Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 9320 |
| ensemblid | ENSG00000153827.15 |
| hgncid | 12306 |
| symbol | TRIP12 |
| name | thyroid hormone receptor interactor 12 |
| refseq_nuc | NM_001348323.3 |
| refseq_prot | NP_001335252.1 |
| ensembl_nuc | ENST00000675903.1 |
| ensembl_prot | ENSP00000502713.1 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 229763837 |
| end | 229922009 |
| strand | - |
| ver | v1.2 |
| region | chr2:229763837-229922009 |
| region5000 | chr2:229758837-229927009 |
| regionname0 | TRIP12_chr2_229763837_229922009 |
| regionname5000 | TRIP12_chr2_229758837_229927009 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 2067 | 329 | 92 | 64 | 113 | 16 | 42 | 85 | TRIP12_chr2_229758837_229927009 | TRIP12 | MSNRP others(2062): Show |
chr2 | 229758837 | 229927009 |
| a0002 | 0/0 | 2067 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | MSNRP others(2062): Show |
chr2 | 229758837 | 229927009 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 6201 | 149 | 68 | 29 | 37 | 4 | 10 | TRIP12_chr2_229758837_229927009 | TRIP12 | ATGTC others(6196): Show |
chr2 | 229758837 | 229927009 | ||
| a0001c0002 | 0/0 | 6201 | 112 | 12 | 29 | 43 | 8 | 20 | TRIP12_chr2_229758837_229927009 | TRIP12 | ATGTC others(6196): Show |
chr2 | 229758837 | 229927009 | ||
| a0001c0003 | 0/1 | 6201 | 53 | 9 | 6 | 24 | 4 | 9 | TRIP12_chr2_229758837_229927009 | TRIP12 | ATGTC others(6196): Show |
chr2 | 229758837 | 229927009 | ||
| a0001c0004 | 0/0 | 6201 | 8 | 0 | 0 | 8 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | ATGTC others(6196): Show |
chr2 | 229758837 | 229927009 | ||
| a0001c0005 | 0/0 | 6201 | 3 | 3 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | ATGTC others(6196): Show |
chr2 | 229758837 | 229927009 | ||
| a0001c0007 | 0/0 | 6201 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | ATGTC others(6196): Show |
chr2 | 229758837 | 229927009 | ||
| a0001c0008 | 0/0 | 6201 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | ATGTC others(6196): Show |
chr2 | 229758837 | 229927009 | ||
| a0001c0009 | 0/0 | 6201 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | ATGTC others(6196): Show |
chr2 | 229758837 | 229927009 | ||
| a0001c0010 | 0/0 | 6201 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | ATGTC others(6196): Show |
chr2 | 229758837 | 229927009 | ||
| a0002c0006 | 0/0 | 6201 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | ATGTC others(6196): Show |
chr2 | 229758837 | 229927009 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 10100 | 94 | 30 | 18 | 35 | 3 | 7 | TRIP12_chr2_229758837_229927009 | TRIP12 | GCTGC others(10095): Show |
chr2 | 229758837 | 229927009 |
| a0001c0001t0004 | 0/0 | 10100 | 14 | 13 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | GCTGC others(10095): Show |
chr2 | 229758837 | 229927009 |
| a0001c0001t0005 | 0/0 | 10101 | 8 | 2 | 3 | 1 | 0 | 2 | TRIP12_chr2_229758837_229927009 | TRIP12 | GCTGC others(10096): Show |
chr2 | 229758837 | 229927009 |
| a0001c0001t0009 | 0/0 | 10099 | 6 | 6 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | GCTGC others(10094): Show |
chr2 | 229758837 | 229927009 |
| a0001c0001t0010 | 0/0 | 10099 | 5 | 3 | 2 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | GCTGC others(10094): Show |
chr2 | 229758837 | 229927009 |
| a0001c0001t0011 | 0/0 | 10100 | 5 | 5 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | GCTGC others(10095): Show |
chr2 | 229758837 | 229927009 |
| a0001c0001t0012 | 0/0 | 10100 | 4 | 2 | 2 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | GCTGC others(10095): Show |
chr2 | 229758837 | 229927009 |
| a0001c0001t0014 | 0/0 | 10100 | 3 | 3 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | GCTGC others(10095): Show |
chr2 | 229758837 | 229927009 |
| a0001c0001t0016 | 0/0 | 10100 | 2 | 0 | 2 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | GCTGC others(10095): Show |
chr2 | 229758837 | 229927009 |
| a0001c0001t0019 | 0/0 | 10100 | 2 | 2 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | GCTGC others(10095): Show |
chr2 | 229758837 | 229927009 |
| a0001c0001t0024 | 0/0 | 10100 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | GCTGC others(10095): Show |
chr2 | 229758837 | 229927009 |
| a0001c0001t0025 | 0/0 | 10100 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | GCTGC others(10095): Show |
chr2 | 229758837 | 229927009 |
| a0001c0001t0026 | 0/0 | 10100 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | GCTGC others(10095): Show |
chr2 | 229758837 | 229927009 |
| a0001c0001t0027 | 0/0 | 10100 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | GCTGC others(10095): Show |
chr2 | 229758837 | 229927009 |
| a0001c0001t0030 | 0/0 | 10100 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | GCTGC others(10095): Show |
chr2 | 229758837 | 229927009 |
| a0001c0001t0031 | 0/0 | 10100 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | GCTGC others(10095): Show |
chr2 | 229758837 | 229927009 |
| a0001c0002t0001 | 0/0 | 10100 | 24 | 0 | 6 | 9 | 1 | 8 | TRIP12_chr2_229758837_229927009 | TRIP12 | GCTGC others(10095): Show |
chr2 | 229758837 | 229927009 |
| a0001c0002t0002 | 0/0 | 10100 | 37 | 6 | 8 | 15 | 5 | 3 | TRIP12_chr2_229758837_229927009 | TRIP12 | GCTGC others(10095): Show |
chr2 | 229758837 | 229927009 |
| a0001c0002t0003 | 0/0 | 10100 | 28 | 1 | 10 | 8 | 2 | 7 | TRIP12_chr2_229758837_229927009 | TRIP12 | GCTGC others(10095): Show |
chr2 | 229758837 | 229927009 |
| a0001c0002t0005 | 0/0 | 10101 | 2 | 1 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | GCTGC others(10096): Show |
chr2 | 229758837 | 229927009 |
| a0001c0002t0008 | 0/0 | 10102 | 6 | 0 | 0 | 6 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | GCTGC others(10097): Show |
chr2 | 229758837 | 229927009 |
| a0001c0002t0013 | 0/0 | 10101 | 3 | 0 | 2 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | GCTGC others(10096): Show |
chr2 | 229758837 | 229927009 |
| a0001c0002t0017 | 0/0 | 10100 | 2 | 0 | 0 | 2 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | GCTGC others(10095): Show |
chr2 | 229758837 | 229927009 |
| a0001c0002t0018 | 0/0 | 10100 | 2 | 2 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | GCTGC others(10095): Show |
chr2 | 229758837 | 229927009 |
| a0001c0002t0020 | 0/0 | 10100 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | GCTGC others(10095): Show |
chr2 | 229758837 | 229927009 |
| a0001c0002t0022 | 0/0 | 10101 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | GCTGC others(10096): Show |
chr2 | 229758837 | 229927009 |
| a0001c0002t0023 | 0/0 | 10101 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | GCTGC others(10096): Show |
chr2 | 229758837 | 229927009 |
| a0001c0002t0028 | 0/0 | 10100 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | GCTGC others(10095): Show |
chr2 | 229758837 | 229927009 |
| a0001c0002t0029 | 0/0 | 10100 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | GCTGC others(10095): Show |
chr2 | 229758837 | 229927009 |
| a0001c0002t0033 | 0/0 | 10100 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | GCTGC others(10095): Show |
chr2 | 229758837 | 229927009 |
| a0001c0002t0034 | 0/0 | 10100 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | GCTGC others(10095): Show |
chr2 | 229758837 | 229927009 |
| a0001c0002t0035 | 0/0 | 10100 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | GCTGC others(10095): Show |
chr2 | 229758837 | 229927009 |
| a0001c0003t0001 | 0/0 | 10100 | 31 | 6 | 1 | 18 | 1 | 5 | TRIP12_chr2_229758837_229927009 | TRIP12 | GCTGC others(10095): Show |
chr2 | 229758837 | 229927009 |
| a0001c0003t0005 | 0/0 | 10101 | 2 | 0 | 0 | 1 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | GCTGC others(10096): Show |
chr2 | 229758837 | 229927009 |
| a0001c0003t0006 | 0/0 | 10100 | 8 | 0 | 3 | 0 | 2 | 3 | TRIP12_chr2_229758837_229927009 | TRIP12 | GCTGC others(10095): Show |
chr2 | 229758837 | 229927009 |
| a0001c0003t0007 | 0/1 | 10100 | 6 | 0 | 1 | 3 | 1 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | GCTGC others(10095): Show |
chr2 | 229758837 | 229927009 |
| a0001c0003t0015 | 0/0 | 10100 | 3 | 3 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | GCTGC others(10095): Show |
chr2 | 229758837 | 229927009 |
| a0001c0003t0021 | 0/0 | 10101 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | GCTGC others(10096): Show |
chr2 | 229758837 | 229927009 |
| a0001c0003t0032 | 0/0 | 10100 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | GCTGC others(10095): Show |
chr2 | 229758837 | 229927009 |
| a0001c0003t0036 | 0/0 | 10101 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | GCTGC others(10096): Show |
chr2 | 229758837 | 229927009 |
| a0001c0004t0003 | 0/0 | 10100 | 8 | 0 | 0 | 8 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | GCTGC others(10095): Show |
chr2 | 229758837 | 229927009 |
| a0001c0005t0001 | 0/0 | 10100 | 3 | 3 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | GCTGC others(10095): Show |
chr2 | 229758837 | 229927009 |
| a0001c0007t0005 | 0/0 | 10101 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | GCTGC others(10096): Show |
chr2 | 229758837 | 229927009 |
| a0001c0008t0001 | 0/0 | 10100 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | GCTGC others(10095): Show |
chr2 | 229758837 | 229927009 |
| a0001c0009t0007 | 0/0 | 10100 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | GCTGC others(10095): Show |
chr2 | 229758837 | 229927009 |
| a0001c0010t0001 | 0/0 | 10100 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | GCTGC others(10095): Show |
chr2 | 229758837 | 229927009 |
| a0002c0006t0001 | 0/0 | 10100 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | GCTGC others(10095): Show |
chr2 | 229758837 | 229927009 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0176 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0004g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0004g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0004g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0004g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0004g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0004g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0004g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0004g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0004g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0004g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0004g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0004g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0004g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0005g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0005g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0005g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0005g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0005g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0005g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0005g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0005g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0009g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0009g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0009g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0009g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0009g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0009g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0010g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0010g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0010g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0010g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0010g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0011g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0011g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0011g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0011g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0011g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0012g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0012g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0012g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0012g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0014g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0014g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0014g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0016g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0016g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0019g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0019g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0024g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0025g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0026g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0027g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0030g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0031g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0002g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0002g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0002g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0002g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0002g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0002g0298 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0002g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0002g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0002g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0002g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0002g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0002g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0002g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0002g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0002g0308 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0002g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0002g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0002g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0002g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0002g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0002g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0002g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0003g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0003g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0003g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0003g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0003g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0003g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0003g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0003g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0003g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0003g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0003g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0003g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0003g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0003g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0003g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0003g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0003g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0003g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0003g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0005g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0005g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0008g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0008g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0008g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0008g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0008g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0008g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0013g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0013g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0013g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0017g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0017g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0018g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0018g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0020g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0022g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0023g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0028g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0029g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0033g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0034g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0035g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0003t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0003t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0003t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0003t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0003t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0003t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0003t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0003t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0003t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0003t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0003t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0003t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0003t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0003t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0003t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0003t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0003t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0003t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0003t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0003t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0003t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0003t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0003t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0003t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0003t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0003t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0003t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0003t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0003t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0003t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0003t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0003t0005g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0003t0005g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0003t0006g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0003t0006g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0003t0006g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0003t0006g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0003t0006g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0003t0006g0327 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0003t0006g0328 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0003t0006g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0003t0007g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0003t0007g0196 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0003t0007g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0003t0007g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0003t0007g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0003t0007g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0003t0015g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0003t0015g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0003t0015g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0003t0021g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0003t0032g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0003t0036g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0004t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0004t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0004t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0004t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0004t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0004t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0004t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0004t0003g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0005t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0005t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0005t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0007t0005g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0008t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0009t0007g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0010t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0002c0006t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0170 | EUR | GBR | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG00099 | hp2 | a0001 | c0003 | t0001 | g0115 | EUR | GBR | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG00140 | hp1 | a0001 | c0003 | t0006 | g0327 | EUR | GBR | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG00140 | hp2 | a0001 | c0002 | t0002 | g0298 | EUR | GBR | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG00280 | hp1 | a0001 | c0003 | t0007 | g0159 | EUR | FIN | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG00280 | hp2 | a0001 | c0001 | t0030 | g0123 | EUR | FIN | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG00323 | hp1 | a0001 | c0002 | t0003 | g0037 | EUR | FIN | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG00323 | hp2 | a0001 | c0002 | t0002 | g0307 | EUR | FIN | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | CHS | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG00408 | hp2 | a0001 | c0003 | t0001 | g0111 | EAS | CHS | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG00423 | hp1 | a0001 | c0002 | t0002 | g0280 | EAS | CHS | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | CHS | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG00438 | hp1 | a0001 | c0002 | t0005 | g0007 | EAS | CHS | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | CHS | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG00544 | hp1 | a0001 | c0003 | t0001 | g0100 | EAS | CHS | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0056 | EAS | CHS | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG00558 | hp1 | a0001 | c0003 | t0007 | g0238 | EAS | CHS | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG00558 | hp2 | a0001 | c0001 | t0024 | g0239 | EAS | CHS | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG00597 | hp1 | a0001 | c0002 | t0023 | g0021 | EAS | CHS | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG00597 | hp2 | a0001 | c0001 | t0005 | g0019 | EAS | CHS | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG00621 | hp1 | a0001 | c0002 | t0003 | g0061 | EAS | CHS | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | CHS | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG00639 | hp1 | a0001 | c0001 | t0012 | g0140 | AMR | PUR | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | PUR | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG00642 | hp1 | a0001 | c0002 | t0003 | g0043 | AMR | PUR | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | CHS | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG00673 | hp2 | a0001 | c0002 | t0002 | g0294 | EAS | CHS | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG00733 | hp1 | a0001 | c0002 | t0003 | g0078 | AMR | PUR | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0033 | AMR | PUR | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG00735 | hp2 | a0001 | c0002 | t0013 | g0005 | AMR | PUR | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG00741 | hp1 | a0001 | c0003 | t0006 | g0329 | AMR | PUR | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG00741 | hp2 | a0001 | c0001 | t0010 | g0251 | AMR | PUR | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG01070 | hp2 | a0001 | c0002 | t0001 | g0059 | AMR | PUR | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG01071 | hp1 | a0001 | c0002 | t0002 | g0306 | AMR | PUR | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0077 | AMR | PUR | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG01074 | hp1 | a0001 | c0001 | t0016 | g0160 | AMR | PUR | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG01074 | hp2 | a0001 | c0002 | t0003 | g0066 | AMR | PUR | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG01081 | hp1 | a0001 | c0002 | t0035 | g0297 | AMR | PUR | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG01099 | hp1 | a0001 | c0001 | t0005 | g0014 | AMR | PUR | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG01099 | hp2 | a0001 | c0002 | t0013 | g0008 | AMR | PUR | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG01106 | hp1 | a0001 | c0001 | t0010 | g0253 | AMR | PUR | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG01106 | hp2 | a0001 | c0002 | t0003 | g0069 | AMR | PUR | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG01109 | hp1 | a0001 | c0003 | t0001 | g0177 | AMR | PUR | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG01109 | hp2 | a0001 | c0001 | t0012 | g0168 | AMR | PUR | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG01167 | hp1 | a0001 | c0002 | t0003 | g0036 | AMR | PUR | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG01167 | hp2 | a0001 | c0003 | t0006 | g0326 | AMR | PUR | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG01168 | hp2 | a0001 | c0002 | t0001 | g0034 | AMR | PUR | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG01169 | hp1 | a0001 | c0002 | t0003 | g0038 | AMR | PUR | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG01175 | hp1 | a0001 | c0001 | t0005 | g0020 | AMR | PUR | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG01175 | hp2 | a0001 | c0002 | t0003 | g0026 | AMR | PUR | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG01243 | hp1 | a0001 | c0001 | t0004 | g0262 | AMR | PUR | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0028 | AMR | CLM | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG01255 | hp2 | a0001 | c0002 | t0003 | g0272 | AMR | CLM | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | CLM | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG01257 | hp2 | a0001 | c0002 | t0003 | g0024 | AMR | CLM | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG01261 | hp1 | a0001 | c0003 | t0036 | g0321 | AMR | CLM | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG01261 | hp2 | a0001 | c0001 | t0005 | g0018 | AMR | CLM | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | CLM | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG01346 | hp2 | a0001 | c0002 | t0001 | g0089 | AMR | CLM | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG01358 | hp1 | a0001 | c0002 | t0033 | g0041 | AMR | CLM | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | CLM | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | CLM | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG01433 | hp2 | a0001 | c0003 | t0006 | g0322 | AMR | CLM | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG01496 | hp1 | a0001 | c0002 | t0002 | g0299 | AMR | CLM | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | CLM | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG01515 | hp1 | a0001 | c0003 | t0006 | g0328 | EUR | IBS | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG01515 | hp2 | a0001 | c0002 | t0003 | g0025 | EUR | IBS | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0138 | EUR | IBS | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG01516 | hp2 | a0001 | c0002 | t0002 | g0296 | EUR | IBS | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG01884 | hp1 | a0001 | c0001 | t0011 | g0114 | AFR | ACB | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG01891 | hp1 | a0001 | c0002 | t0022 | g0006 | AFR | ACB | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG01891 | hp2 | a0001 | c0001 | t0004 | g0259 | AFR | ACB | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG01928 | hp1 | a0001 | c0002 | t0002 | g0320 | AMR | PEL | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PEL | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG01934 | hp1 | a0001 | c0002 | t0003 | g0062 | AMR | PEL | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0246 | AMR | PEL | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG01952 | hp1 | a0001 | c0002 | t0002 | g0283 | AMR | PEL | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG01952 | hp2 | a0001 | c0001 | t0026 | g0247 | AMR | PEL | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG01975 | hp1 | a0001 | c0002 | t0002 | g0290 | AMR | PEL | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG01978 | hp1 | a0001 | c0001 | t0016 | g0141 | AMR | PEL | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG01978 | hp2 | a0001 | c0002 | t0029 | g0060 | AMR | PEL | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG01993 | hp1 | a0001 | c0002 | t0002 | g0291 | AMR | PEL | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0274 | AMR | PEL | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG02027 | hp1 | a0001 | c0002 | t0001 | g0074 | EAS | KHV | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | KHV | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG02055 | hp1 | a0001 | c0001 | t0005 | g0011 | AFR | ACB | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG02055 | hp2 | a0001 | c0001 | t0009 | g0268 | AFR | ACB | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG02056 | hp1 | a0001 | c0004 | t0003 | g0082 | EAS | KHV | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG02056 | hp2 | a0001 | c0003 | t0001 | g0228 | EAS | KHV | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | KHV | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG02080 | hp2 | a0001 | c0002 | t0002 | g0301 | EAS | KHV | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | KHV | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG02083 | hp2 | a0001 | c0002 | t0001 | g0057 | EAS | KHV | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG02129 | hp2 | a0001 | c0004 | t0003 | g0084 | EAS | KHV | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG02145 | hp1 | a0001 | c0001 | t0004 | g0264 | AFR | ACB | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG02145 | hp2 | a0001 | c0001 | t0005 | g0003 | AFR | ACB | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG02257 | hp2 | a0001 | c0001 | t0019 | g0317 | AFR | ACB | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | ACB | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG02258 | hp2 | a0001 | c0001 | t0012 | g0143 | AFR | ACB | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG02280 | hp1 | a0001 | c0002 | t0002 | g0302 | AFR | ACB | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG02280 | hp2 | a0001 | c0001 | t0009 | g0148 | AFR | ACB | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG02293 | hp1 | a0001 | c0003 | t0007 | g0222 | AMR | PEL | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG02293 | hp2 | a0001 | c0002 | t0002 | g0285 | AMR | PEL | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PEL | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG02300 | hp2 | a0001 | c0002 | t0002 | g0305 | AMR | PEL | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG02602 | hp1 | a0001 | c0002 | t0013 | g0004 | SAS | PJL | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG02602 | hp2 | a0001 | c0002 | t0002 | g0309 | SAS | PJL | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | GWD | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG02630 | hp2 | a0001 | c0001 | t0004 | g0001 | AFR | GWD | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG02647 | hp1 | a0001 | c0001 | t0027 | g0169 | AFR | GWD | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG02647 | hp2 | a0001 | c0001 | t0004 | g0260 | AFR | GWD | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG02683 | hp1 | a0001 | c0003 | t0006 | g0324 | SAS | PJL | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG02683 | hp2 | a0001 | c0002 | t0001 | g0063 | SAS | PJL | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG02698 | hp1 | a0001 | c0003 | t0005 | g0012 | SAS | PJL | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG02698 | hp2 | a0001 | c0001 | t0005 | g0015 | SAS | PJL | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG02717 | hp1 | a0001 | c0001 | t0014 | g0112 | AFR | GWD | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | GWD | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG02723 | hp2 | a0001 | c0001 | t0011 | g0225 | AFR | GWD | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG02735 | hp2 | a0001 | c0002 | t0001 | g0029 | SAS | PJL | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG02809 | hp1 | a0001 | c0001 | t0025 | g0241 | AFR | GWD | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG02809 | hp2 | a0001 | c0001 | t0004 | g0261 | AFR | GWD | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG02818 | hp1 | a0001 | c0002 | t0002 | g0310 | AFR | GWD | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG02818 | hp2 | a0001 | c0001 | t0014 | g0107 | AFR | GWD | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG02886 | hp1 | a0001 | c0005 | t0001 | g0217 | AFR | GWD | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG02886 | hp2 | a0001 | c0002 | t0002 | g0311 | AFR | GWD | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | GWD | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | GWD | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG02896 | hp2 | a0001 | c0001 | t0009 | g0146 | AFR | GWD | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | GWD | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | GWD | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0258 | AFR | ESN | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG02922 | hp2 | a0001 | c0003 | t0015 | g0151 | AFR | ESN | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | ESN | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG02965 | hp2 | a0001 | c0003 | t0015 | g0150 | AFR | ESN | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG02970 | hp1 | a0001 | c0002 | t0018 | g0314 | AFR | ESN | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | ESN | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0255 | AFR | ESN | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | ESN | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG03017 | hp1 | a0001 | c0003 | t0001 | g0204 | SAS | PJL | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG03017 | hp2 | a0001 | c0002 | t0003 | g0042 | SAS | PJL | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG03041 | hp1 | a0001 | c0001 | t0004 | g0254 | AFR | GWD | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | GWD | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | MSL | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | MSL | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG03130 | hp1 | a0001 | c0003 | t0001 | g0092 | AFR | ESN | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG03130 | hp2 | a0001 | c0001 | t0011 | g0226 | AFR | ESN | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | ESN | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0257 | AFR | ESN | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG03195 | hp1 | a0001 | c0001 | t0010 | g0249 | AFR | ESN | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG03195 | hp2 | a0001 | c0003 | t0001 | g0178 | AFR | ESN | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | MSL | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG03209 | hp2 | a0001 | c0001 | t0011 | g0187 | AFR | MSL | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | MSL | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | MSL | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG03239 | hp2 | a0001 | c0010 | t0001 | g0110 | SAS | PJL | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | MSL | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG03453 | hp2 | a0001 | c0003 | t0015 | g0173 | AFR | MSL | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG03490 | hp1 | a0001 | c0002 | t0002 | g0303 | SAS | PJL | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG03490 | hp2 | a0001 | c0003 | t0001 | g0201 | SAS | PJL | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG03491 | hp1 | a0001 | c0003 | t0006 | g0323 | SAS | PJL | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG03491 | hp2 | a0001 | c0002 | t0003 | g0080 | SAS | PJL | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG03492 | hp1 | a0001 | c0002 | t0002 | g0304 | SAS | PJL | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG03492 | hp2 | a0001 | c0003 | t0006 | g0325 | SAS | PJL | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG03516 | hp1 | a0001 | c0001 | t0009 | g0172 | AFR | ESN | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | ESN | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG03540 | hp1 | a0001 | c0003 | t0001 | g0091 | AFR | GWD | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG03540 | hp2 | a0001 | c0002 | t0018 | g0313 | AFR | GWD | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG03579 | hp1 | a0001 | c0001 | t0004 | g0001 | AFR | MSL | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG03579 | hp2 | a0001 | c0003 | t0001 | g0190 | AFR | MSL | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0072 | SAS | PJL | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG03669 | hp2 | a0001 | c0001 | t0031 | g0165 | SAS | PJL | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0240 | SAS | STU | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG03688 | hp2 | a0001 | c0002 | t0003 | g0076 | SAS | STU | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG03704 | hp1 | a0001 | c0002 | t0001 | g0070 | SAS | PJL | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG03704 | hp2 | a0001 | c0002 | t0003 | g0079 | SAS | PJL | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG03710 | hp1 | a0001 | c0008 | t0001 | g0267 | SAS | PJL | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG03710 | hp2 | a0001 | c0002 | t0003 | g0271 | SAS | PJL | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG03834 | hp1 | a0001 | c0002 | t0028 | g0081 | SAS | BEB | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | BEB | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG03927 | hp1 | a0001 | c0002 | t0003 | g0046 | SAS | BEB | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG03927 | hp2 | a0001 | c0007 | t0005 | g0016 | SAS | BEB | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG03942 | hp1 | a0001 | c0003 | t0001 | g0221 | SAS | BEB | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG03942 | hp2 | a0001 | c0002 | t0001 | g0064 | SAS | BEB | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG04184 | hp1 | a0001 | c0002 | t0001 | g0058 | SAS | BEB | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0276 | SAS | BEB | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0065 | SAS | STU | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG04199 | hp2 | a0001 | c0003 | t0001 | g0206 | SAS | STU | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG04204 | hp1 | a0001 | c0001 | t0005 | g0010 | SAS | STU | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0270 | SAS | STU | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG04228 | hp1 | a0001 | c0003 | t0001 | g0102 | SAS | STU | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | STU | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA18522 | hp1 | a0001 | c0005 | t0001 | g0104 | AFR | YRI | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA18522 | hp2 | a0001 | c0001 | t0010 | g0250 | AFR | YRI | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA18612 | hp1 | a0001 | c0003 | t0007 | g0202 | EAS | CHB | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | CHB | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | YRI | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | YRI | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA18941 | hp2 | a0001 | c0002 | t0002 | g0286 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA18944 | hp1 | a0001 | c0002 | t0017 | g0090 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA18944 | hp2 | a0001 | c0003 | t0001 | g0199 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA18945 | hp2 | a0001 | c0002 | t0008 | g0048 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA18951 | hp1 | a0001 | c0004 | t0003 | g0085 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA18951 | hp2 | a0001 | c0003 | t0001 | g0095 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA18952 | hp1 | a0001 | c0002 | t0002 | g0282 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA18953 | hp1 | a0001 | c0002 | t0003 | g0030 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA18954 | hp1 | a0001 | c0002 | t0001 | g0027 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA18954 | hp2 | a0001 | c0003 | t0001 | g0216 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA18956 | hp1 | a0001 | c0002 | t0003 | g0067 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA18957 | hp1 | a0001 | c0002 | t0017 | g0040 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA18960 | hp1 | a0001 | c0002 | t0008 | g0047 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA18960 | hp2 | a0001 | c0003 | t0007 | g0213 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA18964 | hp1 | a0001 | c0003 | t0001 | g0126 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA18964 | hp2 | a0001 | c0002 | t0002 | g0281 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA18968 | hp1 | a0001 | c0003 | t0001 | g0101 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA18968 | hp2 | a0001 | c0002 | t0003 | g0051 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA18969 | hp1 | a0001 | c0002 | t0008 | g0050 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA18971 | hp1 | a0001 | c0003 | t0001 | g0191 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA18972 | hp1 | a0001 | c0002 | t0003 | g0073 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA18973 | hp1 | a0001 | c0002 | t0008 | g0044 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA18975 | hp1 | a0001 | c0002 | t0002 | g0319 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA18975 | hp2 | a0001 | c0003 | t0001 | g0198 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA18977 | hp1 | a0001 | c0002 | t0003 | g0068 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA18981 | hp1 | a0001 | c0002 | t0002 | g0288 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA18981 | hp2 | a0001 | c0003 | t0001 | g0113 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA18988 | hp2 | a0001 | c0002 | t0008 | g0049 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA18989 | hp2 | a0001 | c0004 | t0003 | g0273 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA18992 | hp2 | a0001 | c0002 | t0002 | g0292 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA18993 | hp1 | a0001 | c0003 | t0001 | g0158 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA18994 | hp1 | a0001 | c0002 | t0002 | g0284 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA18994 | hp2 | a0001 | c0003 | t0001 | g0207 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA18998 | hp1 | a0001 | c0009 | t0007 | g0103 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA19003 | hp1 | a0001 | c0003 | t0001 | g0109 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA19003 | hp2 | a0001 | c0002 | t0003 | g0045 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA19007 | hp1 | a0001 | c0003 | t0001 | g0157 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA19007 | hp2 | a0001 | c0002 | t0001 | g0071 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA19011 | hp2 | a0001 | c0004 | t0003 | g0087 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA19030 | hp1 | a0001 | c0002 | t0005 | g0009 | AFR | LWK | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA19030 | hp2 | a0001 | c0002 | t0002 | g0312 | AFR | LWK | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA19043 | hp1 | a0001 | c0002 | t0003 | g0035 | AFR | LWK | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA19043 | hp2 | a0001 | c0002 | t0002 | g0316 | AFR | LWK | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA19055 | hp1 | a0001 | c0002 | t0008 | g0039 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA19057 | hp1 | a0001 | c0002 | t0001 | g0055 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA19057 | hp2 | a0001 | c0003 | t0001 | g0194 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA19063 | hp1 | a0001 | c0002 | t0002 | g0279 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA19063 | hp2 | a0001 | c0003 | t0032 | g0193 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA19066 | hp1 | a0001 | c0002 | t0001 | g0054 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA19066 | hp2 | a0001 | c0003 | t0021 | g0013 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA19070 | hp1 | a0001 | c0002 | t0003 | g0031 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA19075 | hp1 | a0001 | c0002 | t0020 | g0002 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA19077 | hp1 | a0001 | c0004 | t0003 | g0088 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA19077 | hp2 | a0001 | c0003 | t0001 | g0200 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA19079 | hp2 | a0001 | c0002 | t0002 | g0293 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA19080 | hp1 | a0001 | c0002 | t0001 | g0052 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA19082 | hp1 | a0001 | c0002 | t0001 | g0053 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA19082 | hp2 | a0002 | c0006 | t0001 | g0096 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA19083 | hp1 | a0001 | c0003 | t0005 | g0017 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA19083 | hp2 | a0001 | c0002 | t0002 | g0287 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA19084 | hp1 | a0001 | c0002 | t0002 | g0289 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA19085 | hp1 | a0001 | c0004 | t0003 | g0083 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA19088 | hp2 | a0001 | c0002 | t0002 | g0295 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA19090 | hp1 | a0001 | c0003 | t0001 | g0214 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA19090 | hp2 | a0001 | c0004 | t0003 | g0086 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA19240 | hp1 | a0001 | c0002 | t0002 | g0315 | AFR | YRI | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA19240 | hp2 | a0001 | c0001 | t0014 | g0108 | AFR | YRI | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA20129 | hp1 | a0001 | c0001 | t0011 | g0098 | AFR | ASW | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA20129 | hp2 | a0001 | c0001 | t0004 | g0266 | AFR | ASW | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0156 | EUR | TSI | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA20752 | hp2 | a0001 | c0002 | t0002 | g0308 | EUR | TSI | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA20805 | hp1 | a0001 | c0002 | t0002 | g0300 | EUR | TSI | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0075 | EUR | TSI | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0233 | SAS | GIH | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA20905 | hp2 | a0001 | c0002 | t0003 | g0032 | SAS | GIH | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0263 | AFR | ACB | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG02109 | hp2 | a0001 | c0003 | t0001 | g0218 | AFR | ACB | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG02486 | hp1 | a0001 | c0001 | t0004 | g0265 | AFR | ACB | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | ACB | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG02559 | hp1 | a0001 | c0001 | t0009 | g0147 | AFR | ACB | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG02559 | hp2 | a0001 | c0001 | t0019 | g0318 | AFR | ACB | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG03471 | hp1 | a0001 | c0002 | t0034 | g0256 | AFR | MSL | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG03471 | hp2 | a0001 | c0001 | t0010 | g0252 | AFR | MSL | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG06807 | hp1 | a0001 | c0003 | t0001 | g0185 | AFR | USA | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG06807 | hp2 | a0001 | c0001 | t0012 | g0139 | AFR | USA | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA20300 | hp1 | a0001 | c0005 | t0001 | g0219 | AFR | USA | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA20300 | hp2 | a0001 | c0001 | t0009 | g0171 | AFR | USA | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| homoSapiens | chm13v2 | a0001 | c0003 | t0007 | g0196 | REF | REF | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0176 | REF | REF | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:229859081 | A | C | 1 | a0002 | 1 | NA19082.hp2 | missense_variant | MODERATE | c.718T>G | p.Ser240Ala | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/42 | 897/10100 | 718/6204 | 240/2067 | chr2 | 229859081 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:229791997 | C | A | 1 | a0001c0005 | 3 | HG02886.hp1 NA18522.hp1 NA20300.hp1 |
synonymous_variant | LOW | c.4284G>T | p.Leu1428Leu | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 29/42 | 4463/10100 | 4284/6204 | 1428/2067 | chr2 | 229791997 | |||
| chr2:229804142 | T | C | 3 | a0001c0002 a0001c0004 a0001c0009 |
121 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(118): Show |
synonymous_variant | LOW | c.2736A>G | p.Thr912Thr | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 19/42 | 2915/10100 | 2736/6204 | 912/2067 | chr2 | 229804142 | |||
| chr2:229810977 | T | C | 1 | a0001c0007 | 1 | HG03927.hp2 | synonymous_variant | LOW | c.2124A>G | p.Pro708Pro | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 15/42 | 2303/10100 | 2124/6204 | 708/2067 | chr2 | 229810977 | |||
| chr2:229810980 | A | G | 1 | a0001c0004 | 8 | HG02056.hp1 HG02129.hp2 NA18951.hp1 others(5): Show |
synonymous_variant | LOW | c.2121T>C | p.Thr707Thr | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 15/42 | 2300/10100 | 2121/6204 | 707/2067 | chr2 | 229810980 | |||
| chr2:229818487 | T | C | 1 | a0001c0010 | 1 | HG03239.hp2 | synonymous_variant | LOW | c.1476A>G | p.Gln492Gln | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 9/42 | 1655/10100 | 1476/6204 | 492/2067 | chr2 | 229818487 | |||
| chr2:229829239 | A | G | 1 | a0001c0008 | 1 | HG03710.hp1 | synonymous_variant | LOW | c.1404T>C | p.Gly468Gly | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/42 | 1583/10100 | 1404/6204 | 468/2067 | chr2 | 229829239 | |||
| chr2:229859061 | G | C | 5 | a0001c0003 a0001c0005 a0001c0008 others(2): Show |
58 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(55): Show |
synonymous_variant | LOW | c.738C>G | p.Ser246Ser | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/42 | 917/10100 | 738/6204 | 246/2067 | chr2 | 229859061 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:229763964 | A | G | 1 | a0001c0001t0027 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3590T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 42/42 | 3590 | chr2 | 229763964 | ||||||
| chr2:229764415 | G | A | 1 | a0001c0002t0018 | 2 | HG02970.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3139C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 42/42 | 3139 | chr2 | 229764415 | ||||||
| chr2:229764422 | C | T | 5 | a0001c0002t0002 a0001c0002t0018 a0001c0002t0023 others(2): Show |
42 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*3132G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 42/42 | 3132 | chr2 | 229764422 | ||||||
| chr2:229764494 | T | C | 1 | a0001c0002t0028 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3060A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 42/42 | 3060 | chr2 | 229764494 | ||||||
| chr2:229764613 | C | T | 1 | a0001c0003t0015 | 3 | HG02922.hp2 HG02965.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2941G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 42/42 | 2941 | chr2 | 229764613 | ||||||
| chr2:229764667 | T | C | 1 | a0001c0002t0029 | 1 | HG01978.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2887A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 42/42 | 2887 | chr2 | 229764667 | ||||||
| chr2:229764942 | C | T | 1 | a0001c0001t0010 | 5 | HG00741.hp2 HG01106.hp1 HG03195.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2612G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 42/42 | 2612 | chr2 | 229764942 | ||||||
| chr2:229764985 | G | T | 1 | a0001c0001t0026 | 1 | HG01952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2569C>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 42/42 | 2569 | chr2 | 229764985 | ||||||
| chr2:229765012 | A | G | 3 | a0001c0003t0007 a0001c0003t0032 a0001c0009t0007 |
7 | HG00280.hp1 HG00558.hp1 HG02293.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2542T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 42/42 | 2542 | chr2 | 229765012 | ||||||
| chr2:229765142 | T | A | 1 | a0001c0002t0008 | 6 | NA18945.hp2 NA18960.hp1 NA18969.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2412A>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 42/42 | 2412 | chr2 | 229765142 | ||||||
| chr2:229765519 | T | C | 1 | a0001c0002t0008 | 6 | NA18945.hp2 NA18960.hp1 NA18969.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2035A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 42/42 | 2035 | chr2 | 229765519 | ||||||
| chr2:229765793 | A | C | 1 | a0001c0001t0014 | 3 | HG02717.hp1 HG02818.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1761T>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 42/42 | 1761 | chr2 | 229765793 | ||||||
| chr2:229765916 | G | A | 10 | a0001c0002t0003 a0001c0002t0008 a0001c0002t0013 others(7): Show |
52 | HG00323.hp1 HG00621.hp1 HG00642.hp1 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*1638C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 42/42 | 1638 | chr2 | 229765916 | ||||||
| chr2:229765975 | G | A | 2 | a0001c0001t0012 a0001c0001t0016 |
6 | HG00639.hp1 HG01074.hp1 HG01109.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1579C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 42/42 | 1579 | chr2 | 229765975 | ||||||
| chr2:229766109 | TA | T | 2 | a0001c0001t0009 a0001c0001t0010 |
11 | HG00741.hp2 HG01106.hp1 HG02055.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1444delT | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 42/42 | 1444 | chr2 | 229766109 | ||||||
| chr2:229766155 | T | G | 1 | a0001c0001t0030 | 1 | HG00280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1399A>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 42/42 | 1399 | chr2 | 229766155 | ||||||
| chr2:229766288 | A | ACC | 1 | a0001c0002t0008 | 6 | NA18945.hp2 NA18960.hp1 NA18969.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1264_*1265dupGG | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 42/42 | 1265 | chr2 | 229766288 | ||||||
| chr2:229766306 | T | C | 1 | a0001c0001t0031 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1248A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 42/42 | 1248 | chr2 | 229766306 | ||||||
| chr2:229766529 | A | G | 1 | a0001c0002t0017 | 2 | NA18944.hp1 NA18957.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1025T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 42/42 | 1025 | chr2 | 229766529 | ||||||
| chr2:229766610 | A | T | 1 | a0001c0001t0025 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*944T>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 42/42 | 944 | chr2 | 229766610 | ||||||
| chr2:229766645 | T | C | 1 | a0001c0003t0032 | 1 | NA19063.hp2 | 3_prime_UTR_variant | MODIFIER | c.*909A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 42/42 | 909 | chr2 | 229766645 | ||||||
| chr2:229766730 | C | T | 1 | a0001c0001t0011 | 5 | HG01884.hp1 HG02723.hp2 HG03130.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*824G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 42/42 | 824 | chr2 | 229766730 | ||||||
| chr2:229766776 | C | A | 1 | a0001c0003t0021 | 1 | NA19066.hp2 | 3_prime_UTR_variant | MODIFIER | c.*778G>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 42/42 | 778 | chr2 | 229766776 | ||||||
| chr2:229766797 | T | G | 1 | a0001c0001t0004 | 14 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*757A>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 42/42 | 757 | chr2 | 229766797 | ||||||
| chr2:229767074 | G | A | 1 | a0001c0003t0036 | 1 | HG01261.hp1 | 3_prime_UTR_variant | MODIFIER | c.*480C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 42/42 | 480 | chr2 | 229767074 | ||||||
| chr2:229767107 | T | C | 2 | a0001c0002t0022 a0001c0002t0033 |
2 | HG01358.hp1 HG01891.hp1 |
3_prime_UTR_variant | MODIFIER | c.*447A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 42/42 | 447 | chr2 | 229767107 | ||||||
| chr2:229767371 | A | G | 1 | a0001c0001t0016 | 2 | HG01074.hp1 HG01978.hp1 |
3_prime_UTR_variant | MODIFIER | c.*183T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 42/42 | 183 | chr2 | 229767371 | ||||||
| chr2:229767497 | G | T | 1 | a0001c0001t0024 | 1 | HG00558.hp2 | 3_prime_UTR_variant | MODIFIER | c.*57C>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 42/42 | 57 | chr2 | 229767497 | ||||||
| chr2:229767552 | G | A | 6 | a0001c0001t0011 a0001c0001t0019 a0001c0002t0002 others(3): Show |
48 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*2C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 42/42 | 2 | chr2 | 229767552 | ||||||
| chr2:229921921 | G | C | 5 | a0001c0001t0019 a0001c0002t0002 a0001c0002t0018 others(2): Show |
43 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(40): Show |
5_prime_UTR_variant | MODIFIER | c.-91C>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/42 | 41842 | chr2 | 229921921 | ||||||
| chr2:229921947 | A | AC | 9 | a0001c0001t0005 a0001c0002t0005 a0001c0002t0013 others(6): Show |
20 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(17): Show |
5_prime_UTR_variant | MODIFIER | c.-118dupG | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/42 | 41869 | chr2 | 229921947 | ||||||
| chr2:229921947 | A | C | 1 | a0001c0002t0020 | 1 | NA19075.hp1 | 5_prime_UTR_variant | MODIFIER | c.-117T>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/42 | 41868 | chr2 | 229921947 | ||||||
| chr2:229921973 | G | C | 2 | a0001c0003t0006 a0001c0003t0036 |
9 | HG00140.hp1 HG00741.hp1 HG01167.hp2 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-143C>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/42 | 41894 | chr2 | 229921973 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:229767998 | T | C | 24 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0099 others(21): Show |
25 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.6008-248A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 41/41 | chr2 | 229767998 | |||||||
| chr2:229768044 | G | A | 2 | a0001c0003t0006g0323 a0001c0003t0006g0325 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.6008-294C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 41/41 | chr2 | 229768044 | |||||||
| chr2:229768047 | T | C | 5 | a0001c0001t0010g0249 a0001c0001t0010g0250 a0001c0001t0010g0251 others(2): Show |
5 | HG00741.hp2 HG01106.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.6008-297A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 41/41 | chr2 | 229768047 | |||||||
| chr2:229768056 | C | T | 1 | a0001c0002t0002g0307 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.6008-306G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 41/41 | chr2 | 229768056 | |||||||
| chr2:229768223 | C | G | 2 | a0001c0001t0001g0188 a0001c0001t0001g0189 |
2 | HG02723.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.6007+393G>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 41/41 | chr2 | 229768223 | |||||||
| chr2:229768507 | A | T | 5 | a0001c0001t0011g0098 a0001c0001t0011g0114 a0001c0001t0011g0187 others(2): Show |
5 | HG01884.hp1 HG02723.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.6007+109T>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 41/41 | chr2 | 229768507 | |||||||
| chr2:229768555 | T | A | 4 | a0001c0001t0011g0098 a0001c0001t0011g0114 a0001c0001t0011g0225 others(1): Show |
4 | HG01884.hp1 HG02723.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.6007+61A>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 41/41 | chr2 | 229768555 | |||||||
| chr2:229768722 | A | G | 2 | a0001c0002t0003g0032 a0001c0002t0013g0004 |
2 | HG02602.hp1 NA20905.hp2 |
splice_region_variant&intron_variant | LOW | c.5904-3T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 40/41 | chr2 | 229768722 | |||||||
| chr2:229768856 | T | TAAATC | 110 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0099 others(107): Show |
111 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.5904-138_5904-137i others(7): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 40/41 | chr2 | 229768856 | |||||||
| chr2:229769005 | A | AG | 3 | a0001c0002t0003g0078 a0001c0002t0003g0271 a0001c0002t0013g0008 |
3 | HG00733.hp1 HG01099.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.5903+225dupC | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 40/41 | chr2 | 229769005 | |||||||
| chr2:229769059 | T | G | 1 | a0001c0002t0002g0301 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.5903+172A>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 40/41 | chr2 | 229769059 | |||||||
| chr2:229769108 | C | T | 1 | a0001c0001t0001g0180 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.5903+123G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 40/41 | chr2 | 229769108 | |||||||
| chr2:229769398 | C | T | 5 | a0001c0001t0011g0098 a0001c0001t0011g0114 a0001c0001t0011g0187 others(2): Show |
5 | HG01884.hp1 HG02723.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.5809-73G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 39/41 | chr2 | 229769398 | |||||||
| chr2:229769451 | T | C | 1 | a0001c0002t0020g0002 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.5809-126A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 39/41 | chr2 | 229769451 | |||||||
| chr2:229769468 | A | AAT | 22 | a0001c0001t0001g0099 a0001c0001t0001g0153 a0001c0001t0001g0215 others(19): Show |
23 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.5809-144_5809-143i others(4): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 39/41 | chr2 | 229769468 | |||||||
| chr2:229769470 | A | T | 4 | a0001c0002t0001g0053 a0001c0002t0003g0066 a0001c0004t0003g0083 others(1): Show |
4 | HG01074.hp2 NA18951.hp1 NA19082.hp1 others(1): Show |
intron_variant | MODIFIER | c.5809-145T>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 39/41 | chr2 | 229769470 | |||||||
| chr2:229769471 | T | A | 79 | a0001c0001t0009g0268 a0001c0001t0014g0107 a0001c0001t0014g0108 others(76): Show |
79 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.5809-146A>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 39/41 | chr2 | 229769471 | |||||||
| chr2:229769602 | C | T | 1 | a0001c0003t0007g0159 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.5809-277G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 39/41 | chr2 | 229769602 | |||||||
| chr2:229769655 | T | A | 1 | a0001c0003t0005g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.5809-330A>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 39/41 | chr2 | 229769655 | |||||||
| chr2:229769685 | C | T | 5 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0188 others(2): Show |
5 | HG02615.hp2 HG02630.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.5809-360G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 39/41 | chr2 | 229769685 | |||||||
| chr2:229769740 | T | C | 7 | a0001c0001t0001g0269 a0001c0001t0009g0268 a0001c0001t0014g0107 others(4): Show |
7 | HG00639.hp2 HG02055.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.5809-415A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 39/41 | chr2 | 229769740 | |||||||
| chr2:229769882 | A | G | 1 | a0001c0001t0001g0233 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.5809-557T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 39/41 | chr2 | 229769882 | |||||||
| chr2:229769937 | A | G | 2 | a0001c0002t0008g0039 a0001c0002t0008g0047 |
2 | NA18960.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.5809-612T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 39/41 | chr2 | 229769937 | |||||||
| chr2:229769950 | T | C | 5 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0127 others(2): Show |
5 | HG02258.hp1 HG02622.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.5809-625A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 39/41 | chr2 | 229769950 | |||||||
| chr2:229770013 | C | A | 1 | a0001c0004t0003g0082 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.5809-688G>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 39/41 | chr2 | 229770013 | |||||||
| chr2:229770136 | A | G | 1 | a0001c0002t0013g0005 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.5809-811T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 39/41 | chr2 | 229770136 | |||||||
| chr2:229770232 | G | A | 80 | a0001c0002t0001g0027 a0001c0002t0001g0028 a0001c0002t0001g0029 others(77): Show |
80 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.5809-907C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 39/41 | chr2 | 229770232 | |||||||
| chr2:229770383 | T | C | 5 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0188 others(2): Show |
5 | HG02615.hp2 HG02630.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.5809-1058A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 39/41 | chr2 | 229770383 | |||||||
| chr2:229770748 | T | C | 25 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0099 others(22): Show |
26 | HG01106.hp1 HG01243.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.5808+771A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 39/41 | chr2 | 229770748 | |||||||
| chr2:229770814 | A | C | 1 | a0001c0001t0001g0120 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.5808+705T>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 39/41 | chr2 | 229770814 | |||||||
| chr2:229770831 | C | T | 1 | a0001c0002t0028g0081 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.5808+688G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 39/41 | chr2 | 229770831 | |||||||
| chr2:229770866 | A | T | 1 | a0001c0001t0001g0220 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.5808+653T>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 39/41 | chr2 | 229770866 | |||||||
| chr2:229771145 | G | C | 1 | a0001c0003t0001g0199 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.5808+374C>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 39/41 | chr2 | 229771145 | |||||||
| chr2:229771226 | C | G | 2 | a0001c0002t0002g0303 a0001c0002t0002g0304 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.5808+293G>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 39/41 | chr2 | 229771226 | |||||||
| chr2:229771266 | T | C | 1 | a0001c0002t0003g0037 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.5808+253A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 39/41 | chr2 | 229771266 | |||||||
| chr2:229771314 | C | A | 1 | a0001c0001t0001g0120 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.5808+205G>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 39/41 | chr2 | 229771314 | |||||||
| chr2:229771365 | G | A | 2 | a0001c0002t0003g0069 a0001c0002t0013g0005 |
2 | HG00735.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.5808+154C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 39/41 | chr2 | 229771365 | |||||||
| chr2:229771399 | CT | C | 3 | a0001c0002t0003g0051 a0001c0002t0003g0067 a0001c0002t0003g0073 |
3 | NA18956.hp1 NA18968.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.5808+119delA | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 39/41 | chr2 | 229771399 | |||||||
| chr2:229771636 | C | A | 8 | a0001c0001t0004g0001 a0001c0001t0004g0254 a0001c0001t0004g0255 others(5): Show |
9 | HG01891.hp2 HG02109.hp1 HG02630.hp2 others(6): Show |
splice_region_variant&intron_variant | LOW | c.5695-4G>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 38/41 | chr2 | 229771636 | |||||||
| chr2:229771869 | T | G | 1 | a0001c0002t0003g0076 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.5695-237A>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 38/41 | chr2 | 229771869 | |||||||
| chr2:229771924 | C | T | 2 | a0001c0001t0001g0269 a0001c0001t0009g0268 |
2 | HG00639.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.5695-292G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 38/41 | chr2 | 229771924 | |||||||
| chr2:229772367 | A | G | 1 | a0001c0002t0001g0033 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.5695-735T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 38/41 | chr2 | 229772367 | |||||||
| chr2:229772556 | T | C | 176 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0093 others(173): Show |
177 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.5695-924A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 38/41 | chr2 | 229772556 | |||||||
| chr2:229772652 | C | T | 1 | a0001c0001t0001g0276 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.5695-1020G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 38/41 | chr2 | 229772652 | |||||||
| chr2:229772708 | C | T | 7 | a0001c0001t0004g0263 a0001c0001t0004g0266 a0001c0001t0011g0098 others(4): Show |
7 | HG01884.hp1 HG02109.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.5695-1076G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 38/41 | chr2 | 229772708 | |||||||
| chr2:229772781 | T | TTC | 22 | a0001c0001t0001g0099 a0001c0001t0001g0153 a0001c0001t0001g0215 others(19): Show |
23 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.5695-1151_5695-115 others(6): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 38/41 | chr2 | 229772781 | |||||||
| chr2:229772802 | A | G | 1 | a0001c0002t0002g0310 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.5695-1170T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 38/41 | chr2 | 229772802 | |||||||
| chr2:229773080 | CT | C | 77 | a0001c0002t0001g0027 a0001c0002t0001g0028 a0001c0002t0001g0029 others(74): Show |
77 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.5694+1016delA | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 38/41 | chr2 | 229773080 | |||||||
| chr2:229773179 | G | A | 2 | a0001c0002t0003g0036 a0001c0002t0003g0038 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.5694+918C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 38/41 | chr2 | 229773179 | |||||||
| chr2:229773363 | C | T | 10 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0188 others(7): Show |
10 | HG02615.hp2 HG02630.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.5694+734G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 38/41 | chr2 | 229773363 | |||||||
| chr2:229773486 | C | T | 9 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0011g0098 others(6): Show |
9 | HG01884.hp1 HG02257.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.5694+611G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 38/41 | chr2 | 229773486 | |||||||
| chr2:229773743 | G | A | 22 | a0001c0001t0001g0099 a0001c0001t0001g0153 a0001c0001t0001g0215 others(19): Show |
23 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.5694+354C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 38/41 | chr2 | 229773743 | |||||||
| chr2:229773744 | C | A | 22 | a0001c0001t0001g0099 a0001c0001t0001g0153 a0001c0001t0001g0215 others(19): Show |
23 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.5694+353G>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 38/41 | chr2 | 229773744 | |||||||
| chr2:229774002 | T | C | 5 | a0001c0001t0001g0269 a0001c0001t0009g0268 a0001c0001t0014g0107 others(2): Show |
5 | HG00639.hp2 HG02055.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.5694+95A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 38/41 | chr2 | 229774002 | |||||||
| chr2:229774058 | T | C | 1 | a0001c0002t0001g0071 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.5694+39A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 38/41 | chr2 | 229774058 | |||||||
| chr2:229774288 | G | C | 1 | a0001c0001t0001g0120 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.5530-27C>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 37/41 | chr2 | 229774288 | |||||||
| chr2:229774394 | T | C | 1 | a0001c0002t0013g0004 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.5530-133A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 37/41 | chr2 | 229774394 | |||||||
| chr2:229774585 | A | G | 3 | a0001c0001t0014g0107 a0001c0001t0014g0108 a0001c0001t0014g0112 |
3 | HG02717.hp1 HG02818.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.5530-324T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 37/41 | chr2 | 229774585 | |||||||
| chr2:229774829 | TA | T | 7 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0011g0098 others(4): Show |
7 | HG01884.hp1 HG02622.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.5530-569delT | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 37/41 | chr2 | 229774829 | |||||||
| chr2:229775001 | A | T | 1 | a0001c0002t0003g0046 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.5530-740T>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 37/41 | chr2 | 229775001 | |||||||
| chr2:229775238 | T | C | 3 | a0001c0001t0001g0145 a0001c0001t0001g0192 a0001c0001t0001g0197 |
3 | HG01433.hp1 NA18972.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.5530-977A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 37/41 | chr2 | 229775238 | |||||||
| chr2:229775263 | T | C | 19 | a0001c0002t0002g0279 a0001c0002t0002g0280 a0001c0002t0002g0281 others(16): Show |
19 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(16): Show |
intron_variant | MODIFIER | c.5530-1002A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 37/41 | chr2 | 229775263 | |||||||
| chr2:229775269 | T | C | 4 | a0001c0001t0004g0254 a0001c0001t0004g0255 a0001c0001t0004g0259 others(1): Show |
4 | HG01891.hp2 HG02647.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.5530-1008A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 37/41 | chr2 | 229775269 | |||||||
| chr2:229775386 | T | TA | 11 | a0001c0001t0001g0097 a0001c0001t0001g0105 a0001c0001t0001g0129 others(8): Show |
11 | HG00099.hp1 HG00597.hp2 HG00673.hp1 others(8): Show |
intron_variant | MODIFIER | c.5530-1126dupT | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 37/41 | chr2 | 229775386 | |||||||
| chr2:229775386 | TA | T | 58 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0099 others(55): Show |
59 | HG00639.hp2 HG01070.hp2 HG01243.hp1 others(56): Show |
intron_variant | MODIFIER | c.5530-1126delT | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 37/41 | chr2 | 229775386 | |||||||
| chr2:229775572 | T | A | 2 | a0001c0001t0001g0269 a0001c0001t0009g0268 |
2 | HG00639.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.5530-1311A>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 37/41 | chr2 | 229775572 | |||||||
| chr2:229775637 | T | C | 11 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0188 others(8): Show |
11 | HG02109.hp2 HG02615.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.5530-1376A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 37/41 | chr2 | 229775637 | |||||||
| chr2:229775656 | C | T | 11 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0188 others(8): Show |
11 | HG02109.hp2 HG02615.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.5530-1395G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 37/41 | chr2 | 229775656 | |||||||
| chr2:229776070 | C | G | 1 | a0001c0002t0003g0030 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.5529+1245G>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 37/41 | chr2 | 229776070 | |||||||
| chr2:229776626 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.5529+689G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 37/41 | chr2 | 229776626 | |||||||
| chr2:229776698 | C | T | 3 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0005g0003 |
3 | HG02145.hp2 HG02257.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.5529+617G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 37/41 | chr2 | 229776698 | |||||||
| chr2:229776822 | A | T | 1 | a0001c0001t0001g0211 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.5529+493T>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 37/41 | chr2 | 229776822 | |||||||
| chr2:229776823 | A | C | 1 | a0001c0001t0001g0211 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.5529+492T>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 37/41 | chr2 | 229776823 | |||||||
| chr2:229776824 | G | T | 1 | a0001c0001t0001g0211 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.5529+491C>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 37/41 | chr2 | 229776824 | |||||||
| chr2:229776826 | T | G | 1 | a0001c0001t0001g0211 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.5529+489A>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 37/41 | chr2 | 229776826 | |||||||
| chr2:229776827 | C | T | 1 | a0001c0001t0001g0211 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.5529+488G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 37/41 | chr2 | 229776827 | |||||||
| chr2:229776828 | A | C | 1 | a0001c0001t0001g0211 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.5529+487T>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 37/41 | chr2 | 229776828 | |||||||
| chr2:229776829 | A | T | 1 | a0001c0001t0001g0211 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.5529+486T>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 37/41 | chr2 | 229776829 | |||||||
| chr2:229776831 | G | T | 1 | a0001c0001t0001g0211 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.5529+484C>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 37/41 | chr2 | 229776831 | |||||||
| chr2:229776834 | A | T | 1 | a0001c0001t0001g0211 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.5529+481T>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 37/41 | chr2 | 229776834 | |||||||
| chr2:229776836 | C | T | 1 | a0001c0001t0001g0211 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.5529+479G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 37/41 | chr2 | 229776836 | |||||||
| chr2:229776838 | A | T | 1 | a0001c0001t0001g0211 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.5529+477T>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 37/41 | chr2 | 229776838 | |||||||
| chr2:229776841 | A | T | 1 | a0001c0001t0001g0211 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.5529+474T>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 37/41 | chr2 | 229776841 | |||||||
| chr2:229776842 | G | T | 1 | a0001c0001t0001g0211 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.5529+473C>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 37/41 | chr2 | 229776842 | |||||||
| chr2:229776843 | A | T | 1 | a0001c0001t0001g0211 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.5529+472T>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 37/41 | chr2 | 229776843 | |||||||
| chr2:229776845 | G | C | 1 | a0001c0001t0001g0211 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.5529+470C>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 37/41 | chr2 | 229776845 | |||||||
| chr2:229776848 | A | T | 1 | a0001c0001t0001g0211 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.5529+467T>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 37/41 | chr2 | 229776848 | |||||||
| chr2:229776850 | A | T | 1 | a0001c0001t0001g0211 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.5529+465T>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 37/41 | chr2 | 229776850 | |||||||
| chr2:229776851 | G | T | 1 | a0001c0001t0001g0211 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.5529+464C>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 37/41 | chr2 | 229776851 | |||||||
| chr2:229776852 | A | T | 1 | a0001c0001t0001g0211 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.5529+463T>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 37/41 | chr2 | 229776852 | |||||||
| chr2:229776857 | C | T | 1 | a0001c0001t0001g0211 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.5529+458G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 37/41 | chr2 | 229776857 | |||||||
| chr2:229776858 | C | T | 1 | a0001c0001t0001g0211 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.5529+457G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 37/41 | chr2 | 229776858 | |||||||
| chr2:229776860 | C | T | 1 | a0001c0001t0001g0211 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.5529+455G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 37/41 | chr2 | 229776860 | |||||||
| chr2:229776862 | A | T | 1 | a0001c0001t0001g0211 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.5529+453T>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 37/41 | chr2 | 229776862 | |||||||
| chr2:229776863 | A | T | 1 | a0001c0001t0001g0211 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.5529+452T>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 37/41 | chr2 | 229776863 | |||||||
| chr2:229776864 | A | T | 1 | a0001c0001t0001g0211 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.5529+451T>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 37/41 | chr2 | 229776864 | |||||||
| chr2:229776870 | T | G | 1 | a0001c0001t0001g0211 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.5529+445A>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 37/41 | chr2 | 229776870 | |||||||
| chr2:229776872 | C | G | 1 | a0001c0001t0001g0211 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.5529+443G>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 37/41 | chr2 | 229776872 | |||||||
| chr2:229776873 | C | A | 1 | a0001c0001t0001g0211 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.5529+442G>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 37/41 | chr2 | 229776873 | |||||||
| chr2:229776874 | A | G | 1 | a0001c0001t0001g0211 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.5529+441T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 37/41 | chr2 | 229776874 | |||||||
| chr2:229776896 | T | C | 318 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0093 others(315): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(316): Show |
intron_variant | MODIFIER | c.5529+419A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 37/41 | chr2 | 229776896 | |||||||
| chr2:229777047 | T | C | 108 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0099 others(105): Show |
109 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.5529+268A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 37/41 | chr2 | 229777047 | |||||||
| chr2:229777154 | C | T | 52 | a0001c0002t0003g0024 a0001c0002t0003g0025 a0001c0002t0003g0026 others(49): Show |
52 | HG00323.hp1 HG00621.hp1 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.5529+161G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 37/41 | chr2 | 229777154 | |||||||
| chr2:229777493 | T | C | 2 | a0001c0001t0001g0166 a0001c0001t0001g0167 |
2 | HG02080.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.5365-14A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 36/41 | chr2 | 229777493 | |||||||
| chr2:229777606 | T | C | 3 | a0001c0001t0014g0107 a0001c0001t0014g0108 a0001c0001t0014g0112 |
3 | HG02717.hp1 HG02818.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.5365-127A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 36/41 | chr2 | 229777606 | |||||||
| chr2:229777862 | G | A | 10 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0188 others(7): Show |
10 | HG02615.hp2 HG02630.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.5365-383C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 36/41 | chr2 | 229777862 | |||||||
| chr2:229777868 | G | A | 9 | a0001c0001t0001g0203 a0001c0001t0001g0208 a0001c0001t0001g0209 others(6): Show |
9 | HG00423.hp2 HG00438.hp2 NA18952.hp2 others(6): Show |
intron_variant | MODIFIER | c.5365-389C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 36/41 | chr2 | 229777868 | |||||||
| chr2:229777886 | C | T | 3 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0005g0003 |
3 | HG02145.hp2 HG02257.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.5365-407G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 36/41 | chr2 | 229777886 | |||||||
| chr2:229777936 | A | C | 80 | a0001c0001t0005g0010 a0001c0002t0001g0027 a0001c0002t0001g0028 others(77): Show |
80 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.5365-457T>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 36/41 | chr2 | 229777936 | |||||||
| chr2:229778143 | C | T | 2 | a0001c0002t0003g0024 a0001c0002t0003g0025 |
2 | HG01257.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.5364+290G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 36/41 | chr2 | 229778143 | |||||||
| chr2:229778263 | C | T | 1 | a0001c0003t0006g0324 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.5364+170G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 36/41 | chr2 | 229778263 | |||||||
| chr2:229778280 | C | T | 1 | a0001c0001t0001g0205 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.5364+153G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 36/41 | chr2 | 229778280 | |||||||
| chr2:229778321 | T | G | 1 | a0001c0003t0001g0095 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.5364+112A>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 36/41 | chr2 | 229778321 | |||||||
| chr2:229778739 | T | C | 1 | a0001c0002t0002g0293 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.5209+137A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 35/41 | chr2 | 229778739 | |||||||
| chr2:229779036 | G | A | 3 | a0001c0005t0001g0104 a0001c0005t0001g0217 a0001c0005t0001g0219 |
3 | HG02886.hp1 NA18522.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.5095-46C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 34/41 | chr2 | 229779036 | |||||||
| chr2:229779258 | CAT | C | 5 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0127 others(2): Show |
5 | HG02258.hp1 HG02622.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.5095-270_5095-269d others(4): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 34/41 | chr2 | 229779258 | |||||||
| chr2:229779572 | T | C | 1 | a0001c0001t0009g0146 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.5095-582A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 34/41 | chr2 | 229779572 | |||||||
| chr2:229779612 | C | A | 1 | a0001c0003t0001g0194 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.5095-622G>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 34/41 | chr2 | 229779612 | |||||||
| chr2:229779979 | C | T | 2 | a0001c0002t0003g0035 a0001c0002t0003g0037 |
2 | HG00323.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.5095-989G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 34/41 | chr2 | 229779979 | |||||||
| chr2:229780435 | G | A | 4 | a0001c0001t0004g0254 a0001c0001t0004g0255 a0001c0001t0004g0259 others(1): Show |
4 | HG01891.hp2 HG02647.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.5095-1445C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 34/41 | chr2 | 229780435 | |||||||
| chr2:229780760 | T | C | 1 | a0001c0003t0032g0193 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.5095-1770A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 34/41 | chr2 | 229780760 | |||||||
| chr2:229780810 | T | C | 2 | a0001c0001t0001g0269 a0001c0001t0009g0268 |
2 | HG00639.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.5095-1820A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 34/41 | chr2 | 229780810 | |||||||
| chr2:229780963 | C | G | 1 | a0001c0003t0001g0111 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.5095-1973G>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 34/41 | chr2 | 229780963 | |||||||
| chr2:229781063 | G | C | 1 | a0001c0001t0001g0170 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.5095-2073C>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 34/41 | chr2 | 229781063 | |||||||
| chr2:229781164 | G | A | 9 | a0001c0001t0001g0099 a0001c0001t0001g0153 a0001c0001t0001g0215 others(6): Show |
9 | HG02055.hp1 HG02486.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.5095-2174C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 34/41 | chr2 | 229781164 | |||||||
| chr2:229781234 | T | C | 29 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0099 others(26): Show |
30 | HG00639.hp2 HG01243.hp1 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.5095-2244A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 34/41 | chr2 | 229781234 | |||||||
| chr2:229781471 | G | T | 5 | a0001c0002t0002g0312 a0001c0002t0002g0315 a0001c0002t0002g0316 others(2): Show |
5 | HG02970.hp1 HG03540.hp2 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.5095-2481C>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 34/41 | chr2 | 229781471 | |||||||
| chr2:229781540 | A | G | 44 | a0001c0001t0019g0317 a0001c0001t0019g0318 a0001c0002t0002g0279 others(41): Show |
44 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(41): Show |
intron_variant | MODIFIER | c.5095-2550T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 34/41 | chr2 | 229781540 | |||||||
| chr2:229781644 | G | A | 1 | a0001c0002t0003g0030 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.5095-2654C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 34/41 | chr2 | 229781644 | |||||||
| chr2:229781677 | A | T | 1 | a0001c0001t0001g0236 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.5095-2687T>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 34/41 | chr2 | 229781677 | |||||||
| chr2:229781790 | T | A | 1 | a0001c0001t0001g0236 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.5095-2800A>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 34/41 | chr2 | 229781790 | |||||||
| chr2:229781982 | A | C | 172 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0093 others(169): Show |
173 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.5095-2992T>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 34/41 | chr2 | 229781982 | |||||||
| chr2:229782137 | A | C | 4 | a0001c0001t0011g0098 a0001c0001t0011g0114 a0001c0001t0011g0225 others(1): Show |
4 | HG01884.hp1 HG02723.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.5095-3147T>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 34/41 | chr2 | 229782137 | |||||||
| chr2:229782812 | T | G | 1 | a0001c0001t0019g0317 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.5094+2945A>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 34/41 | chr2 | 229782812 | |||||||
| chr2:229782833 | T | C | 5 | a0001c0002t0002g0312 a0001c0002t0002g0315 a0001c0002t0002g0316 others(2): Show |
5 | HG02970.hp1 HG03540.hp2 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.5094+2924A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 34/41 | chr2 | 229782833 | |||||||
| chr2:229783047 | G | A | 1 | a0001c0003t0006g0324 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.5094+2710C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 34/41 | chr2 | 229783047 | |||||||
| chr2:229783187 | T | A | 89 | a0001c0001t0001g0097 a0001c0001t0001g0105 a0001c0001t0001g0106 others(86): Show |
89 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.5094+2570A>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 34/41 | chr2 | 229783187 | |||||||
| chr2:229783219 | A | G | 1 | a0001c0002t0002g0301 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.5094+2538T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 34/41 | chr2 | 229783219 | |||||||
| chr2:229783332 | C | A | 5 | a0001c0001t0011g0098 a0001c0001t0011g0114 a0001c0001t0011g0187 others(2): Show |
5 | HG01884.hp1 HG02723.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.5094+2425G>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 34/41 | chr2 | 229783332 | |||||||
| chr2:229783385 | T | C | 8 | a0001c0004t0003g0082 a0001c0004t0003g0083 a0001c0004t0003g0084 others(5): Show |
8 | HG02056.hp1 HG02129.hp2 NA18951.hp1 others(5): Show |
intron_variant | MODIFIER | c.5094+2372A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 34/41 | chr2 | 229783385 | |||||||
| chr2:229783395 | C | T | 1 | a0001c0001t0001g0181 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.5094+2362G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 34/41 | chr2 | 229783395 | |||||||
| chr2:229783396 | A | G | 1 | a0001c0001t0001g0181 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.5094+2361T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 34/41 | chr2 | 229783396 | |||||||
| chr2:229783479 | C | T | 1 | a0001c0002t0002g0296 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.5094+2278G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 34/41 | chr2 | 229783479 | |||||||
| chr2:229783526 | G | C | 4 | a0001c0003t0001g0218 a0001c0005t0001g0104 a0001c0005t0001g0217 others(1): Show |
4 | HG02109.hp2 HG02886.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.5094+2231C>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 34/41 | chr2 | 229783526 | |||||||
| chr2:229783668 | G | A | 1 | a0001c0002t0001g0028 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.5094+2089C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 34/41 | chr2 | 229783668 | |||||||
| chr2:229783718 | G | A | 1 | a0001c0002t0002g0312 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.5094+2039C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 34/41 | chr2 | 229783718 | |||||||
| chr2:229783737 | C | T | 13 | a0001c0001t0004g0001 a0001c0001t0004g0254 a0001c0001t0004g0255 others(10): Show |
14 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.5094+2020G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 34/41 | chr2 | 229783737 | |||||||
| chr2:229783810 | T | A | 2 | a0001c0001t0001g0210 a0001c0002t0033g0041 |
2 | HG01358.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.5094+1947A>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 34/41 | chr2 | 229783810 | |||||||
| chr2:229783810 | T | TA | 48 | a0001c0001t0001g0116 a0001c0001t0001g0152 a0001c0001t0001g0229 others(45): Show |
48 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(45): Show |
intron_variant | MODIFIER | c.5094+1946dupT | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 34/41 | chr2 | 229783810 | |||||||
| chr2:229783810 | T | TAA | 6 | a0001c0001t0014g0107 a0001c0001t0014g0108 a0001c0001t0014g0112 others(3): Show |
6 | HG02717.hp1 HG02818.hp2 NA18964.hp2 others(3): Show |
intron_variant | MODIFIER | c.5094+1945_5094+194 others(6): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 34/41 | chr2 | 229783810 | |||||||
| chr2:229783810 | TA | T | 11 | a0001c0001t0001g0248 a0001c0001t0004g0261 a0001c0001t0004g0264 others(8): Show |
11 | HG00408.hp1 HG01515.hp1 HG01515.hp2 others(8): Show |
intron_variant | MODIFIER | c.5094+1946delT | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 34/41 | chr2 | 229783810 | |||||||
| chr2:229783846 | C | T | 1 | a0001c0002t0002g0298 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.5094+1911G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 34/41 | chr2 | 229783846 | |||||||
| chr2:229784075 | A | G | 1 | a0001c0002t0028g0081 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.5094+1682T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 34/41 | chr2 | 229784075 | |||||||
| chr2:229784106 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.5094+1651C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 34/41 | chr2 | 229784106 | |||||||
| chr2:229784110 | C | CA | 27 | a0001c0001t0001g0099 a0001c0001t0001g0133 a0001c0001t0001g0153 others(24): Show |
28 | HG01243.hp1 HG01884.hp2 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.5094+1646dupT | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 34/41 | chr2 | 229784110 | |||||||
| chr2:229784154 | C | A | 1 | a0001c0001t0001g0120 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.5094+1603G>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 34/41 | chr2 | 229784154 | |||||||
| chr2:229784372 | AAT | A | 22 | a0001c0001t0001g0099 a0001c0001t0001g0153 a0001c0001t0001g0215 others(19): Show |
23 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.5094+1383_5094+138 others(6): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 34/41 | chr2 | 229784372 | |||||||
| chr2:229784426 | T | A | 65 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0093 others(62): Show |
65 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.5094+1331A>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 34/41 | chr2 | 229784426 | |||||||
| chr2:229784513 | GA | G | 7 | a0001c0001t0001g0149 a0001c0001t0001g0236 a0001c0001t0004g0254 others(4): Show |
7 | HG01074.hp2 HG01891.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.5094+1243delT | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 34/41 | chr2 | 229784513 | |||||||
| chr2:229784533 | A | AC | 271 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0093 others(268): Show |
272 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(269): Show |
intron_variant | MODIFIER | c.5094+1223_5094+122 others(5): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 34/41 | chr2 | 229784533 | |||||||
| chr2:229784535 | G | A | 2 | a0001c0002t0003g0066 a0001c0002t0029g0060 |
2 | HG01074.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.5094+1222C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 34/41 | chr2 | 229784535 | |||||||
| chr2:229784802 | C | T | 1 | a0001c0002t0002g0308 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.5094+955G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 34/41 | chr2 | 229784802 | |||||||
| chr2:229784821 | T | A | 1 | a0001c0001t0001g0120 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.5094+936A>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 34/41 | chr2 | 229784821 | |||||||
| chr2:229784835 | G | A | 1 | a0001c0003t0007g0222 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.5094+922C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 34/41 | chr2 | 229784835 | |||||||
| chr2:229784988 | A | G | 1 | a0001c0002t0003g0271 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.5094+769T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 34/41 | chr2 | 229784988 | |||||||
| chr2:229785263 | A | G | 1 | a0001c0002t0001g0055 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.5094+494T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 34/41 | chr2 | 229785263 | |||||||
| chr2:229785277 | C | T | 7 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0011g0098 others(4): Show |
7 | HG01884.hp1 HG02622.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.5094+480G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 34/41 | chr2 | 229785277 | |||||||
| chr2:229785379 | C | G | 1 | a0001c0001t0001g0163 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.5094+378G>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 34/41 | chr2 | 229785379 | |||||||
| chr2:229785429 | T | A | 2 | a0001c0001t0001g0022 a0001c0001t0005g0003 |
2 | HG02145.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.5094+328A>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 34/41 | chr2 | 229785429 | |||||||
| chr2:229785458 | T | C | 2 | a0001c0002t0002g0306 a0001c0002t0002g0308 |
2 | HG01071.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.5094+299A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 34/41 | chr2 | 229785458 | |||||||
| chr2:229786184 | T | C | 1 | a0001c0001t0001g0097 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.4996-329A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 33/41 | chr2 | 229786184 | |||||||
| chr2:229786245 | T | C | 10 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0188 others(7): Show |
10 | HG02615.hp2 HG02630.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.4996-390A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 33/41 | chr2 | 229786245 | |||||||
| chr2:229786257 | C | T | 52 | a0001c0002t0003g0024 a0001c0002t0003g0025 a0001c0002t0003g0026 others(49): Show |
52 | HG00323.hp1 HG00621.hp1 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.4996-402G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 33/41 | chr2 | 229786257 | |||||||
| chr2:229786301 | C | T | 1 | a0001c0008t0001g0267 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.4996-446G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 33/41 | chr2 | 229786301 | |||||||
| chr2:229786306 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4996-451C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 33/41 | chr2 | 229786306 | |||||||
| chr2:229786396 | C | CT | 188 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0097 others(185): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.4996-542dupA | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 33/41 | chr2 | 229786396 | |||||||
| chr2:229786396 | C | CTT | 29 | a0001c0001t0001g0132 a0001c0001t0001g0135 a0001c0001t0001g0174 others(26): Show |
29 | HG00423.hp2 HG00621.hp2 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.4996-543_4996-542d others(4): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 33/41 | chr2 | 229786396 | |||||||
| chr2:229786396 | CT | C | 78 | a0001c0001t0001g0269 a0001c0001t0009g0268 a0001c0001t0014g0107 others(75): Show |
78 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.4996-542delA | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 33/41 | chr2 | 229786396 | |||||||
| chr2:229786401 | T | G | 5 | a0001c0002t0001g0070 a0001c0002t0001g0074 a0001c0002t0003g0069 others(2): Show |
5 | HG01106.hp2 HG02027.hp1 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.4996-546A>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 33/41 | chr2 | 229786401 | |||||||
| chr2:229786402 | T | G | 73 | a0001c0002t0001g0027 a0001c0002t0001g0028 a0001c0002t0001g0029 others(70): Show |
73 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.4996-547A>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 33/41 | chr2 | 229786402 | |||||||
| chr2:229786430 | G | A | 2 | a0001c0001t0010g0249 a0001c0001t0010g0250 |
2 | HG03195.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.4996-575C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 33/41 | chr2 | 229786430 | |||||||
| chr2:229786473 | C | T | 1 | a0001c0001t0004g0254 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.4996-618G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 33/41 | chr2 | 229786473 | |||||||
| chr2:229786541 | G | A | 2 | a0001c0001t0001g0269 a0001c0001t0009g0268 |
2 | HG00639.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.4996-686C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 33/41 | chr2 | 229786541 | |||||||
| chr2:229786564 | A | AT | 73 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0116 others(70): Show |
73 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.4996-710dupA | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 33/41 | chr2 | 229786564 | |||||||
| chr2:229786564 | A | ATT | 15 | a0001c0001t0001g0097 a0001c0001t0001g0119 a0001c0001t0001g0133 others(12): Show |
15 | HG00423.hp2 HG00673.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.4996-711_4996-710d others(4): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 33/41 | chr2 | 229786564 | |||||||
| chr2:229786564 | AT | A | 55 | a0001c0001t0001g0093 a0001c0001t0001g0117 a0001c0001t0004g0001 others(52): Show |
56 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.4996-710delA | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 33/41 | chr2 | 229786564 | |||||||
| chr2:229786564 | ATT | A | 97 | a0001c0001t0001g0094 a0001c0001t0001g0099 a0001c0001t0001g0174 others(94): Show |
97 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.4996-711_4996-710d others(4): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 33/41 | chr2 | 229786564 | |||||||
| chr2:229786564 | ATTT | A | 15 | a0001c0001t0001g0120 a0001c0001t0001g0153 a0001c0001t0001g0215 others(12): Show |
15 | HG00639.hp2 HG02083.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.4996-712_4996-710d others(5): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 33/41 | chr2 | 229786564 | |||||||
| chr2:229786668 | C | T | 2 | a0001c0001t0019g0317 a0001c0001t0019g0318 |
2 | HG02257.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.4996-813G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 33/41 | chr2 | 229786668 | |||||||
| chr2:229786669 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4996-814C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 33/41 | chr2 | 229786669 | |||||||
| chr2:229786703 | C | T | 5 | a0001c0002t0002g0299 a0001c0002t0002g0300 a0001c0002t0002g0301 others(2): Show |
5 | HG01496.hp1 HG02080.hp2 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.4995+802G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 33/41 | chr2 | 229786703 | |||||||
| chr2:229786805 | C | G | 5 | a0001c0001t0010g0249 a0001c0001t0010g0250 a0001c0001t0010g0251 others(2): Show |
5 | HG00741.hp2 HG01106.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.4995+700G>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 33/41 | chr2 | 229786805 | |||||||
| chr2:229787094 | C | T | 10 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0188 others(7): Show |
10 | HG02615.hp2 HG02630.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.4995+411G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 33/41 | chr2 | 229787094 | |||||||
| chr2:229787213 | T | C | 1 | a0001c0002t0005g0007 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.4995+292A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 33/41 | chr2 | 229787213 | |||||||
| chr2:229787215 | C | T | 1 | a0001c0002t0005g0007 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.4995+290G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 33/41 | chr2 | 229787215 | |||||||
| chr2:229787216 | A | G | 11 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0188 others(8): Show |
11 | HG00438.hp1 HG02615.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.4995+289T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 33/41 | chr2 | 229787216 | |||||||
| chr2:229787217 | G | T | 1 | a0001c0002t0005g0007 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.4995+288C>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 33/41 | chr2 | 229787217 | |||||||
| chr2:229787218 | T | C | 1 | a0001c0002t0005g0007 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.4995+287A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 33/41 | chr2 | 229787218 | |||||||
| chr2:229787219 | G | T | 1 | a0001c0002t0005g0007 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.4995+286C>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 33/41 | chr2 | 229787219 | |||||||
| chr2:229787220 | A | T | 1 | a0001c0002t0005g0007 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.4995+285T>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 33/41 | chr2 | 229787220 | |||||||
| chr2:229787474 | G | C | 1 | a0001c0001t0001g0120 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4995+31C>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 33/41 | chr2 | 229787474 | |||||||
| chr2:229787828 | TC | T | 323 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0093 others(320): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(321): Show |
intron_variant | MODIFIER | c.4839-168delG | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 32/41 | chr2 | 229787828 | |||||||
| chr2:229788233 | T | C | 13 | a0001c0001t0004g0001 a0001c0001t0004g0254 a0001c0001t0004g0255 others(10): Show |
14 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.4838+565A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 32/41 | chr2 | 229788233 | |||||||
| chr2:229788421 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.4838+377G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 32/41 | chr2 | 229788421 | |||||||
| chr2:229788496 | G | C | 3 | a0001c0001t0014g0107 a0001c0001t0014g0108 a0001c0001t0014g0112 |
3 | HG02717.hp1 HG02818.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.4838+302C>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 32/41 | chr2 | 229788496 | |||||||
| chr2:229788534 | C | T | 1 | a0001c0005t0001g0104 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.4838+264G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 32/41 | chr2 | 229788534 | |||||||
| chr2:229788617 | C | G | 1 | a0001c0001t0010g0253 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.4838+181G>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 32/41 | chr2 | 229788617 | |||||||
| chr2:229789027 | T | C | 7 | a0001c0001t0001g0119 a0001c0001t0009g0146 a0001c0001t0009g0147 others(4): Show |
7 | HG02280.hp2 HG02559.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.4696-87A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 31/41 | chr2 | 229789027 | |||||||
| chr2:229789840 | C | T | 2 | a0001c0001t0001g0093 a0001c0001t0001g0094 |
2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.4544-78G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 30/41 | chr2 | 229789840 | |||||||
| chr2:229789864 | T | C | 2 | a0001c0001t0001g0093 a0001c0001t0001g0094 |
2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.4544-102A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 30/41 | chr2 | 229789864 | |||||||
| chr2:229789918 | C | G | 1 | a0001c0002t0002g0312 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.4544-156G>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 30/41 | chr2 | 229789918 | |||||||
| chr2:229789966 | T | C | 176 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0093 others(173): Show |
177 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.4544-204A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 30/41 | chr2 | 229789966 | |||||||
| chr2:229790022 | C | T | 1 | a0001c0002t0002g0319 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.4544-260G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 30/41 | chr2 | 229790022 | |||||||
| chr2:229790156 | A | C | 5 | a0001c0001t0011g0098 a0001c0001t0011g0114 a0001c0001t0011g0187 others(2): Show |
5 | HG01884.hp1 HG02723.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.4544-394T>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 30/41 | chr2 | 229790156 | |||||||
| chr2:229790325 | T | C | 1 | a0001c0002t0013g0008 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.4544-563A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 30/41 | chr2 | 229790325 | |||||||
| chr2:229790335 | A | G | 5 | a0001c0001t0011g0098 a0001c0001t0011g0114 a0001c0001t0011g0187 others(2): Show |
5 | HG01884.hp1 HG02723.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.4544-573T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 30/41 | chr2 | 229790335 | |||||||
| chr2:229790540 | AG | A | 81 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0005g0003 others(78): Show |
81 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.4543+583delC | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 30/41 | chr2 | 229790540 | |||||||
| chr2:229790542 | G | C | 1 | a0001c0002t0002g0319 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.4543+582C>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 30/41 | chr2 | 229790542 | |||||||
| chr2:229790700 | C | T | 6 | a0001c0002t0001g0029 a0001c0002t0001g0059 a0001c0002t0001g0075 others(3): Show |
6 | HG01070.hp2 HG01071.hp2 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.4543+424G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 30/41 | chr2 | 229790700 | |||||||
| chr2:229790779 | T | A | 22 | a0001c0001t0001g0099 a0001c0001t0001g0153 a0001c0001t0001g0215 others(19): Show |
23 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.4543+345A>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 30/41 | chr2 | 229790779 | |||||||
| chr2:229790897 | GT | G | 269 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0093 others(266): Show |
270 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.4543+226delA | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 30/41 | chr2 | 229790897 | |||||||
| chr2:229790909 | A | G | 1 | a0001c0002t0003g0061 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.4543+215T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 30/41 | chr2 | 229790909 | |||||||
| chr2:229791017 | C | T | 318 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0093 others(315): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(316): Show |
intron_variant | MODIFIER | c.4543+107G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 30/41 | chr2 | 229791017 | |||||||
| chr2:229791729 | C | T | 4 | a0001c0001t0009g0268 a0001c0001t0014g0107 a0001c0001t0014g0108 others(1): Show |
4 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.4415+137G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 29/41 | chr2 | 229791729 | |||||||
| chr2:229792122 | C | A | 1 | a0001c0002t0003g0046 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.4215+31G>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 28/41 | chr2 | 229792122 | |||||||
| chr2:229792412 | T | G | 1 | a0001c0001t0009g0268 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.4142-186A>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 27/41 | chr2 | 229792412 | |||||||
| chr2:229792474 | T | C | 1 | a0001c0003t0006g0326 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.4142-248A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 27/41 | chr2 | 229792474 | |||||||
| chr2:229792606 | A | G | 166 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0099 others(163): Show |
167 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.4141+367T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 27/41 | chr2 | 229792606 | |||||||
| chr2:229792694 | T | C | 1 | a0001c0001t0011g0187 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.4141+279A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 27/41 | chr2 | 229792694 | |||||||
| chr2:229792780 | G | T | 269 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0093 others(266): Show |
270 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.4141+193C>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 27/41 | chr2 | 229792780 | |||||||
| chr2:229792922 | T | C | 3 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0005g0003 |
3 | HG02145.hp2 HG02257.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.4141+51A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 27/41 | chr2 | 229792922 | |||||||
| chr2:229793546 | A | C | 1 | a0001c0001t0010g0249 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3969-401T>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 26/41 | chr2 | 229793546 | |||||||
| chr2:229793572 | C | A | 2 | a0001c0002t0003g0045 a0001c0002t0020g0002 |
2 | NA19003.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.3969-427G>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 26/41 | chr2 | 229793572 | |||||||
| chr2:229793617 | T | C | 3 | a0001c0001t0012g0139 a0001c0001t0012g0140 a0001c0001t0012g0168 |
3 | HG00639.hp1 HG01109.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.3969-472A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 26/41 | chr2 | 229793617 | |||||||
| chr2:229793713 | C | G | 89 | a0001c0001t0001g0097 a0001c0001t0001g0105 a0001c0001t0001g0106 others(86): Show |
89 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.3969-568G>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 26/41 | chr2 | 229793713 | |||||||
| chr2:229793850 | G | GT | 94 | a0001c0001t0001g0097 a0001c0001t0001g0105 a0001c0001t0001g0106 others(91): Show |
94 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.3969-706dupA | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 26/41 | chr2 | 229793850 | |||||||
| chr2:229793928 | T | C | 4 | a0001c0001t0009g0268 a0001c0001t0014g0107 a0001c0001t0014g0108 others(1): Show |
4 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.3969-783A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 26/41 | chr2 | 229793928 | |||||||
| chr2:229794245 | T | A | 1 | a0001c0001t0009g0268 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3968+934A>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 26/41 | chr2 | 229794245 | |||||||
| chr2:229794303 | G | A | 1 | a0001c0002t0002g0311 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3968+876C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 26/41 | chr2 | 229794303 | |||||||
| chr2:229794329 | G | A | 52 | a0001c0002t0003g0024 a0001c0002t0003g0025 a0001c0002t0003g0026 others(49): Show |
52 | HG00323.hp1 HG00621.hp1 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.3968+850C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 26/41 | chr2 | 229794329 | |||||||
| chr2:229794534 | T | C | 2 | a0001c0003t0006g0322 a0001c0003t0036g0321 |
2 | HG01261.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.3968+645A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 26/41 | chr2 | 229794534 | |||||||
| chr2:229794566 | AAAAT | A | 172 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0099 others(169): Show |
173 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.3968+609_3968+612d others(6): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 26/41 | chr2 | 229794566 | |||||||
| chr2:229794630 | G | C | 1 | a0001c0003t0006g0328 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.3968+549C>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 26/41 | chr2 | 229794630 | |||||||
| chr2:229795368 | T | C | 1 | a0001c0001t0001g0149 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.3817-38A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 25/41 | chr2 | 229795368 | |||||||
| chr2:229795387 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3817-57G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 25/41 | chr2 | 229795387 | |||||||
| chr2:229795670 | T | C | 1 | a0001c0001t0009g0268 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3817-340A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 25/41 | chr2 | 229795670 | |||||||
| chr2:229795946 | T | C | 10 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0188 others(7): Show |
10 | HG02615.hp2 HG02630.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.3817-616A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 25/41 | chr2 | 229795946 | |||||||
| chr2:229796223 | A | T | 1 | a0001c0002t0003g0035 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3816+368T>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 25/41 | chr2 | 229796223 | |||||||
| chr2:229796372 | T | C | 1 | a0001c0001t0001g0120 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3816+219A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 25/41 | chr2 | 229796372 | |||||||
| chr2:229796824 | G | A | 1 | a0001c0001t0001g0180 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.3625-42C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 24/41 | chr2 | 229796824 | |||||||
| chr2:229796887 | A | G | 22 | a0001c0001t0001g0099 a0001c0001t0001g0153 a0001c0001t0001g0215 others(19): Show |
23 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.3625-105T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 24/41 | chr2 | 229796887 | |||||||
| chr2:229796893 | G | C | 2 | a0001c0003t0006g0322 a0001c0003t0036g0321 |
2 | HG01261.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.3625-111C>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 24/41 | chr2 | 229796893 | |||||||
| chr2:229796945 | AAC | A | 170 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0093 others(167): Show |
171 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.3625-165_3625-164d others(4): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 24/41 | chr2 | 229796945 | |||||||
| chr2:229797003 | TAAG | T | 3 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0005g0003 |
3 | HG02145.hp2 HG02257.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.3625-224_3625-222d others(5): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 24/41 | chr2 | 229797003 | |||||||
| chr2:229797489 | T | C | 1 | a0001c0002t0005g0009 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3624+201A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 24/41 | chr2 | 229797489 | |||||||
| chr2:229798075 | A | G | 182 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0093 others(179): Show |
183 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(180): Show |
intron_variant | MODIFIER | c.3483-244T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 23/41 | chr2 | 229798075 | |||||||
| chr2:229798149 | C | T | 1 | a0001c0003t0001g0206 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.3483-318G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 23/41 | chr2 | 229798149 | |||||||
| chr2:229798150 | A | G | 1 | a0001c0003t0001g0206 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.3483-319T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 23/41 | chr2 | 229798150 | |||||||
| chr2:229798231 | G | A | 3 | a0001c0002t0003g0042 a0001c0002t0003g0043 a0001c0002t0003g0272 |
3 | HG00642.hp1 HG01255.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.3483-400C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 23/41 | chr2 | 229798231 | |||||||
| chr2:229798380 | T | C | 11 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0188 others(8): Show |
11 | HG02109.hp2 HG02615.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.3482+495A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 23/41 | chr2 | 229798380 | |||||||
| chr2:229798464 | T | TA | 8 | a0001c0001t0004g0262 a0001c0001t0005g0011 a0001c0001t0011g0098 others(5): Show |
8 | HG01243.hp1 HG01261.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.3482+410dupT | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 23/41 | chr2 | 229798464 | |||||||
| chr2:229798464 | TA | T | 12 | a0001c0001t0010g0249 a0001c0001t0010g0250 a0001c0001t0010g0251 others(9): Show |
12 | HG00741.hp2 HG01106.hp1 HG02970.hp1 others(9): Show |
intron_variant | MODIFIER | c.3482+410delT | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 23/41 | chr2 | 229798464 | |||||||
| chr2:229798633 | G | A | 3 | a0001c0001t0014g0107 a0001c0001t0014g0108 a0001c0001t0014g0112 |
3 | HG02717.hp1 HG02818.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3482+242C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 23/41 | chr2 | 229798633 | |||||||
| chr2:229798724 | G | T | 1 | a0001c0001t0001g0120 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3482+151C>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 23/41 | chr2 | 229798724 | |||||||
| chr2:229798727 | A | C | 108 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0099 others(105): Show |
109 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.3482+148T>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 23/41 | chr2 | 229798727 | |||||||
| chr2:229798852 | A | G | 1 | a0001c0001t0009g0268 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3482+23T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 23/41 | chr2 | 229798852 | |||||||
| chr2:229798860 | C | T | 126 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0099 others(123): Show |
127 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.3482+15G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 23/41 | chr2 | 229798860 | |||||||
| chr2:229799182 | T | C | 1 | a0001c0001t0001g0138 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.3307+101A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 22/41 | chr2 | 229799182 | |||||||
| chr2:229799470 | A | C | 11 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0188 others(8): Show |
11 | HG02109.hp2 HG02615.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.3207-87T>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 21/41 | chr2 | 229799470 | |||||||
| chr2:229799709 | A | C | 5 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0127 others(2): Show |
5 | HG02258.hp1 HG02622.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.3207-326T>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 21/41 | chr2 | 229799709 | |||||||
| chr2:229799731 | C | A | 1 | a0001c0001t0001g0174 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3207-348G>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 21/41 | chr2 | 229799731 | |||||||
| chr2:229799772 | CA | C | 20 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0269 others(17): Show |
21 | HG00639.hp2 HG01243.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.3207-390delT | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 21/41 | chr2 | 229799772 | |||||||
| chr2:229799772 | CAA | C | 9 | a0001c0001t0001g0099 a0001c0001t0001g0153 a0001c0001t0001g0215 others(6): Show |
9 | HG02055.hp1 HG02486.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.3207-391_3207-390d others(4): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 21/41 | chr2 | 229799772 | |||||||
| chr2:229799875 | A | G | 1 | a0001c0002t0003g0073 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.3207-492T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 21/41 | chr2 | 229799875 | |||||||
| chr2:229799901 | G | A | 24 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0099 others(21): Show |
25 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.3207-518C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 21/41 | chr2 | 229799901 | |||||||
| chr2:229799962 | T | G | 1 | a0001c0001t0001g0170 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.3207-579A>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 21/41 | chr2 | 229799962 | |||||||
| chr2:229800103 | C | A | 3 | a0001c0002t0002g0282 a0001c0002t0002g0286 a0001c0002t0002g0288 |
3 | NA18941.hp2 NA18952.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.3207-720G>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 21/41 | chr2 | 229800103 | |||||||
| chr2:229800271 | G | C | 1 | a0001c0001t0001g0246 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.3207-888C>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 21/41 | chr2 | 229800271 | |||||||
| chr2:229800294 | G | A | 1 | a0001c0001t0001g0174 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3207-911C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 21/41 | chr2 | 229800294 | |||||||
| chr2:229800316 | T | C | 3 | a0001c0001t0014g0107 a0001c0001t0014g0108 a0001c0001t0014g0112 |
3 | HG02717.hp1 HG02818.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3207-933A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 21/41 | chr2 | 229800316 | |||||||
| chr2:229800477 | A | G | 169 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0099 others(166): Show |
170 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.3207-1094T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 21/41 | chr2 | 229800477 | |||||||
| chr2:229800587 | T | C | 111 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0099 others(108): Show |
112 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(109): Show |
intron_variant | MODIFIER | c.3207-1204A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 21/41 | chr2 | 229800587 | |||||||
| chr2:229800644 | C | A | 1 | a0001c0003t0001g0178 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.3207-1261G>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 21/41 | chr2 | 229800644 | |||||||
| chr2:229800967 | C | A | 1 | a0001c0001t0001g0174 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3206+1285G>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 21/41 | chr2 | 229800967 | |||||||
| chr2:229801062 | C | T | 1 | a0001c0002t0001g0028 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.3206+1190G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 21/41 | chr2 | 229801062 | |||||||
| chr2:229801214 | A | C | 2 | a0001c0001t0001g0269 a0001c0001t0009g0268 |
2 | HG00639.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.3206+1038T>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 21/41 | chr2 | 229801214 | |||||||
| chr2:229801270 | A | G | 8 | a0001c0002t0002g0280 a0001c0002t0002g0281 a0001c0002t0002g0287 others(5): Show |
8 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(5): Show |
intron_variant | MODIFIER | c.3206+982T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 21/41 | chr2 | 229801270 | |||||||
| chr2:229801529 | G | C | 1 | a0001c0001t0001g0205 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3206+723C>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 21/41 | chr2 | 229801529 | |||||||
| chr2:229801594 | A | G | 1 | a0001c0003t0001g0092 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3206+658T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 21/41 | chr2 | 229801594 | |||||||
| chr2:229801600 | A | G | 2 | a0001c0002t0017g0040 a0001c0002t0017g0090 |
2 | NA18944.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.3206+652T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 21/41 | chr2 | 229801600 | |||||||
| chr2:229802182 | A | G | 93 | a0001c0001t0001g0097 a0001c0001t0001g0105 a0001c0001t0001g0106 others(90): Show |
93 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.3206+70T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 21/41 | chr2 | 229802182 | |||||||
| chr2:229802596 | G | A | 2 | a0001c0001t0019g0317 a0001c0001t0019g0318 |
2 | HG02257.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.2999-137C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 20/41 | chr2 | 229802596 | |||||||
| chr2:229802723 | G | A | 1 | a0001c0002t0001g0054 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.2999-264C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 20/41 | chr2 | 229802723 | |||||||
| chr2:229802823 | T | C | 80 | a0001c0002t0001g0027 a0001c0002t0001g0028 a0001c0002t0001g0029 others(77): Show |
80 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.2999-364A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 20/41 | chr2 | 229802823 | |||||||
| chr2:229802854 | C | T | 318 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0093 others(315): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(316): Show |
intron_variant | MODIFIER | c.2999-395G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 20/41 | chr2 | 229802854 | |||||||
| chr2:229803012 | T | A | 1 | a0001c0001t0001g0232 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.2999-553A>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 20/41 | chr2 | 229803012 | |||||||
| chr2:229803015 | G | T | 3 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0005g0003 |
3 | HG02145.hp2 HG02257.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.2998+556C>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 20/41 | chr2 | 229803015 | |||||||
| chr2:229803073 | C | G | 80 | a0001c0002t0001g0027 a0001c0002t0001g0028 a0001c0002t0001g0029 others(77): Show |
80 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.2998+498G>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 20/41 | chr2 | 229803073 | |||||||
| chr2:229803132 | T | C | 7 | a0001c0002t0002g0296 a0001c0002t0002g0305 a0001c0002t0002g0306 others(4): Show |
7 | HG00323.hp2 HG01071.hp1 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.2998+439A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 20/41 | chr2 | 229803132 | |||||||
| chr2:229803185 | T | G | 12 | a0001c0001t0001g0153 a0001c0001t0001g0215 a0001c0001t0001g0227 others(9): Show |
12 | HG00639.hp2 HG02055.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.2998+386A>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 20/41 | chr2 | 229803185 | |||||||
| chr2:229803308 | T | A | 3 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0278 |
3 | NA18945.hp1 NA18953.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.2998+263A>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 20/41 | chr2 | 229803308 | |||||||
| chr2:229803315 | T | C | 2 | a0001c0002t0001g0071 a0001c0009t0007g0103 |
2 | NA18998.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.2998+256A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 20/41 | chr2 | 229803315 | |||||||
| chr2:229803375 | A | C | 2 | a0001c0003t0001g0178 a0001c0003t0001g0185 |
2 | HG03195.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2998+196T>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 20/41 | chr2 | 229803375 | |||||||
| chr2:229803423 | C | T | 2 | a0001c0001t0001g0093 a0001c0001t0001g0094 |
2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2998+148G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 20/41 | chr2 | 229803423 | |||||||
| chr2:229804252 | G | A | 271 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0093 others(268): Show |
272 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(269): Show |
intron_variant | MODIFIER | c.2651-25C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 18/41 | chr2 | 229804252 | |||||||
| chr2:229804266 | T | G | 121 | a0001c0002t0001g0027 a0001c0002t0001g0028 a0001c0002t0001g0029 others(118): Show |
121 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.2651-39A>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 18/41 | chr2 | 229804266 | |||||||
| chr2:229804516 | T | C | 2 | a0001c0001t0001g0093 a0001c0001t0001g0094 |
2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2651-289A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 18/41 | chr2 | 229804516 | |||||||
| chr2:229804589 | C | T | 1 | a0001c0001t0004g0260 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2651-362G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 18/41 | chr2 | 229804589 | |||||||
| chr2:229804590 | C | G | 177 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0093 others(174): Show |
178 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.2651-363G>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 18/41 | chr2 | 229804590 | |||||||
| chr2:229804671 | G | A | 1 | a0001c0002t0008g0049 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.2651-444C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 18/41 | chr2 | 229804671 | |||||||
| chr2:229804766 | T | A | 11 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0188 others(8): Show |
11 | HG02109.hp2 HG02615.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.2651-539A>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 18/41 | chr2 | 229804766 | |||||||
| chr2:229804889 | C | T | 1 | a0001c0003t0001g0199 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.2651-662G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 18/41 | chr2 | 229804889 | |||||||
| chr2:229804905 | ATTAAT | A | 24 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0099 others(21): Show |
25 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.2651-683_2651-679d others(7): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 18/41 | chr2 | 229804905 | |||||||
| chr2:229805105 | C | A | 4 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 others(1): Show |
4 | HG01928.hp2 HG02300.hp1 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.2650+625G>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 18/41 | chr2 | 229805105 | |||||||
| chr2:229805191 | C | T | 1 | a0001c0003t0006g0327 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2650+539G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 18/41 | chr2 | 229805191 | |||||||
| chr2:229805222 | A | AAACAAC | 34 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0005g0003 others(31): Show |
34 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.2650+502_2650+507d others(8): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 18/41 | chr2 | 229805222 | |||||||
| chr2:229805222 | A | AAACAACA others(2): Show |
68 | a0001c0001t0001g0106 a0001c0001t0012g0139 a0001c0001t0012g0140 others(65): Show |
68 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(65): Show |
intron_variant | MODIFIER | c.2650+499_2650+507d others(11): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 18/41 | chr2 | 229805222 | |||||||
| chr2:229805222 | A | AAACAACA others(5): Show |
98 | a0001c0001t0001g0097 a0001c0001t0001g0105 a0001c0001t0001g0116 others(95): Show |
98 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.2650+496_2650+507d others(14): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 18/41 | chr2 | 229805222 | |||||||
| chr2:229805222 | A | AAACAACA others(8): Show |
28 | a0001c0001t0001g0120 a0001c0001t0001g0145 a0001c0001t0001g0174 others(25): Show |
29 | HG01884.hp1 HG01891.hp2 HG02083.hp2 others(26): Show |
intron_variant | MODIFIER | c.2650+493_2650+507d others(17): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 18/41 | chr2 | 229805222 | |||||||
| chr2:229805222 | A | AAACAACA others(11): Show |
17 | a0001c0001t0001g0099 a0001c0001t0001g0153 a0001c0001t0001g0230 others(14): Show |
17 | HG00323.hp1 HG01243.hp1 HG01993.hp2 others(14): Show |
intron_variant | MODIFIER | c.2650+490_2650+507d others(20): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 18/41 | chr2 | 229805222 | |||||||
| chr2:229805222 | A | AAACAACA others(14): Show |
40 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0215 others(37): Show |
40 | HG00642.hp1 HG00733.hp1 HG01099.hp2 others(37): Show |
intron_variant | MODIFIER | c.2650+487_2650+507d others(23): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 18/41 | chr2 | 229805222 | |||||||
| chr2:229805222 | A | AAACAACA others(17): Show |
29 | a0001c0002t0001g0028 a0001c0002t0001g0029 a0001c0002t0001g0052 others(26): Show |
29 | HG00438.hp1 HG00544.hp2 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.2650+484_2650+507d others(26): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 18/41 | chr2 | 229805222 | |||||||
| chr2:229805222 | A | AAACAACA others(20): Show |
9 | a0001c0002t0001g0033 a0001c0002t0001g0034 a0001c0002t0001g0071 others(6): Show |
9 | HG00735.hp1 HG00735.hp2 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.2650+507_2650+508i others(29): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 18/41 | chr2 | 229805222 | |||||||
| chr2:229805222 | A | AAACAACA others(23): Show |
1 | a0001c0009t0007g0103 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.2650+507_2650+508i others(32): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 18/41 | chr2 | 229805222 | |||||||
| chr2:229805346 | T | G | 1 | a0001c0002t0002g0294 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2650+384A>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 18/41 | chr2 | 229805346 | |||||||
| chr2:229805416 | T | C | 3 | a0001c0003t0015g0150 a0001c0003t0015g0151 a0001c0003t0015g0173 |
3 | HG02922.hp2 HG02965.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2650+314A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 18/41 | chr2 | 229805416 | |||||||
| chr2:229805425 | G | A | 1 | a0002c0006t0001g0096 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.2650+305C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 18/41 | chr2 | 229805425 | |||||||
| chr2:229805434 | T | C | 1 | a0001c0002t0001g0058 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2650+296A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 18/41 | chr2 | 229805434 | |||||||
| chr2:229805501 | G | A | 29 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0099 others(26): Show |
30 | HG00639.hp2 HG01243.hp1 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.2650+229C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 18/41 | chr2 | 229805501 | |||||||
| chr2:229806290 | G | A | 1 | a0001c0003t0001g0190 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2497-407C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 17/41 | chr2 | 229806290 | |||||||
| chr2:229806355 | C | CT | 24 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0099 others(21): Show |
25 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.2497-473dupA | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 17/41 | chr2 | 229806355 | |||||||
| chr2:229806393 | C | T | 1 | a0001c0003t0015g0150 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2497-510G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 17/41 | chr2 | 229806393 | |||||||
| chr2:229806623 | G | C | 1 | a0001c0002t0003g0080 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2497-740C>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 17/41 | chr2 | 229806623 | |||||||
| chr2:229806656 | C | T | 3 | a0001c0001t0004g0261 a0001c0001t0004g0264 a0001c0001t0004g0265 |
3 | HG02145.hp1 HG02486.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.2497-773G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 17/41 | chr2 | 229806656 | |||||||
| chr2:229807638 | T | A | 3 | a0001c0002t0003g0076 a0001c0002t0003g0079 a0001c0002t0028g0081 |
3 | HG03688.hp2 HG03704.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.2496+70A>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 17/41 | chr2 | 229807638 | |||||||
| chr2:229807874 | A | G | 1 | a0001c0002t0003g0045 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2340-10T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 16/41 | chr2 | 229807874 | |||||||
| chr2:229808024 | G | A | 2 | a0001c0002t0003g0045 a0001c0002t0020g0002 |
2 | NA19003.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.2340-160C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 16/41 | chr2 | 229808024 | |||||||
| chr2:229808136 | T | C | 1 | a0001c0002t0001g0055 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2339+116A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 16/41 | chr2 | 229808136 | |||||||
| chr2:229808213 | G | A | 1 | a0001c0002t0002g0300 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2339+39C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 16/41 | chr2 | 229808213 | |||||||
| chr2:229808393 | C | G | 1 | a0001c0001t0001g0132 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2222-24G>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 15/41 | chr2 | 229808393 | |||||||
| chr2:229808489 | A | G | 5 | a0001c0001t0011g0098 a0001c0001t0011g0114 a0001c0001t0011g0187 others(2): Show |
5 | HG01884.hp1 HG02723.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.2222-120T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 15/41 | chr2 | 229808489 | |||||||
| chr2:229808581 | G | A | 29 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0099 others(26): Show |
30 | HG00639.hp2 HG01243.hp1 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.2222-212C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 15/41 | chr2 | 229808581 | |||||||
| chr2:229808591 | C | T | 1 | a0001c0002t0003g0061 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2222-222G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 15/41 | chr2 | 229808591 | |||||||
| chr2:229808674 | C | T | 1 | a0001c0002t0035g0297 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2222-305G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 15/41 | chr2 | 229808674 | |||||||
| chr2:229808694 | A | G | 1 | a0001c0001t0001g0208 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.2222-325T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 15/41 | chr2 | 229808694 | |||||||
| chr2:229808891 | G | C | 24 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0099 others(21): Show |
25 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.2222-522C>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 15/41 | chr2 | 229808891 | |||||||
| chr2:229808936 | G | A | 24 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0099 others(21): Show |
25 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.2222-567C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 15/41 | chr2 | 229808936 | |||||||
| chr2:229809101 | A | C | 1 | a0001c0001t0001g0120 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2222-732T>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 15/41 | chr2 | 229809101 | |||||||
| chr2:229809116 | T | C | 2 | a0001c0001t0001g0269 a0001c0001t0009g0268 |
2 | HG00639.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.2222-747A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 15/41 | chr2 | 229809116 | |||||||
| chr2:229809233 | T | C | 3 | a0001c0001t0014g0107 a0001c0001t0014g0108 a0001c0001t0014g0112 |
3 | HG02717.hp1 HG02818.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2222-864A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 15/41 | chr2 | 229809233 | |||||||
| chr2:229809272 | T | C | 24 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0099 others(21): Show |
25 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.2222-903A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 15/41 | chr2 | 229809272 | |||||||
| chr2:229809282 | G | T | 2 | a0001c0001t0001g0269 a0001c0001t0009g0268 |
2 | HG00639.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.2222-913C>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 15/41 | chr2 | 229809282 | |||||||
| chr2:229809345 | C | T | 1 | a0001c0008t0001g0267 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2222-976G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 15/41 | chr2 | 229809345 | |||||||
| chr2:229809466 | A | T | 3 | a0001c0002t0003g0024 a0001c0002t0003g0025 a0001c0002t0003g0026 |
3 | HG01175.hp2 HG01257.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.2222-1097T>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 15/41 | chr2 | 229809466 | |||||||
| chr2:229809500 | C | A | 11 | a0001c0002t0002g0279 a0001c0002t0002g0282 a0001c0002t0002g0283 others(8): Show |
11 | HG01952.hp1 HG01975.hp1 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.2222-1131G>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 15/41 | chr2 | 229809500 | |||||||
| chr2:229809551 | C | T | 1 | a0001c0003t0001g0221 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2222-1182G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 15/41 | chr2 | 229809551 | |||||||
| chr2:229809959 | TATC | T | 3 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0005g0003 |
3 | HG02145.hp2 HG02257.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.2221+918_2221+920d others(5): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 15/41 | chr2 | 229809959 | |||||||
| chr2:229810010 | T | A | 3 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0005g0003 |
3 | HG02145.hp2 HG02257.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.2221+870A>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 15/41 | chr2 | 229810010 | |||||||
| chr2:229810114 | C | T | 4 | a0001c0002t0001g0052 a0001c0002t0001g0053 a0001c0002t0001g0055 others(1): Show |
4 | HG00544.hp2 NA19057.hp1 NA19080.hp1 others(1): Show |
intron_variant | MODIFIER | c.2221+766G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 15/41 | chr2 | 229810114 | |||||||
| chr2:229810313 | T | C | 7 | a0001c0001t0001g0153 a0001c0001t0001g0215 a0001c0001t0001g0227 others(4): Show |
7 | HG02486.hp2 HG02895.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.2221+567A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 15/41 | chr2 | 229810313 | |||||||
| chr2:229810327 | T | C | 1 | a0001c0002t0013g0004 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2221+553A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 15/41 | chr2 | 229810327 | |||||||
| chr2:229810337 | A | T | 2 | a0001c0001t0001g0269 a0001c0001t0009g0268 |
2 | HG00639.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.2221+543T>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 15/41 | chr2 | 229810337 | |||||||
| chr2:229810379 | G | C | 1 | a0001c0001t0001g0105 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.2221+501C>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 15/41 | chr2 | 229810379 | |||||||
| chr2:229810852 | T | C | 3 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0005g0003 |
3 | HG02145.hp2 HG02257.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.2221+28A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 15/41 | chr2 | 229810852 | |||||||
| chr2:229811350 | A | C | 5 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0127 others(2): Show |
5 | HG02258.hp1 HG02622.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1987-146T>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 13/41 | chr2 | 229811350 | |||||||
| chr2:229811427 | CT | C | 10 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0188 others(7): Show |
10 | HG02615.hp2 HG02630.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.1987-224delA | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 13/41 | chr2 | 229811427 | |||||||
| chr2:229811518 | T | C | 1 | a0001c0001t0001g0244 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1987-314A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 13/41 | chr2 | 229811518 | |||||||
| chr2:229811571 | G | A | 326 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0093 others(323): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.1987-367C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 13/41 | chr2 | 229811571 | |||||||
| chr2:229811718 | T | C | 1 | a0001c0002t0001g0033 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1987-514A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 13/41 | chr2 | 229811718 | |||||||
| chr2:229811843 | T | A | 8 | a0001c0004t0003g0082 a0001c0004t0003g0083 a0001c0004t0003g0084 others(5): Show |
8 | HG02056.hp1 HG02129.hp2 NA18951.hp1 others(5): Show |
intron_variant | MODIFIER | c.1987-639A>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 13/41 | chr2 | 229811843 | |||||||
| chr2:229811956 | C | T | 1 | a0001c0002t0001g0027 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1987-752G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 13/41 | chr2 | 229811956 | |||||||
| chr2:229812000 | T | TAAAGAAT others(330): Show |
1 | a0001c0001t0027g0169 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1987-797_1987-796i others(339): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 13/41 | chr2 | 229812000 | |||||||
| chr2:229812006 | A | T | 3 | a0001c0001t0014g0107 a0001c0001t0014g0108 a0001c0001t0014g0112 |
3 | HG02717.hp1 HG02818.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1987-802T>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 13/41 | chr2 | 229812006 | |||||||
| chr2:229812329 | C | T | 41 | a0001c0002t0002g0279 a0001c0002t0002g0280 a0001c0002t0002g0281 others(38): Show |
41 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(38): Show |
intron_variant | MODIFIER | c.1987-1125G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 13/41 | chr2 | 229812329 | |||||||
| chr2:229812422 | A | T | 2 | a0001c0002t0002g0310 a0001c0002t0002g0311 |
2 | HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1987-1218T>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 13/41 | chr2 | 229812422 | |||||||
| chr2:229812527 | C | T | 7 | a0001c0001t0001g0153 a0001c0001t0001g0215 a0001c0001t0001g0227 others(4): Show |
7 | HG02486.hp2 HG02895.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1987-1323G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 13/41 | chr2 | 229812527 | |||||||
| chr2:229812595 | C | T | 3 | a0001c0001t0001g0175 a0001c0001t0001g0188 a0001c0001t0001g0189 |
3 | HG02615.hp2 HG02723.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1986+1275G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 13/41 | chr2 | 229812595 | |||||||
| chr2:229812658 | T | C | 2 | a0001c0001t0001g0133 a0001c0001t0001g0183 |
2 | HG01884.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1986+1212A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 13/41 | chr2 | 229812658 | |||||||
| chr2:229812667 | G | A | 29 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0099 others(26): Show |
30 | HG00639.hp2 HG01243.hp1 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.1986+1203C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 13/41 | chr2 | 229812667 | |||||||
| chr2:229812743 | C | T | 4 | a0001c0001t0004g0254 a0001c0001t0004g0255 a0001c0001t0004g0259 others(1): Show |
4 | HG01891.hp2 HG02647.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1986+1127G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 13/41 | chr2 | 229812743 | |||||||
| chr2:229812815 | A | T | 1 | a0001c0002t0001g0054 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1986+1055T>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 13/41 | chr2 | 229812815 | |||||||
| chr2:229812822 | CA | C | 41 | a0001c0002t0002g0279 a0001c0002t0002g0280 a0001c0002t0002g0281 others(38): Show |
41 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(38): Show |
intron_variant | MODIFIER | c.1986+1047delT | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 13/41 | chr2 | 229812822 | |||||||
| chr2:229813242 | C | G | 2 | a0001c0002t0002g0306 a0001c0002t0002g0308 |
2 | HG01071.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1986+628G>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 13/41 | chr2 | 229813242 | |||||||
| chr2:229813395 | C | A | 5 | a0001c0001t0011g0098 a0001c0001t0011g0114 a0001c0001t0011g0187 others(2): Show |
5 | HG01884.hp1 HG02723.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1986+475G>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 13/41 | chr2 | 229813395 | |||||||
| chr2:229813445 | G | A | 1 | a0001c0002t0003g0080 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1986+425C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 13/41 | chr2 | 229813445 | |||||||
| chr2:229813487 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1986+383C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 13/41 | chr2 | 229813487 | |||||||
| chr2:229813707 | C | G | 5 | a0001c0003t0001g0158 a0001c0003t0001g0200 a0001c0003t0001g0207 others(2): Show |
5 | NA18954.hp2 NA18993.hp1 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.1986+163G>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 13/41 | chr2 | 229813707 | |||||||
| chr2:229814040 | T | C | 1 | a0001c0001t0001g0229 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1825-9A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 12/41 | chr2 | 229814040 | |||||||
| chr2:229814214 | C | G | 1 | a0001c0002t0002g0310 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1824+19G>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 12/41 | chr2 | 229814214 | |||||||
| chr2:229814349 | A | C | 4 | a0001c0003t0001g0218 a0001c0005t0001g0104 a0001c0005t0001g0217 others(1): Show |
4 | HG02109.hp2 HG02886.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1732-24T>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 11/41 | chr2 | 229814349 | |||||||
| chr2:229814423 | T | G | 3 | a0001c0003t0001g0178 a0001c0003t0001g0185 a0001c0003t0001g0190 |
3 | HG03195.hp2 HG03579.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1732-98A>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 11/41 | chr2 | 229814423 | |||||||
| chr2:229814576 | T | C | 1 | a0001c0002t0002g0316 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1732-251A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 11/41 | chr2 | 229814576 | |||||||
| chr2:229814616 | C | T | 1 | a0001c0003t0001g0095 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1732-291G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 11/41 | chr2 | 229814616 | |||||||
| chr2:229814738 | G | A | 1 | a0001c0001t0011g0187 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1731+361C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 11/41 | chr2 | 229814738 | |||||||
| chr2:229815092 | G | A | 3 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0005g0003 |
3 | HG02145.hp2 HG02257.hp1 HG02615.hp1 |
splice_region_variant&intron_variant | LOW | c.1731+7C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 11/41 | chr2 | 229815092 | |||||||
| chr2:229815461 | G | A | 3 | a0001c0001t0014g0107 a0001c0001t0014g0108 a0001c0001t0014g0112 |
3 | HG02717.hp1 HG02818.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1600-153C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 9/41 | chr2 | 229815461 | |||||||
| chr2:229815492 | C | A | 4 | a0001c0001t0001g0125 a0001c0001t0001g0156 a0001c0001t0001g0179 others(1): Show |
4 | HG00280.hp2 HG01243.hp2 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.1600-184G>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 9/41 | chr2 | 229815492 | |||||||
| chr2:229815519 | TA | T | 24 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0099 others(21): Show |
25 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.1600-212delT | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 9/41 | chr2 | 229815519 | |||||||
| chr2:229815651 | C | T | 3 | a0001c0001t0004g0261 a0001c0001t0004g0264 a0001c0001t0004g0265 |
3 | HG02145.hp1 HG02486.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1600-343G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 9/41 | chr2 | 229815651 | |||||||
| chr2:229815708 | CA | C | 22 | a0001c0001t0001g0099 a0001c0001t0001g0153 a0001c0001t0001g0215 others(19): Show |
23 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.1600-401delT | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 9/41 | chr2 | 229815708 | |||||||
| chr2:229815856 | C | G | 1 | a0001c0001t0001g0224 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1600-548G>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 9/41 | chr2 | 229815856 | |||||||
| chr2:229816149 | A | G | 1 | a0001c0002t0002g0284 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1600-841T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 9/41 | chr2 | 229816149 | |||||||
| chr2:229816264 | T | C | 3 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0005g0003 |
3 | HG02145.hp2 HG02257.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1600-956A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 9/41 | chr2 | 229816264 | |||||||
| chr2:229816325 | T | TA | 88 | a0001c0001t0001g0097 a0001c0001t0001g0105 a0001c0001t0001g0106 others(85): Show |
88 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.1600-1018dupT | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 9/41 | chr2 | 229816325 | |||||||
| chr2:229816325 | TA | T | 37 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0099 others(34): Show |
38 | HG00639.hp2 HG00741.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.1600-1018delT | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 9/41 | chr2 | 229816325 | |||||||
| chr2:229816509 | T | G | 1 | a0001c0003t0001g0199 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1600-1201A>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 9/41 | chr2 | 229816509 | |||||||
| chr2:229816599 | T | C | 1 | a0001c0002t0002g0315 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1600-1291A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 9/41 | chr2 | 229816599 | |||||||
| chr2:229816710 | T | C | 6 | a0001c0003t0001g0091 a0001c0003t0001g0092 a0001c0003t0001g0177 others(3): Show |
6 | HG01109.hp1 HG03130.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.1600-1402A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 9/41 | chr2 | 229816710 | |||||||
| chr2:229817189 | A | G | 80 | a0001c0002t0001g0027 a0001c0002t0001g0028 a0001c0002t0001g0029 others(77): Show |
80 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.1599+1175T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 9/41 | chr2 | 229817189 | |||||||
| chr2:229817302 | A | G | 2 | a0001c0001t0019g0317 a0001c0001t0019g0318 |
2 | HG02257.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.1599+1062T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 9/41 | chr2 | 229817302 | |||||||
| chr2:229817346 | T | G | 41 | a0001c0002t0002g0279 a0001c0002t0002g0280 a0001c0002t0002g0281 others(38): Show |
41 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(38): Show |
intron_variant | MODIFIER | c.1599+1018A>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 9/41 | chr2 | 229817346 | |||||||
| chr2:229817419 | T | A | 1 | a0001c0001t0001g0181 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1599+945A>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 9/41 | chr2 | 229817419 | |||||||
| chr2:229817641 | G | A | 1 | a0001c0001t0001g0156 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1599+723C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 9/41 | chr2 | 229817641 | |||||||
| chr2:229817672 | G | A | 1 | a0001c0002t0002g0283 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1599+692C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 9/41 | chr2 | 229817672 | |||||||
| chr2:229817939 | T | C | 1 | a0001c0004t0003g0087 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1599+425A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 9/41 | chr2 | 229817939 | |||||||
| chr2:229818088 | A | C | 1 | a0001c0003t0001g0191 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1599+276T>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 9/41 | chr2 | 229818088 | |||||||
| chr2:229818655 | T | C | 3 | a0001c0001t0014g0107 a0001c0001t0014g0108 a0001c0001t0014g0112 |
3 | HG02717.hp1 HG02818.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1451-143A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229818655 | |||||||
| chr2:229818737 | T | G | 7 | a0001c0001t0001g0233 a0001c0001t0001g0234 a0001c0001t0001g0235 others(4): Show |
7 | HG00558.hp2 NA18945.hp1 NA18953.hp2 others(4): Show |
intron_variant | MODIFIER | c.1451-225A>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229818737 | |||||||
| chr2:229818779 | A | G | 5 | a0001c0001t0001g0269 a0001c0001t0009g0268 a0001c0001t0014g0107 others(2): Show |
5 | HG00639.hp2 HG02055.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1451-267T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229818779 | |||||||
| chr2:229818992 | G | A | 1 | a0001c0001t0001g0233 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1451-480C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229818992 | |||||||
| chr2:229819039 | A | C | 1 | a0001c0003t0001g0214 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1451-527T>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229819039 | |||||||
| chr2:229819040 | C | CCA | 62 | a0001c0001t0001g0116 a0001c0001t0001g0122 a0001c0001t0001g0127 others(59): Show |
62 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.1451-530_1451-529d others(4): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229819040 | |||||||
| chr2:229819040 | C | CCACA | 17 | a0001c0001t0001g0093 a0001c0001t0001g0097 a0001c0001t0001g0105 others(14): Show |
17 | HG00140.hp2 HG00597.hp2 HG00673.hp1 others(14): Show |
intron_variant | MODIFIER | c.1451-532_1451-529d others(6): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229819040 | |||||||
| chr2:229819040 | C | CCACACA | 15 | a0001c0001t0001g0119 a0001c0001t0001g0121 a0001c0001t0001g0174 others(12): Show |
15 | HG01070.hp1 HG01928.hp1 HG01934.hp1 others(12): Show |
intron_variant | MODIFIER | c.1451-534_1451-529d others(8): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229819040 | |||||||
| chr2:229819040 | C | CCACACAC others(1): Show |
9 | a0001c0001t0001g0099 a0001c0001t0001g0120 a0001c0001t0001g0184 others(6): Show |
9 | HG00639.hp2 HG02486.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.1451-536_1451-529d others(10): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229819040 | |||||||
| chr2:229819040 | C | CCACACAC others(9): Show |
1 | a0001c0001t0005g0011 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1451-544_1451-529d others(18): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229819040 | |||||||
| chr2:229819040 | CCA | C | 60 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0094 others(57): Show |
60 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(57): Show |
intron_variant | MODIFIER | c.1451-530_1451-529d others(4): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229819040 | |||||||
| chr2:229819040 | CCACA | C | 45 | a0001c0001t0014g0107 a0001c0001t0014g0108 a0001c0001t0014g0112 others(42): Show |
45 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(42): Show |
intron_variant | MODIFIER | c.1451-532_1451-529d others(6): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229819040 | |||||||
| chr2:229819040 | CCACACA | C | 17 | a0001c0002t0001g0027 a0001c0002t0001g0028 a0001c0002t0001g0033 others(14): Show |
17 | HG00735.hp1 HG01081.hp1 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.1451-534_1451-529d others(8): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229819040 | |||||||
| chr2:229819040 | CCACACAC others(1): Show |
C | 8 | a0001c0002t0001g0052 a0001c0002t0001g0053 a0001c0002t0001g0054 others(5): Show |
8 | HG00544.hp1 HG00544.hp2 NA18992.hp2 others(5): Show |
intron_variant | MODIFIER | c.1451-536_1451-529d others(10): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229819040 | |||||||
| chr2:229819040 | CCACACAC others(3): Show |
C | 10 | a0001c0004t0003g0082 a0001c0004t0003g0083 a0001c0004t0003g0084 others(7): Show |
10 | HG02056.hp1 HG02129.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.1451-538_1451-529d others(12): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229819040 | |||||||
| chr2:229819040 | CCACACAC others(5): Show |
C | 2 | a0001c0002t0002g0299 a0001c0002t0002g0300 |
2 | HG01496.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1451-540_1451-529d others(14): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229819040 | |||||||
| chr2:229819080 | ACACAC | A | 14 | a0001c0001t0001g0145 a0001c0001t0001g0149 a0001c0001t0001g0181 others(11): Show |
14 | HG00423.hp2 HG00438.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.1451-573_1451-569d others(7): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229819080 | |||||||
| chr2:229819082 | ACAC | A | 12 | a0001c0001t0001g0106 a0001c0001t0001g0130 a0001c0001t0001g0156 others(9): Show |
12 | HG00099.hp1 HG00642.hp2 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.1451-573_1451-571d others(5): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229819082 | |||||||
| chr2:229819084 | AC | A | 4 | a0001c0001t0001g0131 a0001c0001t0001g0163 a0001c0001t0001g0182 others(1): Show |
4 | HG00280.hp2 HG00733.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.1451-573delG | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229819084 | |||||||
| chr2:229819180 | T | C | 1 | a0001c0001t0001g0274 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1451-668A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229819180 | |||||||
| chr2:229819246 | A | T | 3 | a0001c0001t0014g0107 a0001c0001t0014g0108 a0001c0001t0014g0112 |
3 | HG02717.hp1 HG02818.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1451-734T>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229819246 | |||||||
| chr2:229819259 | G | C | 308 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0093 others(305): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.1451-747C>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229819259 | |||||||
| chr2:229819365 | C | T | 49 | a0001c0001t0001g0097 a0001c0001t0001g0105 a0001c0001t0001g0116 others(46): Show |
49 | HG00408.hp1 HG00558.hp2 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.1451-853G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229819365 | |||||||
| chr2:229819388 | T | C | 201 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0097 others(198): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.1451-876A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229819388 | |||||||
| chr2:229819436 | G | A | 1 | a0001c0001t0009g0172 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1451-924C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229819436 | |||||||
| chr2:229819554 | T | A | 1 | a0001c0002t0013g0004 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1451-1042A>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229819554 | |||||||
| chr2:229819580 | T | C | 107 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0099 others(104): Show |
108 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.1451-1068A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229819580 | |||||||
| chr2:229819643 | T | C | 1 | a0001c0001t0011g0226 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1451-1131A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229819643 | |||||||
| chr2:229819656 | T | G | 1 | a0001c0001t0011g0226 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1451-1144A>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229819656 | |||||||
| chr2:229819734 | A | G | 1 | a0001c0001t0001g0275 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1451-1222T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229819734 | |||||||
| chr2:229820053 | A | G | 1 | a0001c0004t0003g0082 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1451-1541T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229820053 | |||||||
| chr2:229820086 | G | A | 2 | a0001c0002t0003g0069 a0001c0002t0013g0005 |
2 | HG00735.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.1451-1574C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229820086 | |||||||
| chr2:229820254 | T | C | 4 | a0001c0003t0006g0326 a0001c0003t0006g0327 a0001c0003t0006g0328 others(1): Show |
4 | HG00140.hp1 HG00741.hp1 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.1451-1742A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229820254 | |||||||
| chr2:229820416 | T | C | 315 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0093 others(312): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.1451-1904A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229820416 | |||||||
| chr2:229820504 | C | G | 38 | a0001c0003t0001g0095 a0001c0003t0001g0100 a0001c0003t0001g0101 others(35): Show |
38 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(35): Show |
intron_variant | MODIFIER | c.1451-1992G>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229820504 | |||||||
| chr2:229820613 | T | C | 2 | a0001c0002t0018g0313 a0001c0002t0018g0314 |
2 | HG02970.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1451-2101A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229820613 | |||||||
| chr2:229820652 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1451-2140C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229820652 | |||||||
| chr2:229820926 | T | C | 1 | a0001c0002t0002g0309 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1451-2414A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229820926 | |||||||
| chr2:229821128 | T | A | 2 | a0001c0003t0001g0194 a0001c0003t0001g0214 |
2 | NA19057.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.1451-2616A>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229821128 | |||||||
| chr2:229821172 | T | G | 80 | a0001c0002t0001g0027 a0001c0002t0001g0028 a0001c0002t0001g0029 others(77): Show |
80 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.1451-2660A>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229821172 | |||||||
| chr2:229821251 | C | A | 3 | a0001c0001t0001g0124 a0001c0001t0001g0154 a0001c0001t0001g0155 |
3 | HG01168.hp1 HG01169.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.1451-2739G>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229821251 | |||||||
| chr2:229821567 | A | T | 42 | a0001c0002t0002g0279 a0001c0002t0002g0280 a0001c0002t0002g0281 others(39): Show |
42 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(39): Show |
intron_variant | MODIFIER | c.1451-3055T>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229821567 | |||||||
| chr2:229821840 | T | C | 2 | a0001c0001t0001g0269 a0001c0001t0009g0268 |
2 | HG00639.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.1451-3328A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229821840 | |||||||
| chr2:229821952 | C | G | 1 | a0001c0005t0001g0219 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1451-3440G>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229821952 | |||||||
| chr2:229822141 | A | G | 3 | a0001c0001t0014g0107 a0001c0001t0014g0108 a0001c0001t0014g0112 |
3 | HG02717.hp1 HG02818.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1451-3629T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229822141 | |||||||
| chr2:229822174 | GA | G | 3 | a0001c0001t0014g0107 a0001c0001t0014g0108 a0001c0001t0014g0112 |
3 | HG02717.hp1 HG02818.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1451-3663delT | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229822174 | |||||||
| chr2:229822252 | CAG | C | 25 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0099 others(22): Show |
26 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1451-3742_1451-374 others(6): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229822252 | |||||||
| chr2:229822326 | T | G | 1 | a0001c0002t0001g0028 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1451-3814A>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229822326 | |||||||
| chr2:229822380 | A | G | 1 | a0001c0002t0002g0312 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1451-3868T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229822380 | |||||||
| chr2:229822462 | A | T | 1 | a0001c0003t0001g0091 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1451-3950T>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229822462 | |||||||
| chr2:229822463 | G | C | 1 | a0001c0003t0001g0091 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1451-3951C>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229822463 | |||||||
| chr2:229822736 | GA | G | 7 | a0001c0001t0001g0153 a0001c0001t0001g0215 a0001c0001t0001g0227 others(4): Show |
7 | HG02486.hp2 HG02895.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1451-4225delT | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229822736 | |||||||
| chr2:229822769 | T | C | 4 | a0001c0001t0004g0254 a0001c0001t0004g0255 a0001c0001t0004g0259 others(1): Show |
4 | HG01891.hp2 HG02647.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1451-4257A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229822769 | |||||||
| chr2:229822791 | T | C | 5 | a0001c0001t0010g0249 a0001c0001t0010g0250 a0001c0001t0010g0251 others(2): Show |
5 | HG00741.hp2 HG01106.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1451-4279A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229822791 | |||||||
| chr2:229822906 | C | T | 3 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0005g0003 |
3 | HG02145.hp2 HG02257.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1451-4394G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229822906 | |||||||
| chr2:229822921 | G | C | 1 | a0001c0001t0011g0098 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1451-4409C>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229822921 | |||||||
| chr2:229822971 | T | C | 3 | a0001c0001t0001g0243 a0001c0001t0001g0245 a0001c0002t0003g0046 |
3 | HG02896.hp1 HG02897.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1451-4459A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229822971 | |||||||
| chr2:229823119 | A | G | 1 | a0001c0001t0001g0180 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1451-4607T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229823119 | |||||||
| chr2:229823333 | C | T | 3 | a0001c0003t0001g0178 a0001c0003t0001g0185 a0001c0003t0001g0190 |
3 | HG03195.hp2 HG03579.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1451-4821G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229823333 | |||||||
| chr2:229823634 | C | T | 3 | a0001c0001t0014g0107 a0001c0001t0014g0108 a0001c0001t0014g0112 |
3 | HG02717.hp1 HG02818.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1451-5122G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229823634 | |||||||
| chr2:229823659 | G | A | 1 | a0001c0002t0003g0271 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1451-5147C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229823659 | |||||||
| chr2:229823674 | C | CA | 70 | a0001c0001t0004g0258 a0001c0001t0005g0018 a0001c0001t0009g0146 others(67): Show |
70 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.1451-5163dupT | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229823674 | |||||||
| chr2:229823684 | A | C | 1 | a0001c0001t0016g0141 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1451-5172T>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229823684 | |||||||
| chr2:229823699 | C | A | 151 | a0001c0001t0001g0097 a0001c0001t0001g0105 a0001c0001t0001g0106 others(148): Show |
151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.1451-5187G>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229823699 | |||||||
| chr2:229823758 | G | A | 2 | a0001c0001t0001g0133 a0001c0001t0001g0183 |
2 | HG01884.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1451-5246C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229823758 | |||||||
| chr2:229823770 | T | C | 5 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0127 others(2): Show |
5 | HG02258.hp1 HG02622.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1451-5258A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229823770 | |||||||
| chr2:229823798 | G | A | 5 | a0001c0001t0010g0249 a0001c0001t0010g0250 a0001c0001t0010g0251 others(2): Show |
5 | HG00741.hp2 HG01106.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1451-5286C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229823798 | |||||||
| chr2:229823804 | TG | T | 4 | a0001c0001t0001g0153 a0001c0001t0001g0227 a0001c0001t0001g0230 others(1): Show |
4 | HG02895.hp2 HG02897.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1451-5293delC | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229823804 | |||||||
| chr2:229823807 | C | T | 1 | a0001c0001t0004g0258 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1451-5295G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229823807 | |||||||
| chr2:229823981 | C | T | 2 | a0001c0001t0001g0269 a0001c0001t0009g0268 |
2 | HG00639.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.1450+5212G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229823981 | |||||||
| chr2:229824029 | C | T | 7 | a0001c0001t0001g0153 a0001c0001t0001g0215 a0001c0001t0001g0227 others(4): Show |
7 | HG02486.hp2 HG02895.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1450+5164G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229824029 | |||||||
| chr2:229824270 | A | C | 42 | a0001c0002t0002g0279 a0001c0002t0002g0280 a0001c0002t0002g0281 others(39): Show |
42 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(39): Show |
intron_variant | MODIFIER | c.1450+4923T>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229824270 | |||||||
| chr2:229824272 | T | A | 2 | a0001c0002t0003g0045 a0001c0002t0020g0002 |
2 | NA19003.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.1450+4921A>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229824272 | |||||||
| chr2:229824296 | T | C | 3 | a0001c0001t0014g0107 a0001c0001t0014g0108 a0001c0001t0014g0112 |
3 | HG02717.hp1 HG02818.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1450+4897A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229824296 | |||||||
| chr2:229824305 | A | C | 58 | a0001c0003t0001g0091 a0001c0003t0001g0092 a0001c0003t0001g0095 others(55): Show |
58 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.1450+4888T>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229824305 | |||||||
| chr2:229824349 | A | C | 2 | a0001c0002t0018g0313 a0001c0002t0018g0314 |
2 | HG02970.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1450+4844T>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229824349 | |||||||
| chr2:229824363 | G | A | 2 | a0001c0002t0002g0310 a0001c0002t0002g0311 |
2 | HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1450+4830C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229824363 | |||||||
| chr2:229824624 | T | C | 1 | a0001c0001t0005g0015 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1450+4569A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229824624 | |||||||
| chr2:229824625 | G | C | 42 | a0001c0002t0002g0279 a0001c0002t0002g0280 a0001c0002t0002g0281 others(39): Show |
42 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(39): Show |
intron_variant | MODIFIER | c.1450+4568C>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229824625 | |||||||
| chr2:229824715 | C | T | 1 | a0001c0002t0003g0031 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1450+4478G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229824715 | |||||||
| chr2:229824763 | G | C | 1 | a0001c0003t0005g0017 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1450+4430C>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229824763 | |||||||
| chr2:229824830 | G | A | 2 | a0001c0001t0012g0140 a0001c0001t0012g0168 |
2 | HG00639.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.1450+4363C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229824830 | |||||||
| chr2:229824857 | A | G | 24 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0099 others(21): Show |
25 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.1450+4336T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229824857 | |||||||
| chr2:229825196 | T | C | 1 | a0001c0008t0001g0267 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1450+3997A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229825196 | |||||||
| chr2:229825500 | G | C | 2 | a0001c0002t0002g0310 a0001c0002t0002g0311 |
2 | HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1450+3693C>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229825500 | |||||||
| chr2:229825961 | C | T | 22 | a0001c0001t0001g0099 a0001c0001t0001g0153 a0001c0001t0001g0215 others(19): Show |
23 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.1450+3232G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229825961 | |||||||
| chr2:229826121 | GAGA | G | 3 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0005g0003 |
3 | HG02145.hp2 HG02257.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1450+3069_1450+307 others(7): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229826121 | |||||||
| chr2:229826228 | C | A | 1 | a0001c0001t0001g0275 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1450+2965G>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229826228 | |||||||
| chr2:229826296 | C | T | 5 | a0001c0001t0011g0098 a0001c0001t0011g0114 a0001c0001t0011g0187 others(2): Show |
5 | HG01884.hp1 HG02723.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1450+2897G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229826296 | |||||||
| chr2:229826324 | C | A | 1 | a0001c0001t0004g0262 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1450+2869G>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229826324 | |||||||
| chr2:229826378 | C | G | 2 | a0001c0001t0001g0093 a0001c0001t0001g0094 |
2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1450+2815G>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229826378 | |||||||
| chr2:229826539 | A | T | 1 | a0001c0002t0028g0081 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1450+2654T>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229826539 | |||||||
| chr2:229826642 | T | C | 7 | a0001c0001t0001g0153 a0001c0001t0001g0215 a0001c0001t0001g0227 others(4): Show |
7 | HG02486.hp2 HG02895.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1450+2551A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229826642 | |||||||
| chr2:229827154 | C | A | 150 | a0001c0001t0001g0097 a0001c0001t0001g0105 a0001c0001t0001g0106 others(147): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.1450+2039G>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229827154 | |||||||
| chr2:229827186 | A | C | 5 | a0001c0001t0010g0249 a0001c0001t0010g0250 a0001c0001t0010g0251 others(2): Show |
5 | HG00741.hp2 HG01106.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1450+2007T>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229827186 | |||||||
| chr2:229827195 | G | A | 1 | a0001c0002t0013g0005 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1450+1998C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229827195 | |||||||
| chr2:229827481 | T | A | 62 | a0001c0001t0001g0120 a0001c0001t0010g0253 a0001c0001t0014g0108 others(59): Show |
62 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(59): Show |
intron_variant | MODIFIER | c.1450+1712A>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229827481 | |||||||
| chr2:229827526 | G | A | 1 | a0001c0001t0005g0015 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1450+1667C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229827526 | |||||||
| chr2:229827558 | T | A | 2 | a0001c0001t0001g0099 a0001c0001t0005g0011 |
2 | HG02055.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1450+1635A>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229827558 | |||||||
| chr2:229827616 | G | C | 1 | a0001c0001t0001g0269 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1450+1577C>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229827616 | |||||||
| chr2:229827660 | C | T | 316 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0093 others(313): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.1450+1533G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229827660 | |||||||
| chr2:229827704 | T | C | 24 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0099 others(21): Show |
25 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.1450+1489A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229827704 | |||||||
| chr2:229827834 | A | T | 106 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0099 others(103): Show |
107 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.1450+1359T>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229827834 | |||||||
| chr2:229827863 | G | C | 3 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0005g0003 |
3 | HG02145.hp2 HG02257.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1450+1330C>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229827863 | |||||||
| chr2:229828040 | T | C | 7 | a0001c0002t0001g0029 a0001c0002t0001g0059 a0001c0002t0001g0075 others(4): Show |
7 | HG01070.hp2 HG01071.hp2 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.1450+1153A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229828040 | |||||||
| chr2:229828342 | GT | G | 59 | a0001c0001t0001g0124 a0001c0001t0001g0154 a0001c0002t0002g0298 others(56): Show |
59 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(56): Show |
intron_variant | MODIFIER | c.1450+850delA | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229828342 | |||||||
| chr2:229828494 | G | A | 316 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0093 others(313): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.1450+699C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229828494 | |||||||
| chr2:229828568 | T | G | 1 | a0001c0002t0003g0043 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1450+625A>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229828568 | |||||||
| chr2:229828628 | G | A | 2 | a0001c0001t0019g0317 a0001c0001t0019g0318 |
2 | HG02257.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.1450+565C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229828628 | |||||||
| chr2:229828771 | A | AAT | 5 | a0001c0001t0010g0249 a0001c0001t0010g0250 a0001c0001t0010g0251 others(2): Show |
5 | HG00741.hp2 HG01106.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1450+421_1450+422i others(4): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229828771 | |||||||
| chr2:229828773 | A | T | 309 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0093 others(306): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.1450+420T>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229828773 | |||||||
| chr2:229828787 | A | T | 1 | a0001c0001t0001g0133 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1450+406T>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229828787 | |||||||
| chr2:229829412 | G | C | 2 | a0001c0001t0001g0099 a0001c0001t0005g0011 |
2 | HG02055.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1355-124C>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 7/41 | chr2 | 229829412 | |||||||
| chr2:229829446 | C | T | 2 | a0001c0002t0001g0027 a0001c0002t0001g0054 |
2 | NA18954.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.1355-158G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 7/41 | chr2 | 229829446 | |||||||
| chr2:229829696 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1355-408G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 7/41 | chr2 | 229829696 | |||||||
| chr2:229830076 | A | C | 3 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0005g0003 |
3 | HG02145.hp2 HG02257.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1354+680T>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 7/41 | chr2 | 229830076 | |||||||
| chr2:229830079 | C | T | 25 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0099 others(22): Show |
26 | HG00639.hp2 HG01243.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.1354+677G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 7/41 | chr2 | 229830079 | |||||||
| chr2:229830294 | T | A | 1 | a0001c0002t0034g0256 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1354+462A>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 7/41 | chr2 | 229830294 | |||||||
| chr2:229830532 | A | T | 1 | a0001c0003t0006g0324 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1354+224T>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 7/41 | chr2 | 229830532 | |||||||
| chr2:229830742 | A | C | 2 | a0001c0002t0002g0299 a0001c0002t0002g0300 |
2 | HG01496.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1354+14T>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 7/41 | chr2 | 229830742 | |||||||
| chr2:229831139 | T | C | 7 | a0001c0001t0001g0153 a0001c0001t0001g0215 a0001c0001t0001g0227 others(4): Show |
7 | HG02486.hp2 HG02895.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1271-300A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 6/41 | chr2 | 229831139 | |||||||
| chr2:229831156 | A | C | 1 | a0001c0002t0003g0068 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1271-317T>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 6/41 | chr2 | 229831156 | |||||||
| chr2:229831205 | A | G | 1 | a0001c0002t0018g0313 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1271-366T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 6/41 | chr2 | 229831205 | |||||||
| chr2:229831242 | T | C | 5 | a0001c0001t0001g0116 a0001c0001t0001g0121 a0001c0001t0001g0122 others(2): Show |
5 | HG01070.hp1 HG01081.hp2 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.1271-403A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 6/41 | chr2 | 229831242 | |||||||
| chr2:229831865 | G | GT | 45 | a0001c0001t0011g0098 a0001c0001t0011g0114 a0001c0001t0011g0187 others(42): Show |
45 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(42): Show |
intron_variant | MODIFIER | c.1271-1027dupA | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 6/41 | chr2 | 229831865 | |||||||
| chr2:229831871 | T | G | 1 | a0001c0003t0001g0206 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1271-1032A>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 6/41 | chr2 | 229831871 | |||||||
| chr2:229831873 | TG | T | 24 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0099 others(21): Show |
25 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.1271-1035delC | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 6/41 | chr2 | 229831873 | |||||||
| chr2:229831874 | G | T | 302 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0097 others(299): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.1271-1035C>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 6/41 | chr2 | 229831874 | |||||||
| chr2:229831887 | G | GT | 145 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0127 others(142): Show |
145 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.1271-1049dupA | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 6/41 | chr2 | 229831887 | |||||||
| chr2:229831887 | G | GTT | 58 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0005g0003 others(55): Show |
58 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.1271-1050_1271-104 others(6): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 6/41 | chr2 | 229831887 | |||||||
| chr2:229831891 | T | G | 2 | a0001c0001t0001g0093 a0001c0001t0001g0094 |
2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1271-1052A>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 6/41 | chr2 | 229831891 | |||||||
| chr2:229832276 | C | T | 2 | a0001c0001t0009g0147 a0001c0001t0009g0148 |
2 | HG02280.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1271-1437G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 6/41 | chr2 | 229832276 | |||||||
| chr2:229832305 | C | T | 1 | a0001c0002t0001g0058 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1271-1466G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 6/41 | chr2 | 229832305 | |||||||
| chr2:229832410 | C | T | 2 | a0001c0001t0001g0093 a0001c0001t0001g0094 |
2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1271-1571G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 6/41 | chr2 | 229832410 | |||||||
| chr2:229832421 | A | G | 1 | a0001c0001t0004g0263 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1271-1582T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 6/41 | chr2 | 229832421 | |||||||
| chr2:229832853 | T | G | 2 | a0001c0001t0001g0138 a0001c0001t0001g0276 |
2 | HG01516.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1271-2014A>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 6/41 | chr2 | 229832853 | |||||||
| chr2:229832862 | T | C | 2 | a0001c0001t0001g0093 a0001c0001t0001g0094 |
2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1271-2023A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 6/41 | chr2 | 229832862 | |||||||
| chr2:229832986 | A | C | 24 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0099 others(21): Show |
25 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.1271-2147T>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 6/41 | chr2 | 229832986 | |||||||
| chr2:229833143 | G | A | 41 | a0001c0002t0002g0279 a0001c0002t0002g0280 a0001c0002t0002g0281 others(38): Show |
41 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(38): Show |
intron_variant | MODIFIER | c.1271-2304C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 6/41 | chr2 | 229833143 | |||||||
| chr2:229833169 | G | A | 3 | a0001c0002t0003g0042 a0001c0002t0003g0043 a0001c0002t0003g0272 |
3 | HG00642.hp1 HG01255.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.1271-2330C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 6/41 | chr2 | 229833169 | |||||||
| chr2:229833345 | G | A | 1 | a0001c0002t0003g0051 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1271-2506C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 6/41 | chr2 | 229833345 | |||||||
| chr2:229833382 | G | T | 1 | a0001c0002t0003g0045 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1271-2543C>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 6/41 | chr2 | 229833382 | |||||||
| chr2:229833629 | G | A | 1 | a0001c0009t0007g0103 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1271-2790C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 6/41 | chr2 | 229833629 | |||||||
| chr2:229833640 | G | A | 1 | a0001c0001t0001g0231 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1271-2801C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 6/41 | chr2 | 229833640 | |||||||
| chr2:229833651 | G | A | 3 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0005g0003 |
3 | HG02145.hp2 HG02257.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1271-2812C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 6/41 | chr2 | 229833651 | |||||||
| chr2:229833738 | ATATGAGT | A | 3 | a0001c0001t0001g0132 a0001c0001t0001g0138 a0001c0001t0001g0276 |
3 | HG00621.hp2 HG01516.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1271-2906_1271-290 others(11): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 6/41 | chr2 | 229833738 | |||||||
| chr2:229833969 | T | C | 3 | a0001c0001t0014g0107 a0001c0001t0014g0108 a0001c0001t0014g0112 |
3 | HG02717.hp1 HG02818.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1270+2879A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 6/41 | chr2 | 229833969 | |||||||
| chr2:229834295 | A | T | 1 | a0001c0002t0001g0027 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1270+2553T>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 6/41 | chr2 | 229834295 | |||||||
| chr2:229834313 | G | A | 1 | a0001c0001t0001g0105 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1270+2535C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 6/41 | chr2 | 229834313 | |||||||
| chr2:229834365 | T | C | 6 | a0001c0001t0001g0242 a0001c0001t0001g0243 a0001c0001t0001g0244 others(3): Show |
6 | HG02109.hp2 HG02809.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1270+2483A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 6/41 | chr2 | 229834365 | |||||||
| chr2:229834555 | T | G | 1 | a0001c0003t0001g0191 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1270+2293A>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 6/41 | chr2 | 229834555 | |||||||
| chr2:229834568 | C | T | 2 | a0001c0002t0003g0079 a0001c0002t0028g0081 |
2 | HG03704.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1270+2280G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 6/41 | chr2 | 229834568 | |||||||
| chr2:229834569 | G | C | 2 | a0001c0001t0019g0317 a0001c0001t0019g0318 |
2 | HG02257.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.1270+2279C>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 6/41 | chr2 | 229834569 | |||||||
| chr2:229834891 | A | G | 19 | a0001c0002t0003g0032 a0001c0002t0003g0046 a0001c0002t0008g0039 others(16): Show |
19 | HG01358.hp1 HG01891.hp1 HG02056.hp1 others(16): Show |
intron_variant | MODIFIER | c.1270+1957T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 6/41 | chr2 | 229834891 | |||||||
| chr2:229834945 | A | G | 5 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0127 others(2): Show |
5 | HG02258.hp1 HG02622.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1270+1903T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 6/41 | chr2 | 229834945 | |||||||
| chr2:229834965 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1270+1883G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 6/41 | chr2 | 229834965 | |||||||
| chr2:229835075 | A | G | 4 | a0001c0002t0002g0283 a0001c0002t0002g0285 a0001c0002t0002g0290 others(1): Show |
4 | HG01952.hp1 HG01975.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.1270+1773T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 6/41 | chr2 | 229835075 | |||||||
| chr2:229835226 | G | A | 5 | a0001c0001t0009g0146 a0001c0001t0009g0147 a0001c0001t0009g0148 others(2): Show |
5 | HG02280.hp2 HG02559.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1270+1622C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 6/41 | chr2 | 229835226 | |||||||
| chr2:229835335 | G | A | 3 | a0001c0001t0001g0175 a0001c0001t0001g0188 a0001c0001t0001g0189 |
3 | HG02615.hp2 HG02723.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1270+1513C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 6/41 | chr2 | 229835335 | |||||||
| chr2:229835371 | G | A | 2 | a0001c0001t0001g0093 a0001c0001t0001g0094 |
2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1270+1477C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 6/41 | chr2 | 229835371 | |||||||
| chr2:229835399 | A | G | 3 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0278 |
3 | NA18945.hp1 NA18953.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.1270+1449T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 6/41 | chr2 | 229835399 | |||||||
| chr2:229835490 | T | C | 6 | a0001c0002t0003g0024 a0001c0002t0003g0025 a0001c0002t0003g0026 others(3): Show |
6 | HG00642.hp1 HG01175.hp2 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.1270+1358A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 6/41 | chr2 | 229835490 | |||||||
| chr2:229835616 | A | T | 1 | a0001c0001t0001g0223 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1270+1232T>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 6/41 | chr2 | 229835616 | |||||||
| chr2:229835693 | T | C | 2 | a0001c0001t0001g0269 a0001c0001t0009g0268 |
2 | HG00639.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.1270+1155A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 6/41 | chr2 | 229835693 | |||||||
| chr2:229835791 | C | A | 1 | a0001c0001t0001g0137 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1270+1057G>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 6/41 | chr2 | 229835791 | |||||||
| chr2:229835796 | G | C | 1 | a0001c0003t0007g0202 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1270+1052C>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 6/41 | chr2 | 229835796 | |||||||
| chr2:229836019 | C | A | 5 | a0001c0003t0001g0158 a0001c0003t0001g0200 a0001c0003t0001g0207 others(2): Show |
5 | NA18954.hp2 NA18993.hp1 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.1270+829G>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 6/41 | chr2 | 229836019 | |||||||
| chr2:229836019 | CAAG | C | 3 | a0001c0001t0014g0107 a0001c0001t0014g0108 a0001c0001t0014g0112 |
3 | HG02717.hp1 HG02818.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1270+826_1270+828d others(5): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 6/41 | chr2 | 229836019 | |||||||
| chr2:229836081 | C | A | 1 | a0001c0004t0003g0084 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1270+767G>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 6/41 | chr2 | 229836081 | |||||||
| chr2:229836278 | G | A | 17 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0099 others(14): Show |
18 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.1270+570C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 6/41 | chr2 | 229836278 | |||||||
| chr2:229836329 | C | T | 1 | a0001c0002t0001g0089 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1270+519G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 6/41 | chr2 | 229836329 | |||||||
| chr2:229836452 | C | G | 78 | a0001c0002t0001g0027 a0001c0002t0001g0028 a0001c0002t0001g0029 others(75): Show |
78 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.1270+396G>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 6/41 | chr2 | 229836452 | |||||||
| chr2:229836785 | C | A | 33 | a0001c0001t0001g0097 a0001c0001t0001g0105 a0001c0001t0001g0124 others(30): Show |
33 | HG00408.hp1 HG00558.hp2 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.1270+63G>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 6/41 | chr2 | 229836785 | |||||||
| chr2:229837090 | C | T | 6 | a0001c0002t0001g0029 a0001c0002t0001g0059 a0001c0002t0001g0075 others(3): Show |
6 | HG01070.hp2 HG01071.hp2 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.1134-106G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 5/41 | chr2 | 229837090 | |||||||
| chr2:229837107 | A | G | 2 | a0001c0002t0001g0053 a0001c0002t0001g0056 |
2 | HG00544.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.1134-123T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 5/41 | chr2 | 229837107 | |||||||
| chr2:229837191 | C | T | 1 | a0001c0002t0035g0297 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1134-207G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 5/41 | chr2 | 229837191 | |||||||
| chr2:229837194 | G | A | 1 | a0001c0001t0027g0169 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1134-210C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 5/41 | chr2 | 229837194 | |||||||
| chr2:229837237 | G | T | 4 | a0001c0003t0001g0158 a0001c0003t0001g0200 a0001c0003t0001g0216 others(1): Show |
4 | NA18954.hp2 NA18993.hp1 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.1134-253C>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 5/41 | chr2 | 229837237 | |||||||
| chr2:229837710 | G | A | 4 | a0001c0001t0001g0120 a0001c0001t0014g0107 a0001c0001t0014g0108 others(1): Show |
4 | HG02717.hp1 HG02818.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1134-726C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 5/41 | chr2 | 229837710 | |||||||
| chr2:229837922 | T | G | 79 | a0001c0002t0001g0027 a0001c0002t0001g0028 a0001c0002t0001g0029 others(76): Show |
79 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.1134-938A>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 5/41 | chr2 | 229837922 | |||||||
| chr2:229838354 | G | C | 1 | a0001c0001t0001g0167 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1134-1370C>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 5/41 | chr2 | 229838354 | |||||||
| chr2:229838563 | G | C | 2 | a0001c0001t0019g0317 a0001c0001t0019g0318 |
2 | HG02257.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.1134-1579C>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 5/41 | chr2 | 229838563 | |||||||
| chr2:229838800 | A | G | 1 | a0001c0003t0006g0326 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1134-1816T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 5/41 | chr2 | 229838800 | |||||||
| chr2:229838910 | G | A | 317 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0093 others(314): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.1133+1912C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 5/41 | chr2 | 229838910 | |||||||
| chr2:229838917 | T | A | 1 | a0001c0002t0001g0063 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1133+1905A>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 5/41 | chr2 | 229838917 | |||||||
| chr2:229838953 | G | A | 1 | a0001c0002t0001g0063 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1133+1869C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 5/41 | chr2 | 229838953 | |||||||
| chr2:229839005 | C | A | 1 | a0001c0002t0002g0311 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1133+1817G>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 5/41 | chr2 | 229839005 | |||||||
| chr2:229839058 | A | G | 103 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0153 others(100): Show |
104 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.1133+1764T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 5/41 | chr2 | 229839058 | |||||||
| chr2:229839059 | T | C | 152 | a0001c0001t0001g0097 a0001c0001t0001g0105 a0001c0001t0001g0106 others(149): Show |
152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.1133+1763A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 5/41 | chr2 | 229839059 | |||||||
| chr2:229839107 | G | A | 3 | a0001c0001t0014g0107 a0001c0001t0014g0108 a0001c0001t0014g0112 |
3 | HG02717.hp1 HG02818.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1133+1715C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 5/41 | chr2 | 229839107 | |||||||
| chr2:229839191 | G | A | 1 | a0001c0002t0003g0031 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1133+1631C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 5/41 | chr2 | 229839191 | |||||||
| chr2:229839192 | G | T | 1 | a0001c0001t0001g0192 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1133+1630C>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 5/41 | chr2 | 229839192 | |||||||
| chr2:229839198 | C | A | 1 | a0001c0002t0034g0256 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1133+1624G>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 5/41 | chr2 | 229839198 | |||||||
| chr2:229839443 | C | T | 2 | a0001c0003t0007g0159 a0001c0003t0007g0222 |
2 | HG00280.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.1133+1379G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 5/41 | chr2 | 229839443 | |||||||
| chr2:229839444 | G | A | 7 | a0001c0001t0001g0099 a0001c0001t0005g0011 a0001c0001t0011g0098 others(4): Show |
7 | HG01884.hp1 HG02055.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1133+1378C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 5/41 | chr2 | 229839444 | |||||||
| chr2:229839556 | A | G | 267 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0093 others(264): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.1133+1266T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 5/41 | chr2 | 229839556 | |||||||
| chr2:229839571 | C | T | 5 | a0001c0001t0009g0146 a0001c0001t0009g0147 a0001c0001t0009g0148 others(2): Show |
5 | HG02280.hp2 HG02559.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1133+1251G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 5/41 | chr2 | 229839571 | |||||||
| chr2:229839628 | G | A | 2 | a0001c0001t0019g0317 a0001c0001t0019g0318 |
2 | HG02257.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.1133+1194C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 5/41 | chr2 | 229839628 | |||||||
| chr2:229839640 | T | C | 1 | a0001c0002t0028g0081 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1133+1182A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 5/41 | chr2 | 229839640 | |||||||
| chr2:229839795 | C | T | 1 | a0001c0001t0004g0262 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1133+1027G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 5/41 | chr2 | 229839795 | |||||||
| chr2:229839867 | T | C | 1 | a0001c0003t0001g0198 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1133+955A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 5/41 | chr2 | 229839867 | |||||||
| chr2:229840069 | G | T | 3 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0005g0003 |
3 | HG02145.hp2 HG02257.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1133+753C>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 5/41 | chr2 | 229840069 | |||||||
| chr2:229840132 | C | T | 1 | a0001c0001t0004g0257 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1133+690G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 5/41 | chr2 | 229840132 | |||||||
| chr2:229840230 | C | T | 263 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0093 others(260): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.1133+592G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 5/41 | chr2 | 229840230 | |||||||
| chr2:229840418 | A | C | 1 | a0001c0002t0002g0279 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1133+404T>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 5/41 | chr2 | 229840418 | |||||||
| chr2:229840424 | G | A | 2 | a0001c0001t0019g0317 a0001c0001t0019g0318 |
2 | HG02257.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.1133+398C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 5/41 | chr2 | 229840424 | |||||||
| chr2:229840800 | T | TA | 29 | a0001c0001t0001g0023 a0001c0001t0001g0093 a0001c0001t0001g0094 others(26): Show |
30 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.1133+21dupT | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 5/41 | chr2 | 229840800 | |||||||
| chr2:229840800 | TA | T | 79 | a0001c0001t0001g0192 a0001c0002t0001g0027 a0001c0002t0001g0028 others(76): Show |
79 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.1133+21delT | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 5/41 | chr2 | 229840800 | |||||||
| chr2:229841867 | G | A | 1 | a0001c0002t0001g0033 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1028-940C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229841867 | |||||||
| chr2:229841950 | C | A | 1 | a0001c0002t0002g0296 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1028-1023G>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229841950 | |||||||
| chr2:229842535 | A | G | 1 | a0001c0003t0001g0113 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1028-1608T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229842535 | |||||||
| chr2:229842698 | AC | A | 89 | a0001c0001t0001g0097 a0001c0001t0001g0105 a0001c0001t0001g0106 others(86): Show |
89 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.1028-1772delG | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229842698 | |||||||
| chr2:229842938 | T | C | 1 | a0001c0002t0002g0296 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1028-2011A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229842938 | |||||||
| chr2:229842971 | C | T | 8 | a0001c0004t0003g0082 a0001c0004t0003g0083 a0001c0004t0003g0084 others(5): Show |
8 | HG02056.hp1 HG02129.hp2 NA18951.hp1 others(5): Show |
intron_variant | MODIFIER | c.1028-2044G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229842971 | |||||||
| chr2:229843050 | TTC | T | 3 | a0001c0001t0014g0107 a0001c0001t0014g0108 a0001c0001t0014g0112 |
3 | HG02717.hp1 HG02818.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1028-2125_1028-212 others(6): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229843050 | |||||||
| chr2:229843069 | A | C | 314 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0093 others(311): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.1028-2142T>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229843069 | |||||||
| chr2:229843071 | T | C | 3 | a0001c0001t0014g0107 a0001c0001t0014g0108 a0001c0001t0014g0112 |
3 | HG02717.hp1 HG02818.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1028-2144A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229843071 | |||||||
| chr2:229843503 | G | A | 1 | a0001c0001t0005g0015 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1028-2576C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229843503 | |||||||
| chr2:229843580 | A | G | 152 | a0001c0001t0001g0097 a0001c0001t0001g0105 a0001c0001t0001g0106 others(149): Show |
152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.1028-2653T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229843580 | |||||||
| chr2:229843933 | A | C | 1 | a0001c0001t0001g0120 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1028-3006T>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229843933 | |||||||
| chr2:229843958 | T | TA | 7 | a0001c0001t0001g0119 a0001c0001t0009g0146 a0001c0001t0009g0147 others(4): Show |
7 | HG02280.hp2 HG02559.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1028-3032dupT | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229843958 | |||||||
| chr2:229843959 | A | T | 3 | a0001c0004t0003g0082 a0001c0004t0003g0084 a0001c0004t0003g0086 |
3 | HG02056.hp1 HG02129.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1028-3032T>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229843959 | |||||||
| chr2:229844011 | C | A | 3 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0005g0003 |
3 | HG02145.hp2 HG02257.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1028-3084G>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229844011 | |||||||
| chr2:229844163 | T | C | 3 | a0001c0001t0014g0107 a0001c0001t0014g0108 a0001c0001t0014g0112 |
3 | HG02717.hp1 HG02818.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1028-3236A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229844163 | |||||||
| chr2:229844366 | A | G | 2 | a0001c0001t0001g0093 a0001c0001t0001g0094 |
2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1028-3439T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229844366 | |||||||
| chr2:229844482 | A | G | 89 | a0001c0001t0001g0097 a0001c0001t0001g0105 a0001c0001t0001g0106 others(86): Show |
89 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.1028-3555T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229844482 | |||||||
| chr2:229844483 | T | G | 1 | a0001c0001t0009g0268 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1028-3556A>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229844483 | |||||||
| chr2:229844733 | ATCT | A | 78 | a0001c0002t0001g0027 a0001c0002t0001g0028 a0001c0002t0001g0029 others(75): Show |
78 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.1028-3809_1028-380 others(7): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229844733 | |||||||
| chr2:229844869 | A | C | 7 | a0001c0003t0001g0113 a0001c0003t0001g0191 a0001c0003t0001g0194 others(4): Show |
7 | HG02056.hp2 NA18944.hp2 NA18971.hp1 others(4): Show |
intron_variant | MODIFIER | c.1028-3942T>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229844869 | |||||||
| chr2:229844871 | T | C | 1 | a0001c0003t0007g0238 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1028-3944A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229844871 | |||||||
| chr2:229845206 | T | C | 1 | a0001c0001t0001g0175 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1028-4279A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229845206 | |||||||
| chr2:229845208 | G | C | 3 | a0001c0001t0004g0261 a0001c0001t0004g0264 a0001c0001t0004g0265 |
3 | HG02145.hp1 HG02486.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1028-4281C>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229845208 | |||||||
| chr2:229845334 | C | G | 1 | a0001c0001t0001g0244 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1028-4407G>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229845334 | |||||||
| chr2:229845377 | A | T | 3 | a0001c0001t0004g0261 a0001c0001t0004g0264 a0001c0001t0004g0265 |
3 | HG02145.hp1 HG02486.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1028-4450T>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229845377 | |||||||
| chr2:229845532 | G | C | 79 | a0001c0002t0001g0027 a0001c0002t0001g0028 a0001c0002t0001g0029 others(76): Show |
79 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.1028-4605C>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229845532 | |||||||
| chr2:229845673 | T | C | 1 | a0001c0002t0001g0064 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1028-4746A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229845673 | |||||||
| chr2:229845759 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1028-4832G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229845759 | |||||||
| chr2:229845843 | T | C | 17 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0099 others(14): Show |
18 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.1028-4916A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229845843 | |||||||
| chr2:229845866 | GA | G | 205 | a0001c0001t0001g0097 a0001c0001t0001g0105 a0001c0001t0001g0106 others(202): Show |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.1028-4940delT | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229845866 | |||||||
| chr2:229845956 | C | T | 1 | a0001c0002t0002g0305 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1028-5029G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229845956 | |||||||
| chr2:229845998 | G | T | 1 | a0001c0001t0001g0181 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1028-5071C>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229845998 | |||||||
| chr2:229846014 | C | CA | 17 | a0001c0001t0001g0022 a0001c0001t0001g0093 a0001c0001t0001g0094 others(14): Show |
17 | HG01168.hp2 HG01257.hp2 HG01515.hp2 others(14): Show |
intron_variant | MODIFIER | c.1028-5088dupT | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229846014 | |||||||
| chr2:229846014 | C | CAA | 72 | a0001c0001t0001g0153 a0001c0002t0001g0027 a0001c0002t0001g0028 others(69): Show |
72 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.1028-5089_1028-508 others(6): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229846014 | |||||||
| chr2:229846014 | CA | C | 146 | a0001c0001t0001g0097 a0001c0001t0001g0105 a0001c0001t0001g0106 others(143): Show |
146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.1028-5088delT | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229846014 | |||||||
| chr2:229846055 | G | A | 1 | a0001c0002t0013g0008 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1028-5128C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229846055 | |||||||
| chr2:229846292 | TG | T | 15 | a0001c0001t0001g0099 a0001c0001t0004g0001 a0001c0001t0004g0254 others(12): Show |
16 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.1028-5366delC | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229846292 | |||||||
| chr2:229846496 | T | G | 1 | a0001c0001t0001g0136 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1028-5569A>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229846496 | |||||||
| chr2:229846501 | G | A | 1 | a0001c0002t0003g0272 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1028-5574C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229846501 | |||||||
| chr2:229846610 | G | A | 1 | a0001c0002t0003g0043 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1028-5683C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229846610 | |||||||
| chr2:229846674 | T | TA | 206 | a0001c0001t0001g0097 a0001c0001t0001g0105 a0001c0001t0001g0106 others(203): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.1028-5748dupT | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229846674 | |||||||
| chr2:229846752 | G | C | 78 | a0001c0002t0001g0027 a0001c0002t0001g0028 a0001c0002t0001g0029 others(75): Show |
78 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.1028-5825C>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229846752 | |||||||
| chr2:229847311 | C | T | 1 | a0001c0002t0001g0065 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1028-6384G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229847311 | |||||||
| chr2:229847458 | T | G | 42 | a0001c0002t0002g0279 a0001c0002t0002g0280 a0001c0002t0002g0281 others(39): Show |
42 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(39): Show |
intron_variant | MODIFIER | c.1028-6531A>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229847458 | |||||||
| chr2:229847876 | T | C | 1 | a0001c0002t0028g0081 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1028-6949A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229847876 | |||||||
| chr2:229847913 | A | G | 1 | a0001c0002t0001g0055 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1028-6986T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229847913 | |||||||
| chr2:229848079 | C | T | 1 | a0001c0002t0001g0063 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1028-7152G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229848079 | |||||||
| chr2:229848158 | T | C | 2 | a0001c0001t0001g0116 a0001c0001t0001g0152 |
2 | HG01346.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.1028-7231A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229848158 | |||||||
| chr2:229848317 | G | GC | 18 | a0001c0001t0001g0097 a0001c0001t0001g0106 a0001c0001t0001g0120 others(15): Show |
18 | HG00438.hp1 HG00673.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.1028-7391dupG | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229848317 | |||||||
| chr2:229848326 | G | C | 16 | a0001c0001t0001g0183 a0001c0001t0005g0003 a0001c0001t0005g0011 others(13): Show |
16 | HG00544.hp2 HG00642.hp1 HG00673.hp2 others(13): Show |
intron_variant | MODIFIER | c.1028-7399C>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229848326 | |||||||
| chr2:229848326 | G | GC | 52 | a0001c0001t0001g0099 a0001c0001t0001g0124 a0001c0001t0001g0128 others(49): Show |
52 | HG00408.hp2 HG00423.hp1 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.1028-7400dupG | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229848326 | |||||||
| chr2:229848333 | C | A | 1 | a0001c0003t0007g0222 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1028-7406G>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229848333 | |||||||
| chr2:229848334 | C | A | 1 | a0001c0001t0001g0184 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1028-7407G>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229848334 | |||||||
| chr2:229848335 | A | C | 9 | a0001c0001t0001g0099 a0001c0001t0001g0128 a0001c0001t0001g0180 others(6): Show |
9 | HG00673.hp2 HG02055.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1028-7408T>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229848335 | |||||||
| chr2:229848490 | A | G | 1 | a0001c0002t0003g0042 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1028-7563T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229848490 | |||||||
| chr2:229848606 | T | C | 6 | a0001c0003t0001g0091 a0001c0003t0001g0092 a0001c0003t0001g0177 others(3): Show |
6 | HG01109.hp1 HG03130.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.1028-7679A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229848606 | |||||||
| chr2:229848717 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1028-7790C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229848717 | |||||||
| chr2:229848739 | T | C | 2 | a0001c0001t0001g0133 a0001c0001t0001g0183 |
2 | HG01884.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1028-7812A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229848739 | |||||||
| chr2:229849062 | G | A | 2 | a0001c0001t0001g0099 a0001c0001t0005g0011 |
2 | HG02055.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1028-8135C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229849062 | |||||||
| chr2:229849174 | T | C | 1 | a0001c0002t0002g0289 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1028-8247A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229849174 | |||||||
| chr2:229849176 | G | C | 1 | a0001c0002t0001g0027 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1028-8249C>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229849176 | |||||||
| chr2:229849309 | A | G | 44 | a0001c0001t0019g0317 a0001c0001t0019g0318 a0001c0002t0002g0279 others(41): Show |
44 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(41): Show |
intron_variant | MODIFIER | c.1028-8382T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229849309 | |||||||
| chr2:229849320 | C | T | 1 | a0001c0002t0002g0293 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1028-8393G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229849320 | |||||||
| chr2:229849512 | T | A | 326 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0093 others(323): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.1028-8585A>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229849512 | |||||||
| chr2:229849529 | C | T | 17 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0099 others(14): Show |
18 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.1028-8602G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229849529 | |||||||
| chr2:229849617 | C | T | 1 | a0002c0006t0001g0096 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1028-8690G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229849617 | |||||||
| chr2:229849680 | T | G | 1 | a0001c0002t0003g0043 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1028-8753A>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229849680 | |||||||
| chr2:229849700 | A | G | 1 | a0001c0001t0010g0252 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1028-8773T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229849700 | |||||||
| chr2:229849726 | A | T | 1 | a0001c0002t0001g0028 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1028-8799T>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229849726 | |||||||
| chr2:229849809 | G | C | 5 | a0001c0001t0001g0269 a0001c0001t0009g0268 a0001c0001t0014g0107 others(2): Show |
5 | HG00639.hp2 HG02055.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1028-8882C>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229849809 | |||||||
| chr2:229849811 | C | A | 1 | a0001c0002t0002g0279 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1028-8884G>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229849811 | |||||||
| chr2:229849905 | T | C | 17 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0099 others(14): Show |
18 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.1027+8867A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229849905 | |||||||
| chr2:229849916 | T | A | 2 | a0001c0001t0001g0269 a0001c0001t0009g0268 |
2 | HG00639.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.1027+8856A>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229849916 | |||||||
| chr2:229849935 | C | CA | 146 | a0001c0001t0001g0097 a0001c0001t0001g0105 a0001c0001t0001g0106 others(143): Show |
146 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.1027+8836dupT | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229849935 | |||||||
| chr2:229849935 | C | CAA | 59 | a0001c0001t0030g0123 a0001c0003t0001g0091 a0001c0003t0001g0092 others(56): Show |
59 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.1027+8835_1027+883 others(6): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229849935 | |||||||
| chr2:229849935 | CA | C | 13 | a0001c0001t0004g0001 a0001c0001t0004g0254 a0001c0001t0004g0255 others(10): Show |
14 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1027+8836delT | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229849935 | |||||||
| chr2:229850056 | T | G | 7 | a0001c0002t0001g0027 a0001c0002t0001g0052 a0001c0002t0001g0053 others(4): Show |
7 | HG00544.hp2 HG02083.hp2 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.1027+8716A>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229850056 | |||||||
| chr2:229850080 | G | A | 3 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0005g0003 |
3 | HG02145.hp2 HG02257.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1027+8692C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229850080 | |||||||
| chr2:229850215 | C | T | 1 | a0001c0002t0002g0296 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1027+8557G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229850215 | |||||||
| chr2:229850292 | TAA | T | 13 | a0001c0001t0004g0001 a0001c0001t0004g0254 a0001c0001t0004g0255 others(10): Show |
14 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1027+8478_1027+847 others(6): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229850292 | |||||||
| chr2:229850357 | T | A | 2 | a0001c0001t0001g0166 a0001c0001t0001g0167 |
2 | HG02080.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.1027+8415A>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229850357 | |||||||
| chr2:229850527 | T | C | 5 | a0001c0002t0001g0033 a0001c0002t0001g0034 a0001c0002t0001g0063 others(2): Show |
5 | HG00735.hp1 HG01168.hp2 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.1027+8245A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229850527 | |||||||
| chr2:229850575 | C | G | 2 | a0001c0002t0001g0071 a0001c0002t0001g0074 |
2 | HG02027.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.1027+8197G>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229850575 | |||||||
| chr2:229850683 | G | A | 3 | a0001c0002t0003g0024 a0001c0002t0003g0025 a0001c0002t0003g0026 |
3 | HG01175.hp2 HG01257.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.1027+8089C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229850683 | |||||||
| chr2:229850693 | C | T | 58 | a0001c0003t0001g0091 a0001c0003t0001g0092 a0001c0003t0001g0095 others(55): Show |
58 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.1027+8079G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229850693 | |||||||
| chr2:229850789 | G | A | 1 | a0001c0003t0001g0214 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1027+7983C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229850789 | |||||||
| chr2:229850868 | G | T | 2 | a0001c0002t0001g0071 a0001c0002t0001g0074 |
2 | HG02027.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.1027+7904C>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229850868 | |||||||
| chr2:229850869 | C | T | 2 | a0001c0002t0001g0071 a0001c0002t0001g0074 |
2 | HG02027.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.1027+7903G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229850869 | |||||||
| chr2:229851003 | C | G | 1 | a0001c0002t0003g0066 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1027+7769G>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229851003 | |||||||
| chr2:229851075 | C | T | 1 | a0001c0003t0001g0177 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1027+7697G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229851075 | |||||||
| chr2:229851099 | C | T | 1 | a0001c0001t0001g0269 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1027+7673G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229851099 | |||||||
| chr2:229851144 | G | A | 1 | a0001c0003t0001g0207 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1027+7628C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229851144 | |||||||
| chr2:229851210 | T | C | 1 | a0001c0001t0001g0182 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1027+7562A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229851210 | |||||||
| chr2:229851233 | C | T | 1 | a0001c0002t0003g0031 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1027+7539G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229851233 | |||||||
| chr2:229851272 | A | G | 1 | a0001c0002t0008g0044 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1027+7500T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229851272 | |||||||
| chr2:229851316 | G | A | 1 | a0001c0001t0001g0236 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1027+7456C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229851316 | |||||||
| chr2:229851321 | T | A | 2 | a0001c0001t0001g0099 a0001c0001t0005g0011 |
2 | HG02055.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1027+7451A>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229851321 | |||||||
| chr2:229851506 | A | C | 5 | a0001c0001t0001g0269 a0001c0001t0009g0268 a0001c0001t0014g0107 others(2): Show |
5 | HG00639.hp2 HG02055.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1027+7266T>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229851506 | |||||||
| chr2:229851526 | G | C | 1 | a0001c0001t0001g0120 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1027+7246C>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229851526 | |||||||
| chr2:229851529 | C | T | 2 | a0001c0001t0001g0184 a0001c0001t0005g0019 |
2 | HG00597.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.1027+7243G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229851529 | |||||||
| chr2:229851536 | T | C | 1 | a0001c0003t0001g0191 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1027+7236A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229851536 | |||||||
| chr2:229851545 | G | A | 4 | a0001c0002t0002g0283 a0001c0002t0002g0285 a0001c0002t0002g0290 others(1): Show |
4 | HG01952.hp1 HG01975.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.1027+7227C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229851545 | |||||||
| chr2:229851789 | G | A | 1 | a0001c0001t0001g0269 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1027+6983C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229851789 | |||||||
| chr2:229851822 | C | A | 1 | a0001c0002t0003g0272 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1027+6950G>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229851822 | |||||||
| chr2:229851824 | G | A | 5 | a0001c0001t0011g0098 a0001c0001t0011g0114 a0001c0001t0011g0187 others(2): Show |
5 | HG01884.hp1 HG02723.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1027+6948C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229851824 | |||||||
| chr2:229851857 | C | T | 2 | a0001c0003t0006g0323 a0001c0003t0006g0325 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1027+6915G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229851857 | |||||||
| chr2:229852003 | C | T | 2 | a0001c0001t0001g0093 a0001c0001t0001g0094 |
2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1027+6769G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229852003 | |||||||
| chr2:229852116 | A | T | 1 | a0001c0001t0001g0211 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1027+6656T>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229852116 | |||||||
| chr2:229852209 | A | C | 1 | a0001c0001t0001g0211 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1027+6563T>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229852209 | |||||||
| chr2:229852218 | T | A | 1 | a0001c0001t0001g0211 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1027+6554A>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229852218 | |||||||
| chr2:229852220 | A | G | 1 | a0001c0001t0001g0211 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1027+6552T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229852220 | |||||||
| chr2:229852227 | T | A | 1 | a0001c0001t0001g0211 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1027+6545A>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229852227 | |||||||
| chr2:229852231 | C | G | 1 | a0001c0001t0001g0211 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1027+6541G>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229852231 | |||||||
| chr2:229852234 | T | G | 1 | a0001c0001t0001g0211 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1027+6538A>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229852234 | |||||||
| chr2:229852235 | A | T | 1 | a0001c0001t0001g0211 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1027+6537T>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229852235 | |||||||
| chr2:229852244 | G | A | 1 | a0001c0001t0001g0211 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1027+6528C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229852244 | |||||||
| chr2:229852245 | C | T | 1 | a0001c0001t0001g0211 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1027+6527G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229852245 | |||||||
| chr2:229852265 | TTTTCTAT others(3): Show |
T | 1 | a0001c0001t0001g0211 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1027+6497_1027+650 others(14): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229852265 | |||||||
| chr2:229852278 | G | A | 1 | a0001c0001t0001g0211 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1027+6494C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229852278 | |||||||
| chr2:229852292 | T | A | 42 | a0001c0002t0002g0279 a0001c0002t0002g0280 a0001c0002t0002g0281 others(39): Show |
42 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(39): Show |
intron_variant | MODIFIER | c.1027+6480A>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229852292 | |||||||
| chr2:229852364 | A | T | 6 | a0001c0001t0001g0269 a0001c0001t0009g0268 a0001c0003t0001g0177 others(3): Show |
6 | HG00639.hp2 HG01109.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.1027+6408T>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229852364 | |||||||
| chr2:229852410 | T | C | 2 | a0001c0001t0001g0099 a0001c0001t0005g0011 |
2 | HG02055.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1027+6362A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229852410 | |||||||
| chr2:229852457 | A | G | 1 | a0001c0002t0002g0283 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1027+6315T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229852457 | |||||||
| chr2:229852511 | T | C | 1 | a0001c0001t0001g0156 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1027+6261A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229852511 | |||||||
| chr2:229852689 | A | G | 7 | a0001c0001t0001g0153 a0001c0001t0001g0215 a0001c0001t0001g0227 others(4): Show |
7 | HG02486.hp2 HG02895.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1027+6083T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229852689 | |||||||
| chr2:229852864 | T | C | 1 | a0001c0001t0010g0252 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1027+5908A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229852864 | |||||||
| chr2:229852946 | G | T | 78 | a0001c0002t0001g0027 a0001c0002t0001g0028 a0001c0002t0001g0029 others(75): Show |
78 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.1027+5826C>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229852946 | |||||||
| chr2:229853267 | T | C | 1 | a0001c0001t0001g0125 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1027+5505A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229853267 | |||||||
| chr2:229853487 | G | C | 269 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0093 others(266): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.1027+5285C>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229853487 | |||||||
| chr2:229853565 | G | A | 3 | a0001c0001t0014g0107 a0001c0001t0014g0108 a0001c0001t0014g0112 |
3 | HG02717.hp1 HG02818.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1027+5207C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229853565 | |||||||
| chr2:229853679 | A | AATAC | 7 | a0001c0002t0002g0296 a0001c0002t0002g0305 a0001c0002t0002g0306 others(4): Show |
7 | HG00323.hp2 HG01071.hp1 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.1027+5089_1027+509 others(8): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229853679 | |||||||
| chr2:229853679 | AATACATA others(1): Show |
A | 90 | a0001c0001t0001g0097 a0001c0001t0001g0105 a0001c0001t0001g0106 others(87): Show |
90 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.1027+5085_1027+509 others(12): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229853679 | |||||||
| chr2:229853865 | A | C | 1 | a0001c0002t0003g0062 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1027+4907T>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229853865 | |||||||
| chr2:229853946 | A | G | 2 | a0001c0001t0001g0269 a0001c0001t0009g0268 |
2 | HG00639.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.1027+4826T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229853946 | |||||||
| chr2:229854017 | G | C | 7 | a0001c0001t0001g0153 a0001c0001t0001g0215 a0001c0001t0001g0227 others(4): Show |
7 | HG02486.hp2 HG02895.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1027+4755C>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229854017 | |||||||
| chr2:229854165 | C | G | 57 | a0001c0003t0001g0091 a0001c0003t0001g0092 a0001c0003t0001g0095 others(54): Show |
57 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(54): Show |
intron_variant | MODIFIER | c.1027+4607G>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229854165 | |||||||
| chr2:229854319 | T | C | 1 | a0001c0002t0003g0080 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1027+4453A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229854319 | |||||||
| chr2:229854436 | A | G | 3 | a0001c0004t0003g0082 a0001c0004t0003g0084 a0001c0004t0003g0086 |
3 | HG02056.hp1 HG02129.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1027+4336T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229854436 | |||||||
| chr2:229854447 | T | A | 2 | a0001c0002t0002g0299 a0001c0002t0002g0300 |
2 | HG01496.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1027+4325A>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229854447 | |||||||
| chr2:229854840 | A | C | 5 | a0001c0001t0009g0146 a0001c0001t0009g0147 a0001c0001t0009g0148 others(2): Show |
5 | HG02280.hp2 HG02559.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1027+3932T>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229854840 | |||||||
| chr2:229855031 | C | T | 9 | a0001c0002t0002g0296 a0001c0002t0002g0298 a0001c0002t0002g0305 others(6): Show |
9 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(6): Show |
intron_variant | MODIFIER | c.1027+3741G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229855031 | |||||||
| chr2:229855185 | T | C | 1 | a0001c0002t0003g0272 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1027+3587A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229855185 | |||||||
| chr2:229855543 | T | C | 1 | a0001c0003t0005g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1027+3229A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229855543 | |||||||
| chr2:229855603 | T | TA | 8 | a0001c0001t0001g0120 a0001c0001t0004g0001 a0001c0001t0004g0258 others(5): Show |
9 | HG01243.hp1 HG02109.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1027+3168dupT | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229855603 | |||||||
| chr2:229855619 | A | G | 1 | a0001c0001t0001g0195 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1027+3153T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229855619 | |||||||
| chr2:229855620 | A | G | 1 | a0001c0001t0001g0189 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1027+3152T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229855620 | |||||||
| chr2:229855621 | A | G | 8 | a0001c0001t0001g0269 a0001c0001t0009g0268 a0001c0001t0012g0139 others(5): Show |
8 | HG00639.hp1 HG00639.hp2 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.1027+3151T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229855621 | |||||||
| chr2:229855622 | AAAG | A | 14 | a0001c0001t0001g0105 a0001c0001t0001g0122 a0001c0001t0001g0124 others(11): Show |
14 | HG00099.hp1 HG00733.hp2 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.1027+3147_1027+314 others(7): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229855622 | |||||||
| chr2:229855623 | AAG | A | 85 | a0001c0001t0001g0097 a0001c0001t0001g0106 a0001c0001t0001g0116 others(82): Show |
85 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.1027+3147_1027+314 others(6): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229855623 | |||||||
| chr2:229855624 | AG | A | 90 | a0001c0001t0001g0099 a0001c0001t0001g0175 a0001c0001t0001g0197 others(87): Show |
90 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.1027+3147delC | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229855624 | |||||||
| chr2:229855625 | G | A | 134 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0093 others(131): Show |
135 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.1027+3147C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229855625 | |||||||
| chr2:229855677 | T | A | 5 | a0001c0001t0001g0153 a0001c0001t0001g0227 a0001c0001t0001g0229 others(2): Show |
5 | HG02895.hp2 HG02897.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.1027+3095A>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229855677 | |||||||
| chr2:229855716 | G | A | 1 | a0001c0002t0002g0319 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1027+3056C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229855716 | |||||||
| chr2:229855753 | T | C | 1 | a0001c0001t0001g0174 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1027+3019A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229855753 | |||||||
| chr2:229856041 | GA | G | 14 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0004g0001 others(11): Show |
15 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.1027+2730delT | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229856041 | |||||||
| chr2:229856075 | A | AT | 7 | a0001c0001t0001g0153 a0001c0001t0001g0215 a0001c0001t0001g0227 others(4): Show |
7 | HG02486.hp2 HG02895.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1027+2696dupA | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229856075 | |||||||
| chr2:229856085 | A | C | 7 | a0001c0001t0001g0153 a0001c0001t0001g0215 a0001c0001t0001g0227 others(4): Show |
7 | HG02486.hp2 HG02895.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1027+2687T>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229856085 | |||||||
| chr2:229856676 | T | TA | 13 | a0001c0001t0004g0001 a0001c0001t0004g0254 a0001c0001t0004g0255 others(10): Show |
14 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1027+2095dupT | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229856676 | |||||||
| chr2:229857202 | C | T | 1 | a0001c0002t0002g0291 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1027+1570G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229857202 | |||||||
| chr2:229857239 | A | G | 1 | a0001c0001t0001g0149 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1027+1533T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229857239 | |||||||
| chr2:229857281 | A | T | 1 | a0001c0002t0005g0009 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1027+1491T>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229857281 | |||||||
| chr2:229857497 | C | T | 6 | a0001c0003t0001g0113 a0001c0003t0001g0191 a0001c0003t0001g0194 others(3): Show |
6 | HG02056.hp2 NA18971.hp1 NA18981.hp2 others(3): Show |
intron_variant | MODIFIER | c.1027+1275G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229857497 | |||||||
| chr2:229857637 | C | CA | 78 | a0001c0002t0001g0027 a0001c0002t0001g0028 a0001c0002t0001g0029 others(75): Show |
78 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.1027+1134dupT | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229857637 | |||||||
| chr2:229857744 | C | T | 5 | a0001c0001t0010g0249 a0001c0001t0010g0250 a0001c0001t0010g0251 others(2): Show |
5 | HG00741.hp2 HG01106.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1027+1028G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229857744 | |||||||
| chr2:229857857 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1027+915G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229857857 | |||||||
| chr2:229858294 | C | T | 2 | a0001c0001t0001g0093 a0001c0001t0001g0094 |
2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1027+478G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229858294 | |||||||
| chr2:229858295 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1027+477C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229858295 | |||||||
| chr2:229858341 | C | T | 78 | a0001c0002t0001g0027 a0001c0002t0001g0028 a0001c0002t0001g0029 others(75): Show |
78 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.1027+431G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229858341 | |||||||
| chr2:229858611 | A | G | 1 | a0001c0003t0001g0115 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1027+161T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229858611 | |||||||
| chr2:229859822 | A | G | 1 | a0001c0002t0003g0080 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.225-248T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 3/41 | chr2 | 229859822 | |||||||
| chr2:229859848 | G | C | 1 | a0001c0001t0001g0175 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.225-274C>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 3/41 | chr2 | 229859848 | |||||||
| chr2:229860252 | C | T | 41 | a0001c0002t0002g0279 a0001c0002t0002g0280 a0001c0002t0002g0281 others(38): Show |
41 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(38): Show |
intron_variant | MODIFIER | c.224+154G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 3/41 | chr2 | 229860252 | |||||||
| chr2:229860265 | C | A | 1 | a0001c0001t0001g0182 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.224+141G>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 3/41 | chr2 | 229860265 | |||||||
| chr2:229860714 | G | A | 4 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 others(1): Show |
4 | HG01928.hp2 HG02300.hp1 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.99-183C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229860714 | |||||||
| chr2:229860918 | T | C | 8 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 others(5): Show |
8 | HG00408.hp1 HG01928.hp2 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.99-387A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229860918 | |||||||
| chr2:229861132 | G | A | 1 | a0001c0001t0001g0180 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.99-601C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229861132 | |||||||
| chr2:229861179 | C | T | 1 | a0001c0001t0001g0167 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.99-648G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229861179 | |||||||
| chr2:229861402 | A | G | 2 | a0001c0001t0001g0093 a0001c0001t0001g0094 |
2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.99-871T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229861402 | |||||||
| chr2:229861452 | G | A | 1 | a0001c0001t0011g0098 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.99-921C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229861452 | |||||||
| chr2:229861558 | C | T | 1 | a0001c0002t0005g0009 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.99-1027G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229861558 | |||||||
| chr2:229861901 | A | G | 1 | a0001c0001t0001g0131 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.99-1370T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229861901 | |||||||
| chr2:229861987 | T | TA | 5 | a0001c0001t0001g0153 a0001c0001t0001g0227 a0001c0001t0001g0229 others(2): Show |
5 | HG02895.hp2 HG02897.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.99-1457dupT | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229861987 | |||||||
| chr2:229862393 | G | A | 79 | a0001c0002t0001g0027 a0001c0002t0001g0028 a0001c0002t0001g0029 others(76): Show |
79 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.99-1862C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229862393 | |||||||
| chr2:229862402 | T | C | 1 | a0001c0002t0002g0280 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.99-1871A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229862402 | |||||||
| chr2:229862613 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.99-2082C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229862613 | |||||||
| chr2:229862621 | T | G | 79 | a0001c0002t0001g0027 a0001c0002t0001g0028 a0001c0002t0001g0029 others(76): Show |
79 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.99-2090A>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229862621 | |||||||
| chr2:229862646 | T | C | 17 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0099 others(14): Show |
18 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.99-2115A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229862646 | |||||||
| chr2:229862797 | C | T | 2 | a0001c0001t0001g0269 a0001c0001t0009g0268 |
2 | HG00639.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.99-2266G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229862797 | |||||||
| chr2:229862958 | G | A | 6 | a0001c0001t0010g0249 a0001c0001t0010g0250 a0001c0001t0010g0251 others(3): Show |
6 | HG00741.hp2 HG01106.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.99-2427C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229862958 | |||||||
| chr2:229863058 | T | A | 1 | a0001c0002t0005g0009 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.99-2527A>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229863058 | |||||||
| chr2:229863178 | G | A | 1 | a0001c0001t0001g0023 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.99-2647C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229863178 | |||||||
| chr2:229863219 | A | G | 1 | a0001c0002t0003g0061 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.99-2688T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229863219 | |||||||
| chr2:229863250 | G | GA | 7 | a0001c0001t0001g0161 a0001c0001t0004g0001 a0001c0001t0004g0258 others(4): Show |
8 | HG02080.hp2 HG02109.hp1 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.99-2720dupT | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229863250 | |||||||
| chr2:229863378 | CCTAT | C | 9 | a0001c0001t0001g0153 a0001c0001t0001g0215 a0001c0001t0001g0227 others(6): Show |
9 | HG02486.hp2 HG02895.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.99-2851_99-2848del others(4): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229863378 | |||||||
| chr2:229863405 | T | C | 1 | a0001c0002t0003g0051 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.99-2874A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229863405 | |||||||
| chr2:229863427 | A | C | 7 | a0001c0001t0001g0153 a0001c0001t0001g0215 a0001c0001t0001g0227 others(4): Show |
7 | HG02486.hp2 HG02895.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.99-2896T>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229863427 | |||||||
| chr2:229863630 | T | C | 1 | a0001c0002t0002g0319 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.99-3099A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229863630 | |||||||
| chr2:229863854 | T | C | 2 | a0001c0002t0001g0070 a0001c0002t0003g0079 |
2 | HG03704.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.99-3323A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229863854 | |||||||
| chr2:229864001 | T | TGAGA | 3 | a0001c0001t0001g0120 a0001c0002t0002g0299 a0001c0002t0002g0307 |
3 | HG00323.hp2 HG01496.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.99-3471_99-3470ins others(4): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229864001 | |||||||
| chr2:229864001 | TGAAA | T | 25 | a0001c0001t0001g0117 a0001c0001t0001g0144 a0001c0001t0001g0227 others(22): Show |
25 | HG00140.hp1 HG00423.hp1 HG01167.hp2 others(22): Show |
intron_variant | MODIFIER | c.99-3474_99-3471del others(4): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229864001 | |||||||
| chr2:229864001 | TGAAAGA | T | 5 | a0001c0001t0010g0251 a0001c0001t0010g0252 a0001c0002t0002g0310 others(2): Show |
5 | HG00741.hp2 HG02818.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.99-3476_99-3471del others(6): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229864001 | |||||||
| chr2:229864001 | TGAAAGAG others(1): Show |
T | 18 | a0001c0001t0001g0215 a0001c0001t0001g0231 a0001c0001t0010g0253 others(15): Show |
18 | HG00558.hp1 HG00741.hp1 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.99-3478_99-3471del others(8): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229864001 | |||||||
| chr2:229864001 | TGAAAGAG others(3): Show |
T | 31 | a0001c0003t0001g0091 a0001c0003t0001g0092 a0001c0003t0001g0095 others(28): Show |
31 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(28): Show |
intron_variant | MODIFIER | c.99-3480_99-3471del others(10): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229864001 | |||||||
| chr2:229864001 | TGAAAGAG others(5): Show |
T | 3 | a0001c0002t0002g0319 a0001c0003t0001g0157 a0001c0003t0001g0228 |
3 | HG02056.hp2 NA18975.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.99-3482_99-3471del others(12): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229864001 | |||||||
| chr2:229864001 | TGAAAGAG others(7): Show |
T | 10 | a0001c0001t0001g0137 a0001c0001t0001g0186 a0001c0001t0001g0195 others(7): Show |
10 | HG00408.hp1 HG01934.hp2 HG01952.hp2 others(7): Show |
intron_variant | MODIFIER | c.99-3484_99-3471del others(14): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229864001 | |||||||
| chr2:229864001 | TGAAAGAG others(9): Show |
T | 59 | a0001c0001t0001g0097 a0001c0001t0001g0105 a0001c0001t0001g0119 others(56): Show |
59 | HG00099.hp1 HG00438.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.99-3486_99-3471del others(16): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229864001 | |||||||
| chr2:229864001 | TGAAAGAG others(11): Show |
T | 1 | a0001c0008t0001g0267 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.99-3488_99-3471del others(18): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229864001 | |||||||
| chr2:229864001 | TGAAAGAG others(23): Show |
T | 1 | a0001c0001t0030g0123 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.99-3500_99-3471del others(30): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229864001 | |||||||
| chr2:229864002 | GAA | G | 19 | a0001c0001t0001g0118 a0001c0001t0001g0127 a0001c0001t0001g0229 others(16): Show |
19 | HG00597.hp1 HG01516.hp2 HG01928.hp1 others(16): Show |
intron_variant | MODIFIER | c.99-3473_99-3472del others(2): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229864002 | |||||||
| chr2:229864004 | A | AAG | 4 | a0001c0002t0003g0024 a0001c0002t0003g0025 a0001c0002t0003g0042 others(1): Show |
4 | HG01257.hp2 HG01358.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.99-3475_99-3474dup others(2): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229864004 | |||||||
| chr2:229864004 | A | AAGAG | 7 | a0001c0002t0003g0026 a0001c0002t0003g0076 a0001c0002t0008g0039 others(4): Show |
7 | HG01175.hp2 HG03688.hp2 NA18960.hp1 others(4): Show |
intron_variant | MODIFIER | c.99-3477_99-3474dup others(4): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229864004 | |||||||
| chr2:229864004 | A | AAGAGAG | 4 | a0001c0002t0003g0038 a0001c0002t0003g0068 a0001c0002t0008g0048 others(1): Show |
4 | HG01169.hp1 HG03834.hp1 NA18945.hp2 others(1): Show |
intron_variant | MODIFIER | c.99-3479_99-3474dup others(6): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229864004 | |||||||
| chr2:229864004 | A | AAGAGAGA others(1): Show |
5 | a0001c0002t0003g0031 a0001c0002t0003g0043 a0001c0002t0020g0002 others(2): Show |
5 | HG00642.hp1 HG01891.hp1 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.99-3481_99-3474dup others(8): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229864004 | |||||||
| chr2:229864004 | A | AAGAGAGA others(3): Show |
3 | a0001c0002t0003g0037 a0001c0002t0003g0272 a0001c0002t0017g0040 |
3 | HG00323.hp1 HG01255.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.99-3483_99-3474dup others(10): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229864004 | |||||||
| chr2:229864004 | A | AAGAGAGA others(5): Show |
6 | a0001c0002t0003g0032 a0001c0002t0003g0066 a0001c0002t0003g0067 others(3): Show |
6 | HG01074.hp2 HG01106.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.99-3485_99-3474dup others(12): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229864004 | |||||||
| chr2:229864004 | A | AAGAGAGA others(11): Show |
3 | a0001c0002t0001g0027 a0001c0002t0003g0061 a0001c0002t0003g0080 |
3 | HG00621.hp1 HG03491.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.99-3491_99-3474dup others(18): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229864004 | |||||||
| chr2:229864004 | A | AAGAGAGA others(15): Show |
1 | a0001c0002t0003g0035 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.99-3495_99-3474dup others(22): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229864004 | |||||||
| chr2:229864004 | A | AGAGAGAG others(6): Show |
2 | a0001c0002t0005g0009 a0001c0002t0013g0005 |
2 | HG00735.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.99-3474_99-3473ins others(13): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229864004 | |||||||
| chr2:229864004 | A | AGAGAGAG others(8): Show |
2 | a0001c0002t0003g0045 a0001c0002t0003g0051 |
2 | NA18968.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.99-3474_99-3473ins others(15): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229864004 | |||||||
| chr2:229864004 | A | G | 49 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0106 others(46): Show |
50 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(47): Show |
intron_variant | MODIFIER | c.99-3473T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229864004 | |||||||
| chr2:229864004 | AAG | A | 6 | a0001c0004t0003g0082 a0001c0004t0003g0083 a0001c0004t0003g0086 others(3): Show |
6 | HG02056.hp1 NA18989.hp2 NA19011.hp2 others(3): Show |
intron_variant | MODIFIER | c.99-3475_99-3474del others(2): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229864004 | |||||||
| chr2:229864004 | AAGAGAGA others(5): Show |
A | 1 | a0001c0004t0003g0085 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.99-3485_99-3474del others(12): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229864004 | |||||||
| chr2:229864027 | AGAGAGAG others(27): Show |
A | 1 | a0001c0001t0004g0254 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.99-3530_99-3497del others(34): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229864027 | |||||||
| chr2:229864029 | AGAGAGAG others(15): Show |
A | 1 | a0001c0001t0012g0139 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.99-3520_99-3499del others(22): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229864029 | |||||||
| chr2:229864031 | AGAGAGAG others(23): Show |
A | 3 | a0001c0001t0004g0255 a0001c0001t0004g0259 a0001c0001t0004g0260 |
3 | HG01891.hp2 HG02647.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.99-3530_99-3501del others(30): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229864031 | |||||||
| chr2:229864033 | AGAGAGAG others(11): Show |
A | 12 | a0001c0001t0001g0116 a0001c0001t0001g0121 a0001c0001t0001g0122 others(9): Show |
12 | HG00639.hp1 HG01070.hp1 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.99-3520_99-3503del others(18): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229864033 | |||||||
| chr2:229864033 | AGAGAGAG others(13): Show |
A | 2 | a0001c0001t0001g0106 a0001c0001t0024g0239 |
2 | HG00558.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.99-3522_99-3503del others(20): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229864033 | |||||||
| chr2:229864033 | AGAGAGAG others(19): Show |
A | 1 | a0001c0001t0004g0262 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.99-3528_99-3503del others(26): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229864033 | |||||||
| chr2:229864035 | AGAGAGAG others(9): Show |
A | 6 | a0001c0001t0001g0224 a0001c0001t0001g0234 a0001c0001t0001g0235 others(3): Show |
6 | HG00423.hp2 HG01993.hp2 HG04184.hp2 others(3): Show |
intron_variant | MODIFIER | c.99-3520_99-3505del others(16): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229864035 | |||||||
| chr2:229864035 | AGAGAGAG others(11): Show |
A | 2 | a0001c0001t0019g0317 a0001c0001t0019g0318 |
2 | HG02257.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.99-3522_99-3505del others(18): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229864035 | |||||||
| chr2:229864035 | AGAGAGAG others(15): Show |
A | 2 | a0001c0001t0001g0022 a0001c0001t0005g0003 |
2 | HG02145.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.99-3526_99-3505del others(22): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229864035 | |||||||
| chr2:229864035 | AGAGAGAG others(19): Show |
A | 7 | a0001c0001t0004g0001 a0001c0001t0004g0258 a0001c0001t0004g0261 others(4): Show |
8 | HG02109.hp1 HG02145.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.99-3530_99-3505del others(26): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229864035 | |||||||
| chr2:229864037 | AGAGAGAG others(15): Show |
A | 2 | a0001c0001t0001g0099 a0001c0001t0005g0011 |
2 | HG02055.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.99-3528_99-3507del others(22): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229864037 | |||||||
| chr2:229864037 | AGAGAGAG others(17): Show |
A | 1 | a0001c0001t0004g0257 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.99-3530_99-3507del others(24): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229864037 | |||||||
| chr2:229864039 | AGAGAGAG others(3): Show |
A | 1 | a0001c0001t0001g0269 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.99-3518_99-3509del others(10): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229864039 | |||||||
| chr2:229864039 | AGAGAGAG others(5): Show |
A | 2 | a0001c0001t0011g0098 a0001c0003t0005g0017 |
2 | NA19083.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.99-3520_99-3509del others(12): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229864039 | |||||||
| chr2:229864039 | AGAGAGAG others(15): Show |
A | 1 | a0001c0001t0001g0093 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.99-3530_99-3509del others(22): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229864039 | |||||||
| chr2:229864041 | AGAGAGAG others(3): Show |
A | 2 | a0001c0001t0011g0225 a0001c0001t0011g0226 |
2 | HG02723.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.99-3520_99-3511del others(10): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229864041 | |||||||
| chr2:229864041 | AGAGAGAG others(9): Show |
A | 1 | a0001c0001t0001g0023 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.99-3526_99-3511del others(16): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229864041 | |||||||
| chr2:229864041 | AGAGAGAG others(13): Show |
A | 1 | a0001c0001t0001g0094 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.99-3530_99-3511del others(20): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229864041 | |||||||
| chr2:229864043 | A | T | 3 | a0001c0001t0001g0229 a0001c0001t0010g0249 a0001c0001t0010g0250 |
3 | HG03195.hp1 NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.99-3512T>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229864043 | |||||||
| chr2:229864043 | AGAGAGTG others(9): Show |
A | 1 | a0001c0001t0014g0112 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.99-3528_99-3513del others(16): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229864043 | |||||||
| chr2:229864045 | A | T | 15 | a0001c0001t0001g0227 a0001c0001t0001g0229 a0001c0001t0001g0230 others(12): Show |
15 | HG00741.hp2 HG01106.hp1 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.99-3514T>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229864045 | |||||||
| chr2:229864047 | A | AGAGAGAG others(23): Show |
1 | a0001c0002t0003g0062 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.99-3517_99-3516ins others(30): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229864047 | |||||||
| chr2:229864047 | A | AGAGAGAG others(19): Show |
1 | a0001c0002t0001g0057 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.99-3517_99-3516ins others(26): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229864047 | |||||||
| chr2:229864047 | A | AGAGAGAG others(23): Show |
1 | a0001c0002t0001g0052 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.99-3517_99-3516ins others(30): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229864047 | |||||||
| chr2:229864047 | A | AGAGAGAG others(17): Show |
1 | a0001c0002t0001g0064 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.99-3517_99-3516ins others(24): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229864047 | |||||||
| chr2:229864047 | A | AGAGAGAG others(13): Show |
1 | a0001c0002t0001g0034 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.99-3517_99-3516ins others(20): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229864047 | |||||||
| chr2:229864047 | A | AGAGAGAG others(17): Show |
1 | a0001c0002t0001g0054 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.99-3517_99-3516ins others(24): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229864047 | |||||||
| chr2:229864047 | A | AGAGAGAG others(19): Show |
1 | a0001c0002t0001g0071 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.99-3517_99-3516ins others(26): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229864047 | |||||||
| chr2:229864047 | A | AGAGAGAG others(11): Show |
1 | a0001c0002t0001g0065 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.99-3517_99-3516ins others(18): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229864047 | |||||||
| chr2:229864047 | A | AGAGAGAG others(11): Show |
1 | a0001c0002t0001g0028 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.99-3517_99-3516ins others(18): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229864047 | |||||||
| chr2:229864047 | A | AGAGAGAG others(9): Show |
1 | a0001c0002t0001g0063 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.99-3517_99-3516ins others(16): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229864047 | |||||||
| chr2:229864047 | A | AGAGAGAG others(13): Show |
1 | a0001c0002t0001g0055 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.99-3517_99-3516ins others(20): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229864047 | |||||||
| chr2:229864047 | A | AGAGAGAG others(7): Show |
2 | a0001c0002t0001g0033 a0001c0002t0013g0008 |
2 | HG00735.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.99-3517_99-3516ins others(14): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229864047 | |||||||
| chr2:229864047 | A | AGAGAGAG others(3): Show |
1 | a0001c0002t0003g0046 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.99-3517_99-3516ins others(10): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229864047 | |||||||
| chr2:229864047 | A | AGAGAGAG others(9): Show |
2 | a0001c0002t0001g0053 a0001c0002t0001g0089 |
2 | HG01346.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.99-3517_99-3516ins others(16): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229864047 | |||||||
| chr2:229864047 | A | AGAGAGAG others(11): Show |
2 | a0001c0002t0001g0070 a0001c0002t0003g0079 |
2 | HG03704.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.99-3517_99-3516ins others(18): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229864047 | |||||||
| chr2:229864047 | A | AGAGAGAG others(7): Show |
1 | a0001c0002t0001g0075 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.99-3517_99-3516ins others(14): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229864047 | |||||||
| chr2:229864047 | A | AGAGAGAG others(11): Show |
1 | a0001c0002t0005g0007 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.99-3517_99-3516ins others(18): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229864047 | |||||||
| chr2:229864047 | A | AGAGAGTG others(5): Show |
1 | a0001c0002t0001g0074 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.99-3517_99-3516ins others(12): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229864047 | |||||||
| chr2:229864047 | A | AGAGTGAG others(3): Show |
2 | a0001c0002t0001g0029 a0001c0002t0001g0270 |
2 | HG02735.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.99-3517_99-3516ins others(10): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229864047 | |||||||
| chr2:229864047 | A | AGAGTGAG others(5): Show |
3 | a0001c0002t0001g0059 a0001c0002t0001g0072 a0001c0002t0001g0077 |
3 | HG01070.hp2 HG01071.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.99-3517_99-3516ins others(12): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229864047 | |||||||
| chr2:229864047 | A | T | 28 | a0001c0001t0001g0153 a0001c0001t0001g0227 a0001c0001t0001g0229 others(25): Show |
28 | HG00140.hp1 HG00741.hp1 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.99-3516T>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229864047 | |||||||
| chr2:229864047 | AGT | A | 5 | a0001c0001t0001g0175 a0001c0001t0001g0188 a0001c0001t0001g0189 others(2): Show |
5 | HG02615.hp2 HG02723.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.99-3518_99-3517del others(2): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229864047 | |||||||
| chr2:229864047 | AGTGT | A | 4 | a0001c0001t0001g0245 a0001c0002t0002g0294 a0001c0002t0002g0295 others(1): Show |
4 | HG00140.hp2 HG00673.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.99-3520_99-3517del others(4): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229864047 | |||||||
| chr2:229864047 | AGTGTGTG others(5): Show |
A | 1 | a0001c0001t0014g0108 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.99-3528_99-3517del others(12): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229864047 | |||||||
| chr2:229864049 | T | A | 103 | a0001c0001t0001g0097 a0001c0001t0001g0105 a0001c0001t0001g0117 others(100): Show |
103 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.99-3518A>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229864049 | |||||||
| chr2:229864051 | T | A | 4 | a0001c0001t0001g0243 a0001c0002t0001g0027 a0001c0002t0003g0035 others(1): Show |
4 | HG02897.hp2 HG03471.hp1 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.99-3520A>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229864051 | |||||||
| chr2:229864053 | T | A | 2 | a0001c0001t0001g0269 a0001c0001t0009g0268 |
2 | HG00639.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.99-3522A>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229864053 | |||||||
| chr2:229864057 | T | A | 1 | a0001c0001t0014g0107 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.99-3526A>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229864057 | |||||||
| chr2:229864059 | T | A | 1 | a0001c0001t0014g0107 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.99-3528A>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229864059 | |||||||
| chr2:229864077 | T | C | 5 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0233 others(2): Show |
5 | HG02145.hp2 HG02257.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.99-3546A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229864077 | |||||||
| chr2:229864089 | C | T | 1 | a0001c0003t0006g0322 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.99-3558G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229864089 | |||||||
| chr2:229864216 | A | G | 17 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0099 others(14): Show |
18 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.99-3685T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229864216 | |||||||
| chr2:229864302 | T | C | 1 | a0001c0003t0001g0100 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.99-3771A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229864302 | |||||||
| chr2:229864496 | A | G | 5 | a0001c0002t0001g0033 a0001c0002t0001g0034 a0001c0002t0001g0063 others(2): Show |
5 | HG00735.hp1 HG01168.hp2 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.99-3965T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229864496 | |||||||
| chr2:229864693 | T | C | 2 | a0001c0001t0001g0269 a0001c0001t0009g0268 |
2 | HG00639.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.99-4162A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229864693 | |||||||
| chr2:229864705 | T | C | 41 | a0001c0002t0002g0279 a0001c0002t0002g0280 a0001c0002t0002g0281 others(38): Show |
41 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(38): Show |
intron_variant | MODIFIER | c.99-4174A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229864705 | |||||||
| chr2:229864845 | T | C | 6 | a0001c0003t0001g0113 a0001c0003t0001g0191 a0001c0003t0001g0194 others(3): Show |
6 | HG02056.hp2 NA18971.hp1 NA18981.hp2 others(3): Show |
intron_variant | MODIFIER | c.99-4314A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229864845 | |||||||
| chr2:229865139 | C | T | 1 | a0001c0001t0001g0156 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.99-4608G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229865139 | |||||||
| chr2:229865213 | G | A | 3 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0005g0003 |
3 | HG02145.hp2 HG02257.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.99-4682C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229865213 | |||||||
| chr2:229865223 | A | G | 6 | a0001c0002t0008g0039 a0001c0002t0008g0044 a0001c0002t0008g0047 others(3): Show |
6 | NA18945.hp2 NA18960.hp1 NA18969.hp1 others(3): Show |
intron_variant | MODIFIER | c.99-4692T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229865223 | |||||||
| chr2:229865240 | C | T | 2 | a0001c0003t0006g0323 a0001c0003t0006g0325 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.99-4709G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229865240 | |||||||
| chr2:229865329 | AAAAAAAA others(8): Show |
A | 1 | a0001c0002t0002g0302 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.99-4813_99-4799del others(15): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229865329 | |||||||
| chr2:229865329 | AAAAAAAA others(12): Show |
A | 1 | a0001c0001t0001g0269 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.99-4817_99-4799del others(19): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229865329 | |||||||
| chr2:229865331 | AAAAAAAA others(10): Show |
A | 1 | a0001c0001t0001g0130 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.99-4817_99-4801del others(17): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229865331 | |||||||
| chr2:229865332 | AAAAAAAA others(5): Show |
A | 8 | a0001c0002t0002g0296 a0001c0002t0002g0298 a0001c0002t0002g0305 others(5): Show |
8 | HG00140.hp2 HG00323.hp2 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.99-4813_99-4802del others(12): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229865332 | |||||||
| chr2:229865332 | AAAAAAAA others(9): Show |
A | 160 | a0001c0001t0001g0023 a0001c0001t0001g0097 a0001c0001t0001g0105 others(157): Show |
160 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.99-4817_99-4802del others(16): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229865332 | |||||||
| chr2:229865333 | AAAAAAAA others(8): Show |
A | 6 | a0001c0001t0001g0022 a0001c0001t0001g0116 a0001c0001t0001g0152 others(3): Show |
6 | HG00099.hp1 HG01346.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.99-4817_99-4803del others(15): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229865333 | |||||||
| chr2:229865334 | AAAAAAAA others(7): Show |
A | 1 | a0001c0001t0005g0003 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.99-4817_99-4804del others(14): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229865334 | |||||||
| chr2:229865340 | AAAAG | A | 33 | a0001c0001t0011g0098 a0001c0001t0011g0114 a0001c0001t0011g0187 others(30): Show |
33 | HG00423.hp1 HG00597.hp1 HG01496.hp1 others(30): Show |
intron_variant | MODIFIER | c.99-4813_99-4810del others(4): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229865340 | |||||||
| chr2:229865341 | AAAGAAAG | A | 61 | a0001c0001t0014g0107 a0001c0002t0001g0027 a0001c0002t0001g0028 others(58): Show |
61 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.99-4817_99-4811del others(7): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229865341 | |||||||
| chr2:229865342 | AAGAAAG | A | 29 | a0001c0001t0001g0093 a0001c0001t0001g0099 a0001c0001t0004g0001 others(26): Show |
30 | HG00621.hp1 HG01070.hp2 HG01346.hp2 others(27): Show |
intron_variant | MODIFIER | c.99-4817_99-4812del others(6): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229865342 | |||||||
| chr2:229865343 | AGAAAG | A | 5 | a0001c0001t0001g0094 a0001c0001t0004g0262 a0001c0001t0004g0264 others(2): Show |
5 | HG01071.hp2 HG01243.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.99-4817_99-4813del others(5): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229865343 | |||||||
| chr2:229865428 | T | C | 3 | a0001c0001t0012g0139 a0001c0001t0012g0140 a0001c0001t0012g0168 |
3 | HG00639.hp1 HG01109.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.99-4897A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229865428 | |||||||
| chr2:229865535 | TATGCATG others(15): Show |
T | 19 | a0001c0002t0002g0279 a0001c0002t0002g0280 a0001c0002t0002g0281 others(16): Show |
19 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(16): Show |
intron_variant | MODIFIER | c.99-5026_99-5005del others(22): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229865535 | |||||||
| chr2:229865621 | A | T | 1 | a0001c0002t0001g0058 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.99-5090T>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229865621 | |||||||
| chr2:229865656 | C | T | 1 | a0001c0002t0001g0071 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.99-5125G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229865656 | |||||||
| chr2:229865821 | G | A | 17 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0099 others(14): Show |
18 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.99-5290C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229865821 | |||||||
| chr2:229865828 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.99-5297C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229865828 | |||||||
| chr2:229865871 | C | T | 1 | a0001c0001t0001g0276 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.99-5340G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229865871 | |||||||
| chr2:229865982 | C | T | 7 | a0001c0001t0001g0153 a0001c0001t0001g0215 a0001c0001t0001g0227 others(4): Show |
7 | HG02486.hp2 HG02895.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.99-5451G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229865982 | |||||||
| chr2:229866108 | T | C | 1 | a0001c0003t0006g0326 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.99-5577A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229866108 | |||||||
| chr2:229866294 | T | C | 1 | a0001c0001t0001g0120 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.99-5763A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229866294 | |||||||
| chr2:229866614 | C | T | 2 | a0001c0001t0001g0269 a0001c0001t0009g0268 |
2 | HG00639.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.99-6083G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229866614 | |||||||
| chr2:229866621 | C | T | 1 | a0001c0001t0001g0145 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.99-6090G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229866621 | |||||||
| chr2:229866681 | C | T | 89 | a0001c0001t0001g0097 a0001c0001t0001g0105 a0001c0001t0001g0106 others(86): Show |
89 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.99-6150G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229866681 | |||||||
| chr2:229866785 | G | A | 7 | a0001c0001t0001g0153 a0001c0001t0001g0215 a0001c0001t0001g0227 others(4): Show |
7 | HG02486.hp2 HG02895.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.99-6254C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229866785 | |||||||
| chr2:229866917 | T | G | 1 | a0002c0006t0001g0096 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.99-6386A>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229866917 | |||||||
| chr2:229867097 | G | GT | 152 | a0001c0001t0001g0097 a0001c0001t0001g0105 a0001c0001t0001g0106 others(149): Show |
152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.99-6567dupA | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229867097 | |||||||
| chr2:229867109 | G | T | 6 | a0001c0001t0010g0249 a0001c0001t0010g0250 a0001c0001t0010g0251 others(3): Show |
6 | HG00741.hp2 HG01106.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.99-6578C>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229867109 | |||||||
| chr2:229867110 | T | G | 1 | a0001c0002t0028g0081 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.99-6579A>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229867110 | |||||||
| chr2:229867167 | G | GT | 34 | a0001c0002t0002g0279 a0001c0002t0002g0280 a0001c0002t0002g0281 others(31): Show |
34 | HG00140.hp2 HG00423.hp1 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.99-6637dupA | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229867167 | |||||||
| chr2:229867171 | G | GT | 6 | a0001c0002t0002g0295 a0001c0002t0002g0296 a0001c0002t0002g0300 others(3): Show |
6 | HG00323.hp2 HG01071.hp1 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.99-6641dupA | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229867171 | |||||||
| chr2:229867171 | G | GTTTT | 20 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0099 others(17): Show |
21 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.99-6644_99-6641dup others(4): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229867171 | |||||||
| chr2:229867171 | G | GTTTTT | 73 | a0001c0002t0001g0027 a0001c0002t0001g0028 a0001c0002t0001g0029 others(70): Show |
73 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.99-6645_99-6641dup others(5): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229867171 | |||||||
| chr2:229867171 | G | T | 43 | a0001c0001t0001g0022 a0001c0001t0005g0003 a0001c0001t0010g0249 others(40): Show |
43 | HG00140.hp2 HG00423.hp1 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.99-6640C>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229867171 | |||||||
| chr2:229867171 | GT | G | 155 | a0001c0001t0001g0097 a0001c0001t0001g0106 a0001c0001t0001g0116 others(152): Show |
155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.99-6641delA | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229867171 | |||||||
| chr2:229867176 | T | G | 7 | a0001c0001t0001g0153 a0001c0001t0001g0215 a0001c0001t0001g0227 others(4): Show |
7 | HG02486.hp2 HG02895.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.99-6645A>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229867176 | |||||||
| chr2:229867199 | T | G | 2 | a0001c0001t0004g0263 a0001c0001t0004g0266 |
2 | HG02109.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.99-6668A>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229867199 | |||||||
| chr2:229867261 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.99-6730C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229867261 | |||||||
| chr2:229867306 | C | T | 5 | a0001c0001t0011g0098 a0001c0001t0011g0114 a0001c0001t0011g0187 others(2): Show |
5 | HG01884.hp1 HG02723.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.99-6775G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229867306 | |||||||
| chr2:229867338 | A | G | 2 | a0001c0002t0003g0045 a0001c0002t0020g0002 |
2 | NA19003.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.99-6807T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229867338 | |||||||
| chr2:229867496 | A | G | 7 | a0001c0003t0001g0113 a0001c0003t0001g0191 a0001c0003t0001g0194 others(4): Show |
7 | HG02056.hp2 NA18944.hp2 NA18971.hp1 others(4): Show |
intron_variant | MODIFIER | c.99-6965T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229867496 | |||||||
| chr2:229867678 | C | T | 1 | a0001c0002t0002g0294 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.99-7147G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229867678 | |||||||
| chr2:229868095 | G | T | 317 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0093 others(314): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.99-7564C>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229868095 | |||||||
| chr2:229868117 | G | A | 1 | a0001c0003t0005g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.99-7586C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229868117 | |||||||
| chr2:229868158 | G | C | 1 | a0001c0001t0001g0174 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.99-7627C>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229868158 | |||||||
| chr2:229868259 | C | T | 40 | a0001c0002t0002g0279 a0001c0002t0002g0280 a0001c0002t0002g0281 others(37): Show |
40 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(37): Show |
intron_variant | MODIFIER | c.99-7728G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229868259 | |||||||
| chr2:229868352 | C | T | 2 | a0001c0001t0001g0269 a0001c0001t0009g0268 |
2 | HG00639.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.99-7821G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229868352 | |||||||
| chr2:229868473 | C | G | 317 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0093 others(314): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.99-7942G>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229868473 | |||||||
| chr2:229868494 | C | A | 4 | a0001c0003t0001g0218 a0001c0005t0001g0104 a0001c0005t0001g0217 others(1): Show |
4 | HG02109.hp2 HG02886.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.99-7963G>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229868494 | |||||||
| chr2:229868619 | A | C | 1 | a0001c0001t0010g0252 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.99-8088T>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229868619 | |||||||
| chr2:229868790 | T | C | 5 | a0001c0001t0014g0107 a0001c0001t0014g0108 a0001c0001t0014g0112 others(2): Show |
5 | HG02257.hp2 HG02559.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.99-8259A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229868790 | |||||||
| chr2:229868979 | G | C | 1 | a0001c0003t0006g0324 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.99-8448C>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229868979 | |||||||
| chr2:229869104 | C | A | 7 | a0001c0001t0001g0119 a0001c0001t0009g0146 a0001c0001t0009g0147 others(4): Show |
7 | HG02280.hp2 HG02559.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.99-8573G>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229869104 | |||||||
| chr2:229869115 | G | A | 1 | a0001c0001t0009g0268 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.99-8584C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229869115 | |||||||
| chr2:229869149 | T | A | 1 | a0001c0001t0001g0275 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.99-8618A>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229869149 | |||||||
| chr2:229869340 | C | T | 1 | a0001c0003t0006g0324 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.99-8809G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229869340 | |||||||
| chr2:229869365 | C | T | 58 | a0001c0003t0001g0091 a0001c0003t0001g0092 a0001c0003t0001g0095 others(55): Show |
58 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.99-8834G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229869365 | |||||||
| chr2:229869815 | C | A | 78 | a0001c0002t0001g0027 a0001c0002t0001g0028 a0001c0002t0001g0029 others(75): Show |
78 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.99-9284G>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229869815 | |||||||
| chr2:229870056 | G | A | 1 | a0001c0001t0001g0197 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.99-9525C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229870056 | |||||||
| chr2:229870207 | T | C | 2 | a0001c0001t0001g0269 a0001c0001t0009g0268 |
2 | HG00639.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.99-9676A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229870207 | |||||||
| chr2:229870449 | A | G | 1 | a0001c0002t0001g0052 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.98+9533T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229870449 | |||||||
| chr2:229870750 | G | C | 1 | a0001c0001t0001g0120 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.98+9232C>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229870750 | |||||||
| chr2:229871050 | C | T | 3 | a0001c0001t0014g0107 a0001c0001t0014g0108 a0001c0001t0014g0112 |
3 | HG02717.hp1 HG02818.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.98+8932G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229871050 | |||||||
| chr2:229871183 | A | AGAGGGGA others(13): Show |
5 | a0001c0001t0011g0098 a0001c0001t0011g0114 a0001c0001t0011g0187 others(2): Show |
5 | HG01884.hp1 HG02723.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.98+8779_98+8798dup others(20): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229871183 | |||||||
| chr2:229871193 | AGAGGGGA others(3): Show |
A | 5 | a0001c0001t0010g0249 a0001c0001t0010g0250 a0001c0001t0010g0251 others(2): Show |
5 | HG00741.hp2 HG01106.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.98+8779_98+8788del others(10): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229871193 | |||||||
| chr2:229871284 | C | A | 1 | a0001c0001t0001g0125 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.98+8698G>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229871284 | |||||||
| chr2:229871310 | T | C | 3 | a0001c0001t0014g0107 a0001c0001t0014g0108 a0001c0001t0014g0112 |
3 | HG02717.hp1 HG02818.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.98+8672A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229871310 | |||||||
| chr2:229871409 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.98+8573C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229871409 | |||||||
| chr2:229871417 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.98+8565C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229871417 | |||||||
| chr2:229871620 | G | A | 1 | a0001c0002t0005g0009 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.98+8362C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229871620 | |||||||
| chr2:229871809 | A | T | 5 | a0001c0001t0011g0098 a0001c0001t0011g0114 a0001c0001t0011g0187 others(2): Show |
5 | HG01884.hp1 HG02723.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.98+8173T>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229871809 | |||||||
| chr2:229871841 | T | G | 1 | a0001c0002t0002g0302 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.98+8141A>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229871841 | |||||||
| chr2:229871907 | T | C | 1 | a0001c0002t0001g0028 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.98+8075A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229871907 | |||||||
| chr2:229871965 | G | A | 58 | a0001c0003t0001g0091 a0001c0003t0001g0092 a0001c0003t0001g0095 others(55): Show |
58 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.98+8017C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229871965 | |||||||
| chr2:229872061 | A | G | 1 | a0001c0001t0001g0180 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.98+7921T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229872061 | |||||||
| chr2:229872104 | T | TA | 15 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0188 others(12): Show |
15 | HG01074.hp2 HG01099.hp2 HG01978.hp2 others(12): Show |
intron_variant | MODIFIER | c.98+7877dupT | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229872104 | |||||||
| chr2:229872104 | T | TAA | 64 | a0001c0001t0001g0245 a0001c0002t0001g0028 a0001c0002t0001g0029 others(61): Show |
64 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.98+7876_98+7877dup others(2): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229872104 | |||||||
| chr2:229872104 | T | TAAA | 37 | a0001c0001t0001g0242 a0001c0002t0001g0027 a0001c0002t0001g0033 others(34): Show |
37 | HG00140.hp2 HG00423.hp1 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.98+7875_98+7877dup others(3): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229872104 | |||||||
| chr2:229872104 | TA | T | 110 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0097 others(107): Show |
110 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.98+7877delT | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229872104 | |||||||
| chr2:229872104 | TAAAAAAA others(5): Show |
T | 7 | a0001c0001t0004g0254 a0001c0001t0004g0255 a0001c0001t0004g0259 others(4): Show |
7 | HG00642.hp1 HG01255.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.98+7866_98+7877del others(12): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229872104 | |||||||
| chr2:229872104 | TAAAAAAA others(6): Show |
T | 13 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0099 others(10): Show |
14 | HG01243.hp1 HG02055.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.98+7865_98+7877del others(13): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229872104 | |||||||
| chr2:229872113 | A | G | 54 | a0001c0003t0001g0091 a0001c0003t0001g0092 a0001c0003t0001g0095 others(51): Show |
54 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(51): Show |
intron_variant | MODIFIER | c.98+7869T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229872113 | |||||||
| chr2:229872114 | A | G | 106 | a0001c0001t0001g0097 a0001c0001t0001g0105 a0001c0001t0001g0106 others(103): Show |
106 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.98+7868T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229872114 | |||||||
| chr2:229872115 | A | G | 2 | a0001c0001t0001g0149 a0001c0001t0001g0195 |
2 | HG02027.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.98+7867T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229872115 | |||||||
| chr2:229872141 | T | C | 1 | a0001c0002t0003g0026 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.98+7841A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229872141 | |||||||
| chr2:229872199 | C | T | 1 | a0001c0002t0003g0061 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.98+7783G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229872199 | |||||||
| chr2:229872295 | G | C | 2 | a0001c0002t0002g0299 a0001c0002t0002g0300 |
2 | HG01496.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.98+7687C>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229872295 | |||||||
| chr2:229872769 | T | A | 3 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0005g0003 |
3 | HG02145.hp2 HG02257.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.98+7213A>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229872769 | |||||||
| chr2:229872892 | A | C | 1 | a0001c0002t0005g0009 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.98+7090T>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229872892 | |||||||
| chr2:229873047 | C | A | 2 | a0001c0001t0001g0269 a0001c0001t0009g0268 |
2 | HG00639.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.98+6935G>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229873047 | |||||||
| chr2:229873135 | A | C | 1 | a0001c0003t0001g0199 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.98+6847T>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229873135 | |||||||
| chr2:229873514 | T | C | 5 | a0001c0001t0010g0249 a0001c0001t0010g0250 a0001c0001t0010g0251 others(2): Show |
5 | HG00741.hp2 HG01106.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.98+6468A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229873514 | |||||||
| chr2:229873735 | A | G | 4 | a0001c0003t0001g0218 a0001c0005t0001g0104 a0001c0005t0001g0217 others(1): Show |
4 | HG02109.hp2 HG02886.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.98+6247T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229873735 | |||||||
| chr2:229874036 | TTAAAA | T | 35 | a0001c0002t0002g0279 a0001c0002t0002g0280 a0001c0002t0002g0281 others(32): Show |
35 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(32): Show |
intron_variant | MODIFIER | c.98+5941_98+5945del others(5): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229874036 | |||||||
| chr2:229874049 | T | TA | 9 | a0001c0001t0001g0117 a0001c0001t0001g0153 a0001c0001t0001g0215 others(6): Show |
9 | HG02486.hp2 HG02895.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.98+5932dupT | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229874049 | |||||||
| chr2:229874252 | T | C | 9 | a0001c0003t0006g0322 a0001c0003t0006g0323 a0001c0003t0006g0324 others(6): Show |
9 | HG00140.hp1 HG00741.hp1 HG01167.hp2 others(6): Show |
intron_variant | MODIFIER | c.98+5730A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229874252 | |||||||
| chr2:229874371 | A | G | 1 | a0001c0002t0002g0280 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.98+5611T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229874371 | |||||||
| chr2:229874493 | G | C | 79 | a0001c0002t0001g0027 a0001c0002t0001g0028 a0001c0002t0001g0029 others(76): Show |
79 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.98+5489C>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229874493 | |||||||
| chr2:229874960 | A | G | 10 | a0001c0002t0002g0296 a0001c0002t0002g0298 a0001c0002t0002g0302 others(7): Show |
10 | HG00140.hp2 HG00323.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.98+5022T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229874960 | |||||||
| chr2:229875220 | C | T | 1 | a0001c0001t0010g0251 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.98+4762G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229875220 | |||||||
| chr2:229875340 | T | C | 2 | a0001c0001t0001g0093 a0001c0001t0001g0094 |
2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.98+4642A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229875340 | |||||||
| chr2:229875576 | A | T | 317 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0093 others(314): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.98+4406T>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229875576 | |||||||
| chr2:229875610 | G | A | 3 | a0001c0002t0001g0063 a0001c0002t0001g0064 a0001c0002t0001g0065 |
3 | HG02683.hp2 HG03942.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.98+4372C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229875610 | |||||||
| chr2:229875972 | G | C | 1 | a0001c0002t0018g0313 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.98+4010C>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229875972 | |||||||
| chr2:229876560 | C | G | 2 | a0001c0001t0001g0099 a0001c0001t0005g0011 |
2 | HG02055.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.98+3422G>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229876560 | |||||||
| chr2:229876699 | G | A | 15 | a0001c0001t0001g0099 a0001c0001t0004g0001 a0001c0001t0004g0254 others(12): Show |
16 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.98+3283C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229876699 | |||||||
| chr2:229876871 | G | A | 1 | a0001c0002t0001g0028 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.98+3111C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229876871 | |||||||
| chr2:229876897 | T | G | 1 | a0001c0003t0001g0214 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.98+3085A>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229876897 | |||||||
| chr2:229877017 | A | G | 1 | a0001c0002t0001g0028 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.98+2965T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229877017 | |||||||
| chr2:229877248 | A | G | 1 | a0001c0002t0033g0041 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.98+2734T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229877248 | |||||||
| chr2:229877357 | T | C | 1 | a0001c0001t0001g0023 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.98+2625A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229877357 | |||||||
| chr2:229877455 | C | T | 3 | a0001c0001t0014g0107 a0001c0001t0014g0108 a0001c0001t0014g0112 |
3 | HG02717.hp1 HG02818.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.98+2527G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229877455 | |||||||
| chr2:229877545 | A | G | 2 | a0001c0001t0001g0269 a0001c0001t0009g0268 |
2 | HG00639.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.98+2437T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229877545 | |||||||
| chr2:229877552 | A | T | 1 | a0001c0001t0001g0120 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.98+2430T>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229877552 | |||||||
| chr2:229877580 | T | C | 1 | a0001c0001t0001g0120 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.98+2402A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229877580 | |||||||
| chr2:229877610 | G | T | 2 | a0001c0001t0001g0130 a0001c0001t0001g0162 |
2 | HG01257.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.98+2372C>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229877610 | |||||||
| chr2:229877703 | C | T | 43 | a0001c0003t0001g0095 a0001c0003t0001g0100 a0001c0003t0001g0101 others(40): Show |
43 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(40): Show |
intron_variant | MODIFIER | c.98+2279G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229877703 | |||||||
| chr2:229877780 | G | A | 5 | a0001c0001t0010g0249 a0001c0001t0010g0250 a0001c0001t0010g0251 others(2): Show |
5 | HG00741.hp2 HG01106.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.98+2202C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229877780 | |||||||
| chr2:229878257 | C | T | 3 | a0001c0001t0014g0107 a0001c0001t0014g0108 a0001c0001t0014g0112 |
3 | HG02717.hp1 HG02818.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.98+1725G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229878257 | |||||||
| chr2:229878283 | C | T | 5 | a0001c0001t0010g0249 a0001c0001t0010g0250 a0001c0001t0010g0251 others(2): Show |
5 | HG00741.hp2 HG01106.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.98+1699G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229878283 | |||||||
| chr2:229878443 | T | A | 4 | a0001c0001t0014g0107 a0001c0001t0014g0108 a0001c0001t0014g0112 others(1): Show |
4 | HG02717.hp1 HG02818.hp2 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.98+1539A>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229878443 | |||||||
| chr2:229878469 | C | T | 1 | a0001c0002t0002g0312 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.98+1513G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229878469 | |||||||
| chr2:229878674 | G | A | 8 | a0001c0002t0002g0296 a0001c0002t0002g0305 a0001c0002t0002g0306 others(5): Show |
8 | HG00323.hp2 HG01071.hp1 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.98+1308C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229878674 | |||||||
| chr2:229878682 | G | A | 1 | a0001c0001t0011g0187 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.98+1300C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229878682 | |||||||
| chr2:229878698 | A | G | 1 | a0001c0001t0001g0120 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.98+1284T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229878698 | |||||||
| chr2:229878703 | C | T | 1 | a0001c0001t0025g0241 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.98+1279G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229878703 | |||||||
| chr2:229878789 | A | G | 1 | a0001c0001t0001g0023 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.98+1193T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229878789 | |||||||
| chr2:229878796 | A | C | 1 | a0001c0001t0001g0023 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.98+1186T>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229878796 | |||||||
| chr2:229878814 | C | A | 1 | a0001c0001t0001g0023 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.98+1168G>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229878814 | |||||||
| chr2:229878818 | G | C | 1 | a0001c0001t0001g0023 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.98+1164C>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229878818 | |||||||
| chr2:229878825 | G | A | 1 | a0001c0001t0001g0023 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.98+1157C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229878825 | |||||||
| chr2:229878826 | C | A | 1 | a0001c0001t0001g0023 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.98+1156G>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229878826 | |||||||
| chr2:229878829 | A | G | 1 | a0001c0001t0001g0023 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.98+1153T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229878829 | |||||||
| chr2:229878861 | T | C | 1 | a0001c0001t0001g0023 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.98+1121A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229878861 | |||||||
| chr2:229878862 | G | A | 1 | a0001c0001t0001g0023 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.98+1120C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229878862 | |||||||
| chr2:229878871 | C | A | 1 | a0001c0001t0001g0023 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.98+1111G>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229878871 | |||||||
| chr2:229878872 | G | A | 1 | a0001c0001t0001g0269 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.98+1110C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229878872 | |||||||
| chr2:229878878 | G | A | 2 | a0001c0001t0001g0023 a0001c0001t0004g0262 |
2 | HG01243.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.98+1104C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229878878 | |||||||
| chr2:229878887 | A | C | 16 | a0001c0001t0001g0099 a0001c0001t0001g0231 a0001c0001t0004g0001 others(13): Show |
17 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.98+1095T>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229878887 | |||||||
| chr2:229878902 | T | C | 1 | a0001c0001t0004g0257 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.98+1080A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229878902 | |||||||
| chr2:229878971 | A | G | 268 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0093 others(265): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.98+1011T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229878971 | |||||||
| chr2:229878979 | G | A | 1 | a0001c0002t0003g0068 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.98+1003C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229878979 | |||||||
| chr2:229879237 | C | T | 1 | a0001c0002t0003g0062 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.98+745G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229879237 | |||||||
| chr2:229879292 | T | C | 1 | a0001c0002t0002g0295 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.98+690A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229879292 | |||||||
| chr2:229879330 | G | C | 1 | a0001c0002t0003g0068 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.98+652C>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229879330 | |||||||
| chr2:229879536 | A | G | 5 | a0001c0001t0011g0098 a0001c0001t0011g0114 a0001c0001t0011g0187 others(2): Show |
5 | HG01884.hp1 HG02723.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.98+446T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229879536 | |||||||
| chr2:229879844 | T | C | 1 | a0001c0001t0001g0120 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.98+138A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229879844 | |||||||
| chr2:229879854 | C | T | 317 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0093 others(314): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.98+128G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229879854 | |||||||
| chr2:229879857 | G | C | 1 | a0001c0003t0001g0100 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.98+125C>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229879857 | |||||||
| chr2:229880211 | T | C | 2 | a0001c0001t0001g0246 a0001c0001t0026g0247 |
2 | HG01934.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.-49-83A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229880211 | |||||||
| chr2:229880495 | A | G | 5 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0127 others(2): Show |
5 | HG02258.hp1 HG02622.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-49-367T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229880495 | |||||||
| chr2:229880813 | G | A | 1 | a0001c0002t0002g0301 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-49-685C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229880813 | |||||||
| chr2:229880837 | G | T | 35 | a0001c0002t0002g0279 a0001c0002t0002g0280 a0001c0002t0002g0281 others(32): Show |
35 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(32): Show |
intron_variant | MODIFIER | c.-49-709C>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229880837 | |||||||
| chr2:229880838 | G | T | 2 | a0001c0001t0001g0269 a0001c0001t0009g0268 |
2 | HG00639.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.-49-710C>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229880838 | |||||||
| chr2:229880848 | G | A | 2 | a0001c0001t0001g0243 a0001c0001t0001g0245 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-49-720C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229880848 | |||||||
| chr2:229881118 | C | CT | 18 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0099 others(15): Show |
19 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.-49-991dupA | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229881118 | |||||||
| chr2:229881144 | C | G | 5 | a0001c0001t0011g0098 a0001c0001t0011g0114 a0001c0001t0011g0187 others(2): Show |
5 | HG01884.hp1 HG02723.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-49-1016G>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229881144 | |||||||
| chr2:229881173 | G | A | 1 | a0001c0001t0001g0142 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-49-1045C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229881173 | |||||||
| chr2:229881647 | T | C | 2 | a0001c0001t0001g0269 a0001c0001t0009g0268 |
2 | HG00639.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.-49-1519A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229881647 | |||||||
| chr2:229881750 | T | C | 1 | a0001c0001t0001g0161 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-49-1622A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229881750 | |||||||
| chr2:229882037 | C | T | 1 | a0001c0001t0027g0169 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-49-1909G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229882037 | |||||||
| chr2:229882158 | T | C | 4 | a0001c0003t0001g0218 a0001c0005t0001g0104 a0001c0005t0001g0217 others(1): Show |
4 | HG02109.hp2 HG02886.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49-2030A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229882158 | |||||||
| chr2:229882294 | G | T | 2 | a0001c0002t0017g0040 a0001c0002t0017g0090 |
2 | NA18944.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.-49-2166C>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229882294 | |||||||
| chr2:229882301 | G | C | 1 | a0001c0003t0001g0201 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-49-2173C>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229882301 | |||||||
| chr2:229883113 | C | A | 1 | a0001c0001t0001g0120 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-49-2985G>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229883113 | |||||||
| chr2:229883169 | A | C | 3 | a0001c0002t0003g0078 a0001c0002t0003g0271 a0001c0002t0013g0008 |
3 | HG00733.hp1 HG01099.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.-49-3041T>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229883169 | |||||||
| chr2:229883184 | T | C | 1 | a0001c0003t0006g0327 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-49-3056A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229883184 | |||||||
| chr2:229883463 | G | A | 3 | a0001c0003t0001g0178 a0001c0003t0001g0185 a0001c0003t0001g0190 |
3 | HG03195.hp2 HG03579.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-49-3335C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229883463 | |||||||
| chr2:229883833 | C | T | 5 | a0001c0002t0002g0299 a0001c0002t0002g0300 a0001c0002t0002g0301 others(2): Show |
5 | HG01496.hp1 HG02080.hp2 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.-49-3705G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229883833 | |||||||
| chr2:229883914 | C | G | 23 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0099 others(20): Show |
24 | HG00639.hp2 HG01243.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.-49-3786G>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229883914 | |||||||
| chr2:229884095 | T | C | 5 | a0001c0001t0010g0249 a0001c0001t0010g0250 a0001c0001t0010g0251 others(2): Show |
5 | HG00741.hp2 HG01106.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-49-3967A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229884095 | |||||||
| chr2:229884106 | C | CA | 8 | a0001c0001t0001g0192 a0001c0001t0001g0275 a0001c0001t0004g0254 others(5): Show |
8 | HG01891.hp2 HG02647.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.-49-3979dupT | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229884106 | |||||||
| chr2:229884118 | C | A | 1 | a0001c0002t0003g0030 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-49-3990G>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229884118 | |||||||
| chr2:229884175 | T | G | 1 | a0001c0002t0001g0072 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-49-4047A>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229884175 | |||||||
| chr2:229884236 | C | CT | 154 | a0001c0001t0001g0097 a0001c0001t0001g0105 a0001c0001t0001g0116 others(151): Show |
154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.-49-4109dupA | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229884236 | |||||||
| chr2:229884236 | C | CTT | 11 | a0001c0001t0001g0119 a0001c0001t0001g0121 a0001c0001t0001g0153 others(8): Show |
11 | HG00280.hp2 HG01070.hp1 HG01358.hp2 others(8): Show |
intron_variant | MODIFIER | c.-49-4110_-49-4109d others(4): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229884236 | |||||||
| chr2:229884236 | CT | C | 19 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0099 others(16): Show |
20 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.-49-4109delA | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229884236 | |||||||
| chr2:229884358 | T | C | 5 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0127 others(2): Show |
5 | HG02258.hp1 HG02622.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-49-4230A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229884358 | |||||||
| chr2:229884418 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-49-4290C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229884418 | |||||||
| chr2:229884442 | G | A | 151 | a0001c0001t0001g0097 a0001c0001t0001g0105 a0001c0001t0001g0106 others(148): Show |
151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.-49-4314C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229884442 | |||||||
| chr2:229884540 | C | T | 1 | a0001c0003t0005g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-49-4412G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229884540 | |||||||
| chr2:229885093 | CTA | C | 5 | a0001c0002t0002g0312 a0001c0002t0002g0315 a0001c0002t0002g0316 others(2): Show |
5 | HG02970.hp1 HG03540.hp2 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.-49-4967_-49-4966d others(4): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229885093 | |||||||
| chr2:229885193 | G | A | 1 | a0001c0002t0029g0060 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-49-5065C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229885193 | |||||||
| chr2:229885687 | A | G | 1 | a0001c0001t0001g0105 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-49-5559T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229885687 | |||||||
| chr2:229885773 | A | G | 3 | a0001c0001t0014g0107 a0001c0001t0014g0108 a0001c0001t0014g0112 |
3 | HG02717.hp1 HG02818.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-49-5645T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229885773 | |||||||
| chr2:229886145 | A | G | 1 | a0001c0001t0009g0268 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-49-6017T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229886145 | |||||||
| chr2:229886166 | T | C | 1 | a0001c0001t0031g0165 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-49-6038A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229886166 | |||||||
| chr2:229886197 | G | A | 7 | a0001c0001t0001g0153 a0001c0001t0001g0215 a0001c0001t0001g0227 others(4): Show |
7 | HG02486.hp2 HG02895.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.-49-6069C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229886197 | |||||||
| chr2:229886376 | G | A | 5 | a0001c0001t0010g0249 a0001c0001t0010g0250 a0001c0001t0010g0251 others(2): Show |
5 | HG00741.hp2 HG01106.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-49-6248C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229886376 | |||||||
| chr2:229886398 | A | G | 1 | a0001c0003t0001g0199 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-49-6270T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229886398 | |||||||
| chr2:229886466 | A | AT | 7 | a0001c0001t0001g0195 a0001c0001t0001g0236 a0001c0001t0011g0098 others(4): Show |
7 | HG01884.hp1 HG02027.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.-49-6339dupA | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229886466 | |||||||
| chr2:229886466 | AT | A | 26 | a0001c0001t0001g0099 a0001c0001t0001g0117 a0001c0001t0004g0001 others(23): Show |
27 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.-49-6339delA | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229886466 | |||||||
| chr2:229886726 | C | A | 1 | a0001c0003t0001g0201 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-49-6598G>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229886726 | |||||||
| chr2:229886877 | T | C | 1 | a0001c0001t0001g0232 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.-49-6749A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229886877 | |||||||
| chr2:229887001 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-49-6873G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229887001 | |||||||
| chr2:229887460 | A | G | 1 | a0001c0007t0005g0016 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-49-7332T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229887460 | |||||||
| chr2:229887481 | A | G | 42 | a0001c0001t0005g0015 a0001c0002t0002g0279 a0001c0002t0002g0280 others(39): Show |
42 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(39): Show |
intron_variant | MODIFIER | c.-49-7353T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229887481 | |||||||
| chr2:229887600 | A | T | 2 | a0001c0003t0001g0157 a0001c0003t0001g0198 |
2 | NA18975.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.-49-7472T>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229887600 | |||||||
| chr2:229887810 | GCAT | G | 4 | a0001c0001t0001g0242 a0001c0001t0001g0243 a0001c0001t0001g0245 others(1): Show |
4 | HG02809.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-49-7685_-49-7683d others(5): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229887810 | |||||||
| chr2:229888248 | T | C | 151 | a0001c0001t0001g0097 a0001c0001t0001g0105 a0001c0001t0001g0106 others(148): Show |
151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.-49-8120A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229888248 | |||||||
| chr2:229889104 | G | A | 1 | a0001c0002t0002g0289 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-49-8976C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229889104 | |||||||
| chr2:229889168 | G | A | 4 | a0001c0003t0006g0326 a0001c0003t0006g0327 a0001c0003t0006g0328 others(1): Show |
4 | HG00140.hp1 HG00741.hp1 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.-49-9040C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229889168 | |||||||
| chr2:229889187 | G | C | 1 | a0001c0001t0001g0120 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-49-9059C>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229889187 | |||||||
| chr2:229889268 | C | T | 1 | a0001c0008t0001g0267 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-49-9140G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229889268 | |||||||
| chr2:229889293 | A | T | 2 | a0001c0001t0001g0269 a0001c0001t0009g0268 |
2 | HG00639.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.-49-9165T>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229889293 | |||||||
| chr2:229889331 | T | C | 3 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0005g0003 |
3 | HG02145.hp2 HG02257.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.-49-9203A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229889331 | |||||||
| chr2:229889423 | T | C | 2 | a0001c0001t0019g0317 a0001c0001t0019g0318 |
2 | HG02257.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.-49-9295A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229889423 | |||||||
| chr2:229889433 | A | C | 19 | a0001c0002t0002g0279 a0001c0002t0002g0280 a0001c0002t0002g0281 others(16): Show |
19 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(16): Show |
intron_variant | MODIFIER | c.-49-9305T>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229889433 | |||||||
| chr2:229889599 | T | C | 18 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0099 others(15): Show |
19 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.-49-9471A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229889599 | |||||||
| chr2:229889602 | T | C | 326 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0093 others(323): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.-49-9474A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229889602 | |||||||
| chr2:229889948 | A | G | 18 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0099 others(15): Show |
19 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.-49-9820T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229889948 | |||||||
| chr2:229890072 | G | A | 2 | a0001c0002t0002g0303 a0001c0002t0002g0304 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-49-9944C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229890072 | |||||||
| chr2:229890080 | C | CT | 6 | a0001c0001t0001g0174 a0001c0002t0002g0312 a0001c0002t0002g0315 others(3): Show |
6 | HG02970.hp1 HG03540.hp2 NA18906.hp2 others(3): Show |
intron_variant | MODIFIER | c.-49-9953dupA | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229890080 | |||||||
| chr2:229890080 | CT | C | 178 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0093 others(175): Show |
179 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.-49-9953delA | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229890080 | |||||||
| chr2:229890080 | CTT | C | 91 | a0001c0001t0001g0097 a0001c0001t0001g0105 a0001c0001t0001g0106 others(88): Show |
91 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.-49-9954_-49-9953d others(4): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229890080 | |||||||
| chr2:229890125 | G | T | 2 | a0001c0001t0001g0093 a0001c0001t0001g0094 |
2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-49-9997C>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229890125 | |||||||
| chr2:229890166 | G | A | 6 | a0001c0002t0001g0029 a0001c0002t0001g0059 a0001c0002t0001g0075 others(3): Show |
6 | HG01070.hp2 HG01071.hp2 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.-49-10038C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229890166 | |||||||
| chr2:229890393 | C | G | 2 | a0001c0001t0001g0269 a0001c0001t0009g0268 |
2 | HG00639.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.-49-10265G>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229890393 | |||||||
| chr2:229890739 | G | A | 41 | a0001c0002t0002g0279 a0001c0002t0002g0280 a0001c0002t0002g0281 others(38): Show |
41 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(38): Show |
intron_variant | MODIFIER | c.-49-10611C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229890739 | |||||||
| chr2:229890808 | C | T | 3 | a0001c0001t0014g0107 a0001c0001t0014g0108 a0001c0001t0014g0112 |
3 | HG02717.hp1 HG02818.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-49-10680G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229890808 | |||||||
| chr2:229891241 | T | C | 2 | a0001c0001t0001g0093 a0001c0001t0001g0094 |
2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-49-11113A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229891241 | |||||||
| chr2:229891309 | C | T | 3 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0005g0003 |
3 | HG02145.hp2 HG02257.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.-49-11181G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229891309 | |||||||
| chr2:229891519 | T | C | 1 | a0001c0001t0001g0212 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-49-11391A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229891519 | |||||||
| chr2:229891673 | T | C | 152 | a0001c0001t0001g0097 a0001c0001t0001g0105 a0001c0001t0001g0106 others(149): Show |
152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.-49-11545A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229891673 | |||||||
| chr2:229891908 | T | A | 4 | a0001c0002t0002g0283 a0001c0002t0002g0285 a0001c0002t0002g0290 others(1): Show |
4 | HG01952.hp1 HG01975.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49-11780A>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229891908 | |||||||
| chr2:229892266 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-49-12138C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229892266 | |||||||
| chr2:229892384 | G | A | 1 | a0001c0002t0003g0061 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-49-12256C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229892384 | |||||||
| chr2:229892734 | T | C | 89 | a0001c0001t0001g0097 a0001c0001t0001g0105 a0001c0001t0001g0106 others(86): Show |
89 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.-49-12606A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229892734 | |||||||
| chr2:229892753 | C | A | 1 | a0001c0001t0001g0242 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-49-12625G>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229892753 | |||||||
| chr2:229892820 | T | C | 317 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0093 others(314): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.-49-12692A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229892820 | |||||||
| chr2:229892879 | T | A | 1 | a0001c0001t0004g0262 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-49-12751A>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229892879 | |||||||
| chr2:229892925 | C | T | 1 | a0001c0002t0005g0009 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-49-12797G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229892925 | |||||||
| chr2:229893261 | C | T | 1 | a0001c0001t0001g0186 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-49-13133G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229893261 | |||||||
| chr2:229893427 | C | T | 5 | a0001c0001t0001g0269 a0001c0001t0009g0268 a0001c0001t0014g0107 others(2): Show |
5 | HG00639.hp2 HG02055.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-49-13299G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229893427 | |||||||
| chr2:229893493 | A | AT | 206 | a0001c0001t0001g0023 a0001c0001t0001g0097 a0001c0001t0001g0105 others(203): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.-49-13366dupA | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229893493 | |||||||
| chr2:229893796 | T | G | 2 | a0001c0004t0003g0083 a0001c0004t0003g0085 |
2 | NA18951.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.-49-13668A>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229893796 | |||||||
| chr2:229893844 | A | G | 78 | a0001c0002t0001g0027 a0001c0002t0001g0028 a0001c0002t0001g0029 others(75): Show |
78 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.-49-13716T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229893844 | |||||||
| chr2:229893922 | G | A | 1 | a0001c0002t0002g0320 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-49-13794C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229893922 | |||||||
| chr2:229893958 | C | T | 1 | a0001c0003t0007g0202 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-49-13830G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229893958 | |||||||
| chr2:229894004 | A | G | 2 | a0001c0001t0001g0269 a0001c0001t0009g0268 |
2 | HG00639.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.-49-13876T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229894004 | |||||||
| chr2:229894288 | A | C | 1 | a0001c0001t0001g0094 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-49-14160T>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229894288 | |||||||
| chr2:229894388 | G | A | 1 | a0001c0001t0010g0252 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-49-14260C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229894388 | |||||||
| chr2:229894488 | T | C | 1 | a0001c0001t0001g0237 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.-49-14360A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229894488 | |||||||
| chr2:229894633 | A | C | 2 | a0001c0001t0001g0269 a0001c0001t0009g0268 |
2 | HG00639.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.-49-14505T>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229894633 | |||||||
| chr2:229894798 | T | C | 1 | a0001c0001t0001g0195 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-49-14670A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229894798 | |||||||
| chr2:229894970 | G | C | 4 | a0001c0003t0001g0218 a0001c0005t0001g0104 a0001c0005t0001g0217 others(1): Show |
4 | HG02109.hp2 HG02886.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49-14842C>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229894970 | |||||||
| chr2:229894983 | C | A | 78 | a0001c0002t0001g0027 a0001c0002t0001g0028 a0001c0002t0001g0029 others(75): Show |
78 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.-49-14855G>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229894983 | |||||||
| chr2:229895034 | C | T | 1 | a0001c0001t0005g0010 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-49-14906G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229895034 | |||||||
| chr2:229895038 | A | G | 5 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0127 others(2): Show |
5 | HG02258.hp1 HG02622.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-49-14910T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229895038 | |||||||
| chr2:229895150 | A | G | 1 | a0001c0001t0004g0254 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-49-15022T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229895150 | |||||||
| chr2:229895172 | T | C | 1 | a0001c0002t0003g0069 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-49-15044A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229895172 | |||||||
| chr2:229895513 | A | C | 1 | a0001c0003t0001g0101 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-49-15385T>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229895513 | |||||||
| chr2:229895526 | G | C | 5 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0127 others(2): Show |
5 | HG02258.hp1 HG02622.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-49-15398C>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229895526 | |||||||
| chr2:229895607 | T | C | 1 | a0001c0002t0002g0294 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-49-15479A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229895607 | |||||||
| chr2:229895934 | C | T | 7 | a0001c0001t0001g0153 a0001c0001t0001g0215 a0001c0001t0001g0227 others(4): Show |
7 | HG02486.hp2 HG02895.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.-49-15806G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229895934 | |||||||
| chr2:229896043 | C | T | 1 | a0001c0002t0002g0301 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-49-15915G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229896043 | |||||||
| chr2:229896098 | G | A | 1 | a0001c0001t0001g0212 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-49-15970C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229896098 | |||||||
| chr2:229896520 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-49-16392C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229896520 | |||||||
| chr2:229896599 | A | G | 326 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0093 others(323): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.-49-16471T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229896599 | |||||||
| chr2:229896673 | A | G | 3 | a0001c0001t0014g0107 a0001c0001t0014g0108 a0001c0001t0014g0112 |
3 | HG02717.hp1 HG02818.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-49-16545T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229896673 | |||||||
| chr2:229896678 | A | T | 1 | a0001c0001t0001g0119 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-49-16550T>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229896678 | |||||||
| chr2:229897395 | C | A | 1 | a0001c0001t0001g0120 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-49-17267G>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229897395 | |||||||
| chr2:229897520 | C | T | 1 | a0001c0002t0003g0035 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-49-17392G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229897520 | |||||||
| chr2:229897529 | T | A | 1 | a0001c0001t0001g0195 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-49-17401A>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229897529 | |||||||
| chr2:229897583 | G | A | 5 | a0001c0001t0011g0098 a0001c0001t0011g0114 a0001c0001t0011g0187 others(2): Show |
5 | HG01884.hp1 HG02723.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-49-17455C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229897583 | |||||||
| chr2:229897584 | T | G | 1 | a0001c0002t0003g0062 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-49-17456A>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229897584 | |||||||
| chr2:229897833 | C | A | 23 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0099 others(20): Show |
24 | HG00639.hp2 HG01243.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.-49-17705G>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229897833 | |||||||
| chr2:229897833 | C | T | 78 | a0001c0002t0001g0027 a0001c0002t0001g0028 a0001c0002t0001g0029 others(75): Show |
78 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.-49-17705G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229897833 | |||||||
| chr2:229898105 | G | A | 1 | a0001c0002t0002g0308 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-49-17977C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229898105 | |||||||
| chr2:229898162 | A | G | 1 | a0001c0002t0034g0256 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-49-18034T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229898162 | |||||||
| chr2:229898219 | C | T | 5 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0127 others(2): Show |
5 | HG02258.hp1 HG02622.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-49-18091G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229898219 | |||||||
| chr2:229898274 | T | G | 18 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0099 others(15): Show |
19 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.-49-18146A>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229898274 | |||||||
| chr2:229898447 | T | G | 1 | a0001c0002t0003g0062 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-49-18319A>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229898447 | |||||||
| chr2:229898492 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-49-18364C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229898492 | |||||||
| chr2:229898614 | TA | T | 4 | a0001c0001t0011g0098 a0001c0001t0011g0114 a0001c0001t0011g0225 others(1): Show |
4 | HG01884.hp1 HG02723.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-49-18487delT | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229898614 | |||||||
| chr2:229898773 | C | T | 3 | a0001c0001t0014g0107 a0001c0001t0014g0108 a0001c0001t0014g0112 |
3 | HG02717.hp1 HG02818.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-49-18645G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229898773 | |||||||
| chr2:229898831 | A | G | 5 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0127 others(2): Show |
5 | HG02258.hp1 HG02622.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-49-18703T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229898831 | |||||||
| chr2:229898855 | CTAATT | C | 78 | a0001c0002t0001g0027 a0001c0002t0001g0028 a0001c0002t0001g0029 others(75): Show |
78 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.-49-18732_-49-1872 others(9): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229898855 | |||||||
| chr2:229898928 | C | A | 1 | a0001c0002t0005g0009 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-49-18800G>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229898928 | |||||||
| chr2:229898974 | C | A | 164 | a0001c0001t0001g0097 a0001c0001t0001g0105 a0001c0001t0001g0106 others(161): Show |
164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.-49-18846G>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229898974 | |||||||
| chr2:229899279 | G | A | 1 | a0001c0002t0002g0284 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-49-19151C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229899279 | |||||||
| chr2:229899510 | G | A | 52 | a0001c0002t0003g0024 a0001c0002t0003g0025 a0001c0002t0003g0026 others(49): Show |
52 | HG00323.hp1 HG00621.hp1 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.-49-19382C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229899510 | |||||||
| chr2:229899532 | T | C | 2 | a0001c0001t0001g0093 a0001c0001t0001g0094 |
2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-49-19404A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229899532 | |||||||
| chr2:229899703 | T | C | 2 | a0001c0002t0002g0299 a0001c0002t0002g0300 |
2 | HG01496.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-49-19575A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229899703 | |||||||
| chr2:229899741 | A | C | 9 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0188 others(6): Show |
9 | HG02615.hp2 HG02723.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.-49-19613T>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229899741 | |||||||
| chr2:229899926 | C | T | 1 | a0001c0002t0005g0009 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-49-19798G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229899926 | |||||||
| chr2:229899957 | C | G | 1 | a0001c0001t0001g0230 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-49-19829G>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229899957 | |||||||
| chr2:229899957 | C | T | 5 | a0001c0001t0010g0249 a0001c0001t0010g0250 a0001c0001t0010g0251 others(2): Show |
5 | HG00741.hp2 HG01106.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-49-19829G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229899957 | |||||||
| chr2:229900072 | T | G | 101 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0099 others(98): Show |
102 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.-49-19944A>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229900072 | |||||||
| chr2:229900126 | A | G | 1 | a0001c0002t0002g0285 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-49-19998T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229900126 | |||||||
| chr2:229900351 | C | G | 1 | a0001c0002t0003g0067 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-49-20223G>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229900351 | |||||||
| chr2:229900600 | C | T | 19 | a0001c0002t0002g0279 a0001c0002t0002g0280 a0001c0002t0002g0281 others(16): Show |
19 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(16): Show |
intron_variant | MODIFIER | c.-49-20472G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229900600 | |||||||
| chr2:229900679 | T | C | 2 | a0001c0003t0007g0159 a0001c0003t0007g0222 |
2 | HG00280.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.-49-20551A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229900679 | |||||||
| chr2:229900973 | G | A | 1 | a0001c0002t0002g0300 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-49-20845C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229900973 | |||||||
| chr2:229901047 | C | T | 1 | a0001c0001t0009g0268 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-50+20833G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229901047 | |||||||
| chr2:229901083 | G | A | 1 | a0001c0003t0001g0126 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-50+20797C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229901083 | |||||||
| chr2:229901087 | C | T | 3 | a0001c0003t0015g0150 a0001c0003t0015g0151 a0001c0003t0015g0173 |
3 | HG02922.hp2 HG02965.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-50+20793G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229901087 | |||||||
| chr2:229901091 | G | A | 1 | a0001c0003t0036g0321 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-50+20789C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229901091 | |||||||
| chr2:229901229 | C | T | 2 | a0001c0001t0001g0099 a0001c0001t0005g0011 |
2 | HG02055.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-50+20651G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229901229 | |||||||
| chr2:229901230 | G | A | 3 | a0001c0001t0001g0175 a0001c0001t0001g0188 a0001c0001t0001g0189 |
3 | HG02615.hp2 HG02723.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-50+20650C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229901230 | |||||||
| chr2:229901320 | A | C | 33 | a0001c0001t0001g0106 a0001c0001t0001g0125 a0001c0001t0001g0130 others(30): Show |
33 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(30): Show |
intron_variant | MODIFIER | c.-50+20560T>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229901320 | |||||||
| chr2:229901492 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-50+20388C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229901492 | |||||||
| chr2:229901523 | T | C | 2 | a0001c0001t0001g0243 a0001c0001t0001g0245 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-50+20357A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229901523 | |||||||
| chr2:229901527 | G | A | 3 | a0001c0001t0014g0107 a0001c0001t0014g0108 a0001c0001t0014g0112 |
3 | HG02717.hp1 HG02818.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-50+20353C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229901527 | |||||||
| chr2:229901616 | GTC | G | 78 | a0001c0002t0001g0027 a0001c0002t0001g0028 a0001c0002t0001g0029 others(75): Show |
78 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.-50+20262_-50+2026 others(6): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229901616 | |||||||
| chr2:229901619 | T | A | 78 | a0001c0002t0001g0027 a0001c0002t0001g0028 a0001c0002t0001g0029 others(75): Show |
78 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.-50+20261A>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229901619 | |||||||
| chr2:229901620 | G | A | 78 | a0001c0002t0001g0027 a0001c0002t0001g0028 a0001c0002t0001g0029 others(75): Show |
78 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.-50+20260C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229901620 | |||||||
| chr2:229901620 | G | GA | 236 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0093 others(233): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.-50+20259dupT | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229901620 | |||||||
| chr2:229901797 | G | A | 3 | a0001c0001t0001g0175 a0001c0001t0001g0188 a0001c0001t0001g0189 |
3 | HG02615.hp2 HG02723.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-50+20083C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229901797 | |||||||
| chr2:229901852 | G | A | 89 | a0001c0001t0001g0097 a0001c0001t0001g0105 a0001c0001t0001g0106 others(86): Show |
89 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.-50+20028C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229901852 | |||||||
| chr2:229902230 | A | G | 14 | a0001c0001t0001g0097 a0001c0001t0001g0105 a0001c0001t0001g0129 others(11): Show |
14 | HG00558.hp2 HG00597.hp2 HG00673.hp1 others(11): Show |
intron_variant | MODIFIER | c.-50+19650T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229902230 | |||||||
| chr2:229902246 | T | C | 1 | a0001c0002t0001g0058 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-50+19634A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229902246 | |||||||
| chr2:229902312 | G | A | 2 | a0001c0001t0001g0269 a0001c0001t0009g0268 |
2 | HG00639.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.-50+19568C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229902312 | |||||||
| chr2:229902374 | C | T | 3 | a0001c0001t0001g0119 a0001c0001t0001g0269 a0001c0001t0009g0268 |
3 | HG00639.hp2 HG02055.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-50+19506G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229902374 | |||||||
| chr2:229902447 | T | C | 1 | a0001c0001t0027g0169 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-50+19433A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229902447 | |||||||
| chr2:229902850 | T | G | 1 | a0001c0002t0001g0074 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-50+19030A>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229902850 | |||||||
| chr2:229903011 | T | TTTTTC | 4 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0269 others(1): Show |
4 | HG00639.hp2 HG02055.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-50+18868_-50+1886 others(9): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229903011 | |||||||
| chr2:229903012 | T | TTTTC | 19 | a0001c0001t0001g0099 a0001c0001t0004g0001 a0001c0001t0004g0254 others(16): Show |
20 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.-50+18867_-50+1886 others(8): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229903012 | |||||||
| chr2:229903013 | T | TTTC | 214 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0097 others(211): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.-50+18866_-50+1886 others(7): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229903013 | |||||||
| chr2:229903015 | T | C | 78 | a0001c0002t0001g0027 a0001c0002t0001g0028 a0001c0002t0001g0029 others(75): Show |
78 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.-50+18865A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229903015 | |||||||
| chr2:229903017 | TC | T | 72 | a0001c0002t0001g0027 a0001c0002t0001g0028 a0001c0002t0001g0029 others(69): Show |
72 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.-50+18862delG | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229903017 | |||||||
| chr2:229903018 | C | CT | 160 | a0001c0001t0001g0097 a0001c0001t0001g0105 a0001c0001t0001g0106 others(157): Show |
160 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(157): Show |
intron_variant | MODIFIER | c.-50+18861dupA | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229903018 | |||||||
| chr2:229903018 | C | T | 25 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0099 others(22): Show |
26 | HG00639.hp2 HG01175.hp2 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.-50+18862G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229903018 | |||||||
| chr2:229903019 | T | C | 1 | a0001c0002t0002g0281 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-50+18861A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229903019 | |||||||
| chr2:229903170 | T | C | 1 | a0001c0007t0005g0016 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-50+18710A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229903170 | |||||||
| chr2:229903196 | T | C | 1 | a0001c0002t0005g0007 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-50+18684A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229903196 | |||||||
| chr2:229903232 | G | T | 13 | a0001c0001t0004g0001 a0001c0001t0004g0254 a0001c0001t0004g0255 others(10): Show |
14 | HG01891.hp2 HG02109.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.-50+18648C>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229903232 | |||||||
| chr2:229903280 | C | T | 18 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0099 others(15): Show |
19 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.-50+18600G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229903280 | |||||||
| chr2:229903496 | G | A | 2 | a0001c0003t0006g0323 a0001c0003t0006g0325 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-50+18384C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229903496 | |||||||
| chr2:229903717 | T | C | 3 | a0001c0001t0014g0107 a0001c0001t0014g0108 a0001c0001t0014g0112 |
3 | HG02717.hp1 HG02818.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-50+18163A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229903717 | |||||||
| chr2:229903728 | G | T | 1 | a0001c0003t0001g0091 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-50+18152C>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229903728 | |||||||
| chr2:229903788 | G | C | 79 | a0001c0002t0001g0027 a0001c0002t0001g0028 a0001c0002t0001g0029 others(76): Show |
79 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.-50+18092C>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229903788 | |||||||
| chr2:229903834 | G | T | 78 | a0001c0002t0001g0027 a0001c0002t0001g0028 a0001c0002t0001g0029 others(75): Show |
78 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.-50+18046C>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229903834 | |||||||
| chr2:229903866 | CA | C | 7 | a0001c0001t0001g0117 a0001c0001t0001g0124 a0001c0001t0001g0127 others(4): Show |
7 | HG01168.hp1 HG02300.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-50+18013delT | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229903866 | |||||||
| chr2:229904274 | C | T | 2 | a0001c0001t0001g0093 a0001c0001t0001g0094 |
2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-50+17606G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229904274 | |||||||
| chr2:229904416 | C | CA | 228 | a0001c0001t0001g0097 a0001c0001t0001g0105 a0001c0001t0001g0106 others(225): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.-50+17463dupT | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229904416 | |||||||
| chr2:229904416 | C | CAA | 35 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0099 others(32): Show |
36 | HG00597.hp1 HG01168.hp2 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.-50+17462_-50+1746 others(6): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229904416 | |||||||
| chr2:229904475 | A | C | 149 | a0001c0001t0001g0097 a0001c0001t0001g0105 a0001c0001t0001g0106 others(146): Show |
149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.-50+17405T>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229904475 | |||||||
| chr2:229904477 | G | A | 2 | a0001c0001t0001g0188 a0001c0001t0001g0189 |
2 | HG02723.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-50+17403C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229904477 | |||||||
| chr2:229904583 | C | T | 1 | a0001c0003t0001g0095 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-50+17297G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229904583 | |||||||
| chr2:229904800 | G | A | 1 | a0001c0001t0012g0143 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-50+17080C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229904800 | |||||||
| chr2:229904875 | T | C | 2 | a0001c0001t0001g0269 a0001c0001t0009g0268 |
2 | HG00639.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.-50+17005A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229904875 | |||||||
| chr2:229904921 | G | C | 78 | a0001c0002t0001g0027 a0001c0002t0001g0028 a0001c0002t0001g0029 others(75): Show |
78 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.-50+16959C>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229904921 | |||||||
| chr2:229905106 | C | T | 2 | a0001c0001t0001g0269 a0001c0001t0009g0268 |
2 | HG00639.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.-50+16774G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229905106 | |||||||
| chr2:229905134 | C | T | 2 | a0001c0001t0001g0156 a0001c0001t0030g0123 |
2 | HG00280.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-50+16746G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229905134 | |||||||
| chr2:229905143 | A | G | 10 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0099 others(7): Show |
10 | HG01243.hp1 HG02055.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.-50+16737T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229905143 | |||||||
| chr2:229905274 | C | CA | 9 | a0001c0001t0001g0128 a0001c0001t0001g0188 a0001c0001t0001g0189 others(6): Show |
9 | HG01070.hp2 HG01071.hp2 HG01346.hp2 others(6): Show |
intron_variant | MODIFIER | c.-50+16605dupT | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229905274 | |||||||
| chr2:229905274 | CA | C | 17 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0215 others(14): Show |
17 | HG00639.hp2 HG00741.hp2 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.-50+16605delT | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229905274 | |||||||
| chr2:229905375 | A | G | 317 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0093 others(314): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.-50+16505T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229905375 | |||||||
| chr2:229905515 | AAC | A | 88 | a0001c0001t0001g0097 a0001c0001t0001g0105 a0001c0001t0001g0106 others(85): Show |
88 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.-50+16363_-50+1636 others(6): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229905515 | |||||||
| chr2:229905681 | T | C | 1 | a0001c0001t0001g0120 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-50+16199A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229905681 | |||||||
| chr2:229905800 | G | A | 1 | a0001c0001t0001g0274 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-50+16080C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229905800 | |||||||
| chr2:229906189 | C | G | 78 | a0001c0002t0001g0027 a0001c0002t0001g0028 a0001c0002t0001g0029 others(75): Show |
78 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.-50+15691G>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229906189 | |||||||
| chr2:229906303 | C | CA | 92 | a0001c0001t0001g0097 a0001c0001t0001g0116 a0001c0001t0001g0119 others(89): Show |
92 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.-50+15576dupT | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229906303 | |||||||
| chr2:229906303 | CA | C | 19 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0099 others(16): Show |
20 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.-50+15576delT | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229906303 | |||||||
| chr2:229906310 | A | C | 6 | a0001c0002t0003g0035 a0001c0002t0003g0036 a0001c0002t0003g0037 others(3): Show |
6 | HG00323.hp1 HG01074.hp2 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.-50+15570T>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229906310 | |||||||
| chr2:229906314 | A | G | 2 | a0001c0001t0001g0093 a0001c0001t0001g0094 |
2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-50+15566T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229906314 | |||||||
| chr2:229906397 | A | T | 174 | a0001c0001t0001g0094 a0001c0001t0001g0097 a0001c0001t0001g0105 others(171): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.-50+15483T>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229906397 | |||||||
| chr2:229906588 | C | T | 5 | a0001c0001t0010g0249 a0001c0001t0010g0250 a0001c0001t0010g0251 others(2): Show |
5 | HG00741.hp2 HG01106.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-50+15292G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229906588 | |||||||
| chr2:229906633 | T | C | 2 | a0001c0001t0009g0171 a0001c0001t0009g0172 |
2 | HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-50+15247A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229906633 | |||||||
| chr2:229906724 | C | CA | 8 | a0001c0001t0001g0120 a0001c0001t0010g0249 a0001c0001t0010g0250 others(5): Show |
8 | HG00741.hp2 HG01106.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.-50+15155dupT | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229906724 | |||||||
| chr2:229906938 | A | G | 14 | a0001c0001t0004g0001 a0001c0001t0004g0254 a0001c0001t0004g0255 others(11): Show |
15 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.-50+14942T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229906938 | |||||||
| chr2:229906975 | T | A | 1 | a0001c0001t0001g0231 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-50+14905A>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229906975 | |||||||
| chr2:229907395 | C | T | 1 | a0001c0001t0001g0248 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-50+14485G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229907395 | |||||||
| chr2:229907736 | G | A | 1 | a0001c0002t0003g0026 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-50+14144C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229907736 | |||||||
| chr2:229907781 | C | A | 1 | a0001c0003t0001g0095 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-50+14099G>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229907781 | |||||||
| chr2:229907784 | C | CAG | 326 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0093 others(323): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.-50+14094_-50+1409 others(6): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229907784 | |||||||
| chr2:229907868 | T | A | 1 | a0001c0002t0002g0301 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-50+14012A>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229907868 | |||||||
| chr2:229907909 | A | C | 2 | a0001c0002t0003g0032 a0001c0002t0013g0004 |
2 | HG02602.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-50+13971T>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229907909 | |||||||
| chr2:229907962 | C | G | 78 | a0001c0002t0001g0027 a0001c0002t0001g0028 a0001c0002t0001g0029 others(75): Show |
78 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.-50+13918G>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229907962 | |||||||
| chr2:229908073 | C | T | 1 | a0001c0001t0001g0179 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-50+13807G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229908073 | |||||||
| chr2:229908317 | A | G | 1 | a0001c0003t0001g0204 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-50+13563T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229908317 | |||||||
| chr2:229908429 | CG | C | 18 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0099 others(15): Show |
19 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.-50+13450delC | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229908429 | |||||||
| chr2:229908482 | C | T | 9 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0188 others(6): Show |
9 | HG02615.hp2 HG02723.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.-50+13398G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229908482 | |||||||
| chr2:229908540 | C | A | 2 | a0001c0002t0001g0059 a0001c0002t0001g0077 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-50+13340G>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229908540 | |||||||
| chr2:229908576 | C | T | 4 | a0001c0002t0003g0062 a0001c0002t0003g0078 a0001c0002t0003g0271 others(1): Show |
4 | HG00733.hp1 HG01099.hp2 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50+13304G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229908576 | |||||||
| chr2:229908601 | G | A | 3 | a0001c0001t0014g0107 a0001c0001t0014g0108 a0001c0001t0014g0112 |
3 | HG02717.hp1 HG02818.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-50+13279C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229908601 | |||||||
| chr2:229908825 | C | T | 1 | a0001c0002t0003g0078 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-50+13055G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229908825 | |||||||
| chr2:229908858 | G | A | 1 | a0001c0002t0002g0302 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-50+13022C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229908858 | |||||||
| chr2:229908912 | C | T | 78 | a0001c0002t0001g0027 a0001c0002t0001g0028 a0001c0002t0001g0029 others(75): Show |
78 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.-50+12968G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229908912 | |||||||
| chr2:229908930 | A | C | 1 | a0001c0003t0001g0221 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-50+12950T>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229908930 | |||||||
| chr2:229909025 | G | A | 5 | a0001c0001t0010g0249 a0001c0001t0010g0250 a0001c0001t0010g0251 others(2): Show |
5 | HG00741.hp2 HG01106.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-50+12855C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229909025 | |||||||
| chr2:229909089 | C | CA | 252 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0097 others(249): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.-50+12790dupT | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229909089 | |||||||
| chr2:229909089 | C | CAA | 16 | a0001c0001t0001g0153 a0001c0001t0001g0156 a0001c0001t0001g0215 others(13): Show |
16 | HG00544.hp1 HG01070.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.-50+12789_-50+1279 others(6): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229909089 | |||||||
| chr2:229909159 | A | G | 1 | a0001c0001t0010g0252 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-50+12721T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229909159 | |||||||
| chr2:229909340 | G | C | 3 | a0001c0001t0014g0107 a0001c0001t0014g0108 a0001c0001t0014g0112 |
3 | HG02717.hp1 HG02818.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-50+12540C>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229909340 | |||||||
| chr2:229909387 | A | C | 1 | a0001c0002t0001g0028 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-50+12493T>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229909387 | |||||||
| chr2:229909390 | A | C | 120 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0093 others(117): Show |
121 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.-50+12490T>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229909390 | |||||||
| chr2:229909392 | A | C | 16 | a0001c0001t0001g0099 a0001c0001t0004g0001 a0001c0001t0004g0254 others(13): Show |
17 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.-50+12488T>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229909392 | |||||||
| chr2:229909472 | C | T | 3 | a0001c0001t0014g0107 a0001c0001t0014g0108 a0001c0001t0014g0112 |
3 | HG02717.hp1 HG02818.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-50+12408G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229909472 | |||||||
| chr2:229909543 | G | A | 3 | a0001c0001t0014g0107 a0001c0001t0014g0108 a0001c0001t0014g0112 |
3 | HG02717.hp1 HG02818.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-50+12337C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229909543 | |||||||
| chr2:229909557 | T | TA | 10 | a0001c0001t0001g0144 a0001c0001t0001g0183 a0001c0001t0001g0184 others(7): Show |
10 | HG01884.hp1 HG02630.hp1 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.-50+12322dupT | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229909557 | |||||||
| chr2:229909888 | A | G | 5 | a0001c0001t0010g0249 a0001c0001t0010g0250 a0001c0001t0010g0251 others(2): Show |
5 | HG00741.hp2 HG01106.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-50+11992T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229909888 | |||||||
| chr2:229909948 | A | G | 2 | a0001c0001t0001g0093 a0001c0001t0001g0094 |
2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-50+11932T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229909948 | |||||||
| chr2:229910288 | T | C | 1 | a0001c0003t0007g0222 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-50+11592A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229910288 | |||||||
| chr2:229910715 | T | A | 2 | a0001c0001t0010g0249 a0001c0001t0010g0250 |
2 | HG03195.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-50+11165A>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229910715 | |||||||
| chr2:229910871 | T | C | 7 | a0001c0001t0001g0153 a0001c0001t0001g0215 a0001c0001t0001g0227 others(4): Show |
7 | HG02486.hp2 HG02895.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.-50+11009A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229910871 | |||||||
| chr2:229910871 | T | G | 1 | a0001c0001t0001g0120 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-50+11009A>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229910871 | |||||||
| chr2:229910977 | T | C | 1 | a0001c0003t0005g0012 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-50+10903A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229910977 | |||||||
| chr2:229911062 | C | T | 1 | a0001c0004t0003g0083 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-50+10818G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229911062 | |||||||
| chr2:229911097 | G | A | 4 | a0001c0001t0004g0254 a0001c0001t0004g0255 a0001c0001t0004g0259 others(1): Show |
4 | HG01891.hp2 HG02647.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50+10783C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229911097 | |||||||
| chr2:229911200 | C | T | 1 | a0001c0001t0001g0269 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-50+10680G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229911200 | |||||||
| chr2:229911304 | G | C | 1 | a0001c0001t0001g0170 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-50+10576C>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229911304 | |||||||
| chr2:229911640 | C | T | 2 | a0001c0003t0006g0322 a0001c0003t0036g0321 |
2 | HG01261.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.-50+10240G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229911640 | |||||||
| chr2:229911662 | G | A | 1 | a0001c0002t0003g0031 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-50+10218C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229911662 | |||||||
| chr2:229911706 | T | C | 1 | a0001c0002t0003g0026 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-50+10174A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229911706 | |||||||
| chr2:229911790 | T | C | 3 | a0001c0001t0014g0107 a0001c0001t0014g0108 a0001c0001t0014g0112 |
3 | HG02717.hp1 HG02818.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-50+10090A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229911790 | |||||||
| chr2:229912035 | T | G | 1 | a0001c0002t0002g0294 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-50+9845A>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229912035 | |||||||
| chr2:229912064 | C | T | 7 | a0001c0001t0001g0153 a0001c0001t0001g0215 a0001c0001t0001g0227 others(4): Show |
7 | HG02486.hp2 HG02895.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.-50+9816G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229912064 | |||||||
| chr2:229912728 | A | T | 101 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0099 others(98): Show |
102 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.-50+9152T>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229912728 | |||||||
| chr2:229912740 | C | G | 101 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0099 others(98): Show |
102 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.-50+9140G>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229912740 | |||||||
| chr2:229912869 | G | GT | 5 | a0001c0001t0010g0249 a0001c0001t0010g0250 a0001c0001t0010g0251 others(2): Show |
5 | HG00741.hp2 HG01106.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-50+9010dupA | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229912869 | |||||||
| chr2:229913457 | T | C | 1 | a0001c0003t0007g0202 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-50+8423A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229913457 | |||||||
| chr2:229913669 | C | T | 18 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0099 others(15): Show |
19 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.-50+8211G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229913669 | |||||||
| chr2:229913694 | C | T | 1 | a0001c0002t0003g0031 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-50+8186G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229913694 | |||||||
| chr2:229913706 | T | C | 18 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0099 others(15): Show |
19 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.-50+8174A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229913706 | |||||||
| chr2:229914046 | T | C | 18 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0099 others(15): Show |
19 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.-50+7834A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229914046 | |||||||
| chr2:229914184 | G | A | 3 | a0001c0001t0004g0261 a0001c0001t0004g0264 a0001c0001t0004g0265 |
3 | HG02145.hp1 HG02486.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.-50+7696C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229914184 | |||||||
| chr2:229914217 | T | A | 5 | a0001c0001t0011g0098 a0001c0001t0011g0114 a0001c0001t0011g0187 others(2): Show |
5 | HG01884.hp1 HG02723.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-50+7663A>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229914217 | |||||||
| chr2:229914526 | A | C | 3 | a0001c0002t0002g0306 a0001c0002t0002g0307 a0001c0002t0002g0308 |
3 | HG00323.hp2 HG01071.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.-50+7354T>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229914526 | |||||||
| chr2:229914718 | G | A | 13 | a0001c0001t0001g0145 a0001c0001t0001g0186 a0001c0001t0001g0192 others(10): Show |
13 | HG00423.hp2 HG00438.hp2 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.-50+7162C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229914718 | |||||||
| chr2:229914909 | C | G | 101 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0099 others(98): Show |
102 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.-50+6971G>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229914909 | |||||||
| chr2:229915081 | G | A | 3 | a0001c0002t0003g0078 a0001c0002t0003g0271 a0001c0002t0013g0008 |
3 | HG00733.hp1 HG01099.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.-50+6799C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229915081 | |||||||
| chr2:229915126 | A | G | 1 | a0001c0002t0020g0002 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-50+6754T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229915126 | |||||||
| chr2:229915137 | G | A | 5 | a0001c0001t0009g0146 a0001c0001t0009g0147 a0001c0001t0009g0148 others(2): Show |
5 | HG02280.hp2 HG02559.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.-50+6743C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229915137 | |||||||
| chr2:229915336 | C | T | 1 | a0001c0003t0001g0100 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-50+6544G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229915336 | |||||||
| chr2:229915442 | A | T | 2 | a0001c0001t0001g0099 a0001c0001t0005g0011 |
2 | HG02055.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-50+6438T>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229915442 | |||||||
| chr2:229915529 | C | T | 2 | a0001c0001t0001g0269 a0001c0001t0009g0268 |
2 | HG00639.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.-50+6351G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229915529 | |||||||
| chr2:229915531 | G | C | 2 | a0001c0001t0001g0269 a0001c0001t0009g0268 |
2 | HG00639.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.-50+6349C>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229915531 | |||||||
| chr2:229915532 | T | A | 2 | a0001c0001t0001g0269 a0001c0001t0009g0268 |
2 | HG00639.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.-50+6348A>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229915532 | |||||||
| chr2:229915591 | G | C | 1 | a0001c0002t0029g0060 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-50+6289C>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229915591 | |||||||
| chr2:229915631 | A | AAAG | 317 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0093 others(314): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.-50+6246_-50+6248d others(5): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229915631 | |||||||
| chr2:229915692 | TA | T | 167 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0097 others(164): Show |
167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.-50+6187delT | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229915692 | |||||||
| chr2:229915706 | A | T | 5 | a0001c0001t0001g0269 a0001c0001t0009g0268 a0001c0001t0014g0107 others(2): Show |
5 | HG00639.hp2 HG02055.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-50+6174T>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229915706 | |||||||
| chr2:229915707 | A | T | 8 | a0001c0001t0001g0269 a0001c0001t0009g0268 a0001c0001t0014g0107 others(5): Show |
8 | HG00639.hp2 HG02055.hp2 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.-50+6173T>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229915707 | |||||||
| chr2:229915919 | T | G | 43 | a0001c0001t0019g0317 a0001c0001t0019g0318 a0001c0002t0002g0279 others(40): Show |
43 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(40): Show |
intron_variant | MODIFIER | c.-50+5961A>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229915919 | |||||||
| chr2:229916144 | G | A | 1 | a0001c0003t0001g0204 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-50+5736C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229916144 | |||||||
| chr2:229916331 | T | C | 1 | a0001c0001t0001g0149 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-50+5549A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229916331 | |||||||
| chr2:229916485 | G | A | 3 | a0001c0003t0015g0150 a0001c0003t0015g0151 a0001c0003t0015g0173 |
3 | HG02922.hp2 HG02965.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-50+5395C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229916485 | |||||||
| chr2:229916536 | CA | C | 165 | a0001c0001t0001g0097 a0001c0001t0001g0105 a0001c0001t0001g0106 others(162): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.-50+5343delT | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229916536 | |||||||
| chr2:229916680 | A | T | 4 | a0001c0001t0001g0116 a0001c0001t0001g0121 a0001c0001t0001g0122 others(1): Show |
4 | HG01070.hp1 HG01081.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50+5200T>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229916680 | |||||||
| chr2:229916860 | T | TA | 264 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0093 others(261): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.-50+5019dupT | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229916860 | |||||||
| chr2:229916902 | G | A | 3 | a0001c0001t0014g0107 a0001c0001t0014g0108 a0001c0001t0014g0112 |
3 | HG02717.hp1 HG02818.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-50+4978C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229916902 | |||||||
| chr2:229916913 | T | C | 5 | a0001c0001t0001g0269 a0001c0001t0009g0268 a0001c0001t0014g0107 others(2): Show |
5 | HG00639.hp2 HG02055.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-50+4967A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229916913 | |||||||
| chr2:229917208 | A | G | 270 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0093 others(267): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.-50+4672T>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229917208 | |||||||
| chr2:229917373 | T | C | 1 | a0001c0003t0001g0206 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-50+4507A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229917373 | |||||||
| chr2:229917374 | C | T | 18 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0099 others(15): Show |
19 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.-50+4506G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229917374 | |||||||
| chr2:229917380 | C | CA | 27 | a0001c0001t0001g0022 a0001c0001t0001g0179 a0001c0001t0001g0180 others(24): Show |
27 | HG01109.hp1 HG01243.hp2 HG01975.hp1 others(24): Show |
intron_variant | MODIFIER | c.-50+4499dupT | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229917380 | |||||||
| chr2:229917380 | C | CAA | 12 | a0001c0001t0001g0023 a0001c0001t0001g0192 a0001c0002t0002g0292 others(9): Show |
12 | HG00597.hp1 HG00673.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.-50+4498_-50+4499d others(4): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229917380 | |||||||
| chr2:229917380 | C | CAAA | 6 | a0001c0001t0024g0239 a0001c0003t0001g0092 a0001c0003t0006g0326 others(3): Show |
6 | HG00140.hp1 HG00558.hp1 HG00558.hp2 others(3): Show |
intron_variant | MODIFIER | c.-50+4497_-50+4499d others(5): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229917380 | |||||||
| chr2:229917380 | C | CAAAAA | 6 | a0001c0001t0001g0195 a0001c0001t0001g0197 a0001c0001t0019g0317 others(3): Show |
6 | HG01433.hp1 HG02027.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.-50+4495_-50+4499d others(7): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229917380 | |||||||
| chr2:229917380 | C | CAAAAAA | 11 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0019g0318 others(8): Show |
11 | HG02559.hp2 HG02630.hp1 HG03017.hp1 others(8): Show |
intron_variant | MODIFIER | c.-50+4494_-50+4499d others(8): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229917380 | |||||||
| chr2:229917380 | C | CAAAAAAA | 7 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0210 others(4): Show |
7 | HG00438.hp2 HG01515.hp1 NA18952.hp2 others(4): Show |
intron_variant | MODIFIER | c.-50+4493_-50+4499d others(9): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229917380 | |||||||
| chr2:229917380 | C | CAAAAAAA others(3): Show |
4 | a0001c0001t0005g0020 a0001c0002t0002g0305 a0001c0003t0001g0214 others(1): Show |
4 | HG01175.hp1 HG02300.hp2 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.-50+4490_-50+4499d others(12): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229917380 | |||||||
| chr2:229917380 | C | CAAAAAAA others(4): Show |
9 | a0001c0001t0001g0215 a0001c0001t0001g0220 a0001c0002t0002g0306 others(6): Show |
9 | HG00323.hp2 HG01071.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.-50+4489_-50+4499d others(13): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229917380 | |||||||
| chr2:229917380 | C | CAAAAAAA others(5): Show |
2 | a0001c0002t0002g0320 a0001c0003t0007g0222 |
2 | HG01928.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.-50+4488_-50+4499d others(14): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229917380 | |||||||
| chr2:229917380 | C | CAAAAAAA others(6): Show |
5 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0011g0225 others(2): Show |
5 | HG00423.hp2 HG02723.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-50+4487_-50+4499d others(15): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229917380 | |||||||
| chr2:229917380 | C | CAAAAAAA others(7): Show |
1 | a0001c0001t0001g0277 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-50+4486_-50+4499d others(16): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229917380 | |||||||
| chr2:229917380 | C | CAAAAAAA others(10): Show |
1 | a0001c0001t0001g0227 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-50+4483_-50+4499d others(19): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229917380 | |||||||
| chr2:229917380 | C | CAAAAAAA others(11): Show |
1 | a0001c0003t0001g0228 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-50+4482_-50+4499d others(20): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229917380 | |||||||
| chr2:229917380 | C | CAAAAAAA others(14): Show |
1 | a0001c0001t0001g0229 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-50+4479_-50+4499d others(23): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229917380 | |||||||
| chr2:229917380 | C | CAAAAAAA others(17): Show |
1 | a0001c0001t0001g0230 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-50+4476_-50+4499d others(26): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229917380 | |||||||
| chr2:229917380 | C | CAAAAAAA others(26): Show |
1 | a0001c0001t0001g0231 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-50+4467_-50+4499d others(35): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229917380 | |||||||
| chr2:229917380 | C | CAAAAAAA others(33): Show |
1 | a0001c0002t0002g0309 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-50+4499_-50+4500i others(42): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229917380 | |||||||
| chr2:229917380 | CA | C | 48 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(45): Show |
48 | HG00280.hp2 HG00408.hp1 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.-50+4499delT | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229917380 | |||||||
| chr2:229917380 | CAA | C | 9 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0118 others(6): Show |
9 | HG00741.hp2 HG01934.hp2 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.-50+4498_-50+4499d others(4): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229917380 | |||||||
| chr2:229917380 | CAAAAA | C | 27 | a0001c0001t0001g0094 a0001c0002t0001g0063 a0001c0002t0001g0064 others(24): Show |
27 | HG00099.hp2 HG00438.hp1 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.-50+4495_-50+4499d others(7): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229917380 | |||||||
| chr2:229917380 | CAAAAAA | C | 48 | a0001c0001t0001g0093 a0001c0001t0001g0269 a0001c0001t0011g0114 others(45): Show |
48 | HG00323.hp1 HG00544.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.-50+4494_-50+4499d others(8): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229917380 | |||||||
| chr2:229917380 | CAAAAAAA | C | 8 | a0001c0001t0004g0266 a0001c0001t0009g0268 a0001c0001t0014g0112 others(5): Show |
8 | HG00408.hp2 HG02055.hp2 HG02698.hp1 others(5): Show |
intron_variant | MODIFIER | c.-50+4493_-50+4499d others(9): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229917380 | |||||||
| chr2:229917380 | CAAAAAAA others(1): Show |
C | 16 | a0001c0001t0001g0099 a0001c0001t0001g0105 a0001c0001t0001g0106 others(13): Show |
17 | HG00544.hp1 HG01243.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.-50+4492_-50+4499d others(10): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229917380 | |||||||
| chr2:229917380 | CAAAAAAA others(2): Show |
C | 10 | a0001c0001t0004g0255 a0001c0001t0004g0257 a0001c0001t0004g0258 others(7): Show |
10 | HG01516.hp2 HG01891.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.-50+4491_-50+4499d others(11): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229917380 | |||||||
| chr2:229917380 | CAAAAAAA others(3): Show |
C | 3 | a0001c0001t0004g0254 a0001c0001t0010g0250 a0001c0002t0002g0280 |
3 | HG00423.hp1 HG03041.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-50+4490_-50+4499d others(12): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229917380 | |||||||
| chr2:229917380 | CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0001g0097 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-50+4488_-50+4499d others(14): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229917380 | |||||||
| chr2:229917380 | CAAAAAAA others(7): Show |
C | 1 | a0002c0006t0001g0096 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-50+4486_-50+4499d others(16): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229917380 | |||||||
| chr2:229917380 | CAAAAAAA others(10): Show |
C | 2 | a0001c0002t0002g0279 a0001c0003t0001g0095 |
2 | NA18951.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.-50+4483_-50+4499d others(19): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229917380 | |||||||
| chr2:229917380 | CAAAAAAA others(17): Show |
C | 2 | a0001c0002t0003g0024 a0001c0002t0003g0025 |
2 | HG01257.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.-50+4476_-50+4499d others(26): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229917380 | |||||||
| chr2:229917380 | CAAAAAAA others(19): Show |
C | 1 | a0001c0002t0002g0310 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-50+4474_-50+4499d others(28): Show |
TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229917380 | |||||||
| chr2:229917595 | A | C | 2 | a0001c0001t0001g0093 a0001c0001t0001g0094 |
2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-50+4285T>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229917595 | |||||||
| chr2:229917598 | C | T | 1 | a0001c0001t0005g0010 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-50+4282G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229917598 | |||||||
| chr2:229917639 | C | T | 1 | a0001c0001t0010g0249 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-50+4241G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229917639 | |||||||
| chr2:229917803 | G | A | 1 | a0001c0001t0001g0232 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.-50+4077C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229917803 | |||||||
| chr2:229917901 | T | C | 1 | a0001c0002t0002g0295 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-50+3979A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229917901 | |||||||
| chr2:229917996 | C | T | 1 | a0001c0003t0001g0092 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-50+3884G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229917996 | |||||||
| chr2:229918556 | GT | G | 8 | a0001c0001t0001g0233 a0001c0001t0001g0234 a0001c0001t0001g0235 others(5): Show |
8 | HG00558.hp1 HG00558.hp2 NA18945.hp1 others(5): Show |
intron_variant | MODIFIER | c.-50+3323delA | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229918556 | |||||||
| chr2:229919013 | A | C | 2 | a0001c0001t0001g0269 a0001c0001t0009g0268 |
2 | HG00639.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.-50+2867T>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229919013 | |||||||
| chr2:229919284 | C | T | 1 | a0001c0002t0001g0028 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-50+2596G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229919284 | |||||||
| chr2:229919393 | C | T | 1 | a0001c0003t0001g0091 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-50+2487G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229919393 | |||||||
| chr2:229919409 | T | C | 8 | a0001c0004t0003g0082 a0001c0004t0003g0083 a0001c0004t0003g0084 others(5): Show |
8 | HG02056.hp1 HG02129.hp2 NA18951.hp1 others(5): Show |
intron_variant | MODIFIER | c.-50+2471A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229919409 | |||||||
| chr2:229919414 | T | TA | 77 | a0001c0002t0001g0028 a0001c0002t0001g0029 a0001c0002t0001g0033 others(74): Show |
77 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.-50+2465dupT | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229919414 | |||||||
| chr2:229919677 | A | C | 19 | a0001c0002t0002g0279 a0001c0002t0002g0280 a0001c0002t0002g0281 others(16): Show |
19 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(16): Show |
intron_variant | MODIFIER | c.-50+2203T>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229919677 | |||||||
| chr2:229919735 | T | A | 1 | a0001c0002t0002g0320 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-50+2145A>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229919735 | |||||||
| chr2:229919906 | C | A | 1 | a0001c0002t0001g0089 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-50+1974G>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229919906 | |||||||
| chr2:229919985 | G | A | 1 | a0001c0001t0001g0240 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-50+1895C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229919985 | |||||||
| chr2:229919995 | T | C | 5 | a0001c0001t0001g0242 a0001c0001t0001g0243 a0001c0001t0001g0244 others(2): Show |
5 | HG02809.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.-50+1885A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229919995 | |||||||
| chr2:229920208 | T | C | 1 | a0001c0002t0017g0090 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-50+1672A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229920208 | |||||||
| chr2:229920347 | G | A | 3 | a0001c0001t0001g0246 a0001c0001t0001g0248 a0001c0001t0026g0247 |
3 | HG00408.hp1 HG01934.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.-50+1533C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229920347 | |||||||
| chr2:229920912 | A | C | 34 | a0001c0002t0002g0279 a0001c0002t0002g0280 a0001c0002t0002g0281 others(31): Show |
34 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(31): Show |
intron_variant | MODIFIER | c.-50+968T>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229920912 | |||||||
| chr2:229921065 | C | T | 3 | a0001c0002t0003g0024 a0001c0002t0003g0025 a0001c0002t0003g0026 |
3 | HG01175.hp2 HG01257.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.-50+815G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229921065 | |||||||
| chr2:229921140 | C | A | 3 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0005g0003 |
3 | HG02145.hp2 HG02257.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.-50+740G>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229921140 | |||||||
| chr2:229921274 | G | A | 5 | a0001c0001t0010g0249 a0001c0001t0010g0250 a0001c0001t0010g0251 others(2): Show |
5 | HG00741.hp2 HG01106.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-50+606C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229921274 | |||||||
| chr2:229921377 | C | T | 78 | a0001c0002t0001g0027 a0001c0002t0001g0028 a0001c0002t0001g0029 others(75): Show |
78 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.-50+503G>A | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229921377 | |||||||
| chr2:229921412 | T | C | 14 | a0001c0001t0004g0001 a0001c0001t0004g0254 a0001c0001t0004g0255 others(11): Show |
15 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.-50+468A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229921412 | |||||||
| chr2:229921624 | T | C | 1 | a0001c0008t0001g0267 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-50+256A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229921624 | |||||||
| chr2:229921721 | G | A | 2 | a0001c0001t0001g0269 a0001c0001t0009g0268 |
2 | HG00639.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.-50+159C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229921721 | |||||||
| chr2:229921804 | C | G | 3 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0005g0003 |
3 | HG02145.hp2 HG02257.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.-50+76G>C | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229921804 | |||||||
| chr2:229921808 | G | C | 1 | a0001c0002t0020g0002 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-50+72C>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229921808 | |||||||
| chr2:229921808 | G | GC | 16 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0276 others(13): Show |
16 | HG00597.hp2 HG00741.hp1 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.-50+71dupG | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229921808 |