Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 9319 |
| ensemblid | ENSG00000071539.14 |
| hgncid | 12307 |
| symbol | TRIP13 |
| name | thyroid hormone receptor interactor 13 |
| refseq_nuc | NM_004237.4 |
| refseq_prot | NP_004228.1 |
| ensembl_nuc | ENST00000166345.8 |
| ensembl_prot | ENSP00000166345.3 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 892884 |
| end | 918120 |
| strand | + |
| ver | v1.2 |
| region | chr5:892884-918120 |
| region5000 | chr5:887884-923120 |
| regionname0 | TRIP13_chr5_892884_918120 |
| regionname5000 | TRIP13_chr5_887884_923120 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 432 | 395 | 93 | 78 | 162 | 16 | 44 | 124 | TRIP13_chr5_887884_923120 | TRIP13 | MDEAV others(427): Show |
chr5 | 887884 | 923120 |
| a0002 | 0/0 | 432 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | MDEAV others(427): Show |
chr5 | 887884 | 923120 |
| a0003 | 0/0 | 432 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | MDEAV others(427): Show |
chr5 | 887884 | 923120 |
| a0004 | 0/0 | 432 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | MDEAV others(427): Show |
chr5 | 887884 | 923120 |
| a0005 | 0/0 | 432 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | MDEAV others(427): Show |
chr5 | 887884 | 923120 |
| a0006 | 0/0 | 432 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | MDEAV others(427): Show |
chr5 | 887884 | 923120 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1296 | 386 | 92 | 74 | 159 | 16 | 43 | TRIP13_chr5_887884_923120 | TRIP13 | ATGGA others(1291): Show |
chr5 | 887884 | 923120 | ||
| a0001c0002 | 0/0 | 1296 | 4 | 0 | 3 | 0 | 0 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | ATGGA others(1291): Show |
chr5 | 887884 | 923120 | ||
| a0001c0005 | 0/0 | 1296 | 2 | 1 | 1 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | ATGGA others(1291): Show |
chr5 | 887884 | 923120 | ||
| a0001c0007 | 0/0 | 1296 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | ATGGA others(1291): Show |
chr5 | 887884 | 923120 | ||
| a0001c0009 | 0/0 | 1296 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | ATGGA others(1291): Show |
chr5 | 887884 | 923120 | ||
| a0001c0010 | 0/0 | 1296 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | ATGGA others(1291): Show |
chr5 | 887884 | 923120 | ||
| a0002c0004 | 0/0 | 1296 | 2 | 0 | 0 | 2 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | ATGGA others(1291): Show |
chr5 | 887884 | 923120 | ||
| a0003c0003 | 0/0 | 1296 | 2 | 2 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | ATGGA others(1291): Show |
chr5 | 887884 | 923120 | ||
| a0004c0006 | 0/0 | 1296 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | ATGGA others(1291): Show |
chr5 | 887884 | 923120 | ||
| a0005c0011 | 0/0 | 1296 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | ATGGA others(1291): Show |
chr5 | 887884 | 923120 | ||
| a0006c0008 | 0/0 | 1296 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | ATGGA others(1291): Show |
chr5 | 887884 | 923120 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2431 | 261 | 30 | 48 | 133 | 14 | 34 | TRIP13_chr5_887884_923120 | TRIP13 | AGATT others(2426): Show |
chr5 | 887884 | 923120 |
| a0001c0001t0002 | 0/0 | 2431 | 115 | 62 | 23 | 24 | 0 | 6 | TRIP13_chr5_887884_923120 | TRIP13 | AGATT others(2426): Show |
chr5 | 887884 | 923120 |
| a0001c0001t0003 | 0/0 | 2431 | 2 | 0 | 1 | 0 | 1 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | AGATT others(2426): Show |
chr5 | 887884 | 923120 |
| a0001c0001t0004 | 0/0 | 2431 | 2 | 0 | 2 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | AGATT others(2426): Show |
chr5 | 887884 | 923120 |
| a0001c0001t0005 | 0/0 | 2431 | 2 | 0 | 0 | 0 | 0 | 2 | TRIP13_chr5_887884_923120 | TRIP13 | AGATT others(2426): Show |
chr5 | 887884 | 923120 |
| a0001c0001t0006 | 0/0 | 2431 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | AGATT others(2426): Show |
chr5 | 887884 | 923120 |
| a0001c0001t0007 | 0/0 | 2431 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | AGATT others(2426): Show |
chr5 | 887884 | 923120 |
| a0001c0001t0008 | 0/0 | 2431 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | AGATT others(2426): Show |
chr5 | 887884 | 923120 |
| a0001c0001t0009 | 0/0 | 2431 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | AGATT others(2426): Show |
chr5 | 887884 | 923120 |
| a0001c0002t0002 | 0/0 | 2431 | 4 | 0 | 3 | 0 | 0 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | AGATT others(2426): Show |
chr5 | 887884 | 923120 |
| a0001c0005t0002 | 0/0 | 2431 | 2 | 1 | 1 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | AGATT others(2426): Show |
chr5 | 887884 | 923120 |
| a0001c0007t0001 | 0/0 | 2431 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | AGATT others(2426): Show |
chr5 | 887884 | 923120 |
| a0001c0009t0001 | 0/0 | 2431 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | AGATT others(2426): Show |
chr5 | 887884 | 923120 |
| a0001c0010t0001 | 0/0 | 2431 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | AGATT others(2426): Show |
chr5 | 887884 | 923120 |
| a0002c0004t0001 | 0/0 | 2431 | 2 | 0 | 0 | 2 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | AGATT others(2426): Show |
chr5 | 887884 | 923120 |
| a0003c0003t0002 | 0/0 | 2431 | 2 | 2 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | AGATT others(2426): Show |
chr5 | 887884 | 923120 |
| a0004c0006t0002 | 0/0 | 2431 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | AGATT others(2426): Show |
chr5 | 887884 | 923120 |
| a0005c0011t0001 | 0/0 | 2431 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | AGATT others(2426): Show |
chr5 | 887884 | 923120 |
| a0006c0008t0001 | 0/0 | 2431 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | AGATT others(2426): Show |
chr5 | 887884 | 923120 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 1/0 | 65 | 1 | 16 | 34 | 2 | 11 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0003 | 0/0 | 15 | 1 | 3 | 7 | 2 | 2 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0004 | 0/0 | 14 | 0 | 0 | 13 | 0 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0005 | 0/0 | 11 | 0 | 2 | 9 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0006 | 0/0 | 10 | 0 | 1 | 9 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0007 | 0/0 | 8 | 0 | 6 | 1 | 0 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0009 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0015 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0018 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0019 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0025 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0047 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0049 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0094 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0002g0002 | 0/0 | 33 | 0 | 16 | 12 | 0 | 5 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0002g0008 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0002g0010 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0002g0011 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0002g0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0002g0014 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0002g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0002g0020 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0002g0027 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0002g0028 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0002g0029 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0002g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0002g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0002g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0002g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0002g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0003g0001 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0004g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0004g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0005g0033 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0006g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0007g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0008g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0001t0009g0001 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0002t0002g0012 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0005t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0005t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0007t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0009t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0001c0010t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0002c0004t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0003c0003t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0003c0003t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0004c0006t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0005c0011t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| a0006c0008t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0036 | EUR | GBR | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0149 | EUR | GBR | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0001 | EUR | GBR | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0095 | EUR | GBR | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0037 | EUR | FIN | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0142 | EUR | FIN | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0089 | EUR | FIN | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | CHS | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | CHS | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | CHS | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | CHS | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | CHS | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG00673 | hp2 | a0002 | c0004 | t0001 | g0048 | EAS | CHS | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG00735 | hp1 | a0001 | c0001 | t0004 | g0091 | AMR | PUR | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0029 | AMR | PUR | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0105 | AMR | PUR | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0101 | AMR | PUR | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG01109 | hp2 | a0001 | c0001 | t0004 | g0090 | AMR | PUR | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0029 | AMR | PUR | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0029 | AMR | PUR | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG01175 | hp2 | a0001 | c0002 | t0002 | g0012 | AMR | PUR | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG01243 | hp1 | a0001 | c0005 | t0002 | g0156 | AMR | PUR | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | CLM | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | CLM | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | CLM | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | CLM | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG01433 | hp1 | a0001 | c0002 | t0002 | g0012 | AMR | CLM | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG01516 | hp1 | a0001 | c0001 | t0009 | g0001 | EUR | IBS | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0047 | EUR | IBS | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0047 | EUR | IBS | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | ACB | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | ACB | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0027 | AFR | ACB | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0098 | AMR | PEL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PEL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02027 | hp1 | a0002 | c0004 | t0001 | g0048 | EAS | KHV | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | KHV | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0116 | AFR | ACB | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0110 | EAS | KHV | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | KHV | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02083 | hp2 | a0001 | c0001 | t0007 | g0080 | EAS | KHV | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | KHV | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | KHV | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0030 | AFR | ACB | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02148 | hp2 | a0001 | c0002 | t0002 | g0012 | AMR | PEL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CDX | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | CDX | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | ACB | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | ACB | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0103 | AMR | PEL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0028 | AFR | ACB | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0054 | AFR | ACB | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | ACB | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | ACB | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | GWD | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0119 | AFR | GWD | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | GWD | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | GWD | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | GWD | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | PJL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02698 | hp2 | a0001 | c0001 | t0008 | g0050 | SAS | PJL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0014 | AFR | GWD | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | GWD | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0100 | AFR | GWD | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | GWD | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | GWD | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0052 | AFR | GWD | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | GWD | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0057 | AFR | GWD | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0052 | AFR | ESN | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | ESN | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0020 | AFR | ESN | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0106 | AFR | ESN | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0117 | AFR | ESN | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | ESN | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02976 | hp2 | a0003 | c0003 | t0002 | g0017 | AFR | ESN | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0140 | AFR | GWD | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0058 | AFR | GWD | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0020 | AFR | MSL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | MSL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0107 | AFR | ESN | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0115 | AFR | ESN | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | ESN | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0020 | AFR | ESN | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | ESN | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0056 | AFR | MSL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | MSL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | MSL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | MSL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0113 | SAS | PJL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | MSL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | MSL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0154 | AFR | MSL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | MSL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG03491 | hp1 | a0001 | c0001 | t0005 | g0033 | SAS | PJL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG03492 | hp1 | a0001 | c0001 | t0005 | g0033 | SAS | PJL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | ESN | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0027 | AFR | ESN | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG03540 | hp1 | a0003 | c0003 | t0002 | g0120 | AFR | GWD | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG03540 | hp2 | a0004 | c0006 | t0002 | g0017 | AFR | GWD | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | MSL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG03579 | hp2 | a0001 | c0005 | t0002 | g0155 | AFR | MSL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0049 | SAS | STU | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | BEB | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | BEB | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | BEB | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | BEB | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | BEB | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | BEB | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0146 | SAS | STU | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | BEB | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | STU | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0078 | SAS | STU | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | STU | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | STU | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | YRI | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0020 | AFR | YRI | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHB | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | CHB | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0051 | AFR | YRI | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | YRI | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA18945 | hp1 | a0005 | c0011 | t0001 | g0001 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA18952 | hp1 | a0001 | c0009 | t0001 | g0006 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA18987 | hp1 | a0001 | c0010 | t0001 | g0044 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA19003 | hp1 | a0001 | c0001 | t0006 | g0138 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA19012 | hp2 | a0001 | c0007 | t0001 | g0005 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0118 | AFR | LWK | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0099 | AFR | LWK | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | LWK | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | LWK | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA19059 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA19059 | hp2 | a0006 | c0008 | t0001 | g0136 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | YRI | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0027 | AFR | YRI | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | ASW | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0141 | AFR | ASW | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0076 | EUR | TSI | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0147 | EUR | TSI | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA20905 | hp1 | a0001 | c0002 | t0002 | g0012 | SAS | GIH | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | CLM | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | ACB | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0051 | AFR | ACB | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0055 | AFR | ACB | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | ACB | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0053 | AFR | MSL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0028 | AFR | MSL | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0028 | AFR | USA | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | USA | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | USA | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0030 | AFR | USA | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0094 | REF | REF | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0001 | REF | REF | TRIP13_chr5_887884_923120 | TRIP13 | chr5 | 887884 | 923120 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:896683 | T | C | 2 | a0003 a0004 |
3 | HG02976.hp2 HG03540.hp1 HG03540.hp2 |
missense_variant | MODERATE | c.277T>C | p.Cys93Arg | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/13 | 392/2431 | 277/1299 | 93/432 | chr5 | 896683 | |||
| chr5:901428 | C | T | 1 | a0005 | 1 | NA18945.hp1 | missense_variant | MODERATE | c.532C>T | p.His178Tyr | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 5/13 | 647/2431 | 532/1299 | 178/432 | chr5 | 901428 | |||
| chr5:911847 | T | A | 1 | a0006 | 1 | NA19059.hp2 | missense_variant | MODERATE | c.871T>A | p.Ser291Thr | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 10/13 | 986/2431 | 871/1299 | 291/432 | chr5 | 911847 | |||
| chr5:917030 | G | A | 1 | a0004 | 1 | HG03540.hp2 | missense_variant | MODERATE | c.1226G>A | p.Gly409Glu | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 13/13 | 1341/2431 | 1226/1299 | 409/432 | chr5 | 917030 | |||
| chr5:917098 | A | G | 1 | a0002 | 2 | HG00673.hp2 HG02027.hp1 |
missense_variant | MODERATE | c.1294A>G | p.Ile432Val | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 13/13 | 1409/2431 | 1294/1299 | 432/432 | chr5 | 917098 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:907190 | G | A | 1 | a0001c0007 | 1 | NA19012.hp2 | synonymous_variant | LOW | c.669G>A | p.Ser223Ser | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 7/13 | 784/2431 | 669/1299 | 223/432 | chr5 | 907190 | |||
| chr5:908420 | C | T | 1 | a0001c0010 | 1 | NA18987.hp1 | synonymous_variant | LOW | c.825C>T | p.Arg275Arg | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/13 | 940/2431 | 825/1299 | 275/432 | chr5 | 908420 | |||
| chr5:911882 | C | G | 1 | a0001c0005 | 2 | HG01243.hp1 HG03579.hp2 |
synonymous_variant | LOW | c.906C>G | p.Thr302Thr | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 10/13 | 1021/2431 | 906/1299 | 302/432 | chr5 | 911882 | |||
| chr5:911903 | C | T | 1 | a0001c0009 | 1 | NA18952.hp1 | synonymous_variant | LOW | c.927C>T | p.Phe309Phe | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 10/13 | 1042/2431 | 927/1299 | 309/432 | chr5 | 911903 | |||
| chr5:914549 | T | C | 1 | a0001c0002 | 4 | HG01175.hp2 HG01433.hp1 HG02148.hp2 others(1): Show |
synonymous_variant | LOW | c.1105T>C | p.Leu369Leu | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 11/13 | 1220/2431 | 1105/1299 | 369/432 | chr5 | 914549 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:917209 | G | A | 1 | a0001c0001t0006 | 1 | NA19003.hp1 | 3_prime_UTR_variant | MODIFIER | c.*106G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 13/13 | 106 | chr5 | 917209 | ||||||
| chr5:917236 | A | C | 1 | a0001c0001t0005 | 2 | HG03491.hp1 HG03492.hp1 |
3_prime_UTR_variant | MODIFIER | c.*133A>C | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 13/13 | 133 | chr5 | 917236 | ||||||
| chr5:917296 | T | C | 1 | a0001c0001t0007 | 1 | HG02083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*193T>C | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 13/13 | 193 | chr5 | 917296 | ||||||
| chr5:917479 | G | T | 1 | a0001c0001t0004 | 2 | HG00735.hp1 HG01109.hp2 |
3_prime_UTR_variant | MODIFIER | c.*376G>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 13/13 | 376 | chr5 | 917479 | ||||||
| chr5:917549 | G | A | 1 | a0001c0001t0008 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*446G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 13/13 | 446 | chr5 | 917549 | ||||||
| chr5:917582 | T | G | 1 | a0001c0001t0003 | 2 | HG00140.hp1 HG01346.hp2 |
3_prime_UTR_variant | MODIFIER | c.*479T>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 13/13 | 479 | chr5 | 917582 | ||||||
| chr5:917763 | A | G | 5 | a0001c0001t0002 a0001c0002t0002 a0001c0005t0002 others(2): Show |
124 | HG00408.hp2 HG00544.hp1 HG00621.hp1 others(121): Show |
3_prime_UTR_variant | MODIFIER | c.*660A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 13/13 | 660 | chr5 | 917763 | ||||||
| chr5:918110 | T | C | 1 | a0001c0001t0009 | 1 | HG01516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1007T>C | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 13/13 | 1007 | chr5 | 918110 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:893106 | C | G | 1 | a0001c0001t0002g0010 | 6 | HG02486.hp1 HG02818.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.92+16C>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 1/12 | chr5 | 893106 | |||||||
| chr5:893106 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.92+16C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 1/12 | chr5 | 893106 | |||||||
| chr5:893115 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.92+25C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 1/12 | chr5 | 893115 | |||||||
| chr5:893241 | C | G | 27 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0047 others(24): Show |
60 | HG00099.hp2 HG00323.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.92+151C>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 1/12 | chr5 | 893241 | |||||||
| chr5:893272 | C | T | 1 | a0001c0001t0001g0046 | 2 | NA18980.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.92+182C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 1/12 | chr5 | 893272 | |||||||
| chr5:893310 | C | G | 10 | a0001c0001t0002g0020 a0001c0001t0002g0028 a0001c0001t0002g0029 others(7): Show |
19 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.92+220C>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 1/12 | chr5 | 893310 | |||||||
| chr5:893337 | T | A | 5 | a0001c0001t0002g0010 a0001c0001t0002g0053 a0001c0001t0002g0054 others(2): Show |
13 | HG01175.hp2 HG01433.hp1 HG02148.hp2 others(10): Show |
intron_variant | MODIFIER | c.92+247T>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 1/12 | chr5 | 893337 | |||||||
| chr5:893349 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.92+259C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 1/12 | chr5 | 893349 | |||||||
| chr5:893377 | ACCCTGC | A | 18 | a0001c0001t0002g0010 a0001c0001t0002g0013 a0001c0001t0002g0014 others(15): Show |
40 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(37): Show |
intron_variant | MODIFIER | c.92+297_92+302delTG others(4): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 893377 | ||||||
| chr5:893488 | G | A | 1 | a0001c0001t0002g0056 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.92+398G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 1/12 | chr5 | 893488 | |||||||
| chr5:893510 | G | C | 1 | a0001c0001t0002g0154 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.92+420G>C | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 1/12 | chr5 | 893510 | |||||||
| chr5:893580 | T | A | 4 | a0001c0001t0002g0053 a0001c0001t0002g0054 a0001c0001t0002g0055 others(1): Show |
7 | HG01175.hp2 HG01433.hp1 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.92+490T>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 1/12 | chr5 | 893580 | |||||||
| chr5:893649 | G | T | 1 | a0001c0001t0001g0139 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.92+559G>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 1/12 | chr5 | 893649 | |||||||
| chr5:893895 | C | A | 1 | a0001c0001t0001g0059 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.92+805C>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 1/12 | chr5 | 893895 | |||||||
| chr5:894028 | C | T | 1 | a0001c0001t0002g0011 | 5 | HG02559.hp2 HG02630.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.93-759C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 1/12 | chr5 | 894028 | |||||||
| chr5:894090 | G | T | 30 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0018 others(27): Show |
61 | HG00438.hp1 HG00609.hp1 HG01099.hp1 others(58): Show |
intron_variant | MODIFIER | c.93-697G>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 1/12 | chr5 | 894090 | |||||||
| chr5:894245 | A | G | 1 | a0001c0001t0001g0121 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.93-542A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 1/12 | chr5 | 894245 | |||||||
| chr5:894324 | A | G | 32 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0013 others(29): Show |
65 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(62): Show |
intron_variant | MODIFIER | c.93-463A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 1/12 | chr5 | 894324 | |||||||
| chr5:894468 | C | G | 32 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0013 others(29): Show |
65 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(62): Show |
intron_variant | MODIFIER | c.93-319C>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 1/12 | chr5 | 894468 | |||||||
| chr5:894492 | G | A | 11 | a0001c0001t0002g0008 a0001c0001t0002g0020 a0001c0001t0002g0029 others(8): Show |
25 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.93-295G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 1/12 | chr5 | 894492 | |||||||
| chr5:894508 | G | A | 10 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0027 others(7): Show |
21 | HG01175.hp2 HG01433.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.93-279G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 1/12 | chr5 | 894508 | |||||||
| chr5:894542 | G | A | 1 | a0001c0001t0001g0031 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.93-245G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 1/12 | chr5 | 894542 | |||||||
| chr5:894976 | A | C | 1 | a0001c0001t0006g0138 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.258+24A>C | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 2/12 | chr5 | 894976 | |||||||
| chr5:894996 | CA | C | 83 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0018 others(80): Show |
185 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(182): Show |
intron_variant | MODIFIER | c.258+48delA | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 894996 | ||||||
| chr5:895287 | T | C | 1 | a0001c0001t0001g0142 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.258+335T>C | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 2/12 | chr5 | 895287 | |||||||
| chr5:895289 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.258+337G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 2/12 | chr5 | 895289 | |||||||
| chr5:895488 | GACTTATC | G | 21 | a0001c0001t0002g0002 a0001c0001t0002g0011 a0001c0001t0002g0038 others(18): Show |
59 | HG00408.hp2 HG00544.hp1 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.258+542_258+548del others(7): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 895488 | ||||||
| chr5:895558 | G | C | 1 | a0001c0001t0001g0032 | 2 | HG03831.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.258+606G>C | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 2/12 | chr5 | 895558 | |||||||
| chr5:895561 | C | A | 1 | a0001c0001t0006g0138 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.258+609C>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 2/12 | chr5 | 895561 | |||||||
| chr5:895567 | G | A | 11 | a0001c0001t0002g0008 a0001c0001t0002g0020 a0001c0001t0002g0029 others(8): Show |
25 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.258+615G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 2/12 | chr5 | 895567 | |||||||
| chr5:895923 | T | C | 3 | a0001c0001t0002g0028 a0001c0001t0002g0140 a0001c0001t0002g0141 |
5 | HG02280.hp1 HG03041.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.259-742T>C | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 2/12 | chr5 | 895923 | |||||||
| chr5:896068 | CTG | C | 1 | a0001c0001t0001g0021 | 3 | HG01123.hp1 HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.259-594_259-593del others(2): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 896068 | ||||||
| chr5:896121 | G | A | 2 | a0001c0001t0002g0053 a0001c0001t0002g0054 |
2 | HG02280.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.259-544G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 2/12 | chr5 | 896121 | |||||||
| chr5:896140 | C | T | 3 | a0001c0001t0002g0028 a0001c0001t0002g0140 a0001c0001t0002g0141 |
5 | HG02280.hp1 HG03041.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.259-525C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 2/12 | chr5 | 896140 | |||||||
| chr5:896158 | T | A | 1 | a0001c0001t0002g0027 | 3 | HG01891.hp2 HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.259-507T>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 2/12 | chr5 | 896158 | |||||||
| chr5:896182 | G | A | 4 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0057 others(1): Show |
10 | HG01884.hp2 HG02451.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.259-483G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 2/12 | chr5 | 896182 | |||||||
| chr5:896218 | G | T | 4 | a0001c0001t0002g0053 a0001c0001t0002g0054 a0001c0001t0002g0055 others(1): Show |
7 | HG01175.hp2 HG01433.hp1 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.259-447G>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 2/12 | chr5 | 896218 | |||||||
| chr5:896297 | A | G | 11 | a0001c0001t0002g0008 a0001c0001t0002g0020 a0001c0001t0002g0029 others(8): Show |
25 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.259-368A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 2/12 | chr5 | 896297 | |||||||
| chr5:896429 | C | T | 1 | a0001c0001t0002g0027 | 3 | HG01891.hp2 HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.259-236C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 2/12 | chr5 | 896429 | |||||||
| chr5:896542 | G | T | 11 | a0001c0001t0002g0008 a0001c0001t0002g0020 a0001c0001t0002g0029 others(8): Show |
25 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.259-123G>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 2/12 | chr5 | 896542 | |||||||
| chr5:896611 | C | G | 32 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0013 others(29): Show |
65 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(62): Show |
intron_variant | MODIFIER | c.259-54C>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 2/12 | chr5 | 896611 | |||||||
| chr5:896867 | C | CG | 5 | a0001c0001t0001g0122 a0001c0001t0002g0010 a0001c0001t0002g0028 others(2): Show |
12 | HG02280.hp1 HG02486.hp1 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.388+73_388+74insG | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 896867 | |||||||
| chr5:896868 | A | G | 83 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0018 others(80): Show |
185 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(182): Show |
intron_variant | MODIFIER | c.388+74A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 896868 | |||||||
| chr5:896870 | G | A | 1 | a0001c0001t0002g0098 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.388+76G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 896870 | |||||||
| chr5:897067 | G | T | 1 | a0003c0003t0002g0120 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.388+273G>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 897067 | |||||||
| chr5:897138 | C | G | 1 | a0001c0001t0001g0137 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.388+344C>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 897138 | |||||||
| chr5:897138 | CGGCTTCA others(59): Show |
C | 1 | a0001c0001t0001g0152 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.388+488_388+553del others(66): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 897138 | ||||||
| chr5:897189 | A | G | 1 | a0001c0001t0001g0045 | 2 | NA18983.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.388+395A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 897189 | |||||||
| chr5:897223 | T | C | 1 | a0001c0001t0002g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.388+429T>C | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 897223 | |||||||
| chr5:897255 | A | G | 1 | a0001c0001t0001g0045 | 2 | NA18983.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.388+461A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 897255 | |||||||
| chr5:897268 | C | G | 2 | a0001c0001t0001g0096 a0001c0001t0001g0097 |
2 | HG04199.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.388+474C>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 897268 | |||||||
| chr5:897282 | G | T | 1 | a0001c0001t0002g0027 | 3 | HG01891.hp2 HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.388+488G>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 897282 | |||||||
| chr5:897321 | A | G | 9 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0045 others(6): Show |
18 | HG00140.hp2 HG00438.hp1 HG01123.hp1 others(15): Show |
intron_variant | MODIFIER | c.388+527A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 897321 | |||||||
| chr5:897345 | TCATTCAG others(125): Show |
T | 4 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0005t0002g0155 others(1): Show |
4 | HG01243.hp1 HG02896.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.388+554_388+685del | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 897345 | ||||||
| chr5:897348 | T | G | 14 | a0001c0001t0001g0045 a0001c0001t0002g0002 a0001c0001t0002g0008 others(11): Show |
35 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(32): Show |
intron_variant | MODIFIER | c.388+554T>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 897348 | |||||||
| chr5:897348 | T | TTCAGTGT others(59): Show |
1 | a0001c0001t0002g0100 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.388+592_388+593ins others(66): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 897348 | ||||||
| chr5:897348 | T | TTCAGTGT others(125): Show |
1 | a0001c0001t0002g0002 | 3 | NA18612.hp2 NA18947.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.388+592_388+593ins others(132): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 897348 | ||||||
| chr5:897348 | T | TTCAGTGT others(191): Show |
2 | a0001c0001t0002g0002 a0001c0001t0002g0038 |
3 | HG02300.hp1 NA18988.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.388+592_388+593ins others(198): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 897348 | ||||||
| chr5:897348 | T | TTCAGTGT others(59): Show |
1 | a0001c0001t0001g0043 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.388+617_388+682dup others(66): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 897348 | ||||||
| chr5:897348 | TTCAGTGT others(125): Show |
T | 1 | a0001c0001t0001g0046 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.388+683_388+814del | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 897348 | ||||||
| chr5:897348 | TTCAGTGT others(191): Show |
T | 6 | a0001c0001t0001g0004 a0001c0001t0001g0041 a0001c0001t0001g0042 others(3): Show |
18 | HG00609.hp1 HG02080.hp1 NA18951.hp1 others(15): Show |
intron_variant | MODIFIER | c.388+683_388+880del | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 897348 | ||||||
| chr5:897348 | TTCAGTGT others(323): Show |
T | 1 | a0001c0001t0001g0004 | 2 | HG02027.hp2 NA18943.hp2 |
intron_variant | MODIFIER | c.388+683_388+1012de others(1): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 897348 | ||||||
| chr5:897348 | TTCAGTGT others(653): Show |
T | 1 | a0001c0001t0002g0053 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.388+683_388+1342de others(1): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 897348 | ||||||
| chr5:897348 | TTCAGTGT others(983): Show |
T | 1 | a0001c0001t0001g0001 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.388+683_388+1672de others(1): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 897348 | ||||||
| chr5:897348 | TTCAGTGT others(1115): Show |
T | 1 | a0001c0001t0008g0050 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.388+683_388+1804de others(1): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 897348 | ||||||
| chr5:897376 | G | GGATGGGC others(191): Show |
12 | a0001c0001t0002g0002 a0001c0001t0002g0039 a0001c0001t0002g0098 others(9): Show |
41 | HG00408.hp2 HG00544.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.388+592_388+593ins others(198): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 897376 | ||||||
| chr5:897387 | G | A | 34 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0011 others(31): Show |
71 | HG01081.hp2 HG01099.hp2 HG01109.hp1 others(68): Show |
intron_variant | MODIFIER | c.388+593G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 897387 | |||||||
| chr5:897411 | TCAGTCAG others(59): Show |
T | 8 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0032 others(5): Show |
13 | HG00609.hp2 HG01106.hp1 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.388+683_388+748del others(66): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 897411 | ||||||
| chr5:897411 | TCAGTCAG others(587): Show |
T | 3 | a0001c0001t0002g0010 a0001c0001t0002g0054 a0001c0001t0002g0055 |
8 | HG02280.hp2 HG02486.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.388+683_388+1276de others(1): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 897411 | ||||||
| chr5:897411 | TCAGTCAG others(785): Show |
T | 1 | a0001c0002t0002g0012 | 3 | HG01175.hp2 HG01433.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.388+683_388+1474de others(1): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 897411 | ||||||
| chr5:897411 | TCAGTCAG others(851): Show |
T | 1 | a0001c0002t0002g0012 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.388+683_388+1540de others(1): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 897411 | ||||||
| chr5:897414 | G | GTCAGTGT others(59): Show |
2 | a0001c0001t0002g0117 a0001c0001t0002g0119 |
2 | HG02572.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.388+658_388+659ins others(66): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 897414 | ||||||
| chr5:897434 | G | A | 1 | a0001c0001t0002g0027 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.388+640G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 897434 | |||||||
| chr5:897442 | G | A | 1 | a0001c0001t0002g0002 | 3 | NA18612.hp2 NA18947.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.388+648G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 897442 | |||||||
| chr5:897453 | G | A | 19 | a0001c0001t0002g0008 a0001c0001t0002g0011 a0001c0001t0002g0017 others(16): Show |
38 | HG01081.hp2 HG01099.hp2 HG01168.hp2 others(35): Show |
intron_variant | MODIFIER | c.388+659G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 897453 | |||||||
| chr5:897477 | G | T | 142 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(139): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.388+683G>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 897477 | |||||||
| chr5:897508 | G | A | 1 | a0001c0001t0002g0100 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.388+714G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 897508 | |||||||
| chr5:897508 | G | GGATGGGC others(59): Show |
2 | a0001c0001t0002g0011 a0001c0001t0002g0107 |
6 | HG02559.hp2 HG02630.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.388+779_388+780ins others(66): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 897508 | ||||||
| chr5:897519 | G | A | 6 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0101 others(3): Show |
6 | HG01109.hp1 HG01243.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.388+725G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 897519 | |||||||
| chr5:897543 | T | G | 2 | a0001c0001t0001g0045 a0001c0001t0002g0102 |
3 | NA18948.hp2 NA18983.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.388+749T>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 897543 | |||||||
| chr5:897574 | G | A | 21 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0022 others(18): Show |
48 | HG00099.hp2 HG00323.hp1 HG00673.hp2 others(45): Show |
intron_variant | MODIFIER | c.388+780G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 897574 | |||||||
| chr5:897585 | G | A | 2 | a0001c0005t0002g0155 a0001c0005t0002g0156 |
2 | HG01243.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.388+791G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 897585 | |||||||
| chr5:897640 | G | A | 1 | a0001c0001t0001g0049 | 2 | HG01106.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.388+846G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 897640 | |||||||
| chr5:897675 | T | G | 1 | a0001c0001t0001g0061 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.388+881T>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 897675 | |||||||
| chr5:897696 | A | G | 3 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0058 |
9 | HG01884.hp2 HG02451.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.388+902A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 897696 | |||||||
| chr5:897741 | TCAGTCAG others(125): Show |
T | 1 | a0001c0001t0002g0056 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.388+1211_388+1342d others(2): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 897741 | ||||||
| chr5:897741 | TCAGTCAG others(257): Show |
T | 1 | a0001c0001t0002g0101 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.388+1079_388+1342d others(2): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 897741 | ||||||
| chr5:897762 | A | G | 3 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0058 |
9 | HG01884.hp2 HG02451.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.388+968A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 897762 | |||||||
| chr5:897807 | T | G | 4 | a0001c0001t0001g0046 a0001c0001t0002g0028 a0001c0001t0002g0140 others(1): Show |
6 | HG02280.hp1 HG03041.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.388+1013T>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 897807 | |||||||
| chr5:897807 | T | TCAGTCAG others(59): Show |
2 | a0001c0001t0002g0002 a0001c0001t0002g0099 |
4 | NA18612.hp2 NA18947.hp2 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.388+1079_388+1144d others(68): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 897807 | ||||||
| chr5:897807 | T | TCAGTCAG others(191): Show |
1 | a0001c0001t0001g0019 | 3 | HG02257.hp1 HG02258.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.388+1078_388+1079i others(200): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 897807 | ||||||
| chr5:897807 | TCAGTCAG others(59): Show |
T | 4 | a0001c0001t0001g0001 a0001c0001t0001g0045 a0001c0001t0001g0132 others(1): Show |
6 | HG01433.hp2 HG03491.hp1 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.388+1079_388+1144d others(68): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 897807 | ||||||
| chr5:897810 | G | A | 1 | a0001c0001t0001g0009 | 2 | NA18966.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.388+1016G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 897810 | |||||||
| chr5:897828 | A | G | 4 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0057 others(1): Show |
10 | HG01884.hp2 HG02451.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.388+1034A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 897828 | |||||||
| chr5:897849 | G | A | 5 | a0001c0001t0001g0009 a0001c0001t0001g0133 a0001c0001t0001g0134 others(2): Show |
9 | HG00438.hp1 NA18969.hp2 NA18970.hp2 others(6): Show |
intron_variant | MODIFIER | c.388+1055G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 897849 | |||||||
| chr5:897849 | G | GGCAGGCC others(59): Show |
1 | a0001c0001t0001g0019 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.388+1078_388+1079i others(68): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 897849 | ||||||
| chr5:897873 | G | T | 51 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0018 others(48): Show |
88 | HG00438.hp1 HG01081.hp2 HG01099.hp1 others(85): Show |
intron_variant | MODIFIER | c.388+1079G>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 897873 | |||||||
| chr5:897873 | GCAGTCAG others(59): Show |
G | 8 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0041 others(5): Show |
21 | HG00609.hp1 HG02080.hp1 HG03669.hp1 others(18): Show |
intron_variant | MODIFIER | c.388+1145_388+1210d others(68): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 897873 | ||||||
| chr5:897873 | GCAGTCAG others(323): Show |
G | 1 | a0001c0001t0001g0049 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.388+1211_388+1540d others(2): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 897873 | ||||||
| chr5:897873 | GCAGTCAG others(587): Show |
G | 1 | a0001c0001t0001g0032 | 2 | HG03831.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.388+1211_388+1804d others(2): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 897873 | ||||||
| chr5:897873 | GCAGTCAG others(719): Show |
G | 1 | a0001c0001t0002g0027 | 3 | HG01891.hp2 HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.388+1211_389-1764d others(2): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 897873 | ||||||
| chr5:897894 | A | G | 4 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0057 others(1): Show |
10 | HG01884.hp2 HG02451.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.388+1100A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 897894 | |||||||
| chr5:897915 | G | A | 9 | a0001c0001t0001g0040 a0001c0001t0001g0044 a0001c0001t0001g0122 others(6): Show |
9 | HG02886.hp1 NA18949.hp2 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.388+1121G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 897915 | |||||||
| chr5:897939 | T | G | 26 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(23): Show |
68 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.388+1145T>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 897939 | |||||||
| chr5:897939 | T | TCAGTCAG others(59): Show |
1 | a0001c0001t0002g0011 | 5 | HG02559.hp2 HG02630.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.388+1211_388+1276d others(68): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 897939 | ||||||
| chr5:897939 | TCAGTCAG others(59): Show |
T | 1 | a0001c0001t0001g0046 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.388+1211_388+1276d others(68): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 897939 | ||||||
| chr5:897939 | TCAGTCAG others(1049): Show |
T | 1 | a0001c0001t0001g0005 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.388+1343_389-1302d others(2): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 897939 | ||||||
| chr5:897960 | A | G | 4 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0057 others(1): Show |
10 | HG01884.hp2 HG02451.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.388+1166A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 897960 | |||||||
| chr5:898005 | G | GCAGTCAG others(125): Show |
3 | a0001c0001t0001g0040 a0001c0001t0002g0100 a0001c0001t0002g0107 |
4 | HG02809.hp1 HG02809.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.388+1276_388+1277i others(134): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 898005 | ||||||
| chr5:898005 | G | GCAGTCAG others(125): Show |
1 | a0001c0001t0002g0002 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.389-1763_389-1632d others(134): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 898005 | ||||||
| chr5:898005 | G | GCAGTCAG others(521): Show |
1 | a0001c0001t0001g0068 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.388+1408_388+1409i others(530): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 898005 | ||||||
| chr5:898005 | G | GCAGTCAG others(587): Show |
1 | a0001c0001t0001g0001 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.388+1408_388+1409i others(596): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 898005 | ||||||
| chr5:898005 | G | T | 26 | a0001c0001t0001g0019 a0001c0001t0001g0123 a0001c0001t0001g0137 others(23): Show |
50 | HG01081.hp2 HG01099.hp2 HG01168.hp2 others(47): Show |
intron_variant | MODIFIER | c.388+1211G>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 898005 | |||||||
| chr5:898005 | GCAGTCAG others(455): Show |
G | 1 | a0001c0001t0001g0001 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.388+1607_389-1632d others(2): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 898005 | ||||||
| chr5:898005 | GCAGTCAG others(1577): Show |
G | 1 | a0001c0001t0001g0124 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.388+1277_389-840de others(1): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 898005 | ||||||
| chr5:898008 | G | T | 2 | a0001c0001t0002g0054 a0001c0001t0002g0055 |
2 | HG02280.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.388+1214G>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 898008 | |||||||
| chr5:898026 | A | G | 5 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0056 others(2): Show |
11 | HG01884.hp2 HG02451.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.388+1232A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 898026 | |||||||
| chr5:898047 | G | A | 3 | a0001c0001t0002g0053 a0001c0001t0002g0054 a0001c0001t0002g0055 |
3 | HG02280.hp2 HG02559.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.388+1253G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 898047 | |||||||
| chr5:898058 | CCCAGGGC others(58): Show |
C | 1 | a0006c0008t0001g0136 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.388+1267_388+1331d others(67): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 898058 | ||||||
| chr5:898071 | T | G | 36 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(33): Show |
54 | HG00438.hp1 HG00609.hp2 HG00738.hp1 others(51): Show |
intron_variant | MODIFIER | c.388+1277T>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 898071 | |||||||
| chr5:898071 | T | TCAGTCAG others(191): Show |
1 | a0001c0001t0001g0137 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.388+1408_388+1409i others(200): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 898071 | ||||||
| chr5:898071 | TCAGTCAG others(785): Show |
T | 1 | a0001c0001t0001g0023 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.388+1409_389-1500d others(2): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 898071 | ||||||
| chr5:898074 | G | T | 1 | a0001c0001t0002g0053 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.388+1280G>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 898074 | |||||||
| chr5:898074 | GTCAGTGT others(1771): Show |
G | 4 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0058 others(1): Show |
10 | HG01884.hp2 HG02055.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.388+1385_389-538de others(1): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 898074 | ||||||
| chr5:898092 | A | G | 2 | a0001c0001t0002g0056 a0001c0001t0002g0057 |
2 | HG02896.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.388+1298A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 898092 | |||||||
| chr5:898113 | G | A | 1 | a0001c0001t0002g0053 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.388+1319G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 898113 | |||||||
| chr5:898137 | T | G | 14 | a0001c0001t0001g0007 a0001c0001t0001g0062 a0001c0001t0001g0063 others(11): Show |
23 | HG01069.hp1 HG01074.hp1 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.388+1343T>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 898137 | |||||||
| chr5:898158 | A | G | 2 | a0001c0001t0002g0056 a0001c0001t0002g0057 |
2 | HG02896.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.388+1364A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 898158 | |||||||
| chr5:898203 | T | G | 4 | a0001c0001t0002g0103 a0001c0001t0002g0104 a0001c0001t0002g0105 others(1): Show |
5 | HG01099.hp2 HG02273.hp2 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.388+1409T>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 898203 | |||||||
| chr5:898206 | GTCAGTGT others(1639): Show |
G | 3 | a0001c0001t0002g0008 a0001c0001t0002g0057 a0001c0001t0002g0115 |
9 | HG01884.hp1 HG02257.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.388+1517_389-538de others(1): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 898206 | ||||||
| chr5:898224 | A | G | 1 | a0001c0001t0002g0056 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.388+1430A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 898224 | |||||||
| chr5:898245 | G | A | 1 | a0001c0002t0002g0012 | 3 | HG01175.hp2 HG01433.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.388+1451G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 898245 | |||||||
| chr5:898269 | T | G | 3 | a0001c0001t0001g0001 a0001c0001t0001g0049 a0001c0001t0005g0033 |
4 | HG01106.hp1 HG02083.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.388+1475T>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 898269 | |||||||
| chr5:898271 | A | G | 2 | a0001c0001t0002g0028 a0001c0001t0002g0141 |
4 | HG02280.hp1 HG03471.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.388+1477A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 898271 | |||||||
| chr5:898272 | G | A | 1 | a0001c0001t0001g0003 | 4 | NA18945.hp2 NA18965.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.388+1478G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 898272 | |||||||
| chr5:898272 | GTCAGTGT others(1573): Show |
G | 6 | a0001c0001t0002g0020 a0001c0001t0002g0029 a0001c0001t0002g0030 others(3): Show |
14 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.388+1583_389-538de others(1): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 898272 | ||||||
| chr5:898290 | A | G | 1 | a0001c0001t0002g0056 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.388+1496A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 898290 | |||||||
| chr5:898311 | G | A | 1 | a0001c0002t0002g0012 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.388+1517G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 898311 | |||||||
| chr5:898335 | T | G | 3 | a0001c0001t0001g0001 a0001c0001t0001g0046 a0001c0001t0005g0033 |
5 | HG01981.hp2 HG03491.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.388+1541T>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 898335 | |||||||
| chr5:898335 | T | TCAGTCAG others(455): Show |
1 | a0001c0001t0001g0043 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.389-1764_389-1763i others(464): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 898335 | ||||||
| chr5:898337 | A | G | 1 | a0001c0001t0002g0028 | 2 | HG02280.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.388+1543A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 898337 | |||||||
| chr5:898356 | A | G | 1 | a0001c0001t0002g0056 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.388+1562A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 898356 | |||||||
| chr5:898401 | T | G | 11 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0041 others(8): Show |
28 | HG00609.hp1 HG00735.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.388+1607T>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 898401 | |||||||
| chr5:898401 | TCAGTCAG others(455): Show |
T | 71 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(68): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.388+1739_389-1500d others(2): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 898401 | ||||||
| chr5:898401 | TCAGTCAG others(653): Show |
T | 3 | a0001c0001t0001g0061 a0001c0001t0001g0077 a0001c0001t0001g0146 |
3 | HG01952.hp2 HG02602.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.388+1739_389-1302d others(2): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 898401 | ||||||
| chr5:898401 | TCAGTCAG others(851): Show |
T | 1 | a0001c0001t0001g0001 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.388+1805_389-1038d others(2): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 898401 | ||||||
| chr5:898422 | A | G | 1 | a0001c0001t0002g0056 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.388+1628A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 898422 | |||||||
| chr5:898467 | T | G | 2 | a0001c0001t0001g0001 a0001c0001t0002g0101 |
2 | HG01109.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.388+1673T>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 898467 | |||||||
| chr5:898467 | TCAGTCAG others(389): Show |
T | 6 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0016 others(3): Show |
14 | HG01167.hp2 HG01934.hp1 HG01975.hp2 others(11): Show |
intron_variant | MODIFIER | c.388+1805_389-1500d others(2): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 898467 | ||||||
| chr5:898467 | TCAGTCAG others(521): Show |
T | 1 | a0001c0001t0001g0005 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.388+1739_389-1434d others(2): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 898467 | ||||||
| chr5:898467 | TCAGTCAG others(719): Show |
T | 1 | a0001c0001t0001g0001 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.388+1739_389-1236d others(2): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 898467 | ||||||
| chr5:898470 | GTCAGTGT others(1375): Show |
G | 1 | a0001c0005t0002g0155 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.388+1781_389-538de others(1): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 898470 | ||||||
| chr5:898488 | A | G | 1 | a0001c0001t0002g0056 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.388+1694A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 898488 | |||||||
| chr5:898533 | T | G | 4 | a0001c0001t0001g0001 a0001c0001t0001g0045 a0001c0001t0001g0068 others(1): Show |
5 | HG00735.hp2 HG01109.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.388+1739T>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 898533 | |||||||
| chr5:898533 | TCAGTCAG others(323): Show |
T | 3 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0062 |
4 | HG00609.hp2 HG03669.hp1 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.389-1829_389-1500d others(2): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 898533 | ||||||
| chr5:898536 | GTCAGTGT others(1309): Show |
G | 1 | a0001c0005t0002g0156 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.388+1847_389-538de others(1): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 898536 | ||||||
| chr5:898545 | T | G | 1 | a0006c0008t0001g0136 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.388+1751T>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 898545 | |||||||
| chr5:898554 | A | G | 1 | a0001c0001t0002g0056 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.388+1760A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 898554 | |||||||
| chr5:898586 | C | T | 1 | a0001c0001t0001g0127 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.388+1792C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 898586 | |||||||
| chr5:898599 | T | G | 2 | a0001c0001t0001g0001 a0001c0001t0009g0001 |
2 | HG01516.hp1 NA19059.hp1 |
intron_variant | MODIFIER | c.388+1805T>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 898599 | |||||||
| chr5:898599 | TCAGTCAG others(257): Show |
T | 2 | a0001c0001t0001g0045 a0001c0001t0005g0033 |
4 | HG03491.hp1 HG03492.hp1 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.389-1763_389-1500d others(2): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 898599 | ||||||
| chr5:898611 | TGGGGAAA others(390): Show |
T | 1 | a0001c0001t0001g0001 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.388+1821_389-1483d others(2): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 898611 | ||||||
| chr5:898665 | T | G | 3 | a0001c0001t0001g0004 a0001c0001t0002g0027 a0001c0002t0002g0012 |
7 | HG01175.hp2 HG01433.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.389-1829T>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 898665 | |||||||
| chr5:898665 | TCAGTCAG others(191): Show |
T | 1 | a0001c0001t0001g0132 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.389-1697_389-1500d others(2): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 898665 | ||||||
| chr5:898707 | G | GGCAGGCC others(125): Show |
1 | a0001c0001t0001g0019 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.389-1656_389-1655i others(134): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 898707 | ||||||
| chr5:898731 | T | G | 7 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0002g0010 others(4): Show |
12 | HG01109.hp1 HG01516.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.389-1763T>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 898731 | |||||||
| chr5:898773 | G | GGCAGGCC others(58): Show |
1 | a0001c0001t0002g0038 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.389-1719_389-1655d others(67): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 898773 | ||||||
| chr5:898797 | T | G | 2 | a0001c0001t0002g0055 a0001c0001t0009g0001 |
2 | HG01516.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.389-1697T>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 898797 | |||||||
| chr5:898797 | TCAGTCAG others(59): Show |
T | 14 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0041 others(11): Show |
37 | HG00438.hp1 HG00609.hp1 HG01099.hp2 others(34): Show |
intron_variant | MODIFIER | c.389-1631_389-1566d others(68): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 898797 | ||||||
| chr5:898797 | TCAGTCAG others(455): Show |
T | 1 | a0001c0001t0002g0056 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.389-1631_389-1170d others(2): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 898797 | ||||||
| chr5:898839 | G | AGCAGGCC others(917): Show |
1 | a0001c0001t0001g0019 | 2 | HG02258.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.389-1656_389-1655i others(926): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 898839 | |||||||
| chr5:898863 | G | GCAGTCAG others(59): Show |
1 | a0001c0001t0001g0040 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.389-1565_389-1500d others(68): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 898863 | ||||||
| chr5:898863 | G | T | 52 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0018 others(49): Show |
108 | HG00408.hp2 HG00544.hp1 HG00621.hp1 others(105): Show |
intron_variant | MODIFIER | c.389-1631G>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 898863 | |||||||
| chr5:898863 | GCAGTCAG others(59): Show |
G | 2 | a0001c0001t0001g0049 a0001c0001t0002g0054 |
2 | HG01106.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.389-1565_389-1500d others(68): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 898863 | ||||||
| chr5:898929 | T | G | 13 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0018 others(10): Show |
28 | HG00609.hp2 HG01167.hp2 HG01175.hp2 others(25): Show |
intron_variant | MODIFIER | c.389-1565T>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 898929 | |||||||
| chr5:898929 | T | TCAGTCAG others(1049): Show |
1 | a0001c0001t0001g0019 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.389-1524_389-1523i others(1058): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 898929 | ||||||
| chr5:898929 | T | TCAGTCAG others(59): Show |
1 | a0001c0001t0001g0068 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.389-1433_389-1368d others(68): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 898929 | ||||||
| chr5:898950 | A | G | 1 | a0001c0001t0002g0055 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.389-1544A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 898950 | |||||||
| chr5:898995 | G | T | 16 | a0001c0001t0001g0019 a0001c0001t0001g0040 a0001c0001t0001g0043 others(13): Show |
48 | HG00408.hp2 HG00544.hp1 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.389-1499G>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 898995 | |||||||
| chr5:898995 | GCAGTCAG others(125): Show |
G | 1 | a0001c0001t0001g0046 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.389-1367_389-1236d others(2): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 898995 | ||||||
| chr5:899016 | A | G | 2 | a0001c0001t0002g0053 a0001c0001t0002g0055 |
2 | HG02559.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.389-1478A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 899016 | |||||||
| chr5:899037 | G | A | 1 | a0001c0001t0002g0017 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.389-1457G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 899037 | |||||||
| chr5:899061 | G | T | 47 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(44): Show |
91 | HG00438.hp1 HG00609.hp1 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.389-1433G>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 899061 | |||||||
| chr5:899061 | GCAGTCAG others(59): Show |
G | 3 | a0001c0001t0001g0132 a0001c0001t0002g0053 a0001c0002t0002g0012 |
5 | HG01175.hp2 HG01433.hp1 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.389-1367_389-1302d others(68): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 899061 | ||||||
| chr5:899082 | A | G | 2 | a0001c0001t0002g0054 a0001c0001t0002g0055 |
2 | HG02280.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.389-1412A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 899082 | |||||||
| chr5:899120 | G | C | 1 | a0001c0001t0001g0006 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.389-1374G>C | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 899120 | |||||||
| chr5:899127 | T | G | 12 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0034 others(9): Show |
27 | HG00609.hp2 HG01167.hp2 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.389-1367T>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 899127 | |||||||
| chr5:899127 | TCAGTCAG others(59): Show |
T | 1 | a0001c0001t0001g0005 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.389-1235_389-1170d others(68): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 899127 | ||||||
| chr5:899143 | G | GAAACAGG others(59): Show |
1 | a0001c0001t0002g0002 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.389-1302_389-1301i others(68): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 899143 | ||||||
| chr5:899148 | A | G | 2 | a0001c0001t0002g0053 a0001c0001t0002g0054 |
2 | HG02280.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.389-1346A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 899148 | |||||||
| chr5:899193 | G | T | 18 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0019 others(15): Show |
51 | HG00408.hp2 HG00621.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.389-1301G>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 899193 | |||||||
| chr5:899214 | A | G | 2 | a0001c0001t0002g0053 a0001c0001t0002g0054 |
2 | HG02280.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.389-1280A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 899214 | |||||||
| chr5:899259 | G | T | 1 | a0001c0001t0001g0019 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.389-1235G>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 899259 | |||||||
| chr5:899259 | GCAGT | G | 3 | a0001c0001t0002g0028 a0001c0001t0002g0140 a0001c0001t0002g0141 |
5 | HG02280.hp1 HG03041.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.389-1230_389-1227d others(6): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 899259 | ||||||
| chr5:899259 | GCAGTCAG others(59): Show |
G | 2 | a0001c0001t0002g0017 a0001c0001t0002g0053 |
2 | HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.389-1103_389-1038d others(68): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 899259 | ||||||
| chr5:899280 | A | G | 2 | a0001c0001t0002g0054 a0001c0002t0002g0012 |
5 | HG01175.hp2 HG01433.hp1 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.389-1214A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 899280 | |||||||
| chr5:899325 | T | G | 20 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(17): Show |
54 | HG00408.hp2 HG00544.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.389-1169T>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 899325 | |||||||
| chr5:899325 | TCAGTCAG others(125): Show |
T | 1 | a0001c0001t0001g0139 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.389-1103_389-972de others(1): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 899325 | ||||||
| chr5:899325 | TCAGTCAG others(191): Show |
T | 5 | a0001c0001t0001g0045 a0001c0001t0001g0132 a0001c0001t0002g0010 others(2): Show |
11 | HG01109.hp1 HG02486.hp1 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.389-839_389-642del | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 899325 | ||||||
| chr5:899346 | A | G | 3 | a0001c0001t0002g0053 a0001c0001t0002g0054 a0001c0002t0002g0012 |
6 | HG01175.hp2 HG01433.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.389-1148A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 899346 | |||||||
| chr5:899369 | C | G | 1 | a0001c0001t0007g0080 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.389-1125C>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 899369 | |||||||
| chr5:899390 | TTCAGTCA others(195): Show |
T | 1 | a0001c0001t0009g0001 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.389-1098_389-897de others(1): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 899390 | ||||||
| chr5:899391 | T | G | 46 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(43): Show |
81 | HG00438.hp1 HG00609.hp1 HG01099.hp1 others(78): Show |
intron_variant | MODIFIER | c.389-1103T>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 899391 | |||||||
| chr5:899391 | T | TCAGTCAG others(2237): Show |
1 | a0001c0001t0001g0019 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.389-1038_389-1037i others(2246): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 899391 | ||||||
| chr5:899391 | TCAGTCAG others(257): Show |
T | 1 | a0001c0001t0002g0055 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.389-971_389-708del | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 899391 | ||||||
| chr5:899412 | A | G | 3 | a0001c0001t0002g0053 a0001c0001t0002g0054 a0001c0002t0002g0012 |
6 | HG01175.hp2 HG01433.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.389-1082A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 899412 | |||||||
| chr5:899457 | G | T | 3 | a0001c0001t0001g0133 a0001c0001t0002g0027 a0001c0001t0002g0056 |
5 | HG01891.hp2 HG03209.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.389-1037G>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 899457 | |||||||
| chr5:899523 | G | GCAGTCAG others(59): Show |
15 | a0001c0001t0001g0018 a0001c0001t0001g0040 a0001c0001t0001g0043 others(12): Show |
43 | HG00408.hp2 HG00544.hp1 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.389-905_389-840dup others(66): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 899523 | ||||||
| chr5:899523 | G | T | 44 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(41): Show |
80 | HG00438.hp1 HG00609.hp1 HG01099.hp1 others(77): Show |
intron_variant | MODIFIER | c.389-971G>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 899523 | |||||||
| chr5:899544 | A | G | 1 | a0001c0001t0002g0056 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.389-950A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 899544 | |||||||
| chr5:899589 | T | G | 5 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0016 others(2): Show |
7 | HG00738.hp2 HG01192.hp1 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.389-905T>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 899589 | |||||||
| chr5:899589 | TCAGTCAG others(125): Show |
T | 1 | a0001c0001t0002g0017 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.389-839_389-708del | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 899589 | ||||||
| chr5:899592 | GTCAGTGT others(253): Show |
G | 1 | a0001c0001t0002g0027 | 3 | HG01891.hp2 HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.389-839_389-580del | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 899592 | ||||||
| chr5:899610 | A | G | 1 | a0001c0001t0002g0056 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.389-884A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 899610 | |||||||
| chr5:899655 | G | GCAGTCAG others(59): Show |
1 | a0001c0001t0002g0002 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.389-774_389-773ins others(66): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 899655 | ||||||
| chr5:899655 | G | T | 37 | a0001c0001t0001g0001 a0001c0001t0002g0002 a0001c0001t0002g0010 others(34): Show |
84 | HG00408.hp2 HG00544.hp1 HG00621.hp1 others(81): Show |
intron_variant | MODIFIER | c.389-839G>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 899655 | |||||||
| chr5:899676 | A | G | 1 | a0001c0001t0002g0056 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.389-818A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 899676 | |||||||
| chr5:899721 | G | T | 19 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0124 others(16): Show |
29 | HG01175.hp2 HG01433.hp1 HG01433.hp2 others(26): Show |
intron_variant | MODIFIER | c.389-773G>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 899721 | |||||||
| chr5:899722 | C | T | 1 | a0001c0001t0001g0001 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.389-772C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 899722 | |||||||
| chr5:899727 | A | C | 1 | a0001c0001t0001g0024 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.389-767A>C | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 899727 | |||||||
| chr5:899763 | G | A | 3 | a0001c0001t0002g0053 a0001c0001t0002g0054 a0001c0001t0002g0055 |
3 | HG02280.hp2 HG02559.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.389-731G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 899763 | |||||||
| chr5:899787 | T | G | 2 | a0001c0001t0001g0007 a0001c0001t0002g0002 |
2 | HG01928.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.389-707T>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 899787 | |||||||
| chr5:899790 | GTCAGTGT others(55): Show |
G | 1 | a0001c0001t0002g0056 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.389-636_389-575del others(62): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 899790 | ||||||
| chr5:899829 | G | A | 4 | a0001c0001t0002g0053 a0001c0001t0002g0054 a0001c0001t0002g0055 others(1): Show |
7 | HG01175.hp2 HG01433.hp1 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.389-665G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 899829 | |||||||
| chr5:899852 | T | TTCAG | 2 | a0001c0001t0001g0015 a0001c0001t0002g0140 |
3 | HG02273.hp1 HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.389-640_389-637dup others(4): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 899852 | ||||||
| chr5:899891 | G | A | 8 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0053 others(5): Show |
17 | HG01175.hp2 HG01433.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.389-603G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 899891 | |||||||
| chr5:899957 | A | G | 25 | a0001c0001t0002g0002 a0001c0001t0002g0011 a0001c0001t0002g0027 others(22): Show |
67 | HG00408.hp2 HG00544.hp1 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.389-537A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 899957 | |||||||
| chr5:899972 | G | A | 1 | a0006c0008t0001g0136 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.389-522G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 899972 | |||||||
| chr5:899981 | T | G | 1 | a0001c0002t0002g0012 | 4 | HG01175.hp2 HG01433.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.389-513T>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 899981 | |||||||
| chr5:900041 | A | G | 16 | a0001c0001t0002g0008 a0001c0001t0002g0013 a0001c0001t0002g0014 others(13): Show |
36 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(33): Show |
intron_variant | MODIFIER | c.389-453A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 900041 | |||||||
| chr5:900145 | C | T | 11 | a0001c0001t0002g0008 a0001c0001t0002g0020 a0001c0001t0002g0029 others(8): Show |
25 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.389-349C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 900145 | |||||||
| chr5:900160 | A | C | 4 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0057 others(1): Show |
10 | HG01884.hp2 HG02451.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.389-334A>C | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 900160 | |||||||
| chr5:900175 | T | G | 83 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0018 others(80): Show |
185 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(182): Show |
intron_variant | MODIFIER | c.389-319T>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 900175 | |||||||
| chr5:900220 | C | T | 1 | a0001c0001t0002g0141 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.389-274C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 3/12 | chr5 | 900220 | |||||||
| chr5:900569 | C | T | 1 | a0006c0008t0001g0136 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.444+20C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 4/12 | chr5 | 900569 | |||||||
| chr5:900642 | G | A | 2 | a0001c0001t0001g0062 a0001c0001t0001g0065 |
2 | NA18961.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.444+93G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 4/12 | chr5 | 900642 | |||||||
| chr5:900659 | C | T | 1 | a0001c0001t0001g0037 | 2 | HG00280.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.444+110C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 4/12 | chr5 | 900659 | |||||||
| chr5:900724 | T | C | 4 | a0001c0001t0002g0053 a0001c0001t0002g0054 a0001c0001t0002g0055 others(1): Show |
7 | HG01175.hp2 HG01433.hp1 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.444+175T>C | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 4/12 | chr5 | 900724 | |||||||
| chr5:900765 | C | T | 11 | a0001c0001t0002g0008 a0001c0001t0002g0020 a0001c0001t0002g0029 others(8): Show |
25 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.444+216C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 4/12 | chr5 | 900765 | |||||||
| chr5:900799 | G | A | 5 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0056 others(2): Show |
11 | HG01884.hp2 HG02451.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.444+250G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 4/12 | chr5 | 900799 | |||||||
| chr5:900944 | T | C | 1 | a0001c0001t0002g0117 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.444+395T>C | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 4/12 | chr5 | 900944 | |||||||
| chr5:900964 | G | A | 1 | a0001c0001t0001g0023 | 3 | NA18943.hp1 NA18960.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.445-377G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 4/12 | chr5 | 900964 | |||||||
| chr5:901004 | A | G | 11 | a0001c0001t0002g0008 a0001c0001t0002g0020 a0001c0001t0002g0029 others(8): Show |
25 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.445-337A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 4/12 | chr5 | 901004 | |||||||
| chr5:901079 | T | A | 4 | a0001c0001t0002g0053 a0001c0001t0002g0054 a0001c0001t0002g0055 others(1): Show |
7 | HG01175.hp2 HG01433.hp1 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.445-262T>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 4/12 | chr5 | 901079 | |||||||
| chr5:901229 | C | T | 2 | a0001c0001t0001g0016 a0001c0001t0001g0093 |
5 | NA18950.hp2 NA19056.hp1 NA19080.hp1 others(2): Show |
intron_variant | MODIFIER | c.445-112C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 4/12 | chr5 | 901229 | |||||||
| chr5:901232 | C | T | 1 | a0001c0001t0002g0010 | 6 | HG02486.hp1 HG02818.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.445-109C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 4/12 | chr5 | 901232 | |||||||
| chr5:901308 | T | C | 16 | a0001c0001t0002g0008 a0001c0001t0002g0013 a0001c0001t0002g0014 others(13): Show |
36 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(33): Show |
intron_variant | MODIFIER | c.445-33T>C | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 4/12 | chr5 | 901308 | |||||||
| chr5:901438 | T | C | 3 | a0001c0001t0002g0028 a0001c0001t0002g0140 a0001c0001t0002g0141 |
5 | HG02280.hp1 HG03041.hp1 HG03471.hp2 others(2): Show |
splice_region_variant&intron_variant | LOW | c.535+7T>C | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 5/12 | chr5 | 901438 | |||||||
| chr5:901518 | G | A | 1 | a0001c0001t0002g0056 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.535+87G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 5/12 | chr5 | 901518 | |||||||
| chr5:901604 | TTTTGTTT others(1): Show |
T | 11 | a0001c0001t0002g0008 a0001c0001t0002g0020 a0001c0001t0002g0029 others(8): Show |
25 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.535+185_535+192del others(8): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr5 | 901604 | ||||||
| chr5:901747 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.535+316C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 5/12 | chr5 | 901747 | |||||||
| chr5:901843 | A | G | 7 | a0001c0001t0002g0017 a0001c0001t0002g0117 a0001c0001t0002g0118 others(4): Show |
8 | HG02572.hp2 HG02970.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.535+412A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 5/12 | chr5 | 901843 | |||||||
| chr5:901868 | C | T | 1 | a0001c0001t0001g0092 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.535+437C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 5/12 | chr5 | 901868 | |||||||
| chr5:901943 | G | A | 3 | a0001c0001t0001g0015 a0001c0001t0001g0031 a0001c0001t0001g0092 |
7 | HG02273.hp1 HG02451.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.535+512G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 5/12 | chr5 | 901943 | |||||||
| chr5:902011 | A | G | 16 | a0001c0001t0002g0008 a0001c0001t0002g0013 a0001c0001t0002g0014 others(13): Show |
36 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(33): Show |
intron_variant | MODIFIER | c.535+580A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 5/12 | chr5 | 902011 | |||||||
| chr5:902205 | G | T | 1 | a0001c0001t0001g0137 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.535+774G>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 5/12 | chr5 | 902205 | |||||||
| chr5:902220 | G | A | 1 | a0001c0001t0002g0027 | 3 | HG01891.hp2 HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.535+789G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 5/12 | chr5 | 902220 | |||||||
| chr5:902243 | T | G | 10 | a0001c0001t0002g0017 a0001c0001t0002g0028 a0001c0001t0002g0117 others(7): Show |
13 | HG02280.hp1 HG02572.hp2 HG02970.hp2 others(10): Show |
intron_variant | MODIFIER | c.535+812T>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 5/12 | chr5 | 902243 | |||||||
| chr5:902465 | C | T | 4 | a0001c0001t0001g0015 a0001c0001t0001g0022 a0001c0001t0001g0031 others(1): Show |
10 | HG02109.hp1 HG02145.hp1 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.535+1034C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 5/12 | chr5 | 902465 | |||||||
| chr5:902560 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.535+1129C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 5/12 | chr5 | 902560 | |||||||
| chr5:902563 | C | T | 11 | a0001c0001t0002g0008 a0001c0001t0002g0020 a0001c0001t0002g0029 others(8): Show |
25 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.535+1132C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 5/12 | chr5 | 902563 | |||||||
| chr5:902587 | G | A | 4 | a0001c0001t0002g0053 a0001c0001t0002g0054 a0001c0001t0002g0055 others(1): Show |
7 | HG01175.hp2 HG01433.hp1 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.535+1156G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 5/12 | chr5 | 902587 | |||||||
| chr5:902590 | G | T | 1 | a0006c0008t0001g0136 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.535+1159G>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 5/12 | chr5 | 902590 | |||||||
| chr5:902614 | A | G | 16 | a0001c0001t0002g0008 a0001c0001t0002g0013 a0001c0001t0002g0014 others(13): Show |
36 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(33): Show |
intron_variant | MODIFIER | c.535+1183A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 5/12 | chr5 | 902614 | |||||||
| chr5:902674 | T | TAAAAG | 20 | a0001c0001t0002g0008 a0001c0001t0002g0013 a0001c0001t0002g0014 others(17): Show |
43 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(40): Show |
intron_variant | MODIFIER | c.535+1245_535+1249d others(7): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr5 | 902674 | ||||||
| chr5:902699 | C | A | 1 | a0001c0001t0001g0066 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.535+1268C>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 5/12 | chr5 | 902699 | |||||||
| chr5:902853 | C | T | 11 | a0001c0001t0002g0008 a0001c0001t0002g0020 a0001c0001t0002g0029 others(8): Show |
25 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.536-1295C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 5/12 | chr5 | 902853 | |||||||
| chr5:902895 | CAGAG | C | 5 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0056 others(2): Show |
11 | HG01884.hp2 HG02451.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.536-1249_536-1246d others(6): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr5 | 902895 | ||||||
| chr5:902902 | A | G | 1 | a0001c0002t0002g0012 | 4 | HG01175.hp2 HG01433.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.536-1246A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 5/12 | chr5 | 902902 | |||||||
| chr5:902910 | C | T | 5 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0056 others(2): Show |
11 | HG01884.hp2 HG02451.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.536-1238C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 5/12 | chr5 | 902910 | |||||||
| chr5:902941 | G | A | 2 | a0001c0001t0001g0047 a0001c0001t0001g0142 |
3 | HG00323.hp1 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.536-1207G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 5/12 | chr5 | 902941 | |||||||
| chr5:902968 | C | G | 2 | a0001c0001t0004g0090 a0001c0001t0004g0091 |
2 | HG00735.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.536-1180C>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 5/12 | chr5 | 902968 | |||||||
| chr5:903018 | G | A | 1 | a0001c0001t0002g0038 | 2 | NA18988.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.536-1130G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 5/12 | chr5 | 903018 | |||||||
| chr5:903036 | A | G | 1 | a0001c0001t0001g0036 | 2 | HG00099.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.536-1112A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 5/12 | chr5 | 903036 | |||||||
| chr5:903073 | C | T | 1 | a0001c0001t0002g0027 | 3 | HG01891.hp2 HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.536-1075C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 5/12 | chr5 | 903073 | |||||||
| chr5:903126 | C | G | 1 | a0001c0002t0002g0012 | 4 | HG01175.hp2 HG01433.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.536-1022C>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 5/12 | chr5 | 903126 | |||||||
| chr5:903162 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.536-986G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 5/12 | chr5 | 903162 | |||||||
| chr5:903206 | A | G | 83 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0018 others(80): Show |
185 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(182): Show |
intron_variant | MODIFIER | c.536-942A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 5/12 | chr5 | 903206 | |||||||
| chr5:903233 | G | C | 12 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0020 others(9): Show |
31 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(28): Show |
intron_variant | MODIFIER | c.536-915G>C | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 5/12 | chr5 | 903233 | |||||||
| chr5:903309 | C | T | 1 | a0001c0002t0002g0012 | 4 | HG01175.hp2 HG01433.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.536-839C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 5/12 | chr5 | 903309 | |||||||
| chr5:903345 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.536-803C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 5/12 | chr5 | 903345 | |||||||
| chr5:903415 | T | C | 4 | a0001c0001t0002g0053 a0001c0001t0002g0054 a0001c0001t0002g0055 others(1): Show |
7 | HG01175.hp2 HG01433.hp1 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.536-733T>C | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 5/12 | chr5 | 903415 | |||||||
| chr5:903484 | C | T | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | HG00621.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.536-664C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 5/12 | chr5 | 903484 | |||||||
| chr5:903535 | G | A | 1 | a0001c0001t0001g0024 | 3 | HG02015.hp1 HG02523.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.536-613G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 5/12 | chr5 | 903535 | |||||||
| chr5:903540 | C | T | 1 | a0001c0001t0001g0088 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.536-608C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 5/12 | chr5 | 903540 | |||||||
| chr5:903644 | A | G | 1 | a0001c0001t0002g0114 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.536-504A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 5/12 | chr5 | 903644 | |||||||
| chr5:903897 | G | A | 1 | a0001c0001t0002g0002 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.536-251G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 5/12 | chr5 | 903897 | |||||||
| chr5:903967 | C | T | 4 | a0001c0001t0001g0044 a0001c0001t0001g0122 a0001c0001t0001g0131 others(1): Show |
4 | NA18949.hp2 NA18965.hp1 NA18987.hp1 others(1): Show |
intron_variant | MODIFIER | c.536-181C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 5/12 | chr5 | 903967 | |||||||
| chr5:904010 | C | T | 5 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0056 others(2): Show |
11 | HG01884.hp2 HG02451.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.536-138C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 5/12 | chr5 | 904010 | |||||||
| chr5:904259 | T | G | 19 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0047 others(16): Show |
45 | HG00099.hp2 HG00323.hp1 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.608+39T>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 6/12 | chr5 | 904259 | |||||||
| chr5:904280 | G | GT | 6 | a0001c0001t0001g0087 a0001c0001t0001g0122 a0001c0001t0001g0130 others(3): Show |
9 | HG01175.hp2 HG01433.hp1 HG02148.hp2 others(6): Show |
intron_variant | MODIFIER | c.608+73dupT | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr5 | 904280 | ||||||
| chr5:904280 | GT | G | 13 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0020 others(10): Show |
32 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(29): Show |
intron_variant | MODIFIER | c.608+73delT | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr5 | 904280 | ||||||
| chr5:904455 | A | G | 2 | a0001c0001t0002g0117 a0001c0001t0002g0119 |
2 | HG02572.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.608+235A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 6/12 | chr5 | 904455 | |||||||
| chr5:904480 | G | C | 1 | a0001c0001t0001g0032 | 2 | HG03831.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.608+260G>C | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 6/12 | chr5 | 904480 | |||||||
| chr5:904609 | A | T | 1 | a0001c0001t0001g0086 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.608+389A>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 6/12 | chr5 | 904609 | |||||||
| chr5:904619 | C | A | 1 | a0001c0001t0002g0056 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.608+399C>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 6/12 | chr5 | 904619 | |||||||
| chr5:904619 | C | G | 5 | a0001c0001t0002g0010 a0001c0001t0002g0013 a0001c0001t0002g0014 others(2): Show |
16 | HG01884.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.608+399C>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 6/12 | chr5 | 904619 | |||||||
| chr5:904857 | A | T | 3 | a0001c0001t0002g0008 a0001c0001t0002g0030 a0001c0001t0002g0116 |
10 | HG01884.hp1 HG02055.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.608+637A>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 6/12 | chr5 | 904857 | |||||||
| chr5:904970 | T | G | 1 | a0001c0001t0002g0103 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.608+750T>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 6/12 | chr5 | 904970 | |||||||
| chr5:905005 | A | T | 1 | a0001c0002t0002g0012 | 4 | HG01175.hp2 HG01433.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.608+785A>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 6/12 | chr5 | 905005 | |||||||
| chr5:905076 | AGT | A | 5 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0056 others(2): Show |
11 | HG01884.hp2 HG02451.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.608+859_608+860del others(2): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr5 | 905076 | ||||||
| chr5:905319 | G | A | 1 | a0001c0002t0002g0012 | 4 | HG01175.hp2 HG01433.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.608+1099G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 6/12 | chr5 | 905319 | |||||||
| chr5:905332 | A | G | 11 | a0001c0001t0002g0008 a0001c0001t0002g0020 a0001c0001t0002g0029 others(8): Show |
25 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.608+1112A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 6/12 | chr5 | 905332 | |||||||
| chr5:905347 | G | T | 1 | a0001c0001t0001g0124 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.608+1127G>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 6/12 | chr5 | 905347 | |||||||
| chr5:905354 | G | C | 1 | a0001c0001t0004g0090 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.608+1134G>C | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 6/12 | chr5 | 905354 | |||||||
| chr5:905394 | G | T | 1 | a0001c0001t0001g0146 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.608+1174G>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 6/12 | chr5 | 905394 | |||||||
| chr5:905578 | G | A | 1 | a0001c0001t0001g0069 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.608+1358G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 6/12 | chr5 | 905578 | |||||||
| chr5:905760 | G | A | 1 | a0001c0001t0002g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.609-1370G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 6/12 | chr5 | 905760 | |||||||
| chr5:905978 | G | A | 1 | a0001c0001t0002g0027 | 3 | HG01891.hp2 HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.609-1152G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 6/12 | chr5 | 905978 | |||||||
| chr5:905996 | A | G | 15 | a0001c0001t0002g0008 a0001c0001t0002g0020 a0001c0001t0002g0029 others(12): Show |
32 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(29): Show |
intron_variant | MODIFIER | c.609-1134A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 6/12 | chr5 | 905996 | |||||||
| chr5:906052 | C | CA | 12 | a0001c0001t0002g0008 a0001c0001t0002g0020 a0001c0001t0002g0029 others(9): Show |
26 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.609-1071dupA | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr5 | 906052 | ||||||
| chr5:906272 | C | T | 1 | a0006c0008t0001g0136 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.609-858C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 6/12 | chr5 | 906272 | |||||||
| chr5:906280 | A | G | 1 | a0001c0001t0002g0058 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.609-850A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 6/12 | chr5 | 906280 | |||||||
| chr5:906284 | T | TC | 12 | a0001c0001t0002g0008 a0001c0001t0002g0020 a0001c0001t0002g0029 others(9): Show |
29 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.609-845dupC | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr5 | 906284 | ||||||
| chr5:906344 | T | TTG | 15 | a0001c0001t0002g0008 a0001c0001t0002g0020 a0001c0001t0002g0029 others(12): Show |
32 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(29): Show |
intron_variant | MODIFIER | c.609-785_609-784ins others(2): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr5 | 906344 | ||||||
| chr5:906367 | A | G | 1 | a0001c0001t0001g0088 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.609-763A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 6/12 | chr5 | 906367 | |||||||
| chr5:906515 | A | G | 2 | a0001c0001t0001g0019 a0001c0001t0001g0043 |
6 | HG02257.hp1 HG02258.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.609-615A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 6/12 | chr5 | 906515 | |||||||
| chr5:906716 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.609-414C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 6/12 | chr5 | 906716 | |||||||
| chr5:906888 | T | C | 1 | a0001c0001t0001g0019 | 4 | HG02257.hp1 HG02258.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.609-242T>C | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 6/12 | chr5 | 906888 | |||||||
| chr5:906979 | C | T | 12 | a0001c0001t0002g0008 a0001c0001t0002g0020 a0001c0001t0002g0029 others(9): Show |
29 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.609-151C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 6/12 | chr5 | 906979 | |||||||
| chr5:907008 | A | G | 2 | a0001c0001t0002g0029 a0001c0001t0002g0052 |
5 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.609-122A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 6/12 | chr5 | 907008 | |||||||
| chr5:907058 | C | T | 1 | a0001c0001t0001g0129 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.609-72C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 6/12 | chr5 | 907058 | |||||||
| chr5:907304 | G | T | 1 | a0006c0008t0001g0136 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.672+111G>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 7/12 | chr5 | 907304 | |||||||
| chr5:907305 | T | G | 1 | a0006c0008t0001g0136 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.672+112T>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 7/12 | chr5 | 907305 | |||||||
| chr5:907390 | G | A | 12 | a0001c0001t0002g0008 a0001c0001t0002g0020 a0001c0001t0002g0029 others(9): Show |
29 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.672+197G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 7/12 | chr5 | 907390 | |||||||
| chr5:907405 | A | G | 1 | a0001c0001t0002g0113 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.672+212A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 7/12 | chr5 | 907405 | |||||||
| chr5:907413 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.672+220C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 7/12 | chr5 | 907413 | |||||||
| chr5:907564 | C | T | 1 | a0001c0001t0002g0010 | 6 | HG02486.hp1 HG02818.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.672+371C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 7/12 | chr5 | 907564 | |||||||
| chr5:907583 | G | A | 1 | a0001c0001t0001g0133 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.672+390G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 7/12 | chr5 | 907583 | |||||||
| chr5:907601 | G | T | 1 | a0001c0001t0001g0128 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.673-387G>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 7/12 | chr5 | 907601 | |||||||
| chr5:907820 | T | A | 4 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0057 others(1): Show |
10 | HG01884.hp2 HG02451.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.673-168T>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 7/12 | chr5 | 907820 | |||||||
| chr5:907941 | C | T | 11 | a0001c0001t0002g0008 a0001c0001t0002g0020 a0001c0001t0002g0029 others(8): Show |
25 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.673-47C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 7/12 | chr5 | 907941 | |||||||
| chr5:908091 | A | G | 1 | a0001c0001t0001g0034 | 2 | NA18990.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.759+17A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 8/12 | chr5 | 908091 | |||||||
| chr5:908312 | G | T | 1 | a0001c0001t0001g0085 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.760-43G>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 8/12 | chr5 | 908312 | |||||||
| chr5:908316 | G | C | 1 | a0001c0001t0001g0031 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.760-39G>C | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 8/12 | chr5 | 908316 | |||||||
| chr5:908473 | A | G | 1 | a0001c0002t0002g0012 | 4 | HG01175.hp2 HG01433.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.866+12A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 908473 | |||||||
| chr5:908475 | G | A | 2 | a0001c0001t0001g0006 a0001c0009t0001g0006 |
11 | HG02004.hp2 HG02015.hp2 NA18949.hp1 others(8): Show |
intron_variant | MODIFIER | c.866+14G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 908475 | |||||||
| chr5:908481 | A | G | 1 | a0001c0002t0002g0012 | 4 | HG01175.hp2 HG01433.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.866+20A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 908481 | |||||||
| chr5:908534 | T | C | 11 | a0001c0001t0002g0008 a0001c0001t0002g0020 a0001c0001t0002g0029 others(8): Show |
25 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.866+73T>C | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 908534 | |||||||
| chr5:908610 | T | C | 1 | a0001c0001t0001g0070 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.866+149T>C | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 908610 | |||||||
| chr5:908647 | T | A | 2 | a0001c0001t0002g0013 a0001c0001t0002g0057 |
5 | HG02451.hp1 HG02630.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.866+186T>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 908647 | |||||||
| chr5:908659 | G | A | 1 | a0001c0001t0001g0032 | 2 | HG03831.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.866+198G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 908659 | |||||||
| chr5:908814 | T | C | 12 | a0001c0001t0002g0008 a0001c0001t0002g0020 a0001c0001t0002g0029 others(9): Show |
29 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.866+353T>C | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 908814 | |||||||
| chr5:908815 | G | A | 12 | a0001c0001t0002g0008 a0001c0001t0002g0020 a0001c0001t0002g0029 others(9): Show |
29 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.866+354G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 908815 | |||||||
| chr5:908819 | A | G | 82 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0018 others(79): Show |
184 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(181): Show |
intron_variant | MODIFIER | c.866+358A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 908819 | |||||||
| chr5:908885 | G | C | 12 | a0001c0001t0002g0008 a0001c0001t0002g0020 a0001c0001t0002g0029 others(9): Show |
29 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.866+424G>C | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 908885 | |||||||
| chr5:908907 | G | A | 7 | a0001c0001t0002g0017 a0001c0001t0002g0117 a0001c0001t0002g0118 others(4): Show |
8 | HG02572.hp2 HG02970.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.866+446G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 908907 | |||||||
| chr5:908953 | G | C | 1 | a0001c0001t0001g0071 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.866+492G>C | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 908953 | |||||||
| chr5:909039 | C | T | 1 | a0001c0001t0002g0118 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.866+578C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 909039 | |||||||
| chr5:909062 | T | C | 3 | a0001c0001t0002g0028 a0001c0001t0002g0140 a0001c0001t0002g0141 |
5 | HG02280.hp1 HG03041.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.866+601T>C | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 909062 | |||||||
| chr5:909208 | C | G | 3 | a0001c0001t0001g0016 a0001c0001t0001g0067 a0001c0001t0001g0093 |
6 | HG02132.hp2 NA18950.hp2 NA19056.hp1 others(3): Show |
intron_variant | MODIFIER | c.866+747C>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 909208 | |||||||
| chr5:909284 | C | T | 23 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0019 others(20): Show |
50 | HG00438.hp1 HG00609.hp1 HG02027.hp2 others(47): Show |
intron_variant | MODIFIER | c.866+823C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 909284 | |||||||
| chr5:909301 | G | T | 1 | a0001c0001t0001g0084 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.866+840G>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 909301 | |||||||
| chr5:909444 | C | T | 1 | a0001c0001t0002g0141 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.866+983C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 909444 | |||||||
| chr5:909505 | C | T | 20 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0041 others(17): Show |
43 | HG00438.hp1 HG00609.hp1 HG02027.hp2 others(40): Show |
intron_variant | MODIFIER | c.866+1044C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 909505 | |||||||
| chr5:909506 | G | A | 1 | a0001c0001t0002g0027 | 3 | HG01891.hp2 HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.866+1045G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 909506 | |||||||
| chr5:909641 | C | T | 7 | a0001c0001t0002g0017 a0001c0001t0002g0117 a0001c0001t0002g0118 others(4): Show |
8 | HG02572.hp2 HG02970.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.866+1180C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 909641 | |||||||
| chr5:909672 | A | C | 1 | a0001c0001t0001g0083 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.866+1211A>C | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 909672 | |||||||
| chr5:909706 | T | A | 1 | a0001c0001t0002g0020 | 4 | HG02965.hp1 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.866+1245T>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 909706 | |||||||
| chr5:909818 | A | T | 2 | a0001c0001t0001g0082 a0001c0001t0001g0084 |
2 | HG00642.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.866+1357A>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 909818 | |||||||
| chr5:909889 | T | C | 1 | a0001c0001t0002g0029 | 3 | HG01081.hp2 HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.866+1428T>C | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 909889 | |||||||
| chr5:909991 | G | GT | 12 | a0001c0001t0002g0008 a0001c0001t0002g0020 a0001c0001t0002g0029 others(9): Show |
29 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.866+1532dupT | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 909991 | ||||||
| chr5:910155 | C | T | 21 | a0001c0001t0002g0002 a0001c0001t0002g0011 a0001c0001t0002g0038 others(18): Show |
59 | HG00408.hp2 HG00544.hp1 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.867-1688C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 910155 | |||||||
| chr5:910165 | C | T | 1 | a0001c0001t0001g0145 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.867-1678C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 910165 | |||||||
| chr5:910166 | G | A | 1 | a0001c0001t0001g0072 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.867-1677G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 910166 | |||||||
| chr5:910300 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.867-1543C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 910300 | |||||||
| chr5:910356 | G | T | 1 | a0002c0004t0001g0048 | 2 | HG00673.hp2 HG02027.hp1 |
intron_variant | MODIFIER | c.867-1487G>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 910356 | |||||||
| chr5:910530 | G | A | 12 | a0001c0001t0002g0008 a0001c0001t0002g0020 a0001c0001t0002g0029 others(9): Show |
29 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.867-1313G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 910530 | |||||||
| chr5:910663 | C | G | 1 | a0001c0002t0002g0012 | 4 | HG01175.hp2 HG01433.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.867-1180C>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 910663 | |||||||
| chr5:910665 | C | T | 2 | a0001c0001t0002g0028 a0001c0001t0002g0141 |
4 | HG02280.hp1 HG03471.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.867-1178C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 910665 | |||||||
| chr5:910671 | T | C | 15 | a0001c0001t0002g0008 a0001c0001t0002g0020 a0001c0001t0002g0029 others(12): Show |
32 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(29): Show |
intron_variant | MODIFIER | c.867-1172T>C | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 910671 | |||||||
| chr5:910777 | C | A | 1 | a0001c0001t0001g0016 | 4 | NA18950.hp2 NA19056.hp1 NA19086.hp1 others(1): Show |
intron_variant | MODIFIER | c.867-1066C>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 910777 | |||||||
| chr5:910868 | G | A | 1 | a0001c0001t0002g0055 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.867-975G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 910868 | |||||||
| chr5:910911 | C | T | 1 | a0001c0001t0002g0118 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.867-932C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 910911 | |||||||
| chr5:910926 | G | A | 1 | a0001c0001t0001g0134 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.867-917G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 910926 | |||||||
| chr5:911061 | C | T | 1 | a0001c0002t0002g0012 | 4 | HG01175.hp2 HG01433.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.867-782C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 911061 | |||||||
| chr5:911115 | C | T | 2 | a0001c0005t0002g0155 a0001c0005t0002g0156 |
2 | HG01243.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.867-728C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 911115 | |||||||
| chr5:911121 | C | T | 1 | a0001c0001t0002g0027 | 3 | HG01891.hp2 HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.867-722C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 911121 | |||||||
| chr5:911247 | G | A | 7 | a0001c0001t0002g0017 a0001c0001t0002g0117 a0001c0001t0002g0118 others(4): Show |
8 | HG02572.hp2 HG02970.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.867-596G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 911247 | |||||||
| chr5:911260 | G | A | 4 | a0001c0001t0002g0020 a0001c0001t0002g0051 a0001c0005t0002g0155 others(1): Show |
8 | HG01243.hp1 HG02486.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.867-583G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 911260 | |||||||
| chr5:911270 | C | G | 1 | a0001c0001t0001g0049 | 2 | HG01106.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.867-573C>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 911270 | |||||||
| chr5:911270 | C | T | 4 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0057 others(1): Show |
10 | HG01884.hp2 HG02451.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.867-573C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 911270 | |||||||
| chr5:911272 | A | T | 5 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0056 others(2): Show |
11 | HG01884.hp2 HG02451.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.867-571A>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 911272 | |||||||
| chr5:911276 | T | C | 1 | a0001c0001t0002g0002 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.867-567T>C | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 911276 | |||||||
| chr5:911291 | G | A | 1 | a0001c0001t0002g0108 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.867-552G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 911291 | |||||||
| chr5:911346 | C | T | 1 | a0001c0001t0002g0112 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.867-497C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 911346 | |||||||
| chr5:911396 | C | G | 1 | a0001c0001t0001g0081 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.867-447C>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 911396 | |||||||
| chr5:911408 | A | G | 1 | a0001c0001t0002g0010 | 6 | HG02486.hp1 HG02818.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.867-435A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 911408 | |||||||
| chr5:911433 | C | T | 1 | a0001c0001t0002g0111 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.867-410C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 911433 | |||||||
| chr5:911444 | G | A | 1 | a0001c0001t0001g0145 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.867-399G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 911444 | |||||||
| chr5:911519 | C | T | 1 | a0001c0001t0007g0080 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.867-324C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 911519 | |||||||
| chr5:911561 | ACT | A | 1 | a0001c0002t0002g0012 | 4 | HG01175.hp2 HG01433.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.867-279_867-278del others(2): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 911561 | ||||||
| chr5:911579 | A | T | 1 | a0001c0001t0002g0112 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.867-264A>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 911579 | |||||||
| chr5:911644 | T | TAGG | 7 | a0001c0001t0002g0020 a0001c0001t0002g0029 a0001c0001t0002g0051 others(4): Show |
17 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.867-197_867-196ins others(3): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 911644 | ||||||
| chr5:911687 | G | A | 1 | a0001c0001t0002g0010 | 6 | HG02486.hp1 HG02818.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.867-156G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 911687 | |||||||
| chr5:911696 | G | A | 30 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0018 others(27): Show |
61 | HG00438.hp1 HG00609.hp1 HG01099.hp1 others(58): Show |
intron_variant | MODIFIER | c.867-147G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 911696 | |||||||
| chr5:911793 | G | C | 1 | a0001c0001t0001g0127 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.867-50G>C | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 9/12 | chr5 | 911793 | |||||||
| chr5:912005 | AT | A | 12 | a0001c0001t0002g0008 a0001c0001t0002g0020 a0001c0001t0002g0029 others(9): Show |
29 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.1020+19delT | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr5 | 912005 | ||||||
| chr5:912078 | C | T | 1 | a0001c0001t0001g0066 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1020+82C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 10/12 | chr5 | 912078 | |||||||
| chr5:912269 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1020+273G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 10/12 | chr5 | 912269 | |||||||
| chr5:912282 | T | G | 1 | a0001c0001t0001g0086 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1020+286T>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 10/12 | chr5 | 912282 | |||||||
| chr5:912343 | C | T | 11 | a0001c0001t0002g0008 a0001c0001t0002g0020 a0001c0001t0002g0029 others(8): Show |
25 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.1020+347C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 10/12 | chr5 | 912343 | |||||||
| chr5:912419 | A | G | 21 | a0001c0001t0002g0008 a0001c0001t0002g0013 a0001c0001t0002g0014 others(18): Show |
46 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(43): Show |
intron_variant | MODIFIER | c.1020+423A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 10/12 | chr5 | 912419 | |||||||
| chr5:912438 | T | A | 3 | a0001c0001t0001g0005 a0001c0001t0001g0034 a0001c0007t0001g0005 |
14 | HG00544.hp2 HG01943.hp2 HG02155.hp1 others(11): Show |
intron_variant | MODIFIER | c.1020+442T>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 10/12 | chr5 | 912438 | |||||||
| chr5:912474 | G | A | 4 | a0001c0001t0001g0025 a0001c0001t0001g0069 a0001c0001t0001g0070 others(1): Show |
6 | HG00738.hp1 HG00741.hp2 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.1020+478G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 10/12 | chr5 | 912474 | |||||||
| chr5:912487 | C | T | 3 | a0001c0001t0002g0053 a0001c0001t0002g0054 a0001c0001t0002g0055 |
3 | HG02280.hp2 HG02559.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1020+491C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 10/12 | chr5 | 912487 | |||||||
| chr5:912520 | C | T | 12 | a0001c0001t0002g0008 a0001c0001t0002g0020 a0001c0001t0002g0029 others(9): Show |
29 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.1020+524C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 10/12 | chr5 | 912520 | |||||||
| chr5:912553 | CGT | C | 4 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0057 others(1): Show |
10 | HG01884.hp2 HG02451.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1020+563_1020+564d others(4): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr5 | 912553 | ||||||
| chr5:912603 | G | A | 1 | a0001c0001t0002g0010 | 6 | HG02486.hp1 HG02818.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.1020+607G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 10/12 | chr5 | 912603 | |||||||
| chr5:912640 | CAT | C | 1 | a0001c0001t0002g0010 | 6 | HG02486.hp1 HG02818.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.1020+645_1020+646d others(4): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 10/12 | chr5 | 912640 | |||||||
| chr5:912776 | G | T | 1 | a0001c0001t0001g0022 | 3 | HG02109.hp1 HG02145.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1020+780G>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 10/12 | chr5 | 912776 | |||||||
| chr5:912800 | T | C | 1 | a0001c0001t0001g0137 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1020+804T>C | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 10/12 | chr5 | 912800 | |||||||
| chr5:913156 | C | G | 1 | a0001c0001t0001g0079 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1020+1160C>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 10/12 | chr5 | 913156 | |||||||
| chr5:913205 | G | A | 1 | a0001c0001t0001g0126 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1020+1209G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 10/12 | chr5 | 913205 | |||||||
| chr5:913226 | T | C | 1 | a0001c0001t0002g0027 | 3 | HG01891.hp2 HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1020+1230T>C | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 10/12 | chr5 | 913226 | |||||||
| chr5:913241 | T | G | 1 | a0001c0001t0001g0074 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1021-1224T>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 10/12 | chr5 | 913241 | |||||||
| chr5:913250 | G | C | 1 | a0001c0001t0002g0104 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1021-1215G>C | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 10/12 | chr5 | 913250 | |||||||
| chr5:913354 | TTTTG | T | 2 | a0001c0001t0002g0020 a0001c0001t0002g0051 |
6 | HG02486.hp2 HG02965.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1021-1099_1021-109 others(8): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr5 | 913354 | ||||||
| chr5:913547 | G | C | 30 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0018 others(27): Show |
61 | HG00438.hp1 HG00609.hp1 HG01099.hp1 others(58): Show |
intron_variant | MODIFIER | c.1021-918G>C | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 10/12 | chr5 | 913547 | |||||||
| chr5:913896 | C | T | 1 | a0001c0001t0001g0148 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1021-569C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 10/12 | chr5 | 913896 | |||||||
| chr5:913938 | C | T | 5 | a0001c0001t0002g0008 a0001c0001t0002g0030 a0001c0001t0002g0115 others(2): Show |
12 | HG01884.hp1 HG02055.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.1021-527C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 10/12 | chr5 | 913938 | |||||||
| chr5:913976 | G | A | 1 | a0001c0001t0001g0126 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1021-489G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 10/12 | chr5 | 913976 | |||||||
| chr5:913983 | G | A | 1 | a0001c0001t0002g0027 | 3 | HG01891.hp2 HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1021-482G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 10/12 | chr5 | 913983 | |||||||
| chr5:913989 | TCAGA | T | 6 | a0001c0001t0002g0020 a0001c0001t0002g0029 a0001c0001t0002g0051 others(3): Show |
13 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.1021-473_1021-470d others(6): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr5 | 913989 | ||||||
| chr5:914194 | C | T | 12 | a0001c0001t0002g0008 a0001c0001t0002g0020 a0001c0001t0002g0029 others(9): Show |
29 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.1021-271C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 10/12 | chr5 | 914194 | |||||||
| chr5:914209 | G | A | 1 | a0001c0001t0002g0053 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1021-256G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 10/12 | chr5 | 914209 | |||||||
| chr5:914241 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1021-224C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 10/12 | chr5 | 914241 | |||||||
| chr5:914278 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1021-187G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 10/12 | chr5 | 914278 | |||||||
| chr5:914340 | G | A | 1 | a0001c0002t0002g0012 | 4 | HG01175.hp2 HG01433.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.1021-125G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 10/12 | chr5 | 914340 | |||||||
| chr5:914660 | C | G | 1 | a0001c0001t0001g0143 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1133+83C>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 11/12 | chr5 | 914660 | |||||||
| chr5:914720 | C | CGT | 32 | a0001c0001t0001g0019 a0001c0001t0001g0042 a0001c0001t0001g0063 others(29): Show |
75 | HG00408.hp2 HG00544.hp1 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.1133+163_1133+164d others(4): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr5 | 914720 | ||||||
| chr5:914720 | C | CGTGT | 12 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0020 others(9): Show |
31 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(28): Show |
intron_variant | MODIFIER | c.1133+161_1133+164d others(6): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr5 | 914720 | ||||||
| chr5:914720 | CGT | C | 1 | a0001c0002t0002g0012 | 4 | HG01175.hp2 HG01433.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.1133+163_1133+164d others(4): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr5 | 914720 | ||||||
| chr5:914720 | CGTGTGTG others(3): Show |
C | 1 | a0001c0001t0001g0137 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1133+155_1133+164d others(12): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr5 | 914720 | ||||||
| chr5:914759 | G | A | 1 | a0001c0001t0001g0041 | 2 | NA18962.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.1133+182G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 11/12 | chr5 | 914759 | |||||||
| chr5:914820 | C | CGT | 15 | a0001c0001t0002g0008 a0001c0001t0002g0020 a0001c0001t0002g0029 others(12): Show |
32 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(29): Show |
intron_variant | MODIFIER | c.1133+243_1133+244i others(4): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 11/12 | chr5 | 914820 | |||||||
| chr5:914821 | A | G | 15 | a0001c0001t0002g0008 a0001c0001t0002g0020 a0001c0001t0002g0029 others(12): Show |
32 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(29): Show |
intron_variant | MODIFIER | c.1133+244A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 11/12 | chr5 | 914821 | |||||||
| chr5:914908 | G | A | 9 | a0001c0001t0002g0008 a0001c0001t0002g0020 a0001c0001t0002g0029 others(6): Show |
23 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.1133+331G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 11/12 | chr5 | 914908 | |||||||
| chr5:915025 | G | T | 1 | a0001c0001t0001g0123 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1133+448G>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 11/12 | chr5 | 915025 | |||||||
| chr5:915050 | G | A | 1 | a0001c0001t0002g0055 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1133+473G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 11/12 | chr5 | 915050 | |||||||
| chr5:915082 | G | A | 5 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0056 others(2): Show |
11 | HG01884.hp2 HG02451.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.1133+505G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 11/12 | chr5 | 915082 | |||||||
| chr5:915310 | C | A | 1 | a0001c0001t0002g0154 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1134-594C>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 11/12 | chr5 | 915310 | |||||||
| chr5:915310 | C | T | 1 | a0001c0001t0002g0113 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1134-594C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 11/12 | chr5 | 915310 | |||||||
| chr5:915367 | A | G | 4 | a0001c0001t0002g0017 a0003c0003t0002g0017 a0003c0003t0002g0120 others(1): Show |
5 | HG02976.hp2 HG03098.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1134-537A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 11/12 | chr5 | 915367 | |||||||
| chr5:915397 | GGGCAGGT others(49): Show |
G | 1 | a0001c0002t0002g0012 | 4 | HG01175.hp2 HG01433.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.1134-494_1134-439d others(58): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr5 | 915397 | ||||||
| chr5:915410 | C | A | 9 | a0001c0001t0002g0008 a0001c0001t0002g0029 a0001c0001t0002g0030 others(6): Show |
19 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.1134-494C>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 11/12 | chr5 | 915410 | |||||||
| chr5:915453 | A | AGGCAGGT others(49): Show |
1 | a0001c0001t0001g0023 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1134-382_1134-327d others(58): Show |
TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr5 | 915453 | ||||||
| chr5:915453 | A | G | 16 | a0001c0001t0002g0008 a0001c0001t0002g0013 a0001c0001t0002g0014 others(13): Show |
36 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(33): Show |
intron_variant | MODIFIER | c.1134-451A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 11/12 | chr5 | 915453 | |||||||
| chr5:915466 | A | C | 11 | a0001c0001t0002g0008 a0001c0001t0002g0020 a0001c0001t0002g0029 others(8): Show |
25 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.1134-438A>C | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 11/12 | chr5 | 915466 | |||||||
| chr5:915488 | G | A | 1 | a0001c0001t0002g0118 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1134-416G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 11/12 | chr5 | 915488 | |||||||
| chr5:915522 | A | C | 1 | a0001c0002t0002g0012 | 4 | HG01175.hp2 HG01433.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.1134-382A>C | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 11/12 | chr5 | 915522 | |||||||
| chr5:915534 | C | A | 1 | a0001c0001t0002g0109 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1134-370C>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 11/12 | chr5 | 915534 | |||||||
| chr5:915562 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1134-342C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 11/12 | chr5 | 915562 | |||||||
| chr5:915564 | C | T | 2 | a0001c0001t0002g0039 a0001c0001t0002g0102 |
3 | NA18948.hp2 NA18994.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.1134-340C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 11/12 | chr5 | 915564 | |||||||
| chr5:915589 | A | G | 12 | a0001c0001t0002g0008 a0001c0001t0002g0020 a0001c0001t0002g0029 others(9): Show |
29 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.1134-315A>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 11/12 | chr5 | 915589 | |||||||
| chr5:915712 | C | T | 1 | a0001c0001t0001g0026 | 3 | NA18977.hp1 NA19057.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.1134-192C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 11/12 | chr5 | 915712 | |||||||
| chr5:915792 | T | C | 12 | a0001c0001t0002g0008 a0001c0001t0002g0020 a0001c0001t0002g0029 others(9): Show |
29 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.1134-112T>C | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 11/12 | chr5 | 915792 | |||||||
| chr5:915828 | G | A | 6 | a0001c0001t0002g0020 a0001c0001t0002g0029 a0001c0001t0002g0051 others(3): Show |
13 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.1134-76G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 11/12 | chr5 | 915828 | |||||||
| chr5:915843 | T | C | 12 | a0001c0001t0002g0008 a0001c0001t0002g0020 a0001c0001t0002g0029 others(9): Show |
29 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.1134-61T>C | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 11/12 | chr5 | 915843 | |||||||
| chr5:915878 | C | G | 1 | a0001c0001t0001g0151 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1134-26C>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 11/12 | chr5 | 915878 | |||||||
| chr5:916027 | C | T | 1 | a0001c0005t0002g0156 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1203+54C>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 12/12 | chr5 | 916027 | |||||||
| chr5:916055 | G | A | 2 | a0001c0001t0002g0108 a0001c0001t0002g0110 |
2 | HG00408.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.1203+82G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 12/12 | chr5 | 916055 | |||||||
| chr5:916167 | G | A | 1 | a0001c0001t0001g0075 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1203+194G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 12/12 | chr5 | 916167 | |||||||
| chr5:916220 | G | A | 1 | a0001c0001t0001g0070 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1203+247G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 12/12 | chr5 | 916220 | |||||||
| chr5:916362 | T | C | 12 | a0001c0001t0002g0008 a0001c0001t0002g0020 a0001c0001t0002g0029 others(9): Show |
29 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.1203+389T>C | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 12/12 | chr5 | 916362 | |||||||
| chr5:916368 | G | A | 1 | a0001c0001t0002g0027 | 3 | HG01891.hp2 HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1203+395G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 12/12 | chr5 | 916368 | |||||||
| chr5:916372 | T | C | 32 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0013 others(29): Show |
65 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(62): Show |
intron_variant | MODIFIER | c.1203+399T>C | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 12/12 | chr5 | 916372 | |||||||
| chr5:916373 | G | T | 12 | a0001c0001t0002g0008 a0001c0001t0002g0020 a0001c0001t0002g0029 others(9): Show |
29 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.1203+400G>T | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 12/12 | chr5 | 916373 | |||||||
| chr5:916617 | G | A | 2 | a0001c0001t0001g0018 a0001c0001t0001g0123 |
5 | HG01099.hp1 HG01891.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.1204-391G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 12/12 | chr5 | 916617 | |||||||
| chr5:916775 | T | G | 12 | a0001c0001t0002g0008 a0001c0001t0002g0020 a0001c0001t0002g0029 others(9): Show |
29 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.1204-233T>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 12/12 | chr5 | 916775 | |||||||
| chr5:916791 | GC | G | 6 | a0001c0001t0002g0008 a0001c0001t0002g0027 a0001c0001t0002g0030 others(3): Show |
18 | HG01175.hp2 HG01433.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.1204-216delC | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 12/12 | chr5 | 916791 | |||||||
| chr5:916792 | C | G | 10 | a0001c0001t0002g0010 a0001c0001t0002g0013 a0001c0001t0002g0014 others(7): Show |
20 | HG01884.hp2 HG02055.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.1204-216C>G | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 12/12 | chr5 | 916792 | |||||||
| chr5:916860 | G | A | 1 | a0001c0002t0002g0012 | 4 | HG01175.hp2 HG01433.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.1204-148G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 12/12 | chr5 | 916860 | |||||||
| chr5:916991 | G | C | 29 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0018 others(26): Show |
60 | HG00438.hp1 HG00609.hp1 HG01099.hp1 others(57): Show |
intron_variant | MODIFIER | c.1204-17G>C | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 12/12 | chr5 | 916991 | |||||||
| chr5:916995 | G | A | 13 | a0001c0001t0001g0060 a0001c0001t0001g0076 a0001c0001t0002g0008 others(10): Show |
27 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.1204-13G>A | TRIP13 | ENSG00000071539.14 | transcript | ENST00000166345.8 | protein_coding | 12/12 | chr5 | 916995 |