Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 9321 |
|---|---|
| ensemblid | ENSG00000100815.12 |
| hgncid | 12305 |
| symbol | TRIP11 |
| name | thyroid hormone receptor interactor 11 |
| refseq_nuc | NM_004239.4 |
| refseq_prot | NP_004230.2 |
| ensembl_nuc | ENST00000267622.8 |
| ensembl_prot | ENSP00000267622.4 |
| mane_status | MANE Select |
| chr | chr14 |
| start | 91965991 |
| end | 92040059 |
| strand | - |
| ver | v1.2 |
| region | chr14:91965991-92040059 |
| region5000 | chr14:91960991-92045059 |
| regionname0 | TRIP11_chr14_91965991_92040059 |
| regionname5000 | TRIP11_chr14_91960991_92045059 |
| 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 | 1979 | 190 | 54 | 46 | 59 | 12 | 17 | 46 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0002 | 0/0 | 1979 | 103 | 22 | 8 | 53 | 4 | 16 | 43 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0003 | 0/0 | 1979 | 28 | 0 | 0 | 24 | 0 | 4 | 21 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0004 | 0/0 | 1979 | 6 | 0 | 2 | 4 | 0 | 0 | 4 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0005 | 0/0 | 1979 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0006 | 0/0 | 1979 | 4 | 0 | 2 | 0 | 0 | 2 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0007 | 0/0 | 1979 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0008 | 0/0 | 1979 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0009 | 0/0 | 1979 | 3 | 2 | 0 | 0 | 0 | 1 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0010 | 0/0 | 1979 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0011 | 0/0 | 1979 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0012 | 0/0 | 1979 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0013 | 0/0 | 1979 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0014 | 0/0 | 1979 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0015 | 0/0 | 1979 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0016 | 0/0 | 1979 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0017 | 0/0 | 1979 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0018 | 0/0 | 1979 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0019 | 0/0 | 1979 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0020 | 0/0 | 1979 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0021 | 0/0 | 1979 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0022 | 0/0 | 1979 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0023 | 0/0 | 1979 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| 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 | 1/1 | 5940 | 164 | 38 | 42 | 56 | 11 | 15 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| c0002 | 0/0 | 5940 | 101 | 21 | 8 | 52 | 4 | 16 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| c0003 | 0/0 | 5940 | 27 | 0 | 0 | 24 | 0 | 3 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| c0004 | 0/0 | 5940 | 8 | 7 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| c0005 | 0/0 | 5940 | 6 | 0 | 2 | 4 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| c0006 | 0/0 | 5940 | 5 | 5 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| c0007 | 0/0 | 5940 | 5 | 5 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| c0008 | 0/0 | 5940 | 4 | 3 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| c0009 | 0/0 | 5940 | 4 | 4 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| c0010 | 0/0 | 5940 | 4 | 4 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| c0011 | 0/0 | 5940 | 4 | 0 | 2 | 0 | 0 | 2 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| c0012 | 0/0 | 5940 | 3 | 2 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| c0013 | 0/0 | 5940 | 2 | 2 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| c0014 | 0/0 | 5940 | 2 | 0 | 2 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| c0015 | 0/0 | 5940 | 2 | 0 | 2 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| c0016 | 0/0 | 5940 | 2 | 0 | 0 | 2 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| c0017 | 0/0 | 5940 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| c0018 | 0/0 | 5940 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| c0019 | 0/0 | 5940 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| c0020 | 0/0 | 5940 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| c0021 | 0/0 | 5940 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| c0022 | 0/0 | 5940 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| c0023 | 0/0 | 5940 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| c0024 | 0/0 | 5940 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| c0025 | 0/0 | 5940 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| c0026 | 0/0 | 5940 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| c0027 | 0/0 | 5940 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| c0028 | 0/0 | 5940 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| c0029 | 0/0 | 5940 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| c0030 | 0/0 | 5940 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| c0031 | 0/0 | 5940 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| c0032 | 0/0 | 5940 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| c0033 | 0/0 | 5940 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| c0034 | 0/0 | 5940 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| c0035 | 0/0 | 5940 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| c0036 | 0/0 | 5940 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| c0037 | 0/0 | 5940 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| 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 | 4057 | 82 | 5 | 27 | 37 | 6 | 6 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| t0002 | 0/0 | 4053 | 79 | 8 | 9 | 42 | 4 | 16 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| t0003 | 0/0 | 4057 | 29 | 7 | 9 | 8 | 3 | 2 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| t0004 | 0/0 | 4058 | 17 | 0 | 2 | 11 | 2 | 2 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| t0005 | 0/0 | 4071 | 11 | 7 | 3 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| t0006 | 0/0 | 4068 | 10 | 0 | 0 | 9 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| t0007 | 0/0 | 4069 | 9 | 0 | 0 | 8 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| t0008 | 0/0 | 4053 | 8 | 8 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| t0009 | 0/1 | 4070 | 7 | 4 | 1 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| t0010 | 0/0 | 4058 | 6 | 1 | 2 | 2 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| t0011 | 0/0 | 4070 | 6 | 0 | 0 | 6 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| t0012 | 0/0 | 4072 | 5 | 1 | 1 | 0 | 0 | 3 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| t0013 | 0/0 | 4040 | 5 | 5 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| t0014 | 0/0 | 4053 | 5 | 0 | 0 | 4 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| t0015 | 0/0 | 4057 | 5 | 5 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| t0016 | 0/0 | 4057 | 4 | 3 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| t0017 | 0/0 | 4057 | 4 | 0 | 0 | 4 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| t0018 | 0/0 | 4059 | 4 | 0 | 1 | 3 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| t0019 | 0/0 | 4072 | 3 | 3 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| t0020 | 0/0 | 4056 | 3 | 3 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| t0021 | 0/0 | 4057 | 3 | 1 | 1 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| t0022 | 0/0 | 4053 | 3 | 3 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| t0023 | 0/0 | 4057 | 2 | 2 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| t0024 | 0/0 | 4079 | 2 | 2 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| t0025 | 0/0 | 4075 | 2 | 2 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| t0026 | 0/0 | 4073 | 2 | 2 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| t0027 | 0/0 | 4073 | 2 | 0 | 0 | 0 | 1 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| t0028 | 0/0 | 4056 | 2 | 1 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| t0029 | 0/0 | 4052 | 2 | 1 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| t0030 | 0/0 | 4074 | 2 | 1 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| t0031 | 0/0 | 4074 | 2 | 2 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| t0032 | 0/0 | 4058 | 2 | 2 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| t0033 | 0/0 | 4058 | 2 | 0 | 1 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| t0034 | 0/0 | 4057 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| t0035 | 0/0 | 4057 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| t0036 | 0/0 | 4058 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| t0037 | 0/0 | 4076 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| t0038 | 0/0 | 4085 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| t0039 | 0/0 | 4084 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| t0040 | 0/0 | 4080 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| t0041 | 0/0 | 4076 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| t0042 | 0/0 | 4052 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| t0043 | 0/0 | 4057 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| t0044 | 0/0 | 4056 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| t0045 | 0/0 | 4058 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| t0046 | 0/0 | 4057 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| t0047 | 0/0 | 4076 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| t0048 | 0/0 | 4071 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| t0049 | 0/0 | 4057 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| t0050 | 0/0 | 4072 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| t0051 | 0/0 | 4057 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| t0052 | 0/0 | 4053 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| t0053 | 0/0 | 4053 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| t0054 | 0/0 | 4053 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| t0055 | 0/0 | 4075 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| t0056 | 0/0 | 4075 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| t0057 | 0/0 | 4073 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| t0058 | 0/0 | 4082 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| t0059 | 0/0 | 4057 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| t0060 | 0/0 | 4057 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| t0061 | 0/0 | 4068 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| t0062 | 0/0 | 4074 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| t0063 | 0/0 | 4053 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| t0064 | 0/0 | 4057 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| t0065 | 0/0 | 4057 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| t0066 | 0/0 | 4057 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| t0067 | 0/0 | 4053 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| 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 | 0 | 0 | 2 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0002 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0005 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0047 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0110 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| 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 | 1/1 | 5940 | 164 | 38 | 42 | 56 | 11 | 15 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0001c0004 | 0/0 | 5940 | 8 | 7 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0001c0007 | 0/0 | 5940 | 5 | 5 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0001c0010 | 0/0 | 5940 | 4 | 4 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0001c0015 | 0/0 | 5940 | 2 | 0 | 2 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0001c0017 | 0/0 | 5940 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0001c0018 | 0/0 | 5940 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0001c0019 | 0/0 | 5940 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0001c0020 | 0/0 | 5940 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0001c0031 | 0/0 | 5940 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0001c0033 | 0/0 | 5940 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0001c0035 | 0/0 | 5940 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0002c0002 | 0/0 | 5940 | 101 | 21 | 8 | 52 | 4 | 16 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0002c0021 | 0/0 | 5940 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0002c0029 | 0/0 | 5940 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0003c0003 | 0/0 | 5940 | 27 | 0 | 0 | 24 | 0 | 3 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0003c0037 | 0/0 | 5940 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0004c0005 | 0/0 | 5940 | 6 | 0 | 2 | 4 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0005c0006 | 0/0 | 5940 | 5 | 5 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0006c0011 | 0/0 | 5940 | 4 | 0 | 2 | 0 | 0 | 2 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0007c0009 | 0/0 | 5940 | 4 | 4 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0008c0008 | 0/0 | 5940 | 4 | 3 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0009c0012 | 0/0 | 5940 | 3 | 2 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0010c0013 | 0/0 | 5940 | 2 | 2 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0011c0016 | 0/0 | 5940 | 2 | 0 | 0 | 2 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0012c0014 | 0/0 | 5940 | 2 | 0 | 2 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0013c0036 | 0/0 | 5940 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0014c0034 | 0/0 | 5940 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0015c0022 | 0/0 | 5940 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0016c0024 | 0/0 | 5940 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0017c0025 | 0/0 | 5940 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0018c0030 | 0/0 | 5940 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0019c0028 | 0/0 | 5940 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0020c0027 | 0/0 | 5940 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0021c0026 | 0/0 | 5940 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0022c0023 | 0/0 | 5940 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0023c0032 | 0/0 | 5940 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 9996 | 73 | 4 | 23 | 34 | 6 | 5 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0001c0001t0003 | 0/0 | 9996 | 25 | 6 | 9 | 7 | 3 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0001c0001t0004 | 0/0 | 9997 | 13 | 0 | 1 | 9 | 1 | 2 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0001c0001t0005 | 0/0 | 10010 | 11 | 7 | 3 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0001c0001t0009 | 0/1 | 10009 | 6 | 4 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0001c0001t0010 | 0/0 | 9997 | 6 | 1 | 2 | 2 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0001c0001t0012 | 0/0 | 10011 | 4 | 1 | 1 | 0 | 0 | 2 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0001c0001t0016 | 0/0 | 9996 | 4 | 3 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0001c0001t0019 | 0/0 | 10011 | 2 | 2 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0001c0001t0023 | 0/0 | 9996 | 2 | 2 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0001c0001t0024 | 0/0 | 10018 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0001c0001t0026 | 0/0 | 10012 | 2 | 2 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0001c0001t0027 | 0/0 | 10012 | 2 | 0 | 0 | 0 | 1 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0001c0001t0028 | 0/0 | 9995 | 2 | 1 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0001c0001t0034 | 0/0 | 9996 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0001c0001t0036 | 0/0 | 9997 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0001c0001t0040 | 0/0 | 10019 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0001c0001t0043 | 0/0 | 9996 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0001c0001t0044 | 0/0 | 9995 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0001c0001t0045 | 0/0 | 9997 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0001c0001t0046 | 0/0 | 9996 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0001c0001t0047 | 0/0 | 10015 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0001c0001t0048 | 0/0 | 10010 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0001c0001t0049 | 0/0 | 9996 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0001c0001t0060 | 0/0 | 9996 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0001c0004t0019 | 0/0 | 10011 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0001c0004t0024 | 0/0 | 10018 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0001c0004t0025 | 0/0 | 10014 | 2 | 2 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0001c0004t0037 | 0/0 | 10015 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0001c0004t0038 | 0/0 | 10024 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0001c0004t0039 | 0/0 | 10023 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0001c0004t0041 | 0/0 | 10015 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0001c0007t0013 | 0/0 | 9979 | 5 | 5 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0001c0010t0020 | 0/0 | 9995 | 3 | 3 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0001c0010t0051 | 0/0 | 9996 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0001c0015t0001 | 0/0 | 9996 | 2 | 0 | 2 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0001c0017t0004 | 0/0 | 9997 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0001c0018t0062 | 0/0 | 10013 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0001c0019t0004 | 0/0 | 9997 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0001c0020t0001 | 0/0 | 9996 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0001c0031t0001 | 0/0 | 9996 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0001c0033t0001 | 0/0 | 9996 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0001c0035t0012 | 0/0 | 10011 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0002c0002t0002 | 0/0 | 9992 | 73 | 8 | 7 | 40 | 4 | 14 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0002c0002t0008 | 0/0 | 9992 | 7 | 7 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0002c0002t0014 | 0/0 | 9992 | 5 | 0 | 0 | 4 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0002c0002t0017 | 0/0 | 9996 | 4 | 0 | 0 | 4 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0002c0002t0021 | 0/0 | 9996 | 3 | 1 | 1 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0002c0002t0022 | 0/0 | 9992 | 3 | 3 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0002c0002t0029 | 0/0 | 9991 | 2 | 1 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0002c0002t0042 | 0/0 | 9991 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0002c0002t0052 | 0/0 | 9992 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0002c0002t0053 | 0/0 | 9992 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0002c0002t0054 | 0/0 | 9992 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0002c0021t0002 | 0/0 | 9992 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0002c0029t0008 | 0/0 | 9992 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0003c0003t0006 | 0/0 | 10007 | 10 | 0 | 0 | 9 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0003c0003t0007 | 0/0 | 10008 | 9 | 0 | 0 | 8 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0003c0003t0011 | 0/0 | 10009 | 6 | 0 | 0 | 6 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0003c0003t0061 | 0/0 | 10007 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0003c0003t0063 | 0/0 | 9992 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0003c0037t0050 | 0/0 | 10011 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0004c0005t0018 | 0/0 | 9998 | 4 | 0 | 1 | 3 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0004c0005t0033 | 0/0 | 9997 | 2 | 0 | 1 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0005c0006t0015 | 0/0 | 9996 | 4 | 4 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0005c0006t0067 | 0/0 | 9992 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0006c0011t0002 | 0/0 | 9992 | 4 | 0 | 2 | 0 | 0 | 2 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0007c0009t0031 | 0/0 | 10013 | 2 | 2 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0007c0009t0056 | 0/0 | 10014 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0007c0009t0057 | 0/0 | 10012 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0008c0008t0030 | 0/0 | 10013 | 2 | 1 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0008c0008t0055 | 0/0 | 10014 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0008c0008t0058 | 0/0 | 10021 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0009c0012t0032 | 0/0 | 9997 | 2 | 2 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0009c0012t0059 | 0/0 | 9996 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0010c0013t0015 | 0/0 | 9996 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0010c0013t0066 | 0/0 | 9996 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0011c0016t0001 | 0/0 | 9996 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0011c0016t0004 | 0/0 | 9997 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0012c0014t0001 | 0/0 | 9996 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0012c0014t0004 | 0/0 | 9997 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0013c0036t0003 | 0/0 | 9996 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0014c0034t0003 | 0/0 | 9996 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0015c0022t0065 | 0/0 | 9996 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0016c0024t0064 | 0/0 | 9996 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0017c0025t0003 | 0/0 | 9996 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0018c0030t0002 | 0/0 | 9992 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0019c0028t0001 | 0/0 | 9996 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0020c0027t0003 | 0/0 | 9996 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0021c0026t0001 | 0/0 | 9996 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0022c0023t0035 | 0/0 | 9996 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| a0023c0032t0009 | 0/0 | 10009 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | copy fasta | chr14 | 91960991 | 92045059 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0001g0047 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0003g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0003g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0003g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0003g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0004g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0004g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0004g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0004g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0004g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0004g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0004g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0004g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0004g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0004g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0004g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0004g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0004g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0005g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0005g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0005g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0005g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0005g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0005g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0005g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0005g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0005g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0005g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0005g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0009g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0009g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0009g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0009g0110 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0009g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0009g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0010g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0010g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0010g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0010g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0010g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0010g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0012g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0012g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0012g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0012g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0016g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0016g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0016g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0016g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0019g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0019g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0023g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0023g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0024g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0026g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0026g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0027g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0027g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0028g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0028g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0034g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0036g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0040g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0043g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0044g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0045g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0046g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0047g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0048g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0049g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0001t0060g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0004t0019g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0004t0024g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0004t0025g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0004t0025g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0004t0037g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0004t0038g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0004t0039g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0004t0041g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0007t0013g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0007t0013g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0007t0013g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0007t0013g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0010t0020g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0010t0020g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0010t0020g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0010t0051g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0015t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0015t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0017t0004g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0018t0062g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0019t0004g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0020t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0031t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0033t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0001c0035t0012g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0002g0005 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0002g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0002g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0002g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0002g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0002g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0002g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0002g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0002g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0002g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0002g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0002g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0002g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0002g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0002g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0002g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0002g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0002g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0002g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0008g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0008g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0008g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0008g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0008g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0008g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0014g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0014g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0014g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0014g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0014g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0017g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0017g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0017g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0017g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0021g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0021g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0021g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0022g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0022g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0022g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0029g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0029g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0042g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0052g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0053g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0002t0054g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0021t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0002c0029t0008g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0003c0003t0006g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0003c0003t0006g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0003c0003t0006g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0003c0003t0006g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0003c0003t0006g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0003c0003t0006g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0003c0003t0006g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0003c0003t0006g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0003c0003t0006g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0003c0003t0006g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0003c0003t0007g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0003c0003t0007g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0003c0003t0007g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0003c0003t0007g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0003c0003t0007g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0003c0003t0007g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0003c0003t0007g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0003c0003t0007g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0003c0003t0007g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0003c0003t0011g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0003c0003t0011g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0003c0003t0011g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0003c0003t0011g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0003c0003t0011g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0003c0003t0011g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0003c0003t0061g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0003c0003t0063g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0003c0037t0050g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0004c0005t0018g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0004c0005t0018g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0004c0005t0018g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0004c0005t0018g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0004c0005t0033g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0004c0005t0033g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0005c0006t0015g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0005c0006t0015g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0005c0006t0015g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0005c0006t0015g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0005c0006t0067g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0006c0011t0002g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0006c0011t0002g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0006c0011t0002g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0006c0011t0002g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0007c0009t0031g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0007c0009t0031g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0007c0009t0056g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0007c0009t0057g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0008c0008t0030g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0008c0008t0030g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0008c0008t0055g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0008c0008t0058g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0009c0012t0032g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0009c0012t0032g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0009c0012t0059g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0010c0013t0015g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0010c0013t0066g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0011c0016t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0011c0016t0004g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0012c0014t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0012c0014t0004g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0013c0036t0003g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0014c0034t0003g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0015c0022t0065g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0016c0024t0064g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0017c0025t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0018c0030t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0019c0028t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0020c0027t0003g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0021c0026t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0022c0023t0035g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| a0023c0032t0009g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0048 | EUR | GBR | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG00099 | hp2 | a0002 | c0002 | t0002 | g0005 | EUR | GBR | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG00140 | hp1 | a0002 | c0002 | t0002 | g0254 | EUR | GBR | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0168 | EUR | GBR | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0181 | EUR | FIN | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0160 | EUR | FIN | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG00323 | hp1 | a0001 | c0001 | t0027 | g0083 | EUR | FIN | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0018 | EUR | FIN | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | CHS | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG00408 | hp2 | a0003 | c0003 | t0007 | g0336 | EAS | CHS | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG00423 | hp1 | a0001 | c0001 | t0004 | g0044 | EAS | CHS | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG00423 | hp2 | a0002 | c0002 | t0002 | g0250 | EAS | CHS | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG00438 | hp1 | a0001 | c0001 | t0004 | g0042 | EAS | CHS | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG00438 | hp2 | a0002 | c0002 | t0002 | g0244 | EAS | CHS | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | CHS | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG00544 | hp2 | a0002 | c0002 | t0002 | g0006 | EAS | CHS | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG00558 | hp2 | a0002 | c0002 | t0014 | g0318 | EAS | CHS | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG00609 | hp1 | a0002 | c0002 | t0002 | g0307 | EAS | CHS | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG00609 | hp2 | a0001 | c0001 | t0034 | g0008 | EAS | CHS | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG00642 | hp1 | a0022 | c0023 | t0035 | g0069 | AMR | PUR | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG00642 | hp2 | a0002 | c0002 | t0002 | g0272 | AMR | PUR | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG00673 | hp1 | a0002 | c0002 | t0002 | g0289 | EAS | CHS | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG00673 | hp2 | a0001 | c0001 | t0046 | g0029 | EAS | CHS | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG00735 | hp1 | a0002 | c0002 | t0002 | g0221 | AMR | PUR | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG00735 | hp2 | a0001 | c0001 | t0044 | g0173 | AMR | PUR | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG00738 | hp1 | a0012 | c0014 | t0004 | g0152 | AMR | PUR | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG00738 | hp2 | a0002 | c0002 | t0002 | g0005 | AMR | PUR | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG01069 | hp1 | a0001 | c0001 | t0005 | g0097 | AMR | PUR | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG01069 | hp2 | a0004 | c0005 | t0018 | g0121 | AMR | PUR | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG01070 | hp2 | a0001 | c0001 | t0003 | g0179 | AMR | PUR | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG01071 | hp2 | a0004 | c0005 | t0033 | g0122 | AMR | PUR | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG01081 | hp1 | a0001 | c0001 | t0016 | g0131 | AMR | PUR | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG01081 | hp2 | a0006 | c0011 | t0002 | g0312 | AMR | PUR | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG01099 | hp1 | a0006 | c0011 | t0002 | g0311 | AMR | PUR | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG01106 | hp2 | a0019 | c0028 | t0001 | g0153 | AMR | PUR | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG01109 | hp1 | a0008 | c0008 | t0030 | g0116 | AMR | PUR | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG01109 | hp2 | a0001 | c0001 | t0010 | g0180 | AMR | PUR | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG01167 | hp2 | a0001 | c0001 | t0005 | g0086 | AMR | PUR | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG01168 | hp1 | a0002 | c0002 | t0002 | g0235 | AMR | PUR | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG01169 | hp1 | a0002 | c0002 | t0002 | g0205 | AMR | PUR | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG01175 | hp2 | a0002 | c0002 | t0021 | g0306 | AMR | PUR | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG01192 | hp2 | a0001 | c0001 | t0012 | g0095 | AMR | PUR | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG01243 | hp1 | a0001 | c0001 | t0005 | g0090 | AMR | PUR | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0184 | AMR | PUR | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | CLM | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG01255 | hp2 | a0001 | c0004 | t0038 | g0211 | AMR | CLM | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG01256 | hp1 | a0023 | c0032 | t0009 | g0091 | AMR | CLM | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG01256 | hp2 | a0001 | c0015 | t0001 | g0157 | AMR | CLM | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG01257 | hp1 | a0002 | c0002 | t0002 | g0294 | AMR | CLM | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG01257 | hp2 | a0001 | c0001 | t0010 | g0194 | AMR | CLM | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG01258 | hp1 | a0001 | c0015 | t0001 | g0158 | AMR | CLM | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG01258 | hp2 | a0002 | c0002 | t0002 | g0295 | AMR | CLM | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | CLM | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG01261 | hp2 | a0001 | c0001 | t0003 | g0190 | AMR | CLM | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | CLM | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0197 | AMR | CLM | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0187 | AMR | CLM | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG01358 | hp2 | a0012 | c0014 | t0001 | g0151 | AMR | CLM | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG01496 | hp1 | a0001 | c0001 | t0047 | g0102 | AMR | CLM | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0186 | AMR | CLM | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG01515 | hp1 | a0001 | c0001 | t0004 | g0144 | EUR | IBS | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0199 | EUR | IBS | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0193 | EUR | IBS | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG01884 | hp1 | a0001 | c0001 | t0009 | g0088 | AFR | ACB | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG01884 | hp2 | a0002 | c0002 | t0002 | g0206 | AFR | ACB | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0040 | AFR | ACB | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG01891 | hp2 | a0001 | c0001 | t0016 | g0134 | AFR | ACB | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PEL | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PEL | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PEL | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | PEL | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PEL | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG01975 | hp2 | a0001 | c0001 | t0003 | g0188 | AMR | PEL | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PEL | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG01978 | hp2 | a0001 | c0018 | t0062 | g0321 | AMR | PEL | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG01981 | hp1 | a0001 | c0001 | t0004 | g0156 | AMR | PEL | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG01981 | hp2 | a0001 | c0001 | t0003 | g0200 | AMR | PEL | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PEL | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG02004 | hp2 | a0001 | c0001 | t0003 | g0191 | AMR | PEL | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG02027 | hp2 | a0017 | c0025 | t0003 | g0182 | EAS | KHV | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG02040 | hp1 | a0011 | c0016 | t0001 | g0013 | EAS | KHV | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG02040 | hp2 | a0003 | c0003 | t0006 | g0334 | EAS | KHV | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG02055 | hp1 | a0010 | c0013 | t0066 | g0355 | AFR | ACB | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG02055 | hp2 | a0008 | c0008 | t0055 | g0115 | AFR | ACB | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG02056 | hp1 | a0002 | c0002 | t0017 | g0247 | EAS | KHV | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG02056 | hp2 | a0001 | c0001 | t0004 | g0020 | EAS | KHV | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG02080 | hp2 | a0002 | c0002 | t0002 | g0245 | EAS | KHV | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG02135 | hp1 | a0002 | c0002 | t0002 | g0263 | EAS | KHV | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG02135 | hp2 | a0001 | c0001 | t0043 | g0032 | EAS | KHV | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG02145 | hp1 | a0001 | c0010 | t0051 | g0177 | AFR | ACB | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG02145 | hp2 | a0001 | c0001 | t0005 | g0140 | AFR | ACB | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | CDX | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG02165 | hp2 | a0003 | c0003 | t0006 | g0343 | EAS | CDX | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG02257 | hp1 | a0007 | c0009 | t0031 | g0117 | AFR | ACB | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | ACB | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG02258 | hp1 | a0015 | c0022 | t0065 | g0357 | AFR | ACB | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG02258 | hp2 | a0001 | c0001 | t0026 | g0107 | AFR | ACB | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG02280 | hp1 | a0001 | c0001 | t0016 | g0133 | AFR | ACB | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG02280 | hp2 | a0001 | c0001 | t0005 | g0085 | AFR | ACB | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG02451 | hp1 | a0005 | c0006 | t0015 | g0351 | AFR | ACB | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG02451 | hp2 | a0001 | c0001 | t0024 | g0092 | AFR | ACB | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG02523 | hp1 | a0001 | c0019 | t0004 | g0041 | EAS | KHV | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG02523 | hp2 | a0002 | c0002 | t0017 | g0240 | EAS | KHV | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG02572 | hp1 | a0002 | c0002 | t0002 | g0249 | AFR | GWD | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG02572 | hp2 | a0001 | c0001 | t0026 | g0096 | AFR | GWD | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG02602 | hp1 | a0002 | c0002 | t0054 | g0290 | SAS | PJL | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG02602 | hp2 | a0001 | c0001 | t0028 | g0183 | SAS | PJL | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG02615 | hp1 | a0002 | c0002 | t0008 | g0226 | AFR | GWD | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG02615 | hp2 | a0005 | c0006 | t0015 | g0354 | AFR | GWD | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0038 | AFR | GWD | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG02622 | hp2 | a0001 | c0001 | t0023 | g0136 | AFR | GWD | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG02630 | hp1 | a0002 | c0029 | t0008 | g0231 | AFR | GWD | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG02630 | hp2 | a0001 | c0004 | t0025 | g0213 | AFR | GWD | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG02647 | hp1 | a0001 | c0001 | t0010 | g0035 | AFR | GWD | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG02647 | hp2 | a0001 | c0001 | t0005 | g0089 | AFR | GWD | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG02683 | hp1 | a0013 | c0036 | t0003 | g0279 | SAS | PJL | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG02683 | hp2 | a0006 | c0011 | t0002 | g0313 | SAS | PJL | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG02698 | hp1 | a0002 | c0002 | t0002 | g0268 | SAS | PJL | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG02698 | hp2 | a0001 | c0001 | t0012 | g0094 | SAS | PJL | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG02717 | hp2 | a0001 | c0001 | t0005 | g0106 | AFR | GWD | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG02723 | hp1 | a0001 | c0001 | t0005 | g0103 | AFR | GWD | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG02723 | hp2 | a0008 | c0008 | t0030 | g0114 | AFR | GWD | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG02735 | hp1 | a0006 | c0011 | t0002 | g0314 | SAS | PJL | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG02735 | hp2 | a0001 | c0001 | t0009 | g0104 | SAS | PJL | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG02738 | hp1 | a0003 | c0003 | t0061 | g0340 | SAS | PJL | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG02738 | hp2 | a0002 | c0002 | t0002 | g0243 | SAS | PJL | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG02809 | hp1 | a0002 | c0002 | t0008 | g0227 | AFR | GWD | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG02809 | hp2 | a0001 | c0007 | t0013 | g0308 | AFR | GWD | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG02818 | hp1 | a0001 | c0001 | t0019 | g0111 | AFR | GWD | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG02818 | hp2 | a0014 | c0034 | t0003 | g0128 | AFR | GWD | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG02886 | hp1 | a0001 | c0001 | t0036 | g0139 | AFR | GWD | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG02886 | hp2 | a0021 | c0026 | t0001 | g0172 | AFR | GWD | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG02896 | hp1 | a0007 | c0009 | t0031 | g0120 | AFR | GWD | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG02896 | hp2 | a0001 | c0001 | t0048 | g0100 | AFR | GWD | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG02897 | hp1 | a0007 | c0009 | t0056 | g0118 | AFR | GWD | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG02897 | hp2 | a0001 | c0001 | t0005 | g0087 | AFR | GWD | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG02922 | hp1 | a0005 | c0006 | t0015 | g0352 | AFR | ESN | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG02922 | hp2 | a0002 | c0002 | t0052 | g0228 | AFR | ESN | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG02965 | hp1 | a0009 | c0012 | t0032 | g0130 | AFR | ESN | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG02965 | hp2 | a0010 | c0013 | t0015 | g0350 | AFR | ESN | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG02970 | hp1 | a0001 | c0007 | t0013 | g0007 | AFR | ESN | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0059 | AFR | ESN | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG02976 | hp1 | a0001 | c0001 | t0049 | g0204 | AFR | ESN | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG02976 | hp2 | a0002 | c0002 | t0008 | g0223 | AFR | ESN | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG03017 | hp1 | a0002 | c0002 | t0002 | g0301 | SAS | PJL | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG03017 | hp2 | a0002 | c0002 | t0002 | g0239 | SAS | PJL | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG03041 | hp1 | a0001 | c0004 | t0039 | g0215 | AFR | GWD | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG03041 | hp2 | a0002 | c0002 | t0029 | g0212 | AFR | GWD | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG03098 | hp1 | a0005 | c0006 | t0067 | g0349 | AFR | MSL | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG03098 | hp2 | a0001 | c0004 | t0041 | g0208 | AFR | MSL | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG03130 | hp1 | a0009 | c0012 | t0032 | g0129 | AFR | ESN | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG03130 | hp2 | a0002 | c0002 | t0002 | g0224 | AFR | ESN | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG03139 | hp1 | a0002 | c0002 | t0002 | g0299 | AFR | ESN | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG03139 | hp2 | a0001 | c0004 | t0025 | g0209 | AFR | ESN | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG03195 | hp1 | a0002 | c0002 | t0008 | g0004 | AFR | ESN | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG03195 | hp2 | a0001 | c0001 | t0009 | g0137 | AFR | ESN | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0037 | AFR | MSL | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG03209 | hp2 | a0001 | c0001 | t0005 | g0105 | AFR | MSL | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG03225 | hp1 | a0002 | c0002 | t0022 | g0296 | AFR | MSL | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG03225 | hp2 | a0001 | c0001 | t0009 | g0138 | AFR | MSL | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG03239 | hp2 | a0002 | c0002 | t0002 | g0260 | SAS | PJL | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG03453 | hp1 | a0001 | c0001 | t0016 | g0132 | AFR | MSL | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG03453 | hp2 | a0002 | c0002 | t0002 | g0229 | AFR | MSL | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG03486 | hp1 | a0001 | c0004 | t0019 | g0207 | AFR | MSL | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG03486 | hp2 | a0001 | c0007 | t0013 | g0309 | AFR | MSL | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG03491 | hp1 | a0003 | c0003 | t0006 | g0339 | SAS | PJL | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG03491 | hp2 | a0001 | c0031 | t0001 | g0145 | SAS | PJL | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG03492 | hp1 | a0002 | c0002 | t0002 | g0219 | SAS | PJL | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG03492 | hp2 | a0003 | c0003 | t0007 | g0338 | SAS | PJL | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG03540 | hp1 | a0016 | c0024 | t0064 | g0356 | AFR | GWD | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG03540 | hp2 | a0001 | c0001 | t0019 | g0108 | AFR | GWD | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG03579 | hp1 | a0001 | c0004 | t0037 | g0214 | AFR | MSL | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG03579 | hp2 | a0001 | c0007 | t0013 | g0310 | AFR | MSL | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG03669 | hp1 | a0002 | c0002 | t0002 | g0280 | SAS | PJL | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG03688 | hp1 | a0002 | c0002 | t0002 | g0232 | SAS | STU | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | STU | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG03710 | hp1 | a0002 | c0002 | t0002 | g0267 | SAS | PJL | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG03710 | hp2 | a0020 | c0027 | t0003 | g0178 | SAS | PJL | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG03831 | hp1 | a0009 | c0012 | t0059 | g0123 | SAS | BEB | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG03831 | hp2 | a0001 | c0001 | t0012 | g0109 | SAS | BEB | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG03834 | hp1 | a0001 | c0001 | t0010 | g0203 | SAS | BEB | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG03834 | hp2 | a0002 | c0002 | t0002 | g0218 | SAS | BEB | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG03927 | hp1 | a0001 | c0035 | t0012 | g0084 | SAS | BEB | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG03927 | hp2 | a0001 | c0001 | t0004 | g0052 | SAS | BEB | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | BEB | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG03942 | hp2 | a0002 | c0002 | t0014 | g0317 | SAS | BEB | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0171 | SAS | STU | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG04115 | hp2 | a0002 | c0002 | t0002 | g0252 | SAS | STU | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG04184 | hp1 | a0001 | c0001 | t0027 | g0112 | SAS | BEB | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG04184 | hp2 | a0001 | c0001 | t0060 | g0316 | SAS | BEB | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG04199 | hp1 | a0002 | c0002 | t0002 | g0302 | SAS | STU | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG04199 | hp2 | a0001 | c0001 | t0004 | g0164 | SAS | STU | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG04204 | hp1 | a0002 | c0002 | t0002 | g0276 | SAS | STU | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG04204 | hp2 | a0003 | c0037 | t0050 | g0079 | SAS | STU | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG04228 | hp1 | a0001 | c0001 | t0005 | g0093 | SAS | STU | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG04228 | hp2 | a0002 | c0002 | t0002 | g0275 | SAS | STU | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA18522 | hp1 | a0001 | c0010 | t0020 | g0175 | AFR | YRI | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA18522 | hp2 | a0001 | c0001 | t0012 | g0101 | AFR | YRI | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA18906 | hp1 | a0002 | c0002 | t0022 | g0298 | AFR | YRI | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA18906 | hp2 | a0002 | c0002 | t0002 | g0300 | AFR | YRI | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0196 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA18939 | hp2 | a0002 | c0002 | t0002 | g0234 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA18941 | hp1 | a0001 | c0001 | t0003 | g0195 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA18942 | hp2 | a0002 | c0002 | t0029 | g0258 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA18945 | hp2 | a0003 | c0003 | t0006 | g0342 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA18946 | hp1 | a0003 | c0003 | t0007 | g0344 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA18948 | hp1 | a0003 | c0003 | t0006 | g0345 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA18948 | hp2 | a0002 | c0002 | t0014 | g0320 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA18949 | hp1 | a0002 | c0002 | t0021 | g0242 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA18949 | hp2 | a0001 | c0001 | t0010 | g0202 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA18950 | hp1 | a0003 | c0003 | t0007 | g0327 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA18950 | hp2 | a0001 | c0001 | t0003 | g0198 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA18952 | hp1 | a0003 | c0003 | t0006 | g0331 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA18953 | hp1 | a0002 | c0002 | t0002 | g0255 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA18954 | hp1 | a0018 | c0030 | t0002 | g0271 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA18954 | hp2 | a0003 | c0003 | t0006 | g0348 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA18956 | hp1 | a0002 | c0002 | t0002 | g0293 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA18956 | hp2 | a0003 | c0003 | t0007 | g0330 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA18957 | hp1 | a0002 | c0021 | t0002 | g0286 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA18959 | hp1 | a0002 | c0002 | t0002 | g0264 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA18959 | hp2 | a0001 | c0001 | t0010 | g0192 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA18961 | hp1 | a0001 | c0001 | t0004 | g0292 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA18961 | hp2 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA18965 | hp2 | a0002 | c0002 | t0002 | g0238 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA18966 | hp1 | a0002 | c0002 | t0002 | g0285 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA18966 | hp2 | a0001 | c0001 | t0004 | g0053 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA18968 | hp1 | a0002 | c0002 | t0002 | g0277 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA18970 | hp2 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA18971 | hp1 | a0003 | c0003 | t0006 | g0323 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA18972 | hp1 | a0001 | c0001 | t0004 | g0028 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA18972 | hp2 | a0002 | c0002 | t0002 | g0283 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA18973 | hp1 | a0002 | c0002 | t0002 | g0270 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA18974 | hp1 | a0003 | c0003 | t0007 | g0329 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA18974 | hp2 | a0002 | c0002 | t0042 | g0288 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA18978 | hp1 | a0001 | c0001 | t0003 | g0189 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA18978 | hp2 | a0001 | c0001 | t0045 | g0080 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA18979 | hp1 | a0001 | c0020 | t0001 | g0026 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA18979 | hp2 | a0002 | c0002 | t0002 | g0241 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA18980 | hp1 | a0004 | c0005 | t0018 | g0124 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA18980 | hp2 | a0003 | c0003 | t0063 | g0337 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA18982 | hp1 | a0002 | c0002 | t0017 | g0265 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA18983 | hp2 | a0002 | c0002 | t0002 | g0261 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA18986 | hp2 | a0004 | c0005 | t0018 | g0127 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA18987 | hp1 | a0002 | c0002 | t0002 | g0217 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA18989 | hp1 | a0004 | c0005 | t0033 | g0125 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA18989 | hp2 | a0003 | c0003 | t0007 | g0347 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA18991 | hp1 | a0002 | c0002 | t0014 | g0315 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA18991 | hp2 | a0011 | c0016 | t0004 | g0011 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA18995 | hp2 | a0002 | c0002 | t0002 | g0282 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA18999 | hp1 | a0002 | c0002 | t0002 | g0259 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA19000 | hp1 | a0002 | c0002 | t0014 | g0319 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA19001 | hp2 | a0003 | c0003 | t0006 | g0346 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA19002 | hp1 | a0002 | c0002 | t0002 | g0287 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA19003 | hp1 | a0002 | c0002 | t0017 | g0278 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA19007 | hp1 | a0002 | c0002 | t0002 | g0262 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA19010 | hp2 | a0002 | c0002 | t0002 | g0303 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA19011 | hp2 | a0002 | c0002 | t0002 | g0246 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0039 | AFR | LWK | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA19030 | hp2 | a0001 | c0001 | t0028 | g0304 | AFR | LWK | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA19043 | hp1 | a0002 | c0002 | t0008 | g0004 | AFR | LWK | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA19043 | hp2 | a0005 | c0006 | t0015 | g0353 | AFR | LWK | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA19054 | hp1 | a0003 | c0003 | t0011 | g0332 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA19054 | hp2 | a0002 | c0002 | t0002 | g0233 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA19064 | hp1 | a0002 | c0002 | t0002 | g0256 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA19064 | hp2 | a0003 | c0003 | t0007 | g0333 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA19067 | hp1 | a0002 | c0002 | t0053 | g0253 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA19067 | hp2 | a0003 | c0003 | t0006 | g0325 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA19072 | hp1 | a0002 | c0002 | t0002 | g0284 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA19072 | hp2 | a0002 | c0002 | t0002 | g0291 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA19077 | hp2 | a0002 | c0002 | t0002 | g0269 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA19078 | hp1 | a0002 | c0002 | t0002 | g0251 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA19078 | hp2 | a0001 | c0001 | t0004 | g0081 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA19079 | hp1 | a0002 | c0002 | t0002 | g0266 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA19079 | hp2 | a0003 | c0003 | t0011 | g0328 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA19080 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA19080 | hp2 | a0002 | c0002 | t0002 | g0248 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA19081 | hp1 | a0002 | c0002 | t0002 | g0236 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA19083 | hp1 | a0001 | c0001 | t0004 | g0066 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA19083 | hp2 | a0003 | c0003 | t0007 | g0324 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA19084 | hp1 | a0001 | c0001 | t0004 | g0034 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA19084 | hp2 | a0003 | c0003 | t0011 | g0322 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA19085 | hp1 | a0002 | c0002 | t0002 | g0281 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA19087 | hp1 | a0001 | c0033 | t0001 | g0078 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA19087 | hp2 | a0002 | c0002 | t0002 | g0257 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA19088 | hp1 | a0004 | c0005 | t0018 | g0126 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA19089 | hp1 | a0002 | c0002 | t0002 | g0237 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA19089 | hp2 | a0003 | c0003 | t0011 | g0326 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA19091 | hp1 | a0001 | c0001 | t0003 | g0185 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA19091 | hp2 | a0003 | c0003 | t0011 | g0335 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA19240 | hp1 | a0002 | c0002 | t0021 | g0216 | AFR | YRI | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0036 | AFR | YRI | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA20129 | hp1 | a0002 | c0002 | t0008 | g0225 | AFR | ASW | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA20129 | hp2 | a0001 | c0007 | t0013 | g0007 | AFR | ASW | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA20752 | hp1 | a0001 | c0017 | t0004 | g0016 | EUR | TSI | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA20752 | hp2 | a0002 | c0002 | t0002 | g0220 | EUR | TSI | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0167 | EUR | TSI | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA20805 | hp2 | a0002 | c0002 | t0002 | g0273 | EUR | TSI | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG02109 | hp1 | a0002 | c0002 | t0002 | g0230 | AFR | ACB | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG02109 | hp2 | a0001 | c0001 | t0040 | g0098 | AFR | ACB | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG02486 | hp1 | a0001 | c0010 | t0020 | g0176 | AFR | ACB | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG02486 | hp2 | a0002 | c0002 | t0022 | g0297 | AFR | ACB | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG02559 | hp1 | a0001 | c0001 | t0023 | g0135 | AFR | ACB | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG02559 | hp2 | a0007 | c0009 | t0057 | g0119 | AFR | ACB | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG03471 | hp1 | a0008 | c0008 | t0058 | g0113 | AFR | MSL | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG03471 | hp2 | a0002 | c0002 | t0002 | g0305 | AFR | MSL | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG06807 | hp1 | a0001 | c0010 | t0020 | g0174 | AFR | USA | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| HG06807 | hp2 | a0001 | c0004 | t0024 | g0210 | AFR | USA | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA18955 | hp1 | a0002 | c0002 | t0002 | g0274 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA18955 | hp2 | a0003 | c0003 | t0011 | g0341 | EAS | JPT | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA20300 | hp1 | a0002 | c0002 | t0008 | g0222 | AFR | USA | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | USA | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | LWK | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| NA21309 | hp2 | a0001 | c0001 | t0009 | g0099 | AFR | LWK | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0009 | g0110 | REF | REF | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0047 | REF | REF | TRIP11_chr14_91960991_92045059 | TRIP11 | chr14 | 91960991 | 92045059 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:91969726
|
C | T | 1 | a0021 | 1 | HG02886.hp2 | missense_variant | MODERATE | c.5887G>A | p.Ala1963Thr | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 21/21 | 6261/9996 | 5887/5940 | 1963/1979 | chr14 | 91969726 | ||
| chr14:91972785
|
T | C | 1 | a0005 | 5 | HG02451.hp1 HG02615.hp2 HG02922.hp1 others(2): Show |
missense_variant | MODERATE | c.5651A>G | p.His1884Arg | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 20/21 | 6025/9996 | 5651/5940 | 1884/1979 | chr14 | 91972785 | ||
| chr14:91974652
|
G | A | 1 | a0020 | 1 | HG03710.hp2 | missense_variant | MODERATE | c.5549C>T | p.Pro1850Leu | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 19/21 | 5923/9996 | 5549/5940 | 1850/1979 | chr14 | 91974652 | ||
| chr14:91974664
|
G | A | 1 | a0019 | 1 | HG01106.hp2 | missense_variant | MODERATE | c.5537C>T | p.Thr1846Ile | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 19/21 | 5911/9996 | 5537/5940 | 1846/1979 | chr14 | 91974664 | ||
| chr14:91974722
|
C | T | 3 | a0002a0006a0018 | 108 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(105): Show |
missense_variant | MODERATE | c.5479G>A | p.Gly1827Ser | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 19/21 | 5853/9996 | 5479/5940 | 1827/1979 | chr14 | 91974722 | ||
| chr14:91988289
|
C | T | 7 | a0004a0005a0007others(4): Show | 22 | HG01069.hp2 HG01071.hp2 HG02055.hp1 others(19): Show |
missense_variant | MODERATE | c.5255G>A | p.Arg1752Lys | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/21 | 5629/9996 | 5255/5940 | 1752/1979 | chr14 | 91988289 | ||
| chr14:91988298
|
T | G | 1 | a0004 | 6 | HG01069.hp2 HG01071.hp2 NA18980.hp1 others(3): Show |
missense_variant | MODERATE | c.5246A>C | p.Glu1749Ala | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/21 | 5620/9996 | 5246/5940 | 1749/1979 | chr14 | 91988298 | ||
| chr14:91993883
|
C | T | 1 | a0003 | 28 | HG00408.hp2 HG02040.hp2 HG02165.hp2 others(25): Show |
missense_variant | MODERATE | c.5086G>A | p.Glu1696Lys | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/21 | 5460/9996 | 5086/5940 | 1696/1979 | chr14 | 91993883 | ||
| chr14:91999405
|
C | T | 1 | a0012 | 2 | HG00738.hp1 HG01358.hp2 |
missense_variant | MODERATE | c.4727G>A | p.Arg1576His | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 13/21 | 5101/9996 | 4727/5940 | 1576/1979 | chr14 | 91999405 | ||
| chr14:91999415
|
T | C | 1 | a0018 | 1 | NA18954.hp1 | missense_variant | MODERATE | c.4717A>G | p.Lys1573Glu | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 13/21 | 5091/9996 | 4717/5940 | 1573/1979 | chr14 | 91999415 | ||
| chr14:92003469
|
T | C | 1 | a0008 | 4 | HG01109.hp1 HG02055.hp2 HG02723.hp2 others(1): Show |
missense_variant | MODERATE | c.4507A>G | p.Met1503Val | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 11/21 | 4881/9996 | 4507/5940 | 1503/1979 | chr14 | 92003469 | ||
| chr14:92003717
|
C | T | 1 | a0017 | 1 | HG02027.hp2 | missense_variant | MODERATE | c.4259G>A | p.Ser1420Asn | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 11/21 | 4633/9996 | 4259/5940 | 1420/1979 | chr14 | 92003717 | ||
| chr14:92003837
|
G | A | 1 | a0011 | 2 | HG02040.hp1 NA18991.hp2 |
missense_variant | MODERATE | c.4139C>T | p.Thr1380Ile | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 11/21 | 4513/9996 | 4139/5940 | 1380/1979 | chr14 | 92003837 | ||
| chr14:92004858
|
T | C | 2 | a0005a0010 | 7 | HG02055.hp1 HG02451.hp1 HG02615.hp2 others(4): Show |
missense_variant | MODERATE | c.3118A>G | p.Ile1040Val | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 11/21 | 3492/9996 | 3118/5940 | 1040/1979 | chr14 | 92004858 | ||
| chr14:92005325
|
T | C | 4 | a0005a0010a0015others(1): Show | 9 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
missense_variant | MODERATE | c.2651A>G | p.Asp884Gly | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 11/21 | 3025/9996 | 2651/5940 | 884/1979 | chr14 | 92005325 | ||
| chr14:92005593
|
C | G | 4 | a0005a0010a0015others(1): Show | 9 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
missense_variant | MODERATE | c.2383G>C | p.Val795Leu | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 11/21 | 2757/9996 | 2383/5940 | 795/1979 | chr14 | 92005593 | ||
| chr14:92005842
|
C | T | 1 | a0022 | 1 | HG00642.hp1 | missense_variant | MODERATE | c.2134G>A | p.Glu712Lys | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 11/21 | 2508/9996 | 2134/5940 | 712/1979 | chr14 | 92005842 | ||
| chr14:92005874
|
T | C | 1 | a0023 | 1 | HG01256.hp1 | missense_variant | MODERATE | c.2102A>G | p.Asn701Ser | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 11/21 | 2476/9996 | 2102/5940 | 701/1979 | chr14 | 92005874 | ||
| chr14:92006024
|
A | G | 1 | a0015 | 1 | HG02258.hp1 | missense_variant | MODERATE | c.1952T>C | p.Val651Ala | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 11/21 | 2326/9996 | 1952/5940 | 651/1979 | chr14 | 92006024 | ||
| chr14:92006072
|
G | C | 1 | a0003 | 28 | HG00408.hp2 HG02040.hp2 HG02165.hp2 others(25): Show |
missense_variant | MODERATE | c.1904C>G | p.Ser635Cys | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 11/21 | 2278/9996 | 1904/5940 | 635/1979 | chr14 | 92006072 | ||
| chr14:92007650
|
T | G | 2 | a0009a0014 | 4 | HG02818.hp2 HG02965.hp1 HG03130.hp1 others(1): Show |
missense_variant | MODERATE | c.1517A>C | p.Glu506Ala | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 10/21 | 1891/9996 | 1517/5940 | 506/1979 | chr14 | 92007650 | ||
| chr14:92025408
|
T | C | 1 | a0013 | 1 | HG02683.hp1 | missense_variant | MODERATE | c.214A>G | p.Lys72Glu | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 3/21 | 588/9996 | 214/5940 | 72/1979 | chr14 | 92025408 | ||
| chr14:92039571
|
T | A | 1 | a0006 | 4 | HG01081.hp2 HG01099.hp1 HG02683.hp2 others(1): Show |
missense_variant | MODERATE | c.115A>T | p.Met39Leu | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 1/21 | 489/9996 | 115/5940 | 39/1979 | chr14 | 92039571 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:91969832
|
C | T | 3 | a0001c0018a0003c0003a0003c0037 | 29 | HG00408.hp2 HG01978.hp2 HG02040.hp2 others(26): Show |
synonymous_variant | LOW | c.5781G>A | p.Ser1927Ser | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 21/21 | 6155/9996 | 5781/5940 | 1927/1979 | chr14 | 91969832 | ||
| chr14:91995382
|
G | A | 1 | a0002c0029 | 1 | HG02630.hp1 | synonymous_variant | LOW | c.5026C>T | p.Leu1676Leu | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 14/21 | 5400/9996 | 5026/5940 | 1676/1979 | chr14 | 91995382 | ||
| chr14:91999320
|
A | G | 1 | a0001c0004 | 8 | HG01255.hp2 HG02630.hp2 HG03041.hp1 others(5): Show |
synonymous_variant | LOW | c.4812T>C | p.Asp1604Asp | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 13/21 | 5186/9996 | 4812/5940 | 1604/1979 | chr14 | 91999320 | ||
| chr14:92003803
|
G | A | 1 | a0001c0015 | 2 | HG01256.hp2 HG01258.hp1 |
synonymous_variant | LOW | c.4173C>T | p.Thr1391Thr | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 11/21 | 4547/9996 | 4173/5940 | 1391/1979 | chr14 | 92003803 | ||
| chr14:92003812
|
G | A | 1 | a0001c0007 | 5 | HG02809.hp2 HG02970.hp1 HG03486.hp2 others(2): Show |
synonymous_variant | LOW | c.4164C>T | p.His1388His | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 11/21 | 4538/9996 | 4164/5940 | 1388/1979 | chr14 | 92003812 | ||
| chr14:92004097
|
G | A | 1 | a0001c0031 | 1 | HG03491.hp2 | synonymous_variant | LOW | c.3879C>T | p.His1293His | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 11/21 | 4253/9996 | 3879/5940 | 1293/1979 | chr14 | 92004097 | ||
| chr14:92004118
|
C | T | 1 | a0007c0009 | 4 | HG02257.hp1 HG02559.hp2 HG02896.hp1 others(1): Show |
synonymous_variant | LOW | c.3858G>A | p.Gln1286Gln | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 11/21 | 4232/9996 | 3858/5940 | 1286/1979 | chr14 | 92004118 | ||
| chr14:92004262
|
C | T | 2 | a0005c0006a0010c0013 | 7 | HG02055.hp1 HG02451.hp1 HG02615.hp2 others(4): Show |
synonymous_variant | LOW | c.3714G>A | p.Glu1238Glu | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 11/21 | 4088/9996 | 3714/5940 | 1238/1979 | chr14 | 92004262 | ||
| chr14:92004670
|
A | G | 4 | a0005c0006a0010c0013a0015c0022others(1): Show | 9 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
synonymous_variant | LOW | c.3306T>C | p.Phe1102Phe | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 11/21 | 3680/9996 | 3306/5940 | 1102/1979 | chr14 | 92004670 | ||
| chr14:92004829
|
C | T | 1 | a0001c0007 | 5 | HG02809.hp2 HG02970.hp1 HG03486.hp2 others(2): Show |
synonymous_variant | LOW | c.3147G>A | p.Leu1049Leu | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 11/21 | 3521/9996 | 3147/5940 | 1049/1979 | chr14 | 92004829 | ||
| chr14:92005045
|
G | A | 1 | a0001c0010 | 4 | HG02145.hp1 HG02486.hp1 HG06807.hp1 others(1): Show |
synonymous_variant | LOW | c.2931C>T | p.Thr977Thr | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 11/21 | 3305/9996 | 2931/5940 | 977/1979 | chr14 | 92005045 | ||
| chr14:92005759
|
A | G | 1 | a0008c0008 | 4 | HG01109.hp1 HG02055.hp2 HG02723.hp2 others(1): Show |
synonymous_variant | LOW | c.2217T>C | p.Tyr739Tyr | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 11/21 | 2591/9996 | 2217/5940 | 739/1979 | chr14 | 92005759 | ||
| chr14:92006446
|
G | A | 1 | a0001c0033 | 1 | NA19087.hp1 | splice_region_variant&synonymous_variant | LOW | c.1530C>T | p.His510His | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 11/21 | 1904/9996 | 1530/5940 | 510/1979 | chr14 | 92006446 | ||
| chr14:92007760
|
T | C | 1 | a0001c0035 | 1 | HG03927.hp1 | synonymous_variant | LOW | c.1407A>G | p.Leu469Leu | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 10/21 | 1781/9996 | 1407/5940 | 469/1979 | chr14 | 92007760 | ||
| chr14:92014303
|
C | T | 1 | a0002c0021 | 1 | NA18957.hp1 | synonymous_variant | LOW | c.1098G>A | p.Lys366Lys | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 7/21 | 1472/9996 | 1098/5940 | 366/1979 | chr14 | 92014303 | ||
| chr14:92015765
|
G | T | 1 | a0001c0020 | 1 | NA18979.hp1 | synonymous_variant | LOW | c.754C>A | p.Arg252Arg | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 6/21 | 1128/9996 | 754/5940 | 252/1979 | chr14 | 92015765 | ||
| chr14:92021652
|
A | G | 1 | a0001c0019 | 1 | HG02523.hp1 | synonymous_variant | LOW | c.492T>C | p.Phe164Phe | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 4/21 | 866/9996 | 492/5940 | 164/1979 | chr14 | 92021652 | ||
| chr14:92021739
|
A | G | 2 | a0001c0018a0003c0003 | 28 | HG00408.hp2 HG01978.hp2 HG02040.hp2 others(25): Show |
synonymous_variant | LOW | c.405T>C | p.Ala135Ala | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 4/21 | 779/9996 | 405/5940 | 135/1979 | chr14 | 92021739 | ||
| chr14:92033210
|
A | G | 1 | a0001c0017 | 1 | NA20752.hp1 | synonymous_variant | LOW | c.183T>C | p.His61His | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/21 | 557/9996 | 183/5940 | 61/1979 | chr14 | 92033210 | ||
| chr14:92033246
|
T | C | 1 | a0003c0037 | 1 | HG04204.hp2 | synonymous_variant | LOW | c.147A>G | p.Leu49Leu | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/21 | 521/9996 | 147/5940 | 49/1979 | chr14 | 92033246 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:91966042
|
A | AT | 3 | a0007c0009t0031a0007c0009t0056a0007c0009t0057 | 4 | HG02257.hp1 HG02559.hp2 HG02896.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3630dupA | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 21/21 | 3630 | chr14 | 91966042 | |||||
| chr14:91966289
|
C | G | 2 | a0002c0002t0008a0002c0029t0008 | 8 | HG02615.hp1 HG02630.hp1 HG02809.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3384G>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 21/21 | 3384 | chr14 | 91966289 | |||||
| chr14:91966300
|
C | T | 15 | a0001c0007t0013a0002c0002t0002a0002c0002t0008others(12): Show | 109 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(106): Show |
3_prime_UTR_variant | MODIFIER | c.*3373G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 21/21 | 3373 | chr14 | 91966300 | |||||
| chr14:91966405
|
A | G | 16 | a0001c0001t0048a0004c0005t0018a0004c0005t0033others(13): Show | 26 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*3268T>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 21/21 | 3268 | chr14 | 91966405 | |||||
| chr14:91966790
|
C | T | 6 | a0005c0006t0015a0005c0006t0067a0010c0013t0015others(3): Show | 9 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2883G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 21/21 | 2883 | chr14 | 91966790 | |||||
| chr14:91966840
|
G | A | 1 | a0002c0002t0022 | 3 | HG02486.hp2 HG03225.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2833C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 21/21 | 2833 | chr14 | 91966840 | |||||
| chr14:91966976
|
TGGTTACT others(5): Show |
T | 1 | a0001c0007t0013 | 5 | HG02809.hp2 HG02970.hp1 HG03486.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2685_*2696delGTCT others(8): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 21/21 | 2685 | chr14 | 91966976 | |||||
| chr14:91967132
|
T | C | 2 | a0001c0010t0020a0001c0010t0051 | 4 | HG02145.hp1 HG02486.hp1 HG06807.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2541A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 21/21 | 2541 | chr14 | 91967132 | |||||
| chr14:91967135
|
C | CT | 10 | a0001c0001t0004a0001c0001t0010a0001c0001t0036others(7): Show | 31 | HG00423.hp1 HG00438.hp1 HG00738.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*2537dupA | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 21/21 | 2537 | chr14 | 91967135 | |||||
| chr14:91967135
|
C | CTTTTTTT others(4): Show |
1 | a0003c0003t0006 | 10 | HG02040.hp2 HG02165.hp2 HG03491.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2527_*2537dupAAAA others(7): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 21/21 | 2537 | chr14 | 91967135 | |||||
| chr14:91967135
|
C | CTTTTTTT others(5): Show |
2 | a0003c0003t0007a0003c0003t0061 | 10 | HG00408.hp2 HG02738.hp1 HG03492.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2526_*2537dupAAAA others(8): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 21/21 | 2537 | chr14 | 91967135 | |||||
| chr14:91967135
|
C | CTTTTTTT others(6): Show |
3 | a0001c0001t0009a0003c0003t0011a0023c0032t0009 | 13 | HG01256.hp1 HG01884.hp1 HG02735.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2525_*2537dupAAAA others(9): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 21/21 | 2537 | chr14 | 91967135 | |||||
| chr14:91967135
|
C | CTTTTTTT others(7): Show |
2 | a0001c0001t0005a0001c0001t0048 | 12 | HG01069.hp1 HG01167.hp2 HG01243.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2524_*2537dupAAAA others(10): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 21/21 | 2537 | chr14 | 91967135 | |||||
| chr14:91967135
|
C | CTTTTTTT others(8): Show |
4 | a0001c0001t0012a0001c0035t0012a0003c0037t0050others(1): Show | 7 | HG01192.hp2 HG02559.hp2 HG02698.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2523_*2537dupAAAA others(11): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 21/21 | 2537 | chr14 | 91967135 | |||||
| chr14:91967135
|
C | CTTTTTTT others(9): Show |
4 | a0001c0001t0019a0001c0001t0027a0001c0004t0019others(1): Show | 7 | HG00323.hp1 HG02257.hp1 HG02818.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2522_*2537dupAAAA others(12): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 21/21 | 2537 | chr14 | 91967135 | |||||
| chr14:91967135
|
C | CTTTTTTT others(10): Show |
4 | a0001c0001t0026a0001c0018t0062a0007c0009t0056others(1): Show | 6 | HG01109.hp1 HG01978.hp2 HG02258.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2521_*2537dupAAAA others(13): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 21/21 | 2537 | chr14 | 91967135 | |||||
| chr14:91967135
|
C | CTTTTTTT others(11): Show |
1 | a0008c0008t0055 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2520_*2537dupAAAA others(14): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 21/21 | 2537 | chr14 | 91967135 | |||||
| chr14:91967135
|
C | CTTTTTTT others(12): Show |
3 | a0001c0001t0047a0001c0004t0025a0001c0004t0037 | 4 | HG01496.hp1 HG02630.hp2 HG03139.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2519_*2537dupAAAA others(15): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 21/21 | 2537 | chr14 | 91967135 | |||||
| chr14:91967135
|
C | CTTTTTTT others(13): Show |
1 | a0001c0004t0041 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2518_*2537dupAAAA others(16): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 21/21 | 2537 | chr14 | 91967135 | |||||
| chr14:91967135
|
C | CTTTTTTT others(16): Show |
2 | a0001c0001t0024a0001c0004t0024 | 2 | HG02451.hp2 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2515_*2537dupAAAA others(19): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 21/21 | 2537 | chr14 | 91967135 | |||||
| chr14:91967135
|
C | CTTTTTTT others(17): Show |
1 | a0001c0001t0040 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2514_*2537dupAAAA others(20): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 21/21 | 2537 | chr14 | 91967135 | |||||
| chr14:91967135
|
C | CTTTTTTT others(18): Show |
1 | a0008c0008t0058 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2537_*2538insAAAA others(21): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 21/21 | 2537 | chr14 | 91967135 | |||||
| chr14:91967135
|
C | CTTTTTTT others(21): Show |
1 | a0001c0004t0039 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2537_*2538insAAAA others(24): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 21/21 | 2537 | chr14 | 91967135 | |||||
| chr14:91967135
|
C | CTTTTTTT others(22): Show |
1 | a0001c0004t0038 | 1 | HG01255.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2537_*2538insAAAA others(25): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 21/21 | 2537 | chr14 | 91967135 | |||||
| chr14:91967135
|
CT | C | 3 | a0001c0001t0028a0001c0001t0044a0001c0010t0020 | 6 | HG00735.hp2 HG02486.hp1 HG02602.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2537delA | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 21/21 | 2537 | chr14 | 91967135 | |||||
| chr14:91967135
|
CTTTT | C | 14 | a0002c0002t0002a0002c0002t0008a0002c0002t0014others(11): Show | 101 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*2534_*2537delAAAA | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 21/21 | 2534 | chr14 | 91967135 | |||||
| chr14:91967135
|
CTTTTT | C | 2 | a0001c0007t0013a0002c0002t0029 | 7 | HG02809.hp2 HG02970.hp1 HG03041.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2533_*2537delAAAA others(1): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 21/21 | 2533 | chr14 | 91967135 | |||||
| chr14:91967181
|
G | A | 2 | a0001c0001t0045a0002c0002t0053 | 2 | NA18978.hp2 NA19067.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2492C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 21/21 | 2492 | chr14 | 91967181 | |||||
| chr14:91967194
|
T | C | 3 | a0001c0001t0016a0001c0001t0023a0001c0001t0036 | 7 | HG01081.hp1 HG01891.hp2 HG02280.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2479A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 21/21 | 2479 | chr14 | 91967194 | |||||
| chr14:91967224
|
C | T | 6 | a0005c0006t0015a0005c0006t0067a0010c0013t0015others(3): Show | 9 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2449G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 21/21 | 2449 | chr14 | 91967224 | |||||
| chr14:91967283
|
C | T | 1 | a0001c0001t0043 | 1 | HG02135.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2390G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 21/21 | 2390 | chr14 | 91967283 | |||||
| chr14:91967297
|
C | T | 6 | a0005c0006t0015a0005c0006t0067a0010c0013t0015others(3): Show | 9 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2376G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 21/21 | 2376 | chr14 | 91967297 | |||||
| chr14:91967456
|
A | G | 1 | a0002c0002t0052 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2217T>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 21/21 | 2217 | chr14 | 91967456 | |||||
| chr14:91967559
|
T | C | 1 | a0001c0001t0034 | 1 | HG00609.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2114A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 21/21 | 2114 | chr14 | 91967559 | |||||
| chr14:91967600
|
A | G | 16 | a0001c0004t0037a0004c0005t0018a0004c0005t0033others(13): Show | 26 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*2073T>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 21/21 | 2073 | chr14 | 91967600 | |||||
| chr14:91967704
|
T | G | 3 | a0007c0009t0031a0007c0009t0056a0007c0009t0057 | 4 | HG02257.hp1 HG02559.hp2 HG02896.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1969A>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 21/21 | 1969 | chr14 | 91967704 | |||||
| chr14:91967885
|
G | A | 1 | a0001c0001t0049 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1788C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 21/21 | 1788 | chr14 | 91967885 | |||||
| chr14:91967929
|
C | T | 16 | a0001c0004t0037a0004c0005t0018a0004c0005t0033others(13): Show | 26 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*1744G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 21/21 | 1744 | chr14 | 91967929 | |||||
| chr14:91968119
|
A | T | 11 | a0001c0004t0037a0004c0005t0018a0004c0005t0033others(8): Show | 18 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1554T>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 21/21 | 1554 | chr14 | 91968119 | |||||
| chr14:91968299
|
T | G | 7 | a0001c0018t0062a0003c0003t0006a0003c0003t0007others(4): Show | 29 | HG00408.hp2 HG01978.hp2 HG02040.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*1374A>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 21/21 | 1374 | chr14 | 91968299 | |||||
| chr14:91968333
|
A | AT | 11 | a0001c0004t0037a0004c0005t0018a0004c0005t0033others(8): Show | 18 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1339dupA | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 21/21 | 1339 | chr14 | 91968333 | |||||
| chr14:91968511
|
A | G | 1 | a0016c0024t0064 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1162T>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 21/21 | 1162 | chr14 | 91968511 | |||||
| chr14:91968550
|
G | A | 1 | a0001c0001t0046 | 1 | HG00673.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1123C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 21/21 | 1123 | chr14 | 91968550 | |||||
| chr14:91968613
|
G | A | 71 | a0001c0001t0003a0001c0001t0005a0001c0001t0009others(68): Show | 258 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(255): Show |
3_prime_UTR_variant | MODIFIER | c.*1060C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 21/21 | 1060 | chr14 | 91968613 | |||||
| chr14:91968629
|
A | G | 2 | a0015c0022t0065a0016c0024t0064 | 2 | HG02258.hp1 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1044T>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 21/21 | 1044 | chr14 | 91968629 | |||||
| chr14:91968721
|
T | A | 15 | a0002c0002t0002a0002c0002t0008a0002c0002t0014others(12): Show | 108 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(105): Show |
3_prime_UTR_variant | MODIFIER | c.*952A>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 21/21 | 952 | chr14 | 91968721 | |||||
| chr14:91968743
|
G | A | 6 | a0005c0006t0015a0005c0006t0067a0010c0013t0015others(3): Show | 9 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*930C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 21/21 | 930 | chr14 | 91968743 | |||||
| chr14:91968786
|
T | C | 1 | a0002c0002t0054 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*887A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 21/21 | 887 | chr14 | 91968786 | |||||
| chr14:91968924
|
C | T | 1 | a0001c0007t0013 | 5 | HG02809.hp2 HG02970.hp1 HG03486.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*749G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 21/21 | 749 | chr14 | 91968924 | |||||
| chr14:91969009
|
G | A | 1 | a0001c0001t0023 | 2 | HG02559.hp1 HG02622.hp2 |
3_prime_UTR_variant | MODIFIER | c.*664C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 21/21 | 664 | chr14 | 91969009 | |||||
| chr14:91969063
|
T | G | 2 | a0001c0010t0020a0001c0010t0051 | 4 | HG02145.hp1 HG02486.hp1 HG06807.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*610A>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 21/21 | 610 | chr14 | 91969063 | |||||
| chr14:91969243
|
T | C | 32 | a0001c0007t0013a0002c0002t0002a0002c0002t0008others(29): Show | 139 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(136): Show |
3_prime_UTR_variant | MODIFIER | c.*430A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 21/21 | 430 | chr14 | 91969243 | |||||
| chr14:91969285
|
CG | C | 8 | a0007c0009t0031a0007c0009t0056a0007c0009t0057others(5): Show | 11 | HG01109.hp1 HG02055.hp2 HG02257.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*387delC | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 21/21 | 387 | chr14 | 91969285 | |||||
| chr14:91969286
|
G | T | 2 | a0004c0005t0018a0004c0005t0033 | 6 | HG01069.hp2 HG01071.hp2 NA18980.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*387C>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 21/21 | 387 | chr14 | 91969286 | |||||
| chr14:91969289
|
T | A | 2 | a0004c0005t0018a0004c0005t0033 | 6 | HG01069.hp2 HG01071.hp2 NA18980.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*384A>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 21/21 | 384 | chr14 | 91969289 | |||||
| chr14:91969289
|
TA | T | 13 | a0001c0001t0019a0001c0001t0024a0001c0001t0026others(10): Show | 16 | HG01255.hp2 HG02109.hp2 HG02258.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*383delT | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 21/21 | 383 | chr14 | 91969289 | |||||
| chr14:91969328
|
A | G | 3 | a0001c0001t0016a0001c0001t0023a0001c0001t0036 | 7 | HG01081.hp1 HG01891.hp2 HG02280.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*345T>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 21/21 | 345 | chr14 | 91969328 | |||||
| chr14:91969385
|
G | T | 1 | a0022c0023t0035 | 1 | HG00642.hp1 | 3_prime_UTR_variant | MODIFIER | c.*288C>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 21/21 | 288 | chr14 | 91969385 | |||||
| chr14:91969427
|
T | C | 4 | a0004c0005t0018a0004c0005t0033a0009c0012t0032others(1): Show | 9 | HG01069.hp2 HG01071.hp2 HG02965.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*246A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 21/21 | 246 | chr14 | 91969427 | |||||
| chr14:92039746
|
G | A | 2 | a0001c0001t0060a0002c0002t0014 | 6 | HG00558.hp2 HG03942.hp2 HG04184.hp2 others(3): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-61C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 1/21 | chr14 | 92039746 | ||||||
| chr14:92039950
|
G | T | 1 | a0001c0001t0034 | 1 | HG00609.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-265C>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 1/21 | chr14 | 92039950 | ||||||
| chr14:92040016
|
G | C | 6 | a0001c0018t0062a0003c0003t0006a0003c0003t0007others(3): Show | 28 | HG00408.hp2 HG01978.hp2 HG02040.hp2 others(25): Show |
5_prime_UTR_variant | MODIFIER | c.-331C>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 1/21 | 331 | chr14 | 92040016 | |||||
| chr14:92040050
|
G | C | 6 | a0005c0006t0015a0005c0006t0067a0010c0013t0015others(3): Show | 9 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-365C>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 1/21 | 365 | chr14 | 92040050 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:91969919
|
C | T | 3 | a0002c0002t0022g0296a0002c0002t0022g0297a0002c0002t0022g0298 | 3 | HG02486.hp2 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.5720-26G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 20/20 | chr14 | 91969919 | ||||||
| chr14:91969961
|
T | TGTAA | 9 | a0005c0006t0015g0351a0005c0006t0015g0352a0005c0006t0015g0353others(6): Show | 9 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.5720-72_5720-69dup others(4): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 20/20 | chr14 | 91969961 | ||||||
| chr14:91969962
|
G | GTACA | 17 | a0004c0005t0018g0121a0004c0005t0018g0124a0004c0005t0018g0126others(14): Show | 17 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.5720-70_5720-69ins others(4): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 20/20 | chr14 | 91969962 | ||||||
| chr14:91969971
|
T | C | 3 | a0001c0001t0003g0186a0001c0001t0003g0188a0001c0001t0003g0197 | 3 | HG01346.hp2 HG01496.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.5720-78A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 20/20 | chr14 | 91969971 | ||||||
| chr14:91970001
|
A | T | 1 | a0001c0001t0049g0204 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.5720-108T>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 20/20 | chr14 | 91970001 | ||||||
| chr14:91970069
|
T | C | 17 | a0004c0005t0018g0121a0004c0005t0018g0124a0004c0005t0018g0126others(14): Show | 17 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.5720-176A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 20/20 | chr14 | 91970069 | ||||||
| chr14:91970122
|
C | T | 2 | a0001c0010t0020g0174a0001c0010t0020g0175 | 2 | HG06807.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.5720-229G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 20/20 | chr14 | 91970122 | ||||||
| chr14:91970172
|
T | C | 26 | a0004c0005t0018g0121a0004c0005t0018g0124a0004c0005t0018g0126others(23): Show | 26 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.5720-279A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 20/20 | chr14 | 91970172 | ||||||
| chr14:91970182
|
G | A | 1 | a0001c0001t0001g0065 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.5720-289C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 20/20 | chr14 | 91970182 | ||||||
| chr14:91970282
|
G | A | 9 | a0005c0006t0015g0351a0005c0006t0015g0352a0005c0006t0015g0353others(6): Show | 9 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.5720-389C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 20/20 | chr14 | 91970282 | ||||||
| chr14:91970311
|
G | A | 1 | a0001c0004t0019g0207 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.5720-418C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 20/20 | chr14 | 91970311 | ||||||
| chr14:91970367
|
C | G | 17 | a0004c0005t0018g0121a0004c0005t0018g0124a0004c0005t0018g0126others(14): Show | 17 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.5720-474G>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 20/20 | chr14 | 91970367 | ||||||
| chr14:91970433
|
T | TA | 47 | a0001c0001t0005g0085a0001c0001t0005g0086a0001c0001t0005g0087others(44): Show | 48 | HG00323.hp1 HG01069.hp1 HG01167.hp2 others(45): Show |
intron_variant | MODIFIER | c.5720-541dupT | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 20/20 | chr14 | 91970433 | ||||||
| chr14:91970617
|
G | T | 26 | a0004c0005t0018g0121a0004c0005t0018g0124a0004c0005t0018g0126others(23): Show | 26 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.5720-724C>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 20/20 | chr14 | 91970617 | ||||||
| chr14:91970655
|
G | A | 9 | a0005c0006t0015g0351a0005c0006t0015g0352a0005c0006t0015g0353others(6): Show | 9 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.5720-762C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 20/20 | chr14 | 91970655 | ||||||
| chr14:91970751
|
A | G | 1 | a0019c0028t0001g0153 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.5720-858T>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 20/20 | chr14 | 91970751 | ||||||
| chr14:91970757
|
G | A | 211 | a0001c0001t0005g0085a0001c0001t0005g0086a0001c0001t0005g0087others(208): Show | 215 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.5720-864C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 20/20 | chr14 | 91970757 | ||||||
| chr14:91970804
|
T | C | 8 | a0001c0004t0019g0207a0001c0004t0024g0210a0001c0004t0025g0209others(5): Show | 8 | HG01255.hp2 HG02630.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.5720-911A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 20/20 | chr14 | 91970804 | ||||||
| chr14:91970930
|
C | T | 4 | a0001c0001t0003g0193a0001c0001t0003g0199a0001c0001t0010g0194others(1): Show | 4 | HG01257.hp2 HG01515.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.5720-1037G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 20/20 | chr14 | 91970930 | ||||||
| chr14:91970946
|
T | A | 4 | a0001c0001t0003g0179a0001c0001t0003g0181a0001c0001t0003g0187others(1): Show | 4 | HG00280.hp1 HG01070.hp2 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.5720-1053A>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 20/20 | chr14 | 91970946 | ||||||
| chr14:91971011
|
T | C | 17 | a0004c0005t0018g0121a0004c0005t0018g0124a0004c0005t0018g0126others(14): Show | 17 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.5720-1118A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 20/20 | chr14 | 91971011 | ||||||
| chr14:91971065
|
G | T | 8 | a0007c0009t0031g0117a0007c0009t0031g0120a0007c0009t0056g0118others(5): Show | 8 | HG01109.hp1 HG02055.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.5720-1172C>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 20/20 | chr14 | 91971065 | ||||||
| chr14:91971305
|
G | A | 1 | a0001c0001t0004g0066 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.5719+1412C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 20/20 | chr14 | 91971305 | ||||||
| chr14:91971451
|
T | C | 1 | a0002c0002t0002g0255 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.5719+1266A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 20/20 | chr14 | 91971451 | ||||||
| chr14:91971456
|
T | A | 2 | a0011c0016t0001g0013a0011c0016t0004g0011 | 2 | HG02040.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.5719+1261A>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 20/20 | chr14 | 91971456 | ||||||
| chr14:91971610
|
G | C | 1 | a0002c0002t0002g0243 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.5719+1107C>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 20/20 | chr14 | 91971610 | ||||||
| chr14:91971795
|
G | A | 9 | a0005c0006t0015g0351a0005c0006t0015g0352a0005c0006t0015g0353others(6): Show | 9 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.5719+922C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 20/20 | chr14 | 91971795 | ||||||
| chr14:91971856
|
C | T | 1 | a0022c0023t0035g0069 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.5719+861G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 20/20 | chr14 | 91971856 | ||||||
| chr14:91971861
|
G | T | 9 | a0004c0005t0018g0121a0004c0005t0018g0124a0004c0005t0018g0126others(6): Show | 9 | HG01069.hp2 HG01071.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.5719+856C>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 20/20 | chr14 | 91971861 | ||||||
| chr14:91971890
|
C | A | 9 | a0005c0006t0015g0351a0005c0006t0015g0352a0005c0006t0015g0353others(6): Show | 9 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.5719+827G>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 20/20 | chr14 | 91971890 | ||||||
| chr14:91971922
|
T | C | 22 | a0001c0001t0049g0204a0001c0010t0020g0174a0001c0010t0020g0175others(19): Show | 22 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.5719+795A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 20/20 | chr14 | 91971922 | ||||||
| chr14:91972018
|
A | C | 1 | a0001c0001t0001g0161 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.5719+699T>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 20/20 | chr14 | 91972018 | ||||||
| chr14:91972067
|
A | T | 1 | a0001c0001t0046g0029 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.5719+650T>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 20/20 | chr14 | 91972067 | ||||||
| chr14:91972077
|
G | A | 17 | a0004c0005t0018g0121a0004c0005t0018g0124a0004c0005t0018g0126others(14): Show | 17 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.5719+640C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 20/20 | chr14 | 91972077 | ||||||
| chr14:91972110
|
C | A | 9 | a0005c0006t0015g0351a0005c0006t0015g0352a0005c0006t0015g0353others(6): Show | 9 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.5719+607G>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 20/20 | chr14 | 91972110 | ||||||
| chr14:91972141
|
T | C | 21 | a0001c0010t0020g0174a0001c0010t0020g0175a0001c0010t0020g0176others(18): Show | 21 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.5719+576A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 20/20 | chr14 | 91972141 | ||||||
| chr14:91972163
|
G | A | 4 | a0001c0010t0020g0174a0001c0010t0020g0175a0001c0010t0020g0176others(1): Show | 4 | HG02145.hp1 HG02486.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.5719+554C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 20/20 | chr14 | 91972163 | ||||||
| chr14:91972245
|
A | G | 7 | a0001c0001t0016g0131a0001c0001t0016g0132a0001c0001t0016g0133others(4): Show | 7 | HG01081.hp1 HG01891.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.5719+472T>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 20/20 | chr14 | 91972245 | ||||||
| chr14:91972403
|
A | G | 211 | a0001c0001t0005g0085a0001c0001t0005g0086a0001c0001t0005g0087others(208): Show | 215 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.5719+314T>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 20/20 | chr14 | 91972403 | ||||||
| chr14:91972411
|
T | C | 1 | a0001c0001t0001g0057 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.5719+306A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 20/20 | chr14 | 91972411 | ||||||
| chr14:91972456
|
G | T | 4 | a0001c0010t0020g0174a0001c0010t0020g0175a0001c0010t0020g0176others(1): Show | 4 | HG02145.hp1 HG02486.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.5719+261C>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 20/20 | chr14 | 91972456 | ||||||
| chr14:91972457
|
A | T | 4 | a0001c0010t0020g0174a0001c0010t0020g0175a0001c0010t0020g0176others(1): Show | 4 | HG02145.hp1 HG02486.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.5719+260T>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 20/20 | chr14 | 91972457 | ||||||
| chr14:91972536
|
G | A | 29 | a0001c0018t0062g0321a0003c0003t0006g0323a0003c0003t0006g0325others(26): Show | 29 | HG00408.hp2 HG01978.hp2 HG02040.hp2 others(26): Show |
intron_variant | MODIFIER | c.5719+181C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 20/20 | chr14 | 91972536 | ||||||
| chr14:91972548
|
CAAAAGCC others(14): Show |
C | 9 | a0005c0006t0015g0351a0005c0006t0015g0352a0005c0006t0015g0353others(6): Show | 9 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.5719+148_5719+168d others(23): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 20/20 | chr14 | 91972548 | ||||||
| chr14:91972561
|
C | T | 1 | a0001c0001t0049g0204 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.5719+156G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 20/20 | chr14 | 91972561 | ||||||
| chr14:91972617
|
T | C | 1 | a0001c0001t0048g0100 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.5719+100A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 20/20 | chr14 | 91972617 | ||||||
| chr14:91972666
|
C | T | 1 | a0006c0011t0002g0311 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.5719+51G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 20/20 | chr14 | 91972666 | ||||||
| chr14:91972925
|
A | C | 4 | a0008c0008t0030g0114a0008c0008t0030g0116a0008c0008t0055g0115others(1): Show | 4 | HG01109.hp1 HG02055.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.5575-64T>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 19/20 | chr14 | 91972925 | ||||||
| chr14:91973025
|
C | CT | 24 | a0001c0001t0001g0166a0001c0001t0001g0171a0001c0001t0005g0089others(21): Show | 24 | HG01978.hp2 HG02055.hp1 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.5575-165dupA | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 19/20 | chr14 | 91973025 | ||||||
| chr14:91973025
|
C | CTTTT | 9 | a0004c0005t0018g0121a0004c0005t0018g0124a0004c0005t0018g0126others(6): Show | 9 | HG01069.hp2 HG01071.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.5575-168_5575-165d others(6): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 19/20 | chr14 | 91973025 | ||||||
| chr14:91973025
|
CT | C | 47 | a0001c0001t0001g0165a0001c0001t0005g0085a0001c0001t0005g0090others(44): Show | 47 | HG00323.hp1 HG01069.hp1 HG01081.hp1 others(44): Show |
intron_variant | MODIFIER | c.5575-165delA | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 19/20 | chr14 | 91973025 | ||||||
| chr14:91973084
|
G | A | 1 | a0001c0001t0004g0164 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.5575-223C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 19/20 | chr14 | 91973084 | ||||||
| chr14:91973088
|
C | T | 1 | a0004c0005t0033g0125 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.5575-227G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 19/20 | chr14 | 91973088 | ||||||
| chr14:91973111
|
C | T | 104 | a0002c0002t0002g0005a0002c0002t0002g0006a0002c0002t0002g0009others(101): Show | 107 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.5575-250G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 19/20 | chr14 | 91973111 | ||||||
| chr14:91973182
|
C | T | 9 | a0005c0006t0015g0351a0005c0006t0015g0352a0005c0006t0015g0353others(6): Show | 9 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.5575-321G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 19/20 | chr14 | 91973182 | ||||||
| chr14:91973276
|
G | A | 1 | a0001c0010t0020g0176 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.5575-415C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 19/20 | chr14 | 91973276 | ||||||
| chr14:91973523
|
T | C | 9 | a0005c0006t0015g0351a0005c0006t0015g0352a0005c0006t0015g0353others(6): Show | 9 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.5575-662A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 19/20 | chr14 | 91973523 | ||||||
| chr14:91973755
|
A | T | 1 | a0001c0010t0051g0177 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.5574+872T>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 19/20 | chr14 | 91973755 | ||||||
| chr14:91973921
|
G | A | 1 | a0001c0001t0004g0020 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.5574+706C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 19/20 | chr14 | 91973921 | ||||||
| chr14:91974005
|
G | A | 2 | a0001c0010t0020g0176a0001c0010t0051g0177 | 2 | HG02145.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.5574+622C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 19/20 | chr14 | 91974005 | ||||||
| chr14:91974007
|
G | A | 2 | a0001c0001t0001g0142a0001c0001t0001g0143 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.5574+620C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 19/20 | chr14 | 91974007 | ||||||
| chr14:91974015
|
G | A | 1 | a0008c0008t0030g0116 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.5574+612C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 19/20 | chr14 | 91974015 | ||||||
| chr14:91974083
|
C | A | 26 | a0004c0005t0018g0121a0004c0005t0018g0124a0004c0005t0018g0126others(23): Show | 26 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.5574+544G>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 19/20 | chr14 | 91974083 | ||||||
| chr14:91974107
|
C | G | 21 | a0001c0010t0020g0174a0001c0010t0020g0175a0001c0010t0020g0176others(18): Show | 21 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.5574+520G>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 19/20 | chr14 | 91974107 | ||||||
| chr14:91974111
|
T | C | 7 | a0005c0006t0015g0351a0005c0006t0015g0352a0005c0006t0015g0353others(4): Show | 7 | HG02055.hp1 HG02451.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.5574+516A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 19/20 | chr14 | 91974111 | ||||||
| chr14:91974115
|
G | C | 9 | a0005c0006t0015g0351a0005c0006t0015g0352a0005c0006t0015g0353others(6): Show | 9 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.5574+512C>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 19/20 | chr14 | 91974115 | ||||||
| chr14:91974169
|
G | A | 46 | a0001c0001t0005g0085a0001c0001t0005g0086a0001c0001t0005g0087others(43): Show | 46 | HG00323.hp1 HG01069.hp1 HG01167.hp2 others(43): Show |
intron_variant | MODIFIER | c.5574+458C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 19/20 | chr14 | 91974169 | ||||||
| chr14:91974338
|
T | C | 1 | a0001c0001t0003g0181 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.5574+289A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 19/20 | chr14 | 91974338 | ||||||
| chr14:91974395
|
T | C | 9 | a0005c0006t0015g0351a0005c0006t0015g0352a0005c0006t0015g0353others(6): Show | 9 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.5574+232A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 19/20 | chr14 | 91974395 | ||||||
| chr14:91974409
|
C | T | 1 | a0002c0002t0021g0216 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.5574+218G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 19/20 | chr14 | 91974409 | ||||||
| chr14:91974541
|
T | A | 21 | a0001c0001t0001g0160a0001c0018t0062g0321a0002c0021t0002g0286others(18): Show | 21 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.5574+86A>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 19/20 | chr14 | 91974541 | ||||||
| chr14:91974542
|
A | C | 2 | a0003c0003t0006g0339a0003c0003t0007g0338 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.5574+85T>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 19/20 | chr14 | 91974542 | ||||||
| chr14:91974542
|
A | T | 30 | a0001c0001t0001g0162a0001c0001t0005g0085a0001c0001t0005g0086others(27): Show | 30 | HG00323.hp1 HG01069.hp1 HG01167.hp2 others(27): Show |
intron_variant | MODIFIER | c.5574+85T>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 19/20 | chr14 | 91974542 | ||||||
| chr14:91974562
|
G | C | 17 | a0004c0005t0018g0121a0004c0005t0018g0124a0004c0005t0018g0126others(14): Show | 17 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.5574+65C>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 19/20 | chr14 | 91974562 | ||||||
| chr14:91974603
|
A | G | 17 | a0004c0005t0018g0121a0004c0005t0018g0124a0004c0005t0018g0126others(14): Show | 17 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.5574+24T>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 19/20 | chr14 | 91974603 | ||||||
| chr14:91974785
|
GA | G | 6 | a0001c0001t0003g0196a0003c0003t0006g0345a0007c0009t0031g0117others(3): Show | 6 | HG02257.hp1 HG02559.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.5458-43delT | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 18/20 | chr14 | 91974785 | ||||||
| chr14:91974879
|
T | C | 1 | a0002c0002t0002g0282 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.5458-136A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 18/20 | chr14 | 91974879 | ||||||
| chr14:91974933
|
C | T | 26 | a0004c0005t0018g0121a0004c0005t0018g0124a0004c0005t0018g0126others(23): Show | 26 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.5458-190G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 18/20 | chr14 | 91974933 | ||||||
| chr14:91975006
|
T | C | 1 | a0001c0004t0019g0207 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.5457+166A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 18/20 | chr14 | 91975006 | ||||||
| chr14:91975035
|
G | A | 1 | a0001c0004t0025g0209 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.5457+137C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 18/20 | chr14 | 91975035 | ||||||
| chr14:91975036
|
T | C | 1 | a0020c0027t0003g0178 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.5457+136A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 18/20 | chr14 | 91975036 | ||||||
| chr14:91975422
|
T | C | 21 | a0001c0010t0020g0174a0001c0010t0020g0175a0001c0010t0020g0176others(18): Show | 21 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.5343-136A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 17/20 | chr14 | 91975422 | ||||||
| chr14:91975798
|
A | G | 4 | a0001c0010t0020g0174a0001c0010t0020g0175a0001c0010t0020g0176others(1): Show | 4 | HG02145.hp1 HG02486.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.5342+310T>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 17/20 | chr14 | 91975798 | ||||||
| chr14:91975826
|
A | T | 19 | a0001c0001t0003g0003a0001c0001t0003g0185a0001c0001t0003g0186others(16): Show | 20 | HG01257.hp2 HG01346.hp2 HG01496.hp2 others(17): Show |
intron_variant | MODIFIER | c.5342+282T>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 17/20 | chr14 | 91975826 | ||||||
| chr14:91975915
|
C | T | 26 | a0004c0005t0018g0121a0004c0005t0018g0124a0004c0005t0018g0126others(23): Show | 26 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.5342+193G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 17/20 | chr14 | 91975915 | ||||||
| chr14:91976033
|
T | C | 28 | a0003c0003t0006g0323a0003c0003t0006g0325a0003c0003t0006g0331others(25): Show | 28 | HG00408.hp2 HG02040.hp2 HG02165.hp2 others(25): Show |
intron_variant | MODIFIER | c.5342+75A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 17/20 | chr14 | 91976033 | ||||||
| chr14:91976400
|
A | T | 9 | a0005c0006t0015g0351a0005c0006t0015g0352a0005c0006t0015g0353others(6): Show | 9 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.5261-211T>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91976400 | ||||||
| chr14:91976562
|
A | G | 1 | a0001c0001t0003g0038 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.5261-373T>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91976562 | ||||||
| chr14:91976620
|
C | T | 1 | a0001c0001t0001g0025 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.5261-431G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91976620 | ||||||
| chr14:91976625
|
T | A | 29 | a0001c0018t0062g0321a0003c0003t0006g0323a0003c0003t0006g0325others(26): Show | 29 | HG00408.hp2 HG01978.hp2 HG02040.hp2 others(26): Show |
intron_variant | MODIFIER | c.5261-436A>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91976625 | ||||||
| chr14:91976829
|
A | G | 1 | a0009c0012t0059g0123 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.5261-640T>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91976829 | ||||||
| chr14:91976847
|
A | G | 9 | a0005c0006t0015g0351a0005c0006t0015g0352a0005c0006t0015g0353others(6): Show | 9 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.5261-658T>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91976847 | ||||||
| chr14:91976912
|
A | G | 3 | a0003c0003t0006g0323a0003c0003t0006g0325a0003c0003t0011g0322 | 3 | NA18971.hp1 NA19067.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.5261-723T>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91976912 | ||||||
| chr14:91976988
|
T | C | 1 | a0001c0004t0041g0208 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.5261-799A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91976988 | ||||||
| chr14:91976997
|
C | T | 1 | a0001c0004t0039g0215 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.5261-808G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91976997 | ||||||
| chr14:91977360
|
T | C | 1 | a0001c0001t0001g0074 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.5261-1171A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91977360 | ||||||
| chr14:91977514
|
G | GAATAGTT others(2): Show |
47 | a0001c0001t0005g0085a0001c0001t0005g0086a0001c0001t0005g0087others(44): Show | 47 | HG00323.hp1 HG01069.hp1 HG01109.hp1 others(44): Show |
intron_variant | MODIFIER | c.5261-1326_5261-132 others(13): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91977514 | ||||||
| chr14:91977563
|
A | G | 7 | a0005c0006t0015g0351a0005c0006t0015g0352a0005c0006t0015g0353others(4): Show | 7 | HG02055.hp1 HG02451.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.5261-1374T>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91977563 | ||||||
| chr14:91977612
|
C | CT | 45 | a0001c0001t0005g0086a0001c0001t0005g0087a0001c0001t0005g0089others(42): Show | 45 | HG00323.hp1 HG01069.hp1 HG01109.hp1 others(42): Show |
intron_variant | MODIFIER | c.5261-1424dupA | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91977612 | ||||||
| chr14:91977612
|
CT | C | 9 | a0005c0006t0015g0351a0005c0006t0015g0352a0005c0006t0015g0353others(6): Show | 9 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.5261-1424delA | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91977612 | ||||||
| chr14:91977659
|
C | CTATTAAC others(5): Show |
211 | a0001c0001t0005g0085a0001c0001t0005g0086a0001c0001t0005g0087others(208): Show | 215 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.5261-1471_5261-147 others(16): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91977659 | ||||||
| chr14:91977660
|
C | T | 211 | a0001c0001t0005g0085a0001c0001t0005g0086a0001c0001t0005g0087others(208): Show | 215 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.5261-1471G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91977660 | ||||||
| chr14:91977733
|
G | T | 1 | a0003c0003t0011g0341 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.5261-1544C>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91977733 | ||||||
| chr14:91977855
|
G | A | 1 | a0002c0002t0022g0298 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.5261-1666C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91977855 | ||||||
| chr14:91978058
|
A | T | 2 | a0001c0001t0001g0057a0001c0001t0046g0029 | 2 | HG00673.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.5261-1869T>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91978058 | ||||||
| chr14:91978361
|
G | T | 1 | a0001c0018t0062g0321 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.5261-2172C>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91978361 | ||||||
| chr14:91978416
|
CCTACCTA others(21): Show |
C | 1 | a0015c0022t0065g0357 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.5261-2255_5261-222 others(32): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91978416 | ||||||
| chr14:91978545
|
T | A | 47 | a0001c0001t0005g0085a0001c0001t0005g0086a0001c0001t0005g0087others(44): Show | 47 | HG00323.hp1 HG01069.hp1 HG01109.hp1 others(44): Show |
intron_variant | MODIFIER | c.5261-2356A>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91978545 | ||||||
| chr14:91978701
|
A | G | 238 | a0001c0001t0003g0003a0001c0001t0003g0179a0001c0001t0003g0181others(235): Show | 243 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.5261-2512T>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91978701 | ||||||
| chr14:91978983
|
G | T | 13 | a0005c0006t0015g0351a0005c0006t0015g0352a0005c0006t0015g0353others(10): Show | 13 | HG02055.hp1 HG02257.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.5261-2794C>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91978983 | ||||||
| chr14:91979083
|
CCT | C | 9 | a0005c0006t0015g0351a0005c0006t0015g0352a0005c0006t0015g0353others(6): Show | 9 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.5261-2896_5261-289 others(6): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91979083 | ||||||
| chr14:91979112
|
T | C | 182 | a0001c0001t0005g0085a0001c0001t0005g0086a0001c0001t0005g0087others(179): Show | 186 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.5261-2923A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91979112 | ||||||
| chr14:91979257
|
C | CA | 57 | a0001c0001t0001g0046a0001c0001t0001g0065a0001c0001t0001g0149others(54): Show | 57 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.5261-3069dupT | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91979257 | ||||||
| chr14:91979257
|
C | CAA | 103 | a0001c0007t0013g0007a0001c0007t0013g0308a0001c0007t0013g0309others(100): Show | 107 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.5261-3070_5261-306 others(6): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91979257 | ||||||
| chr14:91979272
|
A | AAG | 8 | a0005c0006t0015g0352a0005c0006t0015g0353a0005c0006t0015g0354others(5): Show | 8 | HG02055.hp1 HG02258.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.5261-3085_5261-308 others(6): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91979272 | ||||||
| chr14:91979273
|
AG | A | 9 | a0004c0005t0018g0121a0004c0005t0018g0124a0004c0005t0018g0126others(6): Show | 9 | HG01069.hp2 HG01071.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.5261-3085delC | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91979273 | ||||||
| chr14:91979274
|
G | A | 4 | a0001c0010t0020g0174a0001c0010t0020g0175a0001c0010t0020g0176others(1): Show | 4 | HG02145.hp1 HG02486.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.5261-3085C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91979274 | ||||||
| chr14:91979584
|
G | A | 2 | a0001c0001t0003g0193a0001c0001t0003g0199 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.5261-3395C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91979584 | ||||||
| chr14:91979647
|
T | C | 46 | a0001c0001t0005g0085a0001c0001t0005g0086a0001c0001t0005g0087others(43): Show | 46 | HG00323.hp1 HG01069.hp1 HG01109.hp1 others(43): Show |
intron_variant | MODIFIER | c.5261-3458A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91979647 | ||||||
| chr14:91979688
|
C | T | 47 | a0001c0001t0005g0085a0001c0001t0005g0086a0001c0001t0005g0087others(44): Show | 47 | HG00323.hp1 HG01069.hp1 HG01109.hp1 others(44): Show |
intron_variant | MODIFIER | c.5261-3499G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91979688 | ||||||
| chr14:91979691
|
T | C | 46 | a0001c0001t0005g0085a0001c0001t0005g0086a0001c0001t0005g0087others(43): Show | 46 | HG00323.hp1 HG01069.hp1 HG01109.hp1 others(43): Show |
intron_variant | MODIFIER | c.5261-3502A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91979691 | ||||||
| chr14:91979791
|
C | T | 3 | a0001c0001t0003g0190a0001c0001t0003g0191a0001c0001t0003g0200 | 3 | HG01261.hp2 HG01981.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.5261-3602G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91979791 | ||||||
| chr14:91979823
|
T | C | 2 | a0002c0002t0002g0236a0002c0002t0002g0263 | 2 | HG02135.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.5261-3634A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91979823 | ||||||
| chr14:91979884
|
T | C | 1 | a0001c0001t0049g0204 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.5261-3695A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91979884 | ||||||
| chr14:91979918
|
T | G | 1 | a0005c0006t0015g0354 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.5261-3729A>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91979918 | ||||||
| chr14:91979991
|
AAAG | A | 17 | a0001c0010t0020g0174a0001c0010t0020g0175a0001c0010t0020g0176others(14): Show | 17 | HG01069.hp2 HG01071.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.5261-3805_5261-380 others(7): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91979991 | ||||||
| chr14:91980219
|
T | G | 109 | a0001c0007t0013g0007a0001c0007t0013g0308a0001c0007t0013g0309others(106): Show | 113 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.5261-4030A>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91980219 | ||||||
| chr14:91980344
|
T | A | 1 | a0001c0018t0062g0321 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.5261-4155A>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91980344 | ||||||
| chr14:91980344
|
T | G | 28 | a0003c0003t0006g0323a0003c0003t0006g0325a0003c0003t0006g0331others(25): Show | 28 | HG00408.hp2 HG02040.hp2 HG02165.hp2 others(25): Show |
intron_variant | MODIFIER | c.5261-4155A>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91980344 | ||||||
| chr14:91980452
|
C | G | 1 | a0003c0003t0006g0343 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.5261-4263G>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91980452 | ||||||
| chr14:91980474
|
A | G | 17 | a0001c0010t0020g0174a0001c0010t0020g0175a0001c0010t0020g0176others(14): Show | 17 | HG01069.hp2 HG01071.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.5261-4285T>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91980474 | ||||||
| chr14:91980492
|
G | C | 1 | a0002c0002t0002g0230 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.5261-4303C>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91980492 | ||||||
| chr14:91980628
|
C | T | 41 | a0001c0001t0005g0085a0001c0001t0005g0086a0001c0001t0005g0087others(38): Show | 41 | HG00323.hp1 HG01069.hp1 HG01167.hp2 others(38): Show |
intron_variant | MODIFIER | c.5261-4439G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91980628 | ||||||
| chr14:91980682
|
T | C | 4 | a0007c0009t0031g0117a0007c0009t0031g0120a0007c0009t0056g0118others(1): Show | 4 | HG02257.hp1 HG02559.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.5261-4493A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91980682 | ||||||
| chr14:91980806
|
T | C | 17 | a0001c0010t0020g0174a0001c0010t0020g0175a0001c0010t0020g0176others(14): Show | 17 | HG01069.hp2 HG01071.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.5261-4617A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91980806 | ||||||
| chr14:91980821
|
G | C | 1 | a0002c0002t0002g0217 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.5261-4632C>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91980821 | ||||||
| chr14:91980990
|
T | TTA | 10 | a0001c0001t0001g0017a0001c0001t0001g0048a0001c0001t0001g0049others(7): Show | 10 | HG00099.hp1 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.5261-4803_5261-480 others(6): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91980990 | ||||||
| chr14:91981006
|
A | T | 4 | a0001c0010t0020g0174a0001c0010t0020g0175a0001c0010t0020g0176others(1): Show | 4 | HG02145.hp1 HG02486.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.5261-4817T>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91981006 | ||||||
| chr14:91981007
|
TATATA | T | 4 | a0002c0002t0002g0300a0002c0002t0022g0296a0002c0002t0022g0297others(1): Show | 4 | HG02486.hp2 HG03225.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.5261-4823_5261-481 others(9): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91981007 | ||||||
| chr14:91981008
|
A | ATTT | 7 | a0001c0001t0005g0097a0001c0001t0009g0137a0001c0001t0009g0138others(4): Show | 7 | HG01069.hp1 HG01978.hp2 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.5261-4820_5261-481 others(7): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91981008 | ||||||
| chr14:91981008
|
A | T | 2 | a0001c0001t0012g0109a0007c0009t0031g0117 | 2 | HG02257.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.5261-4819T>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91981008 | ||||||
| chr14:91981008
|
ATATAT | A | 13 | a0002c0002t0002g0224a0002c0002t0002g0229a0002c0002t0002g0230others(10): Show | 13 | HG00558.hp2 HG02109.hp1 HG02922.hp2 others(10): Show |
intron_variant | MODIFIER | c.5261-4824_5261-482 others(9): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91981008 | ||||||
| chr14:91981008
|
ATATATT | A | 54 | a0002c0002t0002g0005a0002c0002t0002g0006a0002c0002t0002g0009others(51): Show | 56 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(53): Show |
intron_variant | MODIFIER | c.5261-4825_5261-482 others(10): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91981008 | ||||||
| chr14:91981008
|
ATATATTT | A | 8 | a0001c0001t0003g0190a0002c0002t0002g0238a0002c0002t0002g0239others(5): Show | 8 | HG00438.hp2 HG00673.hp1 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.5261-4826_5261-482 others(11): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91981008 | ||||||
| chr14:91981008
|
ATATATTT others(1): Show |
A | 19 | a0001c0001t0003g0003a0001c0001t0003g0179a0001c0001t0003g0181others(16): Show | 20 | HG00280.hp1 HG01070.hp2 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.5261-4827_5261-482 others(12): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91981008 | ||||||
| chr14:91981008
|
ATATATTT others(6): Show |
A | 2 | a0015c0022t0065g0357a0016c0024t0064g0356 | 2 | HG02258.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.5261-4832_5261-482 others(17): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91981008 | ||||||
| chr14:91981010
|
A | ATT | 6 | a0001c0001t0019g0108a0001c0001t0019g0111a0001c0001t0024g0092others(3): Show | 6 | HG02109.hp2 HG02258.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.5261-4822_5261-482 others(6): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91981010 | ||||||
| chr14:91981010
|
A | ATTT | 10 | a0001c0001t0005g0087a0001c0001t0005g0089a0001c0001t0005g0090others(7): Show | 10 | HG00323.hp1 HG01243.hp1 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.5261-4822_5261-482 others(7): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91981010 | ||||||
| chr14:91981010
|
A | T | 20 | a0001c0001t0001g0159a0001c0001t0005g0086a0001c0001t0005g0093others(17): Show | 20 | HG01069.hp1 HG01167.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.5261-4821T>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91981010 | ||||||
| chr14:91981010
|
ATATT | A | 8 | a0002c0002t0008g0004a0002c0002t0008g0222a0002c0002t0008g0223others(5): Show | 9 | HG02615.hp1 HG02630.hp1 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.5261-4825_5261-482 others(8): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91981010 | ||||||
| chr14:91981010
|
ATATTT | A | 21 | a0002c0002t0002g0255a0002c0002t0008g0225a0002c0002t0008g0227others(18): Show | 21 | HG00408.hp2 HG01175.hp2 HG02040.hp2 others(18): Show |
intron_variant | MODIFIER | c.5261-4826_5261-482 others(9): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91981010 | ||||||
| chr14:91981010
|
ATATTTT | A | 11 | a0002c0002t0002g0205a0002c0002t0002g0235a0002c0002t0002g0248others(8): Show | 11 | HG01168.hp1 HG01169.hp1 NA18948.hp1 others(8): Show |
intron_variant | MODIFIER | c.5261-4827_5261-482 others(10): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91981010 | ||||||
| chr14:91981012
|
A | AT | 7 | a0001c0001t0001g0154a0001c0001t0001g0161a0001c0001t0001g0168others(4): Show | 7 | HG00140.hp2 HG00738.hp1 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.5261-4824dupA | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91981012 | ||||||
| chr14:91981012
|
A | ATATATAT others(21): Show |
2 | a0007c0009t0031g0120a0007c0009t0056g0118 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.5261-4824_5261-482 others(32): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91981012 | ||||||
| chr14:91981012
|
A | ATATATAT others(26): Show |
1 | a0007c0009t0057g0119 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.5261-4824_5261-482 others(37): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91981012 | ||||||
| chr14:91981012
|
A | T | 47 | a0001c0001t0001g0159a0001c0001t0005g0086a0001c0001t0005g0087others(44): Show | 47 | HG00323.hp1 HG01069.hp1 HG01081.hp1 others(44): Show |
intron_variant | MODIFIER | c.5261-4823T>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91981012 | ||||||
| chr14:91981012
|
AT | A | 11 | a0001c0001t0001g0014a0001c0001t0001g0045a0001c0001t0001g0046others(8): Show | 11 | HG00408.hp1 HG00609.hp2 HG00673.hp2 others(8): Show |
intron_variant | MODIFIER | c.5261-4824delA | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91981012 | ||||||
| chr14:91981012
|
ATTTT | A | 6 | a0003c0003t0007g0327a0003c0003t0007g0329a0003c0003t0011g0326others(3): Show | 6 | NA18950.hp1 NA18974.hp1 NA18980.hp1 others(3): Show |
intron_variant | MODIFIER | c.5261-4827_5261-482 others(8): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91981012 | ||||||
| chr14:91981012
|
ATTTTT | A | 9 | a0001c0001t0010g0194a0003c0003t0006g0346a0003c0003t0007g0344others(6): Show | 9 | HG01069.hp2 HG01071.hp2 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.5261-4828_5261-482 others(9): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91981012 | ||||||
| chr14:91981012
|
ATTTTTTT others(6): Show |
A | 7 | a0005c0006t0015g0351a0005c0006t0015g0352a0005c0006t0015g0353others(4): Show | 7 | HG02055.hp1 HG02451.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.5261-4836_5261-482 others(17): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91981012 | ||||||
| chr14:91981013
|
T | TA | 5 | a0001c0001t0004g0066a0001c0007t0013g0007a0001c0007t0013g0309others(2): Show | 6 | HG02970.hp1 HG03486.hp2 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.5261-4825_5261-482 others(5): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91981013 | ||||||
| chr14:91981014
|
T | A | 56 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(53): Show | 58 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.5261-4825A>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91981014 | ||||||
| chr14:91981015
|
T | A | 10 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0056others(7): Show | 11 | HG00408.hp1 HG00609.hp2 HG00673.hp2 others(8): Show |
intron_variant | MODIFIER | c.5261-4826A>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91981015 | ||||||
| chr14:91981016
|
T | A | 14 | a0001c0001t0001g0049a0001c0001t0001g0064a0001c0001t0001g0074others(11): Show | 14 | HG01891.hp1 HG01952.hp2 HG02040.hp1 others(11): Show |
intron_variant | MODIFIER | c.5261-4827A>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91981016 | ||||||
| chr14:91981017
|
T | A | 2 | a0001c0001t0046g0029a0009c0012t0059g0123 | 2 | HG00673.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.5261-4828A>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91981017 | ||||||
| chr14:91981018
|
T | A | 8 | a0001c0001t0003g0036a0001c0001t0003g0037a0001c0001t0003g0038others(5): Show | 8 | HG01891.hp1 HG02622.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.5261-4829A>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91981018 | ||||||
| chr14:91981019
|
T | A | 6 | a0004c0005t0018g0121a0004c0005t0018g0127a0004c0005t0033g0122others(3): Show | 6 | HG01069.hp2 HG01071.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.5261-4830A>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91981019 | ||||||
| chr14:91981020
|
T | A | 3 | a0004c0005t0018g0124a0004c0005t0018g0126a0004c0005t0033g0125 | 3 | NA18980.hp1 NA18989.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.5261-4831A>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91981020 | ||||||
| chr14:91981021
|
T | A | 3 | a0004c0005t0018g0127a0009c0012t0032g0129a0009c0012t0032g0130 | 3 | HG02965.hp1 HG03130.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.5261-4832A>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91981021 | ||||||
| chr14:91981022
|
T | A | 4 | a0001c0010t0020g0174a0001c0010t0020g0175a0001c0010t0020g0176others(1): Show | 4 | HG02145.hp1 HG02486.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.5261-4833A>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91981022 | ||||||
| chr14:91981023
|
T | A | 2 | a0009c0012t0032g0129a0009c0012t0032g0130 | 2 | HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.5261-4834A>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91981023 | ||||||
| chr14:91981024
|
T | A | 2 | a0001c0010t0020g0176a0001c0010t0051g0177 | 2 | HG02145.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.5261-4835A>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91981024 | ||||||
| chr14:91981025
|
T | A | 1 | a0009c0012t0032g0129 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.5261-4836A>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91981025 | ||||||
| chr14:91981086
|
G | A | 1 | a0001c0001t0003g0037 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.5261-4897C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91981086 | ||||||
| chr14:91981096
|
A | C | 17 | a0001c0010t0020g0174a0001c0010t0020g0175a0001c0010t0020g0176others(14): Show | 17 | HG01069.hp2 HG01071.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.5261-4907T>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91981096 | ||||||
| chr14:91981141
|
G | A | 1 | a0007c0009t0057g0119 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.5261-4952C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91981141 | ||||||
| chr14:91981179
|
C | T | 1 | a0001c0001t0027g0083 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.5261-4990G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91981179 | ||||||
| chr14:91981216
|
A | G | 1 | a0001c0001t0012g0101 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.5261-5027T>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91981216 | ||||||
| chr14:91981286
|
G | T | 17 | a0001c0010t0020g0174a0001c0010t0020g0175a0001c0010t0020g0176others(14): Show | 17 | HG01069.hp2 HG01071.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.5261-5097C>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91981286 | ||||||
| chr14:91981327
|
T | G | 4 | a0008c0008t0030g0114a0008c0008t0030g0116a0008c0008t0055g0115others(1): Show | 4 | HG01109.hp1 HG02055.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.5261-5138A>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91981327 | ||||||
| chr14:91981372
|
C | T | 22 | a0004c0005t0018g0121a0004c0005t0018g0124a0004c0005t0018g0126others(19): Show | 22 | HG01069.hp2 HG01071.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.5261-5183G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91981372 | ||||||
| chr14:91981378
|
T | A | 2 | a0002c0002t0002g0245a0002c0002t0002g0289 | 2 | HG00673.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.5261-5189A>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91981378 | ||||||
| chr14:91981392
|
TTTG | T | 47 | a0001c0001t0005g0085a0001c0001t0005g0086a0001c0001t0005g0087others(44): Show | 47 | HG00323.hp1 HG01069.hp1 HG01109.hp1 others(44): Show |
intron_variant | MODIFIER | c.5261-5206_5261-520 others(7): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91981392 | ||||||
| chr14:91981401
|
GT | G | 29 | a0001c0018t0062g0321a0003c0003t0006g0323a0003c0003t0006g0325others(26): Show | 29 | HG00408.hp2 HG01978.hp2 HG02040.hp2 others(26): Show |
intron_variant | MODIFIER | c.5261-5213delA | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91981401 | ||||||
| chr14:91981420
|
C | T | 109 | a0001c0007t0013g0007a0001c0007t0013g0308a0001c0007t0013g0309others(106): Show | 113 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.5261-5231G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91981420 | ||||||
| chr14:91981495
|
T | A | 182 | a0001c0001t0005g0085a0001c0001t0005g0086a0001c0001t0005g0087others(179): Show | 186 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.5261-5306A>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91981495 | ||||||
| chr14:91981732
|
A | C | 4 | a0007c0009t0031g0117a0007c0009t0031g0120a0007c0009t0056g0118others(1): Show | 4 | HG02257.hp1 HG02559.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.5261-5543T>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91981732 | ||||||
| chr14:91981857
|
G | A | 1 | a0001c0001t0049g0204 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.5261-5668C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91981857 | ||||||
| chr14:91981883
|
G | A | 9 | a0004c0005t0018g0121a0004c0005t0018g0124a0004c0005t0018g0126others(6): Show | 9 | HG01069.hp2 HG01071.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.5261-5694C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91981883 | ||||||
| chr14:91981903
|
C | T | 1 | a0001c0004t0038g0211 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.5261-5714G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91981903 | ||||||
| chr14:91981949
|
CA | C | 14 | a0002c0002t0017g0278a0005c0006t0015g0351a0005c0006t0015g0352others(11): Show | 14 | HG02055.hp1 HG02257.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.5261-5761delT | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91981949 | ||||||
| chr14:91982247
|
T | A | 3 | a0001c0001t0016g0133a0001c0001t0016g0134a0001c0001t0036g0139 | 3 | HG01891.hp2 HG02280.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.5260+6037A>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91982247 | ||||||
| chr14:91982477
|
G | C | 6 | a0001c0001t0019g0108a0001c0001t0019g0111a0001c0001t0024g0092others(3): Show | 6 | HG02109.hp2 HG02258.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.5260+5807C>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91982477 | ||||||
| chr14:91982603
|
T | C | 1 | a0001c0001t0012g0101 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.5260+5681A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91982603 | ||||||
| chr14:91982877
|
C | T | 1 | a0002c0002t0002g0267 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.5260+5407G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91982877 | ||||||
| chr14:91982925
|
T | C | 1 | a0006c0011t0002g0313 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.5260+5359A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91982925 | ||||||
| chr14:91982939
|
T | C | 1 | a0002c0002t0014g0319 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.5260+5345A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91982939 | ||||||
| chr14:91982966
|
C | T | 29 | a0001c0018t0062g0321a0003c0003t0006g0323a0003c0003t0006g0325others(26): Show | 29 | HG00408.hp2 HG01978.hp2 HG02040.hp2 others(26): Show |
intron_variant | MODIFIER | c.5260+5318G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91982966 | ||||||
| chr14:91982971
|
G | GA | 29 | a0001c0018t0062g0321a0003c0003t0006g0323a0003c0003t0006g0325others(26): Show | 29 | HG00408.hp2 HG01978.hp2 HG02040.hp2 others(26): Show |
intron_variant | MODIFIER | c.5260+5312_5260+531 others(5): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91982971 | ||||||
| chr14:91982973
|
A | ACGT | 29 | a0001c0018t0062g0321a0003c0003t0006g0323a0003c0003t0006g0325others(26): Show | 29 | HG00408.hp2 HG01978.hp2 HG02040.hp2 others(26): Show |
intron_variant | MODIFIER | c.5260+5310_5260+531 others(7): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91982973 | ||||||
| chr14:91982974
|
T | A | 29 | a0001c0018t0062g0321a0003c0003t0006g0323a0003c0003t0006g0325others(26): Show | 29 | HG00408.hp2 HG01978.hp2 HG02040.hp2 others(26): Show |
intron_variant | MODIFIER | c.5260+5310A>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91982974 | ||||||
| chr14:91983051
|
T | C | 4 | a0001c0007t0013g0007a0001c0007t0013g0308a0001c0007t0013g0309others(1): Show | 5 | HG02809.hp2 HG02970.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.5260+5233A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91983051 | ||||||
| chr14:91983144
|
G | A | 9 | a0005c0006t0015g0351a0005c0006t0015g0352a0005c0006t0015g0353others(6): Show | 9 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.5260+5140C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91983144 | ||||||
| chr14:91983321
|
G | A | 2 | a0001c0001t0005g0103a0001c0001t0005g0106 | 2 | HG02717.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.5260+4963C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91983321 | ||||||
| chr14:91983444
|
A | G | 1 | a0002c0002t0002g0245 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.5260+4840T>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91983444 | ||||||
| chr14:91983518
|
G | C | 1 | a0001c0001t0028g0304 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.5260+4766C>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91983518 | ||||||
| chr14:91983554
|
T | C | 4 | a0007c0009t0031g0117a0007c0009t0031g0120a0007c0009t0056g0118others(1): Show | 4 | HG02257.hp1 HG02559.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.5260+4730A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91983554 | ||||||
| chr14:91983681
|
C | T | 17 | a0004c0005t0018g0121a0004c0005t0018g0124a0004c0005t0018g0126others(14): Show | 17 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.5260+4603G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91983681 | ||||||
| chr14:91983916
|
G | A | 27 | a0001c0001t0003g0003a0001c0001t0003g0179a0001c0001t0003g0181others(24): Show | 28 | HG00280.hp1 HG01070.hp2 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.5260+4368C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91983916 | ||||||
| chr14:91983942
|
T | C | 2 | a0012c0014t0001g0151a0012c0014t0004g0152 | 2 | HG00738.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.5260+4342A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91983942 | ||||||
| chr14:91984029
|
A | T | 2 | a0002c0002t0002g0251a0002c0002t0002g0277 | 2 | NA18968.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.5260+4255T>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91984029 | ||||||
| chr14:91984040
|
C | T | 207 | a0001c0001t0005g0085a0001c0001t0005g0086a0001c0001t0005g0087others(204): Show | 211 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.5260+4244G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91984040 | ||||||
| chr14:91984075
|
T | C | 17 | a0004c0005t0018g0121a0004c0005t0018g0124a0004c0005t0018g0126others(14): Show | 17 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.5260+4209A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91984075 | ||||||
| chr14:91984100
|
T | TA | 11 | a0002c0002t0014g0319a0005c0006t0015g0351a0005c0006t0015g0352others(8): Show | 11 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.5260+4183dupT | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91984100 | ||||||
| chr14:91984218
|
T | C | 1 | a0001c0001t0001g0077 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.5260+4066A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91984218 | ||||||
| chr14:91984317
|
C | CT | 30 | a0001c0001t0001g0001a0001c0001t0001g0030a0001c0001t0001g0043others(27): Show | 32 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(29): Show |
intron_variant | MODIFIER | c.5260+3966dupA | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91984317 | ||||||
| chr14:91984317
|
C | CTT | 42 | a0001c0001t0005g0085a0001c0001t0005g0086a0001c0001t0005g0087others(39): Show | 42 | HG00323.hp1 HG01069.hp1 HG01069.hp2 others(39): Show |
intron_variant | MODIFIER | c.5260+3965_5260+396 others(6): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91984317 | ||||||
| chr14:91984317
|
CT | C | 102 | a0001c0001t0001g0146a0001c0010t0020g0174a0001c0010t0020g0175others(99): Show | 105 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.5260+3966delA | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91984317 | ||||||
| chr14:91984320
|
T | TTC | 7 | a0001c0001t0019g0108a0001c0001t0019g0111a0001c0001t0024g0092others(4): Show | 7 | HG02109.hp2 HG02258.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.5260+3963_5260+396 others(6): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91984320 | ||||||
| chr14:91984333
|
T | G | 1 | a0001c0001t0004g0144 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.5260+3951A>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91984333 | ||||||
| chr14:91984418
|
C | T | 1 | a0001c0001t0001g0167 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.5260+3866G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91984418 | ||||||
| chr14:91984658
|
C | T | 26 | a0004c0005t0018g0121a0004c0005t0018g0124a0004c0005t0018g0126others(23): Show | 26 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.5260+3626G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91984658 | ||||||
| chr14:91984694
|
C | T | 4 | a0008c0008t0030g0114a0008c0008t0030g0116a0008c0008t0055g0115others(1): Show | 4 | HG01109.hp1 HG02055.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.5260+3590G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91984694 | ||||||
| chr14:91984714
|
T | C | 238 | a0001c0001t0003g0003a0001c0001t0003g0179a0001c0001t0003g0181others(235): Show | 243 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.5260+3570A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91984714 | ||||||
| chr14:91984799
|
G | C | 1 | a0001c0001t0001g0031 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.5260+3485C>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91984799 | ||||||
| chr14:91984874
|
T | C | 7 | a0005c0006t0015g0351a0005c0006t0015g0352a0005c0006t0015g0353others(4): Show | 7 | HG02055.hp1 HG02451.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.5260+3410A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91984874 | ||||||
| chr14:91984914
|
A | G | 4 | a0001c0007t0013g0007a0001c0007t0013g0308a0001c0007t0013g0309others(1): Show | 5 | HG02809.hp2 HG02970.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.5260+3370T>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91984914 | ||||||
| chr14:91984942
|
G | C | 17 | a0004c0005t0018g0121a0004c0005t0018g0124a0004c0005t0018g0126others(14): Show | 17 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.5260+3342C>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91984942 | ||||||
| chr14:91984997
|
T | C | 3 | a0007c0009t0031g0120a0007c0009t0056g0118a0007c0009t0057g0119 | 3 | HG02559.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.5260+3287A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91984997 | ||||||
| chr14:91985005
|
A | G | 1 | a0001c0001t0001g0075 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.5260+3279T>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91985005 | ||||||
| chr14:91985014
|
G | A | 17 | a0004c0005t0018g0121a0004c0005t0018g0124a0004c0005t0018g0126others(14): Show | 17 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.5260+3270C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91985014 | ||||||
| chr14:91985071
|
A | T | 2 | a0002c0002t0002g0205a0002c0002t0002g0235 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.5260+3213T>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91985071 | ||||||
| chr14:91985215
|
C | T | 2 | a0001c0001t0001g0019a0001c0001t0004g0028 | 2 | HG01099.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.5260+3069G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91985215 | ||||||
| chr14:91985370
|
A | G | 2 | a0002c0002t0002g0218a0002c0002t0002g0219 | 2 | HG03492.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.5260+2914T>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91985370 | ||||||
| chr14:91985418
|
CT | C | 211 | a0001c0001t0005g0085a0001c0001t0005g0086a0001c0001t0005g0087others(208): Show | 215 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.5260+2865delA | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91985418 | ||||||
| chr14:91985491
|
A | G | 2 | a0001c0001t0003g0193a0001c0001t0003g0199 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.5260+2793T>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91985491 | ||||||
| chr14:91985552
|
A | G | 21 | a0001c0010t0020g0174a0001c0010t0020g0175a0001c0010t0020g0176others(18): Show | 21 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.5260+2732T>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91985552 | ||||||
| chr14:91985590
|
T | C | 4 | a0001c0010t0020g0174a0001c0010t0020g0175a0001c0010t0020g0176others(1): Show | 4 | HG02145.hp1 HG02486.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.5260+2694A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91985590 | ||||||
| chr14:91986107
|
G | C | 1 | a0001c0001t0028g0304 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.5260+2177C>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91986107 | ||||||
| chr14:91986164
|
C | T | 27 | a0001c0001t0003g0003a0001c0001t0003g0179a0001c0001t0003g0181others(24): Show | 28 | HG00280.hp1 HG01070.hp2 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.5260+2120G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91986164 | ||||||
| chr14:91986183
|
T | C | 4 | a0008c0008t0030g0114a0008c0008t0030g0116a0008c0008t0055g0115others(1): Show | 4 | HG01109.hp1 HG02055.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.5260+2101A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91986183 | ||||||
| chr14:91986294
|
A | G | 7 | a0001c0001t0016g0131a0001c0001t0016g0132a0001c0001t0016g0133others(4): Show | 7 | HG01081.hp1 HG01891.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.5260+1990T>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91986294 | ||||||
| chr14:91986347
|
A | G | 1 | a0001c0001t0047g0102 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.5260+1937T>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91986347 | ||||||
| chr14:91986374
|
C | G | 1 | a0016c0024t0064g0356 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.5260+1910G>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91986374 | ||||||
| chr14:91986377
|
C | T | 9 | a0005c0006t0015g0351a0005c0006t0015g0352a0005c0006t0015g0353others(6): Show | 9 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.5260+1907G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91986377 | ||||||
| chr14:91986645
|
A | G | 4 | a0001c0010t0020g0174a0001c0010t0020g0175a0001c0010t0020g0176others(1): Show | 4 | HG02145.hp1 HG02486.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.5260+1639T>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91986645 | ||||||
| chr14:91986712
|
T | C | 1 | a0001c0001t0004g0020 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.5260+1572A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91986712 | ||||||
| chr14:91986802
|
G | A | 17 | a0001c0004t0019g0207a0001c0004t0024g0210a0001c0004t0025g0209others(14): Show | 17 | HG01255.hp2 HG02055.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.5260+1482C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91986802 | ||||||
| chr14:91986860
|
C | T | 9 | a0005c0006t0015g0351a0005c0006t0015g0352a0005c0006t0015g0353others(6): Show | 9 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.5260+1424G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91986860 | ||||||
| chr14:91987002
|
T | G | 211 | a0001c0001t0005g0085a0001c0001t0005g0086a0001c0001t0005g0087others(208): Show | 215 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.5260+1282A>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91987002 | ||||||
| chr14:91987047
|
G | T | 47 | a0001c0001t0005g0085a0001c0001t0005g0086a0001c0001t0005g0087others(44): Show | 47 | HG00323.hp1 HG01069.hp1 HG01109.hp1 others(44): Show |
intron_variant | MODIFIER | c.5260+1237C>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91987047 | ||||||
| chr14:91987213
|
A | T | 211 | a0001c0001t0005g0085a0001c0001t0005g0086a0001c0001t0005g0087others(208): Show | 215 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.5260+1071T>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91987213 | ||||||
| chr14:91987251
|
G | A | 1 | a0001c0001t0028g0304 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.5260+1033C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91987251 | ||||||
| chr14:91987295
|
C | CT | 4 | a0001c0010t0020g0174a0001c0010t0020g0175a0001c0010t0020g0176others(1): Show | 4 | HG02145.hp1 HG02486.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.5260+988dupA | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91987295 | ||||||
| chr14:91987343
|
G | A | 3 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0004g0156 | 3 | HG01952.hp1 HG01981.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.5260+941C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91987343 | ||||||
| chr14:91987397
|
C | T | 7 | a0001c0001t0016g0131a0001c0001t0016g0132a0001c0001t0016g0133others(4): Show | 7 | HG01081.hp1 HG01891.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.5260+887G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91987397 | ||||||
| chr14:91987417
|
G | C | 21 | a0001c0010t0020g0174a0001c0010t0020g0175a0001c0010t0020g0176others(18): Show | 21 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.5260+867C>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91987417 | ||||||
| chr14:91987465
|
C | T | 1 | a0002c0002t0002g0249 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.5260+819G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91987465 | ||||||
| chr14:91987604
|
C | T | 9 | a0005c0006t0015g0351a0005c0006t0015g0352a0005c0006t0015g0353others(6): Show | 9 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.5260+680G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91987604 | ||||||
| chr14:91987657
|
C | T | 1 | a0001c0001t0028g0304 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.5260+627G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91987657 | ||||||
| chr14:91987672
|
T | G | 27 | a0001c0001t0005g0085a0001c0001t0005g0086a0001c0001t0005g0087others(24): Show | 27 | HG00323.hp1 HG01069.hp1 HG01167.hp2 others(24): Show |
intron_variant | MODIFIER | c.5260+612A>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91987672 | ||||||
| chr14:91987899
|
T | C | 2 | a0002c0002t0002g0251a0002c0002t0002g0277 | 2 | NA18968.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.5260+385A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91987899 | ||||||
| chr14:91988106
|
G | A | 9 | a0005c0006t0015g0351a0005c0006t0015g0352a0005c0006t0015g0353others(6): Show | 9 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.5260+178C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91988106 | ||||||
| chr14:91988260
|
A | G | 105 | a0002c0002t0002g0005a0002c0002t0002g0006a0002c0002t0002g0009others(102): Show | 108 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.5260+24T>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 16/20 | chr14 | 91988260 | ||||||
| chr14:91988404
|
A | T | 27 | a0001c0001t0003g0003a0001c0001t0003g0179a0001c0001t0003g0181others(24): Show | 28 | HG00280.hp1 HG01070.hp2 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.5161-21T>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91988404 | ||||||
| chr14:91988633
|
T | TA | 30 | a0001c0001t0001g0077a0001c0001t0003g0003a0001c0001t0003g0179others(27): Show | 31 | HG00280.hp1 HG00609.hp2 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.5161-251dupT | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91988633 | ||||||
| chr14:91988633
|
TA | T | 22 | a0001c0001t0001g0027a0001c0001t0001g0058a0001c0001t0003g0036others(19): Show | 23 | HG01891.hp1 HG02257.hp1 HG02559.hp2 others(20): Show |
intron_variant | MODIFIER | c.5161-251delT | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91988633 | ||||||
| chr14:91988633
|
TAA | T | 111 | a0002c0002t0002g0005a0002c0002t0002g0006a0002c0002t0002g0009others(108): Show | 114 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.5161-252_5161-251d others(4): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91988633 | ||||||
| chr14:91988633
|
TAAAAAAA | T | 9 | a0005c0006t0015g0351a0005c0006t0015g0352a0005c0006t0015g0353others(6): Show | 9 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.5161-257_5161-251d others(9): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91988633 | ||||||
| chr14:91988699
|
A | T | 1 | a0001c0001t0009g0110 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.5161-316T>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91988699 | ||||||
| chr14:91988715
|
TTC | T | 9 | a0005c0006t0015g0351a0005c0006t0015g0352a0005c0006t0015g0353others(6): Show | 9 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.5161-334_5161-333d others(4): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91988715 | ||||||
| chr14:91989011
|
T | A | 105 | a0002c0002t0002g0005a0002c0002t0002g0006a0002c0002t0002g0009others(102): Show | 108 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.5161-628A>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91989011 | ||||||
| chr14:91989071
|
C | T | 4 | a0001c0007t0013g0007a0001c0007t0013g0308a0001c0007t0013g0309others(1): Show | 5 | HG02809.hp2 HG02970.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.5161-688G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91989071 | ||||||
| chr14:91989087
|
A | C | 2 | a0001c0010t0020g0174a0001c0010t0020g0175 | 2 | HG06807.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.5161-704T>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91989087 | ||||||
| chr14:91989143
|
A | C | 105 | a0002c0002t0002g0005a0002c0002t0002g0006a0002c0002t0002g0009others(102): Show | 108 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.5161-760T>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91989143 | ||||||
| chr14:91989166
|
G | T | 22 | a0004c0005t0018g0121a0004c0005t0018g0124a0004c0005t0018g0126others(19): Show | 22 | HG01069.hp2 HG01071.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.5161-783C>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91989166 | ||||||
| chr14:91989235
|
A | G | 3 | a0002c0002t0002g0261a0002c0002t0002g0285a0002c0002t0002g0291 | 3 | NA18966.hp1 NA18983.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.5161-852T>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91989235 | ||||||
| chr14:91989318
|
G | T | 9 | a0005c0006t0015g0351a0005c0006t0015g0352a0005c0006t0015g0353others(6): Show | 9 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.5161-935C>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91989318 | ||||||
| chr14:91989479
|
T | G | 80 | a0002c0002t0002g0005a0002c0002t0002g0006a0002c0002t0002g0009others(77): Show | 82 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.5161-1096A>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91989479 | ||||||
| chr14:91989493
|
T | C | 1 | a0002c0002t0002g0305 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.5161-1110A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91989493 | ||||||
| chr14:91989534
|
G | A | 1 | a0001c0001t0027g0112 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.5161-1151C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91989534 | ||||||
| chr14:91989545
|
C | T | 9 | a0005c0006t0015g0351a0005c0006t0015g0352a0005c0006t0015g0353others(6): Show | 9 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.5161-1162G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91989545 | ||||||
| chr14:91989577
|
C | G | 1 | a0001c0004t0024g0210 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.5161-1194G>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91989577 | ||||||
| chr14:91989636
|
A | G | 4 | a0007c0009t0031g0117a0007c0009t0031g0120a0007c0009t0056g0118others(1): Show | 4 | HG02257.hp1 HG02559.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.5161-1253T>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91989636 | ||||||
| chr14:91989850
|
A | G | 1 | a0001c0001t0001g0149 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.5161-1467T>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91989850 | ||||||
| chr14:91990116
|
C | T | 1 | a0001c0004t0041g0208 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.5161-1733G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91990116 | ||||||
| chr14:91990178
|
GGAAT | G | 47 | a0001c0001t0005g0085a0001c0001t0005g0086a0001c0001t0005g0087others(44): Show | 47 | HG00323.hp1 HG01069.hp1 HG01109.hp1 others(44): Show |
intron_variant | MODIFIER | c.5161-1799_5161-179 others(8): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91990178 | ||||||
| chr14:91990322
|
C | T | 1 | a0001c0018t0062g0321 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.5161-1939G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91990322 | ||||||
| chr14:91990655
|
A | G | 27 | a0001c0001t0005g0085a0001c0001t0005g0086a0001c0001t0005g0087others(24): Show | 27 | HG00323.hp1 HG01069.hp1 HG01167.hp2 others(24): Show |
intron_variant | MODIFIER | c.5161-2272T>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91990655 | ||||||
| chr14:91990887
|
C | T | 14 | a0004c0005t0018g0121a0004c0005t0018g0124a0004c0005t0018g0126others(11): Show | 14 | HG01069.hp2 HG01071.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.5161-2504G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91990887 | ||||||
| chr14:91991007
|
G | A | 14 | a0004c0005t0018g0121a0004c0005t0018g0124a0004c0005t0018g0126others(11): Show | 14 | HG01069.hp2 HG01071.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.5161-2624C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91991007 | ||||||
| chr14:91991052
|
T | A | 27 | a0001c0001t0003g0003a0001c0001t0003g0179a0001c0001t0003g0181others(24): Show | 28 | HG00280.hp1 HG01070.hp2 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.5161-2669A>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91991052 | ||||||
| chr14:91991176
|
T | C | 14 | a0004c0005t0018g0121a0004c0005t0018g0124a0004c0005t0018g0126others(11): Show | 14 | HG01069.hp2 HG01071.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.5160+2633A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91991176 | ||||||
| chr14:91991216
|
C | T | 1 | a0001c0001t0001g0030 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.5160+2593G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91991216 | ||||||
| chr14:91991217
|
A | T | 4 | a0001c0010t0020g0174a0001c0010t0020g0175a0001c0010t0020g0176others(1): Show | 4 | HG02145.hp1 HG02486.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.5160+2592T>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91991217 | ||||||
| chr14:91991243
|
T | C | 14 | a0004c0005t0018g0121a0004c0005t0018g0124a0004c0005t0018g0126others(11): Show | 14 | HG01069.hp2 HG01071.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.5160+2566A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91991243 | ||||||
| chr14:91991309
|
C | T | 3 | a0001c0001t0003g0190a0001c0001t0003g0191a0001c0001t0003g0200 | 3 | HG01261.hp2 HG01981.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.5160+2500G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91991309 | ||||||
| chr14:91991342
|
T | C | 14 | a0004c0005t0018g0121a0004c0005t0018g0124a0004c0005t0018g0126others(11): Show | 14 | HG01069.hp2 HG01071.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.5160+2467A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91991342 | ||||||
| chr14:91991516
|
A | G | 8 | a0001c0004t0019g0207a0001c0004t0024g0210a0001c0004t0025g0209others(5): Show | 8 | HG01255.hp2 HG02630.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.5160+2293T>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91991516 | ||||||
| chr14:91991547
|
T | C | 9 | a0005c0006t0015g0351a0005c0006t0015g0352a0005c0006t0015g0353others(6): Show | 9 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.5160+2262A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91991547 | ||||||
| chr14:91991633
|
T | G | 1 | a0001c0018t0062g0321 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.5160+2176A>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91991633 | ||||||
| chr14:91991724
|
G | A | 253 | a0001c0001t0003g0003a0001c0001t0003g0036a0001c0001t0003g0037others(250): Show | 258 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.5160+2085C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91991724 | ||||||
| chr14:91991811
|
G | A | 9 | a0005c0006t0015g0351a0005c0006t0015g0352a0005c0006t0015g0353others(6): Show | 9 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.5160+1998C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91991811 | ||||||
| chr14:91991855
|
G | A | 9 | a0005c0006t0015g0351a0005c0006t0015g0352a0005c0006t0015g0353others(6): Show | 9 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.5160+1954C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91991855 | ||||||
| chr14:91991882
|
A | G | 4 | a0001c0010t0020g0174a0001c0010t0020g0175a0001c0010t0020g0176others(1): Show | 4 | HG02145.hp1 HG02486.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.5160+1927T>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91991882 | ||||||
| chr14:91991943
|
C | A | 1 | a0002c0002t0002g0284 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.5160+1866G>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91991943 | ||||||
| chr14:91992075
|
G | A | 2 | a0001c0001t0009g0099a0002c0002t0002g0006 | 3 | HG00544.hp2 NA18970.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.5160+1734C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91992075 | ||||||
| chr14:91992079
|
C | A | 1 | a0001c0001t0001g0148 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.5160+1730G>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91992079 | ||||||
| chr14:91992079
|
C | CA | 66 | a0001c0001t0001g0050a0001c0001t0001g0065a0001c0001t0001g0142others(63): Show | 67 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.5160+1729dupT | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91992079 | ||||||
| chr14:91992079
|
C | CAA | 13 | a0001c0001t0001g0141a0001c0001t0001g0150a0001c0001t0001g0162others(10): Show | 13 | HG01243.hp2 HG01261.hp1 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.5160+1728_5160+172 others(6): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91992079 | ||||||
| chr14:91992079
|
CA | C | 170 | a0001c0001t0001g0021a0001c0001t0005g0085a0001c0001t0005g0086others(167): Show | 173 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(170): Show |
intron_variant | MODIFIER | c.5160+1729delT | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91992079 | ||||||
| chr14:91992079
|
CAA | C | 10 | a0001c0001t0049g0204a0002c0002t0017g0278a0003c0003t0007g0344others(7): Show | 10 | HG02258.hp1 HG02451.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.5160+1728_5160+172 others(6): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91992079 | ||||||
| chr14:91992079
|
CAAA | C | 10 | a0004c0005t0018g0121a0004c0005t0018g0124a0004c0005t0018g0126others(7): Show | 10 | HG01069.hp2 HG01071.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.5160+1727_5160+172 others(7): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91992079 | ||||||
| chr14:91992105
|
C | G | 29 | a0001c0018t0062g0321a0003c0003t0006g0323a0003c0003t0006g0325others(26): Show | 29 | HG00408.hp2 HG01978.hp2 HG02040.hp2 others(26): Show |
intron_variant | MODIFIER | c.5160+1704G>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91992105 | ||||||
| chr14:91992212
|
G | C | 1 | a0002c0029t0008g0231 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.5160+1597C>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91992212 | ||||||
| chr14:91992331
|
G | A | 1 | a0002c0002t0021g0216 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.5160+1478C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91992331 | ||||||
| chr14:91992332
|
G | T | 1 | a0002c0002t0021g0216 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.5160+1477C>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91992332 | ||||||
| chr14:91992434
|
T | C | 13 | a0004c0005t0018g0121a0004c0005t0018g0124a0004c0005t0018g0126others(10): Show | 13 | HG01069.hp2 HG01071.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.5160+1375A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91992434 | ||||||
| chr14:91992437
|
A | G | 3 | a0001c0001t0001g0017a0001c0001t0001g0051a0001c0001t0004g0052 | 3 | HG01167.hp1 HG01169.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.5160+1372T>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91992437 | ||||||
| chr14:91992510
|
CACTT | C | 9 | a0005c0006t0015g0351a0005c0006t0015g0352a0005c0006t0015g0353others(6): Show | 9 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.5160+1295_5160+129 others(8): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91992510 | ||||||
| chr14:91992536
|
G | A | 1 | a0001c0001t0003g0037 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.5160+1273C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91992536 | ||||||
| chr14:91992657
|
C | T | 2 | a0001c0004t0025g0213a0001c0004t0037g0214 | 2 | HG02630.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.5160+1152G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91992657 | ||||||
| chr14:91992691
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.5160+1118G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91992691 | ||||||
| chr14:91992692
|
G | A | 6 | a0004c0005t0018g0121a0004c0005t0018g0124a0004c0005t0018g0126others(3): Show | 6 | HG01069.hp2 HG01071.hp2 NA18980.hp1 others(3): Show |
intron_variant | MODIFIER | c.5160+1117C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91992692 | ||||||
| chr14:91992702
|
G | A | 6 | a0004c0005t0018g0121a0004c0005t0018g0124a0004c0005t0018g0126others(3): Show | 6 | HG01069.hp2 HG01071.hp2 NA18980.hp1 others(3): Show |
intron_variant | MODIFIER | c.5160+1107C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91992702 | ||||||
| chr14:91992706
|
G | A | 6 | a0004c0005t0018g0121a0004c0005t0018g0124a0004c0005t0018g0126others(3): Show | 6 | HG01069.hp2 HG01071.hp2 NA18980.hp1 others(3): Show |
intron_variant | MODIFIER | c.5160+1103C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91992706 | ||||||
| chr14:91992711
|
T | C | 6 | a0004c0005t0018g0121a0004c0005t0018g0124a0004c0005t0018g0126others(3): Show | 6 | HG01069.hp2 HG01071.hp2 NA18980.hp1 others(3): Show |
intron_variant | MODIFIER | c.5160+1098A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91992711 | ||||||
| chr14:91992725
|
T | C | 47 | a0001c0001t0003g0003a0001c0001t0003g0179a0001c0001t0003g0181others(44): Show | 48 | HG00280.hp1 HG01069.hp2 HG01070.hp2 others(45): Show |
intron_variant | MODIFIER | c.5160+1084A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91992725 | ||||||
| chr14:91992735
|
T | C | 1 | a0003c0003t0007g0336 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.5160+1074A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91992735 | ||||||
| chr14:91992737
|
G | A | 4 | a0001c0010t0020g0174a0001c0010t0020g0175a0001c0010t0020g0176others(1): Show | 4 | HG02145.hp1 HG02486.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.5160+1072C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91992737 | ||||||
| chr14:91992766
|
G | A | 31 | a0001c0018t0062g0321a0002c0002t0002g0294a0002c0002t0002g0295others(28): Show | 31 | HG00408.hp2 HG01257.hp1 HG01258.hp2 others(28): Show |
intron_variant | MODIFIER | c.5160+1043C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91992766 | ||||||
| chr14:91992839
|
G | C | 9 | a0001c0001t0003g0036a0001c0001t0003g0037a0001c0001t0003g0038others(6): Show | 9 | HG01891.hp1 HG02622.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.5160+970C>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91992839 | ||||||
| chr14:91992876
|
T | C | 1 | a0001c0001t0001g0161 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.5160+933A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91992876 | ||||||
| chr14:91992882
|
A | C | 1 | a0001c0017t0004g0016 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.5160+927T>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91992882 | ||||||
| chr14:91992908
|
C | CA | 36 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0054others(33): Show | 37 | HG00438.hp1 HG00609.hp2 HG00673.hp2 others(34): Show |
intron_variant | MODIFIER | c.5160+900dupT | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91992908 | ||||||
| chr14:91992908
|
C | CAA | 19 | a0001c0001t0001g0030a0001c0001t0001g0063a0001c0001t0001g0065others(16): Show | 19 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.5160+899_5160+900d others(4): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91992908 | ||||||
| chr14:91992908
|
C | CAAA | 11 | a0001c0001t0001g0014a0001c0001t0001g0031a0001c0001t0001g0049others(8): Show | 11 | HG01074.hp1 HG01346.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.5160+898_5160+900d others(5): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91992908 | ||||||
| chr14:91992908
|
CA | C | 59 | a0001c0001t0001g0018a0001c0001t0001g0146a0001c0001t0005g0085others(56): Show | 60 | HG00323.hp1 HG00323.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.5160+900delT | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91992908 | ||||||
| chr14:91992908
|
CAA | C | 78 | a0001c0004t0025g0209a0001c0004t0025g0213a0001c0004t0037g0214others(75): Show | 81 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.5160+899_5160+900d others(4): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91992908 | ||||||
| chr14:91992908
|
CAAA | C | 7 | a0001c0001t0028g0304a0001c0018t0062g0321a0002c0002t0002g0264others(4): Show | 7 | HG01978.hp2 HG02055.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.5160+898_5160+900d others(5): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91992908 | ||||||
| chr14:91992908
|
CAAAA | C | 6 | a0001c0001t0049g0204a0005c0006t0015g0351a0005c0006t0015g0352others(3): Show | 6 | HG02451.hp1 HG02615.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.5160+897_5160+900d others(6): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91992908 | ||||||
| chr14:91992908
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0010g0035 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.5160+889_5160+900d others(14): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91992908 | ||||||
| chr14:91992908
|
CAAAAAAA others(7): Show |
C | 28 | a0001c0010t0051g0177a0003c0003t0006g0323a0003c0003t0006g0325others(25): Show | 28 | HG00408.hp2 HG02040.hp2 HG02145.hp1 others(25): Show |
intron_variant | MODIFIER | c.5160+887_5160+900d others(16): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91992908 | ||||||
| chr14:91992908
|
CAAAAAAA others(8): Show |
C | 4 | a0001c0010t0020g0174a0001c0010t0020g0175a0001c0010t0020g0176others(1): Show | 4 | HG02486.hp1 HG06807.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.5160+886_5160+900d others(17): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91992908 | ||||||
| chr14:91992908
|
CAAAAAAA others(10): Show |
C | 4 | a0004c0005t0018g0124a0004c0005t0018g0126a0004c0005t0018g0127others(1): Show | 4 | NA18980.hp1 NA18986.hp2 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.5160+884_5160+900d others(19): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91992908 | ||||||
| chr14:91992908
|
CAAAAAAA others(11): Show |
C | 9 | a0004c0005t0018g0121a0004c0005t0033g0122a0007c0009t0031g0117others(6): Show | 9 | HG01069.hp2 HG01071.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.5160+883_5160+900d others(20): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91992908 | ||||||
| chr14:91992969
|
G | T | 13 | a0004c0005t0018g0121a0004c0005t0018g0124a0004c0005t0018g0126others(10): Show | 13 | HG01069.hp2 HG01071.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.5160+840C>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91992969 | ||||||
| chr14:91993087
|
T | C | 9 | a0005c0006t0015g0351a0005c0006t0015g0352a0005c0006t0015g0353others(6): Show | 9 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.5160+722A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91993087 | ||||||
| chr14:91993091
|
A | C | 9 | a0005c0006t0015g0351a0005c0006t0015g0352a0005c0006t0015g0353others(6): Show | 9 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.5160+718T>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91993091 | ||||||
| chr14:91993093
|
A | C | 1 | a0015c0022t0065g0357 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.5160+716T>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91993093 | ||||||
| chr14:91993203
|
G | A | 33 | a0001c0007t0013g0007a0001c0007t0013g0308a0001c0007t0013g0309others(30): Show | 34 | HG00408.hp2 HG01978.hp2 HG02040.hp2 others(31): Show |
intron_variant | MODIFIER | c.5160+606C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91993203 | ||||||
| chr14:91993256
|
C | A | 4 | a0001c0010t0020g0174a0001c0010t0020g0175a0001c0010t0020g0176others(1): Show | 4 | HG02145.hp1 HG02486.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.5160+553G>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91993256 | ||||||
| chr14:91993322
|
C | A | 2 | a0007c0009t0031g0120a0007c0009t0056g0118 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.5160+487G>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91993322 | ||||||
| chr14:91993476
|
C | CA | 43 | a0001c0001t0001g0054a0001c0001t0001g0141a0001c0001t0003g0039others(40): Show | 44 | HG00642.hp1 HG00735.hp2 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.5160+332dupT | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91993476 | ||||||
| chr14:91993476
|
C | CAAAAA | 6 | a0005c0006t0015g0351a0005c0006t0015g0352a0005c0006t0015g0353others(3): Show | 6 | HG02055.hp1 HG02451.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.5160+328_5160+332d others(7): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91993476 | ||||||
| chr14:91993476
|
CA | C | 36 | a0001c0001t0001g0051a0001c0001t0009g0137a0001c0001t0010g0192others(33): Show | 36 | HG00408.hp2 HG00609.hp2 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.5160+332delT | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91993476 | ||||||
| chr14:91993578
|
CA | C | 211 | a0001c0001t0005g0085a0001c0001t0005g0086a0001c0001t0005g0087others(208): Show | 215 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.5160+230delT | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91993578 | ||||||
| chr14:91993614
|
C | T | 211 | a0001c0001t0005g0085a0001c0001t0005g0086a0001c0001t0005g0087others(208): Show | 215 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.5160+195G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91993614 | ||||||
| chr14:91993750
|
T | C | 1 | a0001c0001t0027g0083 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.5160+59A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91993750 | ||||||
| chr14:91993754
|
C | A | 105 | a0002c0002t0002g0005a0002c0002t0002g0006a0002c0002t0002g0009others(102): Show | 108 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.5160+55G>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91993754 | ||||||
| chr14:91993787
|
A | G | 1 | a0002c0002t0002g0272 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.5160+22T>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91993787 | ||||||
| chr14:91993788
|
G | A | 13 | a0004c0005t0018g0121a0004c0005t0018g0124a0004c0005t0018g0126others(10): Show | 13 | HG01069.hp2 HG01071.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.5160+21C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 15/20 | chr14 | 91993788 | ||||||
| chr14:91993960
|
A | G | 4 | a0008c0008t0030g0114a0008c0008t0030g0116a0008c0008t0055g0115others(1): Show | 4 | HG01109.hp1 HG02055.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.5057-48T>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 14/20 | chr14 | 91993960 | ||||||
| chr14:91994058
|
C | T | 22 | a0004c0005t0018g0121a0004c0005t0018g0124a0004c0005t0018g0126others(19): Show | 22 | HG01069.hp2 HG01071.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.5057-146G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 14/20 | chr14 | 91994058 | ||||||
| chr14:91994181
|
A | G | 1 | a0002c0002t0022g0296 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.5057-269T>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 14/20 | chr14 | 91994181 | ||||||
| chr14:91994257
|
ACT | A | 8 | a0005c0006t0015g0351a0005c0006t0015g0352a0005c0006t0015g0353others(5): Show | 8 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.5057-347_5057-346d others(4): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 14/20 | chr14 | 91994257 | ||||||
| chr14:91994258
|
C | CT | 59 | a0001c0001t0001g0067a0001c0001t0001g0148a0001c0001t0001g0168others(56): Show | 59 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.5057-347dupA | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 14/20 | chr14 | 91994258 | ||||||
| chr14:91994258
|
C | CTT | 10 | a0001c0001t0027g0112a0001c0004t0025g0213a0001c0004t0041g0208others(7): Show | 10 | HG01109.hp1 HG02630.hp2 HG02738.hp1 others(7): Show |
intron_variant | MODIFIER | c.5057-348_5057-347d others(4): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 14/20 | chr14 | 91994258 | ||||||
| chr14:91994258
|
CT | C | 16 | a0001c0007t0013g0007a0001c0007t0013g0309a0002c0002t0002g0224others(13): Show | 18 | HG02109.hp1 HG02257.hp1 HG02615.hp1 others(15): Show |
intron_variant | MODIFIER | c.5057-347delA | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 14/20 | chr14 | 91994258 | ||||||
| chr14:91994258
|
CTT | C | 13 | a0001c0007t0013g0308a0004c0005t0018g0121a0004c0005t0018g0124others(10): Show | 13 | HG01069.hp2 HG01071.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.5057-348_5057-347d others(4): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 14/20 | chr14 | 91994258 | ||||||
| chr14:91994259
|
T | G | 1 | a0005c0006t0067g0349 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.5057-347A>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 14/20 | chr14 | 91994259 | ||||||
| chr14:91994260
|
T | G | 8 | a0005c0006t0015g0351a0005c0006t0015g0352a0005c0006t0015g0353others(5): Show | 8 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.5057-348A>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 14/20 | chr14 | 91994260 | ||||||
| chr14:91994327
|
C | G | 4 | a0002c0002t0002g0261a0002c0002t0002g0285a0002c0002t0002g0291others(1): Show | 4 | NA18957.hp1 NA18966.hp1 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.5057-415G>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 14/20 | chr14 | 91994327 | ||||||
| chr14:91994331
|
G | A | 1 | a0002c0002t0002g0270 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.5057-419C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 14/20 | chr14 | 91994331 | ||||||
| chr14:91994384
|
C | T | 1 | a0001c0001t0028g0304 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.5057-472G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 14/20 | chr14 | 91994384 | ||||||
| chr14:91994419
|
T | G | 33 | a0001c0001t0001g0050a0001c0001t0001g0065a0001c0001t0001g0141others(30): Show | 33 | HG00140.hp2 HG00280.hp2 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.5057-507A>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 14/20 | chr14 | 91994419 | ||||||
| chr14:91994440
|
C | T | 1 | a0002c0002t0022g0298 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.5057-528G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 14/20 | chr14 | 91994440 | ||||||
| chr14:91994673
|
C | T | 105 | a0002c0002t0002g0005a0002c0002t0002g0006a0002c0002t0002g0009others(102): Show | 108 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.5056+679G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 14/20 | chr14 | 91994673 | ||||||
| chr14:91994728
|
T | C | 4 | a0007c0009t0031g0117a0007c0009t0031g0120a0007c0009t0056g0118others(1): Show | 4 | HG02257.hp1 HG02559.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.5056+624A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 14/20 | chr14 | 91994728 | ||||||
| chr14:91994753
|
A | G | 211 | a0001c0001t0005g0085a0001c0001t0005g0086a0001c0001t0005g0087others(208): Show | 215 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.5056+599T>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 14/20 | chr14 | 91994753 | ||||||
| chr14:91994789
|
A | T | 1 | a0002c0021t0002g0286 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.5056+563T>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 14/20 | chr14 | 91994789 | ||||||
| chr14:91994848
|
C | T | 178 | a0001c0001t0005g0085a0001c0001t0005g0086a0001c0001t0005g0087others(175): Show | 182 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.5056+504G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 14/20 | chr14 | 91994848 | ||||||
| chr14:91994876
|
A | G | 9 | a0005c0006t0015g0351a0005c0006t0015g0352a0005c0006t0015g0353others(6): Show | 9 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.5056+476T>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 14/20 | chr14 | 91994876 | ||||||
| chr14:91994889
|
G | A | 28 | a0003c0003t0006g0323a0003c0003t0006g0325a0003c0003t0006g0331others(25): Show | 28 | HG00408.hp2 HG02040.hp2 HG02165.hp2 others(25): Show |
intron_variant | MODIFIER | c.5056+463C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 14/20 | chr14 | 91994889 | ||||||
| chr14:91995036
|
CATTACTT others(28): Show |
C | 4 | a0001c0001t0001g0171a0002c0002t0022g0296a0002c0002t0022g0297others(1): Show | 4 | HG02486.hp2 HG03225.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.5056+281_5056+315d others(37): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 14/20 | chr14 | 91995036 | ||||||
| chr14:91995062
|
TCTC | T | 102 | a0002c0002t0002g0005a0002c0002t0002g0006a0002c0002t0002g0009others(99): Show | 105 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.5056+287_5056+289d others(5): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 14/20 | chr14 | 91995062 | ||||||
| chr14:91995129
|
A | G | 2 | a0002c0002t0002g0305a0002c0002t0029g0212 | 2 | HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.5056+223T>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 14/20 | chr14 | 91995129 | ||||||
| chr14:91995154
|
A | C | 4 | a0008c0008t0030g0114a0008c0008t0030g0116a0008c0008t0055g0115others(1): Show | 4 | HG01109.hp1 HG02055.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.5056+198T>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 14/20 | chr14 | 91995154 | ||||||
| chr14:91995246
|
A | T | 1 | a0001c0001t0009g0099 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.5056+106T>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 14/20 | chr14 | 91995246 | ||||||
| chr14:91995262
|
C | T | 4 | a0008c0008t0030g0114a0008c0008t0030g0116a0008c0008t0055g0115others(1): Show | 4 | HG01109.hp1 HG02055.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.5056+90G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 14/20 | chr14 | 91995262 | ||||||
| chr14:91995309
|
A | G | 1 | a0001c0001t0001g0055 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.5056+43T>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 14/20 | chr14 | 91995309 | ||||||
| chr14:91995619
|
CT | C | 183 | a0001c0001t0003g0186a0001c0001t0005g0085a0001c0001t0005g0086others(180): Show | 187 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.4893-105delA | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 13/20 | chr14 | 91995619 | ||||||
| chr14:91995701
|
C | T | 47 | a0001c0001t0005g0085a0001c0001t0005g0086a0001c0001t0005g0087others(44): Show | 47 | HG00323.hp1 HG01069.hp1 HG01109.hp1 others(44): Show |
intron_variant | MODIFIER | c.4893-186G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 13/20 | chr14 | 91995701 | ||||||
| chr14:91995718
|
C | T | 109 | a0001c0007t0013g0007a0001c0007t0013g0308a0001c0007t0013g0309others(106): Show | 113 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.4893-203G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 13/20 | chr14 | 91995718 | ||||||
| chr14:91995728
|
G | A | 29 | a0001c0018t0062g0321a0003c0003t0006g0323a0003c0003t0006g0325others(26): Show | 29 | HG00408.hp2 HG01978.hp2 HG02040.hp2 others(26): Show |
intron_variant | MODIFIER | c.4893-213C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 13/20 | chr14 | 91995728 | ||||||
| chr14:91995744
|
T | G | 4 | a0001c0001t0003g0179a0001c0001t0003g0181a0001c0001t0003g0187others(1): Show | 4 | HG00280.hp1 HG01070.hp2 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.4893-229A>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 13/20 | chr14 | 91995744 | ||||||
| chr14:91995769
|
C | T | 1 | a0009c0012t0032g0130 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.4893-254G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 13/20 | chr14 | 91995769 | ||||||
| chr14:91995779
|
C | A | 7 | a0001c0001t0016g0131a0001c0001t0016g0132a0001c0001t0016g0133others(4): Show | 7 | HG01081.hp1 HG01891.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.4893-264G>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 13/20 | chr14 | 91995779 | ||||||
| chr14:91995910
|
CT | C | 47 | a0001c0001t0005g0085a0001c0001t0005g0086a0001c0001t0005g0087others(44): Show | 47 | HG00323.hp1 HG01069.hp1 HG01109.hp1 others(44): Show |
intron_variant | MODIFIER | c.4893-396delA | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 13/20 | chr14 | 91995910 | ||||||
| chr14:91996153
|
T | C | 205 | a0001c0001t0005g0085a0001c0001t0005g0086a0001c0001t0005g0087others(202): Show | 209 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.4893-638A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 13/20 | chr14 | 91996153 | ||||||
| chr14:91996303
|
C | T | 8 | a0005c0006t0015g0351a0005c0006t0015g0352a0005c0006t0015g0354others(5): Show | 8 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.4893-788G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 13/20 | chr14 | 91996303 | ||||||
| chr14:91996858
|
C | T | 1 | a0001c0001t0028g0304 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.4893-1343G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 13/20 | chr14 | 91996858 | ||||||
| chr14:91997107
|
A | T | 3 | a0001c0001t0003g0186a0001c0001t0003g0188a0001c0001t0003g0197 | 3 | HG01346.hp2 HG01496.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.4893-1592T>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 13/20 | chr14 | 91997107 | ||||||
| chr14:91997128
|
A | C | 4 | a0001c0010t0020g0174a0001c0010t0020g0175a0001c0010t0020g0176others(1): Show | 4 | HG02145.hp1 HG02486.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.4893-1613T>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 13/20 | chr14 | 91997128 | ||||||
| chr14:91997194
|
G | A | 9 | a0005c0006t0015g0351a0005c0006t0015g0352a0005c0006t0015g0353others(6): Show | 9 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.4893-1679C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 13/20 | chr14 | 91997194 | ||||||
| chr14:91997277
|
A | G | 27 | a0001c0001t0003g0003a0001c0001t0003g0179a0001c0001t0003g0181others(24): Show | 28 | HG00280.hp1 HG01070.hp2 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.4893-1762T>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 13/20 | chr14 | 91997277 | ||||||
| chr14:91997295
|
A | T | 1 | a0003c0003t0006g0325 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.4893-1780T>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 13/20 | chr14 | 91997295 | ||||||
| chr14:91997369
|
G | A | 17 | a0004c0005t0018g0121a0004c0005t0018g0124a0004c0005t0018g0126others(14): Show | 17 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.4893-1854C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 13/20 | chr14 | 91997369 | ||||||
| chr14:91997374
|
T | C | 17 | a0004c0005t0018g0121a0004c0005t0018g0124a0004c0005t0018g0126others(14): Show | 17 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.4893-1859A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 13/20 | chr14 | 91997374 | ||||||
| chr14:91997378
|
T | A | 1 | a0001c0001t0049g0204 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.4892+1862A>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 13/20 | chr14 | 91997378 | ||||||
| chr14:91997422
|
G | A | 2 | a0001c0007t0013g0007a0001c0007t0013g0310 | 3 | HG02970.hp1 HG03579.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.4892+1818C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 13/20 | chr14 | 91997422 | ||||||
| chr14:91997531
|
A | T | 1 | a0003c0003t0006g0325 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.4892+1709T>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 13/20 | chr14 | 91997531 | ||||||
| chr14:91997847
|
T | C | 1 | a0016c0024t0064g0356 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.4892+1393A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 13/20 | chr14 | 91997847 | ||||||
| chr14:91997869
|
G | A | 1 | a0001c0001t0001g0147 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.4892+1371C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 13/20 | chr14 | 91997869 | ||||||
| chr14:91997879
|
T | C | 4 | a0001c0007t0013g0007a0001c0007t0013g0308a0001c0007t0013g0309others(1): Show | 5 | HG02809.hp2 HG02970.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.4892+1361A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 13/20 | chr14 | 91997879 | ||||||
| chr14:91997967
|
C | G | 30 | a0001c0010t0020g0174a0001c0010t0020g0175a0001c0010t0020g0176others(27): Show | 30 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.4892+1273G>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 13/20 | chr14 | 91997967 | ||||||
| chr14:91997988
|
T | A | 1 | a0002c0002t0002g0280 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.4892+1252A>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 13/20 | chr14 | 91997988 | ||||||
| chr14:91998040
|
G | A | 1 | a0015c0022t0065g0357 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.4892+1200C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 13/20 | chr14 | 91998040 | ||||||
| chr14:91998042
|
T | C | 4 | a0001c0007t0013g0007a0001c0007t0013g0308a0001c0007t0013g0309others(1): Show | 5 | HG02809.hp2 HG02970.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.4892+1198A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 13/20 | chr14 | 91998042 | ||||||
| chr14:91998083
|
G | A | 211 | a0001c0001t0005g0085a0001c0001t0005g0086a0001c0001t0005g0087others(208): Show | 215 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.4892+1157C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 13/20 | chr14 | 91998083 | ||||||
| chr14:91998102
|
T | G | 1 | a0003c0003t0006g0325 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.4892+1138A>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 13/20 | chr14 | 91998102 | ||||||
| chr14:91998196
|
T | C | 1 | a0001c0001t0043g0032 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.4892+1044A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 13/20 | chr14 | 91998196 | ||||||
| chr14:91998274
|
G | A | 1 | a0002c0002t0002g0233 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.4892+966C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 13/20 | chr14 | 91998274 | ||||||
| chr14:91998276
|
T | G | 1 | a0002c0002t0002g0301 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.4892+964A>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 13/20 | chr14 | 91998276 | ||||||
| chr14:91998331
|
T | C | 1 | a0002c0002t0021g0216 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.4892+909A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 13/20 | chr14 | 91998331 | ||||||
| chr14:91998691
|
TA | T | 109 | a0001c0007t0013g0007a0001c0007t0013g0308a0001c0007t0013g0309others(106): Show | 113 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.4892+548delT | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 13/20 | chr14 | 91998691 | ||||||
| chr14:91998720
|
C | A | 30 | a0001c0010t0020g0174a0001c0010t0020g0175a0001c0010t0020g0176others(27): Show | 30 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.4892+520G>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 13/20 | chr14 | 91998720 | ||||||
| chr14:91998785
|
C | A | 1 | a0002c0002t0022g0297 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.4892+455G>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 13/20 | chr14 | 91998785 | ||||||
| chr14:91998898
|
C | T | 27 | a0001c0001t0003g0003a0001c0001t0003g0179a0001c0001t0003g0181others(24): Show | 28 | HG00280.hp1 HG01070.hp2 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.4892+342G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 13/20 | chr14 | 91998898 | ||||||
| chr14:91998921
|
A | G | 30 | a0001c0010t0020g0174a0001c0010t0020g0175a0001c0010t0020g0176others(27): Show | 30 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.4892+319T>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 13/20 | chr14 | 91998921 | ||||||
| chr14:91998961
|
T | G | 1 | a0002c0002t0021g0306 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.4892+279A>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 13/20 | chr14 | 91998961 | ||||||
| chr14:91998975
|
G | C | 29 | a0001c0018t0062g0321a0003c0003t0006g0323a0003c0003t0006g0325others(26): Show | 29 | HG00408.hp2 HG01978.hp2 HG02040.hp2 others(26): Show |
intron_variant | MODIFIER | c.4892+265C>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 13/20 | chr14 | 91998975 | ||||||
| chr14:91999002
|
A | G | 30 | a0001c0010t0020g0174a0001c0010t0020g0175a0001c0010t0020g0176others(27): Show | 30 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.4892+238T>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 13/20 | chr14 | 91999002 | ||||||
| chr14:91999457
|
T | G | 1 | a0001c0001t0001g0058 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.4699-24A>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 12/20 | chr14 | 91999457 | ||||||
| chr14:91999523
|
A | G | 1 | a0002c0002t0002g0236 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.4699-90T>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 12/20 | chr14 | 91999523 | ||||||
| chr14:91999706
|
C | T | 1 | a0001c0001t0009g0099 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.4698+262G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 12/20 | chr14 | 91999706 | ||||||
| chr14:91999767
|
C | T | 105 | a0002c0002t0002g0005a0002c0002t0002g0006a0002c0002t0002g0009others(102): Show | 108 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.4698+201G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 12/20 | chr14 | 91999767 | ||||||
| chr14:92000113
|
T | C | 2 | a0002c0002t0002g0256a0002c0002t0002g0257 | 2 | NA19064.hp1 NA19087.hp2 |
splice_region_variant&intron_variant | LOW | c.4558-5A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 11/20 | chr14 | 92000113 | ||||||
| chr14:92000140
|
A | AAC | 22 | a0001c0010t0020g0174a0001c0010t0020g0175a0001c0010t0020g0176others(19): Show | 22 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.4558-34_4558-33dup others(2): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 11/20 | chr14 | 92000140 | ||||||
| chr14:92000295
|
T | C | 8 | a0007c0009t0031g0117a0007c0009t0031g0120a0007c0009t0056g0118others(5): Show | 8 | HG01109.hp1 HG02055.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.4558-187A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 11/20 | chr14 | 92000295 | ||||||
| chr14:92000364
|
T | C | 9 | a0005c0006t0015g0351a0005c0006t0015g0352a0005c0006t0015g0353others(6): Show | 9 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.4558-256A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 11/20 | chr14 | 92000364 | ||||||
| chr14:92000378
|
C | T | 29 | a0001c0018t0062g0321a0003c0003t0006g0323a0003c0003t0006g0325others(26): Show | 29 | HG00408.hp2 HG01978.hp2 HG02040.hp2 others(26): Show |
intron_variant | MODIFIER | c.4558-270G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 11/20 | chr14 | 92000378 | ||||||
| chr14:92000381
|
T | C | 13 | a0002c0002t0002g0224a0002c0002t0002g0229a0002c0002t0002g0230others(10): Show | 14 | HG02109.hp1 HG02615.hp1 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.4558-273A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 11/20 | chr14 | 92000381 | ||||||
| chr14:92000389
|
C | T | 1 | a0002c0002t0002g0224 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.4558-281G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 11/20 | chr14 | 92000389 | ||||||
| chr14:92000397
|
G | C | 2 | a0002c0002t0002g0251a0002c0002t0002g0277 | 2 | NA18968.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.4558-289C>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 11/20 | chr14 | 92000397 | ||||||
| chr14:92000453
|
G | C | 17 | a0004c0005t0018g0121a0004c0005t0018g0124a0004c0005t0018g0126others(14): Show | 17 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.4558-345C>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 11/20 | chr14 | 92000453 | ||||||
| chr14:92000481
|
G | A | 1 | a0008c0008t0030g0114 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.4558-373C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 11/20 | chr14 | 92000481 | ||||||
| chr14:92000717
|
G | A | 6 | a0002c0002t0002g0305a0002c0002t0021g0306a0002c0002t0022g0296others(3): Show | 6 | HG01175.hp2 HG02486.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.4558-609C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 11/20 | chr14 | 92000717 | ||||||
| chr14:92000736
|
T | C | 211 | a0001c0001t0005g0085a0001c0001t0005g0086a0001c0001t0005g0087others(208): Show | 215 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.4558-628A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 11/20 | chr14 | 92000736 | ||||||
| chr14:92000812
|
T | C | 29 | a0001c0018t0062g0321a0003c0003t0006g0323a0003c0003t0006g0325others(26): Show | 29 | HG00408.hp2 HG01978.hp2 HG02040.hp2 others(26): Show |
intron_variant | MODIFIER | c.4558-704A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 11/20 | chr14 | 92000812 | ||||||
| chr14:92000841
|
T | C | 9 | a0005c0006t0015g0351a0005c0006t0015g0352a0005c0006t0015g0353others(6): Show | 9 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.4558-733A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 11/20 | chr14 | 92000841 | ||||||
| chr14:92000844
|
C | A | 1 | a0002c0002t0002g0284 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.4558-736G>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 11/20 | chr14 | 92000844 | ||||||
| chr14:92000864
|
C | CT | 43 | a0001c0001t0003g0003a0001c0001t0003g0179a0001c0001t0003g0181others(40): Show | 44 | HG00280.hp1 HG01069.hp2 HG01070.hp2 others(41): Show |
intron_variant | MODIFIER | c.4558-757dupA | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 11/20 | chr14 | 92000864 | ||||||
| chr14:92000888
|
T | C | 109 | a0001c0007t0013g0007a0001c0007t0013g0308a0001c0007t0013g0309others(106): Show | 113 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.4558-780A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 11/20 | chr14 | 92000888 | ||||||
| chr14:92000965
|
G | A | 21 | a0001c0010t0020g0174a0001c0010t0020g0175a0001c0010t0020g0176others(18): Show | 21 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.4558-857C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 11/20 | chr14 | 92000965 | ||||||
| chr14:92001366
|
T | C | 1 | a0001c0007t0013g0309 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.4558-1258A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 11/20 | chr14 | 92001366 | ||||||
| chr14:92001374
|
CA | C | 20 | a0001c0010t0020g0174a0001c0010t0020g0175a0001c0010t0020g0176others(17): Show | 20 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.4558-1267delT | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 11/20 | chr14 | 92001374 | ||||||
| chr14:92001375
|
A | G | 10 | a0001c0010t0051g0177a0005c0006t0015g0351a0005c0006t0015g0352others(7): Show | 10 | HG02055.hp1 HG02145.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.4558-1267T>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 11/20 | chr14 | 92001375 | ||||||
| chr14:92001376
|
G | GT | 105 | a0001c0001t0001g0072a0001c0001t0003g0189a0001c0007t0013g0007others(102): Show | 109 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.4558-1269dupA | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 11/20 | chr14 | 92001376 | ||||||
| chr14:92001377
|
T | G | 20 | a0001c0010t0020g0174a0001c0010t0020g0175a0001c0010t0020g0176others(17): Show | 20 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.4558-1269A>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 11/20 | chr14 | 92001377 | ||||||
| chr14:92001390
|
T | C | 4 | a0001c0010t0020g0174a0001c0010t0020g0175a0001c0010t0020g0176others(1): Show | 4 | HG02145.hp1 HG02486.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.4558-1282A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 11/20 | chr14 | 92001390 | ||||||
| chr14:92001491
|
T | C | 1 | a0001c0004t0019g0207 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.4558-1383A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 11/20 | chr14 | 92001491 | ||||||
| chr14:92001528
|
T | C | 1 | a0001c0001t0049g0204 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.4558-1420A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 11/20 | chr14 | 92001528 | ||||||
| chr14:92001556
|
A | C | 4 | a0001c0007t0013g0007a0001c0007t0013g0308a0001c0007t0013g0309others(1): Show | 5 | HG02809.hp2 HG02970.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.4558-1448T>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 11/20 | chr14 | 92001556 | ||||||
| chr14:92001564
|
C | T | 2 | a0001c0004t0019g0207a0001c0004t0039g0215 | 2 | HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.4558-1456G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 11/20 | chr14 | 92001564 | ||||||
| chr14:92001606
|
G | A | 109 | a0001c0007t0013g0007a0001c0007t0013g0308a0001c0007t0013g0309others(106): Show | 113 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.4558-1498C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 11/20 | chr14 | 92001606 | ||||||
| chr14:92001632
|
T | C | 212 | a0001c0001t0005g0085a0001c0001t0005g0086a0001c0001t0005g0087others(209): Show | 216 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.4558-1524A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 11/20 | chr14 | 92001632 | ||||||
| chr14:92001633
|
G | A | 21 | a0001c0010t0020g0174a0001c0010t0020g0175a0001c0010t0020g0176others(18): Show | 21 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.4558-1525C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 11/20 | chr14 | 92001633 | ||||||
| chr14:92001716
|
C | G | 1 | a0001c0001t0003g0036 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.4558-1608G>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 11/20 | chr14 | 92001716 | ||||||
| chr14:92001767
|
T | C | 3 | a0001c0001t0001g0017a0001c0001t0001g0051a0001c0001t0004g0052 | 3 | HG01167.hp1 HG01169.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.4557+1652A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 11/20 | chr14 | 92001767 | ||||||
| chr14:92001953
|
C | T | 9 | a0005c0006t0015g0351a0005c0006t0015g0352a0005c0006t0015g0353others(6): Show | 9 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.4557+1466G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 11/20 | chr14 | 92001953 | ||||||
| chr14:92001959
|
T | G | 2 | a0004c0005t0018g0121a0004c0005t0033g0122 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.4557+1460A>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 11/20 | chr14 | 92001959 | ||||||
| chr14:92002022
|
C | T | 33 | a0001c0001t0005g0085a0001c0001t0005g0086a0001c0001t0005g0087others(30): Show | 33 | HG00323.hp1 HG01069.hp1 HG01167.hp2 others(30): Show |
intron_variant | MODIFIER | c.4557+1397G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 11/20 | chr14 | 92002022 | ||||||
| chr14:92002114
|
G | A | 9 | a0005c0006t0015g0351a0005c0006t0015g0352a0005c0006t0015g0353others(6): Show | 9 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.4557+1305C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 11/20 | chr14 | 92002114 | ||||||
| chr14:92002226
|
G | A | 1 | a0001c0001t0023g0136 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.4557+1193C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 11/20 | chr14 | 92002226 | ||||||
| chr14:92002359
|
T | C | 6 | a0001c0001t0019g0108a0001c0001t0019g0111a0001c0001t0024g0092others(3): Show | 6 | HG02109.hp2 HG02258.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.4557+1060A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 11/20 | chr14 | 92002359 | ||||||
| chr14:92002385
|
C | A | 80 | a0002c0002t0002g0005a0002c0002t0002g0006a0002c0002t0002g0009others(77): Show | 82 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.4557+1034G>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 11/20 | chr14 | 92002385 | ||||||
| chr14:92002763
|
T | C | 2 | a0002c0002t0002g0299a0002c0002t0002g0300 | 2 | HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.4557+656A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 11/20 | chr14 | 92002763 | ||||||
| chr14:92002784
|
T | C | 22 | a0001c0010t0020g0174a0001c0010t0020g0175a0001c0010t0020g0176others(19): Show | 22 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.4557+635A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 11/20 | chr14 | 92002784 | ||||||
| chr14:92002832
|
T | A | 10 | a0004c0005t0018g0121a0004c0005t0018g0124a0004c0005t0018g0126others(7): Show | 10 | HG01069.hp2 HG01071.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.4557+587A>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 11/20 | chr14 | 92002832 | ||||||
| chr14:92002937
|
C | G | 212 | a0001c0001t0005g0085a0001c0001t0005g0086a0001c0001t0005g0087others(209): Show | 216 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.4557+482G>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 11/20 | chr14 | 92002937 | ||||||
| chr14:92002972
|
T | C | 254 | a0001c0001t0003g0003a0001c0001t0003g0036a0001c0001t0003g0037others(251): Show | 259 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.4557+447A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 11/20 | chr14 | 92002972 | ||||||
| chr14:92003005
|
A | G | 22 | a0001c0010t0020g0174a0001c0010t0020g0175a0001c0010t0020g0176others(19): Show | 22 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.4557+414T>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 11/20 | chr14 | 92003005 | ||||||
| chr14:92003035
|
G | A | 21 | a0001c0010t0020g0174a0001c0010t0020g0175a0001c0010t0020g0176others(18): Show | 21 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.4557+384C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 11/20 | chr14 | 92003035 | ||||||
| chr14:92003099
|
C | T | 1 | a0001c0001t0047g0102 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.4557+320G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 11/20 | chr14 | 92003099 | ||||||
| chr14:92003122
|
A | G | 31 | a0001c0010t0020g0174a0001c0010t0020g0175a0001c0010t0020g0176others(28): Show | 31 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.4557+297T>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 11/20 | chr14 | 92003122 | ||||||
| chr14:92003176
|
A | C | 22 | a0001c0010t0020g0174a0001c0010t0020g0175a0001c0010t0020g0176others(19): Show | 22 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.4557+243T>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 11/20 | chr14 | 92003176 | ||||||
| chr14:92006593
|
A | G | 47 | a0001c0001t0005g0085a0001c0001t0005g0086a0001c0001t0005g0087others(44): Show | 48 | HG00323.hp1 HG01069.hp1 HG01167.hp2 others(45): Show |
intron_variant | MODIFIER | c.1528-145T>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 10/20 | chr14 | 92006593 | ||||||
| chr14:92006660
|
G | C | 1 | a0002c0002t0021g0216 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1528-212C>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 10/20 | chr14 | 92006660 | ||||||
| chr14:92006707
|
G | A | 1 | a0001c0018t0062g0321 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1528-259C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 10/20 | chr14 | 92006707 | ||||||
| chr14:92006730
|
C | T | 1 | a0014c0034t0003g0128 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1528-282G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 10/20 | chr14 | 92006730 | ||||||
| chr14:92006818
|
G | A | 1 | a0007c0009t0031g0117 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1528-370C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 10/20 | chr14 | 92006818 | ||||||
| chr14:92006841
|
T | C | 1 | a0001c0018t0062g0321 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1528-393A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 10/20 | chr14 | 92006841 | ||||||
| chr14:92007027
|
T | C | 1 | a0002c0002t0021g0216 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1528-579A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 10/20 | chr14 | 92007027 | ||||||
| chr14:92007031
|
A | AT | 6 | a0001c0001t0003g0200a0001c0001t0004g0042a0001c0007t0013g0007others(3): Show | 7 | HG00438.hp1 HG01981.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1528-584dupA | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 10/20 | chr14 | 92007031 | ||||||
| chr14:92007031
|
AT | A | 51 | a0001c0001t0004g0066a0001c0001t0005g0085a0001c0001t0005g0086others(48): Show | 51 | HG00323.hp1 HG01069.hp1 HG01167.hp2 others(48): Show |
intron_variant | MODIFIER | c.1528-584delA | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 10/20 | chr14 | 92007031 | ||||||
| chr14:92007076
|
A | T | 6 | a0002c0002t0002g0305a0002c0002t0021g0306a0002c0002t0022g0296others(3): Show | 6 | HG01175.hp2 HG02486.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1527+564T>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 10/20 | chr14 | 92007076 | ||||||
| chr14:92007148
|
C | T | 1 | a0001c0001t0049g0204 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1527+492G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 10/20 | chr14 | 92007148 | ||||||
| chr14:92007599
|
T | C | 110 | a0001c0001t0004g0292a0001c0007t0013g0007a0001c0007t0013g0308others(107): Show | 114 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.1527+41A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 10/20 | chr14 | 92007599 | ||||||
| chr14:92007634
|
T | C | 4 | a0001c0010t0020g0174a0001c0010t0020g0175a0001c0010t0020g0176others(1): Show | 4 | HG02145.hp1 HG02486.hp1 HG06807.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.1527+6A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 10/20 | chr14 | 92007634 | ||||||
| chr14:92008086
|
C | T | 10 | a0004c0005t0018g0121a0004c0005t0018g0124a0004c0005t0018g0126others(7): Show | 10 | HG01069.hp2 HG01071.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.1315-234G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 9/20 | chr14 | 92008086 | ||||||
| chr14:92008148
|
C | A | 9 | a0005c0006t0015g0351a0005c0006t0015g0352a0005c0006t0015g0353others(6): Show | 9 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1315-296G>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 9/20 | chr14 | 92008148 | ||||||
| chr14:92008231
|
C | T | 27 | a0001c0001t0003g0003a0001c0001t0003g0179a0001c0001t0003g0181others(24): Show | 28 | HG00280.hp1 HG01070.hp2 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.1315-379G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 9/20 | chr14 | 92008231 | ||||||
| chr14:92008502
|
C | T | 1 | a0001c0001t0001g0075 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1315-650G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 9/20 | chr14 | 92008502 | ||||||
| chr14:92008512
|
G | A | 1 | a0002c0002t0014g0318 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1315-660C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 9/20 | chr14 | 92008512 | ||||||
| chr14:92008545
|
G | A | 5 | a0001c0001t0016g0133a0001c0001t0016g0134a0001c0001t0023g0135others(2): Show | 5 | HG01891.hp2 HG02280.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1315-693C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 9/20 | chr14 | 92008545 | ||||||
| chr14:92008579
|
G | C | 46 | a0001c0001t0005g0085a0001c0001t0005g0086a0001c0001t0005g0087others(43): Show | 47 | HG00323.hp1 HG01069.hp1 HG01167.hp2 others(44): Show |
intron_variant | MODIFIER | c.1315-727C>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 9/20 | chr14 | 92008579 | ||||||
| chr14:92008621
|
T | C | 29 | a0001c0018t0062g0321a0003c0003t0006g0323a0003c0003t0006g0325others(26): Show | 29 | HG00408.hp2 HG01978.hp2 HG02040.hp2 others(26): Show |
intron_variant | MODIFIER | c.1315-769A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 9/20 | chr14 | 92008621 | ||||||
| chr14:92009155
|
A | G | 22 | a0001c0010t0020g0174a0001c0010t0020g0175a0001c0010t0020g0176others(19): Show | 22 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1315-1303T>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 9/20 | chr14 | 92009155 | ||||||
| chr14:92009328
|
C | T | 2 | a0002c0002t0022g0296a0002c0002t0022g0297 | 2 | HG02486.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1315-1476G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 9/20 | chr14 | 92009328 | ||||||
| chr14:92009436
|
G | A | 6 | a0001c0001t0019g0108a0001c0001t0019g0111a0001c0001t0024g0092others(3): Show | 6 | HG02109.hp2 HG02258.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1314+1550C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 9/20 | chr14 | 92009436 | ||||||
| chr14:92009494
|
CAG | C | 4 | a0007c0009t0031g0117a0007c0009t0031g0120a0007c0009t0056g0118others(1): Show | 4 | HG02257.hp1 HG02559.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1314+1490_1314+149 others(6): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 9/20 | chr14 | 92009494 | ||||||
| chr14:92009585
|
ATATAG | A | 7 | a0001c0001t0003g0036a0001c0001t0003g0037a0001c0001t0003g0038others(4): Show | 7 | HG01891.hp1 HG02622.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1314+1396_1314+140 others(9): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 9/20 | chr14 | 92009585 | ||||||
| chr14:92009603
|
C | T | 106 | a0001c0001t0004g0292a0002c0002t0002g0005a0002c0002t0002g0006others(103): Show | 109 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.1314+1383G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 9/20 | chr14 | 92009603 | ||||||
| chr14:92009661
|
A | G | 106 | a0001c0001t0004g0292a0002c0002t0002g0005a0002c0002t0002g0006others(103): Show | 109 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.1314+1325T>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 9/20 | chr14 | 92009661 | ||||||
| chr14:92009833
|
A | T | 1 | a0001c0001t0001g0074 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1314+1153T>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 9/20 | chr14 | 92009833 | ||||||
| chr14:92009922
|
A | G | 9 | a0005c0006t0015g0351a0005c0006t0015g0352a0005c0006t0015g0353others(6): Show | 9 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1314+1064T>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 9/20 | chr14 | 92009922 | ||||||
| chr14:92010336
|
C | T | 6 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(3): Show | 6 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(3): Show |
intron_variant | MODIFIER | c.1314+650G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 9/20 | chr14 | 92010336 | ||||||
| chr14:92010348
|
T | C | 4 | a0009c0012t0032g0129a0009c0012t0032g0130a0009c0012t0059g0123others(1): Show | 4 | HG02818.hp2 HG02965.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1314+638A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 9/20 | chr14 | 92010348 | ||||||
| chr14:92010387
|
G | A | 4 | a0007c0009t0031g0117a0007c0009t0031g0120a0007c0009t0056g0118others(1): Show | 4 | HG02257.hp1 HG02559.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1314+599C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 9/20 | chr14 | 92010387 | ||||||
| chr14:92010461
|
C | T | 1 | a0002c0002t0021g0216 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1314+525G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 9/20 | chr14 | 92010461 | ||||||
| chr14:92010462
|
G | A | 6 | a0004c0005t0018g0121a0004c0005t0018g0124a0004c0005t0018g0126others(3): Show | 6 | HG01069.hp2 HG01071.hp2 NA18980.hp1 others(3): Show |
intron_variant | MODIFIER | c.1314+524C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 9/20 | chr14 | 92010462 | ||||||
| chr14:92010471
|
G | A | 12 | a0002c0002t0002g0005a0002c0002t0002g0205a0002c0002t0002g0206others(9): Show | 13 | HG00099.hp2 HG00642.hp2 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.1314+515C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 9/20 | chr14 | 92010471 | ||||||
| chr14:92010477
|
C | A | 1 | a0001c0001t0001g0068 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1314+509G>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 9/20 | chr14 | 92010477 | ||||||
| chr14:92010486
|
C | T | 1 | a0001c0001t0049g0204 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1314+500G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 9/20 | chr14 | 92010486 | ||||||
| chr14:92010533
|
TA | T | 9 | a0002c0002t0002g0244a0002c0002t0002g0245a0002c0002t0002g0255others(6): Show | 9 | HG00438.hp2 HG00609.hp1 HG00673.hp1 others(6): Show |
intron_variant | MODIFIER | c.1314+452delT | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 9/20 | chr14 | 92010533 | ||||||
| chr14:92010730
|
C | G | 2 | a0002c0002t0002g0305a0002c0002t0029g0212 | 2 | HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1314+256G>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 9/20 | chr14 | 92010730 | ||||||
| chr14:92010772
|
C | T | 6 | a0002c0002t0002g0305a0002c0002t0021g0306a0002c0002t0022g0296others(3): Show | 6 | HG01175.hp2 HG02486.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1314+214G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 9/20 | chr14 | 92010772 | ||||||
| chr14:92010824
|
A | G | 254 | a0001c0001t0003g0003a0001c0001t0003g0036a0001c0001t0003g0037others(251): Show | 259 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.1314+162T>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 9/20 | chr14 | 92010824 | ||||||
| chr14:92010862
|
G | A | 1 | a0002c0002t0002g0243 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1314+124C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 9/20 | chr14 | 92010862 | ||||||
| chr14:92010900
|
A | G | 1 | a0001c0018t0062g0321 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1314+86T>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 9/20 | chr14 | 92010900 | ||||||
| chr14:92011188
|
A | T | 29 | a0001c0018t0062g0321a0003c0003t0006g0323a0003c0003t0006g0325others(26): Show | 29 | HG00408.hp2 HG01978.hp2 HG02040.hp2 others(26): Show |
intron_variant | MODIFIER | c.1228-116T>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 8/20 | chr14 | 92011188 | ||||||
| chr14:92011318
|
C | T | 4 | a0001c0010t0020g0174a0001c0010t0020g0175a0001c0010t0020g0176others(1): Show | 4 | HG02145.hp1 HG02486.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1228-246G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 8/20 | chr14 | 92011318 | ||||||
| chr14:92011384
|
G | A | 6 | a0004c0005t0018g0121a0004c0005t0018g0124a0004c0005t0018g0126others(3): Show | 6 | HG01069.hp2 HG01071.hp2 NA18980.hp1 others(3): Show |
intron_variant | MODIFIER | c.1228-312C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 8/20 | chr14 | 92011384 | ||||||
| chr14:92011446
|
G | A | 29 | a0001c0018t0062g0321a0003c0003t0006g0323a0003c0003t0006g0325others(26): Show | 29 | HG00408.hp2 HG01978.hp2 HG02040.hp2 others(26): Show |
intron_variant | MODIFIER | c.1227+309C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 8/20 | chr14 | 92011446 | ||||||
| chr14:92011467
|
G | C | 3 | a0001c0001t0003g0186a0001c0001t0003g0188a0001c0001t0003g0197 | 3 | HG01346.hp2 HG01496.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.1227+288C>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 8/20 | chr14 | 92011467 | ||||||
| chr14:92011475
|
C | T | 1 | a0014c0034t0003g0128 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1227+280G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 8/20 | chr14 | 92011475 | ||||||
| chr14:92011483
|
C | CA | 105 | a0001c0001t0001g0012a0001c0001t0001g0067a0001c0001t0001g0068others(102): Show | 107 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.1227+271dupT | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 8/20 | chr14 | 92011483 | ||||||
| chr14:92011483
|
C | CAA | 42 | a0002c0002t0002g0224a0002c0002t0002g0229a0002c0002t0002g0230others(39): Show | 43 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.1227+270_1227+271d others(4): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 8/20 | chr14 | 92011483 | ||||||
| chr14:92011483
|
CA | C | 44 | a0001c0001t0001g0064a0001c0001t0005g0085a0001c0001t0005g0086others(41): Show | 45 | HG00323.hp1 HG01069.hp1 HG01167.hp2 others(42): Show |
intron_variant | MODIFIER | c.1227+271delT | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 8/20 | chr14 | 92011483 | ||||||
| chr14:92011483
|
CAAAAAAA others(6): Show |
C | 29 | a0001c0018t0062g0321a0003c0003t0006g0323a0003c0003t0006g0325others(26): Show | 29 | HG00408.hp2 HG01978.hp2 HG02040.hp2 others(26): Show |
intron_variant | MODIFIER | c.1227+259_1227+271d others(15): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 8/20 | chr14 | 92011483 | ||||||
| chr14:92011506
|
A | G | 1 | a0001c0001t0012g0101 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1227+249T>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 8/20 | chr14 | 92011506 | ||||||
| chr14:92011586
|
T | A | 4 | a0001c0010t0020g0174a0001c0010t0020g0175a0001c0010t0020g0176others(1): Show | 4 | HG02145.hp1 HG02486.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1227+169A>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 8/20 | chr14 | 92011586 | ||||||
| chr14:92011651
|
C | A | 1 | a0002c0002t0002g0276 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1227+104G>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 8/20 | chr14 | 92011651 | ||||||
| chr14:92011719
|
T | C | 4 | a0001c0010t0020g0174a0001c0010t0020g0175a0001c0010t0020g0176others(1): Show | 4 | HG02145.hp1 HG02486.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1227+36A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 8/20 | chr14 | 92011719 | ||||||
| chr14:92011854
|
A | G | 47 | a0001c0001t0005g0085a0001c0001t0005g0086a0001c0001t0005g0087others(44): Show | 48 | HG00323.hp1 HG01069.hp1 HG01167.hp2 others(45): Show |
intron_variant | MODIFIER | c.1187-59T>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 7/20 | chr14 | 92011854 | ||||||
| chr14:92011955
|
C | T | 1 | a0016c0024t0064g0356 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1187-160G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 7/20 | chr14 | 92011955 | ||||||
| chr14:92011958
|
A | C | 2 | a0002c0002t0002g0251a0002c0002t0002g0277 | 2 | NA18968.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.1187-163T>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 7/20 | chr14 | 92011958 | ||||||
| chr14:92012011
|
CTA | C | 27 | a0001c0001t0005g0085a0001c0001t0005g0086a0001c0001t0005g0087others(24): Show | 27 | HG00323.hp1 HG01069.hp1 HG01167.hp2 others(24): Show |
intron_variant | MODIFIER | c.1187-218_1187-217d others(4): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 7/20 | chr14 | 92012011 | ||||||
| chr14:92012231
|
C | T | 9 | a0005c0006t0015g0351a0005c0006t0015g0352a0005c0006t0015g0353others(6): Show | 9 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1187-436G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 7/20 | chr14 | 92012231 | ||||||
| chr14:92012246
|
A | C | 1 | a0001c0001t0028g0304 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1187-451T>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 7/20 | chr14 | 92012246 | ||||||
| chr14:92012265
|
T | C | 6 | a0002c0002t0002g0305a0002c0002t0021g0306a0002c0002t0022g0296others(3): Show | 6 | HG01175.hp2 HG02486.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1187-470A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 7/20 | chr14 | 92012265 | ||||||
| chr14:92012411
|
C | T | 1 | a0002c0002t0002g0246 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1187-616G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 7/20 | chr14 | 92012411 | ||||||
| chr14:92012470
|
T | C | 9 | a0005c0006t0015g0351a0005c0006t0015g0352a0005c0006t0015g0353others(6): Show | 9 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1187-675A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 7/20 | chr14 | 92012470 | ||||||
| chr14:92012682
|
C | A | 6 | a0004c0005t0018g0121a0004c0005t0018g0124a0004c0005t0018g0126others(3): Show | 6 | HG01069.hp2 HG01071.hp2 NA18980.hp1 others(3): Show |
intron_variant | MODIFIER | c.1187-887G>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 7/20 | chr14 | 92012682 | ||||||
| chr14:92012691
|
G | A | 2 | a0008c0008t0030g0116a0008c0008t0055g0115 | 2 | HG01109.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.1187-896C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 7/20 | chr14 | 92012691 | ||||||
| chr14:92012719
|
T | C | 28 | a0001c0018t0062g0321a0003c0003t0006g0323a0003c0003t0006g0325others(25): Show | 28 | HG00408.hp2 HG01978.hp2 HG02040.hp2 others(25): Show |
intron_variant | MODIFIER | c.1187-924A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 7/20 | chr14 | 92012719 | ||||||
| chr14:92012784
|
T | C | 10 | a0001c0001t0005g0140a0001c0001t0009g0137a0001c0001t0009g0138others(7): Show | 10 | HG01081.hp1 HG01891.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1187-989A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 7/20 | chr14 | 92012784 | ||||||
| chr14:92012795
|
T | C | 4 | a0008c0008t0030g0114a0008c0008t0030g0116a0008c0008t0055g0115others(1): Show | 4 | HG01109.hp1 HG02055.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1187-1000A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 7/20 | chr14 | 92012795 | ||||||
| chr14:92012797
|
G | T | 2 | a0001c0001t0005g0085a0001c0001t0048g0100 | 2 | HG02280.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1187-1002C>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 7/20 | chr14 | 92012797 | ||||||
| chr14:92012833
|
T | G | 39 | a0001c0001t0005g0085a0001c0001t0005g0086a0001c0001t0005g0087others(36): Show | 39 | HG00323.hp1 HG01069.hp1 HG01167.hp2 others(36): Show |
intron_variant | MODIFIER | c.1187-1038A>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 7/20 | chr14 | 92012833 | ||||||
| chr14:92012953
|
A | G | 60 | a0001c0001t0001g0201a0001c0001t0003g0003a0001c0001t0003g0179others(57): Show | 61 | HG00280.hp1 HG01069.hp2 HG01070.hp2 others(58): Show |
intron_variant | MODIFIER | c.1187-1158T>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 7/20 | chr14 | 92012953 | ||||||
| chr14:92012958
|
G | A | 10 | a0004c0005t0018g0121a0004c0005t0018g0124a0004c0005t0018g0126others(7): Show | 10 | HG01069.hp2 HG01071.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.1187-1163C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 7/20 | chr14 | 92012958 | ||||||
| chr14:92012996
|
C | T | 3 | a0001c0007t0013g0007a0001c0007t0013g0309a0001c0007t0013g0310 | 4 | HG02970.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1187-1201G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 7/20 | chr14 | 92012996 | ||||||
| chr14:92013006
|
C | T | 1 | a0001c0007t0013g0308 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1186+1209G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 7/20 | chr14 | 92013006 | ||||||
| chr14:92013048
|
C | G | 1 | a0001c0001t0049g0204 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1186+1167G>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 7/20 | chr14 | 92013048 | ||||||
| chr14:92013216
|
G | A | 5 | a0002c0002t0002g0305a0002c0002t0021g0216a0002c0002t0022g0296others(2): Show | 5 | HG02486.hp2 HG03225.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1186+999C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 7/20 | chr14 | 92013216 | ||||||
| chr14:92013254
|
G | A | 1 | a0002c0002t0002g0282 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1186+961C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 7/20 | chr14 | 92013254 | ||||||
| chr14:92013260
|
C | T | 18 | a0004c0005t0018g0121a0004c0005t0018g0124a0004c0005t0018g0126others(15): Show | 18 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1186+955G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 7/20 | chr14 | 92013260 | ||||||
| chr14:92013272
|
A | C | 3 | a0001c0001t0003g0190a0001c0001t0003g0191a0001c0001t0003g0200 | 3 | HG01261.hp2 HG01981.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.1186+943T>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 7/20 | chr14 | 92013272 | ||||||
| chr14:92013478
|
AC | A | 7 | a0004c0005t0018g0121a0004c0005t0018g0124a0004c0005t0018g0126others(4): Show | 7 | HG01069.hp2 HG01071.hp2 HG03831.hp1 others(4): Show |
intron_variant | MODIFIER | c.1186+736delG | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 7/20 | chr14 | 92013478 | ||||||
| chr14:92013634
|
CACATAAA others(9): Show |
C | 9 | a0005c0006t0015g0351a0005c0006t0015g0352a0005c0006t0015g0353others(6): Show | 9 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1186+565_1186+580d others(18): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 7/20 | chr14 | 92013634 | ||||||
| chr14:92013663
|
G | A | 1 | a0001c0017t0004g0016 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1186+552C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 7/20 | chr14 | 92013663 | ||||||
| chr14:92013665
|
T | C | 102 | a0001c0001t0004g0292a0001c0001t0060g0316a0002c0002t0002g0005others(99): Show | 105 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.1186+550A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 7/20 | chr14 | 92013665 | ||||||
| chr14:92013690
|
T | C | 32 | a0001c0001t0049g0204a0001c0007t0013g0007a0001c0007t0013g0308others(29): Show | 33 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.1186+525A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 7/20 | chr14 | 92013690 | ||||||
| chr14:92013691
|
GTAAGTAA others(14): Show |
G | 4 | a0001c0001t0060g0316a0002c0002t0014g0315a0002c0002t0014g0318others(1): Show | 4 | HG00558.hp2 HG04184.hp2 NA18948.hp2 others(1): Show |
intron_variant | MODIFIER | c.1186+503_1186+523d others(23): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 7/20 | chr14 | 92013691 | ||||||
| chr14:92013749
|
C | T | 103 | a0001c0001t0004g0292a0001c0001t0060g0316a0002c0002t0002g0005others(100): Show | 106 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.1186+466G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 7/20 | chr14 | 92013749 | ||||||
| chr14:92013757
|
T | C | 2 | a0002c0002t0002g0251a0002c0002t0002g0277 | 2 | NA18968.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.1186+458A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 7/20 | chr14 | 92013757 | ||||||
| chr14:92013832
|
C | T | 13 | a0002c0002t0002g0224a0002c0002t0002g0229a0002c0002t0002g0230others(10): Show | 14 | HG02109.hp1 HG02615.hp1 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.1186+383G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 7/20 | chr14 | 92013832 | ||||||
| chr14:92014057
|
C | T | 1 | a0001c0001t0036g0139 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1186+158G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 7/20 | chr14 | 92014057 | ||||||
| chr14:92014167
|
A | C | 22 | a0001c0010t0020g0174a0001c0010t0020g0175a0001c0010t0020g0176others(19): Show | 22 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1186+48T>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 7/20 | chr14 | 92014167 | ||||||
| chr14:92014598
|
A | C | 22 | a0001c0010t0020g0174a0001c0010t0020g0175a0001c0010t0020g0176others(19): Show | 22 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.824-21T>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 6/20 | chr14 | 92014598 | ||||||
| chr14:92014631
|
C | T | 1 | a0009c0012t0059g0123 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.824-54G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 6/20 | chr14 | 92014631 | ||||||
| chr14:92014658
|
T | G | 1 | a0008c0008t0030g0114 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.824-81A>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 6/20 | chr14 | 92014658 | ||||||
| chr14:92014703
|
A | C | 104 | a0001c0001t0004g0292a0001c0001t0049g0204a0001c0001t0060g0316others(101): Show | 107 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.824-126T>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 6/20 | chr14 | 92014703 | ||||||
| chr14:92014767
|
T | C | 1 | a0017c0025t0003g0182 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.824-190A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 6/20 | chr14 | 92014767 | ||||||
| chr14:92014905
|
A | AT | 164 | a0001c0001t0001g0021a0001c0001t0004g0292a0001c0001t0005g0085others(161): Show | 167 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.824-329dupA | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 6/20 | chr14 | 92014905 | ||||||
| chr14:92014905
|
A | ATT | 15 | a0001c0001t0060g0316a0001c0007t0013g0007a0001c0007t0013g0308others(12): Show | 16 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.824-330_824-329dup others(2): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 6/20 | chr14 | 92014905 | ||||||
| chr14:92014961
|
T | C | 1 | a0001c0001t0001g0068 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.824-384A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 6/20 | chr14 | 92014961 | ||||||
| chr14:92014972
|
C | T | 1 | a0011c0016t0001g0013 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.824-395G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 6/20 | chr14 | 92014972 | ||||||
| chr14:92015100
|
C | T | 1 | a0001c0001t0001g0012 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.824-523G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 6/20 | chr14 | 92015100 | ||||||
| chr14:92015248
|
T | G | 9 | a0005c0006t0015g0351a0005c0006t0015g0352a0005c0006t0015g0353others(6): Show | 9 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.823+448A>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 6/20 | chr14 | 92015248 | ||||||
| chr14:92015487
|
T | C | 1 | a0023c0032t0009g0091 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.823+209A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 6/20 | chr14 | 92015487 | ||||||
| chr14:92015492
|
C | T | 9 | a0005c0006t0015g0351a0005c0006t0015g0352a0005c0006t0015g0353others(6): Show | 9 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.823+204G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 6/20 | chr14 | 92015492 | ||||||
| chr14:92015585
|
G | A | 22 | a0001c0010t0020g0174a0001c0010t0020g0175a0001c0010t0020g0176others(19): Show | 22 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.823+111C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 6/20 | chr14 | 92015585 | ||||||
| chr14:92015613
|
G | A | 9 | a0005c0006t0015g0351a0005c0006t0015g0352a0005c0006t0015g0353others(6): Show | 9 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.823+83C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 6/20 | chr14 | 92015613 | ||||||
| chr14:92015619
|
G | C | 4 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(1): Show | 4 | HG01070.hp1 HG01071.hp1 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.823+77C>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 6/20 | chr14 | 92015619 | ||||||
| chr14:92015666
|
T | A | 13 | a0001c0007t0013g0007a0001c0007t0013g0308a0001c0007t0013g0309others(10): Show | 14 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.823+30A>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 6/20 | chr14 | 92015666 | ||||||
| chr14:92015910
|
T | C | 31 | a0001c0010t0020g0174a0001c0010t0020g0175a0001c0010t0020g0176others(28): Show | 31 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.658-49A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 5/20 | chr14 | 92015910 | ||||||
| chr14:92016137
|
A | G | 9 | a0005c0006t0015g0351a0005c0006t0015g0352a0005c0006t0015g0353others(6): Show | 9 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.658-276T>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 5/20 | chr14 | 92016137 | ||||||
| chr14:92016172
|
A | T | 44 | a0001c0001t0005g0085a0001c0001t0005g0086a0001c0001t0005g0087others(41): Show | 45 | HG00323.hp1 HG01069.hp1 HG01167.hp2 others(42): Show |
intron_variant | MODIFIER | c.658-311T>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 5/20 | chr14 | 92016172 | ||||||
| chr14:92016243
|
C | G | 1 | a0002c0002t0002g0218 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.658-382G>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 5/20 | chr14 | 92016243 | ||||||
| chr14:92016263
|
C | T | 6 | a0004c0005t0018g0121a0004c0005t0018g0124a0004c0005t0018g0126others(3): Show | 6 | HG01069.hp2 HG01071.hp2 NA18980.hp1 others(3): Show |
intron_variant | MODIFIER | c.658-402G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 5/20 | chr14 | 92016263 | ||||||
| chr14:92016303
|
C | A | 4 | a0001c0007t0013g0007a0001c0007t0013g0308a0001c0007t0013g0309others(1): Show | 5 | HG02809.hp2 HG02970.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.658-442G>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 5/20 | chr14 | 92016303 | ||||||
| chr14:92016333
|
G | A | 2 | a0003c0003t0061g0340a0008c0008t0055g0115 | 2 | HG02055.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.658-472C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 5/20 | chr14 | 92016333 | ||||||
| chr14:92016422
|
C | T | 1 | a0001c0001t0001g0023 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.658-561G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 5/20 | chr14 | 92016422 | ||||||
| chr14:92016490
|
C | A | 27 | a0004c0005t0018g0121a0004c0005t0018g0124a0004c0005t0018g0126others(24): Show | 27 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.658-629G>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 5/20 | chr14 | 92016490 | ||||||
| chr14:92016590
|
A | T | 2 | a0002c0002t0002g0303a0002c0002t0029g0258 | 2 | NA18942.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.658-729T>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 5/20 | chr14 | 92016590 | ||||||
| chr14:92016604
|
C | T | 104 | a0001c0001t0004g0292a0001c0001t0049g0204a0001c0001t0060g0316others(101): Show | 107 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.658-743G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 5/20 | chr14 | 92016604 | ||||||
| chr14:92017112
|
C | T | 9 | a0005c0006t0015g0351a0005c0006t0015g0352a0005c0006t0015g0353others(6): Show | 9 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.657+570G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 5/20 | chr14 | 92017112 | ||||||
| chr14:92017169
|
A | G | 1 | a0007c0009t0031g0117 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.657+513T>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 5/20 | chr14 | 92017169 | ||||||
| chr14:92017192
|
G | A | 1 | a0001c0001t0001g0163 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.657+490C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 5/20 | chr14 | 92017192 | ||||||
| chr14:92017502
|
T | C | 1 | a0007c0009t0057g0119 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.657+180A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 5/20 | chr14 | 92017502 | ||||||
| chr14:92017612
|
T | C | 1 | a0017c0025t0003g0182 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.657+70A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 5/20 | chr14 | 92017612 | ||||||
| chr14:92017673
|
T | G | 1 | a0001c0001t0001g0012 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.657+9A>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 5/20 | chr14 | 92017673 | ||||||
| chr14:92017883
|
T | C | 104 | a0001c0001t0004g0292a0001c0001t0049g0204a0001c0001t0060g0316others(101): Show | 107 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.589-133A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 4/20 | chr14 | 92017883 | ||||||
| chr14:92017896
|
G | C | 1 | a0001c0001t0023g0136 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.589-146C>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 4/20 | chr14 | 92017896 | ||||||
| chr14:92017923
|
C | T | 4 | a0001c0010t0020g0174a0001c0010t0020g0175a0001c0010t0020g0176others(1): Show | 4 | HG02145.hp1 HG02486.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.589-173G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 4/20 | chr14 | 92017923 | ||||||
| chr14:92017970
|
G | A | 4 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(1): Show | 4 | NA18946.hp2 NA18983.hp1 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.589-220C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 4/20 | chr14 | 92017970 | ||||||
| chr14:92018019
|
A | T | 2 | a0011c0016t0001g0013a0011c0016t0004g0011 | 2 | HG02040.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.589-269T>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 4/20 | chr14 | 92018019 | ||||||
| chr14:92018049
|
G | A | 1 | a0001c0001t0028g0304 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.589-299C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 4/20 | chr14 | 92018049 | ||||||
| chr14:92018097
|
C | CT | 18 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0003g0189others(15): Show | 18 | HG01069.hp2 HG01070.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.589-348dupA | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 4/20 | chr14 | 92018097 | ||||||
| chr14:92018274
|
A | G | 1 | a0017c0025t0003g0182 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.589-524T>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 4/20 | chr14 | 92018274 | ||||||
| chr14:92018440
|
G | C | 9 | a0005c0006t0015g0351a0005c0006t0015g0352a0005c0006t0015g0353others(6): Show | 9 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.589-690C>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 4/20 | chr14 | 92018440 | ||||||
| chr14:92018729
|
C | A | 1 | a0002c0002t0002g0257 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.589-979G>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 4/20 | chr14 | 92018729 | ||||||
| chr14:92018734
|
G | A | 1 | a0002c0002t0002g0284 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.589-984C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 4/20 | chr14 | 92018734 | ||||||
| chr14:92018739
|
A | G | 13 | a0002c0002t0002g0224a0002c0002t0002g0229a0002c0002t0002g0230others(10): Show | 14 | HG02109.hp1 HG02615.hp1 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.589-989T>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 4/20 | chr14 | 92018739 | ||||||
| chr14:92018775
|
G | A | 1 | a0002c0002t0002g0006 | 2 | HG00544.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.589-1025C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 4/20 | chr14 | 92018775 | ||||||
| chr14:92018832
|
G | T | 9 | a0001c0004t0019g0207a0001c0004t0024g0210a0001c0004t0025g0209others(6): Show | 9 | HG01255.hp2 HG02630.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.589-1082C>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 4/20 | chr14 | 92018832 | ||||||
| chr14:92018837
|
C | T | 1 | a0002c0002t0002g0305 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.589-1087G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 4/20 | chr14 | 92018837 | ||||||
| chr14:92018903
|
G | A | 2 | a0001c0001t0016g0133a0001c0001t0016g0134 | 2 | HG01891.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.589-1153C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 4/20 | chr14 | 92018903 | ||||||
| chr14:92018960
|
C | CA | 48 | a0001c0001t0001g0012a0001c0001t0001g0033a0001c0001t0001g0054others(45): Show | 48 | HG00408.hp2 HG00609.hp1 HG01069.hp2 others(45): Show |
intron_variant | MODIFIER | c.589-1211dupT | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 4/20 | chr14 | 92018960 | ||||||
| chr14:92018960
|
CA | C | 138 | a0001c0001t0004g0292a0001c0001t0005g0085a0001c0001t0005g0086others(135): Show | 141 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.589-1211delT | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 4/20 | chr14 | 92018960 | ||||||
| chr14:92018972
|
A | C | 2 | a0001c0001t0005g0093a0001c0007t0013g0309 | 2 | HG03486.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.589-1222T>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 4/20 | chr14 | 92018972 | ||||||
| chr14:92018978
|
AC | A | 29 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(26): Show | 29 | HG00140.hp2 HG00280.hp2 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.589-1229delG | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 4/20 | chr14 | 92018978 | ||||||
| chr14:92018979
|
C | A | 12 | a0001c0001t0001g0165a0001c0001t0004g0164a0001c0001t0028g0304others(9): Show | 12 | HG02004.hp1 HG02055.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.589-1229G>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 4/20 | chr14 | 92018979 | ||||||
| chr14:92019141
|
C | T | 19 | a0001c0007t0013g0007a0001c0007t0013g0308a0001c0007t0013g0309others(16): Show | 20 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.589-1391G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 4/20 | chr14 | 92019141 | ||||||
| chr14:92019537
|
G | T | 172 | a0001c0001t0004g0292a0001c0001t0005g0085a0001c0001t0005g0086others(169): Show | 176 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.589-1787C>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 4/20 | chr14 | 92019537 | ||||||
| chr14:92019574
|
C | T | 1 | a0001c0001t0004g0144 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.589-1824G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 4/20 | chr14 | 92019574 | ||||||
| chr14:92019761
|
T | C | 19 | a0001c0007t0013g0007a0001c0007t0013g0308a0001c0007t0013g0309others(16): Show | 20 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.588+1795A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 4/20 | chr14 | 92019761 | ||||||
| chr14:92019779
|
A | T | 1 | a0001c0001t0003g0200 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.588+1777T>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 4/20 | chr14 | 92019779 | ||||||
| chr14:92019794
|
A | C | 9 | a0005c0006t0015g0351a0005c0006t0015g0352a0005c0006t0015g0353others(6): Show | 9 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.588+1762T>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 4/20 | chr14 | 92019794 | ||||||
| chr14:92019809
|
G | A | 9 | a0005c0006t0015g0351a0005c0006t0015g0352a0005c0006t0015g0353others(6): Show | 9 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.588+1747C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 4/20 | chr14 | 92019809 | ||||||
| chr14:92019822
|
C | G | 4 | a0001c0007t0013g0007a0001c0007t0013g0308a0001c0007t0013g0309others(1): Show | 5 | HG02809.hp2 HG02970.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.588+1734G>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 4/20 | chr14 | 92019822 | ||||||
| chr14:92019898
|
T | C | 40 | a0001c0001t0005g0085a0001c0001t0005g0086a0001c0001t0005g0087others(37): Show | 40 | HG00323.hp1 HG01069.hp1 HG01167.hp2 others(37): Show |
intron_variant | MODIFIER | c.588+1658A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 4/20 | chr14 | 92019898 | ||||||
| chr14:92019911
|
T | TG | 9 | a0005c0006t0015g0351a0005c0006t0015g0352a0005c0006t0015g0353others(6): Show | 9 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.588+1644dupC | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 4/20 | chr14 | 92019911 | ||||||
| chr14:92019958
|
T | C | 7 | a0001c0010t0020g0174a0001c0010t0020g0175a0001c0010t0020g0176others(4): Show | 7 | HG02145.hp1 HG02486.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.588+1598A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 4/20 | chr14 | 92019958 | ||||||
| chr14:92019962
|
T | C | 1 | a0001c0001t0001g0166 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.588+1594A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 4/20 | chr14 | 92019962 | ||||||
| chr14:92019969
|
A | G | 6 | a0004c0005t0018g0121a0004c0005t0018g0124a0004c0005t0018g0126others(3): Show | 6 | HG01069.hp2 HG01071.hp2 NA18980.hp1 others(3): Show |
intron_variant | MODIFIER | c.588+1587T>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 4/20 | chr14 | 92019969 | ||||||
| chr14:92020121
|
G | A | 1 | a0001c0020t0001g0026 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.588+1435C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 4/20 | chr14 | 92020121 | ||||||
| chr14:92020125
|
G | A | 26 | a0001c0007t0013g0007a0001c0007t0013g0308a0001c0007t0013g0309others(23): Show | 27 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.588+1431C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 4/20 | chr14 | 92020125 | ||||||
| chr14:92020177
|
G | A | 19 | a0001c0007t0013g0007a0001c0007t0013g0308a0001c0007t0013g0309others(16): Show | 20 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.588+1379C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 4/20 | chr14 | 92020177 | ||||||
| chr14:92020270
|
A | G | 9 | a0005c0006t0015g0351a0005c0006t0015g0352a0005c0006t0015g0353others(6): Show | 9 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.588+1286T>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 4/20 | chr14 | 92020270 | ||||||
| chr14:92020379
|
G | C | 3 | a0002c0002t0022g0296a0002c0002t0022g0297a0002c0002t0022g0298 | 3 | HG02486.hp2 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.588+1177C>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 4/20 | chr14 | 92020379 | ||||||
| chr14:92020474
|
T | C | 24 | a0003c0003t0006g0323a0003c0003t0006g0325a0003c0003t0006g0331others(21): Show | 24 | HG00408.hp2 HG02040.hp2 HG02165.hp2 others(21): Show |
intron_variant | MODIFIER | c.588+1082A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 4/20 | chr14 | 92020474 | ||||||
| chr14:92020479
|
T | C | 3 | a0009c0012t0032g0129a0009c0012t0032g0130a0014c0034t0003g0128 | 3 | HG02818.hp2 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.588+1077A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 4/20 | chr14 | 92020479 | ||||||
| chr14:92020543
|
G | A | 1 | a0002c0002t0002g0245 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.588+1013C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 4/20 | chr14 | 92020543 | ||||||
| chr14:92020562
|
C | T | 1 | a0001c0001t0028g0304 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.588+994G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 4/20 | chr14 | 92020562 | ||||||
| chr14:92020661
|
T | C | 1 | a0007c0009t0057g0119 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.588+895A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 4/20 | chr14 | 92020661 | ||||||
| chr14:92020662
|
T | A | 2 | a0007c0009t0031g0120a0007c0009t0056g0118 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.588+894A>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 4/20 | chr14 | 92020662 | ||||||
| chr14:92020662
|
TA | T | 6 | a0004c0005t0018g0121a0004c0005t0018g0124a0004c0005t0018g0126others(3): Show | 6 | HG01069.hp2 HG01071.hp2 NA18980.hp1 others(3): Show |
intron_variant | MODIFIER | c.588+893delT | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 4/20 | chr14 | 92020662 | ||||||
| chr14:92020703
|
T | G | 3 | a0001c0001t0003g0036a0001c0001t0003g0037a0001c0001t0003g0059 | 3 | HG02970.hp2 HG03209.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.588+853A>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 4/20 | chr14 | 92020703 | ||||||
| chr14:92020756
|
G | T | 28 | a0001c0007t0013g0007a0001c0007t0013g0308a0001c0007t0013g0309others(25): Show | 29 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.588+800C>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 4/20 | chr14 | 92020756 | ||||||
| chr14:92020842
|
C | T | 8 | a0001c0010t0020g0174a0001c0010t0020g0175a0001c0010t0020g0176others(5): Show | 8 | HG02145.hp1 HG02486.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.588+714G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 4/20 | chr14 | 92020842 | ||||||
| chr14:92020872
|
C | A | 7 | a0004c0005t0018g0121a0004c0005t0018g0124a0004c0005t0018g0126others(4): Show | 7 | HG01069.hp2 HG01071.hp2 HG03831.hp1 others(4): Show |
intron_variant | MODIFIER | c.588+684G>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 4/20 | chr14 | 92020872 | ||||||
| chr14:92020995
|
G | A | 1 | a0006c0011t0002g0311 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.588+561C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 4/20 | chr14 | 92020995 | ||||||
| chr14:92021069
|
C | CA | 43 | a0001c0001t0001g0012a0001c0001t0003g0199a0001c0001t0005g0085others(40): Show | 43 | HG00323.hp1 HG00642.hp1 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.588+486dupT | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 4/20 | chr14 | 92021069 | ||||||
| chr14:92021123
|
TG | T | 7 | a0001c0010t0020g0174a0001c0010t0020g0175a0001c0010t0020g0176others(4): Show | 7 | HG02145.hp1 HG02486.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.588+432delC | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 4/20 | chr14 | 92021123 | ||||||
| chr14:92021388
|
CA | C | 173 | a0001c0001t0001g0064a0001c0001t0003g0188a0001c0001t0004g0292others(170): Show | 176 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.588+167delT | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 4/20 | chr14 | 92021388 | ||||||
| chr14:92021388
|
CAA | C | 31 | a0001c0001t0005g0086a0001c0007t0013g0007a0001c0007t0013g0308others(28): Show | 32 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.588+166_588+167del others(2): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 4/20 | chr14 | 92021388 | ||||||
| chr14:92021420
|
GACGGAAT others(6): Show |
G | 1 | a0001c0001t0001g0067 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.588+123_588+135del others(13): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 4/20 | chr14 | 92021420 | ||||||
| chr14:92021442
|
T | C | 1 | a0009c0012t0059g0123 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.588+114A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 4/20 | chr14 | 92021442 | ||||||
| chr14:92021521
|
A | G | 1 | a0003c0003t0063g0337 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.588+35T>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 4/20 | chr14 | 92021521 | ||||||
| chr14:92021978
|
T | C | 3 | a0001c0001t0005g0140a0001c0001t0009g0137a0001c0001t0009g0138 | 3 | HG02145.hp2 HG03195.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.313-147A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 3/20 | chr14 | 92021978 | ||||||
| chr14:92021992
|
T | C | 1 | a0001c0001t0001g0025 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.313-161A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 3/20 | chr14 | 92021992 | ||||||
| chr14:92022253
|
G | T | 9 | a0005c0006t0015g0351a0005c0006t0015g0352a0005c0006t0015g0353others(6): Show | 9 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.313-422C>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 3/20 | chr14 | 92022253 | ||||||
| chr14:92022514
|
T | C | 1 | a0001c0001t0001g0055 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.313-683A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 3/20 | chr14 | 92022514 | ||||||
| chr14:92022550
|
C | A | 104 | a0001c0001t0004g0292a0001c0001t0049g0204a0001c0001t0060g0316others(101): Show | 107 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.313-719G>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 3/20 | chr14 | 92022550 | ||||||
| chr14:92022559
|
C | T | 7 | a0002c0002t0002g0244a0002c0002t0002g0245a0002c0002t0002g0255others(4): Show | 7 | HG00438.hp2 HG00609.hp1 HG00673.hp1 others(4): Show |
intron_variant | MODIFIER | c.313-728G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 3/20 | chr14 | 92022559 | ||||||
| chr14:92022590
|
C | T | 3 | a0002c0002t0022g0296a0002c0002t0022g0297a0002c0002t0022g0298 | 3 | HG02486.hp2 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.313-759G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 3/20 | chr14 | 92022590 | ||||||
| chr14:92022830
|
T | C | 97 | a0001c0001t0004g0292a0001c0001t0060g0316a0002c0002t0002g0005others(94): Show | 100 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.313-999A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 3/20 | chr14 | 92022830 | ||||||
| chr14:92022989
|
A | C | 28 | a0001c0007t0013g0007a0001c0007t0013g0308a0001c0007t0013g0309others(25): Show | 29 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.313-1158T>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 3/20 | chr14 | 92022989 | ||||||
| chr14:92023010
|
C | T | 19 | a0001c0007t0013g0007a0001c0007t0013g0308a0001c0007t0013g0309others(16): Show | 20 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.313-1179G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 3/20 | chr14 | 92023010 | ||||||
| chr14:92023046
|
A | G | 1 | a0001c0001t0009g0099 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.313-1215T>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 3/20 | chr14 | 92023046 | ||||||
| chr14:92023184
|
T | A | 1 | a0002c0002t0002g0284 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.313-1353A>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 3/20 | chr14 | 92023184 | ||||||
| chr14:92023198
|
T | C | 7 | a0001c0010t0020g0174a0001c0010t0020g0175a0001c0010t0020g0176others(4): Show | 7 | HG02145.hp1 HG02486.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.313-1367A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 3/20 | chr14 | 92023198 | ||||||
| chr14:92023211
|
G | A | 3 | a0001c0001t0003g0038a0001c0001t0003g0039a0001c0001t0003g0040 | 3 | HG01891.hp1 HG02622.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.313-1380C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 3/20 | chr14 | 92023211 | ||||||
| chr14:92023268
|
C | T | 9 | a0005c0006t0015g0351a0005c0006t0015g0352a0005c0006t0015g0353others(6): Show | 9 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.313-1437G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 3/20 | chr14 | 92023268 | ||||||
| chr14:92023359
|
G | C | 1 | a0001c0001t0001g0056 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.313-1528C>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 3/20 | chr14 | 92023359 | ||||||
| chr14:92023404
|
C | T | 9 | a0005c0006t0015g0351a0005c0006t0015g0352a0005c0006t0015g0353others(6): Show | 9 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.313-1573G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 3/20 | chr14 | 92023404 | ||||||
| chr14:92023857
|
C | CT | 34 | a0001c0001t0001g0010a0001c0001t0004g0081a0001c0001t0016g0133others(31): Show | 35 | HG01069.hp2 HG01071.hp2 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.312+1452dupA | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 3/20 | chr14 | 92023857 | ||||||
| chr14:92024016
|
C | T | 1 | a0001c0001t0016g0132 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.312+1294G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 3/20 | chr14 | 92024016 | ||||||
| chr14:92024031
|
T | C | 1 | a0001c0001t0001g0065 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.312+1279A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 3/20 | chr14 | 92024031 | ||||||
| chr14:92024055
|
GA | G | 9 | a0001c0004t0019g0207a0001c0004t0024g0210a0001c0004t0025g0209others(6): Show | 9 | HG01255.hp2 HG02630.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.312+1254delT | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 3/20 | chr14 | 92024055 | ||||||
| chr14:92024106
|
G | C | 2 | a0002c0002t0022g0296a0002c0002t0022g0297 | 2 | HG02486.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.312+1204C>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 3/20 | chr14 | 92024106 | ||||||
| chr14:92024138
|
G | A | 1 | a0002c0002t0017g0240 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.312+1172C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 3/20 | chr14 | 92024138 | ||||||
| chr14:92024205
|
C | T | 7 | a0004c0005t0018g0121a0004c0005t0018g0124a0004c0005t0018g0126others(4): Show | 7 | HG01069.hp2 HG01071.hp2 HG03831.hp1 others(4): Show |
intron_variant | MODIFIER | c.312+1105G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 3/20 | chr14 | 92024205 | ||||||
| chr14:92024238
|
C | A | 19 | a0001c0007t0013g0007a0001c0007t0013g0308a0001c0007t0013g0309others(16): Show | 20 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.312+1072G>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 3/20 | chr14 | 92024238 | ||||||
| chr14:92024349
|
C | T | 1 | a0009c0012t0059g0123 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.312+961G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 3/20 | chr14 | 92024349 | ||||||
| chr14:92024370
|
C | CA | 124 | a0001c0001t0004g0066a0001c0001t0004g0292a0001c0001t0049g0204others(121): Show | 128 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.312+939dupT | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 3/20 | chr14 | 92024370 | ||||||
| chr14:92024511
|
A | T | 28 | a0001c0007t0013g0007a0001c0007t0013g0308a0001c0007t0013g0309others(25): Show | 29 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.312+799T>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 3/20 | chr14 | 92024511 | ||||||
| chr14:92024575
|
T | C | 19 | a0001c0007t0013g0007a0001c0007t0013g0308a0001c0007t0013g0309others(16): Show | 20 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.312+735A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 3/20 | chr14 | 92024575 | ||||||
| chr14:92024679
|
A | G | 7 | a0001c0010t0020g0174a0001c0010t0020g0175a0001c0010t0020g0176others(4): Show | 7 | HG02145.hp1 HG02486.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.312+631T>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 3/20 | chr14 | 92024679 | ||||||
| chr14:92024915
|
T | C | 4 | a0001c0010t0020g0174a0001c0010t0020g0175a0001c0010t0020g0176others(1): Show | 4 | HG02145.hp1 HG02486.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.312+395A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 3/20 | chr14 | 92024915 | ||||||
| chr14:92025178
|
G | A | 7 | a0004c0005t0018g0121a0004c0005t0018g0124a0004c0005t0018g0126others(4): Show | 7 | HG01069.hp2 HG01071.hp2 HG03831.hp1 others(4): Show |
intron_variant | MODIFIER | c.312+132C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 3/20 | chr14 | 92025178 | ||||||
| chr14:92025207
|
AT | A | 4 | a0008c0008t0030g0114a0008c0008t0030g0116a0008c0008t0055g0115others(1): Show | 4 | HG01109.hp1 HG02055.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.312+102delA | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 3/20 | chr14 | 92025207 | ||||||
| chr14:92025427
|
A | T | 9 | a0005c0006t0015g0351a0005c0006t0015g0352a0005c0006t0015g0353others(6): Show | 9 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
splice_region_variant&intron_variant | LOW | c.202-7T>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92025427 | ||||||
| chr14:92025499
|
C | T | 4 | a0001c0001t0003g0179a0001c0001t0003g0181a0001c0001t0003g0187others(1): Show | 4 | HG00280.hp1 HG01070.hp2 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.202-79G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92025499 | ||||||
| chr14:92025508
|
T | TCCC | 27 | a0001c0001t0005g0085a0001c0001t0005g0086a0001c0001t0005g0087others(24): Show | 27 | HG00323.hp1 HG01167.hp2 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.202-89_202-88insGG others(1): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92025508 | ||||||
| chr14:92025508
|
T | TCCCC | 7 | a0001c0001t0012g0095a0001c0001t0012g0109a0001c0001t0019g0108others(4): Show | 7 | HG01192.hp2 HG02258.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.202-89_202-88insGG others(2): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92025508 | ||||||
| chr14:92025509
|
T | C | 207 | a0001c0001t0004g0292a0001c0001t0005g0085a0001c0001t0005g0086others(204): Show | 211 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.202-89A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92025509 | ||||||
| chr14:92025515
|
C | CA | 19 | a0001c0007t0013g0007a0001c0007t0013g0308a0001c0007t0013g0309others(16): Show | 20 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.202-96_202-95insT | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92025515 | ||||||
| chr14:92025694
|
T | C | 1 | a0001c0001t0001g0057 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.202-274A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92025694 | ||||||
| chr14:92025736
|
C | T | 1 | a0009c0012t0059g0123 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.202-316G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92025736 | ||||||
| chr14:92025878
|
C | CA | 38 | a0001c0001t0001g0067a0001c0001t0001g0071a0001c0001t0004g0081others(35): Show | 38 | HG00323.hp1 HG01069.hp1 HG01167.hp2 others(35): Show |
intron_variant | MODIFIER | c.202-459dupT | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92025878 | ||||||
| chr14:92025878
|
C | CAAAAAAA others(3): Show |
8 | a0005c0006t0015g0351a0005c0006t0015g0352a0005c0006t0015g0353others(5): Show | 8 | HG02258.hp1 HG02451.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.202-468_202-459dup others(10): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92025878 | ||||||
| chr14:92025878
|
C | CAAAAAAA others(4): Show |
1 | a0010c0013t0066g0355 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.202-469_202-459dup others(11): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92025878 | ||||||
| chr14:92025895
|
A | AT | 17 | a0001c0007t0013g0007a0001c0007t0013g0308a0001c0007t0013g0309others(14): Show | 18 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.202-476_202-475ins others(1): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92025895 | ||||||
| chr14:92025895
|
A | T | 2 | a0007c0009t0056g0118a0009c0012t0059g0123 | 2 | HG02897.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.202-475T>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92025895 | ||||||
| chr14:92025954
|
T | C | 1 | a0001c0001t0049g0204 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.202-534A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92025954 | ||||||
| chr14:92025996
|
C | T | 11 | a0002c0002t0002g0224a0002c0002t0002g0229a0002c0002t0002g0230others(8): Show | 12 | HG02109.hp1 HG02615.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.202-576G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92025996 | ||||||
| chr14:92026002
|
A | G | 2 | a0001c0001t0001g0142a0001c0001t0001g0143 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.202-582T>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92026002 | ||||||
| chr14:92026006
|
T | C | 1 | a0001c0001t0001g0072 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.202-586A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92026006 | ||||||
| chr14:92026216
|
A | G | 6 | a0004c0005t0018g0121a0004c0005t0018g0124a0004c0005t0018g0126others(3): Show | 6 | HG01069.hp2 HG01071.hp2 NA18980.hp1 others(3): Show |
intron_variant | MODIFIER | c.202-796T>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92026216 | ||||||
| chr14:92026307
|
T | C | 103 | a0001c0001t0004g0292a0001c0001t0049g0204a0001c0001t0060g0316others(100): Show | 106 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.202-887A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92026307 | ||||||
| chr14:92026365
|
T | C | 4 | a0002c0002t0002g0281a0002c0002t0002g0282a0002c0002t0002g0283others(1): Show | 4 | NA18972.hp2 NA18974.hp2 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.202-945A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92026365 | ||||||
| chr14:92026620
|
G | C | 1 | a0002c0002t0002g0284 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.202-1200C>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92026620 | ||||||
| chr14:92026996
|
CCCGCCCA others(12): Show |
C | 9 | a0001c0004t0019g0207a0001c0004t0024g0210a0001c0004t0025g0209others(6): Show | 9 | HG01255.hp2 HG02630.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.202-1595_202-1577d others(21): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92026996 | ||||||
| chr14:92027004
|
C | G | 3 | a0009c0012t0032g0129a0009c0012t0032g0130a0014c0034t0003g0128 | 3 | HG02818.hp2 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.202-1584G>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92027004 | ||||||
| chr14:92027092
|
A | G | 1 | a0001c0001t0005g0090 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.202-1672T>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92027092 | ||||||
| chr14:92027200
|
T | C | 7 | a0004c0005t0018g0121a0004c0005t0018g0124a0004c0005t0018g0126others(4): Show | 7 | HG01069.hp2 HG01071.hp2 HG03831.hp1 others(4): Show |
intron_variant | MODIFIER | c.202-1780A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92027200 | ||||||
| chr14:92027210
|
G | A | 1 | a0003c0003t0006g0345 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.202-1790C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92027210 | ||||||
| chr14:92027338
|
A | G | 1 | a0002c0002t0021g0242 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.202-1918T>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92027338 | ||||||
| chr14:92027482
|
AT | A | 7 | a0001c0010t0020g0174a0001c0010t0020g0175a0001c0010t0020g0176others(4): Show | 7 | HG02145.hp1 HG02486.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.202-2063delA | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92027482 | ||||||
| chr14:92028086
|
G | A | 43 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(40): Show | 43 | HG00140.hp2 HG00280.hp2 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.202-2666C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92028086 | ||||||
| chr14:92028218
|
T | C | 1 | a0001c0001t0001g0058 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.202-2798A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92028218 | ||||||
| chr14:92028297
|
T | A | 1 | a0001c0001t0036g0139 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.202-2877A>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92028297 | ||||||
| chr14:92028323
|
G | A | 15 | a0004c0005t0018g0121a0004c0005t0018g0124a0004c0005t0018g0126others(12): Show | 15 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.202-2903C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92028323 | ||||||
| chr14:92028393
|
C | T | 4 | a0008c0008t0030g0114a0008c0008t0030g0116a0008c0008t0055g0115others(1): Show | 4 | HG01109.hp1 HG02055.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.202-2973G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92028393 | ||||||
| chr14:92028413
|
C | T | 1 | a0001c0001t0028g0304 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.202-2993G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92028413 | ||||||
| chr14:92028428
|
C | T | 4 | a0008c0008t0030g0114a0008c0008t0030g0116a0008c0008t0055g0115others(1): Show | 4 | HG01109.hp1 HG02055.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.202-3008G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92028428 | ||||||
| chr14:92028453
|
T | G | 7 | a0001c0001t0003g0036a0001c0001t0003g0037a0001c0001t0003g0038others(4): Show | 7 | HG01891.hp1 HG02622.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.202-3033A>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92028453 | ||||||
| chr14:92028926
|
C | T | 1 | a0001c0001t0001g0168 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.202-3506G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92028926 | ||||||
| chr14:92029192
|
A | G | 112 | a0001c0001t0004g0292a0001c0001t0049g0204a0001c0001t0060g0316others(109): Show | 115 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.202-3772T>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92029192 | ||||||
| chr14:92029280
|
A | AT | 40 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0015others(37): Show | 40 | HG00280.hp1 HG00673.hp2 HG01070.hp2 others(37): Show |
intron_variant | MODIFIER | c.202-3861dupA | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92029280 | ||||||
| chr14:92029280
|
AT | A | 6 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0060others(3): Show | 6 | HG00323.hp2 HG01099.hp2 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.202-3861delA | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92029280 | ||||||
| chr14:92029280
|
ATTTT | A | 68 | a0001c0001t0004g0292a0001c0001t0060g0316a0001c0004t0019g0207others(65): Show | 69 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.202-3864_202-3861d others(6): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92029280 | ||||||
| chr14:92029280
|
ATTTTT | A | 68 | a0001c0001t0049g0204a0001c0004t0024g0210a0001c0004t0025g0213others(65): Show | 71 | HG00099.hp2 HG00140.hp1 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.202-3865_202-3861d others(7): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92029280 | ||||||
| chr14:92029280
|
ATTTTTT | A | 19 | a0001c0001t0005g0090a0001c0001t0005g0093a0001c0001t0012g0094others(16): Show | 19 | HG01192.hp2 HG01243.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.202-3866_202-3861d others(8): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92029280 | ||||||
| chr14:92029280
|
ATTTTTTT | A | 35 | a0001c0001t0005g0085a0001c0001t0005g0086a0001c0001t0005g0087others(32): Show | 35 | HG00323.hp1 HG01069.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.202-3867_202-3861d others(9): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92029280 | ||||||
| chr14:92029280
|
ATTTTTTT others(5): Show |
A | 4 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(1): Show | 4 | NA18946.hp2 NA18983.hp1 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.202-3872_202-3861d others(14): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92029280 | ||||||
| chr14:92029280
|
ATTTTTTT others(6): Show |
A | 32 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(29): Show | 32 | HG00140.hp2 HG00280.hp2 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.202-3873_202-3861d others(15): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92029280 | ||||||
| chr14:92029283
|
T | A | 1 | a0006c0011t0002g0311 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.202-3863A>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92029283 | ||||||
| chr14:92029287
|
T | A | 30 | a0001c0018t0062g0321a0002c0002t0002g0289a0002c0002t0014g0318others(27): Show | 30 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(27): Show |
intron_variant | MODIFIER | c.202-3867A>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92029287 | ||||||
| chr14:92029288
|
T | A | 1 | a0010c0013t0066g0355 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.202-3868A>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92029288 | ||||||
| chr14:92029289
|
T | A | 7 | a0005c0006t0015g0351a0005c0006t0015g0352a0005c0006t0015g0353others(4): Show | 7 | HG02451.hp1 HG02615.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.202-3869A>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92029289 | ||||||
| chr14:92029290
|
T | A | 40 | a0001c0018t0062g0321a0003c0003t0006g0323a0003c0003t0006g0325others(37): Show | 40 | HG00408.hp2 HG01069.hp2 HG01071.hp2 others(37): Show |
intron_variant | MODIFIER | c.202-3870A>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92029290 | ||||||
| chr14:92029291
|
T | A | 4 | a0007c0009t0031g0117a0007c0009t0056g0118a0007c0009t0057g0119others(1): Show | 4 | HG02055.hp1 HG02257.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.202-3871A>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92029291 | ||||||
| chr14:92029292
|
T | A | 9 | a0001c0035t0012g0084a0005c0006t0015g0351a0005c0006t0015g0352others(6): Show | 9 | HG02451.hp1 HG02615.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.202-3872A>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92029292 | ||||||
| chr14:92029293
|
T | A | 40 | a0001c0018t0062g0321a0003c0003t0006g0323a0003c0003t0006g0325others(37): Show | 40 | HG00408.hp2 HG01069.hp2 HG01071.hp2 others(37): Show |
intron_variant | MODIFIER | c.202-3873A>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92029293 | ||||||
| chr14:92029294
|
T | A | 3 | a0007c0009t0031g0117a0007c0009t0056g0118a0007c0009t0057g0119 | 3 | HG02257.hp1 HG02559.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.202-3874A>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92029294 | ||||||
| chr14:92029295
|
T | A | 6 | a0005c0006t0015g0351a0005c0006t0015g0352a0005c0006t0015g0353others(3): Show | 6 | HG02451.hp1 HG02615.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.202-3875A>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92029295 | ||||||
| chr14:92029296
|
T | A | 31 | a0001c0001t0001g0167a0001c0018t0062g0321a0003c0003t0006g0323others(28): Show | 31 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.202-3876A>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92029296 | ||||||
| chr14:92029297
|
T | A | 1 | a0007c0009t0031g0117 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.202-3877A>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92029297 | ||||||
| chr14:92029298
|
T | A | 1 | a0002c0002t0054g0290 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.202-3878A>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92029298 | ||||||
| chr14:92029299
|
T | A | 10 | a0003c0003t0006g0343a0003c0003t0007g0344a0004c0005t0018g0121others(7): Show | 10 | HG01069.hp2 HG01071.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.202-3879A>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92029299 | ||||||
| chr14:92029299
|
T | G | 1 | a0002c0002t0002g0291 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.202-3879A>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92029299 | ||||||
| chr14:92029301
|
T | A | 1 | a0001c0020t0001g0026 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.202-3881A>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92029301 | ||||||
| chr14:92029414
|
GC | G | 7 | a0004c0005t0018g0121a0004c0005t0018g0124a0004c0005t0018g0126others(4): Show | 7 | HG01069.hp2 HG01071.hp2 HG03831.hp1 others(4): Show |
intron_variant | MODIFIER | c.201+3777delG | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92029414 | ||||||
| chr14:92029456
|
C | T | 4 | a0003c0003t0006g0348a0009c0012t0032g0129a0009c0012t0032g0130others(1): Show | 4 | HG02818.hp2 HG02965.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.201+3736G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92029456 | ||||||
| chr14:92029537
|
G | A | 9 | a0005c0006t0015g0351a0005c0006t0015g0352a0005c0006t0015g0353others(6): Show | 9 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.201+3655C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92029537 | ||||||
| chr14:92029578
|
A | T | 1 | a0002c0002t0002g0241 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.201+3614T>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92029578 | ||||||
| chr14:92029618
|
T | C | 1 | a0002c0029t0008g0231 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.201+3574A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92029618 | ||||||
| chr14:92029630
|
AAG | A | 30 | a0001c0001t0005g0085a0001c0001t0005g0086a0001c0001t0005g0087others(27): Show | 30 | HG00323.hp1 HG01069.hp1 HG01167.hp2 others(27): Show |
intron_variant | MODIFIER | c.201+3560_201+3561d others(4): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92029630 | ||||||
| chr14:92029633
|
A | G | 30 | a0001c0001t0005g0085a0001c0001t0005g0086a0001c0001t0005g0087others(27): Show | 30 | HG00323.hp1 HG01069.hp1 HG01167.hp2 others(27): Show |
intron_variant | MODIFIER | c.201+3559T>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92029633 | ||||||
| chr14:92029634
|
A | T | 30 | a0001c0001t0005g0085a0001c0001t0005g0086a0001c0001t0005g0087others(27): Show | 30 | HG00323.hp1 HG01069.hp1 HG01167.hp2 others(27): Show |
intron_variant | MODIFIER | c.201+3558T>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92029634 | ||||||
| chr14:92029635
|
A | T | 30 | a0001c0001t0005g0085a0001c0001t0005g0086a0001c0001t0005g0087others(27): Show | 30 | HG00323.hp1 HG01069.hp1 HG01167.hp2 others(27): Show |
intron_variant | MODIFIER | c.201+3557T>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92029635 | ||||||
| chr14:92029636
|
A | T | 30 | a0001c0001t0005g0085a0001c0001t0005g0086a0001c0001t0005g0087others(27): Show | 30 | HG00323.hp1 HG01069.hp1 HG01167.hp2 others(27): Show |
intron_variant | MODIFIER | c.201+3556T>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92029636 | ||||||
| chr14:92029637
|
C | T | 30 | a0001c0001t0005g0085a0001c0001t0005g0086a0001c0001t0005g0087others(27): Show | 30 | HG00323.hp1 HG01069.hp1 HG01167.hp2 others(27): Show |
intron_variant | MODIFIER | c.201+3555G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92029637 | ||||||
| chr14:92029688
|
AAC | A | 8 | a0007c0009t0031g0117a0007c0009t0031g0120a0007c0009t0056g0118others(5): Show | 8 | HG01109.hp1 HG02055.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.201+3502_201+3503d others(4): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92029688 | ||||||
| chr14:92029802
|
G | T | 2 | a0002c0002t0002g0218a0002c0002t0002g0219 | 2 | HG03492.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.201+3390C>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92029802 | ||||||
| chr14:92029899
|
T | C | 1 | a0001c0001t0028g0304 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.201+3293A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92029899 | ||||||
| chr14:92029923
|
C | T | 8 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(5): Show | 8 | HG02056.hp2 NA18952.hp2 NA18979.hp1 others(5): Show |
intron_variant | MODIFIER | c.201+3269G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92029923 | ||||||
| chr14:92030046
|
T | A | 171 | a0001c0001t0004g0292a0001c0001t0005g0085a0001c0001t0005g0086others(168): Show | 175 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.201+3146A>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92030046 | ||||||
| chr14:92030057
|
C | T | 2 | a0002c0002t0002g0218a0002c0002t0002g0219 | 2 | HG03492.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.201+3135G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92030057 | ||||||
| chr14:92030065
|
C | T | 19 | a0001c0007t0013g0007a0001c0007t0013g0308a0001c0007t0013g0309others(16): Show | 20 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.201+3127G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92030065 | ||||||
| chr14:92030083
|
G | A | 19 | a0001c0007t0013g0007a0001c0007t0013g0308a0001c0007t0013g0309others(16): Show | 20 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.201+3109C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92030083 | ||||||
| chr14:92030113
|
C | T | 7 | a0001c0010t0020g0174a0001c0010t0020g0175a0001c0010t0020g0176others(4): Show | 7 | HG02145.hp1 HG02486.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.201+3079G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92030113 | ||||||
| chr14:92030147
|
AG | A | 4 | a0001c0007t0013g0007a0001c0007t0013g0308a0001c0007t0013g0309others(1): Show | 5 | HG02809.hp2 HG02970.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.201+3044delC | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92030147 | ||||||
| chr14:92030154
|
G | A | 4 | a0001c0007t0013g0007a0001c0007t0013g0308a0001c0007t0013g0309others(1): Show | 5 | HG02809.hp2 HG02970.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.201+3038C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92030154 | ||||||
| chr14:92030181
|
G | A | 2 | a0008c0008t0030g0114a0008c0008t0058g0113 | 2 | HG02723.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.201+3011C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92030181 | ||||||
| chr14:92030203
|
C | CA | 15 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0067others(12): Show | 15 | HG00642.hp1 HG01106.hp1 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.201+2988dupT | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92030203 | ||||||
| chr14:92030203
|
CA | C | 175 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(172): Show | 178 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.201+2988delT | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92030203 | ||||||
| chr14:92030203
|
CAA | C | 59 | a0001c0001t0049g0204a0001c0001t0060g0316a0001c0004t0019g0207others(56): Show | 60 | HG00408.hp2 HG00558.hp2 HG01168.hp1 others(57): Show |
intron_variant | MODIFIER | c.201+2987_201+2988d others(4): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92030203 | ||||||
| chr14:92030203
|
CAAA | C | 10 | a0001c0007t0013g0007a0001c0007t0013g0308a0001c0007t0013g0309others(7): Show | 11 | HG01109.hp1 HG02055.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.201+2986_201+2988d others(5): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92030203 | ||||||
| chr14:92030203
|
CAAAA | C | 9 | a0004c0005t0018g0121a0004c0005t0018g0124a0004c0005t0018g0126others(6): Show | 9 | HG01069.hp2 HG01071.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.201+2985_201+2988d others(6): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92030203 | ||||||
| chr14:92030269
|
T | C | 112 | a0001c0001t0004g0292a0001c0001t0049g0204a0001c0001t0060g0316others(109): Show | 115 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.201+2923A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92030269 | ||||||
| chr14:92030405
|
TTTTGAGA others(3): Show |
T | 1 | a0001c0001t0005g0086 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.201+2777_201+2786d others(12): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92030405 | ||||||
| chr14:92030511
|
C | T | 1 | a0001c0001t0001g0021 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.201+2681G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92030511 | ||||||
| chr14:92030587
|
A | G | 9 | a0005c0006t0015g0351a0005c0006t0015g0352a0005c0006t0015g0353others(6): Show | 9 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.201+2605T>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92030587 | ||||||
| chr14:92030626
|
A | G | 28 | a0001c0007t0013g0007a0001c0007t0013g0308a0001c0007t0013g0309others(25): Show | 29 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.201+2566T>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92030626 | ||||||
| chr14:92030627
|
C | T | 1 | a0001c0001t0005g0090 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.201+2565G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92030627 | ||||||
| chr14:92030897
|
CA | C | 112 | a0001c0001t0004g0292a0001c0001t0049g0204a0001c0001t0060g0316others(109): Show | 115 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.201+2294delT | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92030897 | ||||||
| chr14:92030978
|
T | TG | 140 | a0001c0001t0004g0292a0001c0001t0049g0204a0001c0001t0060g0316others(137): Show | 144 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.201+2213dupC | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92030978 | ||||||
| chr14:92031091
|
A | C | 1 | a0001c0001t0004g0020 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.201+2101T>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92031091 | ||||||
| chr14:92031105
|
A | T | 9 | a0005c0006t0015g0351a0005c0006t0015g0352a0005c0006t0015g0353others(6): Show | 9 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.201+2087T>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92031105 | ||||||
| chr14:92031306
|
A | G | 27 | a0001c0001t0001g0201a0001c0001t0003g0003a0001c0001t0003g0179others(24): Show | 28 | HG00280.hp1 HG01070.hp2 HG01074.hp2 others(25): Show |
intron_variant | MODIFIER | c.201+1886T>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92031306 | ||||||
| chr14:92031468
|
T | C | 4 | a0001c0007t0013g0007a0001c0007t0013g0308a0001c0007t0013g0309others(1): Show | 5 | HG02809.hp2 HG02970.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.201+1724A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92031468 | ||||||
| chr14:92031503
|
G | A | 1 | a0001c0001t0001g0071 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.201+1689C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92031503 | ||||||
| chr14:92031593
|
C | T | 9 | a0005c0006t0015g0351a0005c0006t0015g0352a0005c0006t0015g0353others(6): Show | 9 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.201+1599G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92031593 | ||||||
| chr14:92031646
|
C | A | 140 | a0001c0001t0004g0292a0001c0001t0049g0204a0001c0001t0060g0316others(137): Show | 144 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.201+1546G>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92031646 | ||||||
| chr14:92031689
|
A | G | 206 | a0001c0001t0004g0292a0001c0001t0005g0085a0001c0001t0005g0086others(203): Show | 210 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.201+1503T>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92031689 | ||||||
| chr14:92031716
|
T | C | 19 | a0001c0007t0013g0007a0001c0007t0013g0308a0001c0007t0013g0309others(16): Show | 20 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.201+1476A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92031716 | ||||||
| chr14:92031798
|
A | G | 3 | a0001c0001t0005g0087a0001c0001t0005g0089a0001c0001t0009g0088 | 3 | HG01884.hp1 HG02647.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.201+1394T>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92031798 | ||||||
| chr14:92031851
|
T | C | 276 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(273): Show | 281 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.201+1341A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92031851 | ||||||
| chr14:92032013
|
C | T | 4 | a0001c0007t0013g0007a0001c0007t0013g0308a0001c0007t0013g0309others(1): Show | 5 | HG02809.hp2 HG02970.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.201+1179G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92032013 | ||||||
| chr14:92032030
|
C | A | 1 | a0001c0001t0001g0072 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.201+1162G>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92032030 | ||||||
| chr14:92032159
|
C | T | 9 | a0005c0006t0015g0351a0005c0006t0015g0352a0005c0006t0015g0353others(6): Show | 9 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.201+1033G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92032159 | ||||||
| chr14:92032197
|
G | A | 1 | a0008c0008t0058g0113 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.201+995C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92032197 | ||||||
| chr14:92032234
|
G | A | 2 | a0001c0004t0025g0213a0001c0004t0037g0214 | 2 | HG02630.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.201+958C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92032234 | ||||||
| chr14:92032290
|
G | A | 4 | a0001c0007t0013g0007a0001c0007t0013g0308a0001c0007t0013g0309others(1): Show | 5 | HG02809.hp2 HG02970.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.201+902C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92032290 | ||||||
| chr14:92032340
|
G | A | 19 | a0001c0007t0013g0007a0001c0007t0013g0308a0001c0007t0013g0309others(16): Show | 20 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.201+852C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92032340 | ||||||
| chr14:92032363
|
C | G | 1 | a0001c0001t0028g0304 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.201+829G>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92032363 | ||||||
| chr14:92032370
|
C | T | 1 | a0001c0001t0028g0304 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.201+822G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92032370 | ||||||
| chr14:92032371
|
A | G | 1 | a0001c0001t0028g0304 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.201+821T>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92032371 | ||||||
| chr14:92032465
|
C | G | 1 | a0002c0002t0017g0240 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.201+727G>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92032465 | ||||||
| chr14:92032465
|
C | T | 1 | a0001c0001t0028g0304 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.201+727G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92032465 | ||||||
| chr14:92032480
|
T | G | 32 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(29): Show | 32 | HG00140.hp2 HG00280.hp2 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.201+712A>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92032480 | ||||||
| chr14:92032485
|
ATAT | A | 102 | a0001c0001t0004g0292a0001c0001t0060g0316a0002c0002t0002g0005others(99): Show | 105 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.201+704_201+706del others(3): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92032485 | ||||||
| chr14:92032562
|
T | C | 1 | a0001c0033t0001g0078 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.201+630A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92032562 | ||||||
| chr14:92032755
|
C | T | 15 | a0001c0007t0013g0007a0001c0007t0013g0308a0001c0007t0013g0309others(12): Show | 16 | HG01069.hp2 HG01071.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.201+437G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92032755 | ||||||
| chr14:92032767
|
A | G | 1 | a0002c0002t0002g0239 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.201+425T>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92032767 | ||||||
| chr14:92032780
|
C | T | 1 | a0020c0027t0003g0178 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.201+412G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92032780 | ||||||
| chr14:92032832
|
C | A | 24 | a0001c0018t0062g0321a0003c0003t0006g0323a0003c0003t0006g0325others(21): Show | 24 | HG00408.hp2 HG01978.hp2 HG02040.hp2 others(21): Show |
intron_variant | MODIFIER | c.201+360G>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92032832 | ||||||
| chr14:92032832
|
CA | C | 25 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0018others(22): Show | 25 | HG00323.hp2 HG01081.hp1 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.201+359delT | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92032832 | ||||||
| chr14:92032832
|
CAA | C | 14 | a0004c0005t0018g0121a0004c0005t0018g0124a0004c0005t0018g0126others(11): Show | 14 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.201+358_201+359del others(2): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92032832 | ||||||
| chr14:92032836
|
A | C | 4 | a0001c0007t0013g0007a0001c0007t0013g0308a0001c0007t0013g0309others(1): Show | 5 | HG02809.hp2 HG02970.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.201+356T>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92032836 | ||||||
| chr14:92033002
|
A | G | 7 | a0004c0005t0018g0121a0004c0005t0018g0124a0004c0005t0018g0126others(4): Show | 7 | HG01069.hp2 HG01071.hp2 HG03831.hp1 others(4): Show |
intron_variant | MODIFIER | c.201+190T>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92033002 | ||||||
| chr14:92033004
|
T | G | 32 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(29): Show | 32 | HG00140.hp2 HG00280.hp2 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.201+188A>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92033004 | ||||||
| chr14:92033137
|
G | A | 7 | a0001c0001t0001g0014a0001c0001t0001g0073a0001c0001t0001g0074others(4): Show | 7 | HG01074.hp1 HG01934.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.201+55C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92033137 | ||||||
| chr14:92033165
|
A | G | 1 | a0001c0001t0001g0171 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.201+27T>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 2/20 | chr14 | 92033165 | ||||||
| chr14:92033444
|
A | C | 3 | a0003c0003t0006g0323a0003c0003t0006g0325a0003c0003t0011g0322 | 3 | NA18971.hp1 NA19067.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.140-191T>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 1/20 | chr14 | 92033444 | ||||||
| chr14:92033464
|
G | A | 2 | a0002c0002t0002g0294a0002c0002t0002g0295 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.140-211C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 1/20 | chr14 | 92033464 | ||||||
| chr14:92033467
|
C | T | 27 | a0001c0001t0001g0201a0001c0001t0003g0003a0001c0001t0003g0179others(24): Show | 28 | HG00280.hp1 HG01070.hp2 HG01074.hp2 others(25): Show |
intron_variant | MODIFIER | c.140-214G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 1/20 | chr14 | 92033467 | ||||||
| chr14:92033504
|
G | A | 112 | a0001c0001t0004g0292a0001c0001t0049g0204a0001c0001t0060g0316others(109): Show | 115 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.140-251C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 1/20 | chr14 | 92033504 | ||||||
| chr14:92033512
|
G | A | 206 | a0001c0001t0004g0292a0001c0001t0005g0085a0001c0001t0005g0086others(203): Show | 210 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.140-259C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 1/20 | chr14 | 92033512 | ||||||
| chr14:92033640
|
G | GA | 4 | a0007c0009t0031g0117a0007c0009t0031g0120a0007c0009t0056g0118others(1): Show | 4 | HG02257.hp1 HG02559.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.140-388dupT | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 1/20 | chr14 | 92033640 | ||||||
| chr14:92033664
|
T | C | 112 | a0001c0001t0004g0292a0001c0001t0049g0204a0001c0001t0060g0316others(109): Show | 115 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.140-411A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 1/20 | chr14 | 92033664 | ||||||
| chr14:92034155
|
G | C | 4 | a0008c0008t0030g0114a0008c0008t0030g0116a0008c0008t0055g0115others(1): Show | 4 | HG01109.hp1 HG02055.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.140-902C>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 1/20 | chr14 | 92034155 | ||||||
| chr14:92034192
|
G | A | 9 | a0005c0006t0015g0351a0005c0006t0015g0352a0005c0006t0015g0353others(6): Show | 9 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.140-939C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 1/20 | chr14 | 92034192 | ||||||
| chr14:92034336
|
T | C | 3 | a0009c0012t0032g0129a0009c0012t0032g0130a0014c0034t0003g0128 | 3 | HG02818.hp2 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.140-1083A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 1/20 | chr14 | 92034336 | ||||||
| chr14:92034358
|
G | A | 9 | a0005c0006t0015g0351a0005c0006t0015g0352a0005c0006t0015g0353others(6): Show | 9 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.140-1105C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 1/20 | chr14 | 92034358 | ||||||
| chr14:92034382
|
T | C | 28 | a0001c0007t0013g0007a0001c0007t0013g0308a0001c0007t0013g0309others(25): Show | 29 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.140-1129A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 1/20 | chr14 | 92034382 | ||||||
| chr14:92034384
|
C | T | 1 | a0002c0002t0002g0234 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.140-1131G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 1/20 | chr14 | 92034384 | ||||||
| chr14:92034424
|
C | CA | 111 | a0001c0001t0004g0292a0001c0001t0049g0204a0001c0001t0060g0316others(108): Show | 114 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.140-1172dupT | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 1/20 | chr14 | 92034424 | ||||||
| chr14:92034424
|
C | CAAAAAAA others(5): Show |
1 | a0001c0007t0013g0308 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.140-1183_140-1172d others(14): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 1/20 | chr14 | 92034424 | ||||||
| chr14:92034424
|
C | CAAAAAAA others(6): Show |
10 | a0001c0007t0013g0007a0001c0007t0013g0309a0005c0006t0015g0351others(7): Show | 11 | HG02257.hp1 HG02451.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.140-1172_140-1171i others(15): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 1/20 | chr14 | 92034424 | ||||||
| chr14:92034424
|
C | CAAAAAAA others(7): Show |
3 | a0001c0007t0013g0310a0010c0013t0066g0355a0015c0022t0065g0357 | 3 | HG02055.hp1 HG02258.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.140-1172_140-1171i others(16): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 1/20 | chr14 | 92034424 | ||||||
| chr14:92034424
|
C | CAAAAAAA others(9): Show |
10 | a0004c0005t0018g0121a0004c0005t0018g0124a0004c0005t0018g0126others(7): Show | 10 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.140-1172_140-1171i others(18): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 1/20 | chr14 | 92034424 | ||||||
| chr14:92034424
|
C | CAAAAAAA others(10): Show |
1 | a0008c0008t0030g0114 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.140-1172_140-1171i others(19): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 1/20 | chr14 | 92034424 | ||||||
| chr14:92034594
|
C | T | 1 | a0001c0018t0062g0321 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.140-1341G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 1/20 | chr14 | 92034594 | ||||||
| chr14:92034609
|
G | A | 9 | a0005c0006t0015g0351a0005c0006t0015g0352a0005c0006t0015g0353others(6): Show | 9 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.140-1356C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 1/20 | chr14 | 92034609 | ||||||
| chr14:92034618
|
C | T | 19 | a0001c0007t0013g0007a0001c0007t0013g0308a0001c0007t0013g0309others(16): Show | 20 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.140-1365G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 1/20 | chr14 | 92034618 | ||||||
| chr14:92034740
|
C | G | 2 | a0002c0002t0002g0305a0002c0002t0021g0306 | 2 | HG01175.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.140-1487G>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 1/20 | chr14 | 92034740 | ||||||
| chr14:92034744
|
C | T | 7 | a0001c0010t0020g0174a0001c0010t0020g0175a0001c0010t0020g0176others(4): Show | 7 | HG02145.hp1 HG02486.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.140-1491G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 1/20 | chr14 | 92034744 | ||||||
| chr14:92034784
|
G | A | 4 | a0001c0007t0013g0007a0001c0007t0013g0308a0001c0007t0013g0309others(1): Show | 5 | HG02809.hp2 HG02970.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.140-1531C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 1/20 | chr14 | 92034784 | ||||||
| chr14:92035028
|
G | C | 9 | a0005c0006t0015g0351a0005c0006t0015g0352a0005c0006t0015g0353others(6): Show | 9 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.140-1775C>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 1/20 | chr14 | 92035028 | ||||||
| chr14:92035033
|
G | A | 1 | a0001c0018t0062g0321 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.140-1780C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 1/20 | chr14 | 92035033 | ||||||
| chr14:92035150
|
C | CA | 117 | a0001c0001t0004g0292a0001c0001t0005g0086a0001c0001t0005g0087others(114): Show | 119 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.140-1898dupT | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 1/20 | chr14 | 92035150 | ||||||
| chr14:92035532
|
T | C | 28 | a0001c0018t0062g0321a0003c0003t0006g0323a0003c0003t0006g0325others(25): Show | 28 | HG00408.hp2 HG01978.hp2 HG02040.hp2 others(25): Show |
intron_variant | MODIFIER | c.140-2279A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 1/20 | chr14 | 92035532 | ||||||
| chr14:92035534
|
T | TA | 14 | a0001c0001t0001g0171a0001c0001t0004g0081a0001c0007t0013g0007others(11): Show | 15 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.140-2282dupT | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 1/20 | chr14 | 92035534 | ||||||
| chr14:92035534
|
TA | T | 105 | a0001c0001t0001g0015a0001c0001t0004g0292a0001c0001t0049g0204others(102): Show | 108 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.140-2282delT | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 1/20 | chr14 | 92035534 | ||||||
| chr14:92035560
|
T | C | 2 | a0008c0008t0030g0116a0008c0008t0055g0115 | 2 | HG01109.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.140-2307A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 1/20 | chr14 | 92035560 | ||||||
| chr14:92035573
|
ATTTAT | A | 31 | a0001c0001t0005g0085a0001c0001t0005g0086a0001c0001t0005g0087others(28): Show | 31 | HG00323.hp1 HG01069.hp1 HG01167.hp2 others(28): Show |
intron_variant | MODIFIER | c.140-2325_140-2321d others(7): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 1/20 | chr14 | 92035573 | ||||||
| chr14:92035581
|
A | AT | 9 | a0002c0002t0002g0217a0002c0002t0002g0218a0002c0002t0002g0219others(6): Show | 9 | HG00735.hp1 HG02486.hp2 HG03225.hp1 others(6): Show |
intron_variant | MODIFIER | c.140-2329dupA | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 1/20 | chr14 | 92035581 | ||||||
| chr14:92035581
|
A | T | 3 | a0002c0002t0021g0216a0003c0003t0006g0323a0003c0003t0011g0322 | 3 | NA18971.hp1 NA19084.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.140-2328T>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 1/20 | chr14 | 92035581 | ||||||
| chr14:92035585
|
A | AT | 94 | a0001c0001t0004g0292a0001c0001t0049g0204a0001c0001t0060g0316others(91): Show | 97 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.140-2333dupA | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 1/20 | chr14 | 92035585 | ||||||
| chr14:92035585
|
A | ATTTT | 15 | a0001c0007t0013g0007a0001c0007t0013g0308a0001c0007t0013g0309others(12): Show | 16 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.140-2336_140-2333d others(6): Show |
TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 1/20 | chr14 | 92035585 | ||||||
| chr14:92035585
|
A | T | 126 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0014others(123): Show | 126 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.140-2332T>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 1/20 | chr14 | 92035585 | ||||||
| chr14:92035651
|
C | T | 112 | a0001c0001t0004g0292a0001c0001t0049g0204a0001c0001t0060g0316others(109): Show | 115 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.140-2398G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 1/20 | chr14 | 92035651 | ||||||
| chr14:92035726
|
C | T | 2 | a0004c0005t0018g0121a0004c0005t0033g0122 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.140-2473G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 1/20 | chr14 | 92035726 | ||||||
| chr14:92035782
|
T | C | 9 | a0005c0006t0015g0351a0005c0006t0015g0352a0005c0006t0015g0353others(6): Show | 9 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.140-2529A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 1/20 | chr14 | 92035782 | ||||||
| chr14:92035913
|
C | T | 112 | a0001c0001t0004g0292a0001c0001t0049g0204a0001c0001t0060g0316others(109): Show | 115 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.140-2660G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 1/20 | chr14 | 92035913 | ||||||
| chr14:92036141
|
T | G | 206 | a0001c0001t0004g0292a0001c0001t0005g0085a0001c0001t0005g0086others(203): Show | 210 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.140-2888A>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 1/20 | chr14 | 92036141 | ||||||
| chr14:92036293
|
T | C | 1 | a0001c0001t0027g0112 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.140-3040A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 1/20 | chr14 | 92036293 | ||||||
| chr14:92036347
|
G | A | 3 | a0007c0009t0031g0120a0007c0009t0056g0118a0007c0009t0057g0119 | 3 | HG02559.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.140-3094C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 1/20 | chr14 | 92036347 | ||||||
| chr14:92036496
|
C | T | 3 | a0009c0012t0032g0129a0009c0012t0032g0130a0014c0034t0003g0128 | 3 | HG02818.hp2 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.139+3051G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 1/20 | chr14 | 92036496 | ||||||
| chr14:92036515
|
G | C | 3 | a0001c0007t0013g0007a0001c0007t0013g0309a0001c0007t0013g0310 | 4 | HG02970.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.139+3032C>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 1/20 | chr14 | 92036515 | ||||||
| chr14:92036967
|
C | G | 7 | a0004c0005t0018g0121a0004c0005t0018g0124a0004c0005t0018g0126others(4): Show | 7 | HG01069.hp2 HG01071.hp2 HG03831.hp1 others(4): Show |
intron_variant | MODIFIER | c.139+2580G>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 1/20 | chr14 | 92036967 | ||||||
| chr14:92036998
|
G | A | 4 | a0001c0007t0013g0007a0001c0007t0013g0308a0001c0007t0013g0309others(1): Show | 5 | HG02809.hp2 HG02970.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.139+2549C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 1/20 | chr14 | 92036998 | ||||||
| chr14:92037002
|
T | G | 3 | a0002c0002t0022g0296a0002c0002t0022g0297a0002c0002t0022g0298 | 3 | HG02486.hp2 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.139+2545A>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 1/20 | chr14 | 92037002 | ||||||
| chr14:92037031
|
C | G | 31 | a0001c0001t0005g0085a0001c0001t0005g0086a0001c0001t0005g0087others(28): Show | 31 | HG00323.hp1 HG01069.hp1 HG01167.hp2 others(28): Show |
intron_variant | MODIFIER | c.139+2516G>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 1/20 | chr14 | 92037031 | ||||||
| chr14:92037232
|
T | C | 206 | a0001c0001t0004g0292a0001c0001t0005g0085a0001c0001t0005g0086others(203): Show | 210 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.139+2315A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 1/20 | chr14 | 92037232 | ||||||
| chr14:92037475
|
T | C | 1 | a0001c0001t0010g0203 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.139+2072A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 1/20 | chr14 | 92037475 | ||||||
| chr14:92037494
|
T | C | 27 | a0001c0001t0001g0201a0001c0001t0003g0003a0001c0001t0003g0179others(24): Show | 28 | HG00280.hp1 HG01070.hp2 HG01074.hp2 others(25): Show |
intron_variant | MODIFIER | c.139+2053A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 1/20 | chr14 | 92037494 | ||||||
| chr14:92037622
|
C | T | 1 | a0001c0035t0012g0084 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.139+1925G>A | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 1/20 | chr14 | 92037622 | ||||||
| chr14:92037662
|
T | C | 1 | a0001c0004t0039g0215 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.139+1885A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 1/20 | chr14 | 92037662 | ||||||
| chr14:92037674
|
G | A | 3 | a0001c0001t0027g0112a0002c0002t0002g0299a0002c0002t0002g0300 | 3 | HG03139.hp1 HG04184.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.139+1873C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 1/20 | chr14 | 92037674 | ||||||
| chr14:92037867
|
T | G | 28 | a0001c0018t0062g0321a0003c0003t0006g0323a0003c0003t0006g0325others(25): Show | 28 | HG00408.hp2 HG01978.hp2 HG02040.hp2 others(25): Show |
intron_variant | MODIFIER | c.139+1680A>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 1/20 | chr14 | 92037867 | ||||||
| chr14:92037887
|
T | G | 2 | a0002c0002t0002g0301a0002c0002t0002g0302 | 2 | HG03017.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.139+1660A>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 1/20 | chr14 | 92037887 | ||||||
| chr14:92037924
|
C | A | 138 | a0001c0001t0004g0292a0001c0001t0049g0204a0001c0001t0060g0316others(135): Show | 142 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.139+1623G>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 1/20 | chr14 | 92037924 | ||||||
| chr14:92038164
|
A | C | 11 | a0001c0007t0013g0007a0001c0007t0013g0308a0001c0007t0013g0309others(8): Show | 12 | HG01069.hp2 HG01071.hp2 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.139+1383T>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 1/20 | chr14 | 92038164 | ||||||
| chr14:92038258
|
G | A | 1 | a0002c0002t0002g0303 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.139+1289C>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 1/20 | chr14 | 92038258 | ||||||
| chr14:92038400
|
C | G | 1 | a0001c0001t0027g0083 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+1147G>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 1/20 | chr14 | 92038400 | ||||||
| chr14:92038629
|
T | TA | 102 | a0001c0001t0001g0082a0001c0001t0004g0292a0001c0001t0060g0316others(99): Show | 105 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.139+917dupT | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 1/20 | chr14 | 92038629 | ||||||
| chr14:92038734
|
T | C | 1 | a0001c0001t0028g0304 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.139+813A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 1/20 | chr14 | 92038734 | ||||||
| chr14:92038808
|
A | G | 14 | a0001c0007t0013g0007a0001c0007t0013g0308a0001c0007t0013g0309others(11): Show | 15 | HG01069.hp2 HG01071.hp2 HG02809.hp2 others(12): Show |
intron_variant | MODIFIER | c.139+739T>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 1/20 | chr14 | 92038808 | ||||||
| chr14:92038902
|
A | G | 7 | a0005c0006t0015g0351a0005c0006t0015g0352a0005c0006t0015g0353others(4): Show | 7 | HG02055.hp1 HG02451.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.139+645T>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 1/20 | chr14 | 92038902 | ||||||
| chr14:92038913
|
T | C | 2 | a0002c0002t0002g0305a0002c0002t0021g0306 | 2 | HG01175.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.139+634A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 1/20 | chr14 | 92038913 | ||||||
| chr14:92038971
|
C | G | 8 | a0007c0009t0031g0117a0007c0009t0031g0120a0007c0009t0056g0118others(5): Show | 8 | HG01109.hp1 HG02055.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.139+576G>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 1/20 | chr14 | 92038971 | ||||||
| chr14:92039002
|
C | G | 30 | a0001c0001t0005g0085a0001c0001t0005g0086a0001c0001t0005g0087others(27): Show | 30 | HG00323.hp1 HG01069.hp1 HG01167.hp2 others(27): Show |
intron_variant | MODIFIER | c.139+545G>C | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 1/20 | chr14 | 92039002 | ||||||
| chr14:92039003
|
T | C | 1 | a0002c0002t0002g0307 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.139+544A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 1/20 | chr14 | 92039003 | ||||||
| chr14:92039256
|
C | A | 275 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(272): Show | 280 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.139+291G>T | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 1/20 | chr14 | 92039256 | ||||||
| chr14:92039329
|
T | C | 4 | a0001c0007t0013g0007a0001c0007t0013g0308a0001c0007t0013g0309others(1): Show | 5 | HG02809.hp2 HG02970.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.139+218A>G | TRIP11 | ENSG00000100815.12 | transcript | ENST00000267622.8 | protein_coding | 1/20 | chr14 | 92039329 |