| geneid | 8295 |
|---|---|
| ensemblid | ENSG00000196367.15 |
| hgncid | 12347 |
| symbol | TRRAP |
| name | transformation/transcription domain associated protein |
| refseq_nuc | NM_001375524.1 |
| refseq_prot | NP_001362453.1 |
| ensembl_nuc | ENST00000456197.2 |
| ensembl_prot | ENSP00000394645.2 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 98878532 |
| end | 99013241 |
| strand | + |
| ver | v1.2 |
| region | chr7:98878532-99013241 |
| region5000 | chr7:98873532-99018241 |
| regionname0 | TRRAP_chr7_98878532_99013241 |
| regionname5000 | TRRAP_chr7_98873532_99018241 |
| 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 | 3873 | 247 | 80 | 40 | 97 | 12 | 16 | 72 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0002 | 0/0 | 3873 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0003 | 0/0 | 3873 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0004 | 0/0 | 3873 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0005 | 0/0 | 3873 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0006 | 0/0 | 3873 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0007 | 0/0 | 3873 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0008 | 0/0 | 3873 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0009 | 0/0 | 3873 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0010 | 0/0 | 3873 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0011 | 0/0 | 3873 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0012 | 0/0 | 3873 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0013 | 0/0 | 3873 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0014 | 0/0 | 3873 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 11622 | 167 | 25 | 30 | 88 | 10 | 12 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| c0002 | 0/0 | 11622 | 23 | 17 | 5 | 0 | 1 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| c0003 | 0/0 | 11622 | 10 | 7 | 3 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| c0004 | 0/0 | 11622 | 9 | 9 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| c0005 | 0/0 | 11622 | 6 | 6 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| c0006 | 0/0 | 11622 | 4 | 4 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| c0007 | 0/0 | 11622 | 2 | 2 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| c0008 | 0/0 | 11622 | 2 | 2 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| c0009 | 0/0 | 11622 | 2 | 2 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| c0010 | 0/0 | 11622 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| c0011 | 0/0 | 11622 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| c0012 | 0/0 | 11622 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| c0013 | 0/0 | 11622 | 1 | 0 | 0 | 0 | 1 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| c0014 | 0/0 | 11622 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| c0015 | 0/0 | 11622 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| c0016 | 0/0 | 11622 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| c0017 | 0/0 | 11622 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| c0018 | 0/0 | 11622 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| c0019 | 0/0 | 11622 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| c0020 | 0/0 | 11622 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| c0021 | 0/0 | 11622 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| c0022 | 0/0 | 11622 | 1 | 0 | 0 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| c0023 | 0/0 | 11622 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| c0024 | 0/0 | 11622 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| c0025 | 0/0 | 11622 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| c0026 | 0/0 | 11622 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| c0027 | 0/0 | 11622 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| c0028 | 0/0 | 11622 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| c0029 | 0/0 | 11622 | 1 | 0 | 0 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| c0030 | 0/0 | 11622 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| c0031 | 0/0 | 11622 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| c0032 | 0/0 | 11622 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| c0033 | 0/0 | 11622 | 1 | 0 | 0 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| c0034 | 0/0 | 11622 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| c0035 | 0/0 | 11622 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| c0036 | 0/0 | 11622 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| c0037 | 0/0 | 11622 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| c0038 | 0/0 | 11622 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| c0039 | 0/0 | 11622 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| c0040 | 0/0 | 11622 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| c0041 | 0/0 | 11622 | 1 | 0 | 0 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| c0042 | 0/0 | 11622 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| c0043 | 0/0 | 11622 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| c0044 | 0/0 | 11622 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| c0045 | 0/0 | 11622 | 1 | 0 | 0 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| c0046 | 0/0 | 11622 | 1 | 0 | 0 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| 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 | 1054 | 133 | 19 | 22 | 66 | 6 | 18 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| t0002 | 0/0 | 1054 | 92 | 49 | 13 | 27 | 3 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| t0003 | 0/0 | 1054 | 11 | 0 | 0 | 11 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| t0004 | 0/0 | 1054 | 6 | 6 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| t0005 | 0/0 | 1053 | 5 | 5 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| t0006 | 0/0 | 1054 | 5 | 0 | 3 | 0 | 2 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| t0007 | 0/0 | 1054 | 3 | 0 | 2 | 0 | 1 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| t0008 | 0/0 | 1054 | 2 | 2 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| t0009 | 0/0 | 1054 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| t0010 | 0/0 | 1054 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| t0011 | 0/0 | 1054 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| t0012 | 0/0 | 1054 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| t0013 | 0/0 | 1054 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0133 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0227 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 11622 | 167 | 25 | 30 | 88 | 10 | 12 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0001c0002 | 0/0 | 11622 | 23 | 17 | 5 | 0 | 1 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0001c0003 | 0/0 | 11622 | 10 | 7 | 3 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0001c0004 | 0/0 | 11622 | 9 | 9 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0001c0005 | 0/0 | 11622 | 6 | 6 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0001c0006 | 0/0 | 11622 | 4 | 4 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0001c0007 | 0/0 | 11622 | 2 | 2 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0001c0009 | 0/0 | 11622 | 2 | 2 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0001c0010 | 0/0 | 11622 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0001c0011 | 0/0 | 11622 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0001c0012 | 0/0 | 11622 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0001c0013 | 0/0 | 11622 | 1 | 0 | 0 | 0 | 1 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0001c0014 | 0/0 | 11622 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0001c0017 | 0/0 | 11622 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0001c0018 | 0/0 | 11622 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0001c0019 | 0/0 | 11622 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0001c0021 | 0/0 | 11622 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0001c0022 | 0/0 | 11622 | 1 | 0 | 0 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0001c0023 | 0/0 | 11622 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0001c0024 | 0/0 | 11622 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0001c0025 | 0/0 | 11622 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0001c0026 | 0/0 | 11622 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0001c0027 | 0/0 | 11622 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0001c0028 | 0/0 | 11622 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0001c0030 | 0/0 | 11622 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0001c0031 | 0/0 | 11622 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0001c0033 | 0/0 | 11622 | 1 | 0 | 0 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0001c0038 | 0/0 | 11622 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0001c0043 | 0/0 | 11622 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0001c0044 | 0/0 | 11622 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0001c0045 | 0/0 | 11622 | 1 | 0 | 0 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0001c0046 | 0/0 | 11622 | 1 | 0 | 0 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0002c0008 | 0/0 | 11622 | 2 | 2 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0003c0036 | 0/0 | 11622 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0003c0037 | 0/0 | 11622 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0004c0040 | 0/0 | 11622 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0005c0034 | 0/0 | 11622 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0006c0042 | 0/0 | 11622 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0007c0020 | 0/0 | 11622 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0008c0029 | 0/0 | 11622 | 1 | 0 | 0 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0009c0015 | 0/0 | 11622 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0010c0039 | 0/0 | 11622 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0011c0032 | 0/0 | 11622 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0012c0035 | 0/0 | 11622 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0013c0016 | 0/0 | 11622 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0014c0041 | 0/0 | 11622 | 1 | 0 | 0 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 12675 | 113 | 14 | 20 | 59 | 6 | 12 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0001c0001t0002 | 0/0 | 12675 | 36 | 7 | 7 | 20 | 2 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0001c0001t0003 | 0/0 | 12675 | 9 | 0 | 0 | 9 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0001c0001t0005 | 0/0 | 12674 | 3 | 3 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0001c0001t0006 | 0/0 | 12675 | 5 | 0 | 3 | 0 | 2 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0001c0001t0011 | 0/0 | 12675 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0001c0002t0002 | 0/0 | 12675 | 17 | 14 | 3 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0001c0002t0007 | 0/0 | 12675 | 3 | 0 | 2 | 0 | 1 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0001c0002t0009 | 0/0 | 12675 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0001c0002t0010 | 0/0 | 12675 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0001c0002t0012 | 0/0 | 12675 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0001c0003t0002 | 0/0 | 12675 | 10 | 7 | 3 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0001c0004t0002 | 0/0 | 12675 | 9 | 9 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0001c0005t0004 | 0/0 | 12675 | 6 | 6 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0001c0006t0002 | 0/0 | 12675 | 4 | 4 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0001c0007t0001 | 0/0 | 12675 | 2 | 2 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0001c0009t0002 | 0/0 | 12675 | 2 | 2 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0001c0010t0001 | 0/0 | 12675 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0001c0011t0013 | 0/0 | 12675 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0001c0012t0001 | 0/0 | 12675 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0001c0013t0002 | 0/0 | 12675 | 1 | 0 | 0 | 0 | 1 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0001c0014t0002 | 0/0 | 12675 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0001c0017t0001 | 0/0 | 12675 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0001c0018t0002 | 0/0 | 12675 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0001c0019t0001 | 0/0 | 12675 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0001c0021t0001 | 0/0 | 12675 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0001c0022t0001 | 0/0 | 12675 | 1 | 0 | 0 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0001c0023t0002 | 0/0 | 12675 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0001c0024t0001 | 0/0 | 12675 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0001c0025t0001 | 0/0 | 12675 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0001c0026t0003 | 0/0 | 12675 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0001c0027t0001 | 0/0 | 12675 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0001c0028t0002 | 0/0 | 12675 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0001c0030t0001 | 0/0 | 12675 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0001c0031t0002 | 0/0 | 12675 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0001c0033t0001 | 0/0 | 12675 | 1 | 0 | 0 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0001c0038t0001 | 0/0 | 12675 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0001c0043t0002 | 0/0 | 12675 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0001c0044t0002 | 0/0 | 12675 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0001c0045t0001 | 0/0 | 12675 | 1 | 0 | 0 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0001c0046t0001 | 0/0 | 12675 | 1 | 0 | 0 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0002c0008t0008 | 0/0 | 12675 | 2 | 2 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0003c0036t0002 | 0/0 | 12675 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0003c0037t0002 | 0/0 | 12675 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0004c0040t0005 | 0/0 | 12674 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0005c0034t0003 | 0/0 | 12675 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0006c0042t0002 | 0/0 | 12675 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0007c0020t0001 | 0/0 | 12675 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0008c0029t0001 | 0/0 | 12675 | 1 | 0 | 0 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0009c0015t0002 | 0/0 | 12675 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0010c0039t0002 | 0/0 | 12675 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0011c0032t0005 | 0/0 | 12674 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0012c0035t0002 | 0/0 | 12675 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0013c0016t0001 | 0/0 | 12675 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| a0014c0041t0001 | 0/0 | 12675 | 1 | 0 | 0 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | copy fasta | chr7 | 98873532 | 99018241 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0133 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0227 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0002g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0003g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0003g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0003g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0005g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0005g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0005g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0006g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0006g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0006g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0006g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0006g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0001t0011g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0002t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0002t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0002t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0002t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0002t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0002t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0002t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0002t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0002t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0002t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0002t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0002t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0002t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0002t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0002t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0002t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0002t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0002t0007g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0002t0007g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0002t0007g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0002t0009g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0002t0010g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0002t0012g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0003t0002g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0003t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0003t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0003t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0003t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0003t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0003t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0003t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0003t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0004t0002g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0004t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0004t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0004t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0004t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0004t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0004t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0004t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0005t0004g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0005t0004g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0005t0004g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0005t0004g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0005t0004g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0005t0004g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0006t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0006t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0006t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0006t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0007t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0007t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0009t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0009t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0010t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0011t0013g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0012t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0013t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0014t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0017t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0018t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0019t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0021t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0022t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0023t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0024t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0025t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0026t0003g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0027t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0028t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0030t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0031t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0033t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0038t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0043t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0044t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0045t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0001c0046t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0002c0008t0008g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0002c0008t0008g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0003c0036t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0003c0037t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0004c0040t0005g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0005c0034t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0006c0042t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0007c0020t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0008c0029t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0009c0015t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0010c0039t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0011c0032t0005g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0012c0035t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0013c0016t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| a0014c0041t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0107 | EUR | GBR | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG00140 | hp2 | a0001 | c0002 | t0007 | g0157 | EUR | GBR | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG00280 | hp1 | a0001 | c0001 | t0006 | g0214 | EUR | FIN | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0233 | EAS | CHS | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | CHS | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | CHS | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | CHS | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0139 | EAS | CHS | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0220 | EAS | CHS | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | CHS | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0238 | EAS | CHS | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | CHS | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | CHS | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG00621 | hp2 | a0001 | c0030 | t0001 | g0014 | EAS | CHS | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG00642 | hp1 | a0001 | c0001 | t0006 | g0217 | AMR | PUR | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0225 | AMR | PUR | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0211 | AMR | PUR | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG01081 | hp1 | a0001 | c0002 | t0002 | g0187 | AMR | PUR | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG01081 | hp2 | a0001 | c0003 | t0002 | g0003 | AMR | PUR | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0243 | AMR | PUR | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG01106 | hp1 | a0001 | c0001 | t0006 | g0213 | AMR | PUR | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG01167 | hp1 | a0001 | c0003 | t0002 | g0198 | AMR | PUR | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG01169 | hp1 | a0001 | c0027 | t0001 | g0031 | AMR | PUR | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG01169 | hp2 | a0001 | c0003 | t0002 | g0003 | AMR | PUR | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG01192 | hp2 | a0001 | c0024 | t0001 | g0040 | AMR | PUR | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG01243 | hp1 | a0001 | c0002 | t0002 | g0189 | AMR | PUR | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG01243 | hp2 | a0001 | c0002 | t0007 | g0156 | AMR | PUR | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | CLM | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG01257 | hp2 | a0001 | c0002 | t0002 | g0218 | AMR | CLM | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | CLM | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG01346 | hp1 | a0001 | c0002 | t0007 | g0155 | AMR | CLM | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG01358 | hp2 | a0001 | c0001 | t0006 | g0215 | AMR | CLM | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0221 | AMR | CLM | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | CLM | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0033 | EUR | IBS | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0253 | EUR | IBS | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0048 | EUR | IBS | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0226 | EUR | IBS | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG01884 | hp1 | a0001 | c0002 | t0002 | g0016 | AFR | ACB | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0080 | AFR | ACB | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG01891 | hp1 | a0001 | c0002 | t0002 | g0180 | AFR | ACB | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG01891 | hp2 | a0001 | c0007 | t0001 | g0148 | AFR | ACB | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PEL | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0231 | AMR | PEL | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PEL | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | KHV | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | KHV | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | KHV | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | KHV | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG02040 | hp2 | a0013 | c0016 | t0001 | g0232 | EAS | KHV | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG02055 | hp1 | a0004 | c0040 | t0005 | g0162 | AFR | ACB | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG02055 | hp2 | a0001 | c0038 | t0001 | g0086 | AFR | ACB | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG02129 | hp1 | a0001 | c0018 | t0002 | g0245 | EAS | KHV | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | KHV | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | ACB | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0249 | AMR | PEL | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PEL | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG02257 | hp1 | a0001 | c0004 | t0002 | g0171 | AFR | ACB | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG02257 | hp2 | a0001 | c0002 | t0002 | g0163 | AFR | ACB | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG02258 | hp1 | a0001 | c0001 | t0005 | g0161 | AFR | ACB | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0195 | AFR | ACB | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG02280 | hp1 | a0001 | c0010 | t0001 | g0096 | AFR | ACB | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG02280 | hp2 | a0001 | c0003 | t0002 | g0205 | AFR | ACB | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PEL | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0234 | AMR | PEL | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG02451 | hp1 | a0001 | c0002 | t0002 | g0177 | AFR | ACB | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG02451 | hp2 | a0001 | c0003 | t0002 | g0201 | AFR | ACB | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | KHV | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | KHV | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG02572 | hp1 | a0001 | c0003 | t0002 | g0206 | AFR | GWD | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG02615 | hp1 | a0001 | c0003 | t0002 | g0204 | AFR | GWD | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG02622 | hp1 | a0001 | c0005 | t0004 | g0004 | AFR | GWD | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG02622 | hp2 | a0001 | c0004 | t0002 | g0183 | AFR | GWD | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG02630 | hp1 | a0001 | c0005 | t0004 | g0008 | AFR | GWD | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG02630 | hp2 | a0001 | c0001 | t0005 | g0160 | AFR | GWD | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG02647 | hp1 | a0001 | c0004 | t0002 | g0176 | AFR | GWD | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG02647 | hp2 | a0010 | c0039 | t0002 | g0081 | AFR | GWD | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG02683 | hp1 | a0014 | c0041 | t0001 | g0055 | SAS | PJL | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0208 | AFR | GWD | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG02723 | hp2 | a0001 | c0006 | t0002 | g0084 | AFR | GWD | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG02809 | hp1 | a0001 | c0028 | t0002 | g0207 | AFR | GWD | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG02809 | hp2 | a0001 | c0009 | t0002 | g0210 | AFR | GWD | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG02818 | hp1 | a0001 | c0044 | t0002 | g0186 | AFR | GWD | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG02818 | hp2 | a0001 | c0006 | t0002 | g0082 | AFR | GWD | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG02886 | hp1 | a0001 | c0002 | t0002 | g0173 | AFR | GWD | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG02886 | hp2 | a0001 | c0004 | t0002 | g0188 | AFR | GWD | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG02895 | hp1 | a0001 | c0005 | t0004 | g0007 | AFR | GWD | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG02895 | hp2 | a0002 | c0008 | t0008 | g0193 | AFR | GWD | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0197 | AFR | GWD | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG02896 | hp2 | a0001 | c0002 | t0002 | g0165 | AFR | GWD | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0196 | AFR | GWD | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG02897 | hp2 | a0001 | c0005 | t0004 | g0009 | AFR | GWD | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG02965 | hp1 | a0001 | c0004 | t0002 | g0170 | AFR | ESN | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | ESN | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG02970 | hp1 | a0001 | c0006 | t0002 | g0092 | AFR | ESN | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG02970 | hp2 | a0001 | c0002 | t0002 | g0017 | AFR | ESN | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG03017 | hp1 | a0001 | c0046 | t0001 | g0137 | SAS | PJL | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG03098 | hp1 | a0001 | c0002 | t0002 | g0182 | AFR | MSL | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG03098 | hp2 | a0001 | c0011 | t0013 | g0190 | AFR | MSL | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | ESN | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG03130 | hp2 | a0001 | c0005 | t0004 | g0005 | AFR | ESN | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG03139 | hp1 | a0001 | c0004 | t0002 | g0169 | AFR | ESN | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | ESN | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG03209 | hp1 | a0001 | c0002 | t0010 | g0179 | AFR | MSL | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | MSL | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | MSL | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG03225 | hp2 | a0001 | c0002 | t0002 | g0174 | AFR | MSL | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG03239 | hp1 | a0001 | c0022 | t0001 | g0056 | SAS | PJL | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG03239 | hp2 | a0001 | c0033 | t0001 | g0094 | SAS | PJL | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | MSL | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG03486 | hp2 | a0001 | c0002 | t0009 | g0175 | AFR | MSL | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG03516 | hp1 | a0001 | c0003 | t0002 | g0203 | AFR | ESN | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | ESN | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG03540 | hp1 | a0001 | c0002 | t0002 | g0167 | AFR | GWD | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG03540 | hp2 | a0001 | c0007 | t0001 | g0142 | AFR | GWD | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | MSL | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG03579 | hp2 | a0001 | c0043 | t0002 | g0168 | AFR | MSL | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG03704 | hp1 | a0008 | c0029 | t0001 | g0138 | SAS | PJL | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG03942 | hp1 | a0001 | c0045 | t0001 | g0101 | SAS | BEB | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0044 | SAS | BEB | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | STU | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | STU | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA18522 | hp1 | a0001 | c0004 | t0002 | g0002 | AFR | YRI | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA18522 | hp2 | a0001 | c0002 | t0002 | g0166 | AFR | YRI | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | CHB | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA18747 | hp2 | a0001 | c0017 | t0001 | g0131 | EAS | CHB | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA18940 | hp2 | a0003 | c0036 | t0002 | g0256 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA18941 | hp1 | a0001 | c0001 | t0003 | g0089 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA18941 | hp2 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA18944 | hp1 | a0001 | c0025 | t0001 | g0151 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA18948 | hp2 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA18956 | hp1 | a0005 | c0034 | t0003 | g0075 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA18969 | hp1 | a0009 | c0015 | t0002 | g0246 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA18970 | hp2 | a0001 | c0021 | t0001 | g0059 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA18981 | hp2 | a0007 | c0020 | t0001 | g0119 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA18986 | hp2 | a0001 | c0026 | t0003 | g0021 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA18990 | hp2 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA19000 | hp1 | a0001 | c0031 | t0002 | g0255 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA19009 | hp1 | a0012 | c0035 | t0002 | g0254 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA19030 | hp1 | a0001 | c0002 | t0002 | g0181 | AFR | LWK | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0154 | AFR | LWK | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA19043 | hp1 | a0001 | c0004 | t0002 | g0185 | AFR | LWK | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA19043 | hp2 | a0001 | c0003 | t0002 | g0200 | AFR | LWK | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA19065 | hp1 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA19070 | hp1 | a0001 | c0014 | t0002 | g0251 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA19070 | hp2 | a0001 | c0019 | t0001 | g0127 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA19080 | hp1 | a0003 | c0037 | t0002 | g0242 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA19082 | hp1 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA19088 | hp1 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA19240 | hp1 | a0011 | c0032 | t0005 | g0159 | AFR | YRI | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA19240 | hp2 | a0001 | c0002 | t0002 | g0178 | AFR | YRI | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA20129 | hp1 | a0001 | c0004 | t0002 | g0002 | AFR | ASW | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA20129 | hp2 | a0001 | c0023 | t0002 | g0202 | AFR | ASW | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0087 | EUR | TSI | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA20752 | hp2 | a0001 | c0013 | t0002 | g0224 | EUR | TSI | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0098 | EUR | TSI | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA20805 | hp2 | a0001 | c0001 | t0006 | g0216 | EUR | TSI | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | GIH | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | GIH | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG02109 | hp2 | a0001 | c0003 | t0002 | g0199 | AFR | ACB | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG02486 | hp1 | a0001 | c0001 | t0011 | g0209 | AFR | ACB | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG02486 | hp2 | a0001 | c0001 | t0005 | g0158 | AFR | ACB | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG02559 | hp1 | a0001 | c0006 | t0002 | g0083 | AFR | ACB | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG02559 | hp2 | a0002 | c0008 | t0008 | g0192 | AFR | ACB | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG03471 | hp1 | a0001 | c0009 | t0002 | g0164 | AFR | MSL | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG03471 | hp2 | a0006 | c0042 | t0002 | g0184 | AFR | MSL | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG06807 | hp1 | a0001 | c0002 | t0002 | g0172 | AFR | USA | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| HG06807 | hp2 | a0001 | c0012 | t0001 | g0125 | AFR | USA | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA20300 | hp1 | a0001 | c0002 | t0012 | g0194 | AFR | USA | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | USA | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0212 | AFR | LWK | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| NA21309 | hp2 | a0001 | c0005 | t0004 | g0006 | AFR | LWK | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0133 | REF | REF | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0227 | REF | REF | TRRAP_chr7_98873532_99018241 | TRRAP | chr7 | 98873532 | 99018241 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:98910150
|
C | G | 1 | a0014 | 1 | HG02683.hp1 | missense_variant | MODERATE | c.1445C>G | p.Ala482Gly | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 15/73 | 1612/12675 | 1445/11622 | 482/3873 | chr7 | 98910150 | ||
| chr7:98910234
|
C | T | 1 | a0004 | 1 | HG02055.hp1 | missense_variant | MODERATE | c.1529C>T | p.Pro510Leu | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 15/73 | 1696/12675 | 1529/11622 | 510/3873 | chr7 | 98910234 | ||
| chr7:98910275
|
G | A | 1 | a0002 | 2 | HG02559.hp2 HG02895.hp2 |
missense_variant | MODERATE | c.1570G>A | p.Val524Met | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 15/73 | 1737/12675 | 1570/11622 | 524/3873 | chr7 | 98910275 | ||
| chr7:98925217
|
C | A | 1 | a0013 | 1 | HG02040.hp2 | missense_variant | MODERATE | c.2929C>A | p.Leu977Met | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 22/73 | 3096/12675 | 2929/11622 | 977/3873 | chr7 | 98925217 | ||
| chr7:98949523
|
G | T | 1 | a0003 | 2 | NA18940.hp2 NA19080.hp1 |
missense_variant | MODERATE | c.4895G>T | p.Arg1632Leu | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 36/73 | 5062/12675 | 4895/11622 | 1632/3873 | chr7 | 98949523 | ||
| chr7:98949832
|
A | G | 1 | a0012 | 1 | NA19009.hp1 | missense_variant | MODERATE | c.5126A>G | p.Asn1709Ser | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 37/73 | 5293/12675 | 5126/11622 | 1709/3873 | chr7 | 98949832 | ||
| chr7:98950138
|
C | T | 1 | a0005 | 1 | NA18956.hp1 | missense_variant | MODERATE | c.5210C>T | p.Thr1737Ile | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 38/73 | 5377/12675 | 5210/11622 | 1737/3873 | chr7 | 98950138 | ||
| chr7:98956442
|
A | G | 1 | a0011 | 1 | NA19240.hp1 | missense_variant | MODERATE | c.6140A>G | p.Asn2047Ser | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 43/73 | 6307/12675 | 6140/11622 | 2047/3873 | chr7 | 98956442 | ||
| chr7:98956447
|
G | A | 1 | a0006 | 1 | HG03471.hp2 | missense_variant | MODERATE | c.6145G>A | p.Val2049Ile | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 43/73 | 6312/12675 | 6145/11622 | 2049/3873 | chr7 | 98956447 | ||
| chr7:98964749
|
C | T | 1 | a0010 | 1 | HG02647.hp2 | missense_variant | MODERATE | c.6950C>T | p.Ala2317Val | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 48/73 | 7117/12675 | 6950/11622 | 2317/3873 | chr7 | 98964749 | ||
| chr7:98976173
|
G | A | 1 | a0007 | 1 | NA18981.hp2 | missense_variant | MODERATE | c.7864G>A | p.Val2622Ile | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 54/73 | 8031/12675 | 7864/11622 | 2622/3873 | chr7 | 98976173 | ||
| chr7:98976195
|
C | T | 1 | a0008 | 1 | HG03704.hp1 | missense_variant | MODERATE | c.7886C>T | p.Thr2629Met | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 54/73 | 8053/12675 | 7886/11622 | 2629/3873 | chr7 | 98976195 | ||
| chr7:99012141
|
C | T | 1 | a0009 | 1 | NA18969.hp1 | missense_variant | MODERATE | c.11408C>T | p.Thr3803Met | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 73/73 | 11575/12675 | 11408/11622 | 3803/3873 | chr7 | 99012141 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:98897785
|
G | C | 1 | a0001c0010 | 1 | HG02280.hp1 | synonymous_variant | LOW | c.552G>C | p.Val184Val | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 8/73 | 719/12675 | 552/11622 | 184/3873 | chr7 | 98897785 | ||
| chr7:98897848
|
G | A | 1 | a0001c0011 | 1 | HG03098.hp2 | synonymous_variant | LOW | c.615G>A | p.Glu205Glu | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 8/73 | 782/12675 | 615/11622 | 205/3873 | chr7 | 98897848 | ||
| chr7:98899744
|
C | T | 1 | a0001c0046 | 1 | HG03017.hp1 | synonymous_variant | LOW | c.777C>T | p.Ala259Ala | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 10/73 | 944/12675 | 777/11622 | 259/3873 | chr7 | 98899744 | ||
| chr7:98903495
|
C | T | 1 | a0001c0045 | 1 | HG03942.hp1 | synonymous_variant | LOW | c.1014C>T | p.Ile338Ile | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 12/73 | 1181/12675 | 1014/11622 | 338/3873 | chr7 | 98903495 | ||
| chr7:98908818
|
C | T | 8 | a0001c0002a0001c0004a0001c0005others(5): Show | 45 | HG00140.hp2 HG01081.hp1 HG01243.hp1 others(42): Show |
synonymous_variant | LOW | c.1206C>T | p.Phe402Phe | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 14/73 | 1373/12675 | 1206/11622 | 402/3873 | chr7 | 98908818 | ||
| chr7:98910604
|
T | C | 1 | a0001c0012 | 1 | HG06807.hp2 | synonymous_variant | LOW | c.1809T>C | p.Tyr603Tyr | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 16/73 | 1976/12675 | 1809/11622 | 603/3873 | chr7 | 98910604 | ||
| chr7:98917487
|
T | C | 1 | a0001c0013 | 1 | NA20752.hp2 | synonymous_variant | LOW | c.2430T>C | p.Cys810Cys | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 20/73 | 2597/12675 | 2430/11622 | 810/3873 | chr7 | 98917487 | ||
| chr7:98917490
|
C | T | 1 | a0002c0008 | 2 | HG02559.hp2 HG02895.hp2 |
synonymous_variant | LOW | c.2433C>T | p.Leu811Leu | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 20/73 | 2600/12675 | 2433/11622 | 811/3873 | chr7 | 98917490 | ||
| chr7:98917673
|
C | T | 2 | a0001c0006a0010c0039 | 5 | HG02559.hp1 HG02647.hp2 HG02723.hp2 others(2): Show |
synonymous_variant | LOW | c.2616C>T | p.Leu872Leu | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 20/73 | 2783/12675 | 2616/11622 | 872/3873 | chr7 | 98917673 | ||
| chr7:98921818
|
T | C | 2 | a0001c0014a0009c0015 | 2 | NA18969.hp1 NA19070.hp1 |
synonymous_variant | LOW | c.2688T>C | p.Gly896Gly | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 21/73 | 2855/12675 | 2688/11622 | 896/3873 | chr7 | 98921818 | ||
| chr7:98930065
|
G | A | 2 | a0001c0004a0006c0042 | 10 | HG02257.hp1 HG02622.hp2 HG02647.hp1 others(7): Show |
synonymous_variant | LOW | c.3252G>A | p.Ser1084Ser | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 24/73 | 3419/12675 | 3252/11622 | 1084/3873 | chr7 | 98930065 | ||
| chr7:98933261
|
C | T | 1 | a0001c0038 | 1 | HG02055.hp2 | synonymous_variant | LOW | c.3873C>T | p.Pro1291Pro | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 27/73 | 4040/12675 | 3873/11622 | 1291/3873 | chr7 | 98933261 | ||
| chr7:98948325
|
G | T | 1 | a0001c0007 | 2 | HG01891.hp2 HG03540.hp2 |
synonymous_variant | LOW | c.4653G>T | p.Arg1551Arg | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 34/73 | 4820/12675 | 4653/11622 | 1551/3873 | chr7 | 98948325 | ||
| chr7:98950989
|
T | C | 1 | a0001c0017 | 1 | NA18747.hp2 | synonymous_variant | LOW | c.5448T>C | p.Ser1816Ser | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 39/73 | 5615/12675 | 5448/11622 | 1816/3873 | chr7 | 98950989 | ||
| chr7:98955127
|
A | G | 1 | a0001c0033 | 1 | HG03239.hp2 | synonymous_variant | LOW | c.5760A>G | p.Ala1920Ala | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 41/73 | 5927/12675 | 5760/11622 | 1920/3873 | chr7 | 98955127 | ||
| chr7:98956190
|
C | T | 1 | a0003c0037 | 1 | NA19080.hp1 | synonymous_variant | LOW | c.5982C>T | p.Ser1994Ser | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 42/73 | 6149/12675 | 5982/11622 | 1994/3873 | chr7 | 98956190 | ||
| chr7:98956512
|
G | A | 1 | a0001c0018 | 1 | HG02129.hp1 | synonymous_variant | LOW | c.6210G>A | p.Thr2070Thr | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 43/73 | 6377/12675 | 6210/11622 | 2070/3873 | chr7 | 98956512 | ||
| chr7:98958043
|
G | A | 1 | a0001c0019 | 1 | NA19070.hp2 | synonymous_variant | LOW | c.6294G>A | p.Lys2098Lys | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 44/73 | 6461/12675 | 6294/11622 | 2098/3873 | chr7 | 98958043 | ||
| chr7:98962357
|
C | T | 1 | a0001c0031 | 1 | NA19000.hp1 | synonymous_variant | LOW | c.6759C>T | p.Val2253Val | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 47/73 | 6926/12675 | 6759/11622 | 2253/3873 | chr7 | 98962357 | ||
| chr7:98967563
|
A | C | 1 | a0001c0030 | 1 | HG00621.hp2 | synonymous_variant | LOW | c.7377A>C | p.Pro2459Pro | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 51/73 | 7544/12675 | 7377/11622 | 2459/3873 | chr7 | 98967563 | ||
| chr7:98970216
|
C | T | 1 | a0001c0044 | 1 | HG02818.hp1 | synonymous_variant | LOW | c.7617C>T | p.Asp2539Asp | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 52/73 | 7784/12675 | 7617/11622 | 2539/3873 | chr7 | 98970216 | ||
| chr7:98976214
|
G | A | 1 | a0001c0021 | 1 | NA18970.hp2 | synonymous_variant | LOW | c.7905G>A | p.Thr2635Thr | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 54/73 | 8072/12675 | 7905/11622 | 2635/3873 | chr7 | 98976214 | ||
| chr7:98976220
|
C | T | 1 | a0001c0043 | 1 | HG03579.hp2 | synonymous_variant | LOW | c.7911C>T | p.Val2637Val | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 54/73 | 8078/12675 | 7911/11622 | 2637/3873 | chr7 | 98976220 | ||
| chr7:98976557
|
G | A | 1 | a0001c0022 | 1 | HG03239.hp1 | synonymous_variant | LOW | c.8034G>A | p.Ala2678Ala | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 55/73 | 8201/12675 | 8034/11622 | 2678/3873 | chr7 | 98976557 | ||
| chr7:98976953
|
C | T | 1 | a0001c0011 | 1 | HG03098.hp2 | synonymous_variant | LOW | c.8262C>T | p.Ser2754Ser | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 56/73 | 8429/12675 | 8262/11622 | 2754/3873 | chr7 | 98976953 | ||
| chr7:98978240
|
T | C | 1 | a0001c0009 | 2 | HG02809.hp2 HG03471.hp1 |
synonymous_variant | LOW | c.8415T>C | p.Asp2805Asp | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 57/73 | 8582/12675 | 8415/11622 | 2805/3873 | chr7 | 98978240 | ||
| chr7:98984169
|
A | C | 1 | a0001c0028 | 1 | HG02809.hp1 | synonymous_variant | LOW | c.9099A>C | p.Ser3033Ser | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 61/73 | 9266/12675 | 9099/11622 | 3033/3873 | chr7 | 98984169 | ||
| chr7:98984946
|
C | A | 2 | a0001c0003a0001c0023 | 11 | HG01081.hp2 HG01167.hp1 HG01169.hp2 others(8): Show |
splice_region_variant&synonymous_variant | LOW | c.9291C>A | p.Gly3097Gly | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 62/73 | 9458/12675 | 9291/11622 | 3097/3873 | chr7 | 98984946 | ||
| chr7:98994601
|
C | T | 1 | a0001c0023 | 1 | NA20129.hp2 | synonymous_variant | LOW | c.10062C>T | p.Leu3354Leu | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/73 | 10229/12675 | 10062/11622 | 3354/3873 | chr7 | 98994601 | ||
| chr7:99008483
|
C | T | 1 | a0001c0027 | 1 | HG01169.hp1 | synonymous_variant | LOW | c.10860C>T | p.Ile3620Ile | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 70/73 | 11027/12675 | 10860/11622 | 3620/3873 | chr7 | 99008483 | ||
| chr7:99008537
|
G | A | 1 | a0001c0019 | 1 | NA19070.hp2 | synonymous_variant | LOW | c.10914G>A | p.Ala3638Ala | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 70/73 | 11081/12675 | 10914/11622 | 3638/3873 | chr7 | 99008537 | ||
| chr7:99011096
|
G | A | 1 | a0001c0024 | 1 | HG01192.hp2 | synonymous_variant | LOW | c.10983G>A | p.Pro3661Pro | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 71/73 | 11150/12675 | 10983/11622 | 3661/3873 | chr7 | 99011096 | ||
| chr7:99011352
|
A | G | 1 | a0001c0019 | 1 | NA19070.hp2 | synonymous_variant | LOW | c.11154A>G | p.Lys3718Lys | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 72/73 | 11321/12675 | 11154/11622 | 3718/3873 | chr7 | 99011352 | ||
| chr7:99011433
|
C | G | 1 | a0001c0005 | 6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
synonymous_variant | LOW | c.11235C>G | p.Leu3745Leu | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 72/73 | 11402/12675 | 11235/11622 | 3745/3873 | chr7 | 99011433 | ||
| chr7:99012157
|
G | A | 1 | a0001c0025 | 1 | NA18944.hp1 | synonymous_variant | LOW | c.11424G>A | p.Ser3808Ser | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 73/73 | 11591/12675 | 11424/11622 | 3808/3873 | chr7 | 99012157 | ||
| chr7:99012220
|
C | T | 1 | a0001c0026 | 1 | NA18986.hp2 | synonymous_variant | LOW | c.11487C>T | p.Val3829Val | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 73/73 | 11654/12675 | 11487/11622 | 3829/3873 | chr7 | 99012220 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:99012364
|
G | A | 1 | a0002c0008t0008 | 2 | HG02559.hp2 HG02895.hp2 |
3_prime_UTR_variant | MODIFIER | c.*9G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 73/73 | 9 | chr7 | 99012364 | |||||
| chr7:99012369
|
G | A | 1 | a0001c0002t0009 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*14G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 73/73 | 14 | chr7 | 99012369 | |||||
| chr7:99012409
|
G | A | 1 | a0001c0002t0010 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*54G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 73/73 | 54 | chr7 | 99012409 | |||||
| chr7:99012479
|
G | A | 1 | a0001c0001t0011 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*124G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 73/73 | 124 | chr7 | 99012479 | |||||
| chr7:99012500
|
G | A | 1 | a0002c0008t0008 | 2 | HG02559.hp2 HG02895.hp2 |
3_prime_UTR_variant | MODIFIER | c.*145G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 73/73 | 145 | chr7 | 99012500 | |||||
| chr7:99012702
|
G | A | 1 | a0001c0002t0012 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*347G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 73/73 | 347 | chr7 | 99012702 | |||||
| chr7:99012912
|
G | A | 1 | a0001c0005t0004 | 6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*557G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 73/73 | 557 | chr7 | 99012912 | |||||
| chr7:99012964
|
G | A | 1 | a0001c0002t0007 | 3 | HG00140.hp2 HG01243.hp2 HG01346.hp1 |
3_prime_UTR_variant | MODIFIER | c.*609G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 73/73 | 609 | chr7 | 99012964 | |||||
| chr7:99012972
|
T | C | 34 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(31): Show | 128 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(125): Show |
3_prime_UTR_variant | MODIFIER | c.*617T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 73/73 | 617 | chr7 | 99012972 | |||||
| chr7:99013059
|
C | T | 1 | a0001c0001t0006 | 5 | HG00280.hp1 HG00642.hp1 HG01106.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*704C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 73/73 | 704 | chr7 | 99013059 | |||||
| chr7:99013061
|
C | T | 32 | a0001c0001t0002a0001c0001t0005a0001c0001t0006others(29): Show | 118 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(115): Show |
3_prime_UTR_variant | MODIFIER | c.*706C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 73/73 | 706 | chr7 | 99013061 | |||||
| chr7:99013207
|
AT | A | 3 | a0001c0001t0005a0004c0040t0005a0011c0032t0005 | 5 | HG02055.hp1 HG02258.hp1 HG02486.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*863delT | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 73/73 | 863 | INFO_REALIGN_3_PRIME | chr7 | 99013207 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:98878644
|
T | TGGCG | 6 | a0001c0005t0004g0004a0001c0005t0004g0005a0001c0005t0004g0006others(3): Show | 6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-62+16_-62+19dupGG others(2): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 1/72 | INFO_REALIGN_3_PRIME | chr7 | 98878644 | |||||
| chr7:98878765
|
C | A | 2 | a0001c0001t0002g0010a0001c0001t0002g0011 | 2 | HG00544.hp2 HG02027.hp1 |
intron_variant | MODIFIER | c.-62+128C>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 1/72 | chr7 | 98878765 | ||||||
| chr7:98878802
|
C | T | 1 | a0001c0001t0001g0259 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-62+165C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 1/72 | chr7 | 98878802 | ||||||
| chr7:98878806
|
T | C | 209 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(206): Show | 212 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.-62+169T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 1/72 | chr7 | 98878806 | ||||||
| chr7:98878973
|
G | C | 4 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(1): Show | 4 | HG00621.hp2 HG01993.hp2 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.-62+336G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 1/72 | chr7 | 98878973 | ||||||
| chr7:98879068
|
G | T | 1 | a0001c0009t0002g0210 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-62+431G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 1/72 | chr7 | 98879068 | ||||||
| chr7:98879072
|
G | C | 2 | a0001c0002t0002g0016a0001c0002t0002g0017 | 2 | HG01884.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.-62+435G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 1/72 | chr7 | 98879072 | ||||||
| chr7:98879130
|
C | A | 192 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(189): Show | 194 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.-62+493C>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 1/72 | chr7 | 98879130 | ||||||
| chr7:98879183
|
C | T | 2 | a0002c0008t0008g0192a0002c0008t0008g0193 | 2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.-62+546C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 1/72 | chr7 | 98879183 | ||||||
| chr7:98879188
|
C | T | 2 | a0002c0008t0008g0192a0002c0008t0008g0193 | 2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.-62+551C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 1/72 | chr7 | 98879188 | ||||||
| chr7:98879288
|
A | G | 2 | a0001c0001t0001g0257a0001c0001t0001g0258 | 2 | NA18971.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.-62+651A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 1/72 | chr7 | 98879288 | ||||||
| chr7:98879453
|
G | C | 2 | a0002c0008t0008g0192a0002c0008t0008g0193 | 2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.-62+816G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 1/72 | chr7 | 98879453 | ||||||
| chr7:98879593
|
C | T | 1 | a0001c0001t0001g0191 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-62+956C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 1/72 | chr7 | 98879593 | ||||||
| chr7:98879807
|
A | G | 3 | a0001c0001t0002g0208a0001c0001t0011g0209a0001c0028t0002g0207 | 3 | HG02486.hp1 HG02723.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.-62+1170A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 1/72 | chr7 | 98879807 | ||||||
| chr7:98880092
|
A | G | 32 | a0001c0002t0002g0016a0001c0002t0002g0017a0001c0002t0002g0163others(29): Show | 33 | HG01081.hp1 HG01243.hp1 HG01884.hp1 others(30): Show |
intron_variant | MODIFIER | c.-61-998A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 1/72 | chr7 | 98880092 | ||||||
| chr7:98880096
|
A | C | 5 | a0001c0001t0005g0158a0001c0001t0005g0160a0001c0001t0005g0161others(2): Show | 5 | HG02055.hp1 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-61-994A>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 1/72 | chr7 | 98880096 | ||||||
| chr7:98880123
|
A | G | 44 | a0001c0001t0002g0154a0001c0002t0002g0016a0001c0002t0002g0017others(41): Show | 45 | HG00140.hp2 HG01081.hp1 HG01243.hp1 others(42): Show |
intron_variant | MODIFIER | c.-61-967A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 1/72 | chr7 | 98880123 | ||||||
| chr7:98880232
|
GCCTGCTG others(51): Show |
G | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-61-854_-61-797del others(58): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 1/72 | INFO_REALIGN_3_PRIME | chr7 | 98880232 | |||||
| chr7:98880259
|
G | T | 6 | a0001c0005t0004g0004a0001c0005t0004g0005a0001c0005t0004g0006others(3): Show | 6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-61-831G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 1/72 | chr7 | 98880259 | ||||||
| chr7:98880262
|
G | GT | 5 | a0001c0001t0002g0252a0001c0001t0002g0253a0001c0031t0002g0255others(2): Show | 5 | HG01515.hp2 NA18940.hp2 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.-61-811dupT | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 1/72 | INFO_REALIGN_3_PRIME | chr7 | 98880262 | |||||
| chr7:98880262
|
G | GTTTTGT | 62 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(59): Show | 62 | HG00408.hp2 HG00621.hp2 HG00738.hp1 others(59): Show |
intron_variant | MODIFIER | c.-61-824_-61-823ins others(6): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 1/72 | INFO_REALIGN_3_PRIME | chr7 | 98880262 | |||||
| chr7:98880262
|
G | GTTTTGTT | 5 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(2): Show | 5 | HG00423.hp1 HG01358.hp1 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.-61-824_-61-823ins others(7): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 1/72 | INFO_REALIGN_3_PRIME | chr7 | 98880262 | |||||
| chr7:98880262
|
G | GTTTTT | 46 | a0001c0001t0001g0001a0001c0001t0001g0093a0001c0001t0001g0095others(43): Show | 47 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(44): Show |
intron_variant | MODIFIER | c.-61-815_-61-811dup others(5): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 1/72 | INFO_REALIGN_3_PRIME | chr7 | 98880262 | |||||
| chr7:98880262
|
G | GTTTTTT | 17 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0143others(14): Show | 17 | HG00438.hp1 HG00621.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.-61-816_-61-811dup others(6): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 1/72 | INFO_REALIGN_3_PRIME | chr7 | 98880262 | |||||
| chr7:98880262
|
G | T | 6 | a0001c0005t0004g0004a0001c0005t0004g0005a0001c0005t0004g0006others(3): Show | 6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-61-828G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 1/72 | chr7 | 98880262 | ||||||
| chr7:98880262
|
GT | G | 46 | a0001c0001t0002g0080a0001c0001t0002g0154a0001c0001t0002g0219others(43): Show | 47 | HG00438.hp2 HG01081.hp1 HG01243.hp2 others(44): Show |
intron_variant | MODIFIER | c.-61-811delT | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 1/72 | INFO_REALIGN_3_PRIME | chr7 | 98880262 | |||||
| chr7:98880265
|
T | G | 23 | a0001c0001t0002g0195a0001c0001t0002g0196a0001c0001t0002g0197others(20): Show | 24 | HG00280.hp1 HG00642.hp1 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.-61-825T>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 1/72 | chr7 | 98880265 | ||||||
| chr7:98880266
|
T | G | 5 | a0001c0001t0002g0154a0001c0001t0005g0158a0002c0008t0008g0192others(2): Show | 5 | HG02486.hp2 HG02559.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-61-824T>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 1/72 | chr7 | 98880266 | ||||||
| chr7:98880267
|
T | G | 2 | a0001c0001t0001g0018a0001c0002t0002g0163 | 2 | HG02257.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.-61-823T>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 1/72 | chr7 | 98880267 | ||||||
| chr7:98880268
|
T | G | 3 | a0001c0001t0002g0208a0001c0001t0011g0209a0001c0028t0002g0207 | 3 | HG02486.hp1 HG02723.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.-61-822T>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 1/72 | chr7 | 98880268 | ||||||
| chr7:98880335
|
C | T | 1 | a0001c0004t0002g0188 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-61-755C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 1/72 | chr7 | 98880335 | ||||||
| chr7:98880436
|
G | T | 6 | a0001c0001t0002g0080a0001c0006t0002g0082a0001c0006t0002g0083others(3): Show | 6 | HG01884.hp2 HG02559.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.-61-654G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 1/72 | chr7 | 98880436 | ||||||
| chr7:98880474
|
C | T | 1 | a0001c0046t0001g0137 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-61-616C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 1/72 | chr7 | 98880474 | ||||||
| chr7:98880577
|
T | C | 1 | a0008c0029t0001g0138 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-61-513T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 1/72 | chr7 | 98880577 | ||||||
| chr7:98880585
|
A | C | 1 | a0001c0001t0001g0074 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-61-505A>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 1/72 | chr7 | 98880585 | ||||||
| chr7:98880778
|
A | G | 1 | a0001c0002t0002g0163 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-61-312A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 1/72 | chr7 | 98880778 | ||||||
| chr7:98880794
|
A | G | 18 | a0001c0001t0001g0058a0001c0001t0001g0060a0001c0001t0001g0061others(15): Show | 18 | HG00738.hp1 HG01192.hp1 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.-61-296A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 1/72 | chr7 | 98880794 | ||||||
| chr7:98880966
|
A | G | 1 | a0001c0001t0001g0136 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-61-124A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 1/72 | chr7 | 98880966 | ||||||
| chr7:98880982
|
G | A | 2 | a0001c0001t0001g0093a0001c0033t0001g0094 | 2 | HG03239.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.-61-108G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 1/72 | chr7 | 98880982 | ||||||
| chr7:98881057
|
A | G | 43 | a0001c0001t0002g0154a0001c0002t0002g0016a0001c0002t0002g0017others(40): Show | 44 | HG00140.hp2 HG01081.hp1 HG01243.hp1 others(41): Show |
intron_variant | MODIFIER | c.-61-33A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 1/72 | chr7 | 98881057 | ||||||
| chr7:98881401
|
C | T | 2 | a0001c0002t0002g0187a0001c0044t0002g0186 | 2 | HG01081.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.100+151C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 2/72 | chr7 | 98881401 | ||||||
| chr7:98881498
|
G | A | 5 | a0001c0002t0002g0165a0001c0002t0002g0166a0001c0002t0002g0167others(2): Show | 5 | HG02809.hp2 HG02896.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.100+248G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 2/72 | chr7 | 98881498 | ||||||
| chr7:98881508
|
G | T | 127 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(124): Show | 128 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.100+258G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 2/72 | chr7 | 98881508 | ||||||
| chr7:98881544
|
C | T | 11 | a0001c0001t0002g0080a0001c0001t0005g0158a0001c0001t0005g0160others(8): Show | 11 | HG01884.hp2 HG02055.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.100+294C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 2/72 | chr7 | 98881544 | ||||||
| chr7:98881571
|
C | CA | 35 | a0001c0001t0002g0208a0001c0001t0002g0252a0001c0001t0011g0209others(32): Show | 36 | HG01081.hp1 HG01243.hp1 HG01884.hp1 others(33): Show |
intron_variant | MODIFIER | c.100+337dupA | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 2/72 | INFO_REALIGN_3_PRIME | chr7 | 98881571 | |||||
| chr7:98881571
|
C | CAA | 5 | a0001c0001t0002g0154a0001c0002t0007g0155a0001c0002t0007g0156others(2): Show | 5 | HG00140.hp2 HG01243.hp2 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.100+336_100+337dup others(2): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 2/72 | INFO_REALIGN_3_PRIME | chr7 | 98881571 | |||||
| chr7:98881571
|
CA | C | 11 | a0001c0001t0001g0057a0001c0001t0001g0135a0001c0001t0001g0259others(8): Show | 11 | HG01884.hp2 HG02040.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.100+337delA | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 2/72 | INFO_REALIGN_3_PRIME | chr7 | 98881571 | |||||
| chr7:98881608
|
A | G | 1 | a0001c0022t0001g0056 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.100+358A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 2/72 | chr7 | 98881608 | ||||||
| chr7:98881610
|
A | G | 4 | a0001c0004t0002g0183a0001c0004t0002g0185a0001c0004t0002g0188others(1): Show | 4 | HG02622.hp2 HG02886.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.100+360A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 2/72 | chr7 | 98881610 | ||||||
| chr7:98881835
|
C | T | 6 | a0001c0005t0004g0004a0001c0005t0004g0005a0001c0005t0004g0006others(3): Show | 6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.101-140C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 2/72 | chr7 | 98881835 | ||||||
| chr7:98882032
|
C | T | 1 | a0001c0002t0002g0182 | 1 | HG03098.hp1 | splice_region_variant&intron_variant | LOW | c.150+8C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98882032 | ||||||
| chr7:98882084
|
G | A | 11 | a0001c0001t0002g0080a0001c0001t0005g0158a0001c0001t0005g0160others(8): Show | 11 | HG01884.hp2 HG02055.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.150+60G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98882084 | ||||||
| chr7:98882200
|
C | G | 1 | a0001c0001t0001g0078 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.150+176C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98882200 | ||||||
| chr7:98882270
|
T | C | 1 | a0001c0001t0002g0221 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.150+246T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98882270 | ||||||
| chr7:98882363
|
C | CT | 8 | a0001c0001t0006g0213a0001c0001t0006g0214a0001c0001t0006g0215others(5): Show | 8 | HG00280.hp1 HG00642.hp1 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.150+355dupT | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | INFO_REALIGN_3_PRIME | chr7 | 98882363 | |||||
| chr7:98882402
|
G | A | 2 | a0001c0001t0002g0222a0001c0001t0002g0223 | 2 | NA18966.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.150+378G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98882402 | ||||||
| chr7:98882483
|
C | T | 1 | a0001c0001t0002g0250 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.150+459C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98882483 | ||||||
| chr7:98882563
|
A | G | 3 | a0001c0005t0004g0007a0001c0005t0004g0008a0001c0005t0004g0009 | 3 | HG02630.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.150+539A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98882563 | ||||||
| chr7:98882636
|
T | C | 4 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(1): Show | 4 | HG00621.hp2 HG01993.hp2 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.150+612T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98882636 | ||||||
| chr7:98882777
|
G | T | 254 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(251): Show | 257 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.150+753G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98882777 | ||||||
| chr7:98882781
|
C | A | 5 | a0001c0001t0005g0158a0001c0001t0005g0160a0001c0001t0005g0161others(2): Show | 5 | HG02055.hp1 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.150+757C>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98882781 | ||||||
| chr7:98882825
|
AT | A | 3 | a0001c0002t0007g0155a0001c0002t0007g0156a0001c0002t0007g0157 | 3 | HG00140.hp2 HG01243.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.150+806delT | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | INFO_REALIGN_3_PRIME | chr7 | 98882825 | |||||
| chr7:98883099
|
A | C | 210 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(207): Show | 213 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.150+1075A>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98883099 | ||||||
| chr7:98883158
|
A | G | 208 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(205): Show | 211 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.150+1134A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98883158 | ||||||
| chr7:98883217
|
G | T | 2 | a0002c0008t0008g0192a0002c0008t0008g0193 | 2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.150+1193G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98883217 | ||||||
| chr7:98883462
|
A | C | 193 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(190): Show | 195 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.150+1438A>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98883462 | ||||||
| chr7:98883520
|
T | C | 1 | a0001c0002t0002g0182 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.150+1496T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98883520 | ||||||
| chr7:98883813
|
C | T | 66 | a0001c0001t0001g0001a0001c0001t0001g0088a0001c0001t0001g0090others(63): Show | 67 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.150+1789C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98883813 | ||||||
| chr7:98884177
|
C | T | 42 | a0001c0001t0002g0080a0001c0001t0005g0158a0001c0001t0005g0160others(39): Show | 43 | HG01081.hp1 HG01243.hp1 HG01884.hp1 others(40): Show |
intron_variant | MODIFIER | c.150+2153C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98884177 | ||||||
| chr7:98884310
|
T | A | 1 | a0001c0004t0002g0183 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.150+2286T>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98884310 | ||||||
| chr7:98884487
|
A | C | 1 | a0014c0041t0001g0055 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.150+2463A>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98884487 | ||||||
| chr7:98884503
|
A | G | 2 | a0001c0001t0001g0053a0001c0001t0001g0054 | 2 | HG01167.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.150+2479A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98884503 | ||||||
| chr7:98884526
|
T | C | 1 | a0001c0001t0001g0012 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.150+2502T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98884526 | ||||||
| chr7:98884597
|
G | A | 3 | a0001c0001t0002g0195a0001c0001t0002g0196a0001c0001t0002g0197 | 3 | HG02258.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.150+2573G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98884597 | ||||||
| chr7:98884995
|
G | A | 1 | a0001c0001t0001g0085 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.150+2971G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98884995 | ||||||
| chr7:98885062
|
A | G | 1 | a0001c0001t0001g0153 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.150+3038A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98885062 | ||||||
| chr7:98885254
|
A | AT | 133 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(130): Show | 134 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.150+3243dupT | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | INFO_REALIGN_3_PRIME | chr7 | 98885254 | |||||
| chr7:98885306
|
C | T | 1 | a0001c0001t0001g0052 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.150+3282C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98885306 | ||||||
| chr7:98885319
|
C | T | 1 | a0001c0002t0002g0182 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.150+3295C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98885319 | ||||||
| chr7:98885350
|
G | T | 2 | a0001c0002t0002g0166a0001c0002t0002g0167 | 2 | HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.150+3326G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98885350 | ||||||
| chr7:98885368
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.150+3344C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98885368 | ||||||
| chr7:98885385
|
A | G | 2 | a0001c0001t0002g0208a0001c0001t0011g0209 | 2 | HG02486.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.150+3361A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98885385 | ||||||
| chr7:98885408
|
T | C | 1 | a0002c0008t0008g0192 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.150+3384T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98885408 | ||||||
| chr7:98885429
|
G | A | 206 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(203): Show | 209 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.150+3405G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98885429 | ||||||
| chr7:98885449
|
C | T | 16 | a0001c0001t0001g0001a0001c0001t0001g0093a0001c0001t0001g0126others(13): Show | 17 | HG00280.hp2 HG00558.hp2 HG00642.hp2 others(14): Show |
intron_variant | MODIFIER | c.150+3425C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98885449 | ||||||
| chr7:98885485
|
G | A | 3 | a0001c0001t0001g0095a0001c0001t0001g0135a0001c0001t0001g0140 | 3 | HG02572.hp2 HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.150+3461G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98885485 | ||||||
| chr7:98885667
|
A | AAT | 7 | a0001c0001t0002g0080a0001c0001t0002g0219a0001c0001t0002g0220others(4): Show | 7 | HG00140.hp2 HG00438.hp2 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.150+3660_150+3661d others(4): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | INFO_REALIGN_3_PRIME | chr7 | 98885667 | |||||
| chr7:98885667
|
A | AATATAT | 4 | a0001c0004t0002g0002a0001c0004t0002g0169a0001c0004t0002g0170others(1): Show | 5 | HG02257.hp1 HG02965.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.150+3656_150+3661d others(8): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | INFO_REALIGN_3_PRIME | chr7 | 98885667 | |||||
| chr7:98885794
|
G | C | 6 | a0001c0005t0004g0004a0001c0005t0004g0005a0001c0005t0004g0006others(3): Show | 6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.150+3770G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98885794 | ||||||
| chr7:98886033
|
C | T | 2 | a0002c0008t0008g0192a0002c0008t0008g0193 | 2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.150+4009C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98886033 | ||||||
| chr7:98886082
|
C | T | 6 | a0001c0005t0004g0004a0001c0005t0004g0005a0001c0005t0004g0006others(3): Show | 6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.150+4058C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98886082 | ||||||
| chr7:98886299
|
CATAGATA others(31): Show |
C | 2 | a0002c0008t0008g0192a0002c0008t0008g0193 | 2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.151-3994_151-3957d others(40): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | INFO_REALIGN_3_PRIME | chr7 | 98886299 | |||||
| chr7:98886313
|
T | C | 1 | a0001c0002t0002g0163 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.151-4022T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98886313 | ||||||
| chr7:98886335
|
T | G | 1 | a0001c0001t0001g0027 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.151-4000T>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98886335 | ||||||
| chr7:98886355
|
T | G | 1 | a0001c0001t0001g0027 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.151-3980T>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98886355 | ||||||
| chr7:98886357
|
T | G | 1 | a0001c0001t0001g0027 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.151-3978T>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98886357 | ||||||
| chr7:98886389
|
T | C | 10 | a0001c0003t0002g0003a0001c0003t0002g0198a0001c0003t0002g0199others(7): Show | 11 | HG01081.hp2 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.151-3946T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98886389 | ||||||
| chr7:98886437
|
T | C | 32 | a0001c0002t0002g0016a0001c0002t0002g0017a0001c0002t0002g0163others(29): Show | 33 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(30): Show |
intron_variant | MODIFIER | c.151-3898T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98886437 | ||||||
| chr7:98886438
|
A | G | 43 | a0001c0001t0002g0080a0001c0001t0005g0158a0001c0001t0005g0160others(40): Show | 44 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(41): Show |
intron_variant | MODIFIER | c.151-3897A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98886438 | ||||||
| chr7:98886441
|
T | C | 1 | a0001c0001t0001g0126 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.151-3894T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98886441 | ||||||
| chr7:98886449
|
T | G | 43 | a0001c0001t0002g0080a0001c0001t0005g0158a0001c0001t0005g0160others(40): Show | 44 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(41): Show |
intron_variant | MODIFIER | c.151-3886T>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98886449 | ||||||
| chr7:98886595
|
A | G | 3 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0074 | 3 | HG02129.hp2 NA18979.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.151-3740A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98886595 | ||||||
| chr7:98886770
|
G | C | 136 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(133): Show | 137 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.151-3565G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98886770 | ||||||
| chr7:98886770
|
G | T | 1 | a0001c0012t0001g0125 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.151-3565G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98886770 | ||||||
| chr7:98886796
|
C | T | 4 | a0001c0001t0001g0093a0001c0001t0001g0133a0001c0001t0001g0152others(1): Show | 4 | HG02698.hp2 HG03239.hp2 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.151-3539C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98886796 | ||||||
| chr7:98886859
|
G | C | 210 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(207): Show | 213 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.151-3476G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98886859 | ||||||
| chr7:98886912
|
A | T | 1 | a0001c0001t0003g0026 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.151-3423A>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98886912 | ||||||
| chr7:98887096
|
C | CT | 12 | a0001c0001t0002g0154a0001c0002t0007g0155a0001c0002t0007g0156others(9): Show | 12 | HG00140.hp2 HG01243.hp2 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.151-3231dupT | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | INFO_REALIGN_3_PRIME | chr7 | 98887096 | |||||
| chr7:98887143
|
C | T | 1 | a0001c0002t0002g0181 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.151-3192C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98887143 | ||||||
| chr7:98887166
|
C | T | 1 | a0001c0001t0001g0049 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.151-3169C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98887166 | ||||||
| chr7:98887356
|
T | G | 1 | a0001c0001t0002g0208 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.151-2979T>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98887356 | ||||||
| chr7:98887514
|
G | A | 5 | a0001c0001t0005g0158a0001c0001t0005g0160a0001c0001t0005g0161others(2): Show | 5 | HG02055.hp1 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.151-2821G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98887514 | ||||||
| chr7:98887662
|
G | A | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.151-2673G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98887662 | ||||||
| chr7:98887690
|
A | G | 6 | a0001c0005t0004g0004a0001c0005t0004g0005a0001c0005t0004g0006others(3): Show | 6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.151-2645A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98887690 | ||||||
| chr7:98887729
|
C | CA | 67 | a0001c0001t0001g0239a0001c0001t0001g0241a0001c0001t0001g0257others(64): Show | 68 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.151-2585dupA | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | INFO_REALIGN_3_PRIME | chr7 | 98887729 | |||||
| chr7:98887729
|
C | CAA | 115 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(112): Show | 116 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.151-2586_151-2585d others(4): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | INFO_REALIGN_3_PRIME | chr7 | 98887729 | |||||
| chr7:98887729
|
C | CAAA | 24 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(21): Show | 24 | HG00423.hp1 HG00738.hp1 HG01192.hp1 others(21): Show |
intron_variant | MODIFIER | c.151-2587_151-2585d others(5): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | INFO_REALIGN_3_PRIME | chr7 | 98887729 | |||||
| chr7:98887744
|
A | AC | 40 | a0001c0001t0002g0080a0001c0001t0005g0158a0001c0001t0005g0160others(37): Show | 41 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(38): Show |
intron_variant | MODIFIER | c.151-2591_151-2590i others(3): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98887744 | ||||||
| chr7:98887845
|
A | G | 1 | a0001c0001t0001g0124 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.151-2490A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98887845 | ||||||
| chr7:98887864
|
A | G | 1 | a0001c0001t0001g0001 | 2 | HG00280.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.151-2471A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98887864 | ||||||
| chr7:98887894
|
C | A | 1 | a0001c0001t0001g0098 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.151-2441C>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98887894 | ||||||
| chr7:98888102
|
C | T | 1 | a0001c0001t0003g0139 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.151-2233C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98888102 | ||||||
| chr7:98888261
|
A | G | 2 | a0001c0002t0002g0187a0001c0044t0002g0186 | 2 | HG01081.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.151-2074A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98888261 | ||||||
| chr7:98888375
|
T | TA | 6 | a0001c0005t0004g0004a0001c0005t0004g0005a0001c0005t0004g0006others(3): Show | 6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.151-1949dupA | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | INFO_REALIGN_3_PRIME | chr7 | 98888375 | |||||
| chr7:98888446
|
A | G | 1 | a0001c0001t0002g0249 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.151-1889A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98888446 | ||||||
| chr7:98888642
|
C | T | 1 | a0001c0001t0001g0091 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.151-1693C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98888642 | ||||||
| chr7:98888674
|
C | G | 1 | a0001c0002t0012g0194 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.151-1661C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98888674 | ||||||
| chr7:98888684
|
A | G | 6 | a0001c0001t0002g0154a0001c0002t0007g0155a0001c0002t0007g0156others(3): Show | 6 | HG00140.hp2 HG01243.hp2 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.151-1651A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98888684 | ||||||
| chr7:98888714
|
T | C | 32 | a0001c0002t0002g0016a0001c0002t0002g0017a0001c0002t0002g0163others(29): Show | 33 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(30): Show |
intron_variant | MODIFIER | c.151-1621T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98888714 | ||||||
| chr7:98889045
|
CT | C | 175 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(172): Show | 177 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.151-1269delT | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | INFO_REALIGN_3_PRIME | chr7 | 98889045 | |||||
| chr7:98889045
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0002t0012g0194 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.151-1279_151-1269d others(13): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | INFO_REALIGN_3_PRIME | chr7 | 98889045 | |||||
| chr7:98889064
|
T | C | 1 | a0001c0001t0002g0154 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.151-1271T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98889064 | ||||||
| chr7:98889076
|
T | C | 43 | a0001c0001t0002g0080a0001c0001t0005g0158a0001c0001t0005g0160others(40): Show | 44 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(41): Show |
intron_variant | MODIFIER | c.151-1259T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98889076 | ||||||
| chr7:98889230
|
A | T | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.151-1105A>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98889230 | ||||||
| chr7:98889265
|
A | G | 2 | a0001c0001t0006g0216a0001c0001t0006g0217 | 2 | HG00642.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.151-1070A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98889265 | ||||||
| chr7:98889354
|
A | T | 7 | a0001c0002t0002g0163a0001c0002t0002g0177a0001c0002t0002g0178others(4): Show | 7 | HG01257.hp2 HG01891.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.151-981A>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98889354 | ||||||
| chr7:98889386
|
A | G | 2 | a0001c0001t0002g0196a0001c0001t0002g0197 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.151-949A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98889386 | ||||||
| chr7:98889411
|
T | G | 1 | a0001c0001t0001g0078 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.151-924T>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98889411 | ||||||
| chr7:98889538
|
CT | C | 59 | a0001c0001t0002g0080a0001c0001t0002g0154a0001c0001t0002g0195others(56): Show | 60 | HG00140.hp2 HG01081.hp1 HG01081.hp2 others(57): Show |
intron_variant | MODIFIER | c.151-780delT | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | INFO_REALIGN_3_PRIME | chr7 | 98889538 | |||||
| chr7:98889554
|
T | A | 4 | a0001c0001t0002g0154a0001c0002t0007g0155a0001c0002t0007g0156others(1): Show | 4 | HG00140.hp2 HG01243.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.151-781T>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98889554 | ||||||
| chr7:98889555
|
T | A | 6 | a0001c0001t0002g0154a0001c0002t0007g0155a0001c0002t0007g0156others(3): Show | 6 | HG00140.hp2 HG01243.hp2 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.151-780T>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98889555 | ||||||
| chr7:98889555
|
TA | T | 122 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(119): Show | 123 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.151-772delA | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | INFO_REALIGN_3_PRIME | chr7 | 98889555 | |||||
| chr7:98889555
|
TAA | T | 5 | a0001c0001t0001g0060a0001c0001t0001g0069a0001c0001t0001g0100others(2): Show | 5 | HG01169.hp1 HG03017.hp1 NA18957.hp1 others(2): Show |
intron_variant | MODIFIER | c.151-773_151-772del others(2): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | INFO_REALIGN_3_PRIME | chr7 | 98889555 | |||||
| chr7:98889556
|
A | T | 7 | a0001c0001t0001g0030a0001c0001t0001g0072a0001c0001t0002g0228others(4): Show | 7 | HG02148.hp2 NA18942.hp2 NA18944.hp2 others(4): Show |
intron_variant | MODIFIER | c.151-779A>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98889556 | ||||||
| chr7:98889557
|
A | T | 119 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(116): Show | 120 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.151-778A>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98889557 | ||||||
| chr7:98889558
|
A | T | 1 | a0001c0001t0001g0132 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.151-777A>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98889558 | ||||||
| chr7:98889676
|
T | C | 127 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(124): Show | 128 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.151-659T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98889676 | ||||||
| chr7:98889731
|
T | A | 129 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(126): Show | 130 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.151-604T>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98889731 | ||||||
| chr7:98889745
|
G | T | 4 | a0001c0001t0002g0154a0001c0002t0007g0155a0001c0002t0007g0156others(1): Show | 4 | HG00140.hp2 HG01243.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.151-590G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98889745 | ||||||
| chr7:98889810
|
C | T | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.151-525C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 3/72 | chr7 | 98889810 | ||||||
| chr7:98890580
|
C | T | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.261+135C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 4/72 | chr7 | 98890580 | ||||||
| chr7:98890581
|
G | A | 1 | a0001c0001t0001g0123 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.261+136G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 4/72 | chr7 | 98890581 | ||||||
| chr7:98890587
|
T | C | 1 | a0001c0001t0001g0032 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.261+142T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 4/72 | chr7 | 98890587 | ||||||
| chr7:98890720
|
G | C | 1 | a0001c0005t0004g0004 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.261+275G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 4/72 | chr7 | 98890720 | ||||||
| chr7:98890781
|
C | CT | 104 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(101): Show | 105 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.261+360dupT | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 4/72 | INFO_REALIGN_3_PRIME | chr7 | 98890781 | |||||
| chr7:98890781
|
C | CTT | 9 | a0001c0001t0001g0015a0001c0001t0001g0051a0001c0001t0001g0072others(6): Show | 9 | HG01891.hp2 HG03579.hp1 HG03710.hp1 others(6): Show |
intron_variant | MODIFIER | c.261+359_261+360dup others(2): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 4/72 | INFO_REALIGN_3_PRIME | chr7 | 98890781 | |||||
| chr7:98890781
|
CT | C | 6 | a0001c0001t0006g0213a0001c0001t0006g0214a0001c0001t0006g0215others(3): Show | 6 | HG00280.hp1 HG00642.hp1 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.261+360delT | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 4/72 | INFO_REALIGN_3_PRIME | chr7 | 98890781 | |||||
| chr7:98890794
|
TTTTTTTT others(5): Show |
T | 1 | a0004c0040t0005g0162 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.261+350_261+361del others(12): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 4/72 | chr7 | 98890794 | ||||||
| chr7:98890804
|
TTA | T | 7 | a0001c0001t0005g0158a0001c0001t0005g0160a0001c0001t0005g0161others(4): Show | 7 | HG01167.hp1 HG02258.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.261+360_261+361del others(2): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 4/72 | chr7 | 98890804 | ||||||
| chr7:98890805
|
TA | T | 56 | a0001c0001t0001g0085a0001c0001t0002g0080a0001c0001t0002g0154others(53): Show | 58 | HG00140.hp2 HG01081.hp1 HG01081.hp2 others(55): Show |
intron_variant | MODIFIER | c.261+364delA | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 4/72 | INFO_REALIGN_3_PRIME | chr7 | 98890805 | |||||
| chr7:98890806
|
A | T | 133 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(130): Show | 134 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.261+361A>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 4/72 | chr7 | 98890806 | ||||||
| chr7:98890858
|
G | A | 255 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(252): Show | 258 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.261+413G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 4/72 | chr7 | 98890858 | ||||||
| chr7:98891137
|
A | G | 12 | a0001c0001t0002g0154a0001c0002t0007g0155a0001c0002t0007g0156others(9): Show | 12 | HG00140.hp2 HG01243.hp2 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.261+692A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 4/72 | chr7 | 98891137 | ||||||
| chr7:98891145
|
C | T | 1 | a0001c0001t0001g0015 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.261+700C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 4/72 | chr7 | 98891145 | ||||||
| chr7:98891192
|
C | CAT | 8 | a0001c0001t0001g0048a0001c0001t0002g0222a0001c0001t0002g0223others(5): Show | 8 | HG01081.hp1 HG01517.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.261+758_261+759dup others(2): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 4/72 | INFO_REALIGN_3_PRIME | chr7 | 98891192 | |||||
| chr7:98891192
|
C | CATAT | 109 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(106): Show | 110 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.261+756_261+759dup others(4): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 4/72 | INFO_REALIGN_3_PRIME | chr7 | 98891192 | |||||
| chr7:98891192
|
C | CATATAT | 10 | a0001c0001t0001g0033a0001c0001t0001g0061a0001c0001t0001g0071others(7): Show | 10 | HG00642.hp2 HG01515.hp1 HG01975.hp1 others(7): Show |
intron_variant | MODIFIER | c.261+754_261+759dup others(6): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 4/72 | INFO_REALIGN_3_PRIME | chr7 | 98891192 | |||||
| chr7:98891204
|
T | TA | 51 | a0001c0001t0002g0011a0001c0001t0002g0080a0001c0001t0002g0154others(48): Show | 53 | HG00438.hp2 HG01081.hp2 HG01167.hp1 others(50): Show |
intron_variant | MODIFIER | c.261+759_261+760ins others(1): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 4/72 | chr7 | 98891204 | ||||||
| chr7:98891204
|
T | TATA | 10 | a0001c0001t0001g0095a0001c0001t0001g0121a0001c0001t0001g0135others(7): Show | 10 | HG00423.hp2 HG02572.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.261+759_261+760ins others(3): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 4/72 | chr7 | 98891204 | ||||||
| chr7:98891205
|
T | A | 184 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(181): Show | 185 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.261+760T>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 4/72 | chr7 | 98891205 | ||||||
| chr7:98891206
|
T | A | 25 | a0001c0001t0001g0095a0001c0001t0001g0121a0001c0001t0001g0122others(22): Show | 25 | HG00423.hp2 HG01496.hp2 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.261+761T>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 4/72 | chr7 | 98891206 | ||||||
| chr7:98891207
|
T | A | 133 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(130): Show | 134 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.261+762T>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 4/72 | chr7 | 98891207 | ||||||
| chr7:98891208
|
T | A | 16 | a0001c0001t0001g0095a0001c0001t0001g0121a0001c0001t0001g0122others(13): Show | 16 | HG00423.hp2 HG01496.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.261+763T>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 4/72 | chr7 | 98891208 | ||||||
| chr7:98891209
|
T | A | 126 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(123): Show | 127 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.261+764T>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 4/72 | chr7 | 98891209 | ||||||
| chr7:98891210
|
T | A | 13 | a0001c0001t0001g0095a0001c0001t0001g0121a0001c0001t0001g0122others(10): Show | 13 | HG00423.hp2 HG01496.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.261+765T>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 4/72 | chr7 | 98891210 | ||||||
| chr7:98891211
|
T | A | 124 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(121): Show | 125 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.261+766T>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 4/72 | chr7 | 98891211 | ||||||
| chr7:98891212
|
T | A | 4 | a0001c0001t0001g0095a0001c0001t0001g0135a0001c0001t0001g0140others(1): Show | 4 | HG02572.hp2 HG02698.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.261+767T>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 4/72 | chr7 | 98891212 | ||||||
| chr7:98891213
|
T | A | 3 | a0001c0001t0001g0085a0001c0001t0001g0126a0001c0027t0001g0031 | 3 | HG00642.hp2 HG01169.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.261+768T>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 4/72 | chr7 | 98891213 | ||||||
| chr7:98891215
|
T | A | 1 | a0001c0001t0001g0085 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.261+770T>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 4/72 | chr7 | 98891215 | ||||||
| chr7:98891238
|
G | T | 1 | a0001c0001t0001g0120 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.261+793G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 4/72 | chr7 | 98891238 | ||||||
| chr7:98891283
|
C | G | 2 | a0001c0001t0001g0090a0001c0001t0001g0147 | 2 | HG02109.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.261+838C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 4/72 | chr7 | 98891283 | ||||||
| chr7:98891453
|
G | A | 1 | a0001c0013t0002g0224 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.262-971G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 4/72 | chr7 | 98891453 | ||||||
| chr7:98891462
|
A | G | 4 | a0001c0002t0002g0177a0001c0002t0002g0178a0001c0002t0010g0179others(1): Show | 4 | HG02451.hp1 HG03209.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.262-962A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 4/72 | chr7 | 98891462 | ||||||
| chr7:98891536
|
C | CT | 10 | a0001c0001t0001g0146a0001c0002t0002g0165a0001c0002t0002g0166others(7): Show | 10 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.262-871dupT | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 4/72 | INFO_REALIGN_3_PRIME | chr7 | 98891536 | |||||
| chr7:98891598
|
C | G | 1 | a0001c0006t0002g0084 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.262-826C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 4/72 | chr7 | 98891598 | ||||||
| chr7:98891630
|
G | A | 1 | a0001c0004t0002g0188 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.262-794G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 4/72 | chr7 | 98891630 | ||||||
| chr7:98891834
|
G | A | 1 | a0001c0005t0004g0005 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.262-590G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 4/72 | chr7 | 98891834 | ||||||
| chr7:98891905
|
G | A | 1 | a0001c0038t0001g0086 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.262-519G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 4/72 | chr7 | 98891905 | ||||||
| chr7:98892050
|
T | C | 1 | a0001c0003t0002g0199 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.262-374T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 4/72 | chr7 | 98892050 | ||||||
| chr7:98892125
|
A | G | 2 | a0001c0001t0001g0149a0001c0001t0001g0153 | 2 | HG03209.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.262-299A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 4/72 | chr7 | 98892125 | ||||||
| chr7:98892369
|
T | C | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.262-55T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 4/72 | chr7 | 98892369 | ||||||
| chr7:98892796
|
G | A | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.366+268G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 5/72 | chr7 | 98892796 | ||||||
| chr7:98892806
|
C | T | 1 | a0001c0001t0001g0047 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.366+278C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 5/72 | chr7 | 98892806 | ||||||
| chr7:98892890
|
G | C | 2 | a0002c0008t0008g0192a0002c0008t0008g0193 | 2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.366+362G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 5/72 | chr7 | 98892890 | ||||||
| chr7:98893045
|
G | A | 1 | a0001c0001t0002g0154 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.366+517G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 5/72 | chr7 | 98893045 | ||||||
| chr7:98893193
|
A | G | 2 | a0002c0008t0008g0192a0002c0008t0008g0193 | 2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.367-605A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 5/72 | chr7 | 98893193 | ||||||
| chr7:98893198
|
C | A | 1 | a0001c0002t0002g0163 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.367-600C>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 5/72 | chr7 | 98893198 | ||||||
| chr7:98893295
|
A | C | 2 | a0002c0008t0008g0192a0002c0008t0008g0193 | 2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.367-503A>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 5/72 | chr7 | 98893295 | ||||||
| chr7:98893295
|
A | G | 6 | a0001c0005t0004g0004a0001c0005t0004g0005a0001c0005t0004g0006others(3): Show | 6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.367-503A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 5/72 | chr7 | 98893295 | ||||||
| chr7:98893314
|
A | G | 43 | a0001c0001t0002g0080a0001c0001t0005g0158a0001c0001t0005g0160others(40): Show | 44 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(41): Show |
intron_variant | MODIFIER | c.367-484A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 5/72 | chr7 | 98893314 | ||||||
| chr7:98893333
|
G | A | 9 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(6): Show | 9 | HG00738.hp1 HG01192.hp1 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.367-465G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 5/72 | chr7 | 98893333 | ||||||
| chr7:98893344
|
G | A | 1 | a0001c0021t0001g0059 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.367-454G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 5/72 | chr7 | 98893344 | ||||||
| chr7:98893399
|
A | T | 1 | a0001c0002t0002g0174 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.367-399A>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 5/72 | chr7 | 98893399 | ||||||
| chr7:98893428
|
A | G | 1 | a0001c0001t0003g0024 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.367-370A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 5/72 | chr7 | 98893428 | ||||||
| chr7:98893623
|
C | T | 1 | a0001c0002t0002g0218 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.367-175C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 5/72 | chr7 | 98893623 | ||||||
| chr7:98893638
|
T | C | 193 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(190): Show | 195 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.367-160T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 5/72 | chr7 | 98893638 | ||||||
| chr7:98893929
|
T | A | 3 | a0001c0001t0003g0025a0001c0001t0003g0026a0001c0026t0003g0021 | 3 | NA18957.hp2 NA18986.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.450+48T>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 6/72 | chr7 | 98893929 | ||||||
| chr7:98894141
|
C | T | 1 | a0001c0025t0001g0151 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.450+260C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 6/72 | chr7 | 98894141 | ||||||
| chr7:98894166
|
T | C | 6 | a0001c0005t0004g0004a0001c0005t0004g0005a0001c0005t0004g0006others(3): Show | 6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.450+285T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 6/72 | chr7 | 98894166 | ||||||
| chr7:98894219
|
C | A | 1 | a0001c0001t0001g0035 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.450+338C>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 6/72 | chr7 | 98894219 | ||||||
| chr7:98894404
|
A | G | 1 | a0001c0001t0001g0032 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.450+523A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 6/72 | chr7 | 98894404 | ||||||
| chr7:98894422
|
G | A | 203 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(200): Show | 206 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.450+541G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 6/72 | chr7 | 98894422 | ||||||
| chr7:98894522
|
G | T | 1 | a0001c0001t0001g0015 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.450+641G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 6/72 | chr7 | 98894522 | ||||||
| chr7:98894567
|
A | C | 6 | a0001c0005t0004g0004a0001c0005t0004g0005a0001c0005t0004g0006others(3): Show | 6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.450+686A>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 6/72 | chr7 | 98894567 | ||||||
| chr7:98894623
|
G | GT | 138 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(135): Show | 139 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.450+751dupT | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 6/72 | INFO_REALIGN_3_PRIME | chr7 | 98894623 | |||||
| chr7:98894634
|
G | A | 5 | a0001c0001t0005g0158a0001c0001t0005g0160a0001c0001t0005g0161others(2): Show | 5 | HG02055.hp1 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.450+753G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 6/72 | chr7 | 98894634 | ||||||
| chr7:98894715
|
C | T | 2 | a0001c0009t0002g0164a0001c0009t0002g0210 | 2 | HG02809.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.450+834C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 6/72 | chr7 | 98894715 | ||||||
| chr7:98894779
|
A | G | 1 | a0001c0001t0001g0093 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.450+898A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 6/72 | chr7 | 98894779 | ||||||
| chr7:98894783
|
G | GT | 31 | a0001c0001t0001g0258a0001c0001t0002g0011a0001c0001t0002g0080others(28): Show | 31 | HG00438.hp2 HG00642.hp1 HG01081.hp1 others(28): Show |
intron_variant | MODIFIER | c.450+927dupT | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 6/72 | INFO_REALIGN_3_PRIME | chr7 | 98894783 | |||||
| chr7:98894783
|
G | GTT | 8 | a0001c0002t0002g0177a0001c0002t0002g0178a0001c0002t0002g0180others(5): Show | 8 | HG01243.hp1 HG01891.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.450+926_450+927dup others(2): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 6/72 | INFO_REALIGN_3_PRIME | chr7 | 98894783 | |||||
| chr7:98894783
|
GT | G | 48 | a0001c0001t0001g0015a0001c0001t0001g0032a0001c0001t0001g0047others(45): Show | 49 | HG00423.hp1 HG00423.hp2 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.450+927delT | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 6/72 | INFO_REALIGN_3_PRIME | chr7 | 98894783 | |||||
| chr7:98894783
|
GTT | G | 107 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(104): Show | 108 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.450+926_450+927del others(2): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 6/72 | INFO_REALIGN_3_PRIME | chr7 | 98894783 | |||||
| chr7:98894956
|
G | A | 1 | a0001c0001t0001g0114 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.451-808G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 6/72 | chr7 | 98894956 | ||||||
| chr7:98895087
|
G | T | 2 | a0001c0001t0002g0208a0001c0001t0011g0209 | 2 | HG02486.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.451-677G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 6/72 | chr7 | 98895087 | ||||||
| chr7:98895164
|
C | T | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.451-600C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 6/72 | chr7 | 98895164 | ||||||
| chr7:98895166
|
G | A | 1 | a0001c0001t0001g0146 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.451-598G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 6/72 | chr7 | 98895166 | ||||||
| chr7:98895209
|
A | G | 1 | a0001c0001t0003g0089 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.451-555A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 6/72 | chr7 | 98895209 | ||||||
| chr7:98895462
|
C | T | 2 | a0001c0001t0003g0020a0001c0001t0003g0022 | 2 | NA18948.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.451-302C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 6/72 | chr7 | 98895462 | ||||||
| chr7:98895463
|
G | A | 3 | a0001c0001t0001g0095a0001c0001t0001g0135a0001c0001t0001g0140 | 3 | HG02572.hp2 HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.451-301G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 6/72 | chr7 | 98895463 | ||||||
| chr7:98895468
|
A | G | 1 | a0001c0001t0001g0099 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.451-296A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 6/72 | chr7 | 98895468 | ||||||
| chr7:98895566
|
A | T | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.451-198A>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 6/72 | chr7 | 98895566 | ||||||
| chr7:98895659
|
C | T | 6 | a0001c0005t0004g0004a0001c0005t0004g0005a0001c0005t0004g0006others(3): Show | 6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.451-105C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 6/72 | chr7 | 98895659 | ||||||
| chr7:98895913
|
G | T | 1 | a0001c0002t0002g0181 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.507+93G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 7/72 | chr7 | 98895913 | ||||||
| chr7:98895954
|
A | G | 10 | a0001c0003t0002g0003a0001c0003t0002g0198a0001c0003t0002g0199others(7): Show | 11 | HG01081.hp2 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.507+134A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 7/72 | chr7 | 98895954 | ||||||
| chr7:98896224
|
A | T | 7 | a0001c0005t0004g0004a0001c0005t0004g0005a0001c0005t0004g0006others(4): Show | 7 | HG01169.hp1 HG02622.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.507+404A>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 7/72 | chr7 | 98896224 | ||||||
| chr7:98896427
|
C | T | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.507+607C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 7/72 | chr7 | 98896427 | ||||||
| chr7:98896435
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.507+615C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 7/72 | chr7 | 98896435 | ||||||
| chr7:98896437
|
G | A | 6 | a0001c0005t0004g0004a0001c0005t0004g0005a0001c0005t0004g0006others(3): Show | 6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.507+617G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 7/72 | chr7 | 98896437 | ||||||
| chr7:98896544
|
G | C | 2 | a0001c0001t0001g0036a0001c0001t0001g0076 | 2 | HG03704.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.507+724G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 7/72 | chr7 | 98896544 | ||||||
| chr7:98896664
|
G | A | 2 | a0002c0008t0008g0192a0002c0008t0008g0193 | 2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.507+844G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 7/72 | chr7 | 98896664 | ||||||
| chr7:98896792
|
A | C | 9 | a0001c0003t0002g0003a0001c0003t0002g0198a0001c0003t0002g0199others(6): Show | 10 | HG01081.hp2 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.508-949A>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 7/72 | chr7 | 98896792 | ||||||
| chr7:98896910
|
G | C | 1 | a0001c0005t0004g0005 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.508-831G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 7/72 | chr7 | 98896910 | ||||||
| chr7:98896942
|
TC | T | 43 | a0001c0001t0002g0080a0001c0001t0005g0158a0001c0001t0005g0160others(40): Show | 44 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(41): Show |
intron_variant | MODIFIER | c.508-797delC | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 7/72 | INFO_REALIGN_3_PRIME | chr7 | 98896942 | |||||
| chr7:98896971
|
A | C | 3 | a0001c0001t0001g0095a0001c0001t0001g0135a0001c0001t0001g0140 | 3 | HG02572.hp2 HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.508-770A>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 7/72 | chr7 | 98896971 | ||||||
| chr7:98897190
|
G | A | 6 | a0001c0005t0004g0004a0001c0005t0004g0005a0001c0005t0004g0006others(3): Show | 6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.508-551G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 7/72 | chr7 | 98897190 | ||||||
| chr7:98897327
|
G | A | 1 | a0001c0002t0002g0166 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.508-414G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 7/72 | chr7 | 98897327 | ||||||
| chr7:98897480
|
A | G | 3 | a0001c0004t0002g0183a0001c0004t0002g0185a0006c0042t0002g0184 | 3 | HG02622.hp2 HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.508-261A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 7/72 | chr7 | 98897480 | ||||||
| chr7:98897525
|
A | G | 2 | a0001c0001t0001g0098a0001c0001t0003g0139 | 2 | HG00438.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.508-216A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 7/72 | chr7 | 98897525 | ||||||
| chr7:98897676
|
G | GTT | 124 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(121): Show | 125 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.508-62_508-61dupTT | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 7/72 | INFO_REALIGN_3_PRIME | chr7 | 98897676 | |||||
| chr7:98897676
|
G | GTTT | 12 | a0001c0001t0001g0100a0001c0001t0001g0103a0001c0001t0001g0104others(9): Show | 12 | HG00423.hp2 HG01975.hp1 HG02040.hp1 others(9): Show |
intron_variant | MODIFIER | c.508-63_508-61dupTT others(1): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 7/72 | INFO_REALIGN_3_PRIME | chr7 | 98897676 | |||||
| chr7:98897676
|
G | T | 1 | a0001c0001t0003g0024 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.508-65G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 7/72 | chr7 | 98897676 | ||||||
| chr7:98897681
|
G | T | 181 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(178): Show | 183 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(180): Show |
intron_variant | MODIFIER | c.508-60G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 7/72 | chr7 | 98897681 | ||||||
| chr7:98897933
|
A | AT | 11 | a0001c0001t0002g0080a0001c0001t0005g0158a0001c0001t0005g0160others(8): Show | 11 | HG01884.hp2 HG02055.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.633+76dupT | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 8/72 | INFO_REALIGN_3_PRIME | chr7 | 98897933 | |||||
| chr7:98898331
|
G | A | 137 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(134): Show | 138 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.633+465G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 8/72 | chr7 | 98898331 | ||||||
| chr7:98898439
|
C | A | 1 | a0001c0001t0001g0028 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.633+573C>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 8/72 | chr7 | 98898439 | ||||||
| chr7:98898469
|
C | A | 1 | a0001c0017t0001g0131 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.633+603C>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 8/72 | chr7 | 98898469 | ||||||
| chr7:98898707
|
G | C | 130 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(127): Show | 131 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.634-715G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 8/72 | chr7 | 98898707 | ||||||
| chr7:98899015
|
G | T | 1 | a0001c0002t0010g0179 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.634-407G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 8/72 | chr7 | 98899015 | ||||||
| chr7:98899583
|
C | G | 25 | a0001c0002t0002g0016a0001c0002t0002g0017a0001c0002t0002g0165others(22): Show | 26 | HG01081.hp1 HG01243.hp1 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.711+84C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 9/72 | chr7 | 98899583 | ||||||
| chr7:98899884
|
T | C | 2 | a0002c0008t0008g0192a0002c0008t0008g0193 | 2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.800+117T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 10/72 | chr7 | 98899884 | ||||||
| chr7:98899970
|
C | T | 1 | a0001c0001t0001g0130 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.800+203C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 10/72 | chr7 | 98899970 | ||||||
| chr7:98900002
|
G | A | 3 | a0001c0001t0001g0034a0001c0001t0001g0037a0001c0001t0001g0038 | 3 | HG01346.hp2 HG02145.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.800+235G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 10/72 | chr7 | 98900002 | ||||||
| chr7:98900123
|
C | T | 4 | a0001c0001t0002g0154a0001c0002t0007g0155a0001c0002t0007g0156others(1): Show | 4 | HG00140.hp2 HG01243.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.800+356C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 10/72 | chr7 | 98900123 | ||||||
| chr7:98900268
|
A | G | 1 | a0001c0001t0001g0046 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.801-356A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 10/72 | chr7 | 98900268 | ||||||
| chr7:98900290
|
T | C | 1 | a0001c0001t0001g0128 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.801-334T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 10/72 | chr7 | 98900290 | ||||||
| chr7:98900531
|
A | G | 4 | a0001c0001t0005g0158a0001c0001t0005g0160a0001c0001t0005g0161others(1): Show | 4 | HG02258.hp1 HG02486.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.801-93A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 10/72 | chr7 | 98900531 | ||||||
| chr7:98900774
|
A | G | 1 | a0001c0001t0005g0161 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.897+54A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 11/72 | chr7 | 98900774 | ||||||
| chr7:98900846
|
C | T | 2 | a0001c0001t0001g0100a0001c0001t0001g0103 | 2 | NA18957.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.897+126C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 11/72 | chr7 | 98900846 | ||||||
| chr7:98900883
|
T | C | 129 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(126): Show | 130 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.897+163T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 11/72 | chr7 | 98900883 | ||||||
| chr7:98901085
|
G | T | 9 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(6): Show | 9 | HG00738.hp1 HG01192.hp1 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.897+365G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 11/72 | chr7 | 98901085 | ||||||
| chr7:98901337
|
G | A | 1 | a0001c0001t0001g0068 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.897+617G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 11/72 | chr7 | 98901337 | ||||||
| chr7:98901483
|
T | A | 3 | a0001c0001t0002g0208a0001c0001t0011g0209a0001c0028t0002g0207 | 3 | HG02486.hp1 HG02723.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.897+763T>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 11/72 | chr7 | 98901483 | ||||||
| chr7:98901613
|
A | G | 2 | a0001c0001t0001g0097a0001c0001t0001g0110 | 2 | HG01099.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.897+893A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 11/72 | chr7 | 98901613 | ||||||
| chr7:98901927
|
C | T | 5 | a0001c0004t0002g0002a0001c0004t0002g0169a0001c0004t0002g0170others(2): Show | 6 | HG02257.hp1 HG02647.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.897+1207C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 11/72 | chr7 | 98901927 | ||||||
| chr7:98901959
|
G | A | 11 | a0001c0001t0002g0080a0001c0001t0005g0158a0001c0001t0005g0160others(8): Show | 11 | HG01884.hp2 HG02055.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.897+1239G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 11/72 | chr7 | 98901959 | ||||||
| chr7:98901965
|
C | T | 184 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(181): Show | 186 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.897+1245C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 11/72 | chr7 | 98901965 | ||||||
| chr7:98902054
|
C | G | 1 | a0001c0001t0001g0102 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.898-1325C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 11/72 | chr7 | 98902054 | ||||||
| chr7:98902128
|
A | C | 1 | a0001c0002t0012g0194 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.898-1251A>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 11/72 | chr7 | 98902128 | ||||||
| chr7:98902158
|
T | A | 10 | a0001c0003t0002g0003a0001c0003t0002g0198a0001c0003t0002g0199others(7): Show | 11 | HG01081.hp2 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.898-1221T>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 11/72 | chr7 | 98902158 | ||||||
| chr7:98902227
|
T | C | 3 | a0001c0002t0007g0155a0001c0002t0007g0156a0001c0002t0007g0157 | 3 | HG00140.hp2 HG01243.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.898-1152T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 11/72 | chr7 | 98902227 | ||||||
| chr7:98902454
|
G | A | 2 | a0001c0001t0001g0149a0001c0001t0001g0153 | 2 | HG03209.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.898-925G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 11/72 | chr7 | 98902454 | ||||||
| chr7:98902546
|
T | G | 61 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(58): Show | 61 | HG00408.hp2 HG00423.hp1 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.898-833T>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 11/72 | chr7 | 98902546 | ||||||
| chr7:98902592
|
A | ATGGAAC | 61 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(58): Show | 61 | HG00408.hp2 HG00423.hp1 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.898-786_898-781dup others(6): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 11/72 | INFO_REALIGN_3_PRIME | chr7 | 98902592 | |||||
| chr7:98902630
|
T | C | 43 | a0001c0001t0002g0080a0001c0001t0005g0158a0001c0001t0005g0160others(40): Show | 44 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(41): Show |
intron_variant | MODIFIER | c.898-749T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 11/72 | chr7 | 98902630 | ||||||
| chr7:98902699
|
G | A | 184 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(181): Show | 186 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.898-680G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 11/72 | chr7 | 98902699 | ||||||
| chr7:98902882
|
G | A | 1 | a0006c0042t0002g0184 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.898-497G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 11/72 | chr7 | 98902882 | ||||||
| chr7:98902906
|
T | C | 43 | a0001c0001t0002g0080a0001c0001t0005g0158a0001c0001t0005g0160others(40): Show | 44 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(41): Show |
intron_variant | MODIFIER | c.898-473T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 11/72 | chr7 | 98902906 | ||||||
| chr7:98902908
|
T | TA | 21 | a0001c0001t0001g0141a0001c0001t0001g0259a0001c0001t0002g0196others(18): Show | 21 | HG00140.hp2 HG01099.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.898-453dupA | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 11/72 | INFO_REALIGN_3_PRIME | chr7 | 98902908 | |||||
| chr7:98902908
|
T | TAA | 119 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(116): Show | 120 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.898-454_898-453dup others(2): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 11/72 | INFO_REALIGN_3_PRIME | chr7 | 98902908 | |||||
| chr7:98902908
|
T | TAAA | 5 | a0001c0001t0001g0073a0001c0001t0001g0106a0001c0001t0001g0113others(2): Show | 5 | HG00544.hp1 HG00621.hp1 HG02015.hp1 others(2): Show |
intron_variant | MODIFIER | c.898-455_898-453dup others(3): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 11/72 | INFO_REALIGN_3_PRIME | chr7 | 98902908 | |||||
| chr7:98902908
|
TA | T | 11 | a0001c0001t0002g0080a0001c0001t0002g0248a0001c0001t0005g0158others(8): Show | 11 | HG01884.hp2 HG02055.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.898-453delA | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 11/72 | INFO_REALIGN_3_PRIME | chr7 | 98902908 | |||||
| chr7:98903001
|
G | A | 2 | a0001c0001t0002g0196a0001c0001t0002g0197 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.898-378G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 11/72 | chr7 | 98903001 | ||||||
| chr7:98903033
|
G | A | 190 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(187): Show | 192 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.898-346G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 11/72 | chr7 | 98903033 | ||||||
| chr7:98903033
|
G | T | 2 | a0001c0001t0001g0146a0001c0001t0001g0191 | 2 | NA18940.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.898-346G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 11/72 | chr7 | 98903033 | ||||||
| chr7:98903049
|
C | CAA | 192 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(189): Show | 194 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.898-330_898-329ins others(2): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 11/72 | chr7 | 98903049 | ||||||
| chr7:98903053
|
T | C | 1 | a0001c0002t0012g0194 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.898-326T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 11/72 | chr7 | 98903053 | ||||||
| chr7:98903075
|
G | T | 1 | a0001c0001t0001g0018 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.898-304G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 11/72 | chr7 | 98903075 | ||||||
| chr7:98903219
|
A | G | 209 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(206): Show | 212 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.898-160A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 11/72 | chr7 | 98903219 | ||||||
| chr7:98903333
|
C | T | 136 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(133): Show | 137 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.898-46C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 11/72 | chr7 | 98903333 | ||||||
| chr7:98903761
|
G | A | 1 | a0001c0001t0001g0027 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1036+244G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 12/72 | chr7 | 98903761 | ||||||
| chr7:98903817
|
C | T | 4 | a0001c0001t0002g0154a0001c0002t0007g0155a0001c0002t0007g0156others(1): Show | 4 | HG00140.hp2 HG01243.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.1036+300C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 12/72 | chr7 | 98903817 | ||||||
| chr7:98903846
|
G | A | 3 | a0001c0001t0002g0195a0001c0001t0002g0196a0001c0001t0002g0197 | 3 | HG02258.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1036+329G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 12/72 | chr7 | 98903846 | ||||||
| chr7:98903850
|
G | A | 1 | a0001c0001t0002g0195 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1036+333G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 12/72 | chr7 | 98903850 | ||||||
| chr7:98903875
|
A | T | 6 | a0001c0001t0002g0080a0001c0006t0002g0082a0001c0006t0002g0083others(3): Show | 6 | HG01884.hp2 HG02559.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1036+358A>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 12/72 | chr7 | 98903875 | ||||||
| chr7:98903881
|
C | T | 1 | a0001c0038t0001g0086 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1036+364C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 12/72 | chr7 | 98903881 | ||||||
| chr7:98903912
|
C | T | 4 | a0001c0001t0002g0154a0001c0002t0007g0155a0001c0002t0007g0156others(1): Show | 4 | HG00140.hp2 HG01243.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.1036+395C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 12/72 | chr7 | 98903912 | ||||||
| chr7:98903933
|
C | T | 1 | a0001c0001t0001g0057 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1036+416C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 12/72 | chr7 | 98903933 | ||||||
| chr7:98903966
|
C | A | 6 | a0001c0005t0004g0004a0001c0005t0004g0005a0001c0005t0004g0006others(3): Show | 6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1036+449C>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 12/72 | chr7 | 98903966 | ||||||
| chr7:98904087
|
G | A | 1 | a0002c0008t0008g0192 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1036+570G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 12/72 | chr7 | 98904087 | ||||||
| chr7:98904145
|
G | C | 1 | a0001c0001t0001g0076 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1036+628G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 12/72 | chr7 | 98904145 | ||||||
| chr7:98904157
|
G | A | 2 | a0001c0002t0002g0187a0001c0044t0002g0186 | 2 | HG01081.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1036+640G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 12/72 | chr7 | 98904157 | ||||||
| chr7:98904202
|
A | G | 192 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(189): Show | 194 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.1036+685A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 12/72 | chr7 | 98904202 | ||||||
| chr7:98904265
|
C | T | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1036+748C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 12/72 | chr7 | 98904265 | ||||||
| chr7:98904300
|
G | A | 2 | a0001c0001t0002g0208a0001c0001t0011g0209 | 2 | HG02486.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1036+783G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 12/72 | chr7 | 98904300 | ||||||
| chr7:98904408
|
A | C | 136 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(133): Show | 137 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.1036+891A>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 12/72 | chr7 | 98904408 | ||||||
| chr7:98904483
|
C | CA | 45 | a0001c0001t0001g0027a0001c0001t0001g0037a0001c0001t0001g0039others(42): Show | 45 | HG00438.hp2 HG00621.hp1 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.1036+992dupA | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 12/72 | INFO_REALIGN_3_PRIME | chr7 | 98904483 | |||||
| chr7:98904483
|
C | CAA | 5 | a0001c0001t0001g0032a0001c0001t0001g0074a0001c0002t0002g0016others(2): Show | 5 | HG01081.hp1 HG01884.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1036+991_1036+992d others(4): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 12/72 | INFO_REALIGN_3_PRIME | chr7 | 98904483 | |||||
| chr7:98904483
|
CA | C | 21 | a0001c0001t0001g0030a0001c0001t0001g0033a0001c0001t0001g0061others(18): Show | 21 | HG01515.hp1 HG02148.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.1036+992delA | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 12/72 | INFO_REALIGN_3_PRIME | chr7 | 98904483 | |||||
| chr7:98904483
|
CAA | C | 7 | a0001c0003t0002g0003a0001c0003t0002g0199a0001c0003t0002g0200others(4): Show | 8 | HG01081.hp2 HG01169.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1036+991_1036+992d others(4): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 12/72 | INFO_REALIGN_3_PRIME | chr7 | 98904483 | |||||
| chr7:98904483
|
CAAAAAAA others(5): Show |
C | 2 | a0002c0008t0008g0192a0002c0008t0008g0193 | 2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1036+981_1036+992d others(14): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 12/72 | INFO_REALIGN_3_PRIME | chr7 | 98904483 | |||||
| chr7:98904483
|
CAAAAAAA others(6): Show |
C | 10 | a0001c0001t0002g0154a0001c0002t0007g0155a0001c0002t0007g0156others(7): Show | 10 | HG00140.hp2 HG01243.hp2 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.1036+980_1036+992d others(15): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 12/72 | INFO_REALIGN_3_PRIME | chr7 | 98904483 | |||||
| chr7:98904566
|
C | A | 4 | a0001c0004t0002g0002a0001c0004t0002g0169a0001c0004t0002g0170others(1): Show | 5 | HG02257.hp1 HG02965.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1036+1049C>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 12/72 | chr7 | 98904566 | ||||||
| chr7:98904593
|
A | G | 5 | a0001c0006t0002g0082a0001c0006t0002g0083a0001c0006t0002g0084others(2): Show | 5 | HG02559.hp1 HG02647.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1036+1076A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 12/72 | chr7 | 98904593 | ||||||
| chr7:98904668
|
C | T | 1 | a0001c0009t0002g0164 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1036+1151C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 12/72 | chr7 | 98904668 | ||||||
| chr7:98904808
|
A | C | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1036+1291A>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 12/72 | chr7 | 98904808 | ||||||
| chr7:98904878
|
A | G | 1 | a0014c0041t0001g0055 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1037-1299A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 12/72 | chr7 | 98904878 | ||||||
| chr7:98904921
|
G | A | 6 | a0001c0001t0001g0097a0001c0001t0001g0107a0001c0001t0001g0110others(3): Show | 6 | HG00140.hp1 HG01099.hp1 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.1037-1256G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 12/72 | chr7 | 98904921 | ||||||
| chr7:98905140
|
G | A | 1 | a0001c0022t0001g0056 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1037-1037G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 12/72 | chr7 | 98905140 | ||||||
| chr7:98905165
|
G | T | 2 | a0001c0001t0001g0090a0001c0001t0001g0147 | 2 | HG02109.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1037-1012G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 12/72 | chr7 | 98905165 | ||||||
| chr7:98905267
|
G | A | 4 | a0001c0006t0002g0082a0001c0006t0002g0083a0001c0006t0002g0084others(1): Show | 4 | HG02559.hp1 HG02647.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1037-910G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 12/72 | chr7 | 98905267 | ||||||
| chr7:98905552
|
A | G | 1 | a0001c0002t0002g0178 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1037-625A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 12/72 | chr7 | 98905552 | ||||||
| chr7:98905585
|
C | A | 2 | a0001c0001t0002g0208a0001c0001t0011g0209 | 2 | HG02486.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1037-592C>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 12/72 | chr7 | 98905585 | ||||||
| chr7:98905652
|
T | G | 6 | a0001c0001t0002g0080a0001c0006t0002g0082a0001c0006t0002g0083others(3): Show | 6 | HG01884.hp2 HG02559.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1037-525T>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 12/72 | chr7 | 98905652 | ||||||
| chr7:98905697
|
T | G | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1037-480T>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 12/72 | chr7 | 98905697 | ||||||
| chr7:98905724
|
G | T | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1037-453G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 12/72 | chr7 | 98905724 | ||||||
| chr7:98905814
|
C | A | 3 | a0001c0002t0007g0155a0001c0002t0007g0156a0001c0002t0007g0157 | 3 | HG00140.hp2 HG01243.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.1037-363C>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 12/72 | chr7 | 98905814 | ||||||
| chr7:98906043
|
C | G | 1 | a0001c0001t0001g0241 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1037-134C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 12/72 | chr7 | 98906043 | ||||||
| chr7:98906084
|
TG | T | 192 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(189): Show | 195 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.1037-91delG | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 12/72 | INFO_REALIGN_3_PRIME | chr7 | 98906084 | |||||
| chr7:98906099
|
T | A | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1037-78T>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 12/72 | chr7 | 98906099 | ||||||
| chr7:98906157
|
A | G | 1 | a0001c0001t0002g0154 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1037-20A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 12/72 | chr7 | 98906157 | ||||||
| chr7:98906396
|
TTTTTGTT others(3): Show |
T | 4 | a0001c0001t0001g0035a0001c0001t0005g0158a0001c0024t0001g0040others(1): Show | 4 | HG00741.hp1 HG01192.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1115+145_1115+154d others(12): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 13/72 | INFO_REALIGN_3_PRIME | chr7 | 98906396 | |||||
| chr7:98906402
|
T | TTTTA | 40 | a0001c0001t0001g0239a0001c0001t0001g0257a0001c0001t0001g0258others(37): Show | 40 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.1115+191_1115+194d others(6): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 13/72 | INFO_REALIGN_3_PRIME | chr7 | 98906402 | |||||
| chr7:98906402
|
T | TTTTATTT others(1): Show |
8 | a0001c0001t0001g0241a0001c0001t0002g0010a0001c0001t0002g0219others(5): Show | 8 | HG00544.hp2 NA18969.hp1 NA19009.hp1 others(5): Show |
intron_variant | MODIFIER | c.1115+187_1115+194d others(10): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 13/72 | INFO_REALIGN_3_PRIME | chr7 | 98906402 | |||||
| chr7:98906402
|
T | TTTTATTT others(5): Show |
1 | a0002c0008t0008g0193 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1115+183_1115+194d others(14): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 13/72 | INFO_REALIGN_3_PRIME | chr7 | 98906402 | |||||
| chr7:98906402
|
TTTTA | T | 10 | a0001c0001t0002g0080a0001c0001t0005g0160a0001c0001t0005g0161others(7): Show | 10 | HG01884.hp2 HG02055.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1115+191_1115+194d others(6): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 13/72 | INFO_REALIGN_3_PRIME | chr7 | 98906402 | |||||
| chr7:98906402
|
TTTTATTT others(1): Show |
T | 3 | a0001c0001t0001g0041a0001c0002t0012g0194a0001c0025t0001g0151 | 3 | HG00408.hp2 NA18944.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1115+187_1115+194d others(10): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 13/72 | INFO_REALIGN_3_PRIME | chr7 | 98906402 | |||||
| chr7:98906402
|
TTTTATTT others(5): Show |
T | 135 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(132): Show | 137 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.1115+183_1115+194d others(14): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 13/72 | INFO_REALIGN_3_PRIME | chr7 | 98906402 | |||||
| chr7:98906456
|
C | T | 3 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0077 | 3 | HG01358.hp1 HG01943.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.1115+201C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 13/72 | chr7 | 98906456 | ||||||
| chr7:98906476
|
G | A | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1115+221G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 13/72 | chr7 | 98906476 | ||||||
| chr7:98906589
|
T | C | 3 | a0001c0001t0002g0221a0001c0001t0002g0231a0001c0001t0002g0243 | 3 | HG01099.hp2 HG01496.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.1115+334T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 13/72 | chr7 | 98906589 | ||||||
| chr7:98906984
|
A | C | 2 | a0001c0001t0002g0196a0001c0001t0002g0197 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1115+729A>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 13/72 | chr7 | 98906984 | ||||||
| chr7:98906999
|
A | C | 1 | a0001c0001t0001g0066 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1115+744A>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 13/72 | chr7 | 98906999 | ||||||
| chr7:98907046
|
A | G | 136 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(133): Show | 137 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.1115+791A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 13/72 | chr7 | 98907046 | ||||||
| chr7:98907113
|
C | T | 11 | a0001c0001t0002g0080a0001c0001t0005g0158a0001c0001t0005g0160others(8): Show | 11 | HG01884.hp2 HG02055.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1115+858C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 13/72 | chr7 | 98907113 | ||||||
| chr7:98907323
|
C | CA | 5 | a0001c0001t0002g0011a0001c0002t0002g0177a0001c0002t0002g0178others(2): Show | 5 | HG02027.hp1 HG02451.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1115+1080dupA | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 13/72 | INFO_REALIGN_3_PRIME | chr7 | 98907323 | |||||
| chr7:98907441
|
C | T | 2 | a0001c0001t0001g0030a0001c0001t0001g0113 | 2 | HG00544.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.1115+1186C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 13/72 | chr7 | 98907441 | ||||||
| chr7:98907573
|
C | T | 3 | a0001c0001t0002g0195a0001c0001t0002g0196a0001c0001t0002g0197 | 3 | HG02258.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1116-1155C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 13/72 | chr7 | 98907573 | ||||||
| chr7:98907597
|
G | A | 1 | a0001c0002t0002g0163 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1116-1131G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 13/72 | chr7 | 98907597 | ||||||
| chr7:98907703
|
T | G | 2 | a0002c0008t0008g0192a0002c0008t0008g0193 | 2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1116-1025T>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 13/72 | chr7 | 98907703 | ||||||
| chr7:98907727
|
T | C | 258 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(255): Show | 261 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.1116-1001T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 13/72 | chr7 | 98907727 | ||||||
| chr7:98907779
|
C | T | 45 | a0001c0001t0001g0057a0001c0001t0002g0080a0001c0001t0005g0158others(42): Show | 46 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(43): Show |
intron_variant | MODIFIER | c.1116-949C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 13/72 | chr7 | 98907779 | ||||||
| chr7:98907796
|
ATCCCTGA others(34): Show |
A | 6 | a0001c0005t0004g0004a0001c0005t0004g0005a0001c0005t0004g0006others(3): Show | 6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1116-899_1116-859d others(43): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 13/72 | INFO_REALIGN_3_PRIME | chr7 | 98907796 | |||||
| chr7:98907903
|
G | A | 1 | a0001c0001t0001g0013 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1116-825G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 13/72 | chr7 | 98907903 | ||||||
| chr7:98908016
|
T | C | 14 | a0001c0001t0001g0058a0001c0001t0001g0060a0001c0001t0001g0061others(11): Show | 14 | HG00738.hp1 HG01192.hp1 HG01261.hp2 others(11): Show |
intron_variant | MODIFIER | c.1116-712T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 13/72 | chr7 | 98908016 | ||||||
| chr7:98908044
|
G | A | 3 | a0001c0001t0001g0034a0001c0001t0001g0037a0001c0001t0001g0038 | 3 | HG01346.hp2 HG02145.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.1116-684G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 13/72 | chr7 | 98908044 | ||||||
| chr7:98908055
|
G | A | 1 | a0001c0007t0001g0142 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1116-673G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 13/72 | chr7 | 98908055 | ||||||
| chr7:98908163
|
G | A | 2 | a0001c0001t0001g0046a0001c0011t0013g0190 | 2 | HG01943.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1116-565G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 13/72 | chr7 | 98908163 | ||||||
| chr7:98908295
|
A | T | 1 | a0001c0002t0002g0163 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1116-433A>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 13/72 | chr7 | 98908295 | ||||||
| chr7:98909019
|
A | AT | 17 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0039others(14): Show | 17 | HG01081.hp1 HG01993.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.1350+79dupT | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 14/72 | INFO_REALIGN_3_PRIME | chr7 | 98909019 | |||||
| chr7:98909019
|
AT | A | 12 | a0001c0001t0001g0042a0001c0001t0001g0072a0001c0001t0001g0076others(9): Show | 13 | HG01515.hp2 HG01975.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.1350+79delT | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 14/72 | INFO_REALIGN_3_PRIME | chr7 | 98909019 | |||||
| chr7:98909104
|
A | G | 2 | a0002c0008t0008g0192a0002c0008t0008g0193 | 2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1350+142A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 14/72 | chr7 | 98909104 | ||||||
| chr7:98909212
|
CA | C | 67 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(64): Show | 67 | HG00408.hp2 HG00423.hp1 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.1350+251delA | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 14/72 | chr7 | 98909212 | ||||||
| chr7:98909214
|
G | T | 67 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(64): Show | 67 | HG00408.hp2 HG00423.hp1 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.1350+252G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 14/72 | chr7 | 98909214 | ||||||
| chr7:98909319
|
G | A | 1 | a0001c0001t0002g0252 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1350+357G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 14/72 | chr7 | 98909319 | ||||||
| chr7:98909440
|
G | GT | 6 | a0001c0005t0004g0004a0001c0005t0004g0005a0001c0005t0004g0006others(3): Show | 6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1350+484dupT | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 14/72 | INFO_REALIGN_3_PRIME | chr7 | 98909440 | |||||
| chr7:98909661
|
C | T | 1 | a0001c0001t0003g0024 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1351-395C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 14/72 | chr7 | 98909661 | ||||||
| chr7:98909792
|
C | CCTTT | 192 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(189): Show | 194 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.1351-263_1351-260d others(6): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 14/72 | INFO_REALIGN_3_PRIME | chr7 | 98909792 | |||||
| chr7:98910051
|
G | A | 1 | a0001c0017t0001g0131 | 1 | NA18747.hp2 | splice_region_variant&intron_variant | LOW | c.1351-5G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 14/72 | chr7 | 98910051 | ||||||
| chr7:98910824
|
C | T | 1 | a0001c0001t0001g0028 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1812+217C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 16/72 | chr7 | 98910824 | ||||||
| chr7:98910900
|
T | A | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1813-177T>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 16/72 | chr7 | 98910900 | ||||||
| chr7:98910917
|
T | G | 2 | a0002c0008t0008g0192a0002c0008t0008g0193 | 2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1813-160T>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 16/72 | chr7 | 98910917 | ||||||
| chr7:98910951
|
G | A | 43 | a0001c0001t0002g0080a0001c0001t0005g0158a0001c0001t0005g0160others(40): Show | 44 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(41): Show |
intron_variant | MODIFIER | c.1813-126G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 16/72 | chr7 | 98910951 | ||||||
| chr7:98911397
|
T | G | 3 | a0001c0002t0007g0155a0001c0002t0007g0156a0001c0002t0007g0157 | 3 | HG00140.hp2 HG01243.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.2007+126T>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 17/72 | chr7 | 98911397 | ||||||
| chr7:98911751
|
G | A | 6 | a0001c0005t0004g0004a0001c0005t0004g0005a0001c0005t0004g0006others(3): Show | 6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.2008-271G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 17/72 | chr7 | 98911751 | ||||||
| chr7:98911774
|
C | CA | 33 | a0001c0001t0001g0129a0001c0001t0006g0217a0001c0002t0002g0016others(30): Show | 33 | HG00642.hp1 HG01081.hp1 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.2008-233dupA | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 17/72 | INFO_REALIGN_3_PRIME | chr7 | 98911774 | |||||
| chr7:98911774
|
C | CAA | 6 | a0001c0002t0010g0179a0001c0004t0002g0002a0001c0004t0002g0169others(3): Show | 7 | HG02257.hp1 HG02647.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.2008-234_2008-233d others(4): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 17/72 | INFO_REALIGN_3_PRIME | chr7 | 98911774 | |||||
| chr7:98911865
|
A | G | 6 | a0001c0005t0004g0004a0001c0005t0004g0005a0001c0005t0004g0006others(3): Show | 6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.2008-157A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 17/72 | chr7 | 98911865 | ||||||
| chr7:98911927
|
G | C | 15 | a0001c0002t0002g0016a0001c0002t0002g0017a0001c0002t0002g0165others(12): Show | 15 | HG01081.hp1 HG01243.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.2008-95G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 17/72 | chr7 | 98911927 | ||||||
| chr7:98912318
|
A | G | 1 | a0001c0004t0002g0171 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2199+105A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 18/72 | chr7 | 98912318 | ||||||
| chr7:98912387
|
CT | C | 258 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(255): Show | 261 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.2199+187delT | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 18/72 | INFO_REALIGN_3_PRIME | chr7 | 98912387 | |||||
| chr7:98912610
|
A | G | 2 | a0002c0008t0008g0192a0002c0008t0008g0193 | 2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.2199+397A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 18/72 | chr7 | 98912610 | ||||||
| chr7:98912931
|
G | A | 2 | a0001c0002t0002g0180a0001c0002t0002g0218 | 2 | HG01257.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.2199+718G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 18/72 | chr7 | 98912931 | ||||||
| chr7:98913000
|
G | C | 131 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(128): Show | 132 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.2199+787G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 18/72 | chr7 | 98913000 | ||||||
| chr7:98913139
|
CGT | C | 31 | a0001c0002t0002g0016a0001c0002t0002g0017a0001c0002t0002g0163others(28): Show | 32 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(29): Show |
intron_variant | MODIFIER | c.2199+930_2199+931d others(4): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 18/72 | INFO_REALIGN_3_PRIME | chr7 | 98913139 | |||||
| chr7:98913145
|
C | A | 31 | a0001c0002t0002g0016a0001c0002t0002g0017a0001c0002t0002g0163others(28): Show | 32 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(29): Show |
intron_variant | MODIFIER | c.2199+932C>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 18/72 | chr7 | 98913145 | ||||||
| chr7:98913175
|
C | G | 1 | a0002c0008t0008g0192 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2199+962C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 18/72 | chr7 | 98913175 | ||||||
| chr7:98913185
|
G | C | 5 | a0001c0001t0005g0158a0001c0001t0005g0160a0001c0001t0005g0161others(2): Show | 5 | HG02055.hp1 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.2199+972G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 18/72 | chr7 | 98913185 | ||||||
| chr7:98913309
|
G | GT | 12 | a0001c0001t0001g0116a0001c0001t0003g0022a0001c0003t0002g0003others(9): Show | 13 | HG01081.hp2 HG01167.hp1 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.2199+1106dupT | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 18/72 | INFO_REALIGN_3_PRIME | chr7 | 98913309 | |||||
| chr7:98913530
|
C | T | 6 | a0001c0005t0004g0004a0001c0005t0004g0005a0001c0005t0004g0006others(3): Show | 6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.2199+1317C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 18/72 | chr7 | 98913530 | ||||||
| chr7:98913547
|
C | G | 128 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(125): Show | 129 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.2199+1334C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 18/72 | chr7 | 98913547 | ||||||
| chr7:98913568
|
G | C | 128 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(125): Show | 129 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.2199+1355G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 18/72 | chr7 | 98913568 | ||||||
| chr7:98913577
|
T | C | 5 | a0001c0002t0002g0016a0001c0002t0002g0017a0001c0002t0002g0172others(2): Show | 5 | HG01243.hp1 HG01884.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2199+1364T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 18/72 | chr7 | 98913577 | ||||||
| chr7:98913865
|
T | C | 2 | a0001c0001t0001g0122a0001c0001t0001g0145 | 2 | HG01496.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.2199+1652T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 18/72 | chr7 | 98913865 | ||||||
| chr7:98913971
|
G | C | 183 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(180): Show | 185 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.2200-1752G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 18/72 | chr7 | 98913971 | ||||||
| chr7:98914173
|
T | C | 6 | a0001c0005t0004g0004a0001c0005t0004g0005a0001c0005t0004g0006others(3): Show | 6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.2200-1550T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 18/72 | chr7 | 98914173 | ||||||
| chr7:98914242
|
A | T | 61 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(58): Show | 61 | HG00408.hp2 HG00423.hp1 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.2200-1481A>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 18/72 | chr7 | 98914242 | ||||||
| chr7:98914302
|
AAG | A | 2 | a0002c0008t0008g0192a0002c0008t0008g0193 | 2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.2200-1414_2200-141 others(6): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 18/72 | INFO_REALIGN_3_PRIME | chr7 | 98914302 | |||||
| chr7:98914375
|
T | G | 1 | a0001c0001t0002g0154 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2200-1348T>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 18/72 | chr7 | 98914375 | ||||||
| chr7:98914462
|
A | G | 3 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0003g0139 | 3 | HG00438.hp1 HG00544.hp2 HG02027.hp1 |
intron_variant | MODIFIER | c.2200-1261A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 18/72 | chr7 | 98914462 | ||||||
| chr7:98914519
|
A | G | 6 | a0001c0005t0004g0004a0001c0005t0004g0005a0001c0005t0004g0006others(3): Show | 6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.2200-1204A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 18/72 | chr7 | 98914519 | ||||||
| chr7:98914559
|
T | G | 1 | a0001c0019t0001g0127 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.2200-1164T>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 18/72 | chr7 | 98914559 | ||||||
| chr7:98914718
|
C | CA | 110 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(107): Show | 112 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.2200-976dupA | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 18/72 | INFO_REALIGN_3_PRIME | chr7 | 98914718 | |||||
| chr7:98914718
|
C | CAA | 29 | a0001c0001t0001g0018a0001c0001t0001g0028a0001c0001t0001g0035others(26): Show | 29 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(26): Show |
intron_variant | MODIFIER | c.2200-977_2200-976d others(4): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 18/72 | INFO_REALIGN_3_PRIME | chr7 | 98914718 | |||||
| chr7:98914718
|
CA | C | 8 | a0001c0001t0002g0154a0001c0001t0002g0195a0001c0001t0002g0196others(5): Show | 8 | HG00140.hp2 HG01243.hp2 HG01346.hp1 others(5): Show |
intron_variant | MODIFIER | c.2200-976delA | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 18/72 | INFO_REALIGN_3_PRIME | chr7 | 98914718 | |||||
| chr7:98914718
|
CAAAA | C | 27 | a0001c0001t0002g0080a0001c0002t0002g0016a0001c0002t0002g0017others(24): Show | 28 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.2200-979_2200-976d others(6): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 18/72 | INFO_REALIGN_3_PRIME | chr7 | 98914718 | |||||
| chr7:98914718
|
CAAAAA | C | 11 | a0001c0001t0005g0158a0001c0001t0005g0160a0001c0001t0005g0161others(8): Show | 11 | HG02055.hp1 HG02258.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.2200-980_2200-976d others(7): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 18/72 | INFO_REALIGN_3_PRIME | chr7 | 98914718 | |||||
| chr7:98914718
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0022t0001g0056 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2200-987_2200-976d others(14): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 18/72 | INFO_REALIGN_3_PRIME | chr7 | 98914718 | |||||
| chr7:98914718
|
CAAAAAAA others(10): Show |
C | 1 | a0001c0038t0001g0086 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2200-992_2200-976d others(19): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 18/72 | INFO_REALIGN_3_PRIME | chr7 | 98914718 | |||||
| chr7:98914744
|
A | C | 1 | a0001c0002t0010g0179 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2200-979A>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 18/72 | chr7 | 98914744 | ||||||
| chr7:98914756
|
A | G | 2 | a0002c0008t0008g0192a0002c0008t0008g0193 | 2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.2200-967A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 18/72 | chr7 | 98914756 | ||||||
| chr7:98915111
|
G | A | 2 | a0002c0008t0008g0192a0002c0008t0008g0193 | 2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.2200-612G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 18/72 | chr7 | 98915111 | ||||||
| chr7:98915623
|
G | T | 2 | a0002c0008t0008g0192a0002c0008t0008g0193 | 2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.2200-100G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 18/72 | chr7 | 98915623 | ||||||
| chr7:98915660
|
G | A | 3 | a0001c0002t0007g0155a0001c0002t0007g0156a0001c0002t0007g0157 | 3 | HG00140.hp2 HG01243.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.2200-63G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 18/72 | chr7 | 98915660 | ||||||
| chr7:98915677
|
C | T | 134 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(131): Show | 135 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.2200-46C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 18/72 | chr7 | 98915677 | ||||||
| chr7:98915712
|
C | G | 7 | a0001c0002t0002g0187a0001c0004t0002g0002a0001c0004t0002g0169others(4): Show | 8 | HG01081.hp1 HG02257.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.2200-11C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 18/72 | chr7 | 98915712 | ||||||
| chr7:98916137
|
T | C | 2 | a0002c0008t0008g0192a0002c0008t0008g0193 | 2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.2365+249T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 19/72 | chr7 | 98916137 | ||||||
| chr7:98916164
|
A | G | 2 | a0001c0001t0001g0239a0001c0001t0001g0241 | 2 | HG02015.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.2365+276A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 19/72 | chr7 | 98916164 | ||||||
| chr7:98916388
|
G | A | 1 | a0001c0001t0002g0231 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2365+500G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 19/72 | chr7 | 98916388 | ||||||
| chr7:98916419
|
T | C | 3 | a0001c0001t0002g0208a0001c0001t0011g0209a0001c0028t0002g0207 | 3 | HG02486.hp1 HG02723.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2365+531T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 19/72 | chr7 | 98916419 | ||||||
| chr7:98916635
|
C | T | 1 | a0001c0001t0001g0109 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.2365+747C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 19/72 | chr7 | 98916635 | ||||||
| chr7:98916662
|
C | T | 1 | a0001c0001t0001g0132 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2366-761C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 19/72 | chr7 | 98916662 | ||||||
| chr7:98916737
|
G | A | 1 | a0001c0002t0002g0163 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2366-686G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 19/72 | chr7 | 98916737 | ||||||
| chr7:98916811
|
G | T | 2 | a0001c0001t0001g0001a0001c0001t0001g0126 | 3 | HG00280.hp2 HG00642.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.2366-612G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 19/72 | chr7 | 98916811 | ||||||
| chr7:98916831
|
C | T | 6 | a0001c0002t0002g0016a0001c0002t0002g0017a0001c0002t0002g0172others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.2366-592C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 19/72 | chr7 | 98916831 | ||||||
| chr7:98916872
|
C | T | 1 | a0001c0002t0002g0182 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2366-551C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 19/72 | chr7 | 98916872 | ||||||
| chr7:98917123
|
A | G | 1 | a0001c0028t0002g0207 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2366-300A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 19/72 | chr7 | 98917123 | ||||||
| chr7:98917410
|
C | T | 14 | a0001c0001t0001g0058a0001c0001t0001g0060a0001c0001t0001g0061others(11): Show | 14 | HG00738.hp1 HG01192.hp1 HG01261.hp2 others(11): Show |
intron_variant | MODIFIER | c.2366-13C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 19/72 | chr7 | 98917410 | ||||||
| chr7:98917846
|
G | T | 7 | a0001c0002t0002g0163a0001c0002t0002g0177a0001c0002t0002g0178others(4): Show | 7 | HG01257.hp2 HG01891.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.2622+167G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 20/72 | chr7 | 98917846 | ||||||
| chr7:98917877
|
T | G | 12 | a0001c0001t0002g0080a0001c0001t0005g0158a0001c0001t0005g0160others(9): Show | 12 | HG01884.hp2 HG02055.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.2622+198T>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 20/72 | chr7 | 98917877 | ||||||
| chr7:98918120
|
C | CA | 44 | a0001c0001t0001g0105a0001c0001t0001g0143a0001c0001t0002g0080others(41): Show | 45 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(42): Show |
intron_variant | MODIFIER | c.2622+455dupA | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 20/72 | INFO_REALIGN_3_PRIME | chr7 | 98918120 | |||||
| chr7:98918214
|
C | T | 6 | a0001c0005t0004g0004a0001c0005t0004g0005a0001c0005t0004g0006others(3): Show | 6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.2622+535C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 20/72 | chr7 | 98918214 | ||||||
| chr7:98918227
|
C | CT | 29 | a0001c0001t0002g0080a0001c0001t0002g0220a0001c0001t0002g0221others(26): Show | 29 | HG00438.hp1 HG00438.hp2 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.2622+569dupT | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 20/72 | INFO_REALIGN_3_PRIME | chr7 | 98918227 | |||||
| chr7:98918227
|
C | CTT | 9 | a0001c0001t0001g0241a0001c0001t0005g0160a0001c0001t0005g0161others(6): Show | 9 | HG02258.hp1 HG02630.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.2622+568_2622+569d others(4): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 20/72 | INFO_REALIGN_3_PRIME | chr7 | 98918227 | |||||
| chr7:98918227
|
CT | C | 131 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(128): Show | 132 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.2622+569delT | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 20/72 | INFO_REALIGN_3_PRIME | chr7 | 98918227 | |||||
| chr7:98918292
|
G | A | 127 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(124): Show | 128 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.2622+613G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 20/72 | chr7 | 98918292 | ||||||
| chr7:98918317
|
G | A | 1 | a0014c0041t0001g0055 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2622+638G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 20/72 | chr7 | 98918317 | ||||||
| chr7:98918375
|
C | T | 1 | a0001c0006t0002g0092 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2622+696C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 20/72 | chr7 | 98918375 | ||||||
| chr7:98918451
|
A | G | 2 | a0002c0008t0008g0192a0002c0008t0008g0193 | 2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.2622+772A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 20/72 | chr7 | 98918451 | ||||||
| chr7:98918509
|
C | T | 3 | a0001c0002t0007g0155a0001c0002t0007g0156a0001c0002t0007g0157 | 3 | HG00140.hp2 HG01243.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.2622+830C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 20/72 | chr7 | 98918509 | ||||||
| chr7:98918624
|
A | G | 1 | a0001c0001t0001g0191 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.2622+945A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 20/72 | chr7 | 98918624 | ||||||
| chr7:98918660
|
C | G | 2 | a0001c0001t0001g0102a0001c0045t0001g0101 | 2 | HG03710.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.2622+981C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 20/72 | chr7 | 98918660 | ||||||
| chr7:98918710
|
A | G | 2 | a0002c0008t0008g0192a0002c0008t0008g0193 | 2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.2622+1031A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 20/72 | chr7 | 98918710 | ||||||
| chr7:98918747
|
A | G | 4 | a0001c0001t0002g0154a0001c0002t0007g0155a0001c0002t0007g0156others(1): Show | 4 | HG00140.hp2 HG01243.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.2622+1068A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 20/72 | chr7 | 98918747 | ||||||
| chr7:98918905
|
A | C | 1 | a0001c0002t0002g0163 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2622+1226A>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 20/72 | chr7 | 98918905 | ||||||
| chr7:98918984
|
C | CA | 6 | a0001c0001t0001g0120a0001c0001t0001g0149a0001c0001t0001g0153others(3): Show | 6 | HG02027.hp1 HG02630.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.2622+1321dupA | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 20/72 | INFO_REALIGN_3_PRIME | chr7 | 98918984 | |||||
| chr7:98918984
|
CA | C | 7 | a0001c0001t0001g0045a0001c0001t0002g0080a0001c0001t0002g0208others(4): Show | 7 | HG01884.hp2 HG02300.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.2622+1321delA | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 20/72 | INFO_REALIGN_3_PRIME | chr7 | 98918984 | |||||
| chr7:98918996
|
A | G | 6 | a0001c0005t0004g0004a0001c0005t0004g0005a0001c0005t0004g0006others(3): Show | 6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.2622+1317A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 20/72 | chr7 | 98918996 | ||||||
| chr7:98919019
|
T | C | 5 | a0001c0002t0007g0155a0001c0002t0007g0156a0001c0002t0007g0157others(2): Show | 5 | HG00140.hp2 HG01243.hp2 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.2622+1340T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 20/72 | chr7 | 98919019 | ||||||
| chr7:98919178
|
G | A | 1 | a0001c0004t0002g0176 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2622+1499G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 20/72 | chr7 | 98919178 | ||||||
| chr7:98919494
|
C | T | 1 | a0001c0010t0001g0096 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2622+1815C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 20/72 | chr7 | 98919494 | ||||||
| chr7:98919517
|
C | T | 2 | a0001c0001t0002g0196a0001c0001t0002g0197 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2622+1838C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 20/72 | chr7 | 98919517 | ||||||
| chr7:98919529
|
G | A | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2622+1850G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 20/72 | chr7 | 98919529 | ||||||
| chr7:98919578
|
A | G | 43 | a0001c0001t0002g0080a0001c0001t0005g0158a0001c0001t0005g0160others(40): Show | 44 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(41): Show |
intron_variant | MODIFIER | c.2622+1899A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 20/72 | chr7 | 98919578 | ||||||
| chr7:98920066
|
G | A | 6 | a0001c0002t0002g0177a0001c0002t0002g0178a0001c0002t0002g0180others(3): Show | 6 | HG01257.hp2 HG01891.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.2623-1687G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 20/72 | chr7 | 98920066 | ||||||
| chr7:98920425
|
G | T | 1 | a0001c0001t0002g0154 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2623-1328G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 20/72 | chr7 | 98920425 | ||||||
| chr7:98920607
|
C | T | 4 | a0001c0001t0005g0158a0001c0001t0005g0160a0001c0001t0005g0161others(1): Show | 4 | HG02258.hp1 HG02486.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.2623-1146C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 20/72 | chr7 | 98920607 | ||||||
| chr7:98920760
|
A | T | 1 | a0001c0038t0001g0086 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2623-993A>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 20/72 | chr7 | 98920760 | ||||||
| chr7:98920901
|
G | A | 44 | a0001c0001t0001g0141a0001c0001t0002g0080a0001c0001t0005g0158others(41): Show | 45 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(42): Show |
intron_variant | MODIFIER | c.2623-852G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 20/72 | chr7 | 98920901 | ||||||
| chr7:98921032
|
A | G | 1 | a0001c0018t0002g0245 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2623-721A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 20/72 | chr7 | 98921032 | ||||||
| chr7:98921065
|
G | A | 6 | a0001c0005t0004g0004a0001c0005t0004g0005a0001c0005t0004g0006others(3): Show | 6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.2623-688G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 20/72 | chr7 | 98921065 | ||||||
| chr7:98921086
|
C | T | 2 | a0001c0001t0001g0090a0001c0001t0001g0147 | 2 | HG02109.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2623-667C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 20/72 | chr7 | 98921086 | ||||||
| chr7:98921090
|
G | A | 3 | a0001c0002t0007g0155a0001c0002t0007g0156a0001c0002t0007g0157 | 3 | HG00140.hp2 HG01243.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.2623-663G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 20/72 | chr7 | 98921090 | ||||||
| chr7:98921144
|
C | T | 4 | a0001c0004t0002g0002a0001c0004t0002g0169a0001c0004t0002g0170others(1): Show | 5 | HG02257.hp1 HG02965.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2623-609C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 20/72 | chr7 | 98921144 | ||||||
| chr7:98921328
|
G | A | 5 | a0001c0002t0007g0155a0001c0002t0007g0156a0001c0002t0007g0157others(2): Show | 5 | HG00140.hp2 HG01243.hp2 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.2623-425G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 20/72 | chr7 | 98921328 | ||||||
| chr7:98921396
|
A | G | 7 | a0001c0002t0002g0163a0001c0002t0002g0177a0001c0002t0002g0178others(4): Show | 7 | HG01257.hp2 HG01891.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.2623-357A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 20/72 | chr7 | 98921396 | ||||||
| chr7:98921526
|
C | T | 2 | a0001c0001t0001g0049a0001c0001t0001g0052 | 2 | NA19054.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.2623-227C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 20/72 | chr7 | 98921526 | ||||||
| chr7:98921607
|
G | T | 16 | a0001c0001t0001g0239a0001c0001t0001g0241a0001c0001t0001g0257others(13): Show | 16 | HG00558.hp1 HG02015.hp2 HG02040.hp2 others(13): Show |
intron_variant | MODIFIER | c.2623-146G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 20/72 | chr7 | 98921607 | ||||||
| chr7:98922354
|
T | C | 1 | a0001c0009t0002g0210 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2823+401T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 21/72 | chr7 | 98922354 | ||||||
| chr7:98922436
|
C | T | 1 | a0001c0002t0007g0155 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2823+483C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 21/72 | chr7 | 98922436 | ||||||
| chr7:98922437
|
G | A | 3 | a0001c0001t0002g0195a0001c0001t0002g0196a0001c0001t0002g0197 | 3 | HG02258.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2823+484G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 21/72 | chr7 | 98922437 | ||||||
| chr7:98922460
|
T | C | 6 | a0001c0005t0004g0004a0001c0005t0004g0005a0001c0005t0004g0006others(3): Show | 6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.2823+507T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 21/72 | chr7 | 98922460 | ||||||
| chr7:98922508
|
G | C | 6 | a0001c0005t0004g0004a0001c0005t0004g0005a0001c0005t0004g0006others(3): Show | 6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.2823+555G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 21/72 | chr7 | 98922508 | ||||||
| chr7:98922573
|
T | C | 2 | a0001c0002t0002g0180a0001c0002t0002g0218 | 2 | HG01257.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.2823+620T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 21/72 | chr7 | 98922573 | ||||||
| chr7:98922660
|
G | T | 1 | a0001c0002t0002g0182 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2823+707G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 21/72 | chr7 | 98922660 | ||||||
| chr7:98922706
|
C | T | 1 | a0001c0022t0001g0056 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2823+753C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 21/72 | chr7 | 98922706 | ||||||
| chr7:98922752
|
T | C | 4 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(1): Show | 4 | HG00621.hp2 HG01993.hp2 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.2823+799T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 21/72 | chr7 | 98922752 | ||||||
| chr7:98922752
|
T | G | 2 | a0001c0001t0001g0117a0001c0001t0001g0118 | 2 | NA18948.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.2823+799T>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 21/72 | chr7 | 98922752 | ||||||
| chr7:98922880
|
T | C | 1 | a0001c0038t0001g0086 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2823+927T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 21/72 | chr7 | 98922880 | ||||||
| chr7:98922888
|
G | A | 1 | a0001c0002t0002g0187 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2823+935G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 21/72 | chr7 | 98922888 | ||||||
| chr7:98922959
|
C | T | 1 | a0001c0025t0001g0151 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.2823+1006C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 21/72 | chr7 | 98922959 | ||||||
| chr7:98922983
|
C | T | 1 | a0001c0001t0001g0069 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.2823+1030C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 21/72 | chr7 | 98922983 | ||||||
| chr7:98923119
|
C | A | 1 | a0001c0001t0001g0152 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2823+1166C>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 21/72 | chr7 | 98923119 | ||||||
| chr7:98923128
|
A | G | 1 | a0001c0001t0002g0234 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2823+1175A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 21/72 | chr7 | 98923128 | ||||||
| chr7:98923605
|
T | G | 6 | a0001c0005t0004g0004a0001c0005t0004g0005a0001c0005t0004g0006others(3): Show | 6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.2824-1507T>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 21/72 | chr7 | 98923605 | ||||||
| chr7:98923612
|
G | A | 1 | a0001c0021t0001g0059 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2824-1500G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 21/72 | chr7 | 98923612 | ||||||
| chr7:98923655
|
G | A | 43 | a0001c0001t0002g0080a0001c0001t0005g0158a0001c0001t0005g0160others(40): Show | 44 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(41): Show |
intron_variant | MODIFIER | c.2824-1457G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 21/72 | chr7 | 98923655 | ||||||
| chr7:98923716
|
C | T | 2 | a0001c0001t0002g0211a0001c0001t0002g0212 | 2 | HG00741.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2824-1396C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 21/72 | chr7 | 98923716 | ||||||
| chr7:98923853
|
A | C | 43 | a0001c0001t0002g0080a0001c0001t0005g0158a0001c0001t0005g0160others(40): Show | 44 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(41): Show |
intron_variant | MODIFIER | c.2824-1259A>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 21/72 | chr7 | 98923853 | ||||||
| chr7:98924040
|
G | C | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2824-1072G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 21/72 | chr7 | 98924040 | ||||||
| chr7:98924329
|
CTATTAAA others(4): Show |
C | 1 | a0001c0019t0001g0127 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.2824-767_2824-757d others(13): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 21/72 | INFO_REALIGN_3_PRIME | chr7 | 98924329 | |||||
| chr7:98924423
|
C | T | 128 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(125): Show | 129 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.2824-689C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 21/72 | chr7 | 98924423 | ||||||
| chr7:98924546
|
G | A | 2 | a0002c0008t0008g0192a0002c0008t0008g0193 | 2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.2824-566G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 21/72 | chr7 | 98924546 | ||||||
| chr7:98924636
|
C | T | 1 | a0001c0001t0001g0132 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2824-476C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 21/72 | chr7 | 98924636 | ||||||
| chr7:98924688
|
C | CA | 136 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0015others(133): Show | 137 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.2824-406dupA | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 21/72 | INFO_REALIGN_3_PRIME | chr7 | 98924688 | |||||
| chr7:98924688
|
CA | C | 31 | a0001c0001t0001g0141a0001c0001t0002g0080a0001c0001t0005g0158others(28): Show | 31 | HG01257.hp2 HG01884.hp2 HG01891.hp1 others(28): Show |
intron_variant | MODIFIER | c.2824-406delA | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 21/72 | INFO_REALIGN_3_PRIME | chr7 | 98924688 | |||||
| chr7:98924688
|
CAA | C | 22 | a0001c0002t0002g0016a0001c0002t0002g0017a0001c0002t0002g0165others(19): Show | 23 | HG01081.hp1 HG01243.hp1 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.2824-407_2824-406d others(4): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 21/72 | INFO_REALIGN_3_PRIME | chr7 | 98924688 | |||||
| chr7:98924726
|
G | T | 2 | a0001c0001t0002g0196a0001c0001t0002g0197 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2824-386G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 21/72 | chr7 | 98924726 | ||||||
| chr7:98924769
|
C | T | 1 | a0001c0001t0001g0132 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2824-343C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 21/72 | chr7 | 98924769 | ||||||
| chr7:98924792
|
A | G | 3 | a0001c0001t0002g0208a0001c0001t0011g0209a0001c0028t0002g0207 | 3 | HG02486.hp1 HG02723.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2824-320A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 21/72 | chr7 | 98924792 | ||||||
| chr7:98924849
|
A | G | 6 | a0001c0005t0004g0004a0001c0005t0004g0005a0001c0005t0004g0006others(3): Show | 6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.2824-263A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 21/72 | chr7 | 98924849 | ||||||
| chr7:98924865
|
G | A | 2 | a0001c0001t0001g0106a0001c0001t0001g0115 | 2 | HG02015.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.2824-247G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 21/72 | chr7 | 98924865 | ||||||
| chr7:98924873
|
G | A | 3 | a0001c0001t0001g0088a0001c0001t0001g0090a0001c0001t0001g0147 | 3 | HG02109.hp1 HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2824-239G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 21/72 | chr7 | 98924873 | ||||||
| chr7:98924877
|
A | G | 3 | a0001c0001t0001g0088a0001c0001t0001g0090a0001c0001t0001g0147 | 3 | HG02109.hp1 HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2824-235A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 21/72 | chr7 | 98924877 | ||||||
| chr7:98924957
|
T | TA | 11 | a0001c0001t0002g0221a0001c0001t0002g0229a0001c0001t0002g0230others(8): Show | 11 | HG01099.hp2 HG01496.hp1 HG01943.hp2 others(8): Show |
intron_variant | MODIFIER | c.2824-154dupA | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 21/72 | INFO_REALIGN_3_PRIME | chr7 | 98924957 | |||||
| chr7:98924969
|
C | T | 1 | a0001c0030t0001g0014 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2824-143C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 21/72 | chr7 | 98924969 | ||||||
| chr7:98924991
|
C | T | 1 | a0001c0038t0001g0086 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2824-121C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 21/72 | chr7 | 98924991 | ||||||
| chr7:98924999
|
C | T | 3 | a0001c0001t0001g0034a0001c0001t0001g0037a0001c0001t0001g0038 | 3 | HG01346.hp2 HG02145.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.2824-113C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 21/72 | chr7 | 98924999 | ||||||
| chr7:98925004
|
CA | C | 5 | a0001c0001t0001g0146a0001c0001t0001g0149a0001c0002t0007g0155others(2): Show | 5 | HG00140.hp2 HG01243.hp2 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.2824-95delA | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 21/72 | INFO_REALIGN_3_PRIME | chr7 | 98925004 | |||||
| chr7:98925270
|
C | T | 38 | a0001c0001t0002g0080a0001c0002t0002g0016a0001c0002t0002g0017others(35): Show | 39 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(36): Show |
splice_region_variant&intron_variant | LOW | c.2975+7C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 22/72 | chr7 | 98925270 | ||||||
| chr7:98925285
|
G | C | 1 | a0001c0005t0004g0006 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2975+22G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 22/72 | chr7 | 98925285 | ||||||
| chr7:98925299
|
A | T | 6 | a0001c0001t0002g0080a0001c0006t0002g0082a0001c0006t0002g0083others(3): Show | 6 | HG01884.hp2 HG02559.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.2975+36A>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 22/72 | chr7 | 98925299 | ||||||
| chr7:98925340
|
T | G | 40 | a0001c0001t0002g0211a0001c0001t0002g0212a0001c0002t0002g0016others(37): Show | 41 | HG00140.hp2 HG00741.hp2 HG01081.hp1 others(38): Show |
intron_variant | MODIFIER | c.2975+77T>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 22/72 | chr7 | 98925340 | ||||||
| chr7:98925428
|
A | G | 1 | a0001c0001t0001g0146 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.2975+165A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 22/72 | chr7 | 98925428 | ||||||
| chr7:98925682
|
C | T | 1 | a0001c0004t0002g0188 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2975+419C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 22/72 | chr7 | 98925682 | ||||||
| chr7:98925750
|
T | C | 129 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(126): Show | 130 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.2975+487T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 22/72 | chr7 | 98925750 | ||||||
| chr7:98925851
|
A | T | 3 | a0001c0002t0007g0155a0001c0002t0007g0156a0001c0002t0007g0157 | 3 | HG00140.hp2 HG01243.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.2975+588A>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 22/72 | chr7 | 98925851 | ||||||
| chr7:98925902
|
A | G | 1 | a0001c0001t0001g0037 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2975+639A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 22/72 | chr7 | 98925902 | ||||||
| chr7:98926134
|
A | G | 1 | a0001c0001t0002g0233 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2975+871A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 22/72 | chr7 | 98926134 | ||||||
| chr7:98926320
|
C | A | 1 | a0001c0001t0001g0102 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2976-847C>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 22/72 | chr7 | 98926320 | ||||||
| chr7:98926371
|
T | C | 1 | a0001c0001t0002g0249 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.2976-796T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 22/72 | chr7 | 98926371 | ||||||
| chr7:98926829
|
A | G | 1 | a0001c0001t0001g0107 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2976-338A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 22/72 | chr7 | 98926829 | ||||||
| chr7:98926888
|
G | A | 2 | a0001c0001t0002g0230a0012c0035t0002g0254 | 2 | NA19009.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.2976-279G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 22/72 | chr7 | 98926888 | ||||||
| chr7:98927127
|
A | G | 7 | a0001c0002t0002g0187a0001c0004t0002g0002a0001c0004t0002g0169others(4): Show | 8 | HG01081.hp1 HG02257.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.2976-40A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 22/72 | chr7 | 98927127 | ||||||
| chr7:98927718
|
T | A | 4 | a0001c0001t0002g0154a0001c0002t0007g0155a0001c0002t0007g0156others(1): Show | 4 | HG00140.hp2 HG01243.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.3175+352T>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 23/72 | chr7 | 98927718 | ||||||
| chr7:98927784
|
C | G | 1 | a0001c0004t0002g0176 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3175+418C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 23/72 | chr7 | 98927784 | ||||||
| chr7:98927791
|
C | G | 1 | a0001c0001t0001g0121 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.3175+425C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 23/72 | chr7 | 98927791 | ||||||
| chr7:98927825
|
C | T | 1 | a0001c0001t0001g0153 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3175+459C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 23/72 | chr7 | 98927825 | ||||||
| chr7:98927908
|
T | G | 147 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(144): Show | 149 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.3175+542T>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 23/72 | chr7 | 98927908 | ||||||
| chr7:98927956
|
T | C | 1 | a0001c0001t0001g0130 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.3175+590T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 23/72 | chr7 | 98927956 | ||||||
| chr7:98927976
|
C | T | 2 | a0001c0001t0001g0035a0001c0024t0001g0040 | 2 | HG00741.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.3175+610C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 23/72 | chr7 | 98927976 | ||||||
| chr7:98928153
|
G | A | 1 | a0001c0021t0001g0059 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.3175+787G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 23/72 | chr7 | 98928153 | ||||||
| chr7:98928231
|
C | T | 1 | a0001c0001t0001g0051 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.3175+865C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 23/72 | chr7 | 98928231 | ||||||
| chr7:98928579
|
C | T | 13 | a0001c0002t0002g0016a0001c0002t0002g0017a0001c0002t0002g0165others(10): Show | 13 | HG01243.hp1 HG01884.hp1 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.3175+1213C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 23/72 | chr7 | 98928579 | ||||||
| chr7:98928639
|
T | C | 3 | a0001c0001t0001g0105a0001c0001t0001g0112a0001c0001t0001g0114 | 3 | NA18960.hp2 NA19010.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.3175+1273T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 23/72 | chr7 | 98928639 | ||||||
| chr7:98928798
|
G | A | 4 | a0001c0001t0002g0154a0001c0002t0007g0155a0001c0002t0007g0156others(1): Show | 4 | HG00140.hp2 HG01243.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.3176-1191G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 23/72 | chr7 | 98928798 | ||||||
| chr7:98928834
|
C | T | 5 | a0001c0002t0002g0165a0001c0002t0002g0166a0001c0002t0002g0181others(2): Show | 5 | HG02809.hp2 HG02896.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.3176-1155C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 23/72 | chr7 | 98928834 | ||||||
| chr7:98928934
|
C | T | 5 | a0001c0001t0006g0213a0001c0001t0006g0214a0001c0001t0006g0215others(2): Show | 5 | HG00280.hp1 HG00642.hp1 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.3176-1055C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 23/72 | chr7 | 98928934 | ||||||
| chr7:98928940
|
A | AT | 7 | a0001c0001t0001g0116a0001c0001t0005g0161a0001c0006t0002g0082others(4): Show | 7 | HG02258.hp1 HG02559.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.3176-1034dupT | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 23/72 | INFO_REALIGN_3_PRIME | chr7 | 98928940 | |||||
| chr7:98928940
|
AT | A | 9 | a0001c0001t0002g0208a0001c0001t0011g0209a0001c0002t0002g0187others(6): Show | 10 | HG01081.hp1 HG02257.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.3176-1034delT | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 23/72 | INFO_REALIGN_3_PRIME | chr7 | 98928940 | |||||
| chr7:98928991
|
G | A | 1 | a0001c0001t0001g0150 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.3176-998G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 23/72 | chr7 | 98928991 | ||||||
| chr7:98929051
|
C | T | 1 | a0001c0002t0002g0163 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3176-938C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 23/72 | chr7 | 98929051 | ||||||
| chr7:98929101
|
G | A | 44 | a0001c0001t0002g0080a0001c0001t0005g0158a0001c0001t0005g0160others(41): Show | 45 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(42): Show |
intron_variant | MODIFIER | c.3176-888G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 23/72 | chr7 | 98929101 | ||||||
| chr7:98929198
|
C | T | 1 | a0001c0004t0002g0188 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3176-791C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 23/72 | chr7 | 98929198 | ||||||
| chr7:98929226
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.3176-763C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 23/72 | chr7 | 98929226 | ||||||
| chr7:98929392
|
A | G | 1 | a0001c0001t0002g0154 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3176-597A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 23/72 | chr7 | 98929392 | ||||||
| chr7:98929738
|
C | T | 1 | a0001c0003t0002g0199 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3176-251C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 23/72 | chr7 | 98929738 | ||||||
| chr7:98929870
|
G | A | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3176-119G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 23/72 | chr7 | 98929870 | ||||||
| chr7:98929972
|
C | T | 2 | a0001c0001t0001g0090a0001c0001t0001g0147 | 2 | HG02109.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3176-17C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 23/72 | chr7 | 98929972 | ||||||
| chr7:98929973
|
C | T | 2 | a0001c0001t0001g0090a0001c0001t0001g0147 | 2 | HG02109.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3176-16C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 23/72 | chr7 | 98929973 | ||||||
| chr7:98930294
|
C | G | 1 | a0001c0001t0001g0028 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3393+88C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 24/72 | chr7 | 98930294 | ||||||
| chr7:98930295
|
G | A | 11 | a0001c0001t0002g0080a0001c0001t0005g0158a0001c0001t0005g0160others(8): Show | 11 | HG01884.hp2 HG02055.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.3393+89G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 24/72 | chr7 | 98930295 | ||||||
| chr7:98930473
|
G | A | 1 | a0001c0001t0002g0235 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.3394-160G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 24/72 | chr7 | 98930473 | ||||||
| chr7:98930519
|
G | C | 1 | a0001c0001t0001g0087 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.3394-114G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 24/72 | chr7 | 98930519 | ||||||
| chr7:98930526
|
C | T | 1 | a0001c0012t0001g0125 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3394-107C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 24/72 | chr7 | 98930526 | ||||||
| chr7:98930578
|
C | CA | 5 | a0001c0001t0001g0095a0001c0001t0001g0135a0001c0001t0001g0140others(2): Show | 5 | HG02572.hp2 HG02965.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.3394-47dupA | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 24/72 | INFO_REALIGN_3_PRIME | chr7 | 98930578 | |||||
| chr7:98930629
|
C | A | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | splice_region_variant&intron_variant | LOW | c.3394-4C>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 24/72 | chr7 | 98930629 | ||||||
| chr7:98931096
|
T | G | 4 | a0001c0001t0002g0154a0001c0002t0007g0155a0001c0002t0007g0156others(1): Show | 4 | HG00140.hp2 HG01243.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.3591+266T>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 25/72 | chr7 | 98931096 | ||||||
| chr7:98931100
|
A | G | 6 | a0001c0002t0002g0165a0001c0002t0002g0166a0001c0002t0002g0167others(3): Show | 6 | HG02809.hp2 HG02896.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.3591+270A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 25/72 | chr7 | 98931100 | ||||||
| chr7:98931342
|
G | A | 1 | a0001c0002t0002g0218 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.3592-63G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 25/72 | chr7 | 98931342 | ||||||
| chr7:98931697
|
T | G | 2 | a0001c0001t0001g0097a0001c0001t0001g0110 | 2 | HG01099.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.3852+32T>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 26/72 | chr7 | 98931697 | ||||||
| chr7:98931703
|
A | G | 7 | a0001c0002t0002g0016a0001c0002t0002g0017a0001c0002t0002g0167others(4): Show | 7 | HG01243.hp1 HG01884.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.3852+38A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 26/72 | chr7 | 98931703 | ||||||
| chr7:98931718
|
T | A | 1 | a0001c0001t0001g0116 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.3852+53T>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 26/72 | chr7 | 98931718 | ||||||
| chr7:98931973
|
A | C | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3852+308A>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 26/72 | chr7 | 98931973 | ||||||
| chr7:98932470
|
A | G | 12 | a0001c0001t0002g0154a0001c0002t0007g0155a0001c0002t0007g0156others(9): Show | 12 | HG00140.hp2 HG01243.hp2 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.3853-771A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 26/72 | chr7 | 98932470 | ||||||
| chr7:98932538
|
C | G | 13 | a0001c0001t0001g0058a0001c0001t0001g0060a0001c0001t0001g0062others(10): Show | 13 | HG00738.hp1 HG01192.hp1 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.3853-703C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 26/72 | chr7 | 98932538 | ||||||
| chr7:98932608
|
T | C | 1 | a0001c0002t0002g0182 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3853-633T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 26/72 | chr7 | 98932608 | ||||||
| chr7:98932664
|
G | A | 199 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(196): Show | 202 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.3853-577G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 26/72 | chr7 | 98932664 | ||||||
| chr7:98933008
|
A | AT | 151 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(148): Show | 153 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.3853-219dupT | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 26/72 | INFO_REALIGN_3_PRIME | chr7 | 98933008 | |||||
| chr7:98933008
|
A | ATT | 8 | a0001c0001t0002g0154a0001c0002t0002g0016a0001c0002t0002g0017others(5): Show | 8 | HG01243.hp1 HG01884.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.3853-220_3853-219d others(4): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 26/72 | INFO_REALIGN_3_PRIME | chr7 | 98933008 | |||||
| chr7:98933091
|
G | A | 1 | a0001c0001t0001g0121 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.3853-150G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 26/72 | chr7 | 98933091 | ||||||
| chr7:98933118
|
C | T | 1 | a0001c0001t0002g0248 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.3853-123C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 26/72 | chr7 | 98933118 | ||||||
| chr7:98933197
|
C | G | 2 | a0002c0008t0008g0192a0002c0008t0008g0193 | 2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.3853-44C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 26/72 | chr7 | 98933197 | ||||||
| chr7:98933469
|
C | T | 3 | a0001c0001t0002g0195a0001c0001t0002g0196a0001c0001t0002g0197 | 3 | HG02258.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.4014+67C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 27/72 | chr7 | 98933469 | ||||||
| chr7:98933504
|
C | T | 1 | a0001c0002t0002g0182 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.4014+102C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 27/72 | chr7 | 98933504 | ||||||
| chr7:98933505
|
G | A | 1 | a0001c0006t0002g0084 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.4014+103G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 27/72 | chr7 | 98933505 | ||||||
| chr7:98933799
|
ACAT | A | 10 | a0001c0003t0002g0003a0001c0003t0002g0198a0001c0003t0002g0199others(7): Show | 11 | HG01081.hp2 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.4014+400_4014+402d others(5): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 27/72 | INFO_REALIGN_3_PRIME | chr7 | 98933799 | |||||
| chr7:98933999
|
C | T | 10 | a0001c0003t0002g0003a0001c0003t0002g0198a0001c0003t0002g0199others(7): Show | 11 | HG01081.hp2 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.4014+597C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 27/72 | chr7 | 98933999 | ||||||
| chr7:98934017
|
A | G | 1 | a0001c0025t0001g0151 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.4014+615A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 27/72 | chr7 | 98934017 | ||||||
| chr7:98934260
|
C | T | 122 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(119): Show | 123 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.4014+858C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 27/72 | chr7 | 98934260 | ||||||
| chr7:98934261
|
G | T | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4014+859G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 27/72 | chr7 | 98934261 | ||||||
| chr7:98934551
|
A | G | 8 | a0001c0005t0004g0004a0001c0005t0004g0005a0001c0005t0004g0006others(5): Show | 8 | HG02559.hp2 HG02622.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.4015-1028A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 27/72 | chr7 | 98934551 | ||||||
| chr7:98934964
|
A | C | 3 | a0001c0001t0002g0208a0001c0001t0011g0209a0001c0028t0002g0207 | 3 | HG02486.hp1 HG02723.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.4015-615A>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 27/72 | chr7 | 98934964 | ||||||
| chr7:98934980
|
A | G | 1 | a0001c0004t0002g0188 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.4015-599A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 27/72 | chr7 | 98934980 | ||||||
| chr7:98935018
|
G | A | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4015-561G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 27/72 | chr7 | 98935018 | ||||||
| chr7:98935056
|
C | T | 6 | a0001c0005t0004g0004a0001c0005t0004g0005a0001c0005t0004g0006others(3): Show | 6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.4015-523C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 27/72 | chr7 | 98935056 | ||||||
| chr7:98935166
|
T | C | 5 | a0001c0001t0002g0154a0001c0002t0007g0156a0001c0002t0007g0157others(2): Show | 5 | HG00140.hp2 HG01243.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.4015-413T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 27/72 | chr7 | 98935166 | ||||||
| chr7:98935238
|
C | G | 258 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(255): Show | 261 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.4015-341C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 27/72 | chr7 | 98935238 | ||||||
| chr7:98935500
|
T | C | 2 | a0001c0001t0002g0211a0001c0001t0002g0212 | 2 | HG00741.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.4015-79T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 27/72 | chr7 | 98935500 | ||||||
| chr7:98935564
|
T | G | 1 | a0001c0024t0001g0040 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.4015-15T>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 27/72 | chr7 | 98935564 | ||||||
| chr7:98936494
|
A | G | 11 | a0001c0001t0002g0080a0001c0001t0005g0158a0001c0001t0005g0160others(8): Show | 11 | HG01884.hp2 HG02055.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.4112-662A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 28/72 | chr7 | 98936494 | ||||||
| chr7:98936606
|
C | T | 10 | a0001c0003t0002g0003a0001c0003t0002g0198a0001c0003t0002g0199others(7): Show | 11 | HG01081.hp2 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.4112-550C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 28/72 | chr7 | 98936606 | ||||||
| chr7:98936730
|
G | T | 127 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(124): Show | 128 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.4112-426G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 28/72 | chr7 | 98936730 | ||||||
| chr7:98936790
|
G | C | 11 | a0001c0001t0002g0080a0001c0001t0005g0158a0001c0001t0005g0160others(8): Show | 11 | HG01884.hp2 HG02055.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.4112-366G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 28/72 | chr7 | 98936790 | ||||||
| chr7:98936850
|
T | C | 1 | a0001c0001t0002g0236 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.4112-306T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 28/72 | chr7 | 98936850 | ||||||
| chr7:98937034
|
C | T | 3 | a0001c0001t0006g0213a0001c0001t0006g0214a0001c0001t0006g0215 | 3 | HG00280.hp1 HG01106.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.4112-122C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 28/72 | chr7 | 98937034 | ||||||
| chr7:98937297
|
T | A | 43 | a0001c0001t0002g0080a0001c0001t0005g0158a0001c0001t0005g0160others(40): Show | 44 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(41): Show |
intron_variant | MODIFIER | c.4233+20T>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 29/72 | chr7 | 98937297 | ||||||
| chr7:98937323
|
CAT | C | 12 | a0001c0001t0001g0098a0001c0001t0002g0222a0001c0001t0002g0223others(9): Show | 12 | HG01257.hp2 HG01891.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.4233+47_4233+48del others(2): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 29/72 | chr7 | 98937323 | ||||||
| chr7:98937841
|
C | T | 3 | a0001c0001t0002g0208a0001c0001t0011g0209a0001c0028t0002g0207 | 3 | HG02486.hp1 HG02723.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.4404+21C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 30/72 | chr7 | 98937841 | ||||||
| chr7:98937972
|
C | T | 1 | a0001c0031t0002g0255 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.4404+152C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 30/72 | chr7 | 98937972 | ||||||
| chr7:98938333
|
T | C | 4 | a0001c0001t0002g0154a0001c0002t0007g0155a0001c0002t0007g0156others(1): Show | 4 | HG00140.hp2 HG01243.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.4404+513T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 30/72 | chr7 | 98938333 | ||||||
| chr7:98938428
|
C | G | 1 | a0001c0001t0001g0071 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.4404+608C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 30/72 | chr7 | 98938428 | ||||||
| chr7:98938476
|
C | A | 43 | a0001c0001t0002g0080a0001c0001t0005g0158a0001c0001t0005g0160others(40): Show | 44 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(41): Show |
intron_variant | MODIFIER | c.4404+656C>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 30/72 | chr7 | 98938476 | ||||||
| chr7:98938510
|
A | G | 137 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(134): Show | 138 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.4404+690A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 30/72 | chr7 | 98938510 | ||||||
| chr7:98938558
|
A | AAT | 137 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(134): Show | 138 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.4404+748_4404+749d others(4): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 30/72 | INFO_REALIGN_3_PRIME | chr7 | 98938558 | |||||
| chr7:98938578
|
T | C | 1 | a0001c0001t0002g0234 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.4404+758T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 30/72 | chr7 | 98938578 | ||||||
| chr7:98938844
|
T | C | 7 | a0001c0002t0002g0163a0001c0002t0002g0177a0001c0002t0002g0178others(4): Show | 7 | HG01257.hp2 HG01891.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.4404+1024T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 30/72 | chr7 | 98938844 | ||||||
| chr7:98939052
|
C | T | 5 | a0001c0001t0005g0158a0001c0001t0005g0160a0001c0001t0005g0161others(2): Show | 5 | HG02055.hp1 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.4404+1232C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 30/72 | chr7 | 98939052 | ||||||
| chr7:98939059
|
C | G | 1 | a0001c0004t0002g0176 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.4404+1239C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 30/72 | chr7 | 98939059 | ||||||
| chr7:98939093
|
G | A | 2 | a0002c0008t0008g0192a0002c0008t0008g0193 | 2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.4404+1273G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 30/72 | chr7 | 98939093 | ||||||
| chr7:98939321
|
G | A | 61 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(58): Show | 61 | HG00408.hp2 HG00423.hp1 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.4404+1501G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 30/72 | chr7 | 98939321 | ||||||
| chr7:98939474
|
T | C | 1 | a0001c0007t0001g0142 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.4404+1654T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 30/72 | chr7 | 98939474 | ||||||
| chr7:98939537
|
G | T | 1 | a0001c0001t0001g0150 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.4404+1717G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 30/72 | chr7 | 98939537 | ||||||
| chr7:98939609
|
C | G | 11 | a0001c0002t0007g0155a0001c0002t0007g0156a0001c0002t0007g0157others(8): Show | 11 | HG00140.hp2 HG01243.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.4404+1789C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 30/72 | chr7 | 98939609 | ||||||
| chr7:98939693
|
G | A | 1 | a0001c0005t0004g0008 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.4404+1873G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 30/72 | chr7 | 98939693 | ||||||
| chr7:98940250
|
G | A | 1 | a0001c0002t0002g0181 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.4404+2430G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 30/72 | chr7 | 98940250 | ||||||
| chr7:98940279
|
C | T | 1 | a0001c0001t0001g0088 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.4404+2459C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 30/72 | chr7 | 98940279 | ||||||
| chr7:98940379
|
G | A | 43 | a0001c0001t0002g0080a0001c0001t0005g0158a0001c0001t0005g0160others(40): Show | 44 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(41): Show |
intron_variant | MODIFIER | c.4404+2559G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 30/72 | chr7 | 98940379 | ||||||
| chr7:98940422
|
T | C | 6 | a0001c0005t0004g0004a0001c0005t0004g0005a0001c0005t0004g0006others(3): Show | 6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.4405-2527T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 30/72 | chr7 | 98940422 | ||||||
| chr7:98940527
|
A | G | 1 | a0001c0001t0001g0129 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.4405-2422A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 30/72 | chr7 | 98940527 | ||||||
| chr7:98940548
|
C | T | 2 | a0001c0002t0010g0179a0001c0043t0002g0168 | 2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.4405-2401C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 30/72 | chr7 | 98940548 | ||||||
| chr7:98940561
|
C | G | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4405-2388C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 30/72 | chr7 | 98940561 | ||||||
| chr7:98941060
|
C | T | 1 | a0001c0001t0001g0036 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.4405-1889C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 30/72 | chr7 | 98941060 | ||||||
| chr7:98941256
|
A | C | 1 | a0001c0001t0001g0145 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.4405-1693A>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 30/72 | chr7 | 98941256 | ||||||
| chr7:98941337
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.4405-1612G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 30/72 | chr7 | 98941337 | ||||||
| chr7:98941370
|
C | T | 6 | a0001c0001t0002g0080a0001c0006t0002g0082a0001c0006t0002g0083others(3): Show | 6 | HG01884.hp2 HG02559.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.4405-1579C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 30/72 | chr7 | 98941370 | ||||||
| chr7:98941466
|
G | T | 6 | a0001c0001t0002g0080a0001c0006t0002g0082a0001c0006t0002g0083others(3): Show | 6 | HG01884.hp2 HG02559.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.4405-1483G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 30/72 | chr7 | 98941466 | ||||||
| chr7:98941733
|
A | G | 137 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(134): Show | 138 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.4405-1216A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 30/72 | chr7 | 98941733 | ||||||
| chr7:98941847
|
C | CA | 10 | a0001c0003t0002g0003a0001c0003t0002g0198a0001c0003t0002g0199others(7): Show | 11 | HG01081.hp2 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.4405-1099dupA | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 30/72 | INFO_REALIGN_3_PRIME | chr7 | 98941847 | |||||
| chr7:98942243
|
A | G | 6 | a0001c0001t0002g0080a0001c0006t0002g0082a0001c0006t0002g0083others(3): Show | 6 | HG01884.hp2 HG02559.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.4405-706A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 30/72 | chr7 | 98942243 | ||||||
| chr7:98942283
|
C | T | 2 | a0002c0008t0008g0192a0002c0008t0008g0193 | 2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.4405-666C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 30/72 | chr7 | 98942283 | ||||||
| chr7:98942316
|
C | G | 70 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(67): Show | 70 | HG00408.hp2 HG00423.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.4405-633C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 30/72 | chr7 | 98942316 | ||||||
| chr7:98942347
|
C | T | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4405-602C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 30/72 | chr7 | 98942347 | ||||||
| chr7:98942500
|
T | C | 138 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(135): Show | 139 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.4405-449T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 30/72 | chr7 | 98942500 | ||||||
| chr7:98942865
|
T | C | 2 | a0001c0002t0002g0016a0001c0002t0002g0017 | 2 | HG01884.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.4405-84T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 30/72 | chr7 | 98942865 | ||||||
| chr7:98943159
|
T | A | 1 | a0001c0001t0001g0073 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.4473+142T>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 31/72 | chr7 | 98943159 | ||||||
| chr7:98943395
|
C | T | 1 | a0004c0040t0005g0162 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.4473+378C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 31/72 | chr7 | 98943395 | ||||||
| chr7:98943638
|
T | A | 186 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(183): Show | 188 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.4473+621T>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 31/72 | chr7 | 98943638 | ||||||
| chr7:98943753
|
G | A | 3 | a0001c0002t0007g0155a0001c0002t0007g0156a0001c0002t0007g0157 | 3 | HG00140.hp2 HG01243.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.4473+736G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 31/72 | chr7 | 98943753 | ||||||
| chr7:98944051
|
C | T | 1 | a0004c0040t0005g0162 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.4473+1034C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 31/72 | chr7 | 98944051 | ||||||
| chr7:98944052
|
G | A | 3 | a0001c0002t0007g0155a0001c0002t0007g0156a0001c0002t0007g0157 | 3 | HG00140.hp2 HG01243.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.4473+1035G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 31/72 | chr7 | 98944052 | ||||||
| chr7:98944110
|
G | A | 1 | a0001c0004t0002g0185 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4473+1093G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 31/72 | chr7 | 98944110 | ||||||
| chr7:98944146
|
C | T | 1 | a0001c0001t0001g0120 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.4473+1129C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 31/72 | chr7 | 98944146 | ||||||
| chr7:98944171
|
G | A | 1 | a0001c0001t0001g0239 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.4473+1154G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 31/72 | chr7 | 98944171 | ||||||
| chr7:98944281
|
T | TA | 9 | a0001c0001t0002g0195a0001c0001t0005g0158a0001c0001t0005g0160others(6): Show | 9 | HG00140.hp2 HG01243.hp2 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.4473+1273dupA | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 31/72 | INFO_REALIGN_3_PRIME | chr7 | 98944281 | |||||
| chr7:98944380
|
T | C | 1 | a0001c0001t0001g0033 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.4473+1363T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 31/72 | chr7 | 98944380 | ||||||
| chr7:98944741
|
C | T | 1 | a0001c0002t0012g0194 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.4474-1006C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 31/72 | chr7 | 98944741 | ||||||
| chr7:98944742
|
G | A | 2 | a0002c0008t0008g0192a0002c0008t0008g0193 | 2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.4474-1005G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 31/72 | chr7 | 98944742 | ||||||
| chr7:98944993
|
T | C | 44 | a0001c0001t0002g0080a0001c0001t0002g0195a0001c0001t0005g0158others(41): Show | 45 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(42): Show |
intron_variant | MODIFIER | c.4474-754T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 31/72 | chr7 | 98944993 | ||||||
| chr7:98945029
|
T | G | 1 | a0001c0002t0002g0182 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.4474-718T>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 31/72 | chr7 | 98945029 | ||||||
| chr7:98945085
|
G | A | 3 | a0001c0002t0007g0155a0001c0002t0007g0156a0001c0002t0007g0157 | 3 | HG00140.hp2 HG01243.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.4474-662G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 31/72 | chr7 | 98945085 | ||||||
| chr7:98945227
|
C | G | 1 | a0001c0002t0012g0194 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.4474-520C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 31/72 | chr7 | 98945227 | ||||||
| chr7:98945243
|
C | A | 1 | a0001c0004t0002g0176 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.4474-504C>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 31/72 | chr7 | 98945243 | ||||||
| chr7:98945264
|
A | G | 33 | a0001c0001t0002g0195a0001c0002t0002g0016a0001c0002t0002g0017others(30): Show | 34 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(31): Show |
intron_variant | MODIFIER | c.4474-483A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 31/72 | chr7 | 98945264 | ||||||
| chr7:98945485
|
A | C | 38 | a0001c0001t0002g0195a0001c0001t0005g0158a0001c0001t0005g0160others(35): Show | 39 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(36): Show |
intron_variant | MODIFIER | c.4474-262A>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 31/72 | chr7 | 98945485 | ||||||
| chr7:98945629
|
T | G | 1 | a0001c0001t0001g0027 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.4474-118T>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 31/72 | chr7 | 98945629 | ||||||
| chr7:98945989
|
C | T | 5 | a0001c0002t0007g0155a0001c0002t0007g0156a0001c0002t0007g0157others(2): Show | 5 | HG00140.hp2 HG01243.hp2 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.4548+39C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 33/72 | chr7 | 98945989 | ||||||
| chr7:98946279
|
TCA | T | 125 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(122): Show | 126 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.4548+334_4548+335d others(4): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 33/72 | INFO_REALIGN_3_PRIME | chr7 | 98946279 | |||||
| chr7:98946301
|
G | C | 1 | a0001c0001t0001g0018 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.4548+351G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 33/72 | chr7 | 98946301 | ||||||
| chr7:98946323
|
T | C | 9 | a0001c0004t0002g0002a0001c0004t0002g0169a0001c0004t0002g0170others(6): Show | 10 | HG02257.hp1 HG02622.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.4548+373T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 33/72 | chr7 | 98946323 | ||||||
| chr7:98946408
|
G | A | 1 | a0001c0045t0001g0101 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.4548+458G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 33/72 | chr7 | 98946408 | ||||||
| chr7:98946441
|
A | ATGCACTC others(27): Show |
1 | a0001c0001t0001g0128 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.4548+502_4548+535d others(36): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 33/72 | INFO_REALIGN_3_PRIME | chr7 | 98946441 | |||||
| chr7:98946452
|
A | G | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4548+502A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 33/72 | chr7 | 98946452 | ||||||
| chr7:98946481
|
T | TCACACCA others(10): Show |
2 | a0001c0001t0001g0108a0001c0001t0001g0113 | 2 | HG00544.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.4548+556_4548+572d others(19): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 33/72 | INFO_REALIGN_3_PRIME | chr7 | 98946481 | |||||
| chr7:98946583
|
C | CCACATAT others(8): Show |
3 | a0001c0002t0007g0155a0001c0002t0007g0156a0001c0002t0007g0157 | 3 | HG00140.hp2 HG01243.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.4548+648_4548+662d others(17): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 33/72 | INFO_REALIGN_3_PRIME | chr7 | 98946583 | |||||
| chr7:98946654
|
A | G | 1 | a0001c0003t0002g0205 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.4548+704A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 33/72 | chr7 | 98946654 | ||||||
| chr7:98946705
|
T | G | 32 | a0001c0002t0002g0016a0001c0002t0002g0017a0001c0002t0002g0163others(29): Show | 33 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(30): Show |
intron_variant | MODIFIER | c.4548+755T>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 33/72 | chr7 | 98946705 | ||||||
| chr7:98946719
|
T | G | 137 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(134): Show | 138 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.4548+769T>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 33/72 | chr7 | 98946719 | ||||||
| chr7:98946751
|
T | C | 1 | a0001c0001t0001g0091 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.4548+801T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 33/72 | chr7 | 98946751 | ||||||
| chr7:98946925
|
G | C | 3 | a0001c0002t0007g0155a0001c0002t0007g0156a0001c0002t0007g0157 | 3 | HG00140.hp2 HG01243.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.4548+975G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 33/72 | chr7 | 98946925 | ||||||
| chr7:98947113
|
G | A | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4549-1108G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 33/72 | chr7 | 98947113 | ||||||
| chr7:98947160
|
T | C | 2 | a0002c0008t0008g0192a0002c0008t0008g0193 | 2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.4549-1061T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 33/72 | chr7 | 98947160 | ||||||
| chr7:98947276
|
C | G | 2 | a0002c0008t0008g0192a0002c0008t0008g0193 | 2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.4549-945C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 33/72 | chr7 | 98947276 | ||||||
| chr7:98947480
|
G | A | 135 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(132): Show | 136 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.4549-741G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 33/72 | chr7 | 98947480 | ||||||
| chr7:98947519
|
G | A | 1 | a0001c0004t0002g0170 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.4549-702G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 33/72 | chr7 | 98947519 | ||||||
| chr7:98947558
|
C | G | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4549-663C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 33/72 | chr7 | 98947558 | ||||||
| chr7:98947581
|
G | A | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4549-640G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 33/72 | chr7 | 98947581 | ||||||
| chr7:98947671
|
G | A | 1 | a0001c0012t0001g0125 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.4549-550G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 33/72 | chr7 | 98947671 | ||||||
| chr7:98947931
|
T | A | 1 | a0001c0001t0001g0108 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.4549-290T>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 33/72 | chr7 | 98947931 | ||||||
| chr7:98948394
|
G | A | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4668+54G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 34/72 | chr7 | 98948394 | ||||||
| chr7:98948532
|
G | A | 5 | a0001c0002t0007g0155a0001c0002t0007g0156a0001c0002t0007g0157others(2): Show | 5 | HG00140.hp2 HG01243.hp2 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.4669-34G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 34/72 | chr7 | 98948532 | ||||||
| chr7:98948730
|
T | G | 32 | a0001c0002t0002g0016a0001c0002t0002g0017a0001c0002t0002g0163others(29): Show | 33 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(30): Show |
intron_variant | MODIFIER | c.4788+45T>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 35/72 | chr7 | 98948730 | ||||||
| chr7:98948806
|
T | C | 1 | a0001c0001t0001g0150 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.4788+121T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 35/72 | chr7 | 98948806 | ||||||
| chr7:98948853
|
T | G | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4788+168T>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 35/72 | chr7 | 98948853 | ||||||
| chr7:98948990
|
C | T | 1 | a0001c0001t0001g0143 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.4788+305C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 35/72 | chr7 | 98948990 | ||||||
| chr7:98948991
|
G | A | 1 | a0001c0001t0001g0136 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.4788+306G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 35/72 | chr7 | 98948991 | ||||||
| chr7:98949011
|
T | C | 1 | a0001c0001t0001g0120 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.4788+326T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 35/72 | chr7 | 98949011 | ||||||
| chr7:98949095
|
C | T | 5 | a0001c0001t0006g0213a0001c0001t0006g0214a0001c0001t0006g0215others(2): Show | 5 | HG00280.hp1 HG00642.hp1 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.4789-322C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 35/72 | chr7 | 98949095 | ||||||
| chr7:98949276
|
G | C | 33 | a0001c0001t0002g0195a0001c0002t0002g0016a0001c0002t0002g0017others(30): Show | 34 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(31): Show |
intron_variant | MODIFIER | c.4789-141G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 35/72 | chr7 | 98949276 | ||||||
| chr7:98949657
|
C | T | 1 | a0001c0002t0002g0163 | 1 | HG02257.hp2 | splice_region_variant&intron_variant | LOW | c.4954-3C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 36/72 | chr7 | 98949657 | ||||||
| chr7:98949927
|
G | A | 1 | a0001c0001t0003g0025 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.5135+86G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 37/72 | chr7 | 98949927 | ||||||
| chr7:98950356
|
T | C | 3 | a0001c0001t0001g0041a0002c0008t0008g0192a0002c0008t0008g0193 | 3 | HG00408.hp2 HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.5334+94T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 38/72 | chr7 | 98950356 | ||||||
| chr7:98950531
|
A | G | 1 | a0001c0001t0001g0129 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.5334+269A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 38/72 | chr7 | 98950531 | ||||||
| chr7:98951059
|
C | CTG | 15 | a0001c0001t0001g0124a0001c0001t0002g0208a0001c0001t0002g0219others(12): Show | 15 | HG02055.hp2 HG02083.hp1 HG02148.hp1 others(12): Show |
intron_variant | MODIFIER | c.5463+89_5463+90dup others(2): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 39/72 | INFO_REALIGN_3_PRIME | chr7 | 98951059 | |||||
| chr7:98951059
|
C | CTGTG | 24 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0113others(21): Show | 25 | HG00140.hp2 HG00544.hp1 HG00558.hp2 others(22): Show |
intron_variant | MODIFIER | c.5463+87_5463+90dup others(4): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 39/72 | INFO_REALIGN_3_PRIME | chr7 | 98951059 | |||||
| chr7:98951059
|
C | CTGTGTG | 69 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0037others(66): Show | 70 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.5463+85_5463+90dup others(6): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 39/72 | INFO_REALIGN_3_PRIME | chr7 | 98951059 | |||||
| chr7:98951059
|
C | CTGTGTGT others(1): Show |
18 | a0001c0001t0001g0018a0001c0001t0001g0030a0001c0001t0001g0033others(15): Show | 18 | HG00423.hp1 HG00423.hp2 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.5463+83_5463+90dup others(8): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 39/72 | INFO_REALIGN_3_PRIME | chr7 | 98951059 | |||||
| chr7:98951059
|
C | CTGTGTGT others(3): Show |
24 | a0001c0001t0001g0013a0001c0001t0001g0027a0001c0001t0001g0029others(21): Show | 24 | HG00408.hp2 HG01167.hp2 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.5463+81_5463+90dup others(10): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 39/72 | INFO_REALIGN_3_PRIME | chr7 | 98951059 | |||||
| chr7:98951059
|
C | CTGTGTGT others(5): Show |
5 | a0001c0001t0001g0044a0001c0001t0001g0050a0001c0001t0005g0161others(2): Show | 5 | HG02129.hp2 HG02258.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.5463+79_5463+90dup others(12): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 39/72 | INFO_REALIGN_3_PRIME | chr7 | 98951059 | |||||
| chr7:98951059
|
C | CTGTGTGT others(7): Show |
6 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0001g0039others(3): Show | 6 | HG02055.hp1 HG03704.hp2 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.5463+77_5463+90dup others(14): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 39/72 | INFO_REALIGN_3_PRIME | chr7 | 98951059 | |||||
| chr7:98951059
|
C | CTGTGTGT others(9): Show |
1 | a0001c0001t0001g0052 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.5463+75_5463+90dup others(16): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 39/72 | INFO_REALIGN_3_PRIME | chr7 | 98951059 | |||||
| chr7:98951059
|
C | CTGTGTGT others(11): Show |
1 | a0001c0001t0001g0049 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.5463+73_5463+90dup others(18): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 39/72 | INFO_REALIGN_3_PRIME | chr7 | 98951059 | |||||
| chr7:98951059
|
CTG | C | 32 | a0001c0001t0002g0252a0001c0001t0003g0019a0001c0001t0006g0213others(29): Show | 32 | HG00280.hp1 HG00642.hp1 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.5463+89_5463+90del others(2): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 39/72 | INFO_REALIGN_3_PRIME | chr7 | 98951059 | |||||
| chr7:98951180
|
C | T | 3 | a0001c0002t0007g0155a0001c0002t0007g0156a0001c0002t0007g0157 | 3 | HG00140.hp2 HG01243.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.5463+176C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 39/72 | chr7 | 98951180 | ||||||
| chr7:98951219
|
C | G | 129 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(126): Show | 130 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.5463+215C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 39/72 | chr7 | 98951219 | ||||||
| chr7:98951319
|
G | A | 1 | a0001c0002t0007g0157 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.5463+315G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 39/72 | chr7 | 98951319 | ||||||
| chr7:98951562
|
T | C | 192 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(189): Show | 194 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.5463+558T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 39/72 | chr7 | 98951562 | ||||||
| chr7:98951593
|
G | A | 13 | a0001c0001t0001g0058a0001c0001t0001g0060a0001c0001t0001g0062others(10): Show | 13 | HG00738.hp1 HG01192.hp1 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.5463+589G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 39/72 | chr7 | 98951593 | ||||||
| chr7:98951622
|
G | A | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.5463+618G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 39/72 | chr7 | 98951622 | ||||||
| chr7:98951647
|
G | A | 5 | a0001c0006t0002g0082a0001c0006t0002g0083a0001c0006t0002g0084others(2): Show | 5 | HG02559.hp1 HG02647.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.5463+643G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 39/72 | chr7 | 98951647 | ||||||
| chr7:98951965
|
C | T | 2 | a0001c0001t0001g0039a0001c0001t0001g0043 | 2 | NA18960.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.5463+961C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 39/72 | chr7 | 98951965 | ||||||
| chr7:98952312
|
C | A | 198 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(195): Show | 201 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.5464-855C>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 39/72 | chr7 | 98952312 | ||||||
| chr7:98952386
|
A | G | 1 | a0001c0002t0002g0182 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.5464-781A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 39/72 | chr7 | 98952386 | ||||||
| chr7:98952567
|
C | T | 3 | a0001c0001t0002g0208a0001c0001t0011g0209a0001c0028t0002g0207 | 3 | HG02486.hp1 HG02723.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.5464-600C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 39/72 | chr7 | 98952567 | ||||||
| chr7:98952698
|
C | T | 1 | a0001c0001t0002g0154 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.5464-469C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 39/72 | chr7 | 98952698 | ||||||
| chr7:98952753
|
G | C | 2 | a0001c0001t0002g0196a0001c0001t0002g0197 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.5464-414G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 39/72 | chr7 | 98952753 | ||||||
| chr7:98952780
|
C | T | 6 | a0001c0005t0004g0004a0001c0005t0004g0005a0001c0005t0004g0006others(3): Show | 6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.5464-387C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 39/72 | chr7 | 98952780 | ||||||
| chr7:98952822
|
C | A | 126 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(123): Show | 127 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.5464-345C>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 39/72 | chr7 | 98952822 | ||||||
| chr7:98952824
|
T | C | 1 | a0001c0001t0001g0134 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.5464-343T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 39/72 | chr7 | 98952824 | ||||||
| chr7:98953031
|
T | TTG | 6 | a0001c0001t0001g0241a0001c0001t0001g0257a0001c0002t0002g0180others(3): Show | 6 | HG01891.hp1 HG02129.hp1 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.5464-88_5464-87dup others(2): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 39/72 | INFO_REALIGN_3_PRIME | chr7 | 98953031 | |||||
| chr7:98953031
|
T | TTGTG | 3 | a0001c0001t0002g0233a0001c0002t0002g0177a0013c0016t0001g0232 | 3 | HG00408.hp1 HG02040.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.5464-90_5464-87dup others(4): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 39/72 | INFO_REALIGN_3_PRIME | chr7 | 98953031 | |||||
| chr7:98953031
|
T | TTGTGTG | 2 | a0001c0001t0002g0220a0001c0001t0002g0234 | 2 | HG00438.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.5464-92_5464-87dup others(6): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 39/72 | INFO_REALIGN_3_PRIME | chr7 | 98953031 | |||||
| chr7:98953031
|
TTG | T | 11 | a0001c0001t0002g0248a0001c0002t0002g0172a0001c0002t0002g0189others(8): Show | 11 | HG01243.hp1 HG01257.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.5464-88_5464-87del others(2): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 39/72 | INFO_REALIGN_3_PRIME | chr7 | 98953031 | |||||
| chr7:98953031
|
TTGTG | T | 10 | a0001c0001t0002g0250a0001c0001t0006g0213a0001c0001t0006g0215others(7): Show | 10 | HG00140.hp2 HG00642.hp1 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.5464-90_5464-87del others(4): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 39/72 | INFO_REALIGN_3_PRIME | chr7 | 98953031 | |||||
| chr7:98953031
|
TTGTGTG | T | 28 | a0001c0001t0002g0195a0001c0001t0002g0208a0001c0001t0005g0160others(25): Show | 29 | HG00280.hp1 HG01081.hp1 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.5464-92_5464-87del others(6): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 39/72 | INFO_REALIGN_3_PRIME | chr7 | 98953031 | |||||
| chr7:98953031
|
TTGTGTGT others(1): Show |
T | 3 | a0001c0001t0001g0239a0001c0001t0002g0154a0001c0004t0002g0176 | 3 | HG02015.hp2 HG02647.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.5464-94_5464-87del others(8): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 39/72 | INFO_REALIGN_3_PRIME | chr7 | 98953031 | |||||
| chr7:98953031
|
TTGTGTGT others(3): Show |
T | 2 | a0001c0001t0002g0010a0001c0001t0002g0011 | 2 | HG00544.hp2 HG02027.hp1 |
intron_variant | MODIFIER | c.5464-96_5464-87del others(10): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 39/72 | INFO_REALIGN_3_PRIME | chr7 | 98953031 | |||||
| chr7:98953031
|
TTGTGTGT others(5): Show |
T | 4 | a0001c0001t0002g0196a0001c0001t0002g0197a0001c0011t0013g0190others(1): Show | 4 | HG02809.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.5464-98_5464-87del others(12): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 39/72 | INFO_REALIGN_3_PRIME | chr7 | 98953031 | |||||
| chr7:98953031
|
TTGTGTGT others(7): Show |
T | 1 | a0001c0001t0003g0139 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.5464-100_5464-87de others(15): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 39/72 | INFO_REALIGN_3_PRIME | chr7 | 98953031 | |||||
| chr7:98953031
|
TTGTGTGT others(9): Show |
T | 1 | a0011c0032t0005g0159 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.5464-102_5464-87de others(17): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 39/72 | INFO_REALIGN_3_PRIME | chr7 | 98953031 | |||||
| chr7:98953031
|
TTGTGTGT others(11): Show |
T | 1 | a0001c0001t0005g0158 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.5464-104_5464-87de others(19): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 39/72 | INFO_REALIGN_3_PRIME | chr7 | 98953031 | |||||
| chr7:98953031
|
TTGTGTGT others(13): Show |
T | 6 | a0001c0001t0002g0080a0001c0006t0002g0082a0001c0006t0002g0083others(3): Show | 6 | HG01884.hp2 HG02559.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.5464-106_5464-87de others(21): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 39/72 | INFO_REALIGN_3_PRIME | chr7 | 98953031 | |||||
| chr7:98953031
|
TTGTGTGT others(23): Show |
T | 1 | a0001c0001t0001g0047 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.5464-116_5464-87de others(31): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 39/72 | INFO_REALIGN_3_PRIME | chr7 | 98953031 | |||||
| chr7:98953031
|
TTGTGTGT others(25): Show |
T | 125 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(122): Show | 126 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.5464-118_5464-87de others(33): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 39/72 | INFO_REALIGN_3_PRIME | chr7 | 98953031 | |||||
| chr7:98953075
|
GTGTGTT | G | 9 | a0001c0003t0002g0003a0001c0003t0002g0198a0001c0003t0002g0200others(6): Show | 10 | HG01081.hp2 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.5464-90_5464-85del others(6): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 39/72 | INFO_REALIGN_3_PRIME | chr7 | 98953075 | |||||
| chr7:98953463
|
C | T | 1 | a0001c0002t0007g0157 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.5730+30C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 40/72 | chr7 | 98953463 | ||||||
| chr7:98953529
|
C | T | 127 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(124): Show | 128 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.5730+96C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 40/72 | chr7 | 98953529 | ||||||
| chr7:98953691
|
G | C | 1 | a0001c0001t0001g0144 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.5730+258G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 40/72 | chr7 | 98953691 | ||||||
| chr7:98953709
|
C | T | 2 | a0001c0001t0002g0222a0001c0001t0002g0223 | 2 | NA18966.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.5730+276C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 40/72 | chr7 | 98953709 | ||||||
| chr7:98953752
|
G | A | 3 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0077 | 3 | HG01358.hp1 HG01943.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.5730+319G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 40/72 | chr7 | 98953752 | ||||||
| chr7:98953769
|
G | A | 1 | a0001c0001t0002g0154 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.5730+336G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 40/72 | chr7 | 98953769 | ||||||
| chr7:98953898
|
C | G | 1 | a0001c0001t0001g0099 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.5730+465C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 40/72 | chr7 | 98953898 | ||||||
| chr7:98953918
|
G | A | 1 | a0001c0002t0002g0163 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.5730+485G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 40/72 | chr7 | 98953918 | ||||||
| chr7:98954158
|
C | CT | 6 | a0001c0005t0004g0004a0001c0005t0004g0005a0001c0005t0004g0006others(3): Show | 6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.5730+726dupT | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 40/72 | INFO_REALIGN_3_PRIME | chr7 | 98954158 | |||||
| chr7:98954249
|
G | T | 1 | a0001c0010t0001g0096 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.5730+816G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 40/72 | chr7 | 98954249 | ||||||
| chr7:98954344
|
C | T | 126 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(123): Show | 127 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.5731-754C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 40/72 | chr7 | 98954344 | ||||||
| chr7:98954429
|
G | A | 1 | a0001c0045t0001g0101 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.5731-669G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 40/72 | chr7 | 98954429 | ||||||
| chr7:98954444
|
C | T | 1 | a0001c0002t0002g0182 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.5731-654C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 40/72 | chr7 | 98954444 | ||||||
| chr7:98954453
|
A | G | 1 | a0001c0001t0001g0077 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.5731-645A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 40/72 | chr7 | 98954453 | ||||||
| chr7:98954803
|
C | T | 1 | a0001c0002t0002g0182 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.5731-295C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 40/72 | chr7 | 98954803 | ||||||
| chr7:98954852
|
C | T | 1 | a0001c0004t0002g0176 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.5731-246C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 40/72 | chr7 | 98954852 | ||||||
| chr7:98954949
|
G | A | 2 | a0001c0001t0001g0036a0001c0001t0001g0076 | 2 | HG03704.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.5731-149G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 40/72 | chr7 | 98954949 | ||||||
| chr7:98954967
|
A | G | 1 | a0001c0002t0002g0182 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.5731-131A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 40/72 | chr7 | 98954967 | ||||||
| chr7:98955087
|
C | T | 1 | a0001c0001t0001g0037 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.5731-11C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 40/72 | chr7 | 98955087 | ||||||
| chr7:98955335
|
G | A | 11 | a0001c0001t0002g0228a0001c0001t0002g0235a0001c0001t0002g0236others(8): Show | 11 | HG00558.hp1 HG02129.hp1 NA18942.hp2 others(8): Show |
intron_variant | MODIFIER | c.5937+31G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 41/72 | chr7 | 98955335 | ||||||
| chr7:98955738
|
G | C | 1 | a0001c0001t0005g0161 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.5938-408G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 41/72 | chr7 | 98955738 | ||||||
| chr7:98955841
|
T | G | 2 | a0002c0008t0008g0192a0002c0008t0008g0193 | 2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.5938-305T>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 41/72 | chr7 | 98955841 | ||||||
| chr7:98956079
|
G | A | 5 | a0001c0002t0002g0016a0001c0002t0002g0017a0001c0002t0002g0172others(2): Show | 5 | HG01243.hp1 HG01884.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.5938-67G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 41/72 | chr7 | 98956079 | ||||||
| chr7:98956087
|
G | T | 1 | a0001c0001t0001g0030 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.5938-59G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 41/72 | chr7 | 98956087 | ||||||
| chr7:98956116
|
T | TC | 194 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(191): Show | 196 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.5938-28dupC | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 41/72 | INFO_REALIGN_3_PRIME | chr7 | 98956116 | |||||
| chr7:98956122
|
G | C | 1 | a0001c0001t0001g0047 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.5938-24G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 41/72 | chr7 | 98956122 | ||||||
| chr7:98956337
|
G | A | 7 | a0001c0001t0001g0108a0001c0005t0004g0004a0001c0005t0004g0005others(4): Show | 7 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.6096+33G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 42/72 | chr7 | 98956337 | ||||||
| chr7:98956587
|
G | A | 1 | a0001c0002t0010g0179 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.6231+54G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 43/72 | chr7 | 98956587 | ||||||
| chr7:98956614
|
C | G | 1 | a0001c0001t0001g0057 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.6231+81C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 43/72 | chr7 | 98956614 | ||||||
| chr7:98956636
|
G | A | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.6231+103G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 43/72 | chr7 | 98956636 | ||||||
| chr7:98956698
|
A | G | 1 | a0001c0001t0001g0070 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.6231+165A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 43/72 | chr7 | 98956698 | ||||||
| chr7:98956767
|
A | G | 1 | a0001c0001t0001g0133 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.6231+234A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 43/72 | chr7 | 98956767 | ||||||
| chr7:98956769
|
G | A | 1 | a0001c0002t0002g0182 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.6231+236G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 43/72 | chr7 | 98956769 | ||||||
| chr7:98956961
|
G | C | 6 | a0001c0005t0004g0004a0001c0005t0004g0005a0001c0005t0004g0006others(3): Show | 6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.6231+428G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 43/72 | chr7 | 98956961 | ||||||
| chr7:98956987
|
C | T | 2 | a0002c0008t0008g0192a0002c0008t0008g0193 | 2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.6231+454C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 43/72 | chr7 | 98956987 | ||||||
| chr7:98957004
|
T | C | 6 | a0001c0001t0002g0080a0001c0006t0002g0082a0001c0006t0002g0083others(3): Show | 6 | HG01884.hp2 HG02559.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.6231+471T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 43/72 | chr7 | 98957004 | ||||||
| chr7:98957040
|
T | C | 1 | a0001c0001t0001g0015 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.6231+507T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 43/72 | chr7 | 98957040 | ||||||
| chr7:98957075
|
C | T | 3 | a0001c0002t0007g0155a0001c0002t0007g0156a0001c0002t0007g0157 | 3 | HG00140.hp2 HG01243.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.6231+542C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 43/72 | chr7 | 98957075 | ||||||
| chr7:98957227
|
G | A | 1 | a0001c0026t0003g0021 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.6231+694G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 43/72 | chr7 | 98957227 | ||||||
| chr7:98957228
|
A | C | 193 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(190): Show | 195 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.6231+695A>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 43/72 | chr7 | 98957228 | ||||||
| chr7:98957320
|
A | G | 5 | a0001c0001t0002g0228a0001c0001t0002g0247a0001c0001t0002g0248others(2): Show | 5 | NA18942.hp2 NA18944.hp2 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.6232-661A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 43/72 | chr7 | 98957320 | ||||||
| chr7:98957357
|
A | G | 1 | a0001c0001t0002g0195 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.6232-624A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 43/72 | chr7 | 98957357 | ||||||
| chr7:98957552
|
C | T | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.6232-429C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 43/72 | chr7 | 98957552 | ||||||
| chr7:98957586
|
C | T | 2 | a0002c0008t0008g0192a0002c0008t0008g0193 | 2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.6232-395C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 43/72 | chr7 | 98957586 | ||||||
| chr7:98957600
|
T | C | 6 | a0001c0005t0004g0004a0001c0005t0004g0005a0001c0005t0004g0006others(3): Show | 6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.6232-381T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 43/72 | chr7 | 98957600 | ||||||
| chr7:98957621
|
C | T | 1 | a0001c0002t0002g0017 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.6232-360C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 43/72 | chr7 | 98957621 | ||||||
| chr7:98957638
|
A | G | 2 | a0002c0008t0008g0192a0002c0008t0008g0193 | 2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.6232-343A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 43/72 | chr7 | 98957638 | ||||||
| chr7:98957699
|
G | A | 11 | a0001c0002t0002g0187a0001c0004t0002g0002a0001c0004t0002g0169others(8): Show | 12 | HG01081.hp1 HG02257.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.6232-282G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 43/72 | chr7 | 98957699 | ||||||
| chr7:98957853
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.6232-128C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 43/72 | chr7 | 98957853 | ||||||
| chr7:98957940
|
G | A | 1 | a0001c0001t0001g0259 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.6232-41G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 43/72 | chr7 | 98957940 | ||||||
| chr7:98958118
|
G | C | 1 | a0001c0001t0002g0154 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.6342+27G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 44/72 | chr7 | 98958118 | ||||||
| chr7:98958309
|
G | GT | 5 | a0001c0001t0002g0236a0001c0001t0002g0237a0001c0001t0002g0238others(2): Show | 5 | HG00558.hp1 HG01169.hp1 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.6342+229dupT | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 44/72 | INFO_REALIGN_3_PRIME | chr7 | 98958309 | |||||
| chr7:98958319
|
T | C | 1 | a0001c0001t0001g0085 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.6342+228T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 44/72 | chr7 | 98958319 | ||||||
| chr7:98958365
|
C | T | 1 | a0001c0001t0001g0098 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.6342+274C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 44/72 | chr7 | 98958365 | ||||||
| chr7:98958472
|
G | A | 3 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0124 | 3 | HG02083.hp1 NA18948.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.6342+381G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 44/72 | chr7 | 98958472 | ||||||
| chr7:98958497
|
A | T | 6 | a0001c0005t0004g0004a0001c0005t0004g0005a0001c0005t0004g0006others(3): Show | 6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.6342+406A>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 44/72 | chr7 | 98958497 | ||||||
| chr7:98958535
|
A | G | 2 | a0002c0008t0008g0192a0002c0008t0008g0193 | 2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.6342+444A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 44/72 | chr7 | 98958535 | ||||||
| chr7:98958670
|
C | T | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.6342+579C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 44/72 | chr7 | 98958670 | ||||||
| chr7:98958671
|
A | G | 203 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(200): Show | 206 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.6342+580A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 44/72 | chr7 | 98958671 | ||||||
| chr7:98958681
|
C | T | 2 | a0001c0001t0002g0196a0001c0001t0002g0197 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.6342+590C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 44/72 | chr7 | 98958681 | ||||||
| chr7:98958711
|
G | A | 126 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(123): Show | 127 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.6342+620G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 44/72 | chr7 | 98958711 | ||||||
| chr7:98958744
|
C | T | 1 | a0001c0012t0001g0125 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.6343-600C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 44/72 | chr7 | 98958744 | ||||||
| chr7:98959273
|
C | T | 1 | a0001c0002t0002g0177 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.6343-71C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 44/72 | chr7 | 98959273 | ||||||
| chr7:98959339
|
C | T | 48 | a0001c0001t0001g0239a0001c0001t0001g0241a0001c0001t0001g0257others(45): Show | 48 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(45): Show |
splice_region_variant&intron_variant | LOW | c.6343-5C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 44/72 | chr7 | 98959339 | ||||||
| chr7:98959733
|
G | C | 11 | a0001c0002t0007g0155a0001c0002t0007g0156a0001c0002t0007g0157others(8): Show | 11 | HG00140.hp2 HG01243.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.6489+243G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 45/72 | chr7 | 98959733 | ||||||
| chr7:98959754
|
A | G | 2 | a0001c0001t0001g0257a0001c0001t0001g0258 | 2 | NA18971.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.6489+264A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 45/72 | chr7 | 98959754 | ||||||
| chr7:98959882
|
A | G | 1 | a0001c0019t0001g0127 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.6489+392A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 45/72 | chr7 | 98959882 | ||||||
| chr7:98959936
|
T | TA | 12 | a0001c0001t0001g0001a0001c0001t0001g0072a0001c0001t0001g0126others(9): Show | 13 | HG00280.hp2 HG00642.hp2 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.6489+464dupA | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 45/72 | INFO_REALIGN_3_PRIME | chr7 | 98959936 | |||||
| chr7:98959936
|
TA | T | 10 | a0001c0001t0001g0046a0001c0001t0001g0069a0001c0001t0001g0074others(7): Show | 10 | HG01943.hp1 HG02109.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.6489+464delA | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 45/72 | INFO_REALIGN_3_PRIME | chr7 | 98959936 | |||||
| chr7:98959937
|
A | G | 26 | a0001c0001t0002g0195a0001c0002t0002g0016a0001c0002t0002g0017others(23): Show | 27 | HG01081.hp1 HG01243.hp1 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.6489+447A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 45/72 | chr7 | 98959937 | ||||||
| chr7:98959943
|
AAAAAAAA others(5): Show |
A | 5 | a0001c0003t0002g0003a0001c0003t0002g0198a0001c0003t0002g0200others(2): Show | 6 | HG01081.hp2 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.6489+459_6489+470d others(14): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 45/72 | INFO_REALIGN_3_PRIME | chr7 | 98959943 | |||||
| chr7:98959954
|
AG | A | 53 | a0001c0001t0001g0239a0001c0001t0001g0241a0001c0001t0001g0257others(50): Show | 53 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.6489+465delG | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 45/72 | chr7 | 98959954 | ||||||
| chr7:98959955
|
G | A | 58 | a0001c0001t0002g0011a0001c0001t0002g0080a0001c0001t0002g0195others(55): Show | 59 | HG00140.hp2 HG00438.hp2 HG01081.hp1 others(56): Show |
intron_variant | MODIFIER | c.6489+465G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 45/72 | chr7 | 98959955 | ||||||
| chr7:98960232
|
T | C | 2 | a0002c0008t0008g0192a0002c0008t0008g0193 | 2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.6489+742T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 45/72 | chr7 | 98960232 | ||||||
| chr7:98960398
|
A | G | 2 | a0001c0001t0001g0128a0001c0001t0001g0130 | 2 | HG00558.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.6490-863A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 45/72 | chr7 | 98960398 | ||||||
| chr7:98960562
|
A | G | 3 | a0001c0002t0002g0165a0001c0002t0002g0166a0001c0002t0002g0167 | 3 | HG02896.hp2 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.6490-699A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 45/72 | chr7 | 98960562 | ||||||
| chr7:98960604
|
G | A | 2 | a0001c0001t0001g0109a0001c0001t0001g0120 | 2 | NA18982.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.6490-657G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 45/72 | chr7 | 98960604 | ||||||
| chr7:98960690
|
C | G | 1 | a0001c0001t0001g0143 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.6490-571C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 45/72 | chr7 | 98960690 | ||||||
| chr7:98960757
|
TTTTG | T | 3 | a0001c0002t0007g0155a0001c0002t0007g0156a0001c0002t0007g0157 | 3 | HG00140.hp2 HG01243.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.6490-502_6490-499d others(6): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 45/72 | INFO_REALIGN_3_PRIME | chr7 | 98960757 | |||||
| chr7:98960759
|
T | TTG | 7 | a0001c0001t0001g0048a0001c0001t0002g0080a0001c0001t0005g0158others(4): Show | 7 | HG01517.hp1 HG01884.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.6490-472_6490-471d others(4): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 45/72 | INFO_REALIGN_3_PRIME | chr7 | 98960759 | |||||
| chr7:98960759
|
T | TTGTG | 5 | a0001c0006t0002g0082a0001c0006t0002g0083a0001c0006t0002g0084others(2): Show | 5 | HG02559.hp1 HG02647.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.6490-474_6490-471d others(6): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 45/72 | INFO_REALIGN_3_PRIME | chr7 | 98960759 | |||||
| chr7:98960759
|
TTG | T | 174 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(171): Show | 176 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.6490-472_6490-471d others(4): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 45/72 | INFO_REALIGN_3_PRIME | chr7 | 98960759 | |||||
| chr7:98960785
|
G | A | 1 | a0001c0001t0001g0143 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.6490-476G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 45/72 | chr7 | 98960785 | ||||||
| chr7:98961059
|
A | T | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.6490-202A>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 45/72 | chr7 | 98961059 | ||||||
| chr7:98961220
|
T | C | 1 | a0001c0001t0001g0112 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.6490-41T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 45/72 | chr7 | 98961220 | ||||||
| chr7:98961257
|
G | C | 204 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(201): Show | 207 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(204): Show |
splice_region_variant&intron_variant | LOW | c.6490-4G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 45/72 | chr7 | 98961257 | ||||||
| chr7:98961516
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.6703+42C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 46/72 | chr7 | 98961516 | ||||||
| chr7:98961535
|
T | C | 4 | a0001c0002t0002g0177a0001c0002t0002g0178a0001c0002t0010g0179others(1): Show | 4 | HG02451.hp1 HG03209.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.6703+61T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 46/72 | chr7 | 98961535 | ||||||
| chr7:98961554
|
C | T | 1 | a0001c0001t0001g0033 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.6703+80C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 46/72 | chr7 | 98961554 | ||||||
| chr7:98961582
|
A | G | 2 | a0001c0001t0002g0208a0001c0001t0011g0209 | 2 | HG02486.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.6703+108A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 46/72 | chr7 | 98961582 | ||||||
| chr7:98961618
|
T | A | 136 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(133): Show | 137 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.6703+144T>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 46/72 | chr7 | 98961618 | ||||||
| chr7:98961655
|
C | T | 1 | a0001c0004t0002g0188 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.6703+181C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 46/72 | chr7 | 98961655 | ||||||
| chr7:98961812
|
G | A | 1 | a0001c0001t0002g0250 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.6703+338G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 46/72 | chr7 | 98961812 | ||||||
| chr7:98961858
|
T | A | 1 | a0001c0001t0001g0070 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.6703+384T>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 46/72 | chr7 | 98961858 | ||||||
| chr7:98961894
|
T | C | 1 | a0001c0001t0001g0134 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.6704-408T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 46/72 | chr7 | 98961894 | ||||||
| chr7:98961957
|
G | A | 1 | a0001c0001t0003g0022 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.6704-345G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 46/72 | chr7 | 98961957 | ||||||
| chr7:98962056
|
A | T | 6 | a0001c0001t0002g0080a0001c0006t0002g0082a0001c0006t0002g0083others(3): Show | 6 | HG01884.hp2 HG02559.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.6704-246A>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 46/72 | chr7 | 98962056 | ||||||
| chr7:98962454
|
G | A | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.6829+27G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 47/72 | chr7 | 98962454 | ||||||
| chr7:98962587
|
G | A | 1 | a0001c0001t0001g0121 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.6829+160G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 47/72 | chr7 | 98962587 | ||||||
| chr7:98962590
|
T | C | 65 | a0001c0001t0001g0239a0001c0001t0001g0241a0001c0001t0001g0257others(62): Show | 65 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.6829+163T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 47/72 | chr7 | 98962590 | ||||||
| chr7:98962604
|
T | C | 132 | a0001c0001t0001g0239a0001c0001t0001g0241a0001c0001t0001g0257others(129): Show | 134 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.6829+177T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 47/72 | chr7 | 98962604 | ||||||
| chr7:98962620
|
C | T | 43 | a0001c0001t0002g0080a0001c0001t0005g0158a0001c0001t0005g0160others(40): Show | 44 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(41): Show |
intron_variant | MODIFIER | c.6829+193C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 47/72 | chr7 | 98962620 | ||||||
| chr7:98962655
|
G | T | 1 | a0001c0002t0012g0194 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.6829+228G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 47/72 | chr7 | 98962655 | ||||||
| chr7:98962723
|
C | T | 10 | a0001c0003t0002g0003a0001c0003t0002g0198a0001c0003t0002g0199others(7): Show | 11 | HG01081.hp2 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.6829+296C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 47/72 | chr7 | 98962723 | ||||||
| chr7:98962811
|
G | A | 2 | a0001c0001t0001g0039a0001c0001t0001g0043 | 2 | NA18960.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.6829+384G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 47/72 | chr7 | 98962811 | ||||||
| chr7:98963008
|
G | A | 122 | a0001c0001t0001g0239a0001c0001t0001g0241a0001c0001t0001g0257others(119): Show | 124 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.6829+581G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 47/72 | chr7 | 98963008 | ||||||
| chr7:98963027
|
C | G | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.6829+600C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 47/72 | chr7 | 98963027 | ||||||
| chr7:98963176
|
G | A | 12 | a0001c0001t0001g0091a0001c0001t0001g0106a0001c0001t0001g0115others(9): Show | 12 | HG00621.hp1 HG02015.hp1 HG02027.hp2 others(9): Show |
intron_variant | MODIFIER | c.6829+749G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 47/72 | chr7 | 98963176 | ||||||
| chr7:98963194
|
A | G | 2 | a0002c0008t0008g0192a0002c0008t0008g0193 | 2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.6829+767A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 47/72 | chr7 | 98963194 | ||||||
| chr7:98963201
|
A | G | 3 | a0001c0002t0007g0155a0001c0002t0007g0156a0001c0002t0007g0157 | 3 | HG00140.hp2 HG01243.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.6829+774A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 47/72 | chr7 | 98963201 | ||||||
| chr7:98963320
|
G | A | 1 | a0001c0001t0001g0111 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.6829+893G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 47/72 | chr7 | 98963320 | ||||||
| chr7:98963363
|
C | A | 1 | a0001c0002t0002g0165 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.6829+936C>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 47/72 | chr7 | 98963363 | ||||||
| chr7:98963373
|
C | T | 2 | a0002c0008t0008g0192a0002c0008t0008g0193 | 2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.6829+946C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 47/72 | chr7 | 98963373 | ||||||
| chr7:98963424
|
G | A | 1 | a0001c0002t0009g0175 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.6829+997G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 47/72 | chr7 | 98963424 | ||||||
| chr7:98963537
|
G | A | 1 | a0001c0001t0002g0080 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.6830-1092G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 47/72 | chr7 | 98963537 | ||||||
| chr7:98963573
|
C | T | 2 | a0001c0001t0002g0196a0001c0001t0002g0197 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.6830-1056C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 47/72 | chr7 | 98963573 | ||||||
| chr7:98963814
|
C | T | 1 | a0001c0001t0002g0154 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.6830-815C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 47/72 | chr7 | 98963814 | ||||||
| chr7:98963865
|
G | A | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.6830-764G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 47/72 | chr7 | 98963865 | ||||||
| chr7:98963908
|
C | T | 2 | a0002c0008t0008g0192a0002c0008t0008g0193 | 2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.6830-721C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 47/72 | chr7 | 98963908 | ||||||
| chr7:98963919
|
A | G | 1 | a0001c0001t0001g0121 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.6830-710A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 47/72 | chr7 | 98963919 | ||||||
| chr7:98963930
|
A | G | 76 | a0001c0001t0001g0239a0001c0001t0001g0241a0001c0001t0001g0257others(73): Show | 77 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.6830-699A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 47/72 | chr7 | 98963930 | ||||||
| chr7:98963941
|
C | T | 6 | a0001c0005t0004g0004a0001c0005t0004g0005a0001c0005t0004g0006others(3): Show | 6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.6830-688C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 47/72 | chr7 | 98963941 | ||||||
| chr7:98964080
|
T | TA | 17 | a0001c0001t0001g0001a0001c0001t0001g0074a0001c0001t0001g0103others(14): Show | 18 | HG00280.hp2 HG00642.hp2 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.6830-530dupA | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 47/72 | INFO_REALIGN_3_PRIME | chr7 | 98964080 | |||||
| chr7:98964080
|
TA | T | 12 | a0001c0001t0001g0013a0001c0001t0001g0046a0001c0001t0001g0047others(9): Show | 12 | HG01943.hp1 HG02451.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.6830-530delA | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 47/72 | INFO_REALIGN_3_PRIME | chr7 | 98964080 | |||||
| chr7:98964792
|
C | T | 2 | a0001c0001t0002g0196a0001c0001t0002g0197 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.6976+17C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 48/72 | chr7 | 98964792 | ||||||
| chr7:98964898
|
G | A | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.6976+123G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 48/72 | chr7 | 98964898 | ||||||
| chr7:98964924
|
T | C | 1 | a0001c0001t0001g0129 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.6976+149T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 48/72 | chr7 | 98964924 | ||||||
| chr7:98964966
|
T | C | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.6976+191T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 48/72 | chr7 | 98964966 | ||||||
| chr7:98964988
|
C | T | 6 | a0001c0005t0004g0004a0001c0005t0004g0005a0001c0005t0004g0006others(3): Show | 6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.6976+213C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 48/72 | chr7 | 98964988 | ||||||
| chr7:98965026
|
G | A | 2 | a0001c0001t0002g0196a0001c0001t0002g0197 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.6976+251G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 48/72 | chr7 | 98965026 | ||||||
| chr7:98965043
|
G | C | 74 | a0001c0001t0001g0239a0001c0001t0001g0241a0001c0001t0001g0257others(71): Show | 75 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.6976+268G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 48/72 | chr7 | 98965043 | ||||||
| chr7:98965132
|
A | G | 6 | a0001c0005t0004g0004a0001c0005t0004g0005a0001c0005t0004g0006others(3): Show | 6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.6976+357A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 48/72 | chr7 | 98965132 | ||||||
| chr7:98965342
|
T | C | 44 | a0001c0001t0002g0080a0001c0001t0002g0195a0001c0001t0005g0158others(41): Show | 45 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(42): Show |
intron_variant | MODIFIER | c.6977-354T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 48/72 | chr7 | 98965342 | ||||||
| chr7:98965442
|
C | G | 131 | a0001c0001t0001g0239a0001c0001t0001g0241a0001c0001t0001g0257others(128): Show | 133 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.6977-254C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 48/72 | chr7 | 98965442 | ||||||
| chr7:98965521
|
T | C | 131 | a0001c0001t0001g0239a0001c0001t0001g0241a0001c0001t0001g0257others(128): Show | 133 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.6977-175T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 48/72 | chr7 | 98965521 | ||||||
| chr7:98966003
|
A | G | 44 | a0001c0001t0002g0080a0001c0001t0002g0195a0001c0001t0005g0158others(41): Show | 45 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(42): Show |
intron_variant | MODIFIER | c.7176+108A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 49/72 | chr7 | 98966003 | ||||||
| chr7:98966025
|
C | T | 2 | a0002c0008t0008g0192a0002c0008t0008g0193 | 2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.7176+130C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 49/72 | chr7 | 98966025 | ||||||
| chr7:98966456
|
A | G | 3 | a0001c0002t0007g0155a0001c0002t0007g0156a0001c0002t0007g0157 | 3 | HG00140.hp2 HG01243.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.7176+561A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 49/72 | chr7 | 98966456 | ||||||
| chr7:98966541
|
C | T | 1 | a0006c0042t0002g0184 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.7177-500C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 49/72 | chr7 | 98966541 | ||||||
| chr7:98966554
|
G | A | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.7177-487G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 49/72 | chr7 | 98966554 | ||||||
| chr7:98966686
|
GA | G | 12 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0003t0002g0003others(9): Show | 13 | HG00544.hp2 HG01081.hp2 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.7177-343delA | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 49/72 | INFO_REALIGN_3_PRIME | chr7 | 98966686 | |||||
| chr7:98966924
|
T | C | 1 | a0001c0001t0002g0195 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.7177-117T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 49/72 | chr7 | 98966924 | ||||||
| chr7:98966974
|
G | C | 1 | a0001c0002t0002g0182 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.7177-67G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 49/72 | chr7 | 98966974 | ||||||
| chr7:98967374
|
G | A | 2 | a0001c0001t0001g0102a0001c0045t0001g0101 | 2 | HG03710.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.7299-111G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 50/72 | chr7 | 98967374 | ||||||
| chr7:98967705
|
A | G | 6 | a0001c0005t0004g0004a0001c0005t0004g0005a0001c0005t0004g0006others(3): Show | 6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.7512+7A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 51/72 | chr7 | 98967705 | ||||||
| chr7:98967820
|
C | A | 2 | a0001c0002t0007g0155a0001c0002t0007g0157 | 2 | HG00140.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.7512+122C>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 51/72 | chr7 | 98967820 | ||||||
| chr7:98967923
|
T | A | 6 | a0001c0005t0004g0004a0001c0005t0004g0005a0001c0005t0004g0006others(3): Show | 6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.7512+225T>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 51/72 | chr7 | 98967923 | ||||||
| chr7:98967980
|
G | A | 66 | a0001c0001t0001g0239a0001c0001t0001g0241a0001c0001t0001g0257others(63): Show | 67 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.7512+282G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 51/72 | chr7 | 98967980 | ||||||
| chr7:98968024
|
CT | C | 67 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0018others(64): Show | 67 | HG00408.hp2 HG00423.hp1 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.7512+338delT | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 51/72 | INFO_REALIGN_3_PRIME | chr7 | 98968024 | |||||
| chr7:98968316
|
G | A | 2 | a0001c0001t0001g0001a0001c0001t0001g0126 | 3 | HG00280.hp2 HG00642.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.7512+618G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 51/72 | chr7 | 98968316 | ||||||
| chr7:98968336
|
A | G | 1 | a0001c0001t0001g0150 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.7512+638A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 51/72 | chr7 | 98968336 | ||||||
| chr7:98968340
|
A | G | 1 | a0001c0010t0001g0096 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.7512+642A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 51/72 | chr7 | 98968340 | ||||||
| chr7:98968951
|
G | C | 1 | a0001c0001t0001g0128 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.7513-1161G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 51/72 | chr7 | 98968951 | ||||||
| chr7:98969006
|
G | A | 32 | a0001c0002t0002g0016a0001c0002t0002g0017a0001c0002t0002g0163others(29): Show | 33 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(30): Show |
intron_variant | MODIFIER | c.7513-1106G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 51/72 | chr7 | 98969006 | ||||||
| chr7:98969126
|
C | T | 1 | a0001c0027t0001g0031 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.7513-986C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 51/72 | chr7 | 98969126 | ||||||
| chr7:98969157
|
G | A | 1 | a0001c0002t0002g0181 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.7513-955G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 51/72 | chr7 | 98969157 | ||||||
| chr7:98969157
|
G | T | 1 | a0001c0001t0001g0015 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.7513-955G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 51/72 | chr7 | 98969157 | ||||||
| chr7:98969578
|
G | A | 52 | a0001c0001t0001g0239a0001c0001t0001g0241a0001c0001t0001g0257others(49): Show | 52 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.7513-534G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 51/72 | chr7 | 98969578 | ||||||
| chr7:98969637
|
C | T | 1 | a0001c0001t0001g0152 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.7513-475C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 51/72 | chr7 | 98969637 | ||||||
| chr7:98969681
|
C | T | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.7513-431C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 51/72 | chr7 | 98969681 | ||||||
| chr7:98969720
|
C | T | 2 | a0002c0008t0008g0192a0002c0008t0008g0193 | 2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.7513-392C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 51/72 | chr7 | 98969720 | ||||||
| chr7:98969732
|
C | T | 3 | a0001c0002t0007g0155a0001c0002t0007g0156a0001c0002t0007g0157 | 3 | HG00140.hp2 HG01243.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.7513-380C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 51/72 | chr7 | 98969732 | ||||||
| chr7:98970391
|
G | C | 6 | a0001c0005t0004g0004a0001c0005t0004g0005a0001c0005t0004g0006others(3): Show | 6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.7692+100G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 52/72 | chr7 | 98970391 | ||||||
| chr7:98970394
|
C | T | 55 | a0001c0001t0001g0239a0001c0001t0001g0241a0001c0001t0001g0257others(52): Show | 55 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.7692+103C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 52/72 | chr7 | 98970394 | ||||||
| chr7:98970597
|
AT | A | 121 | a0001c0001t0001g0029a0001c0001t0001g0239a0001c0001t0001g0241others(118): Show | 123 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.7692+320delT | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 52/72 | INFO_REALIGN_3_PRIME | chr7 | 98970597 | |||||
| chr7:98970635
|
C | T | 1 | a0001c0002t0002g0163 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.7692+344C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 52/72 | chr7 | 98970635 | ||||||
| chr7:98970663
|
C | T | 1 | a0001c0001t0011g0209 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.7692+372C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 52/72 | chr7 | 98970663 | ||||||
| chr7:98970709
|
C | T | 3 | a0001c0002t0007g0155a0001c0002t0007g0156a0001c0002t0007g0157 | 3 | HG00140.hp2 HG01243.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.7692+418C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 52/72 | chr7 | 98970709 | ||||||
| chr7:98970739
|
C | T | 1 | a0001c0001t0001g0143 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.7692+448C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 52/72 | chr7 | 98970739 | ||||||
| chr7:98970774
|
C | T | 1 | a0001c0001t0001g0064 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.7692+483C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 52/72 | chr7 | 98970774 | ||||||
| chr7:98970782
|
C | T | 1 | a0001c0001t0001g0012 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.7692+491C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 52/72 | chr7 | 98970782 | ||||||
| chr7:98970838
|
C | T | 2 | a0001c0001t0002g0208a0001c0001t0011g0209 | 2 | HG02486.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.7692+547C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 52/72 | chr7 | 98970838 | ||||||
| chr7:98970883
|
G | A | 3 | a0001c0002t0007g0155a0001c0002t0007g0156a0001c0002t0007g0157 | 3 | HG00140.hp2 HG01243.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.7692+592G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 52/72 | chr7 | 98970883 | ||||||
| chr7:98970922
|
T | A | 1 | a0001c0001t0001g0149 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.7692+631T>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 52/72 | chr7 | 98970922 | ||||||
| chr7:98971144
|
C | T | 7 | a0001c0002t0002g0163a0001c0002t0002g0177a0001c0002t0002g0178others(4): Show | 7 | HG01257.hp2 HG01891.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.7693-655C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 52/72 | chr7 | 98971144 | ||||||
| chr7:98971210
|
T | G | 6 | a0001c0002t0002g0165a0001c0002t0002g0166a0001c0002t0002g0167others(3): Show | 6 | HG02809.hp2 HG02896.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.7693-589T>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 52/72 | chr7 | 98971210 | ||||||
| chr7:98971412
|
G | A | 2 | a0001c0001t0001g0069a0001c0001t0001g0070 | 2 | NA18982.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.7693-387G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 52/72 | chr7 | 98971412 | ||||||
| chr7:98971435
|
C | T | 1 | a0001c0004t0002g0188 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.7693-364C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 52/72 | chr7 | 98971435 | ||||||
| chr7:98971436
|
G | A | 5 | a0001c0001t0006g0213a0001c0001t0006g0214a0001c0001t0006g0215others(2): Show | 5 | HG00280.hp1 HG00642.hp1 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.7693-363G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 52/72 | chr7 | 98971436 | ||||||
| chr7:98971570
|
A | G | 1 | a0001c0019t0001g0127 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.7693-229A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 52/72 | chr7 | 98971570 | ||||||
| chr7:98971954
|
G | A | 3 | a0001c0001t0002g0221a0001c0001t0002g0231a0001c0001t0002g0243 | 3 | HG01099.hp2 HG01496.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.7839+9G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 53/72 | chr7 | 98971954 | ||||||
| chr7:98972032
|
C | T | 1 | a0001c0001t0001g0048 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.7839+87C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 53/72 | chr7 | 98972032 | ||||||
| chr7:98972333
|
G | A | 5 | a0001c0001t0001g0128a0001c0001t0001g0130a0001c0001t0001g0134others(2): Show | 5 | HG00558.hp2 HG03710.hp1 NA19011.hp1 others(2): Show |
intron_variant | MODIFIER | c.7839+388G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 53/72 | chr7 | 98972333 | ||||||
| chr7:98972432
|
T | C | 1 | a0001c0001t0001g0113 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.7839+487T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 53/72 | chr7 | 98972432 | ||||||
| chr7:98972569
|
G | A | 10 | a0001c0003t0002g0003a0001c0003t0002g0198a0001c0003t0002g0199others(7): Show | 11 | HG01081.hp2 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.7839+624G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 53/72 | chr7 | 98972569 | ||||||
| chr7:98972605
|
G | A | 1 | a0001c0001t0001g0123 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.7839+660G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 53/72 | chr7 | 98972605 | ||||||
| chr7:98972794
|
G | A | 1 | a0001c0001t0001g0133 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.7839+849G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 53/72 | chr7 | 98972794 | ||||||
| chr7:98973042
|
C | G | 1 | a0001c0001t0001g0129 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.7839+1097C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 53/72 | chr7 | 98973042 | ||||||
| chr7:98973260
|
A | C | 82 | a0001c0001t0001g0239a0001c0001t0001g0241a0001c0001t0001g0257others(79): Show | 83 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.7839+1315A>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 53/72 | chr7 | 98973260 | ||||||
| chr7:98973278
|
C | A | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.7839+1333C>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 53/72 | chr7 | 98973278 | ||||||
| chr7:98973388
|
G | C | 121 | a0001c0001t0001g0239a0001c0001t0001g0241a0001c0001t0001g0257others(118): Show | 123 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.7839+1443G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 53/72 | chr7 | 98973388 | ||||||
| chr7:98973701
|
G | A | 122 | a0001c0001t0001g0239a0001c0001t0001g0241a0001c0001t0001g0257others(119): Show | 124 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.7839+1756G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 53/72 | chr7 | 98973701 | ||||||
| chr7:98973965
|
G | A | 3 | a0001c0002t0007g0155a0001c0002t0007g0156a0001c0002t0007g0157 | 3 | HG00140.hp2 HG01243.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.7839+2020G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 53/72 | chr7 | 98973965 | ||||||
| chr7:98974004
|
A | C | 18 | a0001c0001t0001g0058a0001c0001t0001g0060a0001c0001t0001g0061others(15): Show | 18 | HG00738.hp1 HG01192.hp1 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.7839+2059A>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 53/72 | chr7 | 98974004 | ||||||
| chr7:98974092
|
C | T | 2 | a0001c0001t0002g0208a0001c0001t0011g0209 | 2 | HG02486.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.7840-2057C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 53/72 | chr7 | 98974092 | ||||||
| chr7:98974159
|
A | G | 33 | a0001c0001t0002g0195a0001c0002t0002g0016a0001c0002t0002g0017others(30): Show | 34 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(31): Show |
intron_variant | MODIFIER | c.7840-1990A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 53/72 | chr7 | 98974159 | ||||||
| chr7:98974211
|
T | A | 6 | a0001c0005t0004g0004a0001c0005t0004g0005a0001c0005t0004g0006others(3): Show | 6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.7840-1938T>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 53/72 | chr7 | 98974211 | ||||||
| chr7:98974558
|
C | G | 1 | a0001c0001t0001g0044 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.7840-1591C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 53/72 | chr7 | 98974558 | ||||||
| chr7:98974885
|
A | AT | 65 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0027others(62): Show | 66 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.7840-1258dupT | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 53/72 | INFO_REALIGN_3_PRIME | chr7 | 98974885 | |||||
| chr7:98975030
|
A | G | 132 | a0001c0001t0001g0239a0001c0001t0001g0241a0001c0001t0001g0257others(129): Show | 134 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.7840-1119A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 53/72 | chr7 | 98975030 | ||||||
| chr7:98975098
|
G | A | 1 | a0001c0027t0001g0031 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.7840-1051G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 53/72 | chr7 | 98975098 | ||||||
| chr7:98975389
|
G | A | 2 | a0002c0008t0008g0192a0002c0008t0008g0193 | 2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.7840-760G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 53/72 | chr7 | 98975389 | ||||||
| chr7:98975600
|
C | T | 25 | a0001c0002t0002g0016a0001c0002t0002g0017a0001c0002t0002g0165others(22): Show | 26 | HG01081.hp1 HG01243.hp1 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.7840-549C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 53/72 | chr7 | 98975600 | ||||||
| chr7:98975601
|
G | C | 1 | a0001c0002t0002g0182 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.7840-548G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 53/72 | chr7 | 98975601 | ||||||
| chr7:98975672
|
C | T | 67 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0027others(64): Show | 68 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.7840-477C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 53/72 | chr7 | 98975672 | ||||||
| chr7:98975749
|
A | G | 6 | a0001c0001t0001g0097a0001c0001t0001g0107a0001c0001t0001g0110others(3): Show | 6 | HG00140.hp1 HG01099.hp1 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.7840-400A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 53/72 | chr7 | 98975749 | ||||||
| chr7:98975755
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.7840-394G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 53/72 | chr7 | 98975755 | ||||||
| chr7:98975937
|
G | C | 7 | a0001c0005t0004g0004a0001c0005t0004g0005a0001c0005t0004g0006others(4): Show | 7 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.7840-212G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 53/72 | chr7 | 98975937 | ||||||
| chr7:98976008
|
G | T | 11 | a0001c0001t0002g0080a0001c0001t0005g0158a0001c0001t0005g0160others(8): Show | 11 | HG01884.hp2 HG02055.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.7840-141G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 53/72 | chr7 | 98976008 | ||||||
| chr7:98976065
|
C | G | 2 | a0001c0001t0001g0049a0001c0001t0001g0052 | 2 | NA19054.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.7840-84C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 53/72 | chr7 | 98976065 | ||||||
| chr7:98976106
|
C | T | 1 | a0001c0001t0001g0072 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.7840-43C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 53/72 | chr7 | 98976106 | ||||||
| chr7:98976370
|
G | A | 2 | a0002c0008t0008g0192a0002c0008t0008g0193 | 2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.7959+102G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 54/72 | chr7 | 98976370 | ||||||
| chr7:98976374
|
C | T | 1 | a0001c0002t0002g0182 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.7959+106C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 54/72 | chr7 | 98976374 | ||||||
| chr7:98976375
|
G | T | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.7959+107G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 54/72 | chr7 | 98976375 | ||||||
| chr7:98976877
|
T | C | 2 | a0002c0008t0008g0192a0002c0008t0008g0193 | 2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.8248-62T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 55/72 | chr7 | 98976877 | ||||||
| chr7:98976888
|
GA | G | 3 | a0001c0002t0007g0155a0001c0002t0007g0156a0001c0002t0007g0157 | 3 | HG00140.hp2 HG01243.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.8248-44delA | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 55/72 | INFO_REALIGN_3_PRIME | chr7 | 98976888 | |||||
| chr7:98977087
|
G | A | 2 | a0002c0008t0008g0192a0002c0008t0008g0193 | 2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.8385+11G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 56/72 | chr7 | 98977087 | ||||||
| chr7:98977146
|
T | C | 1 | a0001c0001t0002g0154 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.8385+70T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 56/72 | chr7 | 98977146 | ||||||
| chr7:98977185
|
G | A | 1 | a0001c0019t0001g0127 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.8385+109G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 56/72 | chr7 | 98977185 | ||||||
| chr7:98977207
|
C | G | 131 | a0001c0001t0001g0239a0001c0001t0001g0241a0001c0001t0001g0257others(128): Show | 133 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.8385+131C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 56/72 | chr7 | 98977207 | ||||||
| chr7:98977224
|
C | T | 1 | a0001c0001t0003g0139 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.8385+148C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 56/72 | chr7 | 98977224 | ||||||
| chr7:98977243
|
C | A | 2 | a0001c0001t0001g0100a0001c0001t0001g0103 | 2 | NA18957.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.8385+167C>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 56/72 | chr7 | 98977243 | ||||||
| chr7:98977320
|
C | T | 59 | a0001c0001t0001g0239a0001c0001t0001g0241a0001c0001t0001g0257others(56): Show | 59 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.8385+244C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 56/72 | chr7 | 98977320 | ||||||
| chr7:98977434
|
C | T | 3 | a0001c0002t0007g0155a0001c0002t0007g0156a0001c0002t0007g0157 | 3 | HG00140.hp2 HG01243.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.8385+358C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 56/72 | chr7 | 98977434 | ||||||
| chr7:98977504
|
G | A | 2 | a0001c0001t0001g0053a0001c0001t0001g0054 | 2 | HG01167.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.8385+428G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 56/72 | chr7 | 98977504 | ||||||
| chr7:98977623
|
G | A | 4 | a0001c0001t0001g0018a0001c0001t0001g0039a0001c0001t0001g0043others(1): Show | 4 | HG02683.hp1 HG02683.hp2 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.8385+547G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 56/72 | chr7 | 98977623 | ||||||
| chr7:98977691
|
A | C | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.8386-520A>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 56/72 | chr7 | 98977691 | ||||||
| chr7:98977714
|
A | T | 1 | a0001c0001t0001g0114 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.8386-497A>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 56/72 | chr7 | 98977714 | ||||||
| chr7:98977750
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.8386-461C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 56/72 | chr7 | 98977750 | ||||||
| chr7:98977781
|
C | T | 2 | a0001c0001t0001g0034a0001c0001t0001g0038 | 2 | HG01346.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.8386-430C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 56/72 | chr7 | 98977781 | ||||||
| chr7:98977793
|
C | T | 1 | a0001c0006t0002g0092 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.8386-418C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 56/72 | chr7 | 98977793 | ||||||
| chr7:98977860
|
G | C | 1 | a0001c0001t0002g0252 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.8386-351G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 56/72 | chr7 | 98977860 | ||||||
| chr7:98978351
|
G | A | 1 | a0001c0001t0001g0058 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.8498+28G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 57/72 | chr7 | 98978351 | ||||||
| chr7:98978620
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.8499-149G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 57/72 | chr7 | 98978620 | ||||||
| chr7:98978994
|
C | T | 1 | a0001c0001t0001g0099 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.8634+90C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 58/72 | chr7 | 98978994 | ||||||
| chr7:98979121
|
T | C | 6 | a0001c0005t0004g0004a0001c0005t0004g0005a0001c0005t0004g0006others(3): Show | 6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.8634+217T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 58/72 | chr7 | 98979121 | ||||||
| chr7:98979210
|
C | T | 13 | a0001c0002t0002g0016a0001c0002t0002g0017a0001c0002t0002g0165others(10): Show | 13 | HG01243.hp1 HG01884.hp1 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.8634+306C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 58/72 | chr7 | 98979210 | ||||||
| chr7:98979418
|
A | G | 3 | a0001c0004t0002g0183a0001c0004t0002g0185a0006c0042t0002g0184 | 3 | HG02622.hp2 HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.8634+514A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 58/72 | chr7 | 98979418 | ||||||
| chr7:98980356
|
A | G | 2 | a0001c0002t0002g0187a0001c0044t0002g0186 | 2 | HG01081.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.8635-1413A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 58/72 | chr7 | 98980356 | ||||||
| chr7:98980388
|
C | CAA | 130 | a0001c0001t0001g0239a0001c0001t0001g0241a0001c0001t0001g0257others(127): Show | 132 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.8635-1380_8635-137 others(6): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 58/72 | INFO_REALIGN_3_PRIME | chr7 | 98980388 | |||||
| chr7:98980491
|
CA | C | 119 | a0001c0001t0001g0033a0001c0001t0001g0239a0001c0001t0001g0241others(116): Show | 121 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.8635-1268delA | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 58/72 | INFO_REALIGN_3_PRIME | chr7 | 98980491 | |||||
| chr7:98980571
|
A | G | 10 | a0001c0003t0002g0003a0001c0003t0002g0198a0001c0003t0002g0199others(7): Show | 11 | HG01081.hp2 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.8635-1198A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 58/72 | chr7 | 98980571 | ||||||
| chr7:98980574
|
G | A | 2 | a0001c0001t0002g0208a0001c0001t0011g0209 | 2 | HG02486.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.8635-1195G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 58/72 | chr7 | 98980574 | ||||||
| chr7:98980594
|
G | A | 1 | a0001c0001t0002g0011 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.8635-1175G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 58/72 | chr7 | 98980594 | ||||||
| chr7:98980625
|
A | G | 2 | a0001c0001t0005g0158a0011c0032t0005g0159 | 2 | HG02486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.8635-1144A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 58/72 | chr7 | 98980625 | ||||||
| chr7:98981310
|
G | T | 53 | a0001c0001t0002g0080a0001c0001t0005g0158a0001c0001t0005g0160others(50): Show | 54 | HG00140.hp2 HG01081.hp1 HG01243.hp1 others(51): Show |
intron_variant | MODIFIER | c.8635-459G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 58/72 | chr7 | 98981310 | ||||||
| chr7:98981379
|
G | A | 5 | a0001c0001t0006g0213a0001c0001t0006g0214a0001c0001t0006g0215others(2): Show | 5 | HG00280.hp1 HG00642.hp1 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.8635-390G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 58/72 | chr7 | 98981379 | ||||||
| chr7:98981397
|
G | A | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.8635-372G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 58/72 | chr7 | 98981397 | ||||||
| chr7:98981412
|
T | C | 1 | a0001c0004t0002g0188 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.8635-357T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 58/72 | chr7 | 98981412 | ||||||
| chr7:98981416
|
A | G | 1 | a0001c0004t0002g0188 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.8635-353A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 58/72 | chr7 | 98981416 | ||||||
| chr7:98981696
|
T | G | 5 | a0001c0002t0007g0155a0001c0002t0007g0156a0001c0002t0007g0157others(2): Show | 5 | HG00140.hp2 HG01243.hp2 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.8635-73T>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 58/72 | chr7 | 98981696 | ||||||
| chr7:98981740
|
C | T | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.8635-29C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 58/72 | chr7 | 98981740 | ||||||
| chr7:98982147
|
G | A | 3 | a0001c0002t0007g0155a0001c0002t0007g0156a0001c0002t0007g0157 | 3 | HG00140.hp2 HG01243.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.8826+187G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 59/72 | chr7 | 98982147 | ||||||
| chr7:98982296
|
A | G | 11 | a0001c0001t0002g0221a0001c0001t0002g0229a0001c0001t0002g0230others(8): Show | 11 | HG01099.hp2 HG01496.hp1 HG01943.hp2 others(8): Show |
intron_variant | MODIFIER | c.8826+336A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 59/72 | chr7 | 98982296 | ||||||
| chr7:98982496
|
C | G | 3 | a0001c0001t0002g0208a0001c0001t0011g0209a0001c0028t0002g0207 | 3 | HG02486.hp1 HG02723.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.8826+536C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 59/72 | chr7 | 98982496 | ||||||
| chr7:98982529
|
T | C | 67 | a0001c0001t0001g0239a0001c0001t0001g0241a0001c0001t0001g0257others(64): Show | 67 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.8826+569T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 59/72 | chr7 | 98982529 | ||||||
| chr7:98982616
|
A | G | 1 | a0001c0001t0001g0121 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.8827-648A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 59/72 | chr7 | 98982616 | ||||||
| chr7:98982630
|
C | A | 1 | a0001c0001t0001g0041 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.8827-634C>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 59/72 | chr7 | 98982630 | ||||||
| chr7:98982647
|
G | A | 2 | a0001c0002t0002g0180a0001c0002t0002g0218 | 2 | HG01257.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.8827-617G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 59/72 | chr7 | 98982647 | ||||||
| chr7:98982759
|
CA | C | 258 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(255): Show | 261 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.8827-500delA | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 59/72 | INFO_REALIGN_3_PRIME | chr7 | 98982759 | |||||
| chr7:98983038
|
A | G | 123 | a0001c0001t0001g0239a0001c0001t0001g0241a0001c0001t0001g0257others(120): Show | 125 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.8827-226A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 59/72 | chr7 | 98983038 | ||||||
| chr7:98983144
|
C | A | 1 | a0001c0001t0001g0241 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.8827-120C>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 59/72 | chr7 | 98983144 | ||||||
| chr7:98983189
|
A | G | 5 | a0001c0001t0006g0213a0001c0001t0006g0214a0001c0001t0006g0215others(2): Show | 5 | HG00280.hp1 HG00642.hp1 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.8827-75A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 59/72 | chr7 | 98983189 | ||||||
| chr7:98983234
|
C | T | 1 | a0001c0001t0001g0141 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.8827-30C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 59/72 | chr7 | 98983234 | ||||||
| chr7:98983555
|
G | T | 1 | a0001c0001t0001g0150 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.9022+96G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 60/72 | chr7 | 98983555 | ||||||
| chr7:98983564
|
T | C | 1 | a0001c0002t0002g0163 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.9022+105T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 60/72 | chr7 | 98983564 | ||||||
| chr7:98983570
|
A | C | 1 | a0001c0001t0002g0154 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.9022+111A>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 60/72 | chr7 | 98983570 | ||||||
| chr7:98983572
|
G | T | 52 | a0001c0001t0001g0239a0001c0001t0001g0241a0001c0001t0001g0257others(49): Show | 52 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.9022+113G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 60/72 | chr7 | 98983572 | ||||||
| chr7:98983716
|
G | A | 5 | a0001c0004t0002g0002a0001c0004t0002g0169a0001c0004t0002g0170others(2): Show | 6 | HG02257.hp1 HG02647.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.9022+257G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 60/72 | chr7 | 98983716 | ||||||
| chr7:98983790
|
C | T | 1 | a0001c0002t0012g0194 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.9023-303C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 60/72 | chr7 | 98983790 | ||||||
| chr7:98983810
|
C | G | 1 | a0001c0001t0003g0139 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.9023-283C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 60/72 | chr7 | 98983810 | ||||||
| chr7:98983889
|
C | A | 3 | a0001c0001t0001g0033a0001c0001t0001g0037a0001c0001t0001g0038 | 3 | HG01346.hp2 HG01515.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.9023-204C>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 60/72 | chr7 | 98983889 | ||||||
| chr7:98983960
|
C | T | 6 | a0001c0005t0004g0004a0001c0005t0004g0005a0001c0005t0004g0006others(3): Show | 6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.9023-133C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 60/72 | chr7 | 98983960 | ||||||
| chr7:98983996
|
CAT | C | 7 | a0001c0001t0001g0141a0001c0005t0004g0004a0001c0005t0004g0005others(4): Show | 7 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.9023-96_9023-95del others(2): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 60/72 | chr7 | 98983996 | ||||||
| chr7:98984618
|
A | C | 3 | a0001c0002t0007g0155a0001c0002t0007g0156a0001c0002t0007g0157 | 3 | HG00140.hp2 HG01243.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.9288+260A>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 61/72 | chr7 | 98984618 | ||||||
| chr7:98984667
|
A | G | 1 | a0001c0001t0001g0050 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.9289-277A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 61/72 | chr7 | 98984667 | ||||||
| chr7:98984803
|
C | A | 1 | a0001c0002t0002g0163 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.9289-141C>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 61/72 | chr7 | 98984803 | ||||||
| chr7:98985053
|
G | A | 1 | a0001c0006t0002g0092 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.9389+9G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 62/72 | chr7 | 98985053 | ||||||
| chr7:98985189
|
C | T | 1 | a0001c0027t0001g0031 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.9389+145C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 62/72 | chr7 | 98985189 | ||||||
| chr7:98985219
|
T | G | 3 | a0001c0001t0002g0195a0001c0001t0002g0196a0001c0001t0002g0197 | 3 | HG02258.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.9389+175T>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 62/72 | chr7 | 98985219 | ||||||
| chr7:98985445
|
A | G | 1 | a0001c0002t0007g0155 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.9389+401A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 62/72 | chr7 | 98985445 | ||||||
| chr7:98985525
|
C | T | 129 | a0001c0001t0001g0239a0001c0001t0001g0241a0001c0001t0001g0257others(126): Show | 131 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.9389+481C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 62/72 | chr7 | 98985525 | ||||||
| chr7:98985537
|
A | G | 1 | a0001c0001t0001g0051 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.9389+493A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 62/72 | chr7 | 98985537 | ||||||
| chr7:98985607
|
G | A | 3 | a0001c0001t0006g0213a0001c0001t0006g0214a0001c0001t0006g0215 | 3 | HG00280.hp1 HG01106.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.9389+563G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 62/72 | chr7 | 98985607 | ||||||
| chr7:98985623
|
T | C | 43 | a0001c0001t0002g0080a0001c0001t0005g0158a0001c0001t0005g0160others(40): Show | 44 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(41): Show |
intron_variant | MODIFIER | c.9389+579T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 62/72 | chr7 | 98985623 | ||||||
| chr7:98985709
|
T | C | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.9389+665T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 62/72 | chr7 | 98985709 | ||||||
| chr7:98985759
|
A | C | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.9389+715A>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 62/72 | chr7 | 98985759 | ||||||
| chr7:98985899
|
T | C | 44 | a0001c0001t0002g0080a0001c0001t0002g0195a0001c0001t0005g0158others(41): Show | 45 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(42): Show |
intron_variant | MODIFIER | c.9389+855T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 62/72 | chr7 | 98985899 | ||||||
| chr7:98985954
|
C | G | 1 | a0001c0001t0001g0085 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.9389+910C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 62/72 | chr7 | 98985954 | ||||||
| chr7:98986006
|
C | T | 2 | a0002c0008t0008g0192a0002c0008t0008g0193 | 2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.9389+962C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 62/72 | chr7 | 98986006 | ||||||
| chr7:98986075
|
A | T | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.9389+1031A>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 62/72 | chr7 | 98986075 | ||||||
| chr7:98986168
|
A | C | 44 | a0001c0001t0002g0080a0001c0001t0002g0195a0001c0001t0005g0158others(41): Show | 45 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(42): Show |
intron_variant | MODIFIER | c.9389+1124A>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 62/72 | chr7 | 98986168 | ||||||
| chr7:98986182
|
T | TG | 43 | a0001c0001t0002g0080a0001c0001t0002g0195a0001c0001t0005g0158others(40): Show | 44 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(41): Show |
intron_variant | MODIFIER | c.9389+1139dupG | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 62/72 | INFO_REALIGN_3_PRIME | chr7 | 98986182 | |||||
| chr7:98986558
|
G | C | 1 | a0001c0002t0002g0163 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.9389+1514G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 62/72 | chr7 | 98986558 | ||||||
| chr7:98986640
|
G | A | 3 | a0001c0002t0007g0155a0001c0002t0007g0156a0001c0002t0007g0157 | 3 | HG00140.hp2 HG01243.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.9389+1596G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 62/72 | chr7 | 98986640 | ||||||
| chr7:98986752
|
G | A | 122 | a0001c0001t0001g0239a0001c0001t0001g0241a0001c0001t0001g0257others(119): Show | 124 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.9389+1708G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 62/72 | chr7 | 98986752 | ||||||
| chr7:98986849
|
C | A | 1 | a0001c0001t0005g0161 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.9389+1805C>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 62/72 | chr7 | 98986849 | ||||||
| chr7:98986885
|
G | T | 3 | a0001c0002t0007g0155a0001c0002t0007g0156a0001c0002t0007g0157 | 3 | HG00140.hp2 HG01243.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.9389+1841G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 62/72 | chr7 | 98986885 | ||||||
| chr7:98986953
|
T | G | 122 | a0001c0001t0001g0239a0001c0001t0001g0241a0001c0001t0001g0257others(119): Show | 123 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.9390-1812T>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 62/72 | chr7 | 98986953 | ||||||
| chr7:98987041
|
T | G | 11 | a0001c0002t0002g0187a0001c0004t0002g0002a0001c0004t0002g0169others(8): Show | 12 | HG01081.hp1 HG02257.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.9390-1724T>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 62/72 | chr7 | 98987041 | ||||||
| chr7:98987197
|
C | G | 1 | a0001c0001t0001g0069 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.9390-1568C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 62/72 | chr7 | 98987197 | ||||||
| chr7:98987487
|
T | A | 65 | a0001c0001t0001g0239a0001c0001t0001g0241a0001c0001t0001g0257others(62): Show | 65 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.9390-1278T>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 62/72 | chr7 | 98987487 | ||||||
| chr7:98987522
|
G | C | 1 | a0001c0002t0002g0182 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.9390-1243G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 62/72 | chr7 | 98987522 | ||||||
| chr7:98987529
|
G | T | 43 | a0001c0001t0002g0080a0001c0001t0005g0158a0001c0001t0005g0160others(40): Show | 44 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(41): Show |
intron_variant | MODIFIER | c.9390-1236G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 62/72 | chr7 | 98987529 | ||||||
| chr7:98987692
|
G | T | 1 | a0001c0001t0001g0136 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.9390-1073G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 62/72 | chr7 | 98987692 | ||||||
| chr7:98987809
|
T | C | 1 | a0001c0022t0001g0056 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.9390-956T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 62/72 | chr7 | 98987809 | ||||||
| chr7:98988143
|
C | T | 1 | a0001c0018t0002g0245 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.9390-622C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 62/72 | chr7 | 98988143 | ||||||
| chr7:98988150
|
T | A | 2 | a0001c0002t0002g0180a0001c0002t0002g0218 | 2 | HG01257.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.9390-615T>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 62/72 | chr7 | 98988150 | ||||||
| chr7:98988561
|
A | G | 2 | a0001c0011t0013g0190a0001c0033t0001g0094 | 2 | HG03098.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.9390-204A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 62/72 | chr7 | 98988561 | ||||||
| chr7:98988596
|
G | A | 1 | a0001c0001t0001g0121 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.9390-169G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 62/72 | chr7 | 98988596 | ||||||
| chr7:98988724
|
A | G | 10 | a0001c0003t0002g0003a0001c0003t0002g0198a0001c0003t0002g0199others(7): Show | 11 | HG01081.hp2 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.9390-41A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 62/72 | chr7 | 98988724 | ||||||
| chr7:98988969
|
G | A | 1 | a0001c0001t0001g0041 | 1 | HG00408.hp2 | splice_region_variant&intron_variant | LOW | c.9591+3G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 63/72 | chr7 | 98988969 | ||||||
| chr7:98989056
|
G | A | 6 | a0001c0005t0004g0004a0001c0005t0004g0005a0001c0005t0004g0006others(3): Show | 6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.9591+90G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 63/72 | chr7 | 98989056 | ||||||
| chr7:98989137
|
G | A | 3 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0003g0139 | 3 | HG00438.hp1 HG00544.hp2 HG02027.hp1 |
intron_variant | MODIFIER | c.9591+171G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 63/72 | chr7 | 98989137 | ||||||
| chr7:98989157
|
A | G | 3 | a0001c0001t0002g0208a0001c0001t0011g0209a0001c0028t0002g0207 | 3 | HG02486.hp1 HG02723.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.9591+191A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 63/72 | chr7 | 98989157 | ||||||
| chr7:98989285
|
C | G | 5 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0001g0047others(2): Show | 5 | HG02523.hp1 NA18969.hp2 NA19010.hp2 others(2): Show |
intron_variant | MODIFIER | c.9591+319C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 63/72 | chr7 | 98989285 | ||||||
| chr7:98989321
|
T | C | 132 | a0001c0001t0001g0239a0001c0001t0001g0241a0001c0001t0001g0257others(129): Show | 134 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.9591+355T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 63/72 | chr7 | 98989321 | ||||||
| chr7:98989329
|
AC | A | 5 | a0001c0002t0002g0165a0001c0002t0002g0166a0001c0002t0002g0181others(2): Show | 5 | HG02809.hp2 HG02896.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.9591+364delC | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 63/72 | chr7 | 98989329 | ||||||
| chr7:98989420
|
C | T | 1 | a0001c0001t0003g0026 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.9591+454C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 63/72 | chr7 | 98989420 | ||||||
| chr7:98989499
|
A | G | 1 | a0006c0042t0002g0184 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.9591+533A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 63/72 | chr7 | 98989499 | ||||||
| chr7:98989666
|
C | T | 61 | a0001c0001t0001g0239a0001c0001t0001g0241a0001c0001t0001g0257others(58): Show | 61 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.9591+700C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 63/72 | chr7 | 98989666 | ||||||
| chr7:98989672
|
T | C | 132 | a0001c0001t0001g0239a0001c0001t0001g0241a0001c0001t0001g0257others(129): Show | 134 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.9591+706T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 63/72 | chr7 | 98989672 | ||||||
| chr7:98990196
|
C | T | 1 | a0001c0001t0002g0250 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.9592-259C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 63/72 | chr7 | 98990196 | ||||||
| chr7:98990330
|
A | G | 1 | a0001c0001t0002g0154 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.9592-125A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 63/72 | chr7 | 98990330 | ||||||
| chr7:98990364
|
T | C | 1 | a0001c0001t0001g0044 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.9592-91T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 63/72 | chr7 | 98990364 | ||||||
| chr7:98990367
|
A | G | 62 | a0001c0001t0001g0239a0001c0001t0001g0241a0001c0001t0001g0257others(59): Show | 62 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.9592-88A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 63/72 | chr7 | 98990367 | ||||||
| chr7:98990633
|
G | T | 2 | a0001c0001t0001g0132a0001c0033t0001g0094 | 2 | HG03239.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.9756+14G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 64/72 | chr7 | 98990633 | ||||||
| chr7:98990677
|
G | A | 4 | a0001c0006t0002g0082a0001c0006t0002g0083a0001c0006t0002g0084others(1): Show | 4 | HG02559.hp1 HG02647.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.9756+58G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 64/72 | chr7 | 98990677 | ||||||
| chr7:98990779
|
A | G | 77 | a0001c0001t0001g0239a0001c0001t0001g0241a0001c0001t0001g0257others(74): Show | 78 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.9756+160A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 64/72 | chr7 | 98990779 | ||||||
| chr7:98991054
|
G | A | 1 | a0001c0001t0003g0139 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.9756+435G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 64/72 | chr7 | 98991054 | ||||||
| chr7:98991068
|
A | G | 2 | a0002c0008t0008g0192a0002c0008t0008g0193 | 2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.9756+449A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 64/72 | chr7 | 98991068 | ||||||
| chr7:98991188
|
C | T | 2 | a0001c0001t0001g0097a0001c0001t0001g0110 | 2 | HG01099.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.9756+569C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 64/72 | chr7 | 98991188 | ||||||
| chr7:98991190
|
C | T | 10 | a0001c0003t0002g0003a0001c0003t0002g0198a0001c0003t0002g0199others(7): Show | 11 | HG01081.hp2 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.9756+571C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 64/72 | chr7 | 98991190 | ||||||
| chr7:98991378
|
C | T | 3 | a0001c0002t0007g0155a0001c0002t0007g0156a0001c0002t0007g0157 | 3 | HG00140.hp2 HG01243.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.9756+759C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 64/72 | chr7 | 98991378 | ||||||
| chr7:98991396
|
T | C | 1 | a0001c0001t0001g0133 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.9757-741T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 64/72 | chr7 | 98991396 | ||||||
| chr7:98991407
|
C | T | 2 | a0001c0001t0002g0196a0001c0001t0002g0197 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.9757-730C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 64/72 | chr7 | 98991407 | ||||||
| chr7:98991491
|
G | A | 3 | a0001c0002t0007g0155a0001c0002t0007g0156a0001c0002t0007g0157 | 3 | HG00140.hp2 HG01243.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.9757-646G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 64/72 | chr7 | 98991491 | ||||||
| chr7:98992236
|
C | T | 1 | a0001c0001t0001g0077 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.9847+9C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 65/72 | chr7 | 98992236 | ||||||
| chr7:98992306
|
G | A | 10 | a0001c0003t0002g0003a0001c0003t0002g0198a0001c0003t0002g0199others(7): Show | 11 | HG01081.hp2 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.9847+79G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 65/72 | chr7 | 98992306 | ||||||
| chr7:98992321
|
C | G | 1 | a0001c0001t0002g0235 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.9847+94C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 65/72 | chr7 | 98992321 | ||||||
| chr7:98992428
|
A | G | 190 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0027others(187): Show | 193 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.9847+201A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 65/72 | chr7 | 98992428 | ||||||
| chr7:98992443
|
G | A | 2 | a0001c0017t0001g0131a0001c0030t0001g0014 | 2 | HG00621.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.9847+216G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 65/72 | chr7 | 98992443 | ||||||
| chr7:98992477
|
A | C | 1 | a0001c0001t0002g0154 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.9847+250A>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 65/72 | chr7 | 98992477 | ||||||
| chr7:98992495
|
A | G | 1 | a0001c0004t0002g0188 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.9847+268A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 65/72 | chr7 | 98992495 | ||||||
| chr7:98992560
|
C | CAT | 24 | a0001c0002t0002g0016a0001c0002t0002g0017a0001c0002t0002g0163others(21): Show | 25 | HG01081.hp1 HG01243.hp1 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.9847+333_9847+334i others(4): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 65/72 | chr7 | 98992560 | ||||||
| chr7:98992560
|
C | CGT | 19 | a0001c0001t0001g0032a0001c0001t0001g0068a0001c0001t0001g0072others(16): Show | 19 | HG00140.hp1 HG00544.hp1 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.9847+360_9847+361d others(4): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 65/72 | INFO_REALIGN_3_PRIME | chr7 | 98992560 | |||||
| chr7:98992560
|
C | CGTGT | 3 | a0001c0001t0001g0034a0001c0001t0001g0063a0001c0001t0001g0093 | 3 | HG01192.hp1 HG03017.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.9847+358_9847+361d others(6): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 65/72 | INFO_REALIGN_3_PRIME | chr7 | 98992560 | |||||
| chr7:98992560
|
C | CGTGTGT | 6 | a0001c0005t0004g0004a0001c0005t0004g0005a0001c0005t0004g0006others(3): Show | 6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.9847+356_9847+361d others(8): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 65/72 | INFO_REALIGN_3_PRIME | chr7 | 98992560 | |||||
| chr7:98992560
|
C | CGTGTGTG others(13): Show |
1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.9847+342_9847+361d others(22): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 65/72 | INFO_REALIGN_3_PRIME | chr7 | 98992560 | |||||
| chr7:98992560
|
CGT | C | 65 | a0001c0001t0001g0239a0001c0001t0001g0241a0001c0001t0001g0258others(62): Show | 66 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(63): Show |
intron_variant | MODIFIER | c.9847+360_9847+361d others(4): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 65/72 | INFO_REALIGN_3_PRIME | chr7 | 98992560 | |||||
| chr7:98992561
|
G | A | 11 | a0001c0001t0002g0080a0001c0001t0005g0158a0001c0001t0005g0160others(8): Show | 11 | HG01884.hp2 HG02055.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.9847+334G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 65/72 | chr7 | 98992561 | ||||||
| chr7:98992587
|
GTT | G | 11 | a0001c0001t0002g0080a0001c0001t0005g0158a0001c0001t0005g0160others(8): Show | 11 | HG01884.hp2 HG02055.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.9847+362_9847+363d others(4): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 65/72 | INFO_REALIGN_3_PRIME | chr7 | 98992587 | |||||
| chr7:98992828
|
C | T | 4 | a0001c0004t0002g0183a0001c0004t0002g0185a0001c0004t0002g0188others(1): Show | 4 | HG02622.hp2 HG02886.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.9847+601C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 65/72 | chr7 | 98992828 | ||||||
| chr7:98993216
|
G | T | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.9848-322G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 65/72 | chr7 | 98993216 | ||||||
| chr7:98993229
|
G | A | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.9848-309G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 65/72 | chr7 | 98993229 | ||||||
| chr7:98993255
|
G | A | 2 | a0002c0008t0008g0192a0002c0008t0008g0193 | 2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.9848-283G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 65/72 | chr7 | 98993255 | ||||||
| chr7:98993373
|
C | T | 2 | a0002c0008t0008g0192a0002c0008t0008g0193 | 2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.9848-165C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 65/72 | chr7 | 98993373 | ||||||
| chr7:98993457
|
G | C | 3 | a0001c0001t0002g0208a0001c0001t0011g0209a0001c0028t0002g0207 | 3 | HG02486.hp1 HG02723.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.9848-81G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 65/72 | chr7 | 98993457 | ||||||
| chr7:98993497
|
C | T | 3 | a0001c0005t0004g0007a0001c0005t0004g0008a0001c0005t0004g0009 | 3 | HG02630.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.9848-41C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 65/72 | chr7 | 98993497 | ||||||
| chr7:98993989
|
T | C | 258 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(255): Show | 261 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.10047+252T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 66/72 | chr7 | 98993989 | ||||||
| chr7:98994002
|
A | G | 1 | a0001c0001t0002g0080 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.10047+265A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 66/72 | chr7 | 98994002 | ||||||
| chr7:98994076
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.10047+339G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 66/72 | chr7 | 98994076 | ||||||
| chr7:98994099
|
G | T | 1 | a0001c0002t0012g0194 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.10047+362G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 66/72 | chr7 | 98994099 | ||||||
| chr7:98994257
|
G | A | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.10048-330G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 66/72 | chr7 | 98994257 | ||||||
| chr7:98994312
|
G | A | 2 | a0001c0001t0002g0196a0001c0001t0002g0197 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.10048-275G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 66/72 | chr7 | 98994312 | ||||||
| chr7:98994374
|
A | G | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.10048-213A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 66/72 | chr7 | 98994374 | ||||||
| chr7:98994398
|
C | A | 1 | a0001c0001t0001g0241 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.10048-189C>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 66/72 | chr7 | 98994398 | ||||||
| chr7:98994420
|
G | A | 1 | a0001c0001t0001g0241 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.10048-167G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 66/72 | chr7 | 98994420 | ||||||
| chr7:98994471
|
C | T | 2 | a0001c0001t0002g0208a0001c0001t0011g0209 | 2 | HG02486.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.10048-116C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 66/72 | chr7 | 98994471 | ||||||
| chr7:98994519
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.10048-68C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 66/72 | chr7 | 98994519 | ||||||
| chr7:98994530
|
G | C | 1 | a0001c0001t0001g0085 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.10048-57G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 66/72 | chr7 | 98994530 | ||||||
| chr7:98995188
|
A | C | 44 | a0001c0001t0002g0080a0001c0001t0002g0195a0001c0001t0005g0158others(41): Show | 45 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(42): Show |
intron_variant | MODIFIER | c.10309+340A>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98995188 | ||||||
| chr7:98995269
|
C | T | 3 | a0001c0002t0007g0155a0001c0002t0007g0156a0001c0002t0007g0157 | 3 | HG00140.hp2 HG01243.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.10309+421C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98995269 | ||||||
| chr7:98995323
|
C | T | 1 | a0001c0012t0001g0125 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.10309+475C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98995323 | ||||||
| chr7:98995324
|
G | A | 66 | a0001c0001t0001g0239a0001c0001t0001g0241a0001c0001t0001g0257others(63): Show | 67 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.10309+476G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98995324 | ||||||
| chr7:98995574
|
G | T | 51 | a0001c0001t0001g0239a0001c0001t0001g0241a0001c0001t0001g0257others(48): Show | 51 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.10309+726G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98995574 | ||||||
| chr7:98995812
|
C | T | 3 | a0001c0002t0007g0155a0001c0002t0007g0156a0001c0002t0007g0157 | 3 | HG00140.hp2 HG01243.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.10309+964C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98995812 | ||||||
| chr7:98995869
|
ATGTCCCA others(13): Show |
A | 43 | a0001c0001t0002g0080a0001c0001t0005g0158a0001c0001t0005g0160others(40): Show | 44 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(41): Show |
intron_variant | MODIFIER | c.10309+1031_10309+1 others(26): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | INFO_REALIGN_3_PRIME | chr7 | 98995869 | |||||
| chr7:98995953
|
A | G | 43 | a0001c0001t0002g0080a0001c0001t0005g0158a0001c0001t0005g0160others(40): Show | 44 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(41): Show |
intron_variant | MODIFIER | c.10309+1105A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98995953 | ||||||
| chr7:98995995
|
A | T | 13 | a0001c0002t0002g0016a0001c0002t0002g0017a0001c0002t0002g0165others(10): Show | 13 | HG01243.hp1 HG01884.hp1 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.10309+1147A>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98995995 | ||||||
| chr7:98996057
|
C | T | 1 | a0001c0001t0001g0109 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.10309+1209C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98996057 | ||||||
| chr7:98996109
|
C | T | 10 | a0001c0003t0002g0003a0001c0003t0002g0198a0001c0003t0002g0199others(7): Show | 11 | HG01081.hp2 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.10309+1261C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98996109 | ||||||
| chr7:98996169
|
TC | T | 3 | a0001c0001t0002g0195a0001c0001t0002g0196a0001c0001t0002g0197 | 3 | HG02258.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.10309+1325delC | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | INFO_REALIGN_3_PRIME | chr7 | 98996169 | |||||
| chr7:98996174
|
G | A | 5 | a0001c0001t0001g0058a0001c0001t0001g0068a0001c0001t0001g0069others(2): Show | 5 | NA18966.hp2 NA18970.hp2 NA18982.hp1 others(2): Show |
intron_variant | MODIFIER | c.10309+1326G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98996174 | ||||||
| chr7:98996696
|
C | T | 10 | a0001c0001t0002g0221a0001c0001t0002g0229a0001c0001t0002g0230others(7): Show | 10 | HG01099.hp2 HG01496.hp1 HG01943.hp2 others(7): Show |
intron_variant | MODIFIER | c.10309+1848C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98996696 | ||||||
| chr7:98996843
|
G | T | 1 | a0001c0001t0001g0077 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.10309+1995G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98996843 | ||||||
| chr7:98996866
|
C | G | 2 | a0001c0005t0004g0007a0001c0005t0004g0009 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.10309+2018C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98996866 | ||||||
| chr7:98996904
|
A | C | 1 | a0001c0002t0002g0177 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.10309+2056A>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98996904 | ||||||
| chr7:98996955
|
A | G | 2 | a0001c0001t0002g0211a0001c0001t0002g0212 | 2 | HG00741.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.10309+2107A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98996955 | ||||||
| chr7:98997017
|
A | G | 1 | a0001c0001t0003g0139 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.10309+2169A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98997017 | ||||||
| chr7:98997080
|
C | T | 7 | a0001c0001t0001g0047a0001c0005t0004g0004a0001c0005t0004g0005others(4): Show | 7 | HG02523.hp1 HG02622.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.10309+2232C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98997080 | ||||||
| chr7:98997122
|
A | G | 15 | a0001c0002t0002g0016a0001c0002t0002g0017a0001c0002t0002g0165others(12): Show | 15 | HG01081.hp1 HG01243.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.10309+2274A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98997122 | ||||||
| chr7:98997147
|
A | C | 67 | a0001c0001t0001g0239a0001c0001t0001g0241a0001c0001t0001g0257others(64): Show | 68 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.10309+2299A>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98997147 | ||||||
| chr7:98997179
|
G | A | 4 | a0001c0001t0001g0116a0001c0002t0002g0182a0002c0008t0008g0192others(1): Show | 4 | HG02559.hp2 HG02895.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.10309+2331G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98997179 | ||||||
| chr7:98997221
|
G | A | 122 | a0001c0001t0001g0239a0001c0001t0001g0241a0001c0001t0001g0257others(119): Show | 124 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.10309+2373G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98997221 | ||||||
| chr7:98997483
|
C | CA | 23 | a0001c0001t0001g0015a0001c0001t0001g0029a0001c0001t0001g0033others(20): Show | 23 | HG00438.hp1 HG00621.hp2 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.10309+2664dupA | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | INFO_REALIGN_3_PRIME | chr7 | 98997483 | |||||
| chr7:98997483
|
C | CAA | 7 | a0001c0001t0001g0035a0001c0001t0001g0046a0001c0001t0001g0077others(4): Show | 7 | HG00741.hp1 HG01358.hp1 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.10309+2663_10309+2 others(8): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | INFO_REALIGN_3_PRIME | chr7 | 98997483 | |||||
| chr7:98997483
|
C | CAAAAAAA | 21 | a0001c0001t0001g0241a0001c0001t0001g0257a0001c0001t0001g0258others(18): Show | 21 | HG00558.hp1 HG00642.hp1 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.10309+2658_10309+2 others(13): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | INFO_REALIGN_3_PRIME | chr7 | 98997483 | |||||
| chr7:98997483
|
C | CAAAAAAA others(1): Show |
16 | a0001c0001t0001g0239a0001c0001t0002g0221a0001c0001t0002g0229others(13): Show | 16 | HG00280.hp1 HG00408.hp1 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.10309+2657_10309+2 others(14): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | INFO_REALIGN_3_PRIME | chr7 | 98997483 | |||||
| chr7:98997483
|
C | CAAAAAAA others(2): Show |
7 | a0001c0001t0002g0219a0001c0001t0002g0234a0001c0001t0002g0244others(4): Show | 7 | HG01106.hp1 HG02148.hp1 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.10309+2656_10309+2 others(15): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | INFO_REALIGN_3_PRIME | chr7 | 98997483 | |||||
| chr7:98997483
|
C | CAAAAAAA others(3): Show |
3 | a0001c0001t0002g0220a0003c0037t0002g0242a0012c0035t0002g0254 | 3 | HG00438.hp2 NA19009.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.10309+2655_10309+2 others(16): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | INFO_REALIGN_3_PRIME | chr7 | 98997483 | |||||
| chr7:98997483
|
C | CAAAAAAA others(4): Show |
3 | a0001c0001t0002g0222a0001c0001t0002g0223a0001c0031t0002g0255 | 3 | NA18966.hp1 NA18978.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.10309+2654_10309+2 others(17): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | INFO_REALIGN_3_PRIME | chr7 | 98997483 | |||||
| chr7:98997483
|
C | CAAAAAAA others(6): Show |
1 | a0001c0001t0002g0011 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.10309+2652_10309+2 others(19): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | INFO_REALIGN_3_PRIME | chr7 | 98997483 | |||||
| chr7:98997483
|
C | CAAAAAAA others(7): Show |
1 | a0001c0001t0002g0010 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.10309+2651_10309+2 others(20): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | INFO_REALIGN_3_PRIME | chr7 | 98997483 | |||||
| chr7:98997483
|
CA | C | 80 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0027others(77): Show | 82 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.10309+2664delA | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | INFO_REALIGN_3_PRIME | chr7 | 98997483 | |||||
| chr7:98997483
|
CAA | C | 7 | a0001c0001t0001g0105a0001c0001t0001g0118a0001c0001t0003g0026others(4): Show | 7 | HG02258.hp1 HG02486.hp2 HG03704.hp1 others(4): Show |
intron_variant | MODIFIER | c.10309+2663_10309+2 others(8): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | INFO_REALIGN_3_PRIME | chr7 | 98997483 | |||||
| chr7:98997483
|
CAAAAAAA others(2): Show |
C | 11 | a0001c0001t0002g0080a0001c0003t0002g0003a0001c0003t0002g0198others(8): Show | 12 | HG01081.hp2 HG01167.hp1 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.10309+2656_10309+2 others(15): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | INFO_REALIGN_3_PRIME | chr7 | 98997483 | |||||
| chr7:98997483
|
CAAAAAAA others(3): Show |
C | 1 | a0002c0008t0008g0192 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.10309+2655_10309+2 others(16): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | INFO_REALIGN_3_PRIME | chr7 | 98997483 | |||||
| chr7:98997483
|
CAAAAAAA others(4): Show |
C | 2 | a0001c0021t0001g0059a0001c0038t0001g0086 | 2 | HG02055.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.10309+2654_10309+2 others(17): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | INFO_REALIGN_3_PRIME | chr7 | 98997483 | |||||
| chr7:98997641
|
G | C | 2 | a0002c0008t0008g0192a0002c0008t0008g0193 | 2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.10309+2793G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98997641 | ||||||
| chr7:98997795
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.10309+2947G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98997795 | ||||||
| chr7:98997836
|
T | G | 131 | a0001c0001t0001g0239a0001c0001t0001g0241a0001c0001t0001g0257others(128): Show | 133 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.10309+2988T>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98997836 | ||||||
| chr7:98997995
|
G | A | 5 | a0001c0001t0005g0158a0001c0001t0005g0160a0001c0001t0005g0161others(2): Show | 5 | HG02055.hp1 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.10309+3147G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98997995 | ||||||
| chr7:98998089
|
A | G | 3 | a0001c0001t0001g0143a0002c0008t0008g0192a0002c0008t0008g0193 | 3 | HG02559.hp2 HG02615.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.10309+3241A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98998089 | ||||||
| chr7:98998307
|
G | A | 67 | a0001c0001t0001g0239a0001c0001t0001g0241a0001c0001t0001g0257others(64): Show | 68 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.10309+3459G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98998307 | ||||||
| chr7:98998484
|
G | A | 56 | a0001c0001t0002g0080a0001c0001t0005g0158a0001c0001t0005g0161others(53): Show | 57 | HG00140.hp2 HG01081.hp1 HG01243.hp1 others(54): Show |
intron_variant | MODIFIER | c.10309+3636G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98998484 | ||||||
| chr7:98998503
|
A | G | 3 | a0001c0001t0001g0034a0001c0001t0001g0037a0001c0001t0001g0038 | 3 | HG01346.hp2 HG02145.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.10309+3655A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98998503 | ||||||
| chr7:98998532
|
A | C | 1 | a0001c0001t0001g0070 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.10309+3684A>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98998532 | ||||||
| chr7:98998564
|
C | G | 1 | a0001c0001t0011g0209 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.10309+3716C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98998564 | ||||||
| chr7:98998601
|
C | T | 3 | a0001c0002t0007g0155a0001c0002t0007g0156a0001c0002t0007g0157 | 3 | HG00140.hp2 HG01243.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.10309+3753C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98998601 | ||||||
| chr7:98998659
|
G | A | 1 | a0001c0001t0001g0121 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.10309+3811G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98998659 | ||||||
| chr7:98998700
|
A | G | 2 | a0002c0008t0008g0192a0002c0008t0008g0193 | 2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.10309+3852A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98998700 | ||||||
| chr7:98998762
|
C | T | 2 | a0001c0001t0001g0144a0001c0001t0001g0146 | 2 | HG00621.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.10309+3914C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98998762 | ||||||
| chr7:98998763
|
C | A | 2 | a0001c0001t0001g0102a0001c0045t0001g0101 | 2 | HG03710.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.10309+3915C>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98998763 | ||||||
| chr7:98998785
|
G | A | 121 | a0001c0001t0001g0239a0001c0001t0001g0241a0001c0001t0001g0257others(118): Show | 123 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.10309+3937G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98998785 | ||||||
| chr7:98998800
|
C | T | 3 | a0001c0001t0002g0195a0001c0001t0002g0196a0001c0001t0002g0197 | 3 | HG02258.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.10309+3952C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98998800 | ||||||
| chr7:98998905
|
G | A | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.10309+4057G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98998905 | ||||||
| chr7:98999071
|
A | T | 1 | a0001c0001t0001g0150 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.10309+4223A>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98999071 | ||||||
| chr7:98999115
|
A | G | 3 | a0001c0002t0007g0155a0001c0002t0007g0156a0001c0002t0007g0157 | 3 | HG00140.hp2 HG01243.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.10309+4267A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98999115 | ||||||
| chr7:98999166
|
C | T | 1 | a0001c0002t0009g0175 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.10309+4318C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98999166 | ||||||
| chr7:98999257
|
G | A | 1 | a0001c0004t0002g0183 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.10309+4409G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98999257 | ||||||
| chr7:98999516
|
G | A | 66 | a0001c0001t0001g0239a0001c0001t0001g0241a0001c0001t0001g0257others(63): Show | 67 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.10309+4668G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98999516 | ||||||
| chr7:98999676
|
G | T | 1 | a0001c0022t0001g0056 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.10310-4514G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98999676 | ||||||
| chr7:98999801
|
T | G | 1 | a0001c0004t0002g0176 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.10310-4389T>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98999801 | ||||||
| chr7:98999829
|
C | T | 5 | a0001c0004t0002g0002a0001c0004t0002g0169a0001c0004t0002g0170others(2): Show | 6 | HG02257.hp1 HG02647.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.10310-4361C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98999829 | ||||||
| chr7:98999963
|
A | C | 1 | a0006c0042t0002g0184 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.10310-4227A>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 98999963 | ||||||
| chr7:99000001
|
G | GTTTA | 43 | a0001c0001t0002g0080a0001c0001t0005g0158a0001c0001t0005g0160others(40): Show | 44 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(41): Show |
intron_variant | MODIFIER | c.10310-4169_10310-4 others(10): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | INFO_REALIGN_3_PRIME | chr7 | 99000001 | |||||
| chr7:99000084
|
C | T | 1 | a0001c0001t0001g0045 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.10310-4106C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 99000084 | ||||||
| chr7:99000133
|
G | C | 43 | a0001c0001t0002g0080a0001c0001t0005g0158a0001c0001t0005g0160others(40): Show | 44 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(41): Show |
intron_variant | MODIFIER | c.10310-4057G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 99000133 | ||||||
| chr7:99000382
|
C | T | 1 | a0001c0001t0001g0079 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.10310-3808C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 99000382 | ||||||
| chr7:99000566
|
C | T | 1 | a0001c0001t0002g0223 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.10310-3624C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 99000566 | ||||||
| chr7:99000858
|
C | T | 10 | a0001c0003t0002g0003a0001c0003t0002g0198a0001c0003t0002g0199others(7): Show | 11 | HG01081.hp2 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.10310-3332C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 99000858 | ||||||
| chr7:99000901
|
C | G | 1 | a0008c0029t0001g0138 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.10310-3289C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 99000901 | ||||||
| chr7:99000994
|
A | T | 2 | a0001c0007t0001g0142a0001c0007t0001g0148 | 2 | HG01891.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.10310-3196A>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 99000994 | ||||||
| chr7:99000995
|
A | T | 2 | a0001c0007t0001g0142a0001c0007t0001g0148 | 2 | HG01891.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.10310-3195A>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 99000995 | ||||||
| chr7:99001003
|
A | C | 1 | a0011c0032t0005g0159 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.10310-3187A>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 99001003 | ||||||
| chr7:99001017
|
C | T | 129 | a0001c0001t0001g0239a0001c0001t0001g0241a0001c0001t0001g0257others(126): Show | 131 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.10310-3173C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 99001017 | ||||||
| chr7:99001273
|
C | T | 1 | a0001c0001t0001g0036 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.10310-2917C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 99001273 | ||||||
| chr7:99001516
|
G | C | 2 | a0001c0003t0002g0003a0001c0003t0002g0198 | 3 | HG01081.hp2 HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.10310-2674G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 99001516 | ||||||
| chr7:99001535
|
T | TA | 32 | a0001c0002t0002g0016a0001c0002t0002g0017a0001c0002t0002g0163others(29): Show | 33 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(30): Show |
intron_variant | MODIFIER | c.10310-2646dupA | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | INFO_REALIGN_3_PRIME | chr7 | 99001535 | |||||
| chr7:99001805
|
A | T | 1 | a0001c0002t0002g0178 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.10310-2385A>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 99001805 | ||||||
| chr7:99001911
|
C | T | 128 | a0001c0001t0001g0239a0001c0001t0001g0241a0001c0001t0001g0257others(125): Show | 130 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.10310-2279C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 99001911 | ||||||
| chr7:99001976
|
A | G | 1 | a0001c0001t0002g0154 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.10310-2214A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 99001976 | ||||||
| chr7:99002135
|
TGGTGGGG others(3): Show |
T | 3 | a0001c0002t0007g0155a0001c0002t0007g0156a0001c0002t0007g0157 | 3 | HG00140.hp2 HG01243.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.10310-2049_10310-2 others(16): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | INFO_REALIGN_3_PRIME | chr7 | 99002135 | |||||
| chr7:99002527
|
C | T | 1 | a0001c0001t0001g0033 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.10310-1663C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 99002527 | ||||||
| chr7:99002607
|
T | C | 10 | a0001c0003t0002g0003a0001c0003t0002g0198a0001c0003t0002g0199others(7): Show | 11 | HG01081.hp2 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.10310-1583T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 99002607 | ||||||
| chr7:99002639
|
G | C | 3 | a0001c0002t0007g0155a0001c0002t0007g0156a0001c0002t0007g0157 | 3 | HG00140.hp2 HG01243.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.10310-1551G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 99002639 | ||||||
| chr7:99002731
|
A | C | 2 | a0001c0001t0001g0034a0001c0001t0001g0063 | 2 | HG01192.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.10310-1459A>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 99002731 | ||||||
| chr7:99002836
|
T | C | 1 | a0001c0025t0001g0151 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.10310-1354T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 99002836 | ||||||
| chr7:99002847
|
C | T | 1 | a0001c0001t0006g0214 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.10310-1343C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 99002847 | ||||||
| chr7:99002850
|
G | A | 2 | a0001c0002t0002g0016a0001c0002t0002g0017 | 2 | HG01884.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.10310-1340G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 99002850 | ||||||
| chr7:99002927
|
C | A | 1 | a0001c0001t0001g0033 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.10310-1263C>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 99002927 | ||||||
| chr7:99002938
|
T | G | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.10310-1252T>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 99002938 | ||||||
| chr7:99002999
|
C | T | 1 | a0001c0001t0001g0088 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.10310-1191C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 99002999 | ||||||
| chr7:99003055
|
T | C | 2 | a0001c0001t0001g0109a0001c0001t0001g0120 | 2 | NA18982.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.10310-1135T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 99003055 | ||||||
| chr7:99003104
|
C | G | 1 | a0001c0002t0002g0174 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.10310-1086C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 99003104 | ||||||
| chr7:99003208
|
G | T | 1 | a0001c0001t0001g0130 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.10310-982G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 99003208 | ||||||
| chr7:99003216
|
C | G | 75 | a0001c0001t0001g0239a0001c0001t0001g0241a0001c0001t0001g0257others(72): Show | 76 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.10310-974C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 99003216 | ||||||
| chr7:99003402
|
T | C | 57 | a0001c0001t0001g0239a0001c0001t0001g0241a0001c0001t0001g0257others(54): Show | 57 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.10310-788T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 99003402 | ||||||
| chr7:99003429
|
A | G | 4 | a0001c0001t0005g0158a0001c0001t0005g0160a0001c0001t0005g0161others(1): Show | 4 | HG02258.hp1 HG02486.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.10310-761A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 99003429 | ||||||
| chr7:99003621
|
T | C | 3 | a0001c0002t0007g0155a0001c0002t0007g0156a0001c0002t0007g0157 | 3 | HG00140.hp2 HG01243.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.10310-569T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 99003621 | ||||||
| chr7:99003697
|
C | T | 1 | a0001c0045t0001g0101 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.10310-493C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 99003697 | ||||||
| chr7:99003782
|
G | A | 3 | a0001c0001t0006g0213a0001c0001t0006g0214a0001c0001t0006g0215 | 3 | HG00280.hp1 HG01106.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.10310-408G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 99003782 | ||||||
| chr7:99003821
|
T | C | 1 | a0001c0001t0002g0080 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.10310-369T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 99003821 | ||||||
| chr7:99003854
|
G | A | 2 | a0001c0002t0002g0180a0001c0002t0002g0218 | 2 | HG01257.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.10310-336G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 99003854 | ||||||
| chr7:99003858
|
G | A | 3 | a0001c0001t0001g0034a0001c0001t0001g0037a0001c0001t0001g0038 | 3 | HG01346.hp2 HG02145.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.10310-332G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 99003858 | ||||||
| chr7:99003893
|
G | C | 1 | a0001c0004t0002g0183 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.10310-297G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 99003893 | ||||||
| chr7:99003941
|
C | T | 6 | a0001c0005t0004g0004a0001c0005t0004g0005a0001c0005t0004g0006others(3): Show | 6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.10310-249C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 99003941 | ||||||
| chr7:99003965
|
C | T | 1 | a0001c0001t0001g0093 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.10310-225C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 99003965 | ||||||
| chr7:99003998
|
G | A | 1 | a0007c0020t0001g0119 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.10310-192G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 99003998 | ||||||
| chr7:99004005
|
G | A | 2 | a0001c0001t0002g0208a0001c0001t0011g0209 | 2 | HG02486.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.10310-185G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 99004005 | ||||||
| chr7:99004009
|
G | A | 66 | a0001c0001t0001g0239a0001c0001t0001g0241a0001c0001t0001g0257others(63): Show | 67 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.10310-181G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 99004009 | ||||||
| chr7:99004147
|
C | T | 1 | a0001c0001t0001g0111 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.10310-43C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 67/72 | chr7 | 99004147 | ||||||
| chr7:99004588
|
G | A | 1 | a0001c0001t0001g0048 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.10535+173G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 68/72 | chr7 | 99004588 | ||||||
| chr7:99004700
|
C | T | 2 | a0002c0008t0008g0192a0002c0008t0008g0193 | 2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.10535+285C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 68/72 | chr7 | 99004700 | ||||||
| chr7:99004732
|
T | C | 4 | a0001c0001t0003g0025a0001c0001t0003g0026a0001c0001t0003g0089others(1): Show | 4 | NA18941.hp1 NA18957.hp2 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.10535+317T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 68/72 | chr7 | 99004732 | ||||||
| chr7:99004973
|
C | T | 1 | a0001c0002t0002g0180 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.10536-158C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 68/72 | chr7 | 99004973 | ||||||
| chr7:99004974
|
G | T | 2 | a0001c0001t0001g0001a0001c0001t0001g0126 | 3 | HG00280.hp2 HG00642.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.10536-157G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 68/72 | chr7 | 99004974 | ||||||
| chr7:99005016
|
G | A | 43 | a0001c0001t0002g0080a0001c0001t0005g0158a0001c0001t0005g0160others(40): Show | 44 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(41): Show |
intron_variant | MODIFIER | c.10536-115G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 68/72 | chr7 | 99005016 | ||||||
| chr7:99005037
|
T | TC | 3 | a0001c0001t0001g0052a0001c0001t0001g0070a0001c0001t0002g0222 | 3 | NA18978.hp2 NA18982.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.10536-91dupC | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 68/72 | INFO_REALIGN_3_PRIME | chr7 | 99005037 | |||||
| chr7:99005091
|
G | T | 6 | a0001c0001t0002g0080a0001c0006t0002g0082a0001c0006t0002g0083others(3): Show | 6 | HG01884.hp2 HG02559.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.10536-40G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 68/72 | chr7 | 99005091 | ||||||
| chr7:99005367
|
G | C | 122 | a0001c0001t0001g0239a0001c0001t0001g0241a0001c0001t0001g0257others(119): Show | 124 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.10753+19G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99005367 | ||||||
| chr7:99005472
|
A | G | 1 | a0001c0001t0001g0018 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.10753+124A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99005472 | ||||||
| chr7:99005487
|
G | A | 4 | a0001c0001t0002g0225a0001c0001t0002g0226a0001c0001t0002g0253others(1): Show | 4 | HG00738.hp2 HG01515.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.10753+139G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99005487 | ||||||
| chr7:99005636
|
C | T | 1 | a0001c0001t0001g0085 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.10753+288C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99005636 | ||||||
| chr7:99005662
|
G | A | 121 | a0001c0001t0001g0239a0001c0001t0001g0241a0001c0001t0001g0257others(118): Show | 123 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.10753+314G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99005662 | ||||||
| chr7:99005673
|
ATTTCTT | A | 3 | a0001c0004t0002g0183a0001c0004t0002g0185a0006c0042t0002g0184 | 3 | HG02622.hp2 HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.10753+335_10753+34 others(10): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | INFO_REALIGN_3_PRIME | chr7 | 99005673 | |||||
| chr7:99005843
|
C | T | 57 | a0001c0001t0001g0239a0001c0001t0001g0241a0001c0001t0001g0257others(54): Show | 57 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.10753+495C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99005843 | ||||||
| chr7:99005854
|
G | A | 1 | a0001c0017t0001g0131 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.10753+506G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99005854 | ||||||
| chr7:99005880
|
G | A | 6 | a0001c0002t0002g0165a0001c0002t0002g0166a0001c0002t0002g0167others(3): Show | 6 | HG02809.hp2 HG02896.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.10753+532G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99005880 | ||||||
| chr7:99005933
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.10753+585G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99005933 | ||||||
| chr7:99006041
|
G | A | 1 | a0008c0029t0001g0138 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.10753+693G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99006041 | ||||||
| chr7:99006154
|
T | C | 1 | a0001c0001t0001g0099 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.10753+806T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99006154 | ||||||
| chr7:99006160
|
G | A | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.10753+812G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99006160 | ||||||
| chr7:99006233
|
C | G | 1 | a0001c0001t0001g0088 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.10753+885C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99006233 | ||||||
| chr7:99006248
|
C | T | 1 | a0001c0038t0001g0086 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.10753+900C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99006248 | ||||||
| chr7:99006301
|
C | T | 2 | a0001c0001t0001g0090a0001c0001t0001g0147 | 2 | HG02109.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.10753+953C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99006301 | ||||||
| chr7:99006442
|
T | TGTAGTGT others(12): Show |
1 | a0001c0001t0001g0070 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.10753+1095_10753+1 others(25): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | INFO_REALIGN_3_PRIME | chr7 | 99006442 | |||||
| chr7:99006443
|
G | A | 1 | a0001c0011t0013g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.10753+1095G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99006443 | ||||||
| chr7:99006493
|
T | A | 1 | a0001c0022t0001g0056 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.10753+1145T>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99006493 | ||||||
| chr7:99006503
|
A | G | 132 | a0001c0001t0001g0239a0001c0001t0001g0241a0001c0001t0001g0257others(129): Show | 134 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.10753+1155A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99006503 | ||||||
| chr7:99006605
|
A | G | 1 | a0001c0002t0010g0179 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.10753+1257A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99006605 | ||||||
| chr7:99006773
|
T | C | 2 | a0001c0001t0001g0108a0001c0001t0001g0113 | 2 | HG00544.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.10753+1425T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99006773 | ||||||
| chr7:99006849
|
C | T | 1 | a0001c0002t0002g0167 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.10753+1501C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99006849 | ||||||
| chr7:99007122
|
A | G | 3 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0073 | 3 | NA18978.hp1 NA19000.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.10754-1255A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99007122 | ||||||
| chr7:99007142
|
G | A | 3 | a0001c0001t0001g0095a0001c0001t0001g0135a0001c0001t0001g0140 | 3 | HG02572.hp2 HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.10754-1235G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99007142 | ||||||
| chr7:99007218
|
C | T | 1 | a0001c0001t0002g0231 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.10754-1159C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99007218 | ||||||
| chr7:99007219
|
G | A | 3 | a0001c0002t0007g0155a0001c0002t0007g0156a0001c0002t0007g0157 | 3 | HG00140.hp2 HG01243.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.10754-1158G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99007219 | ||||||
| chr7:99007221
|
C | T | 2 | a0001c0001t0001g0035a0001c0001t0001g0063 | 2 | HG00741.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.10754-1156C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99007221 | ||||||
| chr7:99007240
|
G | A | 2 | a0001c0001t0001g0036a0001c0001t0001g0076 | 2 | HG03704.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.10754-1137G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99007240 | ||||||
| chr7:99007461
|
G | A | 3 | a0001c0001t0002g0195a0001c0001t0002g0196a0001c0001t0002g0197 | 3 | HG02258.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.10754-916G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99007461 | ||||||
| chr7:99007468
|
C | T | 3 | a0001c0001t0002g0195a0001c0001t0002g0196a0001c0001t0002g0197 | 3 | HG02258.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.10754-909C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99007468 | ||||||
| chr7:99007506
|
G | A | 1 | a0001c0001t0002g0154 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.10754-871G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99007506 | ||||||
| chr7:99007667
|
T | C | 1 | a0001c0005t0004g0004 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.10754-710T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99007667 | ||||||
| chr7:99007709
|
C | T | 2 | a0001c0007t0001g0142a0001c0007t0001g0148 | 2 | HG01891.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.10754-668C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99007709 | ||||||
| chr7:99007774
|
G | A | 2 | a0001c0001t0002g0208a0001c0001t0011g0209 | 2 | HG02486.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.10754-603G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99007774 | ||||||
| chr7:99007824
|
CT | C | 36 | a0001c0001t0002g0080a0001c0001t0002g0195a0001c0001t0002g0196others(33): Show | 37 | HG01081.hp2 HG01167.hp1 HG01169.hp2 others(34): Show |
intron_variant | MODIFIER | c.10754-537delT | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | INFO_REALIGN_3_PRIME | chr7 | 99007824 | |||||
| chr7:99007840
|
T | C | 1 | a0001c0028t0002g0207 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.10754-537T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99007840 | ||||||
| chr7:99007936
|
C | G | 1 | a0001c0001t0001g0126 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.10754-441C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99007936 | ||||||
| chr7:99007987
|
G | A | 1 | a0001c0001t0001g0042 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.10754-390G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99007987 | ||||||
| chr7:99008014
|
C | G | 1 | a0001c0017t0001g0131 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.10754-363C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99008014 | ||||||
| chr7:99008032
|
A | G | 1 | a0001c0001t0001g0259 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.10754-345A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99008032 | ||||||
| chr7:99008038
|
A | C | 2 | a0001c0001t0001g0128a0001c0001t0001g0130 | 2 | HG00558.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.10754-339A>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99008038 | ||||||
| chr7:99008093
|
T | G | 9 | a0001c0001t0001g0095a0001c0001t0001g0135a0001c0001t0001g0140others(6): Show | 9 | HG01884.hp2 HG02572.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.10754-284T>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99008093 | ||||||
| chr7:99008113
|
T | C | 5 | a0001c0001t0001g0239a0001c0001t0001g0241a0001c0001t0001g0257others(2): Show | 5 | HG02015.hp2 HG02040.hp2 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.10754-264T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99008113 | ||||||
| chr7:99008152
|
A | G | 1 | a0001c0001t0002g0234 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.10754-225A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99008152 | ||||||
| chr7:99008195
|
G | A | 1 | a0001c0002t0002g0187 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.10754-182G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99008195 | ||||||
| chr7:99008307
|
C | G | 6 | a0001c0001t0005g0158a0001c0001t0005g0160a0001c0001t0005g0161others(3): Show | 6 | HG02055.hp1 HG02258.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.10754-70C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99008307 | ||||||
| chr7:99008311
|
C | T | 2 | a0001c0001t0001g0060a0001c0001t0001g0067 | 2 | NA19079.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.10754-66C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 69/72 | chr7 | 99008311 | ||||||
| chr7:99008671
|
C | G | 1 | a0001c0001t0001g0109 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.10938+110C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 70/72 | chr7 | 99008671 | ||||||
| chr7:99008678
|
G | T | 1 | a0001c0001t0002g0250 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.10938+117G>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 70/72 | chr7 | 99008678 | ||||||
| chr7:99008783
|
G | A | 25 | a0001c0002t0002g0016a0001c0002t0002g0017a0001c0002t0002g0165others(22): Show | 26 | HG01081.hp1 HG01243.hp1 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.10938+222G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 70/72 | chr7 | 99008783 | ||||||
| chr7:99008840
|
C | T | 3 | a0001c0001t0001g0129a0001c0001t0001g0149a0001c0001t0001g0153 | 3 | HG03209.hp2 HG03579.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.10938+279C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 70/72 | chr7 | 99008840 | ||||||
| chr7:99008885
|
A | G | 1 | a0001c0025t0001g0151 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.10938+324A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 70/72 | chr7 | 99008885 | ||||||
| chr7:99008900
|
C | G | 43 | a0001c0001t0002g0080a0001c0001t0005g0158a0001c0001t0005g0160others(40): Show | 44 | HG01081.hp1 HG01243.hp1 HG01257.hp2 others(41): Show |
intron_variant | MODIFIER | c.10938+339C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 70/72 | chr7 | 99008900 | ||||||
| chr7:99009006
|
T | C | 1 | a0001c0001t0001g0069 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.10938+445T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 70/72 | chr7 | 99009006 | ||||||
| chr7:99009031
|
T | C | 1 | a0001c0002t0002g0182 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.10938+470T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 70/72 | chr7 | 99009031 | ||||||
| chr7:99009032
|
C | T | 1 | a0001c0002t0002g0182 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.10938+471C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 70/72 | chr7 | 99009032 | ||||||
| chr7:99009300
|
C | T | 5 | a0001c0004t0002g0002a0001c0004t0002g0169a0001c0004t0002g0170others(2): Show | 6 | HG02257.hp1 HG02647.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.10938+739C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 70/72 | chr7 | 99009300 | ||||||
| chr7:99009371
|
G | C | 2 | a0002c0008t0008g0192a0002c0008t0008g0193 | 2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.10938+810G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 70/72 | chr7 | 99009371 | ||||||
| chr7:99009747
|
G | A | 61 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0154others(58): Show | 62 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.10938+1186G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 70/72 | chr7 | 99009747 | ||||||
| chr7:99009880
|
C | CT | 12 | a0001c0001t0001g0047a0001c0001t0001g0052a0001c0001t0001g0057others(9): Show | 12 | HG00558.hp2 HG01261.hp2 HG02083.hp1 others(9): Show |
intron_variant | MODIFIER | c.10939-1147dupT | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 70/72 | INFO_REALIGN_3_PRIME | chr7 | 99009880 | |||||
| chr7:99009880
|
CT | C | 27 | a0001c0001t0001g0049a0001c0001t0001g0060a0001c0001t0001g0065others(24): Show | 27 | HG01884.hp2 HG01975.hp2 HG02451.hp1 others(24): Show |
intron_variant | MODIFIER | c.10939-1147delT | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 70/72 | INFO_REALIGN_3_PRIME | chr7 | 99009880 | |||||
| chr7:99009880
|
CTT | C | 87 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0195others(84): Show | 89 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.10939-1148_10939-1 others(8): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 70/72 | INFO_REALIGN_3_PRIME | chr7 | 99009880 | |||||
| chr7:99009880
|
CTTT | C | 7 | a0001c0001t0002g0197a0001c0001t0002g0228a0001c0001t0002g0229others(4): Show | 7 | HG01099.hp2 HG01943.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.10939-1149_10939-1 others(9): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 70/72 | INFO_REALIGN_3_PRIME | chr7 | 99009880 | |||||
| chr7:99009882
|
T | C | 1 | a0001c0001t0001g0013 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.10939-1170T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 70/72 | chr7 | 99009882 | ||||||
| chr7:99009905
|
T | A | 5 | a0001c0006t0002g0082a0001c0006t0002g0083a0001c0006t0002g0084others(2): Show | 5 | HG02559.hp1 HG02647.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.10939-1147T>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 70/72 | chr7 | 99009905 | ||||||
| chr7:99009964
|
C | T | 3 | a0001c0002t0007g0155a0001c0002t0007g0156a0001c0002t0007g0157 | 3 | HG00140.hp2 HG01243.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.10939-1088C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 70/72 | chr7 | 99009964 | ||||||
| chr7:99010108
|
G | C | 6 | a0001c0005t0004g0004a0001c0005t0004g0005a0001c0005t0004g0006others(3): Show | 6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.10939-944G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 70/72 | chr7 | 99010108 | ||||||
| chr7:99010281
|
T | C | 1 | a0001c0001t0003g0024 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.10939-771T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 70/72 | chr7 | 99010281 | ||||||
| chr7:99010330
|
C | G | 1 | a0001c0023t0002g0202 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.10939-722C>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 70/72 | chr7 | 99010330 | ||||||
| chr7:99010423
|
G | A | 2 | a0001c0001t0001g0090a0001c0001t0001g0147 | 2 | HG02109.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.10939-629G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 70/72 | chr7 | 99010423 | ||||||
| chr7:99010436
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.10939-616G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 70/72 | chr7 | 99010436 | ||||||
| chr7:99010579
|
A | G | 7 | a0001c0002t0002g0016a0001c0002t0002g0017a0001c0002t0002g0167others(4): Show | 7 | HG01243.hp1 HG01884.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.10939-473A>G | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 70/72 | chr7 | 99010579 | ||||||
| chr7:99010581
|
GAGTCTCT others(12): Show |
G | 3 | a0001c0002t0007g0155a0001c0002t0007g0156a0001c0002t0007g0157 | 3 | HG00140.hp2 HG01243.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.10939-463_10939-44 others(23): Show |
TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 70/72 | INFO_REALIGN_3_PRIME | chr7 | 99010581 | |||||
| chr7:99010609
|
G | A | 2 | a0001c0001t0001g0108a0001c0001t0001g0113 | 2 | HG00544.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.10939-443G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 70/72 | chr7 | 99010609 | ||||||
| chr7:99010697
|
G | A | 6 | a0001c0005t0004g0004a0001c0005t0004g0005a0001c0005t0004g0006others(3): Show | 6 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.10939-355G>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 70/72 | chr7 | 99010697 | ||||||
| chr7:99010862
|
C | T | 1 | a0001c0019t0001g0127 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.10939-190C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 70/72 | chr7 | 99010862 | ||||||
| chr7:99010892
|
C | T | 1 | a0001c0001t0001g0073 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.10939-160C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 70/72 | chr7 | 99010892 | ||||||
| chr7:99010982
|
T | C | 1 | a0001c0002t0002g0166 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.10939-70T>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 70/72 | chr7 | 99010982 | ||||||
| chr7:99010983
|
T | A | 45 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0027others(42): Show | 46 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.10939-69T>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 70/72 | chr7 | 99010983 | ||||||
| chr7:99011288
|
C | T | 1 | a0001c0001t0001g0116 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.11142+33C>T | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 71/72 | chr7 | 99011288 | ||||||
| chr7:99011952
|
T | A | 3 | a0001c0002t0007g0155a0001c0002t0007g0156a0001c0002t0007g0157 | 3 | HG00140.hp2 HG01243.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.11338-119T>A | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 72/72 | chr7 | 99011952 | ||||||
| chr7:99012048
|
G | C | 1 | a0001c0001t0002g0247 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.11338-23G>C | TRRAP | ENSG00000196367.15 | transcript | ENST00000456197.2 | protein_coding | 72/72 | chr7 | 99012048 |