Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 9325 |
|---|---|
| ensemblid | ENSG00000103671.10 |
| hgncid | 12310 |
| symbol | TRIP4 |
| name | thyroid hormone receptor interactor 4 |
| refseq_nuc | NM_016213.5 |
| refseq_prot | NP_057297.2 |
| ensembl_nuc | ENST00000261884.8 |
| ensembl_prot | ENSP00000261884.3 |
| mane_status | MANE Select |
| chr | chr15 |
| start | 64387836 |
| end | 64455303 |
| strand | + |
| ver | v1.2 |
| region | chr15:64387836-64455303 |
| region5000 | chr15:64382836-64460303 |
| regionname0 | TRIP4_chr15_64387836_64455303 |
| regionname5000 | TRIP4_chr15_64382836_64460303 |
| 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 | 581 | 217 | 94 | 32 | 39 | 14 | 36 | 25 | TRIP4_chr15_64382836_64460303 | TRIP4 | copy fasta | chr15 | 64382836 | 64460303 |
| a0002 | 0/0 | 581 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | copy fasta | chr15 | 64382836 | 64460303 |
| a0003 | 0/0 | 581 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | copy fasta | chr15 | 64382836 | 64460303 |
| 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 | 0/1 | 1746 | 123 | 46 | 20 | 27 | 9 | 20 | TRIP4_chr15_64382836_64460303 | TRIP4 | copy fasta | chr15 | 64382836 | 64460303 |
| c0002 | 1/0 | 1746 | 53 | 30 | 0 | 11 | 1 | 10 | TRIP4_chr15_64382836_64460303 | TRIP4 | copy fasta | chr15 | 64382836 | 64460303 |
| c0003 | 0/0 | 1746 | 16 | 3 | 7 | 1 | 3 | 2 | TRIP4_chr15_64382836_64460303 | TRIP4 | copy fasta | chr15 | 64382836 | 64460303 |
| c0004 | 0/0 | 1746 | 9 | 0 | 4 | 0 | 1 | 4 | TRIP4_chr15_64382836_64460303 | TRIP4 | copy fasta | chr15 | 64382836 | 64460303 |
| c0005 | 0/0 | 1746 | 6 | 5 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | copy fasta | chr15 | 64382836 | 64460303 |
| c0006 | 0/0 | 1746 | 5 | 5 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | copy fasta | chr15 | 64382836 | 64460303 |
| c0007 | 0/0 | 1746 | 2 | 2 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | copy fasta | chr15 | 64382836 | 64460303 |
| c0008 | 0/0 | 1746 | 2 | 2 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | copy fasta | chr15 | 64382836 | 64460303 |
| c0009 | 0/0 | 1746 | 2 | 2 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | copy fasta | chr15 | 64382836 | 64460303 |
| c0010 | 0/0 | 1746 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | copy fasta | chr15 | 64382836 | 64460303 |
| c0011 | 0/0 | 1746 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | copy fasta | chr15 | 64382836 | 64460303 |
| 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 | 1/1 | 268 | 215 | 91 | 32 | 40 | 14 | 36 | TRIP4_chr15_64382836_64460303 | TRIP4 | copy fasta | chr15 | 64382836 | 64460303 |
| t0002 | 0/0 | 268 | 5 | 5 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | copy fasta | chr15 | 64382836 | 64460303 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0082 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0151 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| 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 | 0/1 | 1746 | 123 | 46 | 20 | 27 | 9 | 20 | TRIP4_chr15_64382836_64460303 | TRIP4 | copy fasta | chr15 | 64382836 | 64460303 |
| a0001c0002 | 1/0 | 1746 | 53 | 30 | 0 | 11 | 1 | 10 | TRIP4_chr15_64382836_64460303 | TRIP4 | copy fasta | chr15 | 64382836 | 64460303 |
| a0001c0003 | 0/0 | 1746 | 16 | 3 | 7 | 1 | 3 | 2 | TRIP4_chr15_64382836_64460303 | TRIP4 | copy fasta | chr15 | 64382836 | 64460303 |
| a0001c0004 | 0/0 | 1746 | 9 | 0 | 4 | 0 | 1 | 4 | TRIP4_chr15_64382836_64460303 | TRIP4 | copy fasta | chr15 | 64382836 | 64460303 |
| a0001c0005 | 0/0 | 1746 | 6 | 5 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | copy fasta | chr15 | 64382836 | 64460303 |
| a0001c0006 | 0/0 | 1746 | 5 | 5 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | copy fasta | chr15 | 64382836 | 64460303 |
| a0001c0007 | 0/0 | 1746 | 2 | 2 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | copy fasta | chr15 | 64382836 | 64460303 |
| a0001c0008 | 0/0 | 1746 | 2 | 2 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | copy fasta | chr15 | 64382836 | 64460303 |
| a0001c0010 | 0/0 | 1746 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | copy fasta | chr15 | 64382836 | 64460303 |
| a0002c0009 | 0/0 | 1746 | 2 | 2 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | copy fasta | chr15 | 64382836 | 64460303 |
| a0003c0011 | 0/0 | 1746 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | copy fasta | chr15 | 64382836 | 64460303 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2013 | 118 | 41 | 20 | 27 | 9 | 20 | TRIP4_chr15_64382836_64460303 | TRIP4 | copy fasta | chr15 | 64382836 | 64460303 |
| a0001c0001t0002 | 0/0 | 2013 | 5 | 5 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | copy fasta | chr15 | 64382836 | 64460303 |
| a0001c0002t0001 | 1/0 | 2013 | 53 | 30 | 0 | 11 | 1 | 10 | TRIP4_chr15_64382836_64460303 | TRIP4 | copy fasta | chr15 | 64382836 | 64460303 |
| a0001c0003t0001 | 0/0 | 2013 | 16 | 3 | 7 | 1 | 3 | 2 | TRIP4_chr15_64382836_64460303 | TRIP4 | copy fasta | chr15 | 64382836 | 64460303 |
| a0001c0004t0001 | 0/0 | 2013 | 9 | 0 | 4 | 0 | 1 | 4 | TRIP4_chr15_64382836_64460303 | TRIP4 | copy fasta | chr15 | 64382836 | 64460303 |
| a0001c0005t0001 | 0/0 | 2013 | 6 | 5 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | copy fasta | chr15 | 64382836 | 64460303 |
| a0001c0006t0001 | 0/0 | 2013 | 5 | 5 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | copy fasta | chr15 | 64382836 | 64460303 |
| a0001c0007t0001 | 0/0 | 2013 | 2 | 2 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | copy fasta | chr15 | 64382836 | 64460303 |
| a0001c0008t0001 | 0/0 | 2013 | 2 | 2 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | copy fasta | chr15 | 64382836 | 64460303 |
| a0001c0010t0001 | 0/0 | 2013 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | copy fasta | chr15 | 64382836 | 64460303 |
| a0002c0009t0001 | 0/0 | 2013 | 2 | 2 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | copy fasta | chr15 | 64382836 | 64460303 |
| a0003c0011t0001 | 0/0 | 2013 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | copy fasta | chr15 | 64382836 | 64460303 |
| 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 | 2 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0151 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0001t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0082 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0002t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0003t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0003t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0003t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0003t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0003t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0003t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0003t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0003t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0003t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0003t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0003t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0003t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0003t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0003t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0003t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0003t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0004t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0004t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0004t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0004t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0004t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0004t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0004t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0004t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0004t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0005t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0005t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0005t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0005t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0005t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0005t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0006t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0006t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0006t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0006t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0006t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0007t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0007t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0008t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0008t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0001c0010t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0002c0009t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0002c0009t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| a0003c0011t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0003 | t0001 | g0154 | EUR | GBR | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0090 | EUR | GBR | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0110 | EUR | GBR | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0122 | EUR | GBR | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG00323 | hp1 | a0001 | c0004 | t0001 | g0034 | EUR | FIN | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG00323 | hp2 | a0001 | c0003 | t0001 | g0183 | EUR | FIN | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | CHS | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | CHS | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG00621 | hp1 | a0001 | c0002 | t0001 | g0200 | EAS | CHS | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | CHS | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG00642 | hp2 | a0001 | c0003 | t0001 | g0152 | AMR | PUR | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG00733 | hp2 | a0001 | c0003 | t0001 | g0052 | AMR | PUR | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG01074 | hp2 | a0001 | c0003 | t0001 | g0146 | AMR | PUR | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG01109 | hp2 | a0001 | c0005 | t0001 | g0048 | AMR | PUR | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG01168 | hp2 | a0001 | c0004 | t0001 | g0218 | AMR | PUR | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG01169 | hp1 | a0001 | c0004 | t0001 | g0219 | AMR | PUR | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG01256 | hp1 | a0001 | c0003 | t0001 | g0147 | AMR | CLM | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | CLM | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG01261 | hp1 | a0001 | c0004 | t0001 | g0032 | AMR | CLM | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | CLM | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | CLM | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG01496 | hp2 | a0001 | c0003 | t0001 | g0148 | AMR | CLM | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0128 | EUR | IBS | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0126 | EUR | IBS | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0120 | EUR | IBS | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0127 | EUR | IBS | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG01884 | hp1 | a0001 | c0003 | t0001 | g0150 | AFR | ACB | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0056 | AFR | ACB | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | ACB | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG01934 | hp1 | a0001 | c0003 | t0001 | g0153 | AMR | PEL | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG01934 | hp2 | a0001 | c0004 | t0001 | g0035 | AMR | PEL | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PEL | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PEL | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02004 | hp2 | a0001 | c0003 | t0001 | g0108 | AMR | PEL | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02040 | hp1 | a0001 | c0003 | t0001 | g0002 | EAS | KHV | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | ACB | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0217 | AFR | ACB | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02071 | hp2 | a0001 | c0002 | t0001 | g0187 | EAS | KHV | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | KHV | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02083 | hp2 | a0001 | c0002 | t0001 | g0066 | EAS | KHV | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0189 | EAS | KHV | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | ACB | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02145 | hp2 | a0001 | c0002 | t0001 | g0057 | AFR | ACB | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | ACB | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02257 | hp2 | a0001 | c0005 | t0001 | g0197 | AFR | ACB | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02258 | hp2 | a0001 | c0002 | t0001 | g0081 | AFR | ACB | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0054 | AFR | ACB | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02280 | hp2 | a0001 | c0005 | t0001 | g0045 | AFR | ACB | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02451 | hp1 | a0001 | c0008 | t0001 | g0046 | AFR | ACB | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0198 | AFR | GWD | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02572 | hp2 | a0001 | c0005 | t0001 | g0050 | AFR | GWD | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02615 | hp2 | a0001 | c0002 | t0001 | g0074 | AFR | GWD | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02622 | hp1 | a0001 | c0002 | t0001 | g0078 | AFR | GWD | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02622 | hp2 | a0001 | c0006 | t0001 | g0076 | AFR | GWD | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0070 | AFR | GWD | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02698 | hp1 | a0001 | c0004 | t0001 | g0031 | SAS | PJL | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02717 | hp1 | a0001 | c0002 | t0001 | g0079 | AFR | GWD | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02723 | hp1 | a0001 | c0006 | t0001 | g0206 | AFR | GWD | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02735 | hp1 | a0001 | c0004 | t0001 | g0036 | SAS | PJL | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0216 | AFR | GWD | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0214 | AFR | GWD | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02818 | hp2 | a0002 | c0009 | t0001 | g0027 | AFR | GWD | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0067 | AFR | GWD | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02886 | hp2 | a0001 | c0007 | t0001 | g0030 | AFR | GWD | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02895 | hp2 | a0001 | c0002 | t0001 | g0055 | AFR | GWD | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02896 | hp2 | a0001 | c0002 | t0001 | g0212 | AFR | GWD | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02897 | hp2 | a0001 | c0002 | t0001 | g0211 | AFR | GWD | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02922 | hp2 | a0001 | c0006 | t0001 | g0075 | AFR | ESN | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0077 | AFR | ESN | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02970 | hp2 | a0001 | c0002 | t0001 | g0073 | AFR | ESN | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | ESN | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02976 | hp2 | a0001 | c0002 | t0001 | g0208 | AFR | ESN | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03041 | hp1 | a0001 | c0010 | t0001 | g0167 | AFR | GWD | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | MSL | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03098 | hp2 | a0001 | c0002 | t0001 | g0053 | AFR | MSL | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03130 | hp2 | a0001 | c0008 | t0001 | g0047 | AFR | ESN | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | ESN | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03139 | hp2 | a0001 | c0002 | t0001 | g0069 | AFR | ESN | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03195 | hp1 | a0001 | c0002 | t0001 | g0038 | AFR | ESN | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03195 | hp2 | a0001 | c0007 | t0001 | g0029 | AFR | ESN | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | MSL | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | MSL | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03225 | hp2 | a0001 | c0002 | t0001 | g0080 | AFR | MSL | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0215 | AFR | MSL | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03453 | hp2 | a0001 | c0005 | t0001 | g0049 | AFR | MSL | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03486 | hp1 | a0001 | c0006 | t0001 | g0196 | AFR | MSL | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | MSL | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03490 | hp2 | a0001 | c0002 | t0001 | g0083 | SAS | PJL | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0043 | SAS | PJL | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0084 | SAS | PJL | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | ESN | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03516 | hp2 | a0001 | c0002 | t0001 | g0184 | AFR | ESN | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | GWD | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03540 | hp2 | a0001 | c0002 | t0001 | g0064 | AFR | GWD | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0213 | AFR | MSL | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | MSL | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03688 | hp1 | a0001 | c0003 | t0001 | g0111 | SAS | STU | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03688 | hp2 | a0001 | c0002 | t0001 | g0062 | SAS | STU | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03704 | hp1 | a0001 | c0004 | t0001 | g0033 | SAS | PJL | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03704 | hp2 | a0001 | c0004 | t0001 | g0037 | SAS | PJL | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0190 | SAS | BEB | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0145 | SAS | BEB | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | BEB | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03942 | hp2 | a0001 | c0002 | t0001 | g0060 | SAS | BEB | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG04184 | hp1 | a0001 | c0003 | t0001 | g0107 | SAS | BEB | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0085 | SAS | BEB | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0061 | SAS | STU | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | STU | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | STU | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0063 | SAS | STU | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | STU | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | STU | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | YRI | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | YRI | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA18906 | hp2 | a0001 | c0002 | t0001 | g0209 | AFR | YRI | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0192 | EAS | JPT | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA18972 | hp2 | a0001 | c0002 | t0001 | g0188 | EAS | JPT | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA18987 | hp2 | a0001 | c0002 | t0001 | g0099 | EAS | JPT | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA18993 | hp1 | a0001 | c0002 | t0001 | g0191 | EAS | JPT | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA18993 | hp2 | a0003 | c0011 | t0001 | g0114 | EAS | JPT | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA19043 | hp1 | a0001 | c0005 | t0001 | g0051 | AFR | LWK | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | LWK | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA19054 | hp1 | a0001 | c0002 | t0001 | g0194 | EAS | JPT | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA19067 | hp1 | a0001 | c0002 | t0001 | g0195 | EAS | JPT | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA19083 | hp1 | a0001 | c0002 | t0001 | g0044 | EAS | JPT | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | YRI | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0072 | AFR | ASW | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ASW | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0193 | EUR | TSI | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA20752 | hp2 | a0001 | c0003 | t0001 | g0156 | EUR | TSI | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0087 | EUR | TSI | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0131 | EUR | TSI | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | GIH | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0065 | SAS | GIH | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02109 | hp2 | a0001 | c0002 | t0001 | g0039 | AFR | ACB | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02486 | hp1 | a0001 | c0003 | t0001 | g0112 | AFR | ACB | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02486 | hp2 | a0001 | c0006 | t0001 | g0205 | AFR | ACB | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | ACB | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0210 | AFR | ACB | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03471 | hp1 | a0001 | c0002 | t0001 | g0068 | AFR | MSL | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG03471 | hp2 | a0002 | c0009 | t0001 | g0026 | AFR | MSL | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG06807 | hp1 | a0001 | c0002 | t0001 | g0058 | AFR | USA | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | USA | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA20300 | hp1 | a0001 | c0002 | t0001 | g0059 | AFR | USA | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0207 | AFR | USA | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA21309 | hp1 | a0001 | c0003 | t0001 | g0149 | AFR | LWK | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | LWK | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0151 | REF | REF | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| homoSapiens_grch38 | hp1 | a0001 | c0002 | t0001 | g0082 | REF | REF | TRIP4_chr15_64382836_64460303 | TRIP4 | chr15 | 64382836 | 64460303 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:64397652
|
A | G | 1 | a0002 | 2 | HG02818.hp2 HG03471.hp2 |
missense_variant | MODERATE | c.452A>G | p.Asn151Ser | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 4/13 | 480/2013 | 452/1746 | 151/581 | chr15 | 64397652 | ||
| chr15:64406413
|
A | G | 1 | a0003 | 1 | NA18993.hp2 | missense_variant | MODERATE | c.781A>G | p.Lys261Glu | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 6/13 | 809/2013 | 781/1746 | 261/581 | chr15 | 64406413 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:64387884
|
G | C | 1 | a0001c0006 | 5 | HG02486.hp2 HG02622.hp2 HG02723.hp1 others(2): Show |
synonymous_variant | LOW | c.21G>C | p.Val7Val | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/13 | 49/2013 | 21/1746 | 7/581 | chr15 | 64387884 | ||
| chr15:64394099
|
G | A | 1 | a0001c0007 | 2 | HG02886.hp2 HG03195.hp2 |
synonymous_variant | LOW | c.255G>A | p.Gln85Gln | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 2/13 | 283/2013 | 255/1746 | 85/581 | chr15 | 64394099 | ||
| chr15:64397782
|
A | G | 1 | a0001c0008 | 2 | HG02451.hp1 HG03130.hp2 |
synonymous_variant | LOW | c.582A>G | p.Gln194Gln | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 4/13 | 610/2013 | 582/1746 | 194/581 | chr15 | 64397782 | ||
| chr15:64409766
|
C | T | 2 | a0001c0005a0001c0008 | 8 | HG01109.hp2 HG02257.hp2 HG02280.hp2 others(5): Show |
synonymous_variant | LOW | c.981C>T | p.Thr327Thr | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 7/13 | 1009/2013 | 981/1746 | 327/581 | chr15 | 64409766 | ||
| chr15:64414133
|
A | G | 1 | a0001c0004 | 9 | HG00323.hp1 HG01168.hp2 HG01169.hp1 others(6): Show |
synonymous_variant | LOW | c.1092A>G | p.Pro364Pro | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 8/13 | 1120/2013 | 1092/1746 | 364/581 | chr15 | 64414133 | ||
| chr15:64418564
|
C | T | 1 | a0001c0010 | 1 | HG03041.hp1 | synonymous_variant | LOW | c.1194C>T | p.Ala398Ala | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/13 | 1222/2013 | 1194/1746 | 398/581 | chr15 | 64418564 | ||
| chr15:64418628
|
T | C | 1 | a0001c0003 | 16 | HG00099.hp1 HG00323.hp2 HG00642.hp2 others(13): Show |
synonymous_variant | LOW | c.1258T>C | p.Leu420Leu | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/13 | 1286/2013 | 1258/1746 | 420/581 | chr15 | 64418628 | ||
| chr15:64445026
|
G | A | 9 | a0001c0001a0001c0003a0001c0004others(6): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
synonymous_variant | LOW | c.1596G>A | p.Glu532Glu | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/13 | 1624/2013 | 1596/1746 | 532/581 | chr15 | 64445026 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:64455254
|
G | C | 1 | a0001c0001t0002 | 5 | HG02055.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*190G>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 13/13 | 190 | chr15 | 64455254 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:64388027
|
G | A | 1 | a0001c0003t0001g0002 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.101+63G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64388027 | ||||||
| chr15:64388070
|
A | T | 2 | a0001c0004t0001g0218a0001c0004t0001g0219 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.101+106A>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64388070 | ||||||
| chr15:64388084
|
G | A | 1 | a0001c0001t0001g0003 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.101+120G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64388084 | ||||||
| chr15:64388143
|
T | C | 2 | a0001c0004t0001g0218a0001c0004t0001g0219 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.101+179T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64388143 | ||||||
| chr15:64388192
|
C | A | 26 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(23): Show | 27 | HG00642.hp1 HG00733.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.101+228C>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64388192 | ||||||
| chr15:64388193
|
A | G | 5 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0002g0215others(2): Show | 5 | HG02055.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.101+229A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64388193 | ||||||
| chr15:64388210
|
A | G | 6 | a0001c0002t0001g0207a0001c0002t0001g0208a0001c0002t0001g0209others(3): Show | 6 | HG02559.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.101+246A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64388210 | ||||||
| chr15:64388353
|
C | A | 8 | a0001c0002t0001g0207a0001c0002t0001g0208a0001c0002t0001g0209others(5): Show | 8 | HG02559.hp2 HG02886.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.101+389C>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64388353 | ||||||
| chr15:64388904
|
A | G | 3 | a0001c0001t0001g0028a0002c0009t0001g0026a0002c0009t0001g0027 | 3 | HG02818.hp2 HG03471.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.101+940A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64388904 | ||||||
| chr15:64388969
|
A | G | 2 | a0001c0006t0001g0205a0001c0006t0001g0206 | 2 | HG02486.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.101+1005A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64388969 | ||||||
| chr15:64389007
|
GGTTGGGG others(14): Show |
G | 9 | a0001c0004t0001g0031a0001c0004t0001g0032a0001c0004t0001g0033others(6): Show | 9 | HG00323.hp1 HG01168.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.101+1049_101+1069d others(23): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 64389007 | |||||
| chr15:64389031
|
T | G | 5 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0002g0215others(2): Show | 5 | HG02055.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.101+1067T>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64389031 | ||||||
| chr15:64389109
|
A | G | 1 | a0001c0001t0001g0204 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.101+1145A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64389109 | ||||||
| chr15:64389226
|
T | C | 5 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0002g0215others(2): Show | 5 | HG02055.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.101+1262T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64389226 | ||||||
| chr15:64389420
|
C | G | 1 | a0001c0001t0001g0203 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.101+1456C>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64389420 | ||||||
| chr15:64389578
|
A | G | 2 | a0001c0001t0001g0201a0001c0001t0001g0202 | 2 | HG01261.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.101+1614A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64389578 | ||||||
| chr15:64389708
|
C | CT | 10 | a0001c0001t0001g0199a0001c0002t0001g0198a0001c0002t0001g0200others(7): Show | 10 | HG00621.hp1 HG02055.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.101+1764dupT | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 64389708 | |||||
| chr15:64389708
|
CT | C | 15 | a0001c0001t0001g0004a0001c0001t0001g0040a0001c0001t0001g0041others(12): Show | 15 | HG00323.hp1 HG01167.hp2 HG01168.hp2 others(12): Show |
intron_variant | MODIFIER | c.101+1764delT | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 64389708 | |||||
| chr15:64389754
|
G | A | 1 | a0001c0002t0001g0043 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.101+1790G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64389754 | ||||||
| chr15:64389799
|
C | T | 5 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0002g0215others(2): Show | 5 | HG02055.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.101+1835C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64389799 | ||||||
| chr15:64389848
|
C | T | 1 | a0001c0007t0001g0030 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.101+1884C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64389848 | ||||||
| chr15:64389993
|
C | T | 1 | a0001c0006t0001g0196 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.101+2029C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64389993 | ||||||
| chr15:64390047
|
CAAATATA others(30): Show |
C | 2 | a0001c0002t0001g0044a0001c0004t0001g0031 | 2 | HG02698.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.101+2136_101+2172d others(39): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 64390047 | |||||
| chr15:64390154
|
C | A | 14 | a0001c0001t0001g0204a0001c0001t0002g0213a0001c0001t0002g0214others(11): Show | 14 | HG01109.hp2 HG02055.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.101+2190C>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64390154 | ||||||
| chr15:64390160
|
TA | T | 7 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0002g0213others(4): Show | 7 | HG02055.hp2 HG02615.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.101+2206delA | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 64390160 | |||||
| chr15:64390193
|
G | A | 1 | a0001c0003t0001g0052 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.101+2229G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64390193 | ||||||
| chr15:64390203
|
T | C | 8 | a0001c0005t0001g0045a0001c0005t0001g0048a0001c0005t0001g0049others(5): Show | 8 | HG01109.hp2 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.101+2239T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64390203 | ||||||
| chr15:64390242
|
A | G | 12 | a0001c0001t0001g0186a0001c0002t0001g0044a0001c0002t0001g0187others(9): Show | 12 | HG00621.hp1 HG02071.hp2 HG02129.hp1 others(9): Show |
intron_variant | MODIFIER | c.101+2278A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64390242 | ||||||
| chr15:64390318
|
C | T | 1 | a0001c0001t0001g0204 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.101+2354C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64390318 | ||||||
| chr15:64390442
|
C | G | 5 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0002g0215others(2): Show | 5 | HG02055.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.101+2478C>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64390442 | ||||||
| chr15:64390460
|
C | CA | 9 | a0001c0004t0001g0031a0001c0004t0001g0032a0001c0004t0001g0033others(6): Show | 9 | HG00323.hp1 HG01168.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.101+2507dupA | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 64390460 | |||||
| chr15:64390505
|
A | G | 2 | a0001c0001t0001g0042a0001c0001t0001g0185 | 2 | HG02080.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.101+2541A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64390505 | ||||||
| chr15:64390537
|
A | G | 141 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(138): Show | 141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.101+2573A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64390537 | ||||||
| chr15:64390628
|
C | T | 1 | a0001c0002t0001g0184 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.101+2664C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64390628 | ||||||
| chr15:64390664
|
G | T | 12 | a0001c0001t0001g0186a0001c0002t0001g0044a0001c0002t0001g0187others(9): Show | 12 | HG00621.hp1 HG02071.hp2 HG02129.hp1 others(9): Show |
intron_variant | MODIFIER | c.101+2700G>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64390664 | ||||||
| chr15:64390720
|
G | A | 1 | a0001c0005t0001g0045 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.101+2756G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64390720 | ||||||
| chr15:64390861
|
C | T | 6 | a0001c0002t0001g0207a0001c0002t0001g0208a0001c0002t0001g0209others(3): Show | 6 | HG02559.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.101+2897C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64390861 | ||||||
| chr15:64391097
|
T | G | 2 | a0001c0001t0001g0040a0001c0001t0001g0086 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.102-2849T>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64391097 | ||||||
| chr15:64391179
|
C | T | 1 | a0001c0007t0001g0029 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.102-2767C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64391179 | ||||||
| chr15:64391302
|
G | A | 1 | a0001c0001t0001g0204 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.102-2644G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64391302 | ||||||
| chr15:64391359
|
G | C | 14 | a0001c0001t0001g0204a0001c0001t0002g0213a0001c0001t0002g0214others(11): Show | 14 | HG01109.hp2 HG02055.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.102-2587G>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64391359 | ||||||
| chr15:64391447
|
A | G | 1 | a0001c0001t0001g0203 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.102-2499A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64391447 | ||||||
| chr15:64391450
|
C | T | 3 | a0001c0002t0001g0083a0001c0002t0001g0084a0001c0002t0001g0085 | 3 | HG03490.hp2 HG03492.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.102-2496C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64391450 | ||||||
| chr15:64391498
|
A | G | 5 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0002g0215others(2): Show | 5 | HG02055.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.102-2448A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64391498 | ||||||
| chr15:64391682
|
C | A | 12 | a0001c0001t0001g0040a0001c0001t0001g0042a0001c0001t0001g0086others(9): Show | 12 | HG00099.hp2 HG02080.hp2 HG03239.hp2 others(9): Show |
intron_variant | MODIFIER | c.102-2264C>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64391682 | ||||||
| chr15:64391844
|
G | A | 1 | a0001c0008t0001g0046 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.102-2102G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64391844 | ||||||
| chr15:64391883
|
A | G | 8 | a0001c0005t0001g0045a0001c0005t0001g0048a0001c0005t0001g0049others(5): Show | 8 | HG01109.hp2 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.102-2063A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64391883 | ||||||
| chr15:64391889
|
T | C | 8 | a0001c0002t0001g0053a0001c0002t0001g0054a0001c0002t0001g0055others(5): Show | 8 | HG01884.hp2 HG02145.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.102-2057T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64391889 | ||||||
| chr15:64391911
|
C | T | 5 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0002g0215others(2): Show | 5 | HG02055.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.102-2035C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64391911 | ||||||
| chr15:64391970
|
C | CA | 52 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0041others(49): Show | 52 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.102-1952dupA | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 64391970 | |||||
| chr15:64391970
|
C | CAA | 6 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(3): Show | 6 | HG01109.hp1 HG01261.hp2 HG03942.hp2 others(3): Show |
intron_variant | MODIFIER | c.102-1953_102-1952d others(4): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 64391970 | |||||
| chr15:64391970
|
CA | C | 27 | a0001c0001t0001g0023a0001c0001t0002g0215a0001c0001t0002g0216others(24): Show | 27 | HG00323.hp1 HG00323.hp2 HG01168.hp2 others(24): Show |
intron_variant | MODIFIER | c.102-1952delA | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 64391970 | |||||
| chr15:64391970
|
CAA | C | 7 | a0001c0005t0001g0045a0001c0005t0001g0048a0001c0005t0001g0049others(4): Show | 7 | HG01109.hp2 HG02280.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.102-1953_102-1952d others(4): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 64391970 | |||||
| chr15:64392006
|
C | T | 8 | a0001c0001t0001g0041a0001c0001t0001g0097a0001c0001t0001g0120others(5): Show | 8 | HG00140.hp2 HG01109.hp1 HG01167.hp2 others(5): Show |
intron_variant | MODIFIER | c.102-1940C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64392006 | ||||||
| chr15:64392046
|
G | A | 1 | a0001c0001t0001g0124 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.102-1900G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64392046 | ||||||
| chr15:64392073
|
G | C | 1 | a0001c0005t0001g0197 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.102-1873G>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64392073 | ||||||
| chr15:64392112
|
T | C | 2 | a0001c0002t0001g0207a0001c0002t0001g0208 | 2 | HG02976.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.102-1834T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64392112 | ||||||
| chr15:64392306
|
A | C | 1 | a0001c0001t0001g0204 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.102-1640A>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64392306 | ||||||
| chr15:64392599
|
C | T | 1 | a0001c0001t0001g0204 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.102-1347C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64392599 | ||||||
| chr15:64392832
|
C | T | 1 | a0001c0002t0001g0208 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.102-1114C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64392832 | ||||||
| chr15:64393005
|
G | A | 1 | a0001c0001t0001g0098 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.102-941G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64393005 | ||||||
| chr15:64393008
|
G | A | 110 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(107): Show | 110 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(107): Show |
intron_variant | MODIFIER | c.102-938G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64393008 | ||||||
| chr15:64393151
|
A | AT | 13 | a0001c0001t0001g0071a0001c0001t0001g0119a0001c0001t0001g0181others(10): Show | 13 | HG01069.hp1 HG01071.hp1 HG02080.hp2 others(10): Show |
intron_variant | MODIFIER | c.102-775dupT | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 64393151 | |||||
| chr15:64393151
|
AT | A | 16 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(13): Show | 16 | HG00323.hp1 HG00642.hp1 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.102-775delT | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 64393151 | |||||
| chr15:64393338
|
T | TA | 39 | a0001c0001t0001g0041a0001c0001t0001g0095a0001c0001t0001g0097others(36): Show | 39 | HG00140.hp2 HG01069.hp1 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.102-607dupA | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 64393338 | |||||
| chr15:64393446
|
C | T | 3 | a0001c0001t0001g0040a0001c0001t0001g0086a0001c0001t0001g0094 | 3 | HG03491.hp1 HG03492.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.102-500C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64393446 | ||||||
| chr15:64393597
|
C | T | 5 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0002g0215others(2): Show | 5 | HG02055.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.102-349C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64393597 | ||||||
| chr15:64393734
|
C | T | 8 | a0001c0005t0001g0045a0001c0005t0001g0048a0001c0005t0001g0049others(5): Show | 8 | HG01109.hp2 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.102-212C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64393734 | ||||||
| chr15:64393891
|
T | C | 1 | a0001c0001t0001g0105 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.102-55T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64393891 | ||||||
| chr15:64393908
|
T | C | 1 | a0001c0001t0001g0014 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.102-38T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 1/12 | chr15 | 64393908 | ||||||
| chr15:64394188
|
T | A | 13 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(10): Show | 13 | HG02109.hp1 HG02258.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.271+73T>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 2/12 | chr15 | 64394188 | ||||||
| chr15:64394211
|
C | T | 3 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144 | 3 | HG01071.hp2 HG02683.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.271+96C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 2/12 | chr15 | 64394211 | ||||||
| chr15:64394233
|
G | A | 141 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(138): Show | 141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.271+118G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 2/12 | chr15 | 64394233 | ||||||
| chr15:64394429
|
C | A | 8 | a0001c0002t0001g0207a0001c0002t0001g0208a0001c0002t0001g0209others(5): Show | 8 | HG02559.hp2 HG02886.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.271+314C>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 2/12 | chr15 | 64394429 | ||||||
| chr15:64394504
|
C | T | 8 | a0001c0001t0001g0118a0001c0001t0001g0174a0001c0001t0001g0175others(5): Show | 8 | HG02004.hp1 HG02976.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.271+389C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 2/12 | chr15 | 64394504 | ||||||
| chr15:64394567
|
T | A | 9 | a0001c0004t0001g0031a0001c0004t0001g0032a0001c0004t0001g0033others(6): Show | 9 | HG00323.hp1 HG01168.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.271+452T>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 2/12 | chr15 | 64394567 | ||||||
| chr15:64394591
|
C | T | 14 | a0001c0001t0001g0204a0001c0001t0002g0213a0001c0001t0002g0214others(11): Show | 14 | HG01109.hp2 HG02055.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.271+476C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 2/12 | chr15 | 64394591 | ||||||
| chr15:64394604
|
C | CA | 19 | a0001c0001t0001g0071a0001c0001t0001g0118a0001c0001t0001g0119others(16): Show | 19 | HG00323.hp1 HG01168.hp2 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.271+507dupA | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 64394604 | |||||
| chr15:64394724
|
T | C | 1 | a0001c0001t0001g0145 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.271+609T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 2/12 | chr15 | 64394724 | ||||||
| chr15:64395105
|
C | CA | 34 | a0001c0001t0001g0040a0001c0001t0001g0042a0001c0001t0001g0086others(31): Show | 34 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(31): Show |
intron_variant | MODIFIER | c.272-290dupA | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 64395105 | |||||
| chr15:64395360
|
CTGTG | C | 2 | a0001c0002t0001g0072a0001c0002t0001g0073 | 2 | HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.272-28_272-25delGT others(2): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 64395360 | |||||
| chr15:64395582
|
G | A | 2 | a0001c0001t0001g0040a0001c0001t0001g0086 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.405+51G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 3/12 | chr15 | 64395582 | ||||||
| chr15:64395585
|
T | A | 2 | a0001c0001t0001g0186a0001c0002t0001g0200 | 2 | HG00621.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.405+54T>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 3/12 | chr15 | 64395585 | ||||||
| chr15:64395739
|
CT | C | 18 | a0001c0002t0001g0074a0001c0002t0001g0207a0001c0002t0001g0208others(15): Show | 18 | HG00323.hp1 HG01168.hp2 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.405+224delT | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr15 | 64395739 | |||||
| chr15:64395755
|
T | C | 1 | a0001c0001t0002g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.405+224T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 3/12 | chr15 | 64395755 | ||||||
| chr15:64395804
|
G | C | 1 | a0001c0001t0001g0204 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.405+273G>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 3/12 | chr15 | 64395804 | ||||||
| chr15:64395865
|
C | T | 8 | a0001c0002t0001g0207a0001c0002t0001g0208a0001c0002t0001g0209others(5): Show | 8 | HG02559.hp2 HG02886.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.405+334C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 3/12 | chr15 | 64395865 | ||||||
| chr15:64395890
|
G | A | 2 | a0001c0001t0001g0042a0001c0001t0001g0185 | 2 | HG02080.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.405+359G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 3/12 | chr15 | 64395890 | ||||||
| chr15:64395912
|
CTT | C | 141 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(138): Show | 141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.405+394_405+395del others(2): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr15 | 64395912 | |||||
| chr15:64395940
|
G | A | 110 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(107): Show | 110 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(107): Show |
intron_variant | MODIFIER | c.405+409G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 3/12 | chr15 | 64395940 | ||||||
| chr15:64396082
|
G | A | 5 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0002g0215others(2): Show | 5 | HG02055.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.405+551G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 3/12 | chr15 | 64396082 | ||||||
| chr15:64396124
|
G | T | 5 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0002g0215others(2): Show | 5 | HG02055.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.405+593G>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 3/12 | chr15 | 64396124 | ||||||
| chr15:64396131
|
G | A | 141 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(138): Show | 141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.405+600G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 3/12 | chr15 | 64396131 | ||||||
| chr15:64396201
|
G | A | 1 | a0001c0001t0001g0113 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.405+670G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 3/12 | chr15 | 64396201 | ||||||
| chr15:64396266
|
C | CT | 12 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0002g0215others(9): Show | 12 | HG02055.hp2 HG02071.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.405+763dupT | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr15 | 64396266 | |||||
| chr15:64396266
|
CT | C | 34 | a0001c0001t0001g0007a0001c0002t0001g0038a0001c0002t0001g0039others(31): Show | 34 | HG00323.hp1 HG01109.hp2 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.405+763delT | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr15 | 64396266 | |||||
| chr15:64396266
|
CTTTTTTT | C | 5 | a0001c0001t0001g0119a0001c0001t0001g0123a0001c0001t0001g0145others(2): Show | 5 | HG02071.hp1 HG02257.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.405+757_405+763del others(7): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr15 | 64396266 | |||||
| chr15:64396266
|
CTTTTTTT others(1): Show |
C | 104 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(101): Show | 104 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(101): Show |
intron_variant | MODIFIER | c.405+756_405+763del others(8): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr15 | 64396266 | |||||
| chr15:64396266
|
CTTTTTTT others(5): Show |
C | 3 | a0001c0002t0001g0083a0001c0002t0001g0084a0001c0002t0001g0085 | 3 | HG03490.hp2 HG03492.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.405+752_405+763del others(12): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr15 | 64396266 | |||||
| chr15:64396337
|
C | T | 7 | a0001c0005t0001g0045a0001c0005t0001g0048a0001c0005t0001g0049others(4): Show | 7 | HG01109.hp2 HG02280.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.405+806C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 3/12 | chr15 | 64396337 | ||||||
| chr15:64396560
|
T | A | 21 | a0001c0001t0001g0186a0001c0002t0001g0044a0001c0002t0001g0053others(18): Show | 21 | HG00621.hp1 HG01884.hp2 HG02071.hp2 others(18): Show |
intron_variant | MODIFIER | c.405+1029T>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 3/12 | chr15 | 64396560 | ||||||
| chr15:64396707
|
G | C | 1 | a0001c0001t0001g0089 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.406-899G>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 3/12 | chr15 | 64396707 | ||||||
| chr15:64396753
|
G | A | 1 | a0001c0001t0001g0204 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.406-853G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 3/12 | chr15 | 64396753 | ||||||
| chr15:64396842
|
A | G | 8 | a0001c0002t0001g0207a0001c0002t0001g0208a0001c0002t0001g0209others(5): Show | 8 | HG02559.hp2 HG02886.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.406-764A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 3/12 | chr15 | 64396842 | ||||||
| chr15:64396923
|
C | T | 8 | a0001c0002t0001g0207a0001c0002t0001g0208a0001c0002t0001g0209others(5): Show | 8 | HG02559.hp2 HG02886.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.406-683C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 3/12 | chr15 | 64396923 | ||||||
| chr15:64396935
|
T | C | 1 | a0001c0001t0002g0215 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.406-671T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 3/12 | chr15 | 64396935 | ||||||
| chr15:64397043
|
T | C | 1 | a0001c0001t0001g0125 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.406-563T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 3/12 | chr15 | 64397043 | ||||||
| chr15:64397220
|
C | T | 22 | a0001c0001t0001g0204a0001c0001t0002g0213a0001c0001t0002g0214others(19): Show | 22 | HG01109.hp2 HG02055.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.406-386C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 3/12 | chr15 | 64397220 | ||||||
| chr15:64397241
|
T | C | 2 | a0001c0004t0001g0036a0001c0004t0001g0037 | 2 | HG02735.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.406-365T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 3/12 | chr15 | 64397241 | ||||||
| chr15:64397458
|
C | G | 1 | a0001c0003t0001g0156 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.406-148C>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 3/12 | chr15 | 64397458 | ||||||
| chr15:64397939
|
C | T | 1 | a0001c0002t0001g0069 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.618+121C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 4/12 | chr15 | 64397939 | ||||||
| chr15:64397975
|
G | A | 1 | a0001c0001t0001g0174 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.618+157G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 4/12 | chr15 | 64397975 | ||||||
| chr15:64397993
|
C | T | 1 | a0001c0008t0001g0047 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.618+175C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 4/12 | chr15 | 64397993 | ||||||
| chr15:64398190
|
C | T | 111 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(108): Show | 111 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(108): Show |
intron_variant | MODIFIER | c.618+372C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 4/12 | chr15 | 64398190 | ||||||
| chr15:64398322
|
C | G | 5 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0002g0215others(2): Show | 5 | HG02055.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.618+504C>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 4/12 | chr15 | 64398322 | ||||||
| chr15:64398424
|
C | CA | 52 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0096others(49): Show | 52 | HG00323.hp1 HG00621.hp1 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.618+632dupA | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr15 | 64398424 | |||||
| chr15:64398424
|
CA | C | 16 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(13): Show | 17 | HG01167.hp1 HG01167.hp2 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.618+632delA | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr15 | 64398424 | |||||
| chr15:64398527
|
C | T | 1 | a0001c0002t0001g0053 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.618+709C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 4/12 | chr15 | 64398527 | ||||||
| chr15:64398555
|
G | T | 2 | a0001c0007t0001g0029a0001c0007t0001g0030 | 2 | HG02886.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.618+737G>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 4/12 | chr15 | 64398555 | ||||||
| chr15:64398561
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.618+743C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 4/12 | chr15 | 64398561 | ||||||
| chr15:64398573
|
A | G | 141 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(138): Show | 141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.618+755A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 4/12 | chr15 | 64398573 | ||||||
| chr15:64398624
|
A | G | 8 | a0001c0002t0001g0207a0001c0002t0001g0208a0001c0002t0001g0209others(5): Show | 8 | HG02559.hp2 HG02886.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.618+806A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 4/12 | chr15 | 64398624 | ||||||
| chr15:64398667
|
G | A | 5 | a0001c0006t0001g0075a0001c0006t0001g0076a0001c0006t0001g0196others(2): Show | 5 | HG02486.hp2 HG02622.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.618+849G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 4/12 | chr15 | 64398667 | ||||||
| chr15:64398682
|
G | C | 2 | a0001c0001t0001g0018a0001c0001t0001g0019 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.618+864G>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 4/12 | chr15 | 64398682 | ||||||
| chr15:64398939
|
C | CT | 6 | a0001c0002t0001g0039a0001c0002t0001g0068a0001c0002t0001g0209others(3): Show | 6 | HG01109.hp2 HG02109.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.618+1149dupT | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr15 | 64398939 | |||||
| chr15:64398939
|
CT | C | 52 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(49): Show | 53 | HG00642.hp1 HG00733.hp1 HG01069.hp2 others(50): Show |
intron_variant | MODIFIER | c.618+1149delT | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr15 | 64398939 | |||||
| chr15:64398939
|
CTT | C | 19 | a0001c0001t0001g0186a0001c0001t0002g0213a0001c0001t0002g0214others(16): Show | 19 | HG00323.hp1 HG01168.hp2 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.618+1148_618+1149d others(4): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr15 | 64398939 | |||||
| chr15:64398939
|
CTTTTTTT others(4): Show |
C | 2 | a0001c0001t0001g0117a0001c0001t0001g0140 | 2 | HG01192.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.618+1139_618+1149d others(13): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr15 | 64398939 | |||||
| chr15:64398939
|
CTTTTTTT others(5): Show |
C | 108 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(105): Show | 108 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(105): Show |
intron_variant | MODIFIER | c.618+1138_618+1149d others(14): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr15 | 64398939 | |||||
| chr15:64398972
|
C | T | 5 | a0001c0001t0001g0095a0001c0001t0001g0102a0001c0001t0001g0125others(2): Show | 5 | HG02055.hp1 HG02717.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.618+1154C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 4/12 | chr15 | 64398972 | ||||||
| chr15:64398982
|
C | G | 9 | a0001c0004t0001g0031a0001c0004t0001g0032a0001c0004t0001g0033others(6): Show | 9 | HG00323.hp1 HG01168.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.618+1164C>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 4/12 | chr15 | 64398982 | ||||||
| chr15:64398988
|
C | T | 1 | a0001c0005t0001g0197 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.618+1170C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 4/12 | chr15 | 64398988 | ||||||
| chr15:64399018
|
C | T | 1 | a0001c0003t0001g0156 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.618+1200C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 4/12 | chr15 | 64399018 | ||||||
| chr15:64399199
|
A | G | 8 | a0001c0002t0001g0207a0001c0002t0001g0208a0001c0002t0001g0209others(5): Show | 8 | HG02559.hp2 HG02886.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.618+1381A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 4/12 | chr15 | 64399199 | ||||||
| chr15:64399542
|
T | G | 1 | a0001c0002t0001g0081 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.619-1201T>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 4/12 | chr15 | 64399542 | ||||||
| chr15:64399674
|
G | T | 1 | a0001c0001t0001g0004 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.619-1069G>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 4/12 | chr15 | 64399674 | ||||||
| chr15:64399938
|
G | A | 1 | a0001c0001t0002g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.619-805G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 4/12 | chr15 | 64399938 | ||||||
| chr15:64399953
|
T | C | 9 | a0001c0004t0001g0031a0001c0004t0001g0032a0001c0004t0001g0033others(6): Show | 9 | HG00323.hp1 HG01168.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.619-790T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 4/12 | chr15 | 64399953 | ||||||
| chr15:64399995
|
A | G | 1 | a0001c0001t0001g0138 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.619-748A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 4/12 | chr15 | 64399995 | ||||||
| chr15:64400219
|
G | T | 9 | a0001c0004t0001g0031a0001c0004t0001g0032a0001c0004t0001g0033others(6): Show | 9 | HG00323.hp1 HG01168.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.619-524G>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 4/12 | chr15 | 64400219 | ||||||
| chr15:64400408
|
A | G | 8 | a0001c0002t0001g0207a0001c0002t0001g0208a0001c0002t0001g0209others(5): Show | 8 | HG02559.hp2 HG02886.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.619-335A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 4/12 | chr15 | 64400408 | ||||||
| chr15:64400456
|
A | G | 200 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(197): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.619-287A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 4/12 | chr15 | 64400456 | ||||||
| chr15:64400473
|
CT | C | 138 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(135): Show | 138 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(135): Show |
intron_variant | MODIFIER | c.619-254delT | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr15 | 64400473 | |||||
| chr15:64400732
|
C | G | 3 | a0001c0001t0001g0028a0002c0009t0001g0026a0002c0009t0001g0027 | 3 | HG02818.hp2 HG03471.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.619-11C>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 4/12 | chr15 | 64400732 | ||||||
| chr15:64400851
|
G | A | 1 | a0001c0001t0001g0158 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.697+30G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | chr15 | 64400851 | ||||||
| chr15:64400884
|
T | C | 1 | a0001c0001t0001g0175 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.697+63T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | chr15 | 64400884 | ||||||
| chr15:64400950
|
G | GT | 199 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(196): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.697+137dupT | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr15 | 64400950 | |||||
| chr15:64401130
|
A | G | 1 | a0001c0007t0001g0029 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.697+309A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | chr15 | 64401130 | ||||||
| chr15:64401237
|
C | A | 1 | a0001c0003t0001g0146 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.697+416C>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | chr15 | 64401237 | ||||||
| chr15:64401426
|
C | A | 9 | a0001c0004t0001g0031a0001c0004t0001g0032a0001c0004t0001g0033others(6): Show | 9 | HG00323.hp1 HG01168.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.697+605C>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | chr15 | 64401426 | ||||||
| chr15:64401427
|
G | A | 1 | a0001c0004t0001g0032 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.697+606G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | chr15 | 64401427 | ||||||
| chr15:64401594
|
C | G | 8 | a0001c0002t0001g0207a0001c0002t0001g0208a0001c0002t0001g0209others(5): Show | 8 | HG02559.hp2 HG02886.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.697+773C>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | chr15 | 64401594 | ||||||
| chr15:64401925
|
G | C | 1 | a0001c0001t0001g0129 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.697+1104G>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | chr15 | 64401925 | ||||||
| chr15:64401935
|
A | G | 6 | a0001c0001t0001g0174a0001c0001t0001g0176a0001c0001t0001g0177others(3): Show | 6 | HG02004.hp1 HG02976.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.697+1114A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | chr15 | 64401935 | ||||||
| chr15:64402026
|
T | A | 13 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0002g0215others(10): Show | 13 | HG01109.hp2 HG02055.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.697+1205T>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | chr15 | 64402026 | ||||||
| chr15:64402198
|
A | G | 1 | a0001c0001t0001g0204 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.697+1377A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | chr15 | 64402198 | ||||||
| chr15:64402305
|
C | G | 8 | a0001c0005t0001g0045a0001c0005t0001g0048a0001c0005t0001g0049others(5): Show | 8 | HG01109.hp2 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.697+1484C>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | chr15 | 64402305 | ||||||
| chr15:64402448
|
C | T | 2 | a0001c0004t0001g0218a0001c0004t0001g0219 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.697+1627C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | chr15 | 64402448 | ||||||
| chr15:64402524
|
T | A | 3 | a0001c0005t0001g0045a0001c0008t0001g0046a0001c0008t0001g0047 | 3 | HG02280.hp2 HG02451.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.697+1703T>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | chr15 | 64402524 | ||||||
| chr15:64402591
|
T | C | 8 | a0001c0002t0001g0207a0001c0002t0001g0208a0001c0002t0001g0209others(5): Show | 8 | HG02559.hp2 HG02886.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.697+1770T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | chr15 | 64402591 | ||||||
| chr15:64402747
|
A | G | 27 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(24): Show | 28 | HG00642.hp1 HG00733.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.697+1926A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | chr15 | 64402747 | ||||||
| chr15:64402748
|
A | ACTC | 2 | a0001c0007t0001g0029a0001c0007t0001g0030 | 2 | HG02886.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.697+1930_697+1932d others(5): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr15 | 64402748 | |||||
| chr15:64402865
|
G | T | 1 | a0001c0001t0001g0098 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.697+2044G>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | chr15 | 64402865 | ||||||
| chr15:64403180
|
G | A | 6 | a0001c0002t0001g0207a0001c0002t0001g0208a0001c0002t0001g0209others(3): Show | 6 | HG02559.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.697+2359G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | chr15 | 64403180 | ||||||
| chr15:64403313
|
T | C | 143 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(140): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.697+2492T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | chr15 | 64403313 | ||||||
| chr15:64403405
|
C | T | 5 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0002g0215others(2): Show | 5 | HG02055.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.697+2584C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | chr15 | 64403405 | ||||||
| chr15:64403450
|
C | T | 6 | a0001c0002t0001g0207a0001c0002t0001g0208a0001c0002t0001g0209others(3): Show | 6 | HG02559.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.697+2629C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | chr15 | 64403450 | ||||||
| chr15:64403511
|
G | A | 3 | a0001c0002t0001g0072a0001c0002t0001g0073a0001c0002t0001g0074 | 3 | HG02615.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.697+2690G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | chr15 | 64403511 | ||||||
| chr15:64403848
|
A | T | 8 | a0001c0002t0001g0207a0001c0002t0001g0208a0001c0002t0001g0209others(5): Show | 8 | HG02559.hp2 HG02886.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.698-2482A>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | chr15 | 64403848 | ||||||
| chr15:64403914
|
G | A | 4 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(1): Show | 4 | HG03041.hp2 HG04228.hp1 NA19084.hp2 others(1): Show |
intron_variant | MODIFIER | c.698-2416G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | chr15 | 64403914 | ||||||
| chr15:64403984
|
G | T | 1 | a0001c0001t0001g0204 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.698-2346G>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | chr15 | 64403984 | ||||||
| chr15:64404182
|
C | T | 1 | a0001c0001t0001g0204 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.698-2148C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | chr15 | 64404182 | ||||||
| chr15:64404207
|
A | G | 1 | a0001c0001t0001g0023 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.698-2123A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | chr15 | 64404207 | ||||||
| chr15:64404574
|
A | C | 2 | a0001c0001t0001g0136a0001c0001t0001g0137 | 2 | NA18962.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.698-1756A>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | chr15 | 64404574 | ||||||
| chr15:64404603
|
G | A | 3 | a0001c0002t0001g0078a0001c0002t0001g0079a0001c0002t0001g0081 | 3 | HG02258.hp2 HG02622.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.698-1727G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | chr15 | 64404603 | ||||||
| chr15:64404712
|
G | T | 213 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(210): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.698-1618G>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | chr15 | 64404712 | ||||||
| chr15:64404739
|
C | T | 1 | a0001c0001t0001g0203 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.698-1591C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | chr15 | 64404739 | ||||||
| chr15:64404782
|
C | G | 4 | a0001c0002t0001g0053a0001c0002t0001g0056a0001c0002t0001g0059others(1): Show | 4 | HG01884.hp2 HG02572.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.698-1548C>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | chr15 | 64404782 | ||||||
| chr15:64404863
|
G | T | 1 | a0001c0001t0001g0092 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.698-1467G>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | chr15 | 64404863 | ||||||
| chr15:64404952
|
C | T | 8 | a0001c0002t0001g0207a0001c0002t0001g0208a0001c0002t0001g0209others(5): Show | 8 | HG02559.hp2 HG02886.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.698-1378C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | chr15 | 64404952 | ||||||
| chr15:64404981
|
C | T | 1 | a0001c0002t0001g0068 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.698-1349C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | chr15 | 64404981 | ||||||
| chr15:64405223
|
C | T | 1 | a0001c0005t0001g0051 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.698-1107C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | chr15 | 64405223 | ||||||
| chr15:64405242
|
C | T | 8 | a0001c0002t0001g0207a0001c0002t0001g0208a0001c0002t0001g0209others(5): Show | 8 | HG02559.hp2 HG02886.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.698-1088C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | chr15 | 64405242 | ||||||
| chr15:64405255
|
T | C | 142 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.698-1075T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | chr15 | 64405255 | ||||||
| chr15:64405415
|
A | G | 110 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(107): Show | 110 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(107): Show |
intron_variant | MODIFIER | c.698-915A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | chr15 | 64405415 | ||||||
| chr15:64405907
|
G | A | 5 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0002g0215others(2): Show | 5 | HG02055.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.698-423G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | chr15 | 64405907 | ||||||
| chr15:64405915
|
C | T | 1 | a0001c0001t0001g0003 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.698-415C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | chr15 | 64405915 | ||||||
| chr15:64406086
|
G | A | 1 | a0001c0002t0001g0069 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.698-244G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | chr15 | 64406086 | ||||||
| chr15:64406292
|
A | C | 1 | a0001c0001t0001g0102 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.698-38A>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 5/12 | chr15 | 64406292 | ||||||
| chr15:64406637
|
A | G | 2 | a0001c0002t0001g0039a0001c0002t0001g0068 | 2 | HG02109.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.827+178A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 6/12 | chr15 | 64406637 | ||||||
| chr15:64406692
|
G | A | 1 | a0001c0002t0001g0069 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.827+233G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 6/12 | chr15 | 64406692 | ||||||
| chr15:64406736
|
C | T | 7 | a0001c0005t0001g0045a0001c0005t0001g0048a0001c0005t0001g0049others(4): Show | 7 | HG01109.hp2 HG02280.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.827+277C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 6/12 | chr15 | 64406736 | ||||||
| chr15:64406978
|
G | C | 8 | a0001c0002t0001g0207a0001c0002t0001g0208a0001c0002t0001g0209others(5): Show | 8 | HG02559.hp2 HG02886.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.827+519G>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 6/12 | chr15 | 64406978 | ||||||
| chr15:64407003
|
GA | G | 34 | a0001c0001t0001g0040a0001c0001t0001g0042a0001c0001t0001g0086others(31): Show | 34 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(31): Show |
intron_variant | MODIFIER | c.827+545delA | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 6/12 | chr15 | 64407003 | ||||||
| chr15:64407074
|
C | T | 140 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.827+615C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 6/12 | chr15 | 64407074 | ||||||
| chr15:64407166
|
A | C | 2 | a0001c0001t0001g0169a0001c0001t0001g0170 | 2 | NA18942.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.827+707A>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 6/12 | chr15 | 64407166 | ||||||
| chr15:64407199
|
G | T | 140 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.827+740G>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 6/12 | chr15 | 64407199 | ||||||
| chr15:64407355
|
A | T | 1 | a0001c0001t0001g0132 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.827+896A>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 6/12 | chr15 | 64407355 | ||||||
| chr15:64407389
|
C | T | 2 | a0001c0001t0001g0105a0001c0002t0001g0099 | 2 | HG00438.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.827+930C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 6/12 | chr15 | 64407389 | ||||||
| chr15:64407395
|
C | T | 8 | a0001c0002t0001g0207a0001c0002t0001g0208a0001c0002t0001g0209others(5): Show | 8 | HG02559.hp2 HG02886.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.827+936C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 6/12 | chr15 | 64407395 | ||||||
| chr15:64407398
|
T | G | 2 | a0001c0008t0001g0046a0001c0008t0001g0047 | 2 | HG02451.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.827+939T>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 6/12 | chr15 | 64407398 | ||||||
| chr15:64407559
|
C | T | 8 | a0001c0002t0001g0207a0001c0002t0001g0208a0001c0002t0001g0209others(5): Show | 8 | HG02559.hp2 HG02886.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.827+1100C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 6/12 | chr15 | 64407559 | ||||||
| chr15:64407666
|
C | CA | 48 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(45): Show | 49 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.827+1217dupA | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr15 | 64407666 | |||||
| chr15:64407814
|
C | A | 12 | a0001c0001t0001g0095a0001c0001t0001g0102a0001c0001t0001g0125others(9): Show | 12 | HG01071.hp2 HG02055.hp1 HG02683.hp2 others(9): Show |
intron_variant | MODIFIER | c.827+1355C>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 6/12 | chr15 | 64407814 | ||||||
| chr15:64408024
|
G | A | 9 | a0001c0004t0001g0031a0001c0004t0001g0032a0001c0004t0001g0033others(6): Show | 9 | HG00323.hp1 HG01168.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.827+1565G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 6/12 | chr15 | 64408024 | ||||||
| chr15:64408044
|
G | A | 2 | a0001c0001t0001g0087a0001c0001t0001g0090 | 2 | HG00099.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.828-1569G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 6/12 | chr15 | 64408044 | ||||||
| chr15:64408094
|
C | CA | 21 | a0001c0001t0001g0159a0001c0001t0002g0213a0001c0001t0002g0214others(18): Show | 21 | HG02055.hp2 HG02083.hp2 HG02559.hp2 others(18): Show |
intron_variant | MODIFIER | c.828-1503dupA | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr15 | 64408094 | |||||
| chr15:64408139
|
C | G | 12 | a0001c0001t0001g0095a0001c0001t0001g0102a0001c0001t0001g0125others(9): Show | 12 | HG01071.hp2 HG02055.hp1 HG02683.hp2 others(9): Show |
intron_variant | MODIFIER | c.828-1474C>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 6/12 | chr15 | 64408139 | ||||||
| chr15:64408157
|
A | ATT | 5 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0002g0215others(2): Show | 5 | HG02055.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.828-1452_828-1451d others(4): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr15 | 64408157 | |||||
| chr15:64408163
|
G | GT | 28 | a0001c0001t0001g0204a0001c0002t0001g0060a0001c0002t0001g0099others(25): Show | 28 | HG00323.hp1 HG01109.hp2 HG01168.hp2 others(25): Show |
intron_variant | MODIFIER | c.828-1438dupT | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr15 | 64408163 | |||||
| chr15:64408163
|
G | GTT | 104 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(101): Show | 104 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(101): Show |
intron_variant | MODIFIER | c.828-1439_828-1438d others(4): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr15 | 64408163 | |||||
| chr15:64408163
|
G | T | 5 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0002g0215others(2): Show | 5 | HG02055.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.828-1450G>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 6/12 | chr15 | 64408163 | ||||||
| chr15:64408190
|
G | A | 1 | a0001c0005t0001g0197 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.828-1423G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 6/12 | chr15 | 64408190 | ||||||
| chr15:64408249
|
A | AT | 26 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0016others(23): Show | 26 | HG00621.hp1 HG01192.hp1 HG02145.hp1 others(23): Show |
intron_variant | MODIFIER | c.828-1337dupT | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr15 | 64408249 | |||||
| chr15:64408249
|
AT | A | 10 | a0001c0001t0001g0204a0001c0001t0002g0213a0001c0001t0002g0215others(7): Show | 10 | HG02559.hp2 HG02886.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.828-1337delT | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr15 | 64408249 | |||||
| chr15:64408249
|
ATT | A | 23 | a0001c0001t0001g0095a0001c0001t0001g0102a0001c0001t0001g0103others(20): Show | 23 | HG01071.hp2 HG01169.hp1 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.828-1338_828-1337d others(4): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr15 | 64408249 | |||||
| chr15:64408249
|
ATTT | A | 95 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(92): Show | 95 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(92): Show |
intron_variant | MODIFIER | c.828-1339_828-1337d others(5): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr15 | 64408249 | |||||
| chr15:64408249
|
ATTTTTTT others(3): Show |
A | 1 | a0001c0001t0001g0092 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.828-1346_828-1337d others(12): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr15 | 64408249 | |||||
| chr15:64408340
|
G | A | 1 | a0001c0001t0001g0130 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.828-1273G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 6/12 | chr15 | 64408340 | ||||||
| chr15:64408359
|
C | G | 109 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.828-1254C>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 6/12 | chr15 | 64408359 | ||||||
| chr15:64408539
|
GT | G | 140 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.828-1072delT | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr15 | 64408539 | |||||
| chr15:64408547
|
A | G | 1 | a0001c0002t0001g0193 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.828-1066A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 6/12 | chr15 | 64408547 | ||||||
| chr15:64408695
|
G | A | 8 | a0001c0002t0001g0053a0001c0002t0001g0054a0001c0002t0001g0055others(5): Show | 8 | HG01884.hp2 HG02145.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.828-918G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 6/12 | chr15 | 64408695 | ||||||
| chr15:64408843
|
G | T | 8 | a0001c0002t0001g0207a0001c0002t0001g0208a0001c0002t0001g0209others(5): Show | 8 | HG02559.hp2 HG02886.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.828-770G>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 6/12 | chr15 | 64408843 | ||||||
| chr15:64408996
|
C | T | 9 | a0001c0004t0001g0031a0001c0004t0001g0032a0001c0004t0001g0033others(6): Show | 9 | HG00323.hp1 HG01168.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.828-617C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 6/12 | chr15 | 64408996 | ||||||
| chr15:64409083
|
C | T | 1 | a0001c0001t0001g0155 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.828-530C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 6/12 | chr15 | 64409083 | ||||||
| chr15:64409170
|
G | A | 109 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.828-443G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 6/12 | chr15 | 64409170 | ||||||
| chr15:64409190
|
CA | C | 9 | a0001c0002t0001g0099a0001c0005t0001g0045a0001c0005t0001g0048others(6): Show | 9 | HG01109.hp2 HG02257.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.828-409delA | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr15 | 64409190 | |||||
| chr15:64409278
|
G | A | 1 | a0001c0001t0001g0136 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.828-335G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 6/12 | chr15 | 64409278 | ||||||
| chr15:64409528
|
T | C | 1 | a0001c0004t0001g0031 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.828-85T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 6/12 | chr15 | 64409528 | ||||||
| chr15:64409597
|
G | C | 3 | a0001c0002t0001g0072a0001c0002t0001g0073a0001c0002t0001g0074 | 3 | HG02615.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.828-16G>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 6/12 | chr15 | 64409597 | ||||||
| chr15:64409969
|
G | A | 109 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.1043+141G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 7/12 | chr15 | 64409969 | ||||||
| chr15:64410024
|
G | GT | 13 | a0001c0001t0001g0166a0001c0001t0001g0180a0001c0001t0001g0199others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.1043+215dupT | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr15 | 64410024 | |||||
| chr15:64410171
|
G | A | 1 | a0001c0001t0001g0204 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1043+343G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 7/12 | chr15 | 64410171 | ||||||
| chr15:64410334
|
T | A | 1 | a0001c0005t0001g0045 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1043+506T>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 7/12 | chr15 | 64410334 | ||||||
| chr15:64410709
|
T | G | 2 | a0001c0001t0001g0157a0001c0001t0001g0160 | 2 | HG02735.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1043+881T>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 7/12 | chr15 | 64410709 | ||||||
| chr15:64411025
|
G | A | 140 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.1043+1197G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 7/12 | chr15 | 64411025 | ||||||
| chr15:64411110
|
T | A | 14 | a0001c0001t0001g0204a0001c0001t0002g0213a0001c0001t0002g0214others(11): Show | 14 | HG01109.hp2 HG02055.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1043+1282T>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 7/12 | chr15 | 64411110 | ||||||
| chr15:64411492
|
C | T | 1 | a0001c0001t0001g0129 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1043+1664C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 7/12 | chr15 | 64411492 | ||||||
| chr15:64411611
|
A | G | 4 | a0001c0002t0001g0209a0001c0002t0001g0210a0001c0002t0001g0211others(1): Show | 4 | HG02559.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1043+1783A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 7/12 | chr15 | 64411611 | ||||||
| chr15:64411616
|
C | T | 2 | a0001c0001t0001g0110a0001c0001t0001g0128 | 2 | HG00140.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.1043+1788C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 7/12 | chr15 | 64411616 | ||||||
| chr15:64411685
|
G | GT | 133 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(130): Show | 133 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(130): Show |
intron_variant | MODIFIER | c.1043+1869dupT | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr15 | 64411685 | |||||
| chr15:64411741
|
G | A | 1 | a0001c0002t0001g0068 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1043+1913G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 7/12 | chr15 | 64411741 | ||||||
| chr15:64411952
|
A | AT | 218 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(215): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.1043+2125dupT | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr15 | 64411952 | |||||
| chr15:64412063
|
A | T | 200 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(197): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.1044-2022A>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 7/12 | chr15 | 64412063 | ||||||
| chr15:64412069
|
A | T | 140 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.1044-2016A>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 7/12 | chr15 | 64412069 | ||||||
| chr15:64412079
|
T | G | 6 | a0001c0002t0001g0044a0001c0002t0001g0188a0001c0002t0001g0191others(3): Show | 6 | NA18962.hp1 NA18972.hp2 NA18993.hp1 others(3): Show |
intron_variant | MODIFIER | c.1044-2006T>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 7/12 | chr15 | 64412079 | ||||||
| chr15:64412284
|
T | G | 1 | a0001c0005t0001g0197 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1044-1801T>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 7/12 | chr15 | 64412284 | ||||||
| chr15:64412305
|
C | G | 1 | a0001c0004t0001g0037 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1044-1780C>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 7/12 | chr15 | 64412305 | ||||||
| chr15:64412557
|
TA | T | 138 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(135): Show | 138 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.1044-1513delA | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr15 | 64412557 | |||||
| chr15:64412562
|
A | G | 1 | a0001c0001t0001g0204 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1044-1523A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 7/12 | chr15 | 64412562 | ||||||
| chr15:64412645
|
A | ATATAT | 109 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.1044-1438_1044-143 others(9): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr15 | 64412645 | |||||
| chr15:64412682
|
C | T | 1 | a0001c0001t0001g0204 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1044-1403C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 7/12 | chr15 | 64412682 | ||||||
| chr15:64412742
|
G | A | 9 | a0001c0004t0001g0031a0001c0004t0001g0032a0001c0004t0001g0033others(6): Show | 9 | HG00323.hp1 HG01168.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.1044-1343G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 7/12 | chr15 | 64412742 | ||||||
| chr15:64413132
|
A | G | 1 | a0001c0001t0001g0155 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1044-953A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 7/12 | chr15 | 64413132 | ||||||
| chr15:64413347
|
A | G | 2 | a0001c0002t0001g0207a0001c0002t0001g0208 | 2 | HG02976.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1044-738A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 7/12 | chr15 | 64413347 | ||||||
| chr15:64413511
|
G | T | 48 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(45): Show | 49 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.1044-574G>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 7/12 | chr15 | 64413511 | ||||||
| chr15:64413541
|
G | A | 1 | a0001c0002t0001g0081 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1044-544G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 7/12 | chr15 | 64413541 | ||||||
| chr15:64413596
|
T | A | 1 | a0001c0001t0001g0028 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1044-489T>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 7/12 | chr15 | 64413596 | ||||||
| chr15:64413603
|
T | A | 213 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(210): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.1044-482T>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 7/12 | chr15 | 64413603 | ||||||
| chr15:64414039
|
C | T | 1 | a0001c0005t0001g0045 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1044-46C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 7/12 | chr15 | 64414039 | ||||||
| chr15:64414060
|
G | A | 109 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.1044-25G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 7/12 | chr15 | 64414060 | ||||||
| chr15:64414064
|
C | T | 2 | a0001c0002t0001g0064a0001c0002t0001g0067 | 2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1044-21C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 7/12 | chr15 | 64414064 | ||||||
| chr15:64414229
|
C | G | 12 | a0001c0001t0001g0040a0001c0001t0001g0042a0001c0001t0001g0086others(9): Show | 12 | HG00099.hp2 HG02080.hp2 HG03239.hp2 others(9): Show |
intron_variant | MODIFIER | c.1170+18C>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 8/12 | chr15 | 64414229 | ||||||
| chr15:64414298
|
ATACCAAT others(20): Show |
A | 1 | a0001c0002t0001g0062 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1170+107_1170+133d others(29): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr15 | 64414298 | |||||
| chr15:64414403
|
T | C | 14 | a0001c0001t0001g0204a0001c0001t0002g0213a0001c0001t0002g0214others(11): Show | 14 | HG01109.hp2 HG02055.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1170+192T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 8/12 | chr15 | 64414403 | ||||||
| chr15:64414486
|
A | G | 6 | a0001c0002t0001g0207a0001c0002t0001g0208a0001c0002t0001g0209others(3): Show | 6 | HG02559.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1170+275A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 8/12 | chr15 | 64414486 | ||||||
| chr15:64414512
|
C | CT | 14 | a0001c0002t0001g0209a0001c0002t0001g0210a0001c0002t0001g0211others(11): Show | 14 | HG00323.hp1 HG00323.hp2 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.1170+323dupT | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr15 | 64414512 | |||||
| chr15:64414512
|
C | CTT | 101 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(98): Show | 101 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(98): Show |
intron_variant | MODIFIER | c.1170+322_1170+323d others(4): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr15 | 64414512 | |||||
| chr15:64414512
|
C | CTTT | 16 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(13): Show | 16 | HG01109.hp2 HG02055.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.1170+321_1170+323d others(5): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr15 | 64414512 | |||||
| chr15:64414512
|
C | T | 2 | a0001c0001t0001g0089a0001c0001t0001g0092 | 2 | NA18998.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1170+301C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 8/12 | chr15 | 64414512 | ||||||
| chr15:64414578
|
A | G | 9 | a0001c0004t0001g0031a0001c0004t0001g0032a0001c0004t0001g0033others(6): Show | 9 | HG00323.hp1 HG01168.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.1170+367A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 8/12 | chr15 | 64414578 | ||||||
| chr15:64414603
|
G | A | 8 | a0001c0002t0001g0207a0001c0002t0001g0208a0001c0002t0001g0209others(5): Show | 8 | HG02559.hp2 HG02886.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1170+392G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 8/12 | chr15 | 64414603 | ||||||
| chr15:64414621
|
A | G | 5 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0002g0215others(2): Show | 5 | HG02055.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1170+410A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 8/12 | chr15 | 64414621 | ||||||
| chr15:64414641
|
T | C | 6 | a0001c0002t0001g0207a0001c0002t0001g0208a0001c0002t0001g0209others(3): Show | 6 | HG02559.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1170+430T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 8/12 | chr15 | 64414641 | ||||||
| chr15:64414718
|
C | T | 48 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(45): Show | 49 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.1170+507C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 8/12 | chr15 | 64414718 | ||||||
| chr15:64414744
|
C | T | 1 | a0001c0005t0001g0197 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1170+533C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 8/12 | chr15 | 64414744 | ||||||
| chr15:64414760
|
A | G | 6 | a0001c0002t0001g0207a0001c0002t0001g0208a0001c0002t0001g0209others(3): Show | 6 | HG02559.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1170+549A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 8/12 | chr15 | 64414760 | ||||||
| chr15:64414863
|
G | A | 8 | a0001c0005t0001g0045a0001c0005t0001g0048a0001c0005t0001g0049others(5): Show | 8 | HG01109.hp2 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1170+652G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 8/12 | chr15 | 64414863 | ||||||
| chr15:64414923
|
G | A | 1 | a0001c0007t0001g0030 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1170+712G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 8/12 | chr15 | 64414923 | ||||||
| chr15:64415001
|
G | A | 6 | a0001c0002t0001g0207a0001c0002t0001g0208a0001c0002t0001g0209others(3): Show | 6 | HG02559.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1170+790G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 8/12 | chr15 | 64415001 | ||||||
| chr15:64415005
|
G | A | 2 | a0001c0003t0001g0149a0001c0003t0001g0150 | 2 | HG01884.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1170+794G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 8/12 | chr15 | 64415005 | ||||||
| chr15:64415085
|
A | G | 6 | a0001c0002t0001g0184a0001c0006t0001g0075a0001c0006t0001g0076others(3): Show | 6 | HG02486.hp2 HG02622.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1170+874A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 8/12 | chr15 | 64415085 | ||||||
| chr15:64415093
|
T | A | 6 | a0001c0002t0001g0207a0001c0002t0001g0208a0001c0002t0001g0209others(3): Show | 6 | HG02559.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1170+882T>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 8/12 | chr15 | 64415093 | ||||||
| chr15:64415176
|
G | A | 5 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0002g0215others(2): Show | 5 | HG02055.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1170+965G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 8/12 | chr15 | 64415176 | ||||||
| chr15:64415335
|
T | C | 3 | a0001c0005t0001g0045a0001c0008t0001g0046a0001c0008t0001g0047 | 3 | HG02280.hp2 HG02451.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1170+1124T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 8/12 | chr15 | 64415335 | ||||||
| chr15:64415817
|
A | C | 3 | a0001c0005t0001g0045a0001c0008t0001g0046a0001c0008t0001g0047 | 3 | HG02280.hp2 HG02451.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1170+1606A>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 8/12 | chr15 | 64415817 | ||||||
| chr15:64415828
|
C | T | 1 | a0002c0009t0001g0027 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1170+1617C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 8/12 | chr15 | 64415828 | ||||||
| chr15:64416123
|
T | C | 1 | a0001c0001t0001g0204 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1170+1912T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 8/12 | chr15 | 64416123 | ||||||
| chr15:64416226
|
A | G | 27 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(24): Show | 28 | HG00642.hp1 HG00733.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.1170+2015A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 8/12 | chr15 | 64416226 | ||||||
| chr15:64416605
|
A | C | 1 | a0001c0002t0001g0198 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1171-1936A>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 8/12 | chr15 | 64416605 | ||||||
| chr15:64416827
|
G | A | 1 | a0001c0001t0001g0121 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1171-1714G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 8/12 | chr15 | 64416827 | ||||||
| chr15:64417107
|
G | A | 1 | a0001c0002t0001g0060 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1171-1434G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 8/12 | chr15 | 64417107 | ||||||
| chr15:64417467
|
T | A | 8 | a0001c0005t0001g0045a0001c0005t0001g0048a0001c0005t0001g0049others(5): Show | 8 | HG01109.hp2 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1171-1074T>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 8/12 | chr15 | 64417467 | ||||||
| chr15:64417467
|
T | TA | 111 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(108): Show | 111 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(108): Show |
intron_variant | MODIFIER | c.1171-1068dupA | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr15 | 64417467 | |||||
| chr15:64417621
|
T | G | 7 | a0001c0005t0001g0045a0001c0005t0001g0048a0001c0005t0001g0049others(4): Show | 7 | HG01109.hp2 HG02280.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1171-920T>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 8/12 | chr15 | 64417621 | ||||||
| chr15:64417676
|
C | G | 1 | a0001c0002t0001g0068 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1171-865C>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 8/12 | chr15 | 64417676 | ||||||
| chr15:64418068
|
C | A | 1 | a0001c0001t0001g0162 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1171-473C>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 8/12 | chr15 | 64418068 | ||||||
| chr15:64418379
|
T | C | 2 | a0001c0004t0001g0033a0001c0004t0001g0035 | 2 | HG01934.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.1171-162T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 8/12 | chr15 | 64418379 | ||||||
| chr15:64418392
|
G | A | 1 | a0001c0002t0001g0038 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1171-149G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 8/12 | chr15 | 64418392 | ||||||
| chr15:64418494
|
G | A | 1 | a0001c0002t0001g0065 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1171-47G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 8/12 | chr15 | 64418494 | ||||||
| chr15:64418838
|
C | A | 8 | a0001c0002t0001g0207a0001c0002t0001g0208a0001c0002t0001g0209others(5): Show | 8 | HG02559.hp2 HG02886.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1358+110C>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64418838 | ||||||
| chr15:64418975
|
C | T | 57 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(54): Show | 58 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.1358+247C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64418975 | ||||||
| chr15:64419383
|
C | T | 1 | a0001c0005t0001g0197 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1358+655C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64419383 | ||||||
| chr15:64419390
|
T | C | 140 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.1358+662T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64419390 | ||||||
| chr15:64419391
|
G | C | 8 | a0001c0002t0001g0207a0001c0002t0001g0208a0001c0002t0001g0209others(5): Show | 8 | HG02559.hp2 HG02886.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1358+663G>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64419391 | ||||||
| chr15:64419430
|
C | G | 5 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0002g0215others(2): Show | 5 | HG02055.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1358+702C>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64419430 | ||||||
| chr15:64419787
|
A | G | 109 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.1358+1059A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64419787 | ||||||
| chr15:64419827
|
T | G | 3 | a0001c0002t0001g0083a0001c0002t0001g0084a0001c0002t0001g0085 | 3 | HG03490.hp2 HG03492.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.1358+1099T>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64419827 | ||||||
| chr15:64419857
|
C | T | 57 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(54): Show | 58 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.1358+1129C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64419857 | ||||||
| chr15:64419960
|
C | T | 1 | a0001c0010t0001g0167 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1358+1232C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64419960 | ||||||
| chr15:64419965
|
G | A | 3 | a0001c0002t0001g0072a0001c0002t0001g0073a0001c0002t0001g0074 | 3 | HG02615.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1358+1237G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64419965 | ||||||
| chr15:64420143
|
C | T | 1 | a0001c0001t0001g0173 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1358+1415C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64420143 | ||||||
| chr15:64420209
|
C | T | 2 | a0001c0004t0001g0218a0001c0004t0001g0219 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1358+1481C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64420209 | ||||||
| chr15:64420303
|
T | G | 1 | a0001c0001t0001g0159 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1358+1575T>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64420303 | ||||||
| chr15:64420341
|
A | T | 8 | a0001c0002t0001g0207a0001c0002t0001g0208a0001c0002t0001g0209others(5): Show | 8 | HG02559.hp2 HG02886.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1358+1613A>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64420341 | ||||||
| chr15:64420356
|
G | A | 5 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0002g0215others(2): Show | 5 | HG02055.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1358+1628G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64420356 | ||||||
| chr15:64420409
|
A | G | 109 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.1358+1681A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64420409 | ||||||
| chr15:64420433
|
C | G | 2 | a0001c0002t0001g0207a0001c0002t0001g0208 | 2 | HG02976.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1358+1705C>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64420433 | ||||||
| chr15:64420507
|
A | G | 1 | a0001c0005t0001g0197 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1358+1779A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64420507 | ||||||
| chr15:64420529
|
C | CT | 109 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.1358+1813dupT | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr15 | 64420529 | |||||
| chr15:64420609
|
C | T | 1 | a0001c0001t0001g0158 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1358+1881C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64420609 | ||||||
| chr15:64420688
|
T | C | 8 | a0001c0005t0001g0045a0001c0005t0001g0048a0001c0005t0001g0049others(5): Show | 8 | HG01109.hp2 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1358+1960T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64420688 | ||||||
| chr15:64420754
|
G | A | 8 | a0001c0002t0001g0207a0001c0002t0001g0208a0001c0002t0001g0209others(5): Show | 8 | HG02559.hp2 HG02886.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1358+2026G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64420754 | ||||||
| chr15:64420783
|
C | A | 9 | a0001c0004t0001g0031a0001c0004t0001g0032a0001c0004t0001g0033others(6): Show | 9 | HG00323.hp1 HG01168.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.1358+2055C>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64420783 | ||||||
| chr15:64420812
|
G | C | 3 | a0001c0002t0001g0072a0001c0002t0001g0073a0001c0002t0001g0074 | 3 | HG02615.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1358+2084G>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64420812 | ||||||
| chr15:64420900
|
C | G | 1 | a0001c0002t0001g0069 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1358+2172C>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64420900 | ||||||
| chr15:64421070
|
G | T | 1 | a0001c0008t0001g0047 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1358+2342G>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64421070 | ||||||
| chr15:64421285
|
A | C | 1 | a0001c0002t0001g0064 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1358+2557A>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64421285 | ||||||
| chr15:64421295
|
TATA | T | 8 | a0001c0005t0001g0045a0001c0005t0001g0048a0001c0005t0001g0049others(5): Show | 8 | HG01109.hp2 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1358+2571_1358+257 others(7): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr15 | 64421295 | |||||
| chr15:64421326
|
T | C | 9 | a0001c0004t0001g0031a0001c0004t0001g0032a0001c0004t0001g0033others(6): Show | 9 | HG00323.hp1 HG01168.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.1358+2598T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64421326 | ||||||
| chr15:64421334
|
T | A | 1 | a0001c0002t0001g0064 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1358+2606T>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64421334 | ||||||
| chr15:64421351
|
T | C | 1 | a0001c0002t0001g0064 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1358+2623T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64421351 | ||||||
| chr15:64421405
|
C | T | 1 | a0001c0001t0001g0109 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1359-2626C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64421405 | ||||||
| chr15:64421441
|
T | C | 1 | a0001c0002t0001g0038 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1359-2590T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64421441 | ||||||
| chr15:64421567
|
C | G | 2 | a0001c0002t0001g0207a0001c0002t0001g0208 | 2 | HG02976.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1359-2464C>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64421567 | ||||||
| chr15:64421883
|
A | C | 8 | a0001c0002t0001g0207a0001c0002t0001g0208a0001c0002t0001g0209others(5): Show | 8 | HG02559.hp2 HG02886.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1359-2148A>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64421883 | ||||||
| chr15:64421999
|
T | C | 6 | a0001c0002t0001g0207a0001c0002t0001g0208a0001c0002t0001g0209others(3): Show | 6 | HG02559.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1359-2032T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64421999 | ||||||
| chr15:64422028
|
C | CA | 38 | a0001c0001t0001g0136a0001c0001t0001g0186a0001c0002t0001g0039others(35): Show | 38 | HG00621.hp1 HG01884.hp2 HG02071.hp2 others(35): Show |
intron_variant | MODIFIER | c.1359-1989dupA | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr15 | 64422028 | |||||
| chr15:64422265
|
G | A | 2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | HG04228.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1359-1766G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64422265 | ||||||
| chr15:64422309
|
T | C | 1 | a0001c0001t0001g0137 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1359-1722T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64422309 | ||||||
| chr15:64422573
|
A | C | 169 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(166): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.1359-1458A>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64422573 | ||||||
| chr15:64422704
|
T | G | 9 | a0001c0004t0001g0031a0001c0004t0001g0032a0001c0004t0001g0033others(6): Show | 9 | HG00323.hp1 HG01168.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.1359-1327T>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64422704 | ||||||
| chr15:64422807
|
T | C | 6 | a0001c0002t0001g0207a0001c0002t0001g0208a0001c0002t0001g0209others(3): Show | 6 | HG02559.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1359-1224T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64422807 | ||||||
| chr15:64423049
|
T | C | 1 | a0001c0001t0001g0109 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1359-982T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64423049 | ||||||
| chr15:64423108
|
G | C | 167 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(164): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.1359-923G>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64423108 | ||||||
| chr15:64423428
|
T | C | 1 | a0001c0001t0001g0129 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1359-603T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64423428 | ||||||
| chr15:64423461
|
C | CA | 13 | a0001c0002t0001g0062a0001c0002t0001g0065a0001c0002t0001g0069others(10): Show | 13 | HG00323.hp1 HG01169.hp1 HG01261.hp1 others(10): Show |
intron_variant | MODIFIER | c.1359-544dupA | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr15 | 64423461 | |||||
| chr15:64423461
|
CA | C | 55 | a0001c0001t0001g0040a0001c0001t0001g0042a0001c0001t0001g0086others(52): Show | 55 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(52): Show |
intron_variant | MODIFIER | c.1359-544delA | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr15 | 64423461 | |||||
| chr15:64423461
|
CAA | C | 105 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(102): Show | 106 | HG00140.hp2 HG00438.hp1 HG00621.hp2 others(103): Show |
intron_variant | MODIFIER | c.1359-545_1359-544d others(4): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr15 | 64423461 | |||||
| chr15:64423461
|
CAAA | C | 5 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0002g0215others(2): Show | 5 | HG02055.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1359-546_1359-544d others(5): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr15 | 64423461 | |||||
| chr15:64423527
|
G | A | 1 | a0001c0003t0001g0111 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1359-504G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64423527 | ||||||
| chr15:64423813
|
A | C | 4 | a0001c0005t0001g0048a0001c0005t0001g0049a0001c0005t0001g0050others(1): Show | 4 | HG01109.hp2 HG02572.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1359-218A>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64423813 | ||||||
| chr15:64423865
|
T | C | 5 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0002g0215others(2): Show | 5 | HG02055.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1359-166T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 9/12 | chr15 | 64423865 | ||||||
| chr15:64424312
|
C | T | 1 | a0001c0001t0001g0088 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1483+157C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 10/12 | chr15 | 64424312 | ||||||
| chr15:64424382
|
T | C | 1 | a0001c0003t0001g0183 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1483+227T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 10/12 | chr15 | 64424382 | ||||||
| chr15:64424778
|
C | G | 9 | a0001c0004t0001g0031a0001c0004t0001g0032a0001c0004t0001g0033others(6): Show | 9 | HG00323.hp1 HG01168.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.1483+623C>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 10/12 | chr15 | 64424778 | ||||||
| chr15:64424900
|
C | T | 1 | a0001c0003t0001g0156 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1484-640C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 10/12 | chr15 | 64424900 | ||||||
| chr15:64425241
|
G | A | 1 | a0001c0003t0001g0002 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1484-299G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 10/12 | chr15 | 64425241 | ||||||
| chr15:64425273
|
T | A | 3 | a0001c0005t0001g0045a0001c0008t0001g0046a0001c0008t0001g0047 | 3 | HG02280.hp2 HG02451.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1484-267T>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 10/12 | chr15 | 64425273 | ||||||
| chr15:64425295
|
T | C | 1 | a0001c0003t0001g0150 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1484-245T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 10/12 | chr15 | 64425295 | ||||||
| chr15:64425646
|
C | CT | 5 | a0001c0002t0001g0184a0001c0006t0001g0075a0001c0006t0001g0076others(2): Show | 5 | HG02486.hp2 HG02622.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1575+26dupT | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64425646 | |||||
| chr15:64425666
|
G | A | 7 | a0001c0001t0001g0118a0001c0001t0001g0174a0001c0001t0001g0176others(4): Show | 7 | HG02004.hp1 HG02976.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.1575+35G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64425666 | ||||||
| chr15:64425792
|
C | T | 1 | a0001c0001t0001g0129 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1575+161C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64425792 | ||||||
| chr15:64425934
|
T | C | 1 | a0001c0001t0001g0020 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1575+303T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64425934 | ||||||
| chr15:64426133
|
C | T | 1 | a0001c0002t0001g0074 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1575+502C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64426133 | ||||||
| chr15:64426140
|
C | A | 2 | a0001c0001t0001g0116a0001c0001t0001g0163 | 2 | HG00438.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.1575+509C>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64426140 | ||||||
| chr15:64426294
|
TTGCCAGG others(4): Show |
T | 5 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0002g0215others(2): Show | 5 | HG02055.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1575+669_1575+679d others(13): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64426294 | |||||
| chr15:64426320
|
G | C | 1 | a0001c0005t0001g0197 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1575+689G>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64426320 | ||||||
| chr15:64426362
|
G | A | 2 | a0001c0007t0001g0029a0001c0007t0001g0030 | 2 | HG02886.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1575+731G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64426362 | ||||||
| chr15:64426538
|
A | G | 1 | a0001c0001t0001g0165 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1575+907A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64426538 | ||||||
| chr15:64426563
|
G | A | 2 | a0001c0007t0001g0029a0001c0007t0001g0030 | 2 | HG02886.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1575+932G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64426563 | ||||||
| chr15:64426573
|
G | A | 5 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0002g0215others(2): Show | 5 | HG02055.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1575+942G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64426573 | ||||||
| chr15:64426699
|
C | CA | 5 | a0001c0001t0001g0023a0001c0001t0001g0071a0001c0001t0002g0213others(2): Show | 5 | HG02129.hp1 HG02145.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1575+1088dupA | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64426699 | |||||
| chr15:64426699
|
CA | C | 107 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(104): Show | 107 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(104): Show |
intron_variant | MODIFIER | c.1575+1088delA | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64426699 | |||||
| chr15:64426893
|
G | A | 1 | a0001c0010t0001g0167 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1575+1262G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64426893 | ||||||
| chr15:64426939
|
G | A | 28 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(25): Show | 29 | HG00642.hp1 HG00733.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.1575+1308G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64426939 | ||||||
| chr15:64426948
|
C | T | 1 | a0001c0002t0001g0061 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1575+1317C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64426948 | ||||||
| chr15:64426965
|
G | A | 6 | a0001c0002t0001g0207a0001c0002t0001g0208a0001c0002t0001g0209others(3): Show | 6 | HG02559.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1575+1334G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64426965 | ||||||
| chr15:64426993
|
C | T | 1 | a0001c0010t0001g0167 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1575+1362C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64426993 | ||||||
| chr15:64427044
|
A | G | 1 | a0001c0002t0001g0069 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1575+1413A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64427044 | ||||||
| chr15:64427105
|
A | G | 41 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(38): Show | 42 | HG00642.hp1 HG00733.hp1 HG01069.hp2 others(39): Show |
intron_variant | MODIFIER | c.1575+1474A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64427105 | ||||||
| chr15:64427191
|
A | G | 3 | a0001c0006t0001g0076a0001c0006t0001g0205a0001c0006t0001g0206 | 3 | HG02486.hp2 HG02622.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1575+1560A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64427191 | ||||||
| chr15:64427566
|
A | G | 1 | a0001c0005t0001g0050 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1575+1935A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64427566 | ||||||
| chr15:64427665
|
T | C | 24 | a0001c0001t0001g0097a0001c0001t0001g0101a0001c0001t0001g0103others(21): Show | 24 | HG00140.hp2 HG01069.hp1 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.1575+2034T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64427665 | ||||||
| chr15:64427954
|
C | G | 1 | a0001c0001t0001g0129 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1575+2323C>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64427954 | ||||||
| chr15:64427954
|
C | T | 6 | a0001c0002t0001g0207a0001c0002t0001g0208a0001c0002t0001g0209others(3): Show | 6 | HG02559.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1575+2323C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64427954 | ||||||
| chr15:64428047
|
G | C | 1 | a0001c0007t0001g0029 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1575+2416G>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64428047 | ||||||
| chr15:64428234
|
C | A | 1 | a0001c0003t0001g0052 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1575+2603C>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64428234 | ||||||
| chr15:64428381
|
TCTC | T | 8 | a0001c0002t0001g0207a0001c0002t0001g0208a0001c0002t0001g0209others(5): Show | 8 | HG02559.hp2 HG02886.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1575+2753_1575+275 others(7): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64428381 | |||||
| chr15:64428554
|
G | A | 2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | HG04228.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1575+2923G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64428554 | ||||||
| chr15:64428740
|
C | G | 1 | a0001c0001t0001g0161 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1575+3109C>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64428740 | ||||||
| chr15:64429045
|
T | C | 2 | a0001c0007t0001g0029a0001c0007t0001g0030 | 2 | HG02886.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1575+3414T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64429045 | ||||||
| chr15:64429081
|
G | A | 1 | a0001c0002t0001g0039 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1575+3450G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64429081 | ||||||
| chr15:64429178
|
G | A | 1 | a0001c0001t0001g0012 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1575+3547G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64429178 | ||||||
| chr15:64429317
|
C | CA | 6 | a0001c0002t0001g0207a0001c0002t0001g0208a0001c0002t0001g0209others(3): Show | 6 | HG02559.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1575+3694dupA | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64429317 | |||||
| chr15:64429396
|
G | C | 1 | a0001c0001t0001g0136 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1575+3765G>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64429396 | ||||||
| chr15:64429519
|
G | A | 2 | a0001c0001t0001g0100a0001c0001t0001g0151 | 2 | HG01978.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1575+3888G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64429519 | ||||||
| chr15:64429546
|
C | A | 9 | a0001c0004t0001g0031a0001c0004t0001g0032a0001c0004t0001g0033others(6): Show | 9 | HG00323.hp1 HG01168.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.1575+3915C>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64429546 | ||||||
| chr15:64429629
|
A | C | 200 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(197): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.1575+3998A>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64429629 | ||||||
| chr15:64429684
|
A | T | 2 | a0001c0001t0001g0169a0001c0001t0001g0170 | 2 | NA18942.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.1575+4053A>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64429684 | ||||||
| chr15:64429728
|
G | T | 9 | a0001c0004t0001g0031a0001c0004t0001g0032a0001c0004t0001g0033others(6): Show | 9 | HG00323.hp1 HG01168.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.1575+4097G>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64429728 | ||||||
| chr15:64430177
|
C | T | 1 | a0001c0002t0001g0085 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1575+4546C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64430177 | ||||||
| chr15:64430237
|
A | G | 5 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0002g0215others(2): Show | 5 | HG02055.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1575+4606A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64430237 | ||||||
| chr15:64430242
|
C | T | 2 | a0001c0004t0001g0218a0001c0004t0001g0219 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1575+4611C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64430242 | ||||||
| chr15:64430498
|
A | T | 2 | a0001c0004t0001g0036a0001c0004t0001g0037 | 2 | HG02735.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.1575+4867A>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64430498 | ||||||
| chr15:64430502
|
C | CT | 10 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(7): Show | 10 | HG00642.hp1 HG00733.hp1 HG01069.hp2 others(7): Show |
intron_variant | MODIFIER | c.1575+4882dupT | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64430502 | |||||
| chr15:64430643
|
T | C | 1 | a0001c0003t0001g0002 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1575+5012T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64430643 | ||||||
| chr15:64430755
|
A | G | 2 | a0001c0001t0001g0087a0001c0001t0001g0090 | 2 | HG00099.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1575+5124A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64430755 | ||||||
| chr15:64430856
|
C | T | 2 | a0001c0001t0001g0087a0001c0001t0001g0090 | 2 | HG00099.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1575+5225C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64430856 | ||||||
| chr15:64431268
|
G | A | 3 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0128 | 3 | HG00140.hp1 HG01515.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.1575+5637G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64431268 | ||||||
| chr15:64431378
|
G | T | 1 | a0001c0001t0001g0165 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1575+5747G>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64431378 | ||||||
| chr15:64431431
|
C | T | 5 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0002g0215others(2): Show | 5 | HG02055.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1575+5800C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64431431 | ||||||
| chr15:64431469
|
G | A | 3 | a0001c0002t0001g0072a0001c0002t0001g0073a0001c0002t0001g0074 | 3 | HG02615.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1575+5838G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64431469 | ||||||
| chr15:64431677
|
G | T | 1 | a0001c0003t0001g0149 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1575+6046G>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64431677 | ||||||
| chr15:64431831
|
T | TTA | 3 | a0001c0002t0001g0039a0001c0002t0001g0056a0001c0002t0001g0068 | 3 | HG01884.hp2 HG02109.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1575+6216_1575+621 others(6): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64431831 | |||||
| chr15:64431831
|
T | TTATATAT others(3): Show |
1 | a0001c0001t0002g0214 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1575+6208_1575+621 others(14): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64431831 | |||||
| chr15:64431831
|
T | TTATATAT others(19): Show |
1 | a0001c0001t0002g0217 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1575+6217_1575+621 others(30): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64431831 | |||||
| chr15:64431831
|
T | TTATATAT others(21): Show |
1 | a0001c0001t0002g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1575+6217_1575+621 others(32): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64431831 | |||||
| chr15:64431831
|
T | TTATATAT others(25): Show |
2 | a0001c0001t0002g0215a0001c0001t0002g0216 | 2 | HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1575+6217_1575+621 others(36): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64431831 | |||||
| chr15:64431833
|
A | T | 6 | a0001c0002t0001g0207a0001c0002t0001g0208a0001c0002t0001g0209others(3): Show | 6 | HG02559.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1575+6202A>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64431833 | ||||||
| chr15:64431847
|
A | AT | 28 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(25): Show | 29 | HG00642.hp1 HG00733.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.1575+6224dupT | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64431847 | |||||
| chr15:64431847
|
A | ATATATAT others(37): Show |
1 | a0001c0005t0001g0049 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1575+6217_1575+621 others(48): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64431847 | |||||
| chr15:64431847
|
A | ATATATAT others(32): Show |
1 | a0001c0005t0001g0050 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1575+6217_1575+621 others(43): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64431847 | |||||
| chr15:64431847
|
A | ATATATAT others(26): Show |
1 | a0001c0007t0001g0030 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1575+6217_1575+621 others(37): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64431847 | |||||
| chr15:64431847
|
A | ATATATAT others(30): Show |
1 | a0001c0005t0001g0048 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1575+6217_1575+621 others(41): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64431847 | |||||
| chr15:64431847
|
A | ATATATAT others(31): Show |
1 | a0001c0005t0001g0051 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1575+6217_1575+621 others(42): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64431847 | |||||
| chr15:64431847
|
A | ATATATAT others(33): Show |
1 | a0001c0005t0001g0045 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1575+6217_1575+621 others(44): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64431847 | |||||
| chr15:64431847
|
A | ATATATAT others(22): Show |
1 | a0001c0007t0001g0029 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1575+6217_1575+621 others(33): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64431847 | |||||
| chr15:64431847
|
A | ATATATAT others(23): Show |
1 | a0001c0008t0001g0046 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1575+6217_1575+621 others(34): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64431847 | |||||
| chr15:64431847
|
A | ATATATAT others(25): Show |
1 | a0001c0008t0001g0047 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1575+6217_1575+621 others(36): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64431847 | |||||
| chr15:64431847
|
A | ATATATAT others(16): Show |
1 | a0001c0005t0001g0197 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1575+6217_1575+621 others(27): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64431847 | |||||
| chr15:64431847
|
A | ATATATAT others(5): Show |
3 | a0001c0004t0001g0033a0001c0004t0001g0034a0001c0004t0001g0035 | 3 | HG00323.hp1 HG01934.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.1575+6217_1575+621 others(16): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64431847 | |||||
| chr15:64431847
|
A | ATATATAT others(6): Show |
1 | a0001c0004t0001g0032 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1575+6217_1575+621 others(17): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64431847 | |||||
| chr15:64431847
|
A | ATATATAT others(4): Show |
2 | a0001c0004t0001g0036a0001c0004t0001g0037 | 2 | HG02735.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.1575+6217_1575+621 others(15): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64431847 | |||||
| chr15:64431847
|
A | ATATATAT others(5): Show |
1 | a0001c0004t0001g0031 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1575+6217_1575+621 others(16): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64431847 | |||||
| chr15:64431847
|
A | ATATATAT others(6): Show |
2 | a0001c0004t0001g0218a0001c0004t0001g0219 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1575+6217_1575+621 others(17): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64431847 | |||||
| chr15:64431847
|
A | ATATATT | 34 | a0001c0001t0001g0003a0001c0001t0001g0041a0001c0001t0001g0092others(31): Show | 34 | HG00438.hp1 HG00438.hp2 HG00621.hp2 others(31): Show |
intron_variant | MODIFIER | c.1575+6217_1575+621 others(10): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64431847 | |||||
| chr15:64431847
|
A | ATATATTT | 6 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(3): Show | 6 | HG02004.hp1 HG02976.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1575+6217_1575+621 others(11): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64431847 | |||||
| chr15:64431847
|
A | ATATATTT others(14): Show |
2 | a0001c0002t0001g0208a0001c0002t0001g0209 | 2 | HG02976.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1575+6217_1575+621 others(25): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64431847 | |||||
| chr15:64431847
|
A | ATATATTT others(15): Show |
2 | a0001c0002t0001g0207a0001c0002t0001g0210 | 2 | HG02559.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1575+6217_1575+621 others(26): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64431847 | |||||
| chr15:64431847
|
A | ATATTTT | 41 | a0001c0001t0001g0040a0001c0001t0001g0042a0001c0001t0001g0086others(38): Show | 41 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.1575+6217_1575+621 others(10): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64431847 | |||||
| chr15:64431847
|
A | ATATTTTT others(14): Show |
2 | a0001c0002t0001g0211a0001c0002t0001g0212 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1575+6217_1575+621 others(25): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64431847 | |||||
| chr15:64431847
|
A | ATTTTTT | 20 | a0001c0001t0001g0093a0001c0001t0001g0101a0001c0001t0001g0104others(17): Show | 20 | HG00099.hp1 HG00140.hp2 HG01069.hp1 others(17): Show |
intron_variant | MODIFIER | c.1575+6219_1575+622 others(10): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64431847 | |||||
| chr15:64431847
|
A | T | 2 | a0001c0002t0001g0066a0001c0002t0001g0077 | 2 | HG02083.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1575+6216A>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64431847 | ||||||
| chr15:64431849
|
T | A | 5 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0002g0215others(2): Show | 5 | HG02055.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1575+6218T>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64431849 | ||||||
| chr15:64431851
|
T | A | 1 | a0001c0001t0002g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1575+6220T>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64431851 | ||||||
| chr15:64431877
|
C | CT | 10 | a0001c0001t0002g0214a0001c0002t0001g0057a0001c0002t0001g0059others(7): Show | 10 | HG02071.hp2 HG02145.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1575+6270dupT | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64431877 | |||||
| chr15:64431877
|
C | CTT | 5 | a0001c0002t0001g0211a0001c0002t0001g0212a0001c0005t0001g0048others(2): Show | 5 | HG01109.hp2 HG02572.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1575+6269_1575+627 others(6): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64431877 | |||||
| chr15:64431877
|
CT | C | 104 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(101): Show | 104 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(101): Show |
intron_variant | MODIFIER | c.1575+6270delT | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64431877 | |||||
| chr15:64431877
|
CTTTTTTT others(2): Show |
C | 27 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(24): Show | 28 | HG00642.hp1 HG00733.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.1575+6262_1575+627 others(13): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64431877 | |||||
| chr15:64431877
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0004 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1575+6261_1575+627 others(14): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64431877 | |||||
| chr15:64431882
|
T | TC | 9 | a0001c0004t0001g0031a0001c0004t0001g0032a0001c0004t0001g0033others(6): Show | 9 | HG00323.hp1 HG01168.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.1575+6251_1575+625 others(5): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64431882 | ||||||
| chr15:64431884
|
T | C | 1 | a0001c0002t0001g0078 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1575+6253T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64431884 | ||||||
| chr15:64431885
|
T | C | 2 | a0001c0008t0001g0046a0001c0008t0001g0047 | 2 | HG02451.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1575+6254T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64431885 | ||||||
| chr15:64431912
|
C | T | 2 | a0001c0002t0001g0211a0001c0002t0001g0212 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1575+6281C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64431912 | ||||||
| chr15:64431925
|
C | T | 1 | a0001c0001t0001g0120 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1575+6294C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64431925 | ||||||
| chr15:64431964
|
G | C | 1 | a0001c0001t0001g0089 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1575+6333G>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64431964 | ||||||
| chr15:64432047
|
C | T | 4 | a0001c0001t0001g0041a0001c0001t0001g0159a0001c0001t0001g0162others(1): Show | 4 | HG01167.hp2 HG01169.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1575+6416C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64432047 | ||||||
| chr15:64432352
|
G | A | 6 | a0001c0002t0001g0207a0001c0002t0001g0208a0001c0002t0001g0209others(3): Show | 6 | HG02559.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1575+6721G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64432352 | ||||||
| chr15:64432380
|
G | A | 1 | a0001c0001t0001g0131 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1575+6749G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64432380 | ||||||
| chr15:64432436
|
A | AAACC | 166 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(163): Show | 167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.1575+6805_1575+680 others(8): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64432436 | ||||||
| chr15:64432497
|
C | G | 41 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(38): Show | 42 | HG00642.hp1 HG00733.hp1 HG01069.hp2 others(39): Show |
intron_variant | MODIFIER | c.1575+6866C>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64432497 | ||||||
| chr15:64432652
|
C | A | 3 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144 | 3 | HG01071.hp2 HG02683.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.1575+7021C>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64432652 | ||||||
| chr15:64432762
|
T | G | 1 | a0001c0002t0001g0074 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1575+7131T>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64432762 | ||||||
| chr15:64432804
|
G | A | 8 | a0001c0002t0001g0207a0001c0002t0001g0208a0001c0002t0001g0209others(5): Show | 8 | HG02559.hp2 HG02886.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1575+7173G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64432804 | ||||||
| chr15:64432825
|
C | A | 1 | a0001c0002t0001g0074 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1575+7194C>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64432825 | ||||||
| chr15:64432868
|
G | A | 7 | a0001c0005t0001g0045a0001c0005t0001g0048a0001c0005t0001g0049others(4): Show | 7 | HG01109.hp2 HG02280.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1575+7237G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64432868 | ||||||
| chr15:64432869
|
C | T | 1 | a0001c0001t0001g0091 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1575+7238C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64432869 | ||||||
| chr15:64432922
|
A | AAAATAAA others(1): Show |
5 | a0001c0001t0001g0106a0001c0001t0001g0140a0001c0002t0001g0064others(2): Show | 5 | HG01192.hp2 HG01978.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.1575+7311_1575+731 others(12): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64432922 | |||||
| chr15:64432922
|
A | AAAATAAA others(5): Show |
4 | a0001c0005t0001g0048a0001c0005t0001g0050a0001c0008t0001g0046others(1): Show | 4 | HG01109.hp2 HG02451.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.1575+7307_1575+731 others(16): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64432922 | |||||
| chr15:64432922
|
AAAAT | A | 22 | a0001c0001t0001g0101a0001c0001t0001g0186a0001c0002t0001g0044others(19): Show | 22 | HG00621.hp1 HG01884.hp2 HG02071.hp2 others(19): Show |
intron_variant | MODIFIER | c.1575+7315_1575+731 others(8): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64432922 | |||||
| chr15:64432946
|
T | TAAATAAA others(5): Show |
2 | a0001c0005t0001g0049a0001c0005t0001g0051 | 2 | HG03453.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1575+7318_1575+731 others(16): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64432946 | |||||
| chr15:64433167
|
A | G | 1 | a0001c0002t0001g0077 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1575+7536A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64433167 | ||||||
| chr15:64433416
|
C | T | 1 | a0001c0001t0001g0109 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1575+7785C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64433416 | ||||||
| chr15:64433622
|
A | T | 5 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0002g0215others(2): Show | 5 | HG02055.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1575+7991A>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64433622 | ||||||
| chr15:64433748
|
C | T | 1 | a0001c0002t0001g0073 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1575+8117C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64433748 | ||||||
| chr15:64433917
|
AT | A | 165 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(162): Show | 166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.1575+8297delT | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64433917 | |||||
| chr15:64433945
|
C | T | 1 | a0001c0001t0001g0124 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1575+8314C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64433945 | ||||||
| chr15:64434065
|
T | C | 168 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(165): Show | 169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.1575+8434T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64434065 | ||||||
| chr15:64434392
|
T | C | 2 | a0001c0008t0001g0046a0001c0008t0001g0047 | 2 | HG02451.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1575+8761T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64434392 | ||||||
| chr15:64434402
|
G | GA | 163 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(160): Show | 164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.1575+8787dupA | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64434402 | |||||
| chr15:64434838
|
G | A | 3 | a0001c0001t0001g0186a0001c0002t0001g0099a0001c0002t0001g0200 | 3 | HG00621.hp1 NA18987.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.1575+9207G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64434838 | ||||||
| chr15:64434841
|
A | G | 3 | a0001c0002t0001g0072a0001c0002t0001g0073a0001c0002t0001g0074 | 3 | HG02615.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1575+9210A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64434841 | ||||||
| chr15:64434926
|
A | G | 1 | a0001c0001t0001g0155 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1575+9295A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64434926 | ||||||
| chr15:64435004
|
C | G | 108 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(105): Show | 108 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(105): Show |
intron_variant | MODIFIER | c.1575+9373C>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64435004 | ||||||
| chr15:64435213
|
C | CA | 133 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(130): Show | 134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.1575+9606dupA | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64435213 | |||||
| chr15:64435213
|
C | CAA | 17 | a0001c0001t0001g0008a0001c0001t0001g0100a0001c0001t0001g0113others(14): Show | 17 | HG00621.hp2 HG00642.hp2 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.1575+9605_1575+960 others(6): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64435213 | |||||
| chr15:64435213
|
CA | C | 6 | a0001c0002t0001g0184a0001c0006t0001g0075a0001c0006t0001g0076others(3): Show | 6 | HG02486.hp2 HG02622.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1575+9606delA | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64435213 | |||||
| chr15:64435259
|
C | T | 1 | a0001c0001t0001g0119 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1575+9628C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64435259 | ||||||
| chr15:64435260
|
G | A | 1 | a0001c0001t0001g0166 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1575+9629G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64435260 | ||||||
| chr15:64435418
|
C | T | 7 | a0001c0005t0001g0045a0001c0005t0001g0048a0001c0005t0001g0049others(4): Show | 7 | HG01109.hp2 HG02280.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1576-9588C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64435418 | ||||||
| chr15:64435439
|
T | A | 1 | a0001c0002t0001g0198 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1576-9567T>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64435439 | ||||||
| chr15:64435504
|
C | T | 41 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(38): Show | 42 | HG00642.hp1 HG00733.hp1 HG01069.hp2 others(39): Show |
intron_variant | MODIFIER | c.1576-9502C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64435504 | ||||||
| chr15:64435525
|
C | CAAA | 9 | a0001c0004t0001g0031a0001c0004t0001g0032a0001c0004t0001g0033others(6): Show | 9 | HG00323.hp1 HG01168.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.1576-9466_1576-946 others(7): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64435525 | |||||
| chr15:64435525
|
CA | C | 127 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(124): Show | 127 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(124): Show |
intron_variant | MODIFIER | c.1576-9464delA | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64435525 | |||||
| chr15:64435525
|
CAA | C | 5 | a0001c0001t0001g0003a0001c0001t0001g0088a0001c0001t0001g0091others(2): Show | 5 | HG02109.hp2 HG03471.hp1 NA18942.hp1 others(2): Show |
intron_variant | MODIFIER | c.1576-9465_1576-946 others(6): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64435525 | |||||
| chr15:64435541
|
A | T | 2 | a0001c0001t0001g0098a0001c0001t0001g0109 | 2 | HG02683.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.1576-9465A>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64435541 | ||||||
| chr15:64435541
|
AAT | A | 10 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(7): Show | 10 | HG01071.hp2 HG01884.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1576-9462_1576-946 others(6): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64435541 | |||||
| chr15:64435543
|
T | A | 9 | a0001c0004t0001g0031a0001c0004t0001g0032a0001c0004t0001g0033others(6): Show | 9 | HG00323.hp1 HG01168.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.1576-9463T>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64435543 | ||||||
| chr15:64435656
|
T | C | 1 | a0001c0001t0001g0093 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1576-9350T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64435656 | ||||||
| chr15:64435752
|
G | A | 2 | a0001c0001t0001g0110a0001c0001t0001g0128 | 2 | HG00140.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.1576-9254G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64435752 | ||||||
| chr15:64435822
|
T | TA | 105 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0019others(102): Show | 105 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(102): Show |
intron_variant | MODIFIER | c.1576-9163dupA | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64435822 | |||||
| chr15:64435822
|
T | TAA | 23 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(20): Show | 24 | HG00642.hp1 HG00733.hp1 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.1576-9164_1576-916 others(6): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64435822 | |||||
| chr15:64435822
|
TA | T | 8 | a0001c0002t0001g0077a0001c0002t0001g0192a0001c0002t0001g0211others(5): Show | 8 | HG00323.hp1 HG02698.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1576-9163delA | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64435822 | |||||
| chr15:64435848
|
A | G | 1 | a0001c0005t0001g0197 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1576-9158A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64435848 | ||||||
| chr15:64435893
|
G | GA | 164 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(161): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.1576-9099dupA | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64435893 | |||||
| chr15:64436364
|
C | T | 1 | a0001c0001t0001g0087 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1576-8642C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64436364 | ||||||
| chr15:64436375
|
C | T | 1 | a0001c0002t0001g0056 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1576-8631C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64436375 | ||||||
| chr15:64436387
|
T | C | 2 | a0001c0007t0001g0029a0001c0007t0001g0030 | 2 | HG02886.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1576-8619T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64436387 | ||||||
| chr15:64436548
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1576-8458G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64436548 | ||||||
| chr15:64436708
|
CT | C | 123 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0040others(120): Show | 123 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(120): Show |
intron_variant | MODIFIER | c.1576-8281delT | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64436708 | |||||
| chr15:64436708
|
CTT | C | 10 | a0001c0001t0001g0135a0001c0001t0001g0138a0001c0001t0001g0170others(7): Show | 10 | HG01074.hp1 HG01074.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1576-8282_1576-828 others(6): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64436708 | |||||
| chr15:64436725
|
T | A | 3 | a0001c0005t0001g0045a0001c0008t0001g0046a0001c0008t0001g0047 | 3 | HG02280.hp2 HG02451.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1576-8281T>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64436725 | ||||||
| chr15:64436760
|
T | G | 1 | a0001c0002t0001g0077 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1576-8246T>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64436760 | ||||||
| chr15:64436763
|
C | CT | 17 | a0001c0001t0002g0214a0001c0001t0002g0215a0001c0001t0002g0216others(14): Show | 17 | HG02145.hp2 HG02280.hp1 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.1576-8214dupT | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64436763 | |||||
| chr15:64436763
|
C | CTT | 6 | a0001c0001t0002g0213a0001c0001t0002g0217a0001c0002t0001g0074others(3): Show | 6 | HG02055.hp2 HG02615.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1576-8215_1576-821 others(6): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64436763 | |||||
| chr15:64436763
|
C | CTTT | 87 | a0001c0001t0001g0003a0001c0001t0001g0041a0001c0001t0001g0042others(84): Show | 87 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(84): Show |
intron_variant | MODIFIER | c.1576-8216_1576-821 others(7): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64436763 | |||||
| chr15:64436763
|
C | CTTTT | 39 | a0001c0001t0001g0087a0001c0001t0001g0095a0001c0001t0001g0097others(36): Show | 39 | HG00438.hp1 HG00438.hp2 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.1576-8217_1576-821 others(8): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64436763 | |||||
| chr15:64436763
|
C | CTTTTTTT | 10 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(7): Show | 10 | HG00733.hp1 HG01069.hp2 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.1576-8220_1576-821 others(11): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64436763 | |||||
| chr15:64436763
|
C | CTTTTTTT others(1): Show |
12 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(9): Show | 13 | HG00642.hp1 HG02109.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.1576-8221_1576-821 others(12): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64436763 | |||||
| chr15:64436763
|
CTTTTTTT others(3): Show |
C | 2 | a0001c0001t0001g0040a0001c0001t0001g0086 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1576-8223_1576-821 others(14): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64436763 | |||||
| chr15:64437015
|
C | T | 1 | a0001c0001t0001g0204 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1576-7991C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64437015 | ||||||
| chr15:64437263
|
T | TA | 200 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(197): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.1576-7733dupA | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64437263 | |||||
| chr15:64437490
|
G | A | 1 | a0001c0010t0001g0167 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1576-7516G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64437490 | ||||||
| chr15:64437498
|
G | GT | 29 | a0001c0001t0001g0137a0001c0001t0001g0186a0001c0001t0002g0213others(26): Show | 29 | HG00621.hp1 HG02055.hp2 HG02071.hp2 others(26): Show |
intron_variant | MODIFIER | c.1576-7496dupT | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64437498 | |||||
| chr15:64437602
|
C | T | 2 | a0002c0009t0001g0026a0002c0009t0001g0027 | 2 | HG02818.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1576-7404C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64437602 | ||||||
| chr15:64437808
|
C | G | 211 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(208): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.1576-7198C>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64437808 | ||||||
| chr15:64437821
|
A | G | 28 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(25): Show | 29 | HG00642.hp1 HG00733.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.1576-7185A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64437821 | ||||||
| chr15:64438040
|
G | T | 1 | a0001c0010t0001g0167 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1576-6966G>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64438040 | ||||||
| chr15:64438185
|
T | C | 9 | a0001c0004t0001g0031a0001c0004t0001g0032a0001c0004t0001g0033others(6): Show | 9 | HG00323.hp1 HG01168.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.1576-6821T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64438185 | ||||||
| chr15:64438381
|
A | G | 2 | a0001c0004t0001g0218a0001c0004t0001g0219 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1576-6625A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64438381 | ||||||
| chr15:64438397
|
G | T | 9 | a0001c0004t0001g0031a0001c0004t0001g0032a0001c0004t0001g0033others(6): Show | 9 | HG00323.hp1 HG01168.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.1576-6609G>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64438397 | ||||||
| chr15:64438571
|
G | A | 1 | a0001c0002t0001g0039 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1576-6435G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64438571 | ||||||
| chr15:64438623
|
G | C | 9 | a0001c0004t0001g0031a0001c0004t0001g0032a0001c0004t0001g0033others(6): Show | 9 | HG00323.hp1 HG01168.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.1576-6383G>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64438623 | ||||||
| chr15:64438788
|
T | C | 1 | a0001c0005t0001g0197 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1576-6218T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64438788 | ||||||
| chr15:64438834
|
G | A | 1 | a0001c0002t0001g0073 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1576-6172G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64438834 | ||||||
| chr15:64438965
|
A | G | 1 | a0001c0001t0001g0204 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1576-6041A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64438965 | ||||||
| chr15:64439326
|
A | G | 1 | a0001c0002t0001g0069 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1576-5680A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64439326 | ||||||
| chr15:64439367
|
C | T | 8 | a0001c0005t0001g0045a0001c0005t0001g0048a0001c0005t0001g0049others(5): Show | 8 | HG01109.hp2 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1576-5639C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64439367 | ||||||
| chr15:64439480
|
G | A | 108 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(105): Show | 108 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(105): Show |
intron_variant | MODIFIER | c.1576-5526G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64439480 | ||||||
| chr15:64439496
|
A | C | 166 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(163): Show | 167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.1576-5510A>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64439496 | ||||||
| chr15:64439512
|
C | CTTTT | 6 | a0001c0002t0001g0207a0001c0002t0001g0208a0001c0002t0001g0209others(3): Show | 6 | HG02559.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1576-5469_1576-546 others(8): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64439512 | |||||
| chr15:64439512
|
CT | C | 60 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0090others(57): Show | 60 | HG00099.hp2 HG00323.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.1576-5466delT | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64439512 | |||||
| chr15:64439512
|
CTT | C | 125 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(122): Show | 126 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(123): Show |
intron_variant | MODIFIER | c.1576-5467_1576-546 others(6): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64439512 | |||||
| chr15:64439512
|
CTTT | C | 7 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0174others(4): Show | 7 | HG02004.hp1 HG02897.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1576-5468_1576-546 others(7): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64439512 | |||||
| chr15:64440053
|
T | TTA | 33 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(30): Show | 34 | HG00642.hp1 HG00733.hp1 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.1576-4942_1576-494 others(6): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64440053 | |||||
| chr15:64440234
|
ATAAT | A | 2 | a0001c0002t0001g0060a0001c0002t0001g0065 | 2 | HG03942.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1576-4763_1576-476 others(8): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64440234 | |||||
| chr15:64440459
|
C | CT | 169 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(166): Show | 169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.1576-4534dupT | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64440459 | |||||
| chr15:64440459
|
C | CTT | 43 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(40): Show | 44 | HG00323.hp1 HG00642.hp1 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.1576-4535_1576-453 others(6): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64440459 | |||||
| chr15:64440640
|
G | T | 1 | a0001c0001t0001g0204 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1576-4366G>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64440640 | ||||||
| chr15:64440990
|
AT | A | 29 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(26): Show | 30 | HG00642.hp1 HG00733.hp1 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.1576-4002delT | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64440990 | |||||
| chr15:64441005
|
A | T | 2 | a0001c0001t0001g0087a0001c0001t0001g0090 | 2 | HG00099.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1576-4001A>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64441005 | ||||||
| chr15:64441024
|
G | A | 7 | a0001c0001t0001g0118a0001c0001t0001g0174a0001c0001t0001g0176others(4): Show | 7 | HG02004.hp1 HG02976.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.1576-3982G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64441024 | ||||||
| chr15:64441089
|
C | T | 2 | a0002c0009t0001g0026a0002c0009t0001g0027 | 2 | HG02818.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1576-3917C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64441089 | ||||||
| chr15:64441146
|
G | A | 1 | a0001c0002t0001g0038 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1576-3860G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64441146 | ||||||
| chr15:64441221
|
C | G | 1 | a0001c0002t0001g0043 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1576-3785C>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64441221 | ||||||
| chr15:64441305
|
C | T | 2 | a0001c0008t0001g0046a0001c0008t0001g0047 | 2 | HG02451.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1576-3701C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64441305 | ||||||
| chr15:64441430
|
A | C | 1 | a0001c0005t0001g0051 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1576-3576A>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64441430 | ||||||
| chr15:64441698
|
G | A | 4 | a0001c0005t0001g0048a0001c0005t0001g0049a0001c0005t0001g0050others(1): Show | 4 | HG01109.hp2 HG02572.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1576-3308G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64441698 | ||||||
| chr15:64442140
|
C | T | 9 | a0001c0004t0001g0031a0001c0004t0001g0032a0001c0004t0001g0033others(6): Show | 9 | HG00323.hp1 HG01168.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.1576-2866C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64442140 | ||||||
| chr15:64442198
|
CA | C | 106 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(103): Show |
intron_variant | MODIFIER | c.1576-2794delA | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64442198 | |||||
| chr15:64442263
|
G | A | 3 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144 | 3 | HG01071.hp2 HG02683.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.1576-2743G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64442263 | ||||||
| chr15:64442514
|
G | T | 1 | a0001c0001t0001g0123 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1576-2492G>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64442514 | ||||||
| chr15:64442524
|
A | G | 5 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0002g0215others(2): Show | 5 | HG02055.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1576-2482A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64442524 | ||||||
| chr15:64442597
|
T | C | 5 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0002g0215others(2): Show | 5 | HG02055.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1576-2409T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64442597 | ||||||
| chr15:64442624
|
T | TA | 200 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(197): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.1576-2370dupA | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64442624 | |||||
| chr15:64443018
|
C | T | 2 | a0001c0002t0001g0099a0001c0002t0001g0200 | 2 | HG00621.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.1576-1988C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64443018 | ||||||
| chr15:64443081
|
T | C | 1 | a0001c0001t0001g0130 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1576-1925T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64443081 | ||||||
| chr15:64443257
|
G | A | 8 | a0001c0002t0001g0207a0001c0002t0001g0208a0001c0002t0001g0209others(5): Show | 8 | HG02559.hp2 HG02886.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1576-1749G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64443257 | ||||||
| chr15:64443328
|
G | A | 109 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.1576-1678G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64443328 | ||||||
| chr15:64443892
|
A | G | 9 | a0001c0004t0001g0031a0001c0004t0001g0032a0001c0004t0001g0033others(6): Show | 9 | HG00323.hp1 HG01168.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.1576-1114A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64443892 | ||||||
| chr15:64444007
|
G | GTT | 109 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.1576-997_1576-996d others(4): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64444007 | |||||
| chr15:64444088
|
T | C | 109 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.1576-918T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64444088 | ||||||
| chr15:64444175
|
C | G | 8 | a0001c0001t0001g0095a0001c0001t0001g0102a0001c0001t0001g0125others(5): Show | 8 | HG01071.hp2 HG02055.hp1 HG02683.hp2 others(5): Show |
intron_variant | MODIFIER | c.1576-831C>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64444175 | ||||||
| chr15:64444466
|
G | A | 2 | a0001c0007t0001g0029a0001c0007t0001g0030 | 2 | HG02886.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1576-540G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64444466 | ||||||
| chr15:64444506
|
T | C | 9 | a0001c0002t0001g0039a0001c0002t0001g0068a0001c0002t0001g0069others(6): Show | 9 | HG02109.hp2 HG02486.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1576-500T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64444506 | ||||||
| chr15:64444674
|
A | G | 1 | a0001c0001t0001g0204 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1576-332A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64444674 | ||||||
| chr15:64444746
|
C | CT | 48 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(45): Show | 49 | HG00099.hp1 HG00642.hp1 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.1576-240dupT | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64444746 | |||||
| chr15:64444746
|
C | CTT | 147 | a0001c0001t0001g0003a0001c0001t0001g0028a0001c0001t0001g0086others(144): Show | 147 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.1576-241_1576-240d others(4): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 64444746 | |||||
| chr15:64444826
|
G | C | 8 | a0001c0005t0001g0045a0001c0005t0001g0048a0001c0005t0001g0049others(5): Show | 8 | HG01109.hp2 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1576-180G>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64444826 | ||||||
| chr15:64444904
|
G | C | 161 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(158): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.1576-102G>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 11/12 | chr15 | 64444904 | ||||||
| chr15:64445134
|
G | A | 8 | a0001c0002t0001g0053a0001c0002t0001g0054a0001c0002t0001g0055others(5): Show | 8 | HG01884.hp2 HG02145.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1678+26G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64445134 | ||||||
| chr15:64445173
|
A | G | 1 | a0001c0001t0001g0157 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1678+65A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64445173 | ||||||
| chr15:64445412
|
G | A | 8 | a0001c0005t0001g0045a0001c0005t0001g0048a0001c0005t0001g0049others(5): Show | 8 | HG01109.hp2 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1678+304G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64445412 | ||||||
| chr15:64445433
|
C | T | 41 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(38): Show | 42 | HG00642.hp1 HG00733.hp1 HG01069.hp2 others(39): Show |
intron_variant | MODIFIER | c.1678+325C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64445433 | ||||||
| chr15:64445474
|
CA | C | 135 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(132): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.1678+384delA | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 64445474 | |||||
| chr15:64445488
|
A | G | 1 | a0001c0001t0001g0158 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1678+380A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64445488 | ||||||
| chr15:64445539
|
A | G | 1 | a0001c0001t0001g0158 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1678+431A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64445539 | ||||||
| chr15:64445584
|
G | C | 1 | a0001c0001t0001g0089 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1678+476G>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64445584 | ||||||
| chr15:64445608
|
A | C | 1 | a0001c0001t0001g0158 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1678+500A>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64445608 | ||||||
| chr15:64445638
|
C | T | 3 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144 | 3 | HG01071.hp2 HG02683.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.1678+530C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64445638 | ||||||
| chr15:64445659
|
C | T | 6 | a0001c0002t0001g0207a0001c0002t0001g0208a0001c0002t0001g0209others(3): Show | 6 | HG02559.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1678+551C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64445659 | ||||||
| chr15:64445666
|
T | TCAAA | 2 | a0001c0001t0001g0004a0001c0001t0001g0009 | 2 | HG01069.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1678+559_1678+562d others(6): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 64445666 | |||||
| chr15:64445667
|
C | CA | 99 | a0001c0001t0001g0003a0001c0001t0001g0041a0001c0001t0001g0042others(96): Show | 99 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(96): Show |
intron_variant | MODIFIER | c.1678+583dupA | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 64445667 | |||||
| chr15:64445667
|
C | CAA | 10 | a0001c0001t0001g0104a0001c0001t0001g0106a0001c0001t0001g0145others(7): Show | 10 | HG00733.hp2 HG01978.hp2 HG03098.hp1 others(7): Show |
intron_variant | MODIFIER | c.1678+582_1678+583d others(4): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 64445667 | |||||
| chr15:64445667
|
C | CAAACA | 24 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(21): Show | 25 | HG00642.hp1 HG00733.hp1 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.1678+562_1678+563i others(7): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 64445667 | |||||
| chr15:64445667
|
CA | C | 12 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0002g0215others(9): Show | 12 | HG01169.hp1 HG02055.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1678+583delA | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 64445667 | |||||
| chr15:64446002
|
G | A | 1 | a0001c0002t0001g0074 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1678+894G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64446002 | ||||||
| chr15:64446062
|
C | T | 5 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0002g0215others(2): Show | 5 | HG02055.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1678+954C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64446062 | ||||||
| chr15:64446198
|
C | T | 1 | a0001c0001t0001g0158 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1678+1090C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64446198 | ||||||
| chr15:64446230
|
C | A | 3 | a0001c0002t0001g0054a0001c0002t0001g0057a0001c0002t0001g0058 | 3 | HG02145.hp2 HG02280.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1678+1122C>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64446230 | ||||||
| chr15:64446283
|
G | A | 1 | a0002c0009t0001g0027 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1678+1175G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64446283 | ||||||
| chr15:64446363
|
C | T | 28 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(25): Show | 29 | HG00642.hp1 HG00733.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.1678+1255C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64446363 | ||||||
| chr15:64446381
|
C | G | 36 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(33): Show | 37 | HG00642.hp1 HG00733.hp1 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.1678+1273C>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64446381 | ||||||
| chr15:64446406
|
A | AT | 9 | a0001c0001t0001g0095a0001c0001t0001g0102a0001c0001t0001g0104others(6): Show | 9 | HG00642.hp2 HG01169.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1678+1314dupT | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 64446406 | |||||
| chr15:64446427
|
CAG | C | 5 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0002g0215others(2): Show | 5 | HG02055.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1678+1322_1678+132 others(6): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 64446427 | |||||
| chr15:64446523
|
C | G | 200 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(197): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.1678+1415C>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64446523 | ||||||
| chr15:64446565
|
T | C | 5 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0002g0215others(2): Show | 5 | HG02055.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1678+1457T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64446565 | ||||||
| chr15:64446651
|
C | G | 9 | a0001c0002t0001g0039a0001c0002t0001g0068a0001c0002t0001g0069others(6): Show | 9 | HG02109.hp2 HG02486.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1678+1543C>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64446651 | ||||||
| chr15:64446838
|
C | T | 2 | a0001c0007t0001g0029a0001c0007t0001g0030 | 2 | HG02886.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1678+1730C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64446838 | ||||||
| chr15:64447134
|
CA | C | 21 | a0001c0002t0001g0044a0001c0002t0001g0053a0001c0002t0001g0054others(18): Show | 21 | HG00621.hp1 HG01884.hp2 HG02071.hp2 others(18): Show |
intron_variant | MODIFIER | c.1678+2034delA | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 64447134 | |||||
| chr15:64447142
|
A | AC | 7 | a0001c0005t0001g0045a0001c0005t0001g0048a0001c0005t0001g0049others(4): Show | 7 | HG01109.hp2 HG02280.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1678+2035dupC | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 64447142 | |||||
| chr15:64447204
|
C | T | 27 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(24): Show | 28 | HG00642.hp1 HG00733.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.1678+2096C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64447204 | ||||||
| chr15:64447397
|
A | G | 1 | a0001c0001t0001g0158 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1678+2289A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64447397 | ||||||
| chr15:64447431
|
C | A | 108 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(105): Show | 108 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(105): Show |
intron_variant | MODIFIER | c.1678+2323C>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64447431 | ||||||
| chr15:64447526
|
A | G | 3 | a0001c0001t0001g0028a0002c0009t0001g0026a0002c0009t0001g0027 | 3 | HG02818.hp2 HG03471.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1678+2418A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64447526 | ||||||
| chr15:64447991
|
A | G | 1 | a0001c0001t0001g0022 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1678+2883A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64447991 | ||||||
| chr15:64448288
|
A | T | 8 | a0001c0005t0001g0045a0001c0005t0001g0048a0001c0005t0001g0049others(5): Show | 8 | HG01109.hp2 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1678+3180A>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64448288 | ||||||
| chr15:64448305
|
A | G | 1 | a0001c0001t0001g0093 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1678+3197A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64448305 | ||||||
| chr15:64448367
|
T | G | 1 | a0001c0005t0001g0045 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1678+3259T>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64448367 | ||||||
| chr15:64448559
|
G | A | 6 | a0001c0002t0001g0207a0001c0002t0001g0208a0001c0002t0001g0209others(3): Show | 6 | HG02559.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1678+3451G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64448559 | ||||||
| chr15:64448611
|
G | A | 9 | a0001c0004t0001g0031a0001c0004t0001g0032a0001c0004t0001g0033others(6): Show | 9 | HG00323.hp1 HG01168.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.1678+3503G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64448611 | ||||||
| chr15:64448690
|
C | T | 2 | a0001c0007t0001g0029a0001c0007t0001g0030 | 2 | HG02886.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1678+3582C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64448690 | ||||||
| chr15:64448771
|
G | T | 4 | a0001c0002t0001g0209a0001c0002t0001g0210a0001c0002t0001g0211others(1): Show | 4 | HG02559.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1678+3663G>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64448771 | ||||||
| chr15:64448893
|
A | G | 1 | a0001c0002t0001g0184 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1678+3785A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64448893 | ||||||
| chr15:64449054
|
T | G | 1 | a0001c0007t0001g0030 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1678+3946T>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64449054 | ||||||
| chr15:64449212
|
TA | T | 24 | a0001c0001t0001g0003a0001c0001t0001g0041a0001c0001t0001g0096others(21): Show | 24 | HG00438.hp1 HG00438.hp2 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.1678+4116delA | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 64449212 | |||||
| chr15:64449271
|
G | GT | 7 | a0001c0005t0001g0045a0001c0005t0001g0048a0001c0005t0001g0049others(4): Show | 7 | HG01109.hp2 HG02280.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1678+4171dupT | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 64449271 | |||||
| chr15:64449289
|
T | C | 41 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(38): Show | 42 | HG00642.hp1 HG00733.hp1 HG01069.hp2 others(39): Show |
intron_variant | MODIFIER | c.1678+4181T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64449289 | ||||||
| chr15:64449289
|
TG | T | 2 | a0001c0007t0001g0029a0001c0007t0001g0030 | 2 | HG02886.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1678+4182delG | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64449289 | ||||||
| chr15:64449290
|
G | GT | 8 | a0001c0001t0001g0005a0001c0001t0001g0025a0001c0001t0001g0092others(5): Show | 8 | HG00438.hp1 HG00438.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.1678+4194dupT | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 64449290 | |||||
| chr15:64449291
|
T | G | 3 | a0001c0001t0001g0041a0001c0001t0001g0162a0001c0001t0001g0172 | 3 | HG01167.hp2 HG01169.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1678+4183T>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64449291 | ||||||
| chr15:64449296
|
T | G | 9 | a0001c0004t0001g0031a0001c0004t0001g0032a0001c0004t0001g0033others(6): Show | 9 | HG00323.hp1 HG01168.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.1678+4188T>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64449296 | ||||||
| chr15:64449343
|
T | C | 1 | a0001c0005t0001g0197 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1678+4235T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64449343 | ||||||
| chr15:64449444
|
C | T | 74 | a0001c0001t0001g0003a0001c0001t0001g0041a0001c0001t0001g0095others(71): Show | 74 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.1678+4336C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64449444 | ||||||
| chr15:64449562
|
G | A | 28 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(25): Show | 29 | HG00642.hp1 HG00733.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.1678+4454G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64449562 | ||||||
| chr15:64449571
|
C | CAT | 25 | a0001c0001t0001g0003a0001c0001t0001g0041a0001c0001t0001g0096others(22): Show | 25 | HG00438.hp1 HG00438.hp2 HG00621.hp2 others(22): Show |
intron_variant | MODIFIER | c.1678+4477_1678+447 others(6): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 64449571 | |||||
| chr15:64449587
|
A | T | 2 | a0001c0001t0001g0012a0001c0005t0001g0048 | 2 | HG01109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1678+4479A>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64449587 | ||||||
| chr15:64449611
|
CTTAAA | C | 4 | a0001c0004t0001g0031a0001c0004t0001g0033a0001c0004t0001g0034others(1): Show | 4 | HG00323.hp1 HG01934.hp2 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.1678+4509_1678+451 others(9): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 64449611 | |||||
| chr15:64449622
|
G | A | 1 | a0001c0001t0001g0132 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1678+4514G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64449622 | ||||||
| chr15:64449866
|
A | G | 8 | a0001c0005t0001g0045a0001c0005t0001g0048a0001c0005t0001g0049others(5): Show | 8 | HG01109.hp2 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1678+4758A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64449866 | ||||||
| chr15:64450068
|
A | T | 8 | a0001c0001t0001g0097a0001c0001t0001g0120a0001c0001t0001g0121others(5): Show | 8 | HG00140.hp2 HG01109.hp1 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.1679-4929A>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64450068 | ||||||
| chr15:64450151
|
T | C | 2 | a0001c0007t0001g0029a0001c0007t0001g0030 | 2 | HG02886.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1679-4846T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64450151 | ||||||
| chr15:64450384
|
G | C | 2 | a0001c0001t0001g0087a0001c0001t0001g0090 | 2 | HG00099.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1679-4613G>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64450384 | ||||||
| chr15:64450393
|
G | GA | 40 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(37): Show | 41 | HG00642.hp1 HG01069.hp2 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.1679-4583dupA | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 64450393 | |||||
| chr15:64450409
|
A | G | 3 | a0001c0002t0001g0072a0001c0002t0001g0073a0001c0002t0001g0074 | 3 | HG02615.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1679-4588A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64450409 | ||||||
| chr15:64450411
|
A | G | 1 | a0001c0001t0001g0115 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1679-4586A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64450411 | ||||||
| chr15:64450471
|
T | A | 161 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(158): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.1679-4526T>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64450471 | ||||||
| chr15:64450563
|
A | T | 1 | a0001c0007t0001g0030 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1679-4434A>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64450563 | ||||||
| chr15:64451278
|
A | G | 1 | a0001c0002t0001g0184 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1679-3719A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64451278 | ||||||
| chr15:64451369
|
TC | T | 9 | a0001c0004t0001g0031a0001c0004t0001g0032a0001c0004t0001g0033others(6): Show | 9 | HG00323.hp1 HG01168.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.1679-3626delC | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 64451369 | |||||
| chr15:64451465
|
CT | C | 81 | a0001c0001t0001g0040a0001c0001t0001g0042a0001c0001t0001g0086others(78): Show | 81 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(78): Show |
intron_variant | MODIFIER | c.1679-3509delT | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 64451465 | |||||
| chr15:64451465
|
CTT | C | 49 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(46): Show | 50 | HG00642.hp1 HG00733.hp1 HG01069.hp2 others(47): Show |
intron_variant | MODIFIER | c.1679-3510_1679-350 others(6): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 64451465 | |||||
| chr15:64451465
|
CTTT | C | 77 | a0001c0001t0001g0003a0001c0001t0001g0041a0001c0001t0001g0095others(74): Show | 77 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.1679-3511_1679-350 others(7): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 64451465 | |||||
| chr15:64451546
|
A | G | 2 | a0001c0007t0001g0029a0001c0007t0001g0030 | 2 | HG02886.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1679-3451A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64451546 | ||||||
| chr15:64451584
|
A | G | 1 | a0001c0001t0001g0097 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1679-3413A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64451584 | ||||||
| chr15:64451637
|
A | G | 1 | a0001c0007t0001g0029 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1679-3360A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64451637 | ||||||
| chr15:64451684
|
A | T | 5 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0002g0215others(2): Show | 5 | HG02055.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1679-3313A>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64451684 | ||||||
| chr15:64451953
|
CA | C | 193 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(190): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.1679-3029delA | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 64451953 | |||||
| chr15:64451968
|
A | T | 1 | a0001c0001t0001g0094 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1679-3029A>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64451968 | ||||||
| chr15:64452085
|
T | C | 161 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(158): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.1679-2912T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64452085 | ||||||
| chr15:64452591
|
T | C | 9 | a0001c0004t0001g0031a0001c0004t0001g0032a0001c0004t0001g0033others(6): Show | 9 | HG00323.hp1 HG01168.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.1679-2406T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64452591 | ||||||
| chr15:64452680
|
G | C | 3 | a0001c0001t0001g0113a0001c0001t0001g0165a0001c0001t0001g0203 | 3 | NA18972.hp1 NA19084.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1679-2317G>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64452680 | ||||||
| chr15:64452889
|
T | C | 1 | a0001c0010t0001g0167 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1679-2108T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64452889 | ||||||
| chr15:64453000
|
C | T | 1 | a0001c0002t0001g0184 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1679-1997C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64453000 | ||||||
| chr15:64453060
|
C | G | 9 | a0001c0001t0001g0118a0001c0001t0001g0158a0001c0001t0001g0174others(6): Show | 9 | HG02004.hp1 HG02976.hp1 HG03098.hp1 others(6): Show |
intron_variant | MODIFIER | c.1679-1937C>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64453060 | ||||||
| chr15:64453071
|
A | AGCTACAG others(5): Show |
1 | a0001c0002t0001g0195 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1679-1921_1679-191 others(16): Show |
TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 64453071 | |||||
| chr15:64453080
|
G | T | 2 | a0001c0001t0001g0116a0001c0001t0001g0163 | 2 | HG00438.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.1679-1917G>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64453080 | ||||||
| chr15:64453335
|
A | G | 1 | a0001c0002t0001g0079 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1679-1662A>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64453335 | ||||||
| chr15:64453424
|
G | A | 1 | a0001c0004t0001g0033 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1679-1573G>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64453424 | ||||||
| chr15:64454217
|
T | A | 1 | a0001c0001t0001g0071 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1679-780T>A | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64454217 | ||||||
| chr15:64454249
|
C | G | 2 | a0001c0007t0001g0029a0001c0007t0001g0030 | 2 | HG02886.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1679-748C>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64454249 | ||||||
| chr15:64454394
|
C | G | 1 | a0001c0002t0001g0208 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1679-603C>G | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64454394 | ||||||
| chr15:64454598
|
CA | C | 5 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0002g0215others(2): Show | 5 | HG02055.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1679-398delA | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64454598 | ||||||
| chr15:64454600
|
T | C | 5 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0002g0215others(2): Show | 5 | HG02055.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1679-397T>C | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64454600 | ||||||
| chr15:64454627
|
C | T | 5 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0002g0215others(2): Show | 5 | HG02055.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1679-370C>T | TRIP4 | ENSG00000103671.10 | transcript | ENST00000261884.8 | protein_coding | 12/12 | chr15 | 64454627 |