Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| 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 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and 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 | copy fasta | chr2 | 229758837 | 229927009 |
| a0002 | 0/0 | 2067 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 6204 | 149 | 68 | 29 | 37 | 4 | 10 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| c0002 | 0/0 | 6204 | 112 | 12 | 29 | 43 | 8 | 20 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| c0003 | 0/1 | 6204 | 53 | 9 | 6 | 24 | 4 | 9 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| c0004 | 0/0 | 6204 | 8 | 0 | 0 | 8 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| c0005 | 0/0 | 6204 | 3 | 3 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| c0006 | 0/0 | 6204 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| c0007 | 0/0 | 6204 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| c0008 | 0/0 | 6204 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| c0009 | 0/0 | 6204 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| c0010 | 0/0 | 6204 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 3897 | 155 | 39 | 25 | 63 | 5 | 22 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| t0002 | 0/0 | 3897 | 37 | 6 | 8 | 15 | 5 | 3 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| t0003 | 0/0 | 3897 | 36 | 1 | 10 | 16 | 2 | 7 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| t0004 | 0/0 | 3897 | 14 | 13 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| t0005 | 0/0 | 3898 | 13 | 3 | 3 | 3 | 0 | 4 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| t0006 | 0/0 | 3897 | 8 | 0 | 3 | 0 | 2 | 3 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| t0007 | 0/1 | 3897 | 7 | 0 | 1 | 4 | 1 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| t0008 | 0/0 | 3899 | 6 | 0 | 0 | 6 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| t0009 | 0/0 | 3896 | 6 | 6 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| t0010 | 0/0 | 3896 | 5 | 3 | 2 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| t0011 | 0/0 | 3897 | 5 | 5 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| t0012 | 0/0 | 3897 | 4 | 2 | 2 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| t0013 | 0/0 | 3898 | 3 | 0 | 2 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| t0014 | 0/0 | 3897 | 3 | 3 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| t0015 | 0/0 | 3897 | 3 | 3 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| t0016 | 0/0 | 3897 | 2 | 0 | 2 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| t0017 | 0/0 | 3897 | 2 | 0 | 0 | 2 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| t0018 | 0/0 | 3897 | 2 | 2 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| t0019 | 0/0 | 3897 | 2 | 2 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| t0020 | 0/0 | 3897 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| t0021 | 0/0 | 3898 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| t0022 | 0/0 | 3898 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| t0023 | 0/0 | 3898 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| t0024 | 0/0 | 3897 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| t0025 | 0/0 | 3897 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| t0026 | 0/0 | 3897 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| t0027 | 0/0 | 3897 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| t0028 | 0/0 | 3897 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| t0029 | 0/0 | 3897 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| t0030 | 0/0 | 3897 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| t0031 | 0/0 | 3897 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| t0032 | 0/0 | 3897 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| t0033 | 0/0 | 3897 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| t0034 | 0/0 | 3897 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| t0035 | 0/0 | 3897 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| t0036 | 0/0 | 3898 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0176 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0195 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0298 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0308 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0327 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0328 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 6204 | 149 | 68 | 29 | 37 | 4 | 10 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| a0001c0002 | 0/0 | 6204 | 112 | 12 | 29 | 43 | 8 | 20 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| a0001c0003 | 0/1 | 6204 | 53 | 9 | 6 | 24 | 4 | 9 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| a0001c0004 | 0/0 | 6204 | 8 | 0 | 0 | 8 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| a0001c0005 | 0/0 | 6204 | 3 | 3 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| a0001c0007 | 0/0 | 6204 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| a0001c0008 | 0/0 | 6204 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| a0001c0009 | 0/0 | 6204 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| a0001c0010 | 0/0 | 6204 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| a0002c0006 | 0/0 | 6204 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | 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 | copy fasta | chr2 | 229758837 | 229927009 |
| a0001c0001t0004 | 0/0 | 10100 | 14 | 13 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| a0001c0001t0005 | 0/0 | 10101 | 8 | 2 | 3 | 1 | 0 | 2 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| a0001c0001t0009 | 0/0 | 10099 | 6 | 6 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| a0001c0001t0010 | 0/0 | 10099 | 5 | 3 | 2 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| a0001c0001t0011 | 0/0 | 10100 | 5 | 5 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| a0001c0001t0012 | 0/0 | 10100 | 4 | 2 | 2 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| a0001c0001t0014 | 0/0 | 10100 | 3 | 3 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| a0001c0001t0016 | 0/0 | 10100 | 2 | 0 | 2 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| a0001c0001t0019 | 0/0 | 10100 | 2 | 2 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| a0001c0001t0024 | 0/0 | 10100 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| a0001c0001t0025 | 0/0 | 10100 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| a0001c0001t0026 | 0/0 | 10100 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| a0001c0001t0027 | 0/0 | 10100 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| a0001c0001t0030 | 0/0 | 10100 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| a0001c0001t0031 | 0/0 | 10100 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| a0001c0002t0001 | 0/0 | 10100 | 24 | 0 | 6 | 9 | 1 | 8 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| a0001c0002t0002 | 0/0 | 10100 | 37 | 6 | 8 | 15 | 5 | 3 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| a0001c0002t0003 | 0/0 | 10100 | 28 | 1 | 10 | 8 | 2 | 7 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| a0001c0002t0005 | 0/0 | 10101 | 2 | 1 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| a0001c0002t0008 | 0/0 | 10102 | 6 | 0 | 0 | 6 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| a0001c0002t0013 | 0/0 | 10101 | 3 | 0 | 2 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| a0001c0002t0017 | 0/0 | 10100 | 2 | 0 | 0 | 2 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| a0001c0002t0018 | 0/0 | 10100 | 2 | 2 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| a0001c0002t0020 | 0/0 | 10100 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| a0001c0002t0022 | 0/0 | 10101 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| a0001c0002t0023 | 0/0 | 10101 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| a0001c0002t0028 | 0/0 | 10100 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| a0001c0002t0029 | 0/0 | 10100 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| a0001c0002t0033 | 0/0 | 10100 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| a0001c0002t0034 | 0/0 | 10100 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| a0001c0002t0035 | 0/0 | 10100 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| a0001c0003t0001 | 0/0 | 10100 | 31 | 6 | 1 | 18 | 1 | 5 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| a0001c0003t0005 | 0/0 | 10101 | 2 | 0 | 0 | 1 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| a0001c0003t0006 | 0/0 | 10100 | 8 | 0 | 3 | 0 | 2 | 3 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| a0001c0003t0007 | 0/1 | 10100 | 6 | 0 | 1 | 3 | 1 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| a0001c0003t0015 | 0/0 | 10100 | 3 | 3 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| a0001c0003t0021 | 0/0 | 10101 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| a0001c0003t0032 | 0/0 | 10100 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| a0001c0003t0036 | 0/0 | 10101 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| a0001c0004t0003 | 0/0 | 10100 | 8 | 0 | 0 | 8 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| a0001c0005t0001 | 0/0 | 10100 | 3 | 3 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| a0001c0007t0005 | 0/0 | 10101 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| a0001c0008t0001 | 0/0 | 10100 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| a0001c0009t0007 | 0/0 | 10100 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| a0001c0010t0001 | 0/0 | 10100 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| a0002c0006t0001 | 0/0 | 10100 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | copy fasta | chr2 | 229758837 | 229927009 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and 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 | 0 | 1 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 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 |
| a0001c0001t0001g0196 | 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 |
| a0001c0001t0012g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0001t0012g0139 | 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 |
| a0001c0001t0016g0140 | 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 |
| a0001c0002t0002g0314 | 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 |
| 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 |
| a0001c0002t0003g0041 | 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 |
| a0001c0002t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0003g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0003g0050 | 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 |
| a0001c0002t0008g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| a0001c0002t0008g0046 | 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 |
| 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 |
| a0001c0002t0017g0051 | 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 |
| a0001c0002t0018g0316 | 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 |
| a0001c0002t0033g0040 | 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 |
| a0001c0003t0001g0103 | 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 |
| a0001c0003t0007g0195 | 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 |
| a0001c0009t0007g0102 | 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 | g0055 | 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 | g0139 | 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 | g0041 | 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 | g0038 | 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 | g0036 | 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 | g0040 | 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 | g0137 | 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 | g0140 | 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 | g0196 | 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 | g0150 | 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 | g0151 | AFR | ESN | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| HG02970 | hp1 | a0001 | c0002 | t0018 | g0316 | 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 | g0045 | 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 | g0103 | 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 | g0046 | 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 | g0209 | 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 | g0210 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA18957 | hp1 | a0001 | c0002 | t0017 | g0051 | 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 | g0050 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA18969 | hp1 | a0001 | c0002 | t0008 | g0049 | EAS | JPT | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0142 | 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 | g0043 | 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 | g0048 | 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 | g0102 | 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 | g0044 | 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 | g0314 | 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 | g0054 | 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 | g0053 | 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 | g0141 | 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 | g0056 | 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 | g0138 | 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 | hp1 | a0001 | c0003 | t0007 | g0195 | REF | REF | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0176 | REF | REF | TRIP12_chr2_229758837_229927009 | TRIP12 | chr2 | 229758837 | 229927009 |
| 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 |
| 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 | a0001c0002a0001c0004a0001c0009 | 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 | a0001c0003a0001c0005a0001c0008others(2): Show | 59 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(56): 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 |
| 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 | a0001c0002t0002a0001c0002t0018a0001c0002t0023others(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 | a0001c0003t0007a0001c0003t0032a0001c0009t0007 | 8 | HG00280.hp1 HG00558.hp1 HG02293.hp1 others(5): 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 | a0001c0002t0003a0001c0002t0008a0001c0002t0013others(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 | a0001c0001t0012a0001c0001t0016 | 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 | a0001c0001t0009a0001c0001t0010 | 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 | a0001c0002t0022a0001c0002t0033 | 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 | a0001c0001t0011a0001c0001t0019a0001c0002t0002others(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 | a0001c0001t0019a0001c0002t0002a0001c0002t0018others(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 | a0001c0001t0005a0001c0002t0005a0001c0002t0013others(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 | a0001c0003t0006a0001c0003t0036 | 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 |
| 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 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0099others(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 | a0001c0003t0006g0323a0001c0003t0006g0325 | 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 | a0001c0001t0010g0249a0001c0001t0010g0250a0001c0001t0010g0251others(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 | a0001c0001t0001g0188a0001c0001t0001g0189 | 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 | a0001c0001t0011g0098a0001c0001t0011g0114a0001c0001t0011g0187others(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 | a0001c0001t0011g0098a0001c0001t0011g0114a0001c0001t0011g0225others(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 | a0001c0002t0003g0032a0001c0002t0013g0004 | 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 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0099others(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 | a0001c0002t0003g0078a0001c0002t0003g0271a0001c0002t0013g0008 | 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 | a0001c0001t0011g0098a0001c0001t0011g0114a0001c0001t0011g0187others(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 | a0001c0001t0001g0099a0001c0001t0001g0153a0001c0001t0001g0215others(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 | a0001c0002t0001g0056a0001c0002t0003g0066a0001c0004t0003g0083others(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 | a0001c0001t0009g0268a0001c0001t0014g0107a0001c0001t0014g0108others(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 | 2 | a0001c0003t0007g0159a0001c0003t0007g0195 | 2 | HG00280.hp1 homoSapiens_chm13v2.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 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0188others(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 | a0001c0001t0001g0269a0001c0001t0009g0268a0001c0001t0014g0107others(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 | a0001c0002t0008g0039a0001c0002t0008g0047 | 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 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0127others(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 | a0001c0002t0001g0027a0001c0002t0001g0028a0001c0002t0001g0029others(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 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0188others(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 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0099others(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 | a0001c0002t0002g0303a0001c0002t0002g0304 | 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 | a0001c0002t0003g0069a0001c0002t0013g0005 | 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 | a0001c0002t0003g0050a0001c0002t0003g0067a0001c0002t0003g0073 | 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 | a0001c0001t0004g0001a0001c0001t0004g0254a0001c0001t0004g0255others(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 | a0001c0001t0001g0269a0001c0001t0009g0268 | 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 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0093others(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 | a0001c0001t0004g0263a0001c0001t0004g0266a0001c0001t0011g0098others(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 | a0001c0001t0001g0099a0001c0001t0001g0153a0001c0001t0001g0215others(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 | a0001c0002t0001g0027a0001c0002t0001g0028a0001c0002t0001g0029others(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 | a0001c0002t0003g0036a0001c0002t0003g0038 | 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 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0188others(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 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0011g0098others(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 | a0001c0001t0001g0099a0001c0001t0001g0153a0001c0001t0001g0215others(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 | a0001c0001t0001g0099a0001c0001t0001g0153a0001c0001t0001g0215others(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 | ||||||
| chr2:229773981
|
G | A | 1 | a0001c0003t0007g0195 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.5694+116C>T | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 38/41 | chr2 | 229773981 | ||||||
| chr2:229774002
|
T | C | 5 | a0001c0001t0001g0269a0001c0001t0009g0268a0001c0001t0014g0107others(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 | a0001c0001t0014g0107a0001c0001t0014g0108a0001c0001t0014g0112 | 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 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0011g0098others(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 | a0001c0002t0003g0045 | 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 | a0001c0001t0001g0145a0001c0001t0001g0192a0001c0001t0001g0197 | 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 | a0001c0002t0002g0279a0001c0002t0002g0280a0001c0002t0002g0281others(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 | a0001c0001t0004g0254a0001c0001t0004g0255a0001c0001t0004g0259others(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 | a0001c0001t0001g0097a0001c0001t0001g0105a0001c0001t0001g0129others(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 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0099others(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 | a0001c0001t0001g0269a0001c0001t0009g0268 | 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 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0188others(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 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0188others(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 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0005g0003 | 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 | 319 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0093others(316): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(317): 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 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0099others(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 | a0001c0002t0003g0024a0001c0002t0003g0025a0001c0002t0003g0026others(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 | a0001c0001t0001g0166a0001c0001t0001g0167 | 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 | a0001c0001t0014g0107a0001c0001t0014g0108a0001c0001t0014g0112 | 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 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0188others(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 | a0001c0001t0001g0203a0001c0001t0001g0208a0001c0001t0001g0209others(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 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0005g0003 | 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 | a0001c0001t0005g0010a0001c0002t0001g0027a0001c0002t0001g0028others(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 | a0001c0002t0003g0024a0001c0002t0003g0025 | 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 | a0001c0005t0001g0104a0001c0005t0001g0217a0001c0005t0001g0219 | 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 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0127others(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 | a0001c0002t0003g0035a0001c0002t0003g0037 | 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 | a0001c0001t0004g0254a0001c0001t0004g0255a0001c0001t0004g0259others(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 | a0001c0001t0001g0269a0001c0001t0009g0268 | 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 | a0001c0001t0001g0099a0001c0001t0001g0153a0001c0001t0001g0215others(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 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0099others(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 | a0001c0002t0002g0312a0001c0002t0002g0314a0001c0002t0002g0315others(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 | a0001c0001t0019g0317a0001c0001t0019g0318a0001c0002t0002g0279others(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 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0093others(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 | a0001c0001t0011g0098a0001c0001t0011g0114a0001c0001t0011g0225others(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 | a0001c0002t0002g0312a0001c0002t0002g0314a0001c0002t0002g0315others(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 | a0001c0001t0001g0097a0001c0001t0001g0105a0001c0001t0001g0106others(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 | a0001c0001t0011g0098a0001c0001t0011g0114a0001c0001t0011g0187others(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 | a0001c0004t0003g0082a0001c0004t0003g0083a0001c0004t0003g0084others(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 | a0001c0003t0001g0218a0001c0005t0001g0104a0001c0005t0001g0217others(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 | a0001c0001t0004g0001a0001c0001t0004g0254a0001c0001t0004g0255others(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 | a0001c0001t0001g0209a0001c0002t0033g0040 | 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 | a0001c0001t0001g0116a0001c0001t0001g0152a0001c0001t0001g0229others(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 | a0001c0001t0014g0107a0001c0001t0014g0108a0001c0001t0014g0112others(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 | a0001c0001t0001g0248a0001c0001t0004g0261a0001c0001t0004g0264others(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 | a0001c0001t0001g0099a0001c0001t0001g0133a0001c0001t0001g0153others(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 | a0001c0001t0001g0099a0001c0001t0001g0153a0001c0001t0001g0215others(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 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0093others(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 | a0001c0001t0001g0149a0001c0001t0001g0236a0001c0001t0004g0254others(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 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0093others(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 | a0001c0002t0003g0066a0001c0002t0029g0060 | 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 | a0001c0002t0001g0054 | 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 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0011g0098others(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 | a0001c0001t0001g0022a0001c0001t0005g0003 | 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 | a0001c0002t0002g0306a0001c0002t0002g0308 | 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 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0188others(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 | a0001c0002t0003g0024a0001c0002t0003g0025a0001c0002t0003g0026others(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 | 189 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0097others(186): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.4996-542dupA | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 33/41 | chr2 | 229786396 | ||||||
| chr2:229786396
|
C | CTT | 29 | a0001c0001t0001g0132a0001c0001t0001g0135a0001c0001t0001g0174others(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 | a0001c0001t0001g0269a0001c0001t0009g0268a0001c0001t0014g0107others(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 | a0001c0002t0001g0070a0001c0002t0001g0074a0001c0002t0003g0069others(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 | a0001c0002t0001g0027a0001c0002t0001g0028a0001c0002t0001g0029others(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 | a0001c0001t0010g0249a0001c0001t0010g0250 | 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 | a0001c0001t0001g0269a0001c0001t0009g0268 | 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 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0116others(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 | a0001c0001t0001g0097a0001c0001t0001g0119a0001c0001t0001g0133others(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 | a0001c0001t0001g0093a0001c0001t0001g0117a0001c0001t0004g0001others(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 | a0001c0001t0001g0094a0001c0001t0001g0099a0001c0001t0001g0174others(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 | a0001c0001t0001g0120a0001c0001t0001g0153a0001c0001t0001g0215others(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 | a0001c0001t0019g0317a0001c0001t0019g0318 | 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 | a0001c0002t0002g0299a0001c0002t0002g0300a0001c0002t0002g0301others(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 | a0001c0001t0010g0249a0001c0001t0010g0250a0001c0001t0010g0251others(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 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0188others(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 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0188others(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 | 324 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0093others(321): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(322): Show |
intron_variant | MODIFIER | c.4839-168delG | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 32/41 | chr2 | 229787828 | ||||||
| chr2:229788233
|
T | C | 13 | a0001c0001t0004g0001a0001c0001t0004g0254a0001c0001t0004g0255others(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 | a0001c0001t0014g0107a0001c0001t0014g0108a0001c0001t0014g0112 | 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 | a0001c0001t0001g0119a0001c0001t0009g0146a0001c0001t0009g0147others(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 | a0001c0001t0001g0093a0001c0001t0001g0094 | 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 | a0001c0001t0001g0093a0001c0001t0001g0094 | 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 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0093others(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 | a0001c0001t0011g0098a0001c0001t0011g0114a0001c0001t0011g0187others(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 | a0001c0001t0011g0098a0001c0001t0011g0114a0001c0001t0011g0187others(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 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0005g0003others(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 | a0001c0002t0001g0029a0001c0002t0001g0059a0001c0002t0001g0075others(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 | a0001c0001t0001g0099a0001c0001t0001g0153a0001c0001t0001g0215others(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 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0093others(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 | 319 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0093others(316): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(317): 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 | a0001c0001t0009g0268a0001c0001t0014g0107a0001c0001t0014g0108others(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 | a0001c0002t0003g0045 | 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 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0099others(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 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0093others(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 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0005g0003 | 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 | a0001c0002t0003g0044a0001c0002t0020g0002 | 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 | a0001c0001t0012g0138a0001c0001t0012g0139a0001c0001t0012g0168 | 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 | a0001c0001t0001g0097a0001c0001t0001g0105a0001c0001t0001g0106others(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 | a0001c0001t0001g0097a0001c0001t0001g0105a0001c0001t0001g0106others(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 | a0001c0001t0009g0268a0001c0001t0014g0107a0001c0001t0014g0108others(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 | a0001c0002t0003g0024a0001c0002t0003g0025a0001c0002t0003g0026others(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 | a0001c0003t0006g0322a0001c0003t0036g0321 | 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 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0099others(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 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0188others(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 | a0001c0001t0001g0099a0001c0001t0001g0153a0001c0001t0001g0215others(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 | a0001c0003t0006g0322a0001c0003t0036g0321 | 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 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0093others(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 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0005g0003 | 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 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0093others(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 | a0001c0002t0003g0041a0001c0002t0003g0042a0001c0002t0003g0272 | 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 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0188others(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 | a0001c0001t0004g0262a0001c0001t0005g0011a0001c0001t0011g0098others(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 | a0001c0001t0010g0249a0001c0001t0010g0250a0001c0001t0010g0251others(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 | a0001c0001t0014g0107a0001c0001t0014g0108a0001c0001t0014g0112 | 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 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0099others(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 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0099others(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 | a0001c0001t0001g0137 | 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 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0188others(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 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0127others(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 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0269others(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 | a0001c0001t0001g0099a0001c0001t0001g0153a0001c0001t0001g0215others(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 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0099others(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 | a0001c0002t0002g0282a0001c0002t0002g0286a0001c0002t0002g0288 | 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 | a0001c0001t0014g0107a0001c0001t0014g0108a0001c0001t0014g0112 | 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 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0099others(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 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0099others(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 | a0001c0001t0001g0269a0001c0001t0009g0268 | 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 | a0001c0002t0002g0280a0001c0002t0002g0281a0001c0002t0002g0287others(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 | a0001c0002t0017g0051a0001c0002t0017g0090 | 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 | a0001c0001t0001g0097a0001c0001t0001g0105a0001c0001t0001g0106others(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 | a0001c0001t0019g0317a0001c0001t0019g0318 | 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 | a0001c0002t0001g0053 | 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 | a0001c0002t0001g0027a0001c0002t0001g0028a0001c0002t0001g0029others(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 | 319 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0093others(316): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(317): 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 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0005g0003 | 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 | a0001c0002t0001g0027a0001c0002t0001g0028a0001c0002t0001g0029others(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 | a0001c0002t0002g0296a0001c0002t0002g0305a0001c0002t0002g0306others(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 | a0001c0001t0001g0153a0001c0001t0001g0215a0001c0001t0001g0227others(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 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0278 | 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 | a0001c0002t0001g0071a0001c0009t0007g0102 | 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 | a0001c0003t0001g0178a0001c0003t0001g0185 | 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 | a0001c0001t0001g0093a0001c0001t0001g0094 | 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 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0093others(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 | a0001c0002t0001g0027a0001c0002t0001g0028a0001c0002t0001g0029others(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 | a0001c0001t0001g0093a0001c0001t0001g0094 | 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 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0093others(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 | a0001c0002t0008g0048 | 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 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0188others(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 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0099others(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 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136others(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 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0005g0003others(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 |
69 | a0001c0001t0001g0106a0001c0001t0012g0138a0001c0001t0012g0139others(66): Show | 69 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(66): 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 | a0001c0001t0001g0097a0001c0001t0001g0105a0001c0001t0001g0116others(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 | a0001c0001t0001g0120a0001c0001t0001g0145a0001c0001t0001g0174others(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 | a0001c0001t0001g0099a0001c0001t0001g0153a0001c0001t0001g0230others(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 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0215others(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 | a0001c0002t0001g0028a0001c0002t0001g0029a0001c0002t0001g0052others(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 | a0001c0002t0001g0033a0001c0002t0001g0034a0001c0002t0001g0071others(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 | a0001c0009t0007g0102 | 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 | a0001c0003t0015g0150a0001c0003t0015g0151a0001c0003t0015g0173 | 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 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0099others(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 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0099others(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 | a0001c0003t0015g0151 | 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 | a0001c0001t0004g0261a0001c0001t0004g0264a0001c0001t0004g0265 | 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 | a0001c0002t0003g0076a0001c0002t0003g0079a0001c0002t0028g0081 | 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 | a0001c0002t0003g0044 | 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 | a0001c0002t0003g0044a0001c0002t0020g0002 | 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 | a0001c0002t0001g0054 | 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 | a0001c0001t0011g0098a0001c0001t0011g0114a0001c0001t0011g0187others(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 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0099others(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 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0099others(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 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0099others(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 | a0001c0001t0001g0269a0001c0001t0009g0268 | 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 | a0001c0001t0014g0107a0001c0001t0014g0108a0001c0001t0014g0112 | 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 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0099others(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 | a0001c0001t0001g0269a0001c0001t0009g0268 | 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 | a0001c0002t0003g0024a0001c0002t0003g0025a0001c0002t0003g0026 | 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 | a0001c0002t0002g0279a0001c0002t0002g0282a0001c0002t0002g0283others(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 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0005g0003 | 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 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0005g0003 | 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 | a0001c0002t0001g0052a0001c0002t0001g0054a0001c0002t0001g0055others(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 | a0001c0001t0001g0153a0001c0001t0001g0215a0001c0001t0001g0227others(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 | a0001c0001t0001g0269a0001c0001t0009g0268 | 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 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0005g0003 | 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 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0127others(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 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0188others(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 | 327 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0093others(324): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): 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 | a0001c0004t0003g0082a0001c0004t0003g0083a0001c0004t0003g0084others(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 | a0001c0001t0014g0107a0001c0001t0014g0108a0001c0001t0014g0112 | 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 | a0001c0002t0002g0279a0001c0002t0002g0280a0001c0002t0002g0281others(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 | a0001c0002t0002g0310a0001c0002t0002g0311 | 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 | a0001c0001t0001g0153a0001c0001t0001g0215a0001c0001t0001g0227others(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 | a0001c0001t0001g0175a0001c0001t0001g0188a0001c0001t0001g0189 | 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 | a0001c0001t0001g0133a0001c0001t0001g0183 | 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 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0099others(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 | a0001c0001t0004g0254a0001c0001t0004g0255a0001c0001t0004g0259others(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 | a0001c0002t0001g0053 | 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 | a0001c0002t0002g0279a0001c0002t0002g0280a0001c0002t0002g0281others(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 | a0001c0002t0002g0306a0001c0002t0002g0308 | 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 | a0001c0001t0011g0098a0001c0001t0011g0114a0001c0001t0011g0187others(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 | a0001c0003t0001g0158a0001c0003t0001g0200a0001c0003t0001g0207others(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 | a0001c0003t0001g0218a0001c0005t0001g0104a0001c0005t0001g0217others(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 | a0001c0003t0001g0178a0001c0003t0001g0185a0001c0003t0001g0190 | 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 | a0001c0002t0002g0314 | 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 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0005g0003 | 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 | a0001c0001t0014g0107a0001c0001t0014g0108a0001c0001t0014g0112 | 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 | a0001c0001t0001g0125a0001c0001t0001g0156a0001c0001t0001g0179others(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 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0099others(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 | a0001c0001t0004g0261a0001c0001t0004g0264a0001c0001t0004g0265 | 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 | a0001c0001t0001g0099a0001c0001t0001g0153a0001c0001t0001g0215others(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 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0005g0003 | 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 | a0001c0001t0001g0097a0001c0001t0001g0105a0001c0001t0001g0106others(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 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0099others(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 | a0001c0003t0001g0091a0001c0003t0001g0092a0001c0003t0001g0177others(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 | a0001c0002t0001g0027a0001c0002t0001g0028a0001c0002t0001g0029others(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 | a0001c0001t0019g0317a0001c0001t0019g0318 | 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 | a0001c0002t0002g0279a0001c0002t0002g0280a0001c0002t0002g0281others(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 | a0001c0001t0014g0107a0001c0001t0014g0108a0001c0001t0014g0112 | 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 | a0001c0001t0001g0233a0001c0001t0001g0234a0001c0001t0001g0235others(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 | a0001c0001t0001g0269a0001c0001t0009g0268a0001c0001t0014g0107others(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 | a0001c0001t0001g0116a0001c0001t0001g0122a0001c0001t0001g0127others(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 | a0001c0001t0001g0093a0001c0001t0001g0097a0001c0001t0001g0105others(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 | a0001c0001t0001g0119a0001c0001t0001g0121a0001c0001t0001g0174others(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 | a0001c0001t0001g0099a0001c0001t0001g0120a0001c0001t0001g0184others(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 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0094others(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 | 46 | a0001c0001t0014g0107a0001c0001t0014g0108a0001c0001t0014g0112others(43): Show | 46 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(43): 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 | a0001c0002t0001g0027a0001c0002t0001g0028a0001c0002t0001g0033others(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 | a0001c0002t0001g0052a0001c0002t0001g0053a0001c0002t0001g0054others(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 | a0001c0004t0003g0082a0001c0004t0003g0083a0001c0004t0003g0084others(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 | a0001c0002t0002g0299a0001c0002t0002g0300 | 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 | a0001c0001t0001g0145a0001c0001t0001g0149a0001c0001t0001g0181others(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 | a0001c0001t0001g0106a0001c0001t0001g0130a0001c0001t0001g0156others(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 | a0001c0001t0001g0131a0001c0001t0001g0163a0001c0001t0001g0182others(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 | a0001c0001t0014g0107a0001c0001t0014g0108a0001c0001t0014g0112 | 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 | 309 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0093others(306): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): 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 | a0001c0001t0001g0097a0001c0001t0001g0105a0001c0001t0001g0116others(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 | 202 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0097others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): 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 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0099others(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 | a0001c0002t0003g0069a0001c0002t0013g0005 | 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 | a0001c0003t0006g0326a0001c0003t0006g0327a0001c0003t0006g0328others(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 | 316 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0093others(313): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.1451-1904A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229820416 | ||||||
| chr2:229820504
|
C | G | 39 | a0001c0003t0001g0095a0001c0003t0001g0100a0001c0003t0001g0101others(36): Show | 39 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(36): 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 | a0001c0002t0018g0313a0001c0002t0018g0316 | 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 | a0001c0003t0001g0194a0001c0003t0001g0214 | 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 | a0001c0002t0001g0027a0001c0002t0001g0028a0001c0002t0001g0029others(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 | a0001c0001t0001g0124a0001c0001t0001g0154a0001c0001t0001g0155 | 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 | a0001c0002t0002g0279a0001c0002t0002g0280a0001c0002t0002g0281others(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 | a0001c0001t0001g0269a0001c0001t0009g0268 | 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 | a0001c0001t0014g0107a0001c0001t0014g0108a0001c0001t0014g0112 | 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 | a0001c0001t0014g0107a0001c0001t0014g0108a0001c0001t0014g0112 | 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 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0099others(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 | a0001c0001t0001g0153a0001c0001t0001g0215a0001c0001t0001g0227others(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 | a0001c0001t0004g0254a0001c0001t0004g0255a0001c0001t0004g0259others(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 | a0001c0001t0010g0249a0001c0001t0010g0250a0001c0001t0010g0251others(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 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0005g0003 | 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 | a0001c0001t0001g0243a0001c0001t0001g0245a0001c0002t0003g0045 | 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 | a0001c0003t0001g0178a0001c0003t0001g0185a0001c0003t0001g0190 | 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 | a0001c0001t0014g0107a0001c0001t0014g0108a0001c0001t0014g0112 | 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 | a0001c0001t0004g0258a0001c0001t0005g0018a0001c0001t0009g0146others(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 | a0001c0001t0016g0140 | 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 | 152 | a0001c0001t0001g0097a0001c0001t0001g0105a0001c0001t0001g0106others(149): Show | 152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): 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 | a0001c0001t0001g0133a0001c0001t0001g0183 | 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 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0127others(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 | a0001c0001t0010g0249a0001c0001t0010g0250a0001c0001t0010g0251others(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 | a0001c0001t0001g0153a0001c0001t0001g0227a0001c0001t0001g0230others(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 | a0001c0001t0001g0269a0001c0001t0009g0268 | 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 | a0001c0001t0001g0153a0001c0001t0001g0215a0001c0001t0001g0227others(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 | a0001c0002t0002g0279a0001c0002t0002g0280a0001c0002t0002g0281others(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 | a0001c0002t0003g0044a0001c0002t0020g0002 | 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 | a0001c0001t0014g0107a0001c0001t0014g0108a0001c0001t0014g0112 | 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 | 59 | a0001c0003t0001g0091a0001c0003t0001g0092a0001c0003t0001g0095others(56): Show | 59 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(56): 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 | a0001c0002t0018g0313a0001c0002t0018g0316 | 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 | a0001c0002t0002g0310a0001c0002t0002g0311 | 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 | a0001c0002t0002g0279a0001c0002t0002g0280a0001c0002t0002g0281others(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 | a0001c0001t0012g0139a0001c0001t0012g0168 | 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 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0099others(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 | a0001c0002t0002g0310a0001c0002t0002g0311 | 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 | a0001c0001t0001g0099a0001c0001t0001g0153a0001c0001t0001g0215others(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 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0005g0003 | 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 | a0001c0001t0011g0098a0001c0001t0011g0114a0001c0001t0011g0187others(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 | a0001c0001t0001g0093a0001c0001t0001g0094 | 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 | a0001c0001t0001g0153a0001c0001t0001g0215a0001c0001t0001g0227others(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 | 151 | a0001c0001t0001g0097a0001c0001t0001g0105a0001c0001t0001g0106others(148): Show | 151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): 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 | a0001c0001t0010g0249a0001c0001t0010g0250a0001c0001t0010g0251others(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 | 63 | a0001c0001t0001g0120a0001c0001t0010g0253a0001c0001t0014g0108others(60): Show | 63 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(60): 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 | a0001c0001t0001g0099a0001c0001t0005g0011 | 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 | 317 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0093others(314): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): 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 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0099others(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 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0099others(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 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0005g0003 | 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 | a0001c0002t0001g0029a0001c0002t0001g0059a0001c0002t0001g0075others(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 | 60 | a0001c0001t0001g0124a0001c0001t0001g0154a0001c0002t0002g0298others(57): Show | 60 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(57): Show |
intron_variant | MODIFIER | c.1450+850delA | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 8/41 | chr2 | 229828342 | ||||||
| chr2:229828494
|
G | A | 317 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0093others(314): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): 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 | a0001c0002t0003g0041 | 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 | a0001c0001t0019g0317a0001c0001t0019g0318 | 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 | a0001c0001t0010g0249a0001c0001t0010g0250a0001c0001t0010g0251others(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 | 310 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0093others(307): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): 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 | a0001c0001t0001g0099a0001c0001t0005g0011 | 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 | a0001c0002t0001g0027a0001c0002t0001g0053 | 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 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0005g0003 | 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 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0099others(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 | a0001c0002t0002g0299a0001c0002t0002g0300 | 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 | a0001c0001t0001g0153a0001c0001t0001g0215a0001c0001t0001g0227others(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 | a0001c0001t0001g0116a0001c0001t0001g0121a0001c0001t0001g0122others(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 | a0001c0001t0011g0098a0001c0001t0011g0114a0001c0001t0011g0187others(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 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0099others(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 | 303 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0097others(300): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): 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 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0127others(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 | 59 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0005g0003others(56): Show | 59 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(56): 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 | a0001c0001t0001g0093a0001c0001t0001g0094 | 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 | a0001c0001t0009g0147a0001c0001t0009g0148 | 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 | a0001c0001t0001g0093a0001c0001t0001g0094 | 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 | a0001c0001t0001g0137a0001c0001t0001g0276 | 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 | a0001c0001t0001g0093a0001c0001t0001g0094 | 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 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0099others(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 | a0001c0002t0002g0279a0001c0002t0002g0280a0001c0002t0002g0281others(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 | a0001c0002t0003g0041a0001c0002t0003g0042a0001c0002t0003g0272 | 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 | a0001c0002t0003g0050 | 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 | a0001c0002t0003g0044 | 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 | a0001c0009t0007g0102 | 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 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0005g0003 | 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 | a0001c0001t0001g0132a0001c0001t0001g0137a0001c0001t0001g0276 | 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 | a0001c0001t0014g0107a0001c0001t0014g0108a0001c0001t0014g0112 | 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 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0244others(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 | a0001c0002t0003g0079a0001c0002t0028g0081 | 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 | a0001c0001t0019g0317a0001c0001t0019g0318 | 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 | a0001c0002t0003g0032a0001c0002t0003g0045a0001c0002t0008g0039others(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 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0127others(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 | a0001c0002t0002g0283a0001c0002t0002g0285a0001c0002t0002g0290others(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 | a0001c0001t0009g0146a0001c0001t0009g0147a0001c0001t0009g0148others(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 | a0001c0001t0001g0175a0001c0001t0001g0188a0001c0001t0001g0189 | 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 | a0001c0001t0001g0093a0001c0001t0001g0094 | 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 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0278 | 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 | a0001c0002t0003g0024a0001c0002t0003g0025a0001c0002t0003g0026others(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 | a0001c0001t0001g0269a0001c0001t0009g0268 | 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 | a0001c0001t0001g0142 | 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 | a0001c0003t0001g0158a0001c0003t0001g0200a0001c0003t0001g0207others(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 | a0001c0001t0014g0107a0001c0001t0014g0108a0001c0001t0014g0112 | 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 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0099others(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 | a0001c0002t0001g0027a0001c0002t0001g0028a0001c0002t0001g0029others(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 | a0001c0001t0001g0097a0001c0001t0001g0105a0001c0001t0001g0124others(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 | a0001c0002t0001g0029a0001c0002t0001g0059a0001c0002t0001g0075others(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 | a0001c0002t0001g0055a0001c0002t0001g0056 | 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 | a0001c0003t0001g0158a0001c0003t0001g0200a0001c0003t0001g0216others(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 | a0001c0001t0001g0120a0001c0001t0014g0107a0001c0001t0014g0108others(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 | a0001c0002t0001g0027a0001c0002t0001g0028a0001c0002t0001g0029others(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 | a0001c0001t0019g0317a0001c0001t0019g0318 | 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 | 318 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0093others(315): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): 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 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0153others(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 | 153 | a0001c0001t0001g0097a0001c0001t0001g0105a0001c0001t0001g0106others(150): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): 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 | a0001c0001t0014g0107a0001c0001t0014g0108a0001c0001t0014g0112 | 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 | 3 | a0001c0003t0007g0159a0001c0003t0007g0195a0001c0003t0007g0222 | 3 | HG00280.hp1 HG02293.hp1 homoSapiens_chm13v2.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 | a0001c0001t0001g0099a0001c0001t0005g0011a0001c0001t0011g0098others(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 | 268 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0093others(265): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): 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 | a0001c0001t0009g0146a0001c0001t0009g0147a0001c0001t0009g0148others(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 | a0001c0001t0019g0317a0001c0001t0019g0318 | 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 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0005g0003 | 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 | 264 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0093others(261): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): 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 | a0001c0001t0019g0317a0001c0001t0019g0318 | 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 | a0001c0001t0001g0023a0001c0001t0001g0093a0001c0001t0001g0094others(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 | a0001c0001t0001g0192a0001c0002t0001g0027a0001c0002t0001g0028others(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 | a0001c0001t0001g0097a0001c0001t0001g0105a0001c0001t0001g0106others(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 | a0001c0004t0003g0082a0001c0004t0003g0083a0001c0004t0003g0084others(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 | a0001c0001t0014g0107a0001c0001t0014g0108a0001c0001t0014g0112 | 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 | 315 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0093others(312): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): 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 | a0001c0001t0014g0107a0001c0001t0014g0108a0001c0001t0014g0112 | 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 | 153 | a0001c0001t0001g0097a0001c0001t0001g0105a0001c0001t0001g0106others(150): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): 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 | a0001c0001t0001g0119a0001c0001t0009g0146a0001c0001t0009g0147others(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 | a0001c0004t0003g0082a0001c0004t0003g0084a0001c0004t0003g0086 | 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 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0005g0003 | 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 | a0001c0001t0014g0107a0001c0001t0014g0108a0001c0001t0014g0112 | 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 | a0001c0001t0001g0093a0001c0001t0001g0094 | 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 | a0001c0001t0001g0097a0001c0001t0001g0105a0001c0001t0001g0106others(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 | a0001c0002t0001g0027a0001c0002t0001g0028a0001c0002t0001g0029others(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 | a0001c0003t0001g0113a0001c0003t0001g0191a0001c0003t0001g0194others(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 | a0001c0001t0004g0261a0001c0001t0004g0264a0001c0001t0004g0265 | 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 | a0001c0001t0004g0261a0001c0001t0004g0264a0001c0001t0004g0265 | 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 | a0001c0002t0001g0027a0001c0002t0001g0028a0001c0002t0001g0029others(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 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0099others(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 | 206 | a0001c0001t0001g0097a0001c0001t0001g0105a0001c0001t0001g0106others(203): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): 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 | a0001c0001t0001g0022a0001c0001t0001g0093a0001c0001t0001g0094others(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 | a0001c0001t0001g0153a0001c0002t0001g0027a0001c0002t0001g0028others(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 | 147 | a0001c0001t0001g0097a0001c0001t0001g0105a0001c0001t0001g0106others(144): Show | 147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): 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 | a0001c0001t0001g0099a0001c0001t0004g0001a0001c0001t0004g0254others(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 | a0001c0002t0003g0041 | 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 | 207 | a0001c0001t0001g0097a0001c0001t0001g0105a0001c0001t0001g0106others(204): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.1028-5748dupT | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 4/41 | chr2 | 229846674 | ||||||
| chr2:229846752
|
G | C | 78 | a0001c0002t0001g0027a0001c0002t0001g0028a0001c0002t0001g0029others(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 | a0001c0002t0002g0279a0001c0002t0002g0280a0001c0002t0002g0281others(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 | a0001c0002t0001g0054 | 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 | a0001c0001t0001g0116a0001c0001t0001g0152 | 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 | a0001c0001t0001g0097a0001c0001t0001g0106a0001c0001t0001g0120others(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 | a0001c0001t0001g0183a0001c0001t0005g0003a0001c0001t0005g0011others(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 | a0001c0001t0001g0099a0001c0001t0001g0124a0001c0001t0001g0128others(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 | a0001c0001t0001g0099a0001c0001t0001g0128a0001c0001t0001g0180others(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 | a0001c0003t0001g0091a0001c0003t0001g0092a0001c0003t0001g0177others(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 | a0001c0001t0001g0133a0001c0001t0001g0183 | 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 | a0001c0001t0001g0099a0001c0001t0005g0011 | 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 | a0001c0001t0019g0317a0001c0001t0019g0318a0001c0002t0002g0279others(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 | 327 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0093others(324): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): 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 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0099others(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 | a0001c0002t0003g0041 | 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 | a0001c0001t0001g0269a0001c0001t0009g0268a0001c0001t0014g0107others(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 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0099others(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 | a0001c0001t0001g0269a0001c0001t0009g0268 | 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 | a0001c0001t0001g0097a0001c0001t0001g0105a0001c0001t0001g0106others(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 | 60 | a0001c0001t0030g0123a0001c0003t0001g0091a0001c0003t0001g0092others(57): Show | 60 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(57): 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 | a0001c0001t0004g0001a0001c0001t0004g0254a0001c0001t0004g0255others(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 | a0001c0002t0001g0027a0001c0002t0001g0052a0001c0002t0001g0053others(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 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0005g0003 | 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 | a0001c0001t0004g0001a0001c0001t0004g0254a0001c0001t0004g0255others(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 | a0001c0001t0001g0166a0001c0001t0001g0167 | 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 | a0001c0002t0001g0033a0001c0002t0001g0034a0001c0002t0001g0063others(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 | a0001c0002t0001g0071a0001c0002t0001g0074 | 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 | a0001c0002t0003g0024a0001c0002t0003g0025a0001c0002t0003g0026 | 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 | 59 | a0001c0003t0001g0091a0001c0003t0001g0092a0001c0003t0001g0095others(56): Show | 59 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(56): 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 | a0001c0002t0001g0071a0001c0002t0001g0074 | 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 | a0001c0002t0001g0071a0001c0002t0001g0074 | 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 | a0001c0002t0008g0043 | 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 | a0001c0001t0001g0099a0001c0001t0005g0011 | 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 | a0001c0001t0001g0269a0001c0001t0009g0268a0001c0001t0014g0107others(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 | a0001c0001t0001g0184a0001c0001t0005g0019 | 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 | a0001c0002t0002g0283a0001c0002t0002g0285a0001c0002t0002g0290others(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 | a0001c0001t0011g0098a0001c0001t0011g0114a0001c0001t0011g0187others(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 | a0001c0003t0006g0323a0001c0003t0006g0325 | 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 | a0001c0001t0001g0093a0001c0001t0001g0094 | 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 | a0001c0002t0002g0279a0001c0002t0002g0280a0001c0002t0002g0281others(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 | a0001c0001t0001g0269a0001c0001t0009g0268a0001c0003t0001g0177others(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 | a0001c0001t0001g0099a0001c0001t0005g0011 | 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 | a0001c0001t0001g0153a0001c0001t0001g0215a0001c0001t0001g0227others(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 | a0001c0002t0001g0027a0001c0002t0001g0028a0001c0002t0001g0029others(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 | 270 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0093others(267): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): 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 | a0001c0001t0014g0107a0001c0001t0014g0108a0001c0001t0014g0112 | 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 | a0001c0002t0002g0296a0001c0002t0002g0305a0001c0002t0002g0306others(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 | a0001c0001t0001g0097a0001c0001t0001g0105a0001c0001t0001g0106others(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 | a0001c0001t0001g0269a0001c0001t0009g0268 | 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 | a0001c0001t0001g0153a0001c0001t0001g0215a0001c0001t0001g0227others(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 | 58 | a0001c0003t0001g0091a0001c0003t0001g0092a0001c0003t0001g0095others(55): Show | 58 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(55): 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 | a0001c0004t0003g0082a0001c0004t0003g0084a0001c0004t0003g0086 | 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 | a0001c0002t0002g0299a0001c0002t0002g0300 | 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 | a0001c0001t0009g0146a0001c0001t0009g0147a0001c0001t0009g0148others(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 | a0001c0002t0002g0296a0001c0002t0002g0298a0001c0002t0002g0305others(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 | a0001c0001t0001g0120a0001c0001t0004g0001a0001c0001t0004g0258others(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 | a0001c0001t0001g0196 | 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 | a0001c0001t0001g0269a0001c0001t0009g0268a0001c0001t0012g0138others(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 | a0001c0001t0001g0105a0001c0001t0001g0122a0001c0001t0001g0124others(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 | a0001c0001t0001g0097a0001c0001t0001g0106a0001c0001t0001g0116others(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 | a0001c0001t0001g0099a0001c0001t0001g0175a0001c0001t0001g0197others(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 | 135 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0093others(132): Show | 136 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(133): 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 | a0001c0001t0001g0153a0001c0001t0001g0227a0001c0001t0001g0229others(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 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0004g0001others(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 | a0001c0001t0001g0153a0001c0001t0001g0215a0001c0001t0001g0227others(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 | a0001c0001t0001g0153a0001c0001t0001g0215a0001c0001t0001g0227others(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 | a0001c0001t0004g0001a0001c0001t0004g0254a0001c0001t0004g0255others(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 | a0001c0003t0001g0113a0001c0003t0001g0191a0001c0003t0001g0194others(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 | a0001c0002t0001g0027a0001c0002t0001g0028a0001c0002t0001g0029others(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 | a0001c0001t0010g0249a0001c0001t0010g0250a0001c0001t0010g0251others(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 | a0001c0001t0001g0093a0001c0001t0001g0094 | 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 | a0001c0002t0001g0027a0001c0002t0001g0028a0001c0002t0001g0029others(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 | a0001c0002t0002g0279a0001c0002t0002g0280a0001c0002t0002g0281others(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 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136others(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 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136others(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 | a0001c0001t0001g0093a0001c0001t0001g0094 | 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 | a0001c0001t0001g0153a0001c0001t0001g0227a0001c0001t0001g0229others(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 | a0001c0002t0001g0027a0001c0002t0001g0028a0001c0002t0001g0029others(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 | a0001c0002t0001g0027a0001c0002t0001g0028a0001c0002t0001g0029others(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 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0099others(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 | a0001c0001t0001g0269a0001c0001t0009g0268 | 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 | a0001c0001t0010g0249a0001c0001t0010g0250a0001c0001t0010g0251others(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 | a0001c0001t0001g0161a0001c0001t0004g0001a0001c0001t0004g0258others(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 | a0001c0001t0001g0153a0001c0001t0001g0215a0001c0001t0001g0227others(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 | a0001c0002t0003g0050 | 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 | a0001c0001t0001g0153a0001c0001t0001g0215a0001c0001t0001g0227others(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 | a0001c0002t0001g0070a0001c0002t0003g0079 | 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 | a0001c0001t0001g0120a0001c0002t0002g0299a0001c0002t0002g0307 | 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 | a0001c0001t0001g0117a0001c0001t0001g0144a0001c0001t0001g0227others(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 | a0001c0001t0010g0251a0001c0001t0010g0252a0001c0002t0002g0310others(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 | a0001c0001t0001g0215a0001c0001t0001g0231a0001c0001t0010g0253others(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 | 32 | a0001c0003t0001g0091a0001c0003t0001g0092a0001c0003t0001g0095others(29): Show | 32 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(29): 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 | a0001c0002t0002g0319a0001c0003t0001g0157a0001c0003t0001g0228 | 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 | a0001c0001t0001g0142a0001c0001t0001g0186a0001c0001t0001g0196others(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 | a0001c0001t0001g0097a0001c0001t0001g0105a0001c0001t0001g0119others(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 | a0001c0001t0001g0118a0001c0001t0001g0127a0001c0001t0001g0229others(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 | a0001c0002t0003g0024a0001c0002t0003g0025a0001c0002t0003g0042others(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 | a0001c0002t0003g0026a0001c0002t0003g0076a0001c0002t0008g0039others(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 | a0001c0002t0003g0036a0001c0002t0003g0068a0001c0002t0008g0046others(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 | a0001c0002t0003g0031a0001c0002t0003g0041a0001c0002t0020g0002others(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 | a0001c0002t0003g0037a0001c0002t0003g0272a0001c0002t0017g0051 | 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 | a0001c0002t0003g0032a0001c0002t0003g0066a0001c0002t0003g0067others(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 | a0001c0002t0001g0027a0001c0002t0003g0061a0001c0002t0003g0080 | 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 | a0001c0002t0005g0009a0001c0002t0013g0005 | 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 | a0001c0002t0003g0044a0001c0002t0003g0050 | 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 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0106others(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 | a0001c0004t0003g0082a0001c0004t0003g0083a0001c0004t0003g0086others(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 | a0001c0001t0012g0138 | 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 | a0001c0001t0004g0255a0001c0001t0004g0259a0001c0001t0004g0260 | 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 | a0001c0001t0001g0116a0001c0001t0001g0121a0001c0001t0001g0122others(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 | a0001c0001t0001g0106a0001c0001t0024g0239 | 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 | a0001c0001t0001g0224a0001c0001t0001g0234a0001c0001t0001g0235others(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 | a0001c0001t0019g0317a0001c0001t0019g0318 | 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 | a0001c0001t0001g0022a0001c0001t0005g0003 | 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 | a0001c0001t0004g0001a0001c0001t0004g0258a0001c0001t0004g0261others(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 | a0001c0001t0001g0099a0001c0001t0005g0011 | 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 | a0001c0001t0011g0098a0001c0003t0005g0017 | 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 | a0001c0001t0011g0225a0001c0001t0011g0226 | 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 | a0001c0001t0001g0229a0001c0001t0010g0249a0001c0001t0010g0250 | 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 | a0001c0001t0001g0227a0001c0001t0001g0229a0001c0001t0001g0230others(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 | a0001c0002t0001g0053 | 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 | a0001c0002t0001g0054 | 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 | a0001c0002t0001g0033a0001c0002t0013g0008 | 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 | a0001c0002t0003g0045 | 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 | a0001c0002t0001g0056a0001c0002t0001g0089 | 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 | a0001c0002t0001g0070a0001c0002t0003g0079 | 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 | a0001c0002t0001g0029a0001c0002t0001g0270 | 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 | a0001c0002t0001g0059a0001c0002t0001g0072a0001c0002t0001g0077 | 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 | a0001c0001t0001g0153a0001c0001t0001g0227a0001c0001t0001g0229others(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 | a0001c0001t0001g0175a0001c0001t0001g0188a0001c0001t0001g0189others(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 | a0001c0001t0001g0245a0001c0002t0002g0294a0001c0002t0002g0295others(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 | a0001c0001t0001g0097a0001c0001t0001g0105a0001c0001t0001g0117others(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 | a0001c0001t0001g0243a0001c0002t0001g0027a0001c0002t0003g0035others(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 | a0001c0001t0001g0269a0001c0001t0009g0268 | 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 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0233others(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 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0099others(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 | a0001c0002t0001g0033a0001c0002t0001g0034a0001c0002t0001g0063others(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 | a0001c0001t0001g0269a0001c0001t0009g0268 | 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 | a0001c0002t0002g0279a0001c0002t0002g0280a0001c0002t0002g0281others(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 | a0001c0003t0001g0113a0001c0003t0001g0191a0001c0003t0001g0194others(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 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0005g0003 | 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 | a0001c0002t0008g0039a0001c0002t0008g0043a0001c0002t0008g0046others(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 | a0001c0003t0006g0323a0001c0003t0006g0325 | 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 | a0001c0002t0002g0296a0001c0002t0002g0298a0001c0002t0002g0305others(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 | 161 | a0001c0001t0001g0023a0001c0001t0001g0097a0001c0001t0001g0105others(158): Show | 161 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(158): 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 | a0001c0001t0001g0022a0001c0001t0001g0116a0001c0001t0001g0152others(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 | a0001c0001t0011g0098a0001c0001t0011g0114a0001c0001t0011g0187others(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 | a0001c0001t0014g0107a0001c0002t0001g0027a0001c0002t0001g0028others(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 | a0001c0001t0001g0093a0001c0001t0001g0099a0001c0001t0004g0001others(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 | a0001c0001t0001g0094a0001c0001t0004g0262a0001c0001t0004g0264others(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 | a0001c0001t0012g0138a0001c0001t0012g0139a0001c0001t0012g0168 | 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 | a0001c0002t0002g0279a0001c0002t0002g0280a0001c0002t0002g0281others(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 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0099others(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 | a0001c0001t0001g0153a0001c0001t0001g0215a0001c0001t0001g0227others(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 | a0001c0001t0001g0269a0001c0001t0009g0268 | 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 | a0001c0001t0001g0097a0001c0001t0001g0105a0001c0001t0001g0106others(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 | a0001c0001t0001g0153a0001c0001t0001g0215a0001c0001t0001g0227others(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 | 153 | a0001c0001t0001g0097a0001c0001t0001g0105a0001c0001t0001g0106others(150): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.99-6567dupA | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229867097 | ||||||
| chr2:229867109
|
G | T | 6 | a0001c0001t0010g0249a0001c0001t0010g0250a0001c0001t0010g0251others(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 | a0001c0002t0002g0279a0001c0002t0002g0280a0001c0002t0002g0281others(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 | a0001c0002t0002g0295a0001c0002t0002g0296a0001c0002t0002g0300others(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 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0099others(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 | a0001c0002t0001g0027a0001c0002t0001g0028a0001c0002t0001g0029others(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 | a0001c0001t0001g0022a0001c0001t0005g0003a0001c0001t0010g0249others(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 | 156 | a0001c0001t0001g0097a0001c0001t0001g0106a0001c0001t0001g0116others(153): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.99-6641delA | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 2/41 | chr2 | 229867171 | ||||||
| chr2:229867176
|
T | G | 7 | a0001c0001t0001g0153a0001c0001t0001g0215a0001c0001t0001g0227others(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 | a0001c0001t0004g0263a0001c0001t0004g0266 | 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 | a0001c0001t0011g0098a0001c0001t0011g0114a0001c0001t0011g0187others(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 | a0001c0002t0003g0044a0001c0002t0020g0002 | 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 | a0001c0003t0001g0113a0001c0003t0001g0191a0001c0003t0001g0194others(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 | 318 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0093others(315): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): 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 | a0001c0002t0002g0279a0001c0002t0002g0280a0001c0002t0002g0281others(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 | a0001c0001t0001g0269a0001c0001t0009g0268 | 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 | 318 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0093others(315): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): 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 | a0001c0003t0001g0218a0001c0005t0001g0104a0001c0005t0001g0217others(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 | a0001c0001t0014g0107a0001c0001t0014g0108a0001c0001t0014g0112others(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 | a0001c0001t0001g0119a0001c0001t0009g0146a0001c0001t0009g0147others(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 | 59 | a0001c0003t0001g0091a0001c0003t0001g0092a0001c0003t0001g0095others(56): Show | 59 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(56): 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 | a0001c0002t0001g0027a0001c0002t0001g0028a0001c0002t0001g0029others(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 | a0001c0001t0001g0269a0001c0001t0009g0268 | 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 | a0001c0001t0014g0107a0001c0001t0014g0108a0001c0001t0014g0112 | 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 | a0001c0001t0011g0098a0001c0001t0011g0114a0001c0001t0011g0187others(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 | a0001c0001t0010g0249a0001c0001t0010g0250a0001c0001t0010g0251others(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 | a0001c0001t0014g0107a0001c0001t0014g0108a0001c0001t0014g0112 | 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 | a0001c0001t0011g0098a0001c0001t0011g0114a0001c0001t0011g0187others(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 | 59 | a0001c0003t0001g0091a0001c0003t0001g0092a0001c0003t0001g0095others(56): Show | 59 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(56): 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 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0188others(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 | a0001c0001t0001g0245a0001c0002t0001g0028a0001c0002t0001g0029others(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 | a0001c0001t0001g0242a0001c0002t0001g0027a0001c0002t0001g0033others(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 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0097others(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 | a0001c0001t0004g0254a0001c0001t0004g0255a0001c0001t0004g0259others(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 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0099others(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 | 55 | a0001c0003t0001g0091a0001c0003t0001g0092a0001c0003t0001g0095others(52): Show | 55 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(52): 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 | a0001c0001t0001g0097a0001c0001t0001g0105a0001c0001t0001g0106others(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 | a0001c0001t0001g0149a0001c0001t0001g0196 | 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 | a0001c0002t0002g0299a0001c0002t0002g0300 | 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 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0005g0003 | 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 | a0001c0001t0001g0269a0001c0001t0009g0268 | 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 | a0001c0001t0010g0249a0001c0001t0010g0250a0001c0001t0010g0251others(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 | a0001c0003t0001g0218a0001c0005t0001g0104a0001c0005t0001g0217others(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 | a0001c0002t0002g0279a0001c0002t0002g0280a0001c0002t0002g0281others(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 | a0001c0001t0001g0117a0001c0001t0001g0153a0001c0001t0001g0215others(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 | a0001c0003t0006g0322a0001c0003t0006g0323a0001c0003t0006g0324others(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 | a0001c0002t0001g0027a0001c0002t0001g0028a0001c0002t0001g0029others(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 | a0001c0002t0002g0296a0001c0002t0002g0298a0001c0002t0002g0302others(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 | a0001c0001t0001g0093a0001c0001t0001g0094 | 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 | 318 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0093others(315): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): 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 | a0001c0002t0001g0063a0001c0002t0001g0064a0001c0002t0001g0065 | 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 | a0001c0001t0001g0099a0001c0001t0005g0011 | 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 | a0001c0001t0001g0099a0001c0001t0004g0001a0001c0001t0004g0254others(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 | a0001c0002t0033g0040 | 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 | a0001c0001t0014g0107a0001c0001t0014g0108a0001c0001t0014g0112 | 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 | a0001c0001t0001g0269a0001c0001t0009g0268 | 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 | a0001c0001t0001g0130a0001c0001t0001g0162 | 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 | 44 | a0001c0003t0001g0095a0001c0003t0001g0100a0001c0003t0001g0101others(41): Show | 44 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(41): 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 | a0001c0001t0010g0249a0001c0001t0010g0250a0001c0001t0010g0251others(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 | a0001c0001t0014g0107a0001c0001t0014g0108a0001c0001t0014g0112 | 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 | a0001c0001t0010g0249a0001c0001t0010g0250a0001c0001t0010g0251others(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 | a0001c0001t0014g0107a0001c0001t0014g0108a0001c0001t0014g0112others(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 | a0001c0002t0002g0296a0001c0002t0002g0305a0001c0002t0002g0306others(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 | a0001c0001t0001g0023a0001c0001t0004g0262 | 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 | a0001c0001t0001g0099a0001c0001t0001g0231a0001c0001t0004g0001others(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 | 269 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0093others(266): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): 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 | a0001c0001t0011g0098a0001c0001t0011g0114a0001c0001t0011g0187others(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 | 318 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0093others(315): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): 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 | a0001c0001t0001g0246a0001c0001t0026g0247 | 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 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0127others(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 | a0001c0002t0002g0279a0001c0002t0002g0280a0001c0002t0002g0281others(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 | a0001c0001t0001g0269a0001c0001t0009g0268 | 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 | a0001c0001t0001g0243a0001c0001t0001g0245 | 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 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0099others(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 | a0001c0001t0011g0098a0001c0001t0011g0114a0001c0001t0011g0187others(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 | a0001c0001t0001g0141 | 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 | a0001c0001t0001g0269a0001c0001t0009g0268 | 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 | a0001c0003t0001g0218a0001c0005t0001g0104a0001c0005t0001g0217others(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 | a0001c0002t0017g0051a0001c0002t0017g0090 | 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 | a0001c0002t0003g0078a0001c0002t0003g0271a0001c0002t0013g0008 | 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 | a0001c0003t0001g0178a0001c0003t0001g0185a0001c0003t0001g0190 | 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 | a0001c0002t0002g0299a0001c0002t0002g0300a0001c0002t0002g0301others(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 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0099others(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 | a0001c0001t0010g0249a0001c0001t0010g0250a0001c0001t0010g0251others(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 | a0001c0001t0001g0192a0001c0001t0001g0275a0001c0001t0004g0254others(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 | 155 | a0001c0001t0001g0097a0001c0001t0001g0105a0001c0001t0001g0116others(152): Show | 155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.-49-4109dupA | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229884236 | ||||||
| chr2:229884236
|
C | CTT | 11 | a0001c0001t0001g0119a0001c0001t0001g0121a0001c0001t0001g0153others(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 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0099others(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 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0127others(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 | 152 | a0001c0001t0001g0097a0001c0001t0001g0105a0001c0001t0001g0106others(149): Show | 152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): 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 | a0001c0002t0002g0312a0001c0002t0002g0314a0001c0002t0002g0315others(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 | a0001c0001t0014g0107a0001c0001t0014g0108a0001c0001t0014g0112 | 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 | a0001c0001t0001g0153a0001c0001t0001g0215a0001c0001t0001g0227others(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 | a0001c0001t0010g0249a0001c0001t0010g0250a0001c0001t0010g0251others(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 | a0001c0001t0001g0196a0001c0001t0001g0236a0001c0001t0011g0098others(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 | a0001c0001t0001g0099a0001c0001t0001g0117a0001c0001t0004g0001others(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 | a0001c0001t0005g0015a0001c0002t0002g0279a0001c0002t0002g0280others(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 | a0001c0003t0001g0157a0001c0003t0001g0198 | 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 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0245others(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 | 152 | a0001c0001t0001g0097a0001c0001t0001g0105a0001c0001t0001g0106others(149): Show | 152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): 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 | a0001c0003t0006g0326a0001c0003t0006g0327a0001c0003t0006g0328others(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 | a0001c0001t0001g0269a0001c0001t0009g0268 | 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 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0005g0003 | 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 | a0001c0001t0019g0317a0001c0001t0019g0318 | 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 | a0001c0002t0002g0279a0001c0002t0002g0280a0001c0002t0002g0281others(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 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0099others(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 | 327 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0093others(324): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): 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 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0099others(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 | a0001c0002t0002g0303a0001c0002t0002g0304 | 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 | a0001c0001t0001g0174a0001c0002t0002g0312a0001c0002t0002g0314others(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 | 179 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0093others(176): Show | 180 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.-49-9953delA | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229890080 | ||||||
| chr2:229890080
|
CTT | C | 91 | a0001c0001t0001g0097a0001c0001t0001g0105a0001c0001t0001g0106others(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 | a0001c0001t0001g0093a0001c0001t0001g0094 | 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 | a0001c0002t0001g0029a0001c0002t0001g0059a0001c0002t0001g0075others(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 | a0001c0001t0001g0269a0001c0001t0009g0268 | 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 | a0001c0002t0002g0279a0001c0002t0002g0280a0001c0002t0002g0281others(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 | a0001c0001t0014g0107a0001c0001t0014g0108a0001c0001t0014g0112 | 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 | a0001c0001t0001g0093a0001c0001t0001g0094 | 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 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0005g0003 | 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 | 153 | a0001c0001t0001g0097a0001c0001t0001g0105a0001c0001t0001g0106others(150): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): 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 | a0001c0002t0002g0283a0001c0002t0002g0285a0001c0002t0002g0290others(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 | a0001c0001t0001g0097a0001c0001t0001g0105a0001c0001t0001g0106others(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 | 318 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0093others(315): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): 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 | a0001c0001t0001g0269a0001c0001t0009g0268a0001c0001t0014g0107others(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 | 207 | a0001c0001t0001g0023a0001c0001t0001g0097a0001c0001t0001g0105others(204): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.-49-13366dupA | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229893493 | ||||||
| chr2:229893796
|
T | G | 2 | a0001c0004t0003g0083a0001c0004t0003g0085 | 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 | a0001c0002t0001g0027a0001c0002t0001g0028a0001c0002t0001g0029others(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 | a0001c0001t0001g0269a0001c0001t0009g0268 | 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 | a0001c0001t0001g0269a0001c0001t0009g0268 | 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 | a0001c0001t0001g0196 | 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 | a0001c0003t0001g0218a0001c0005t0001g0104a0001c0005t0001g0217others(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 | a0001c0002t0001g0027a0001c0002t0001g0028a0001c0002t0001g0029others(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 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0127others(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 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0127others(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 | a0001c0001t0001g0153a0001c0001t0001g0215a0001c0001t0001g0227others(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 | 327 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0093others(324): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): 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 | a0001c0001t0014g0107a0001c0001t0014g0108a0001c0001t0014g0112 | 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 | a0001c0001t0001g0196 | 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 | a0001c0001t0011g0098a0001c0001t0011g0114a0001c0001t0011g0187others(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 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0099others(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 | a0001c0002t0001g0027a0001c0002t0001g0028a0001c0002t0001g0029others(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 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0127others(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 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0099others(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 | a0001c0001t0011g0098a0001c0001t0011g0114a0001c0001t0011g0225others(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 | a0001c0001t0014g0107a0001c0001t0014g0108a0001c0001t0014g0112 | 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 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0127others(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 | a0001c0002t0001g0027a0001c0002t0001g0028a0001c0002t0001g0029others(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 | 165 | a0001c0001t0001g0097a0001c0001t0001g0105a0001c0001t0001g0106others(162): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): 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 | a0001c0002t0003g0024a0001c0002t0003g0025a0001c0002t0003g0026others(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 | a0001c0001t0001g0093a0001c0001t0001g0094 | 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 | a0001c0002t0002g0299a0001c0002t0002g0300 | 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 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0188others(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 | a0001c0001t0010g0249a0001c0001t0010g0250a0001c0001t0010g0251others(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 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0099others(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 | a0001c0002t0002g0279a0001c0002t0002g0280a0001c0002t0002g0281others(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 | 3 | a0001c0003t0007g0159a0001c0003t0007g0195a0001c0003t0007g0222 | 3 | HG00280.hp1 HG02293.hp1 homoSapiens_chm13v2.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 | a0001c0003t0015g0150a0001c0003t0015g0151a0001c0003t0015g0173 | 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 | a0001c0001t0001g0099a0001c0001t0005g0011 | 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 | a0001c0001t0001g0175a0001c0001t0001g0188a0001c0001t0001g0189 | 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 | a0001c0001t0001g0106a0001c0001t0001g0125a0001c0001t0001g0130others(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 | a0001c0001t0001g0243a0001c0001t0001g0245 | 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 | a0001c0001t0014g0107a0001c0001t0014g0108a0001c0001t0014g0112 | 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 | a0001c0002t0001g0027a0001c0002t0001g0028a0001c0002t0001g0029others(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 | a0001c0002t0001g0027a0001c0002t0001g0028a0001c0002t0001g0029others(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 | a0001c0002t0001g0027a0001c0002t0001g0028a0001c0002t0001g0029others(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 | 237 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0093others(234): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.-50+20259dupT | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229901620 | ||||||
| chr2:229901797
|
G | A | 3 | a0001c0001t0001g0175a0001c0001t0001g0188a0001c0001t0001g0189 | 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 | a0001c0001t0001g0097a0001c0001t0001g0105a0001c0001t0001g0106others(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 | a0001c0001t0001g0097a0001c0001t0001g0105a0001c0001t0001g0129others(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 | a0001c0001t0001g0269a0001c0001t0009g0268 | 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 | a0001c0001t0001g0119a0001c0001t0001g0269a0001c0001t0009g0268 | 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 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0269others(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 | a0001c0001t0001g0099a0001c0001t0004g0001a0001c0001t0004g0254others(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 | 215 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0097others(212): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): 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 | a0001c0002t0001g0027a0001c0002t0001g0028a0001c0002t0001g0029others(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 | a0001c0002t0001g0027a0001c0002t0001g0028a0001c0002t0001g0029others(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 | 161 | a0001c0001t0001g0097a0001c0001t0001g0105a0001c0001t0001g0106others(158): Show | 161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
intron_variant | MODIFIER | c.-50+18861dupA | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229903018 | ||||||
| chr2:229903018
|
C | T | 25 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0099others(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 | a0001c0001t0004g0001a0001c0001t0004g0254a0001c0001t0004g0255others(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 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0099others(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 | a0001c0003t0006g0323a0001c0003t0006g0325 | 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 | a0001c0001t0014g0107a0001c0001t0014g0108a0001c0001t0014g0112 | 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 | a0001c0002t0001g0027a0001c0002t0001g0028a0001c0002t0001g0029others(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 | a0001c0002t0001g0027a0001c0002t0001g0028a0001c0002t0001g0029others(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 | a0001c0001t0001g0117a0001c0001t0001g0124a0001c0001t0001g0127others(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 | a0001c0001t0001g0093a0001c0001t0001g0094 | 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 | 229 | a0001c0001t0001g0097a0001c0001t0001g0105a0001c0001t0001g0106others(226): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.-50+17463dupT | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229904416 | ||||||
| chr2:229904416
|
C | CAA | 35 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0099others(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 | 150 | a0001c0001t0001g0097a0001c0001t0001g0105a0001c0001t0001g0106others(147): Show | 150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): 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 | a0001c0001t0001g0188a0001c0001t0001g0189 | 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 | a0001c0001t0001g0269a0001c0001t0009g0268 | 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 | a0001c0002t0001g0027a0001c0002t0001g0028a0001c0002t0001g0029others(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 | a0001c0001t0001g0269a0001c0001t0009g0268 | 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 | a0001c0001t0001g0156a0001c0001t0030g0123 | 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 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0099others(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 | a0001c0001t0001g0128a0001c0001t0001g0188a0001c0001t0001g0189others(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 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0215others(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 | 318 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0093others(315): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): 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 | a0001c0001t0001g0097a0001c0001t0001g0105a0001c0001t0001g0106others(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 | a0001c0002t0001g0027a0001c0002t0001g0028a0001c0002t0001g0029others(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 | a0001c0001t0001g0097a0001c0001t0001g0116a0001c0001t0001g0119others(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 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0099others(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 | a0001c0002t0003g0035a0001c0002t0003g0036a0001c0002t0003g0037others(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 | a0001c0001t0001g0093a0001c0001t0001g0094 | 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 | 175 | a0001c0001t0001g0094a0001c0001t0001g0097a0001c0001t0001g0105others(172): Show | 175 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(172): 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 | a0001c0001t0010g0249a0001c0001t0010g0250a0001c0001t0010g0251others(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 | a0001c0001t0009g0171a0001c0001t0009g0172 | 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 | a0001c0001t0001g0120a0001c0001t0010g0249a0001c0001t0010g0250others(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 | a0001c0001t0004g0001a0001c0001t0004g0254a0001c0001t0004g0255others(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 | 327 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0093others(324): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): 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 | a0001c0002t0003g0032a0001c0002t0013g0004 | 2 | HG02602.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-50+13971T>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229907909 | ||||||
| chr2:229907941
|
T | C | 328 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0093others(325): Show | 329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.-50+13939A>G | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229907941 | ||||||
| chr2:229907962
|
C | G | 78 | a0001c0002t0001g0027a0001c0002t0001g0028a0001c0002t0001g0029others(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 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0099others(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 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0188others(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 | a0001c0002t0001g0059a0001c0002t0001g0077 | 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 | a0001c0002t0003g0062a0001c0002t0003g0078a0001c0002t0003g0271others(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 | a0001c0001t0014g0107a0001c0001t0014g0108a0001c0001t0014g0112 | 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 | a0001c0002t0001g0027a0001c0002t0001g0028a0001c0002t0001g0029others(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 | a0001c0001t0010g0249a0001c0001t0010g0250a0001c0001t0010g0251others(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 | 253 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0097others(250): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.-50+12790dupT | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229909089 | ||||||
| chr2:229909089
|
C | CAA | 16 | a0001c0001t0001g0153a0001c0001t0001g0156a0001c0001t0001g0215others(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 | a0001c0001t0014g0107a0001c0001t0014g0108a0001c0001t0014g0112 | 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 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0093others(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 | a0001c0001t0001g0099a0001c0001t0004g0001a0001c0001t0004g0254others(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 | a0001c0001t0014g0107a0001c0001t0014g0108a0001c0001t0014g0112 | 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 | a0001c0001t0014g0107a0001c0001t0014g0108a0001c0001t0014g0112 | 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 | a0001c0001t0001g0144a0001c0001t0001g0183a0001c0001t0001g0184others(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 | a0001c0001t0010g0249a0001c0001t0010g0250a0001c0001t0010g0251others(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 | a0001c0001t0001g0093a0001c0001t0001g0094 | 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 | a0001c0001t0010g0249a0001c0001t0010g0250 | 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 | a0001c0001t0001g0153a0001c0001t0001g0215a0001c0001t0001g0227others(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 | a0001c0001t0004g0254a0001c0001t0004g0255a0001c0001t0004g0259others(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 | a0001c0003t0006g0322a0001c0003t0036g0321 | 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 | a0001c0001t0014g0107a0001c0001t0014g0108a0001c0001t0014g0112 | 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 | a0001c0001t0001g0153a0001c0001t0001g0215a0001c0001t0001g0227others(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 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0099others(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 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0099others(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 | a0001c0001t0010g0249a0001c0001t0010g0250a0001c0001t0010g0251others(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 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0099others(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 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0099others(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 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0099others(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 | a0001c0001t0004g0261a0001c0001t0004g0264a0001c0001t0004g0265 | 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 | a0001c0001t0011g0098a0001c0001t0011g0114a0001c0001t0011g0187others(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 | a0001c0002t0002g0306a0001c0002t0002g0307a0001c0002t0002g0308 | 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 | a0001c0001t0001g0145a0001c0001t0001g0186a0001c0001t0001g0192others(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 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0099others(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 | a0001c0002t0003g0078a0001c0002t0003g0271a0001c0002t0013g0008 | 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 | a0001c0001t0009g0146a0001c0001t0009g0147a0001c0001t0009g0148others(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 | a0001c0001t0001g0099a0001c0001t0005g0011 | 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 | a0001c0001t0001g0269a0001c0001t0009g0268 | 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 | a0001c0001t0001g0269a0001c0001t0009g0268 | 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 | a0001c0001t0001g0269a0001c0001t0009g0268 | 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 | 318 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0093others(315): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): 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 | 168 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0097others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.-50+6187delT | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229915692 | ||||||
| chr2:229915706
|
A | T | 5 | a0001c0001t0001g0269a0001c0001t0009g0268a0001c0001t0014g0107others(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 | a0001c0001t0001g0269a0001c0001t0009g0268a0001c0001t0014g0107others(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 | a0001c0001t0019g0317a0001c0001t0019g0318a0001c0002t0002g0279others(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 | a0001c0003t0015g0150a0001c0003t0015g0151a0001c0003t0015g0173 | 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 | 166 | a0001c0001t0001g0097a0001c0001t0001g0105a0001c0001t0001g0106others(163): Show | 166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.-50+5343delT | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229916536 | ||||||
| chr2:229916680
|
A | T | 4 | a0001c0001t0001g0116a0001c0001t0001g0121a0001c0001t0001g0122others(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 | 265 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0093others(262): Show | 266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.-50+5019dupT | TRIP12 | ENSG00000153827.15 | transcript | ENST00000675903.1 | protein_coding | 1/41 | chr2 | 229916860 | ||||||
| chr2:229916902
|
G | A | 3 | a0001c0001t0014g0107a0001c0001t0014g0108a0001c0001t0014g0112 | 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 | a0001c0001t0001g0269a0001c0001t0009g0268a0001c0001t0014g0107others(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 | 271 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0093others(268): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): 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 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0099others(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 | a0001c0001t0001g0022a0001c0001t0001g0179a0001c0001t0001g0180others(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 | a0001c0001t0001g0023a0001c0001t0001g0192a0001c0002t0002g0292others(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 | a0001c0001t0024g0239a0001c0003t0001g0092a0001c0003t0006g0326others(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 | 7 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0019g0317others(4): Show | 7 | HG01433.hp1 HG02027.hp2 HG02257.hp2 others(4): 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 | a0001c0001t0001g0203a0001c0001t0001g0205a0001c0001t0019g0318others(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 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(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 | a0001c0001t0005g0020a0001c0002t0002g0305a0001c0003t0001g0214others(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 | a0001c0001t0001g0215a0001c0001t0001g0220a0001c0002t0002g0306others(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 | a0001c0002t0002g0320a0001c0003t0007g0222 | 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 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0011g0225others(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 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(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 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118others(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 | a0001c0001t0001g0094a0001c0002t0001g0063a0001c0002t0001g0064others(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 | a0001c0001t0001g0093a0001c0001t0001g0269a0001c0001t0011g0114others(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 | a0001c0001t0004g0266a0001c0001t0009g0268a0001c0001t0014g0112others(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 | a0001c0001t0001g0099a0001c0001t0001g0105a0001c0001t0001g0106others(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 | a0001c0001t0004g0255a0001c0001t0004g0257a0001c0001t0004g0258others(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 | a0001c0001t0004g0254a0001c0001t0010g0250a0001c0002t0002g0280 | 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 | a0001c0002t0002g0279a0001c0003t0001g0095 | 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 | a0001c0002t0003g0024a0001c0002t0003g0025 | 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 | a0001c0001t0001g0093a0001c0001t0001g0094 | 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 | a0001c0001t0001g0233a0001c0001t0001g0234a0001c0001t0001g0235others(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 | a0001c0001t0001g0269a0001c0001t0009g0268 | 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 | a0001c0004t0003g0082a0001c0004t0003g0083a0001c0004t0003g0084others(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 | a0001c0002t0001g0028a0001c0002t0001g0029a0001c0002t0001g0033others(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 | a0001c0002t0002g0279a0001c0002t0002g0280a0001c0002t0002g0281others(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 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0244others(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 | a0001c0001t0001g0246a0001c0001t0001g0248a0001c0001t0026g0247 | 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 | a0001c0002t0002g0279a0001c0002t0002g0280a0001c0002t0002g0281others(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 | a0001c0002t0003g0024a0001c0002t0003g0025a0001c0002t0003g0026 | 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 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0005g0003 | 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 | a0001c0001t0010g0249a0001c0001t0010g0250a0001c0001t0010g0251others(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 | a0001c0002t0001g0027a0001c0002t0001g0028a0001c0002t0001g0029others(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 | a0001c0001t0004g0001a0001c0001t0004g0254a0001c0001t0004g0255others(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 | a0001c0001t0001g0269a0001c0001t0009g0268 | 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 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0005g0003 | 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 | a0001c0001t0001g0274a0001c0001t0001g0275a0001c0001t0001g0276others(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 |