2 HG01123.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1801-210T>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 18/28 | chr13 | 98009671 | |||||||
| chr13:98010414 | C | G | 1 | a0006c0016t0003g0047 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.2055+190C>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 20/28 | chr13 | 98010414 | |||||||
| chr13:98010500 | T | C | 5 | a0001c0001t0001g0132 a0001c0001t0001g0208 a0001c0001t0001g0209 others(2): Show |
5 | HG00597.hp1 NA18974.hp2 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.2055+276T>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 20/28 | chr13 | 98010500 | |||||||
| chr13:98010510 | A | G | 4 | a0001c0001t0006g0009 a0001c0001t0006g0331 a0001c0001t0006g0332 others(1): Show |
5 | HG01243.hp1 HG02559.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.2055+286A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 20/28 | chr13 | 98010510 | |||||||
| chr13:98010676 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2055+452C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 20/28 | chr13 | 98010676 | |||||||
| chr13:98010779 | C | CATTTTTT others(12): Show |
1 | a0001c0007t0001g0198 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2055+555_2055+556i others(21): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 20/28 | chr13 | 98010779 | |||||||
| chr13:98010780 | C | CT | 11 | a0001c0001t0001g0011 a0001c0001t0001g0113 a0001c0001t0001g0114 others(8): Show |
11 | HG01884.hp2 HG02258.hp1 HG02735.hp1 others(8): Show |
intron_variant | MODIFIER | c.2055+574dupT | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 20/28 | INFO_REALIGN_3_PRIME | chr13 | 98010780 | ||||||
| chr13:98010780 | C | CTTTTTTT others(3): Show |
4 | a0001c0001t0002g0131 a0001c0001t0002g0155 a0001c0001t0002g0160 others(1): Show |
4 | HG01169.hp2 HG01361.hp2 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.2055+565_2055+574d others(12): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 20/28 | INFO_REALIGN_3_PRIME | chr13 | 98010780 | ||||||
| chr13:98010780 | C | CTTTTTTT others(4): Show |
40 | a0001c0001t0001g0118 a0001c0001t0002g0006 a0001c0001t0002g0007 others(37): Show |
42 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.2055+564_2055+574d others(13): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 20/28 | INFO_REALIGN_3_PRIME | chr13 | 98010780 | ||||||
| chr13:98010780 | C | CTTTTTTT others(5): Show |
22 | a0001c0001t0001g0119 a0001c0001t0002g0039 a0001c0001t0002g0124 others(19): Show |
22 | HG01192.hp1 HG01192.hp2 HG01517.hp1 others(19): Show |
intron_variant | MODIFIER | c.2055+563_2055+574d others(14): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 20/28 | INFO_REALIGN_3_PRIME | chr13 | 98010780 | ||||||
| chr13:98010780 | C | CTTTTTTT others(6): Show |
11 | a0001c0001t0001g0074 a0001c0001t0001g0120 a0001c0001t0001g0188 others(8): Show |
11 | HG01346.hp2 HG01891.hp2 HG01981.hp1 others(8): Show |
intron_variant | MODIFIER | c.2055+562_2055+574d others(15): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 20/28 | INFO_REALIGN_3_PRIME | chr13 | 98010780 | ||||||
| chr13:98010780 | C | CTTTTTTT others(7): Show |
3 | a0001c0001t0001g0096 a0001c0001t0001g0368 a0001c0001t0001g0370 |
3 | HG02630.hp1 HG02818.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2055+561_2055+574d others(16): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 20/28 | INFO_REALIGN_3_PRIME | chr13 | 98010780 | ||||||
| chr13:98010780 | C | CTTTTTTT others(8): Show |
1 | a0001c0001t0006g0009 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2055+560_2055+574d others(17): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 20/28 | INFO_REALIGN_3_PRIME | chr13 | 98010780 | ||||||
| chr13:98010780 | C | CTTTTTTT others(9): Show |
10 | a0001c0001t0001g0350 a0001c0001t0001g0351 a0001c0001t0001g0360 others(7): Show |
10 | HG01109.hp2 HG01123.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.2055+559_2055+574d others(18): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 20/28 | INFO_REALIGN_3_PRIME | chr13 | 98010780 | ||||||
| chr13:98010780 | C | CTTTTTTT others(10): Show |
19 | a0001c0001t0001g0187 a0001c0001t0001g0195 a0001c0001t0001g0202 others(16): Show |
19 | HG00609.hp1 HG02015.hp1 HG02040.hp1 others(16): Show |
intron_variant | MODIFIER | c.2055+558_2055+574d others(19): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 20/28 | INFO_REALIGN_3_PRIME | chr13 | 98010780 | ||||||
| chr13:98010780 | C | CTTTTTTT others(11): Show |
12 | a0001c0001t0001g0132 a0001c0001t0001g0192 a0001c0001t0001g0193 others(9): Show |
12 | HG00597.hp1 HG01975.hp2 HG02071.hp1 others(9): Show |
intron_variant | MODIFIER | c.2055+557_2055+574d others(20): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 20/28 | INFO_REALIGN_3_PRIME | chr13 | 98010780 | ||||||
| chr13:98010780 | C | CTTTTTTT others(12): Show |
7 | a0001c0001t0001g0336 a0001c0001t0018g0190 a0001c0003t0001g0197 others(4): Show |
7 | HG02257.hp2 HG02647.hp2 NA18957.hp1 others(4): Show |
intron_variant | MODIFIER | c.2055+574_2055+575i others(21): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 20/28 | INFO_REALIGN_3_PRIME | chr13 | 98010780 | ||||||
| chr13:98010780 | C | CTTTTTTT others(13): Show |
18 | a0001c0001t0001g0083 a0001c0001t0001g0086 a0001c0001t0001g0088 others(15): Show |
18 | HG00621.hp1 HG01361.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.2055+574_2055+575i others(22): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 20/28 | INFO_REALIGN_3_PRIME | chr13 | 98010780 | ||||||
| chr13:98010780 | C | CTTTTTTT others(14): Show |
11 | a0001c0001t0001g0004 a0001c0001t0001g0091 a0001c0001t0001g0095 others(8): Show |
13 | HG02523.hp1 HG02615.hp1 HG03041.hp1 others(10): Show |
intron_variant | MODIFIER | c.2055+574_2055+575i others(23): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 20/28 | INFO_REALIGN_3_PRIME | chr13 | 98010780 | ||||||
| chr13:98010780 | C | CTTTTTTT others(15): Show |
15 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(12): Show |
15 | HG02258.hp2 HG02280.hp2 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.2055+574_2055+575i others(24): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 20/28 | INFO_REALIGN_3_PRIME | chr13 | 98010780 | ||||||
| chr13:98010780 | C | CTTTTTTT others(16): Show |
15 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0087 others(12): Show |
15 | HG00544.hp1 HG01109.hp1 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.2055+574_2055+575i others(25): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 20/28 | INFO_REALIGN_3_PRIME | chr13 | 98010780 | ||||||
| chr13:98010780 | C | CTTTTTTT others(17): Show |
20 | a0001c0001t0001g0237 a0001c0002t0003g0014 a0001c0002t0003g0018 others(17): Show |
20 | HG00423.hp1 HG00423.hp2 HG00639.hp2 others(17): Show |
intron_variant | MODIFIER | c.2055+574_2055+575i others(26): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 20/28 | INFO_REALIGN_3_PRIME | chr13 | 98010780 | ||||||
| chr13:98010780 | C | CTTTTTTT others(18): Show |
17 | a0001c0001t0001g0094 a0001c0001t0001g0238 a0001c0001t0001g0239 others(14): Show |
18 | HG02055.hp1 HG02080.hp2 HG02132.hp1 others(15): Show |
intron_variant | MODIFIER | c.2055+574_2055+575i others(27): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 20/28 | INFO_REALIGN_3_PRIME | chr13 | 98010780 | ||||||
| chr13:98010780 | C | CTTTTTTT others(19): Show |
7 | a0001c0001t0001g0222 a0001c0001t0001g0225 a0001c0001t0001g0227 others(4): Show |
8 | HG00558.hp2 NA18981.hp1 NA18994.hp2 others(5): Show |
intron_variant | MODIFIER | c.2055+574_2055+575i others(28): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 20/28 | INFO_REALIGN_3_PRIME | chr13 | 98010780 | ||||||
| chr13:98010780 | C | CTTTTTTT others(20): Show |
6 | a0001c0001t0001g0228 a0001c0002t0003g0023 a0001c0002t0003g0038 others(3): Show |
6 | HG00597.hp2 HG03704.hp2 NA18986.hp1 others(3): Show |
intron_variant | MODIFIER | c.2055+574_2055+575i others(29): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 20/28 | INFO_REALIGN_3_PRIME | chr13 | 98010780 | ||||||
| chr13:98010780 | C | CTTTTTTT others(21): Show |
7 | a0001c0001t0001g0229 a0001c0001t0001g0233 a0001c0002t0003g0034 others(4): Show |
7 | HG00438.hp2 HG00558.hp1 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.2055+574_2055+575i others(30): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 20/28 | INFO_REALIGN_3_PRIME | chr13 | 98010780 | ||||||
| chr13:98010780 | C | CTTTTTTT others(22): Show |
2 | a0001c0001t0001g0232 a0001c0001t0001g0235 |
2 | HG00733.hp1 HG01070.hp1 |
intron_variant | MODIFIER | c.2055+574_2055+575i others(31): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 20/28 | INFO_REALIGN_3_PRIME | chr13 | 98010780 | ||||||
| chr13:98010780 | C | CTTTTTTT others(23): Show |
3 | a0001c0001t0001g0224 a0001c0001t0001g0234 a0001c0001t0001g0236 |
3 | HG00741.hp1 HG01071.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.2055+574_2055+575i others(32): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 20/28 | INFO_REALIGN_3_PRIME | chr13 | 98010780 | ||||||
| chr13:98010780 | C | CTTTTTTT others(24): Show |
1 | a0001c0001t0001g0226 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.2055+574_2055+575i others(33): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 20/28 | INFO_REALIGN_3_PRIME | chr13 | 98010780 | ||||||
| chr13:98010780 | C | CTTTTTTT others(25): Show |
2 | a0001c0001t0001g0223 a0001c0002t0003g0035 |
2 | HG02135.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.2055+574_2055+575i others(34): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 20/28 | INFO_REALIGN_3_PRIME | chr13 | 98010780 | ||||||
| chr13:98010780 | C | CTTTTTTT others(26): Show |
2 | a0001c0001t0001g0230 a0001c0001t0001g0231 |
2 | NA18956.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.2055+574_2055+575i others(35): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 20/28 | INFO_REALIGN_3_PRIME | chr13 | 98010780 | ||||||
| chr13:98010780 | C | CTTTTTTT others(27): Show |
1 | a0001c0001t0001g0318 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.2055+574_2055+575i others(36): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 20/28 | INFO_REALIGN_3_PRIME | chr13 | 98010780 | ||||||
| chr13:98010780 | C | CTTTTTTT others(29): Show |
1 | a0001c0002t0003g0030 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2055+574_2055+575i others(38): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 20/28 | INFO_REALIGN_3_PRIME | chr13 | 98010780 | ||||||
| chr13:98010780 | C | T | 1 | a0001c0007t0001g0198 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2055+556C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 20/28 | chr13 | 98010780 | |||||||
| chr13:98010807 | G | A | 1 | a0001c0001t0002g0175 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2055+583G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 20/28 | chr13 | 98010807 | |||||||
| chr13:98010878 | T | G | 7 | a0001c0005t0001g0185 a0001c0005t0001g0344 a0001c0005t0001g0345 others(4): Show |
7 | HG01192.hp2 HG01891.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.2055+654T>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 20/28 | chr13 | 98010878 | |||||||
| chr13:98010902 | T | C | 1 | a0001c0001t0001g0244 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.2055+678T>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 20/28 | chr13 | 98010902 | |||||||
| chr13:98010903 | C | T | 1 | a0001c0001t0001g0244 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.2055+679C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 20/28 | chr13 | 98010903 | |||||||
| chr13:98010925 | C | T | 1 | a0001c0005t0019g0346 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2055+701C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 20/28 | chr13 | 98010925 | |||||||
| chr13:98010956 | T | C | 2 | a0001c0001t0002g0172 a0001c0001t0002g0181 |
2 | HG01255.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.2055+732T>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 20/28 | chr13 | 98010956 | |||||||
| chr13:98011273 | T | G | 16 | a0001c0001t0001g0335 a0001c0001t0001g0336 a0001c0001t0001g0337 others(13): Show |
16 | HG01109.hp2 HG01123.hp1 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.2056-973T>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 20/28 | chr13 | 98011273 | |||||||
| chr13:98011277 | TTTTG | T | 6 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0001g0234 others(3): Show |
6 | HG00733.hp1 HG00741.hp1 HG01070.hp1 others(3): Show |
intron_variant | MODIFIER | c.2056-949_2056-946d others(6): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 20/28 | INFO_REALIGN_3_PRIME | chr13 | 98011277 | ||||||
| chr13:98011337 | C | G | 3 | a0001c0001t0001g0368 a0001c0001t0001g0369 a0001c0001t0001g0370 |
3 | HG02451.hp2 HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.2056-909C>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 20/28 | chr13 | 98011337 | |||||||
| chr13:98011376 | C | T | 101 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(98): Show |
104 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(101): Show |
intron_variant | MODIFIER | c.2056-870C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 20/28 | chr13 | 98011376 | |||||||
| chr13:98011609 | C | T | 1 | a0001c0001t0001g0325 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2056-637C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 20/28 | chr13 | 98011609 | |||||||
| chr13:98011647 | C | T | 70 | a0001c0002t0003g0014 a0001c0002t0003g0015 a0001c0002t0003g0016 others(67): Show |
72 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.2056-599C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 20/28 | chr13 | 98011647 | |||||||
| chr13:98011655 | C | T | 7 | a0001c0005t0001g0185 a0001c0005t0001g0344 a0001c0005t0001g0345 others(4): Show |
7 | HG01192.hp2 HG01891.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.2056-591C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 20/28 | chr13 | 98011655 | |||||||
| chr13:98011687 | A | G | 2 | a0001c0001t0001g0075 a0001c0001t0001g0076 |
2 | HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2056-559A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 20/28 | chr13 | 98011687 | |||||||
| chr13:98011826 | A | G | 2 | a0001c0001t0001g0141 a0001c0001t0001g0262 |
2 | HG01346.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.2056-420A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 20/28 | chr13 | 98011826 | |||||||
| chr13:98011837 | G | A | 1 | a0001c0002t0003g0035 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2056-409G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 20/28 | chr13 | 98011837 | |||||||
| chr13:98011876 | G | A | 2 | a0001c0002t0003g0036 a0001c0002t0003g0037 |
2 | NA18612.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.2056-370G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 20/28 | chr13 | 98011876 | |||||||
| chr13:98011932 | C | G | 3 | a0001c0001t0002g0151 a0001c0001t0002g0152 a0001c0001t0002g0153 |
3 | HG01175.hp1 HG02735.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.2056-314C>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 20/28 | chr13 | 98011932 | |||||||
| chr13:98012231 | A | T | 1 | a0001c0001t0001g0326 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2056-15A>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 20/28 | chr13 | 98012231 | |||||||
| chr13:98012733 | C | T | 1 | a0001c0003t0001g0201 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2152+391C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 21/28 | chr13 | 98012733 | |||||||
| chr13:98012765 | G | A | 1 | a0001c0001t0006g0009 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2152+423G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 21/28 | chr13 | 98012765 | |||||||
| chr13:98012801 | A | AT | 9 | a0001c0001t0001g0182 a0001c0001t0001g0265 a0001c0001t0001g0266 others(6): Show |
9 | HG01934.hp1 HG02135.hp2 HG03516.hp2 others(6): Show |
intron_variant | MODIFIER | c.2152+485dupT | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 21/28 | INFO_REALIGN_3_PRIME | chr13 | 98012801 | ||||||
| chr13:98012801 | A | ATTTTTTT others(4): Show |
1 | a0001c0002t0015g0017 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2152+475_2152+485d others(13): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 21/28 | INFO_REALIGN_3_PRIME | chr13 | 98012801 | ||||||
| chr13:98012801 | A | ATTTTTTT others(5): Show |
1 | a0003c0017t0003g0021 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2152+474_2152+485d others(14): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 21/28 | INFO_REALIGN_3_PRIME | chr13 | 98012801 | ||||||
| chr13:98012801 | A | ATTTTTTT others(6): Show |
2 | a0001c0002t0003g0018 a0001c0002t0003g0020 |
2 | HG01069.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.2152+473_2152+485d others(15): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 21/28 | INFO_REALIGN_3_PRIME | chr13 | 98012801 | ||||||
| chr13:98012801 | A | ATTTTTTT others(7): Show |
2 | a0001c0002t0003g0023 a0001c0002t0003g0030 |
2 | HG02027.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.2152+472_2152+485d others(16): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 21/28 | INFO_REALIGN_3_PRIME | chr13 | 98012801 | ||||||
| chr13:98012801 | A | ATTTTTTT others(8): Show |
1 | a0001c0002t0003g0049 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2152+471_2152+485d others(17): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 21/28 | INFO_REALIGN_3_PRIME | chr13 | 98012801 | ||||||
| chr13:98012801 | A | ATTTTTTT others(11): Show |
1 | a0001c0002t0003g0064 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2152+468_2152+485d others(20): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 21/28 | INFO_REALIGN_3_PRIME | chr13 | 98012801 | ||||||
| chr13:98012801 | AT | A | 7 | a0001c0001t0001g0233 a0001c0001t0001g0244 a0001c0001t0001g0246 others(4): Show |
7 | HG00741.hp2 HG01070.hp2 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.2152+485delT | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 21/28 | INFO_REALIGN_3_PRIME | chr13 | 98012801 | ||||||
| chr13:98012801 | ATT | A | 74 | a0001c0001t0001g0074 a0001c0001t0001g0104 a0001c0001t0001g0119 others(71): Show |
75 | HG00099.hp1 HG00642.hp1 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.2152+484_2152+485d others(4): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 21/28 | INFO_REALIGN_3_PRIME | chr13 | 98012801 | ||||||
| chr13:98012801 | ATTT | A | 89 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(86): Show |
94 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(91): Show |
intron_variant | MODIFIER | c.2152+483_2152+485d others(5): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 21/28 | INFO_REALIGN_3_PRIME | chr13 | 98012801 | ||||||
| chr13:98012801 | ATTTTTTT | A | 9 | a0001c0004t0005g0010 a0001c0004t0005g0352 a0001c0004t0005g0353 others(6): Show |
9 | NA18950.hp2 NA18966.hp1 NA18982.hp1 others(6): Show |
intron_variant | MODIFIER | c.2152+479_2152+485d others(9): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 21/28 | INFO_REALIGN_3_PRIME | chr13 | 98012801 | ||||||
| chr13:98012808 | T | TTTTTTTT others(8): Show |
1 | a0001c0002t0004g0048 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.2152+480_2152+481i others(17): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 21/28 | INFO_REALIGN_3_PRIME | chr13 | 98012808 | ||||||
| chr13:98012809 | T | TTTTTTTT others(7): Show |
1 | a0001c0002t0003g0015 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2152+474_2152+475i others(16): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 21/28 | INFO_REALIGN_3_PRIME | chr13 | 98012809 | ||||||
| chr13:98012809 | T | TTTTTTTT others(6): Show |
3 | a0001c0002t0003g0063 a0001c0002t0003g0070 a0001c0002t0004g0045 |
3 | HG02523.hp2 NA19082.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.2152+479_2152+480i others(15): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 21/28 | INFO_REALIGN_3_PRIME | chr13 | 98012809 | ||||||
| chr13:98012809 | T | TTTTTTTT others(7): Show |
45 | a0001c0002t0003g0016 a0001c0002t0003g0019 a0001c0002t0003g0022 others(42): Show |
47 | HG00423.hp1 HG00423.hp2 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.2152+480_2152+481i others(16): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 21/28 | INFO_REALIGN_3_PRIME | chr13 | 98012809 | ||||||
| chr13:98012809 | T | TTTTTTTT others(8): Show |
5 | a0001c0002t0003g0014 a0001c0002t0003g0024 a0001c0002t0003g0026 others(2): Show |
5 | HG02132.hp2 HG03654.hp2 HG04199.hp1 others(2): Show |
intron_variant | MODIFIER | c.2152+481_2152+482i others(17): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 21/28 | INFO_REALIGN_3_PRIME | chr13 | 98012809 | ||||||
| chr13:98012833 | A | T | 9 | a0001c0004t0005g0010 a0001c0004t0005g0352 a0001c0004t0005g0353 others(6): Show |
9 | NA18950.hp2 NA18966.hp1 NA18982.hp1 others(6): Show |
intron_variant | MODIFIER | c.2152+491A>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 21/28 | chr13 | 98012833 | |||||||
| chr13:98012869 | C | A | 3 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0120 |
3 | HG00639.hp1 HG01517.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.2152+527C>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 21/28 | chr13 | 98012869 | |||||||
| chr13:98013154 | C | T | 39 | a0001c0001t0001g0132 a0001c0001t0001g0137 a0001c0001t0001g0187 others(36): Show |
39 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.2152+812C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 21/28 | chr13 | 98013154 | |||||||
| chr13:98013363 | G | C | 7 | a0001c0005t0001g0185 a0001c0005t0001g0344 a0001c0005t0001g0345 others(4): Show |
7 | HG01192.hp2 HG01891.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.2153-679G>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 21/28 | chr13 | 98013363 | |||||||
| chr13:98013413 | G | A | 1 | a0001c0001t0001g0194 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.2153-629G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 21/28 | chr13 | 98013413 | |||||||
| chr13:98013553 | A | G | 1 | a0001c0004t0005g0355 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.2153-489A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 21/28 | chr13 | 98013553 | |||||||
| chr13:98013808 | A | G | 1 | a0001c0001t0001g0102 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2153-234A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 21/28 | chr13 | 98013808 | |||||||
| chr13:98013928 | C | T | 1 | a0001c0001t0001g0011 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2153-114C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 21/28 | chr13 | 98013928 | |||||||
| chr13:98013968 | C | A | 11 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0224 others(8): Show |
11 | HG00438.hp2 HG00558.hp2 HG02155.hp2 others(8): Show |
intron_variant | MODIFIER | c.2153-74C>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 21/28 | chr13 | 98013968 | |||||||
| chr13:98014295 | T | C | 189 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(186): Show |
195 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(192): Show |
intron_variant | MODIFIER | c.2325+81T>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 22/28 | chr13 | 98014295 | |||||||
| chr13:98014600 | A | T | 2 | a0001c0001t0001g0360 a0001c0001t0001g0365 |
2 | HG02572.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2325+386A>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 22/28 | chr13 | 98014600 | |||||||
| chr13:98014789 | T | G | 1 | a0001c0001t0001g0244 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.2325+575T>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 22/28 | chr13 | 98014789 | |||||||
| chr13:98014834 | TTC | T | 85 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(82): Show |
88 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(85): Show |
intron_variant | MODIFIER | c.2325+624_2325+625d others(4): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 22/28 | INFO_REALIGN_3_PRIME | chr13 | 98014834 | ||||||
| chr13:98014837 | TC | T | 15 | a0001c0001t0001g0335 a0001c0001t0001g0336 a0001c0001t0001g0337 others(12): Show |
15 | HG01109.hp2 HG01123.hp1 HG01975.hp2 others(12): Show |
intron_variant | MODIFIER | c.2325+624delC | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 22/28 | chr13 | 98014837 | |||||||
| chr13:98014838 | C | CT | 8 | a0001c0001t0001g0262 a0001c0005t0001g0185 a0001c0005t0001g0344 others(5): Show |
8 | HG01192.hp2 HG01346.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.2325+638dupT | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 22/28 | INFO_REALIGN_3_PRIME | chr13 | 98014838 | ||||||
| chr13:98014945 | C | T | 11 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(8): Show |
12 | HG02258.hp2 HG02451.hp1 HG02523.hp1 others(9): Show |
intron_variant | MODIFIER | c.2326-585C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 22/28 | chr13 | 98014945 | |||||||
| chr13:98014970 | T | C | 3 | a0001c0001t0001g0222 a0001c0001t0001g0225 a0001c0001t0001g0228 |
3 | NA18999.hp1 NA19005.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.2326-560T>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 22/28 | chr13 | 98014970 | |||||||
| chr13:98015005 | T | A | 1 | a0001c0001t0001g0244 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.2326-525T>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 22/28 | chr13 | 98015005 | |||||||
| chr13:98015064 | T | G | 70 | a0001c0001t0001g0310 a0001c0001t0001g0311 a0001c0001t0001g0312 others(67): Show |
72 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.2326-466T>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 22/28 | chr13 | 98015064 | |||||||
| chr13:98015235 | G | C | 4 | a0001c0001t0002g0163 a0001c0001t0002g0168 a0001c0001t0002g0183 others(1): Show |
4 | HG01346.hp2 HG02602.hp2 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.2326-295G>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 22/28 | chr13 | 98015235 | |||||||
| chr13:98015236 | A | T | 4 | a0001c0001t0002g0163 a0001c0001t0002g0168 a0001c0001t0002g0183 others(1): Show |
4 | HG01346.hp2 HG02602.hp2 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.2326-294A>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 22/28 | chr13 | 98015236 | |||||||
| chr13:98015238 | C | G | 4 | a0001c0001t0002g0163 a0001c0001t0002g0168 a0001c0001t0002g0183 others(1): Show |
4 | HG01346.hp2 HG02602.hp2 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.2326-292C>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 22/28 | chr13 | 98015238 | |||||||
| chr13:98015240 | G | T | 4 | a0001c0001t0002g0163 a0001c0001t0002g0168 a0001c0001t0002g0183 others(1): Show |
4 | HG01346.hp2 HG02602.hp2 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.2326-290G>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 22/28 | chr13 | 98015240 | |||||||
| chr13:98015242 | T | TGTGTG | 4 | a0001c0001t0002g0163 a0001c0001t0002g0168 a0001c0001t0002g0183 others(1): Show |
4 | HG01346.hp2 HG02602.hp2 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.2326-288_2326-287i others(7): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 22/28 | chr13 | 98015242 | |||||||
| chr13:98015242 | T | TTG | 89 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0074 others(86): Show |
94 | HG00597.hp1 HG00621.hp1 HG00639.hp1 others(91): Show |
intron_variant | MODIFIER | c.2326-260_2326-259d others(4): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 22/28 | INFO_REALIGN_3_PRIME | chr13 | 98015242 | ||||||
| chr13:98015242 | T | TTGTG | 8 | a0001c0001t0001g0194 a0001c0001t0001g0202 a0001c0001t0001g0213 others(5): Show |
8 | HG00609.hp1 HG02129.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.2326-262_2326-259d others(6): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 22/28 | INFO_REALIGN_3_PRIME | chr13 | 98015242 | ||||||
| chr13:98015242 | T | TTGTGTG | 116 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0096 others(113): Show |
117 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(114): Show |
intron_variant | MODIFIER | c.2326-264_2326-259d others(8): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 22/28 | INFO_REALIGN_3_PRIME | chr13 | 98015242 | ||||||
| chr13:98015242 | T | TTGTGTGT others(1): Show |
42 | a0001c0001t0001g0095 a0001c0001t0001g0267 a0001c0001t0001g0329 others(39): Show |
42 | HG00099.hp1 HG00642.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.2326-266_2326-259d others(10): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 22/28 | INFO_REALIGN_3_PRIME | chr13 | 98015242 | ||||||
| chr13:98015242 | T | TTGTGTGT others(3): Show |
21 | a0001c0001t0001g0189 a0001c0001t0001g0335 a0001c0001t0001g0339 others(18): Show |
21 | HG01109.hp2 HG01123.hp1 HG01975.hp2 others(18): Show |
intron_variant | MODIFIER | c.2326-268_2326-259d others(12): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 22/28 | INFO_REALIGN_3_PRIME | chr13 | 98015242 | ||||||
| chr13:98015242 | T | TTGTGTGT others(5): Show |
5 | a0001c0001t0001g0336 a0001c0001t0001g0337 a0001c0001t0021g0338 others(2): Show |
5 | HG02647.hp2 HG02818.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.2326-270_2326-259d others(14): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 22/28 | INFO_REALIGN_3_PRIME | chr13 | 98015242 | ||||||
| chr13:98015242 | T | TTGTGTGT others(9): Show |
1 | a0001c0001t0001g0326 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2326-274_2326-259d others(18): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 22/28 | INFO_REALIGN_3_PRIME | chr13 | 98015242 | ||||||
| chr13:98015242 | TTG | T | 4 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0106 others(1): Show |
4 | HG02015.hp2 HG03239.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.2326-260_2326-259d others(4): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 22/28 | INFO_REALIGN_3_PRIME | chr13 | 98015242 | ||||||
| chr13:98015396 | A | C | 5 | a0001c0001t0001g0250 a0001c0001t0001g0252 a0001c0001t0001g0253 others(2): Show |
5 | HG00642.hp2 HG00733.hp2 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.2326-134A>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 22/28 | chr13 | 98015396 | |||||||
| chr13:98016031 | A | G | 1 | a0001c0001t0001g0304 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2493+250A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 24/28 | chr13 | 98016031 | |||||||
| chr13:98016143 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2493+362G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 24/28 | chr13 | 98016143 | |||||||
| chr13:98016362 | C | T | 9 | a0001c0004t0005g0010 a0001c0004t0005g0352 a0001c0004t0005g0353 others(6): Show |
9 | NA18950.hp2 NA18966.hp1 NA18982.hp1 others(6): Show |
intron_variant | MODIFIER | c.2494-367C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 24/28 | chr13 | 98016362 | |||||||
| chr13:98016555 | A | G | 1 | a0001c0001t0001g0326 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2494-174A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 24/28 | chr13 | 98016555 | |||||||
| chr13:98016928 | C | T | 3 | a0001c0001t0001g0368 a0001c0001t0001g0369 a0001c0001t0001g0370 |
3 | HG02451.hp2 HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.2616+77C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 25/28 | chr13 | 98016928 | |||||||
| chr13:98017069 | G | A | 2 | a0001c0001t0001g0246 a0001c0001t0001g0272 |
2 | HG01070.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.2616+218G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 25/28 | chr13 | 98017069 | |||||||
| chr13:98017091 | T | C | 4 | a0001c0001t0001g0138 a0001c0001t0001g0145 a0001c0001t0001g0146 others(1): Show |
4 | NA18966.hp2 NA18975.hp2 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.2616+240T>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 25/28 | chr13 | 98017091 | |||||||
| chr13:98017099 | A | AT | 7 | a0001c0001t0001g0368 a0001c0001t0001g0369 a0001c0001t0001g0370 others(4): Show |
8 | HG01243.hp1 HG02451.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.2616+256dupT | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 25/28 | INFO_REALIGN_3_PRIME | chr13 | 98017099 | ||||||
| chr13:98017213 | C | T | 2 | a0001c0001t0002g0039 a0001c0001t0002g0170 |
2 | HG01978.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.2616+362C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 25/28 | chr13 | 98017213 | |||||||
| chr13:98017241 | C | CAT | 8 | a0001c0001t0001g0325 a0001c0005t0001g0185 a0001c0005t0001g0344 others(5): Show |
8 | HG01192.hp2 HG01891.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.2616+405_2616+406d others(4): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 25/28 | INFO_REALIGN_3_PRIME | chr13 | 98017241 | ||||||
| chr13:98017241 | C | CATAT | 64 | a0001c0001t0001g0310 a0001c0001t0001g0311 a0001c0001t0001g0312 others(61): Show |
66 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.2616+403_2616+406d others(6): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 25/28 | INFO_REALIGN_3_PRIME | chr13 | 98017241 | ||||||
| chr13:98017241 | C | CATATAT | 5 | a0001c0002t0003g0014 a0001c0002t0003g0035 a0001c0002t0003g0054 others(2): Show |
5 | HG02040.hp2 HG02135.hp1 HG04199.hp1 others(2): Show |
intron_variant | MODIFIER | c.2616+401_2616+406d others(8): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 25/28 | INFO_REALIGN_3_PRIME | chr13 | 98017241 | ||||||
| chr13:98017258 | G | A | 1 | a0001c0002t0003g0026 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.2616+407G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 25/28 | chr13 | 98017258 | |||||||
| chr13:98017260 | A | T | 2 | a0001c0001t0001g0137 a0001c0001t0001g0204 |
2 | HG02602.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.2616+409A>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 25/28 | chr13 | 98017260 | |||||||
| chr13:98017284 | C | G | 1 | a0001c0001t0001g0249 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2616+433C>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 25/28 | chr13 | 98017284 | |||||||
| chr13:98017311 | T | C | 70 | a0001c0001t0001g0310 a0001c0001t0001g0311 a0001c0001t0001g0312 others(67): Show |
72 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.2616+460T>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 25/28 | chr13 | 98017311 | |||||||
| chr13:98017502 | G | C | 38 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0075 others(35): Show |
41 | HG01109.hp1 HG01361.hp1 HG01884.hp1 others(38): Show |
intron_variant | MODIFIER | c.2616+651G>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 25/28 | chr13 | 98017502 | |||||||
| chr13:98017505 | G | A | 2 | a0001c0001t0001g0202 a0001c0001t0001g0214 |
2 | HG00609.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.2616+654G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 25/28 | chr13 | 98017505 | |||||||
| chr13:98017601 | C | T | 166 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(163): Show |
172 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(169): Show |
intron_variant | MODIFIER | c.2616+750C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 25/28 | chr13 | 98017601 | |||||||
| chr13:98017824 | A | C | 2 | a0001c0001t0001g0329 a0001c0001t0018g0190 |
2 | HG02257.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2617-661A>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 25/28 | chr13 | 98017824 | |||||||
| chr13:98017891 | C | T | 2 | a0001c0001t0002g0133 a0001c0001t0002g0134 |
2 | NA18952.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.2617-594C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 25/28 | chr13 | 98017891 | |||||||
| chr13:98017982 | A | T | 9 | a0001c0004t0005g0010 a0001c0004t0005g0352 a0001c0004t0005g0353 others(6): Show |
9 | NA18950.hp2 NA18966.hp1 NA18982.hp1 others(6): Show |
intron_variant | MODIFIER | c.2617-503A>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 25/28 | chr13 | 98017982 | |||||||
| chr13:98018215 | T | C | 2 | a0001c0001t0002g0151 a0001c0001t0002g0153 |
2 | HG01175.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.2617-270T>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 25/28 | chr13 | 98018215 | |||||||
| chr13:98018387 | G | C | 246 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(243): Show |
254 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(251): Show |
intron_variant | MODIFIER | c.2617-98G>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 25/28 | chr13 | 98018387 | |||||||
| chr13:98018721 | C | T | 5 | a0001c0002t0003g0025 a0001c0002t0003g0027 a0001c0002t0003g0028 others(2): Show |
5 | HG00423.hp2 HG02155.hp1 HG02523.hp2 others(2): Show |
intron_variant | MODIFIER | c.2836+17C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 26/28 | chr13 | 98018721 | |||||||
| chr13:98018971 | C | CT | 74 | a0001c0001t0001g0316 a0001c0002t0001g0327 a0001c0002t0003g0014 others(71): Show |
76 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.2836+279dupT | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 26/28 | INFO_REALIGN_3_PRIME | chr13 | 98018971 | ||||||
| chr13:98018971 | CT | C | 52 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0039 others(49): Show |
54 | HG00099.hp1 HG00642.hp1 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.2836+279delT | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 26/28 | INFO_REALIGN_3_PRIME | chr13 | 98018971 | ||||||
| chr13:98019024 | C | T | 1 | a0001c0001t0001g0282 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.2836+320C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 26/28 | chr13 | 98019024 | |||||||
| chr13:98019166 | A | G | 1 | a0001c0002t0003g0037 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2837-415A>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 26/28 | chr13 | 98019166 | |||||||
| chr13:98019248 | G | A | 3 | a0001c0001t0001g0003 a0001c0001t0001g0081 a0001c0001t0001g0082 |
4 | HG01884.hp1 HG02486.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2837-333G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 26/28 | chr13 | 98019248 | |||||||
| chr13:98019458 | C | T | 1 | a0001c0002t0003g0070 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2837-123C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 26/28 | chr13 | 98019458 | |||||||
| chr13:98019830 | C | T | 9 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0112 others(6): Show |
11 | HG01192.hp1 HG01243.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.3065+21C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 27/28 | chr13 | 98019830 | |||||||
| chr13:98019886 | T | C | 1 | a0001c0001t0001g0104 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.3065+77T>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 27/28 | chr13 | 98019886 | |||||||
| chr13:98020093 | C | T | 1 | a0001c0002t0003g0071 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.3065+284C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 27/28 | chr13 | 98020093 | |||||||
| chr13:98020127 | G | T | 250 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(247): Show |
258 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(255): Show |
intron_variant | MODIFIER | c.3065+318G>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 27/28 | chr13 | 98020127 | |||||||
| chr13:98020233 | T | C | 1 | a0001c0001t0002g0170 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.3065+424T>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 27/28 | chr13 | 98020233 | |||||||
| chr13:98020372 | CTTGT | C | 9 | a0001c0004t0005g0010 a0001c0004t0005g0352 a0001c0004t0005g0353 others(6): Show |
9 | NA18950.hp2 NA18966.hp1 NA18982.hp1 others(6): Show |
intron_variant | MODIFIER | c.3065+566_3065+569d others(6): Show |
IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr13 | 98020372 | ||||||
| chr13:98020375 | G | T | 1 | a0001c0001t0002g0039 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.3065+566G>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 27/28 | chr13 | 98020375 | |||||||
| chr13:98020424 | A | C | 1 | a0001c0014t0001g0110 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3066-568A>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 27/28 | chr13 | 98020424 | |||||||
| chr13:98020535 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.3066-457G>A | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 27/28 | chr13 | 98020535 | |||||||
| chr13:98020569 | G | C | 1 | a0001c0003t0001g0123 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.3066-423G>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 27/28 | chr13 | 98020569 | |||||||
| chr13:98020586 | A | C | 2 | a0001c0001t0001g0084 a0001c0001t0001g0107 |
2 | HG02451.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.3066-406A>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 27/28 | chr13 | 98020586 | |||||||
| chr13:98020607 | C | T | 1 | a0001c0002t0003g0052 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.3066-385C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 27/28 | chr13 | 98020607 | |||||||
| chr13:98020610 | G | T | 1 | a0001c0005t0019g0346 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3066-382G>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 27/28 | chr13 | 98020610 | |||||||
| chr13:98020668 | G | C | 1 | a0001c0001t0001g0328 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3066-324G>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 27/28 | chr13 | 98020668 | |||||||
| chr13:98020739 | CA | C | 49 | a0001c0001t0001g0132 a0001c0001t0001g0137 a0001c0001t0001g0144 others(46): Show |
49 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.3066-252delA | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 27/28 | chr13 | 98020739 | |||||||
| chr13:98021163 | G | C | 3 | a0001c0001t0001g0368 a0001c0001t0001g0369 a0001c0001t0001g0370 |
3 | HG02451.hp2 HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.3207+30G>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 28/28 | chr13 | 98021163 | |||||||
| chr13:98021173 | C | T | 1 | a0001c0001t0001g0292 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.3207+40C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 28/28 | chr13 | 98021173 | |||||||
| chr13:98021300 | C | T | 1 | a0001c0002t0003g0014 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.3207+167C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 28/28 | chr13 | 98021300 | |||||||
| chr13:98021383 | T | C | 11 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0224 others(8): Show |
11 | HG00438.hp2 HG00558.hp2 HG02155.hp2 others(8): Show |
intron_variant | MODIFIER | c.3207+250T>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 28/28 | chr13 | 98021383 | |||||||
| chr13:98021482 | T | C | 1 | a0001c0001t0001g0107 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3208-254T>C | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 28/28 | chr13 | 98021482 | |||||||
| chr13:98021606 | T | G | 1 | a0001c0001t0009g0320 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.3208-130T>G | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 28/28 | chr13 | 98021606 | |||||||
| chr13:98021697 | C | T | 5 | a0001c0001t0001g0144 a0001c0001t0001g0281 a0001c0001t0001g0298 others(2): Show |
5 | HG00609.hp2 HG02027.hp1 HG03927.hp1 others(2): Show |
intron_variant | MODIFIER | c.3208-39C>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 28/28 | chr13 | 98021697 | |||||||
| chr13:98021703 | G | T | 5 | a0001c0002t0003g0040 a0001c0002t0003g0041 a0001c0002t0003g0043 others(2): Show |
5 | NA18940.hp2 NA18960.hp2 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.3208-33G>T | IPO5 | ENSG00000065150.21 | transcript | ENST00000651721.2 | protein_coding | 28/28 | chr13 | 98021703 |