| geneid | 7874 |
|---|---|
| ensemblid | ENSG00000187555.17 |
| hgncid | 12630 |
| symbol | USP7 |
| name | ubiquitin specific peptidase 7 |
| refseq_nuc | NM_003470.3 |
| refseq_prot | NP_003461.2 |
| ensembl_nuc | ENST00000344836.9 |
| ensembl_prot | ENSP00000343535.4 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 8892097 |
| end | 8963906 |
| strand | - |
| ver | v1.2 |
| region | chr16:8892097-8963906 |
| region5000 | chr16:8887097-8968906 |
| regionname0 | USP7_chr16_8892097_8963906 |
| regionname5000 | USP7_chr16_8887097_8968906 |
| 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 | 1102 | 336 | 90 | 62 | 139 | 8 | 35 | 99 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| a0002 | 0/0 | 1102 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| a0003 | 0/0 | 1102 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| 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 | 3309 | 322 | 87 | 53 | 137 | 8 | 35 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| c0002 | 0/0 | 3309 | 10 | 0 | 8 | 2 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| c0003 | 0/0 | 3309 | 2 | 1 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| c0004 | 0/0 | 3309 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| c0005 | 0/0 | 3309 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| c0006 | 0/0 | 3309 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| c0007 | 0/0 | 3309 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| 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 | 0/0 | 2521 | 134 | 27 | 31 | 57 | 3 | 16 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| t0002 | 0/0 | 2525 | 96 | 19 | 15 | 49 | 1 | 12 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| t0003 | 0/0 | 2522 | 22 | 3 | 2 | 14 | 0 | 3 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| t0004 | 0/0 | 2526 | 16 | 7 | 4 | 4 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| t0005 | 0/0 | 2524 | 9 | 4 | 1 | 4 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| t0006 | 1/0 | 2523 | 7 | 6 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| t0007 | 0/0 | 2523 | 7 | 0 | 3 | 2 | 1 | 1 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| t0008 | 0/0 | 2524 | 5 | 3 | 0 | 0 | 2 | 0 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| t0009 | 0/0 | 2518 | 4 | 3 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| t0010 | 0/0 | 2525 | 3 | 0 | 3 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| t0011 | 0/0 | 2521 | 2 | 0 | 0 | 2 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| t0012 | 0/0 | 2523 | 2 | 2 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| t0013 | 0/0 | 2525 | 2 | 0 | 2 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| t0014 | 0/0 | 2523 | 2 | 2 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| t0015 | 0/1 | 2525 | 2 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| t0016 | 0/0 | 2525 | 2 | 0 | 0 | 0 | 0 | 2 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| t0017 | 0/0 | 2521 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| t0018 | 0/0 | 2522 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| t0019 | 0/0 | 2526 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| t0020 | 0/0 | 2521 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| t0021 | 0/0 | 2521 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| t0022 | 0/0 | 2523 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| t0023 | 0/0 | 2523 | 1 | 0 | 0 | 0 | 1 | 0 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| t0024 | 0/0 | 2525 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| t0025 | 0/0 | 2526 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| t0026 | 0/0 | 2526 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| t0027 | 0/0 | 2526 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| t0028 | 0/0 | 2521 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| t0029 | 0/0 | 2521 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| t0030 | 0/0 | 2521 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| t0031 | 0/0 | 2526 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| t0032 | 0/0 | 2526 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| t0033 | 0/0 | 2524 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| t0034 | 0/0 | 2527 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| t0035 | 0/0 | 2528 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| t0036 | 0/0 | 2525 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| t0037 | 0/0 | 2526 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| t0038 | 0/0 | 2521 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| t0039 | 0/0 | 2521 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0003 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0013 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0318 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0320 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0327 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| 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 | 3309 | 322 | 87 | 53 | 137 | 8 | 35 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| a0001c0002 | 0/0 | 3309 | 10 | 0 | 8 | 2 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| a0001c0003 | 0/0 | 3309 | 2 | 1 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| a0001c0005 | 0/0 | 3309 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| a0001c0006 | 0/0 | 3309 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| a0002c0004 | 0/0 | 3309 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| a0003c0007 | 0/0 | 3309 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5829 | 122 | 26 | 22 | 55 | 3 | 16 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| a0001c0001t0002 | 0/0 | 5833 | 95 | 18 | 15 | 49 | 1 | 12 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| a0001c0001t0003 | 0/0 | 5830 | 21 | 3 | 2 | 14 | 0 | 2 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| a0001c0001t0004 | 0/0 | 5834 | 15 | 6 | 4 | 4 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| a0001c0001t0005 | 0/0 | 5832 | 9 | 4 | 1 | 4 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| a0001c0001t0006 | 1/0 | 5831 | 7 | 6 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| a0001c0001t0007 | 0/0 | 5831 | 7 | 0 | 3 | 2 | 1 | 1 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| a0001c0001t0008 | 0/0 | 5832 | 5 | 3 | 0 | 0 | 2 | 0 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| a0001c0001t0009 | 0/0 | 5826 | 4 | 3 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| a0001c0001t0010 | 0/0 | 5833 | 3 | 0 | 3 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| a0001c0001t0011 | 0/0 | 5829 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| a0001c0001t0012 | 0/0 | 5831 | 2 | 2 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| a0001c0001t0013 | 0/0 | 5833 | 2 | 0 | 2 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| a0001c0001t0014 | 0/0 | 5831 | 2 | 2 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| a0001c0001t0015 | 0/1 | 5833 | 2 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| a0001c0001t0016 | 0/0 | 5833 | 2 | 0 | 0 | 0 | 0 | 2 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| a0001c0001t0017 | 0/0 | 5829 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| a0001c0001t0018 | 0/0 | 5830 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| a0001c0001t0019 | 0/0 | 5834 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| a0001c0001t0020 | 0/0 | 5829 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| a0001c0001t0021 | 0/0 | 5829 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| a0001c0001t0022 | 0/0 | 5831 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| a0001c0001t0023 | 0/0 | 5831 | 1 | 0 | 0 | 0 | 1 | 0 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| a0001c0001t0024 | 0/0 | 5833 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| a0001c0001t0025 | 0/0 | 5834 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| a0001c0001t0026 | 0/0 | 5834 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| a0001c0001t0027 | 0/0 | 5834 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| a0001c0001t0028 | 0/0 | 5829 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| a0001c0001t0029 | 0/0 | 5829 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| a0001c0001t0030 | 0/0 | 5829 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| a0001c0001t0031 | 0/0 | 5834 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| a0001c0001t0032 | 0/0 | 5834 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| a0001c0001t0033 | 0/0 | 5832 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| a0001c0001t0034 | 0/0 | 5835 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| a0001c0001t0035 | 0/0 | 5836 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| a0001c0001t0036 | 0/0 | 5833 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| a0001c0001t0037 | 0/0 | 5834 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| a0001c0001t0038 | 0/0 | 5829 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| a0001c0001t0039 | 0/0 | 5829 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| a0001c0002t0001 | 0/0 | 5829 | 10 | 0 | 8 | 2 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| a0001c0003t0001 | 0/0 | 5829 | 2 | 1 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| a0001c0005t0002 | 0/0 | 5833 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| a0001c0006t0004 | 0/0 | 5834 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| a0002c0004t0011 | 0/0 | 5829 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| a0003c0007t0003 | 0/0 | 5830 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | copy fasta | chr16 | 8887097 | 8968906 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0003g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0003g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0003g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0003g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0003g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0003g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0003g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0003g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0003g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0003g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0003g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0004g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0004g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0004g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0004g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0004g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0004g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0004g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0004g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0004g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0004g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0004g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0004g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0004g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0004g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0005g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0005g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0005g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0005g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0005g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0005g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0005g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0005g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0005g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0006g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0006g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0006g0013 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0006g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0006g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0006g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0007g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0007g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0007g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0007g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0007g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0007g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0008g0320 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0008g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0008g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0008g0327 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0008g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0009g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0009g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0009g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0009g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0010g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0010g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0010g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0011g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0012g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0012g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0013g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0013g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0014g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0014g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0015g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0015g0318 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0016g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0016g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0017g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0018g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0019g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0020g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0021g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0022g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0023g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0024g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0025g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0026g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0027g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0028g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0029g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0030g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0031g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0032g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0033g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0034g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0035g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0036g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0037g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0038g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0039g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0002t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0002t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0002t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0002t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0002t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0003t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0003t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0005t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0006t0004g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0002c0004t0011g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0003c0007t0003g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0008 | g0320 | EUR | GBR | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG00140 | hp2 | a0001 | c0001 | t0023 | g0050 | EUR | GBR | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG00280 | hp1 | a0001 | c0001 | t0007 | g0033 | EUR | FIN | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0242 | EUR | FIN | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0218 | EUR | FIN | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0134 | EUR | FIN | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | CHS | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | CHS | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0282 | EAS | CHS | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | CHS | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | CHS | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | CHS | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | CHS | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | CHS | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0200 | EAS | CHS | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | CHS | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | CHS | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | CHS | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0241 | AMR | PUR | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG00642 | hp2 | a0001 | c0001 | t0007 | g0049 | AMR | PUR | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG00733 | hp1 | a0001 | c0001 | t0003 | g0121 | AMR | PUR | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0300 | AMR | PUR | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01070 | hp1 | a0001 | c0003 | t0001 | g0153 | AMR | PUR | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01070 | hp2 | a0001 | c0001 | t0013 | g0258 | AMR | PUR | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0255 | AMR | PUR | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01071 | hp2 | a0001 | c0001 | t0013 | g0257 | AMR | PUR | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0119 | AMR | PUR | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01099 | hp1 | a0001 | c0001 | t0010 | g0236 | AMR | PUR | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0136 | AMR | PUR | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01106 | hp1 | a0001 | c0001 | t0007 | g0002 | AMR | PUR | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01106 | hp2 | a0001 | c0001 | t0010 | g0280 | AMR | PUR | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01109 | hp1 | a0001 | c0001 | t0007 | g0002 | AMR | PUR | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0254 | AMR | PUR | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01167 | hp1 | a0001 | c0001 | t0005 | g0261 | AMR | PUR | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01169 | hp2 | a0001 | c0001 | t0004 | g0235 | AMR | PUR | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0138 | AMR | PUR | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0077 | AMR | PUR | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0246 | AMR | PUR | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0201 | AMR | CLM | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | CLM | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01257 | hp1 | a0001 | c0001 | t0004 | g0006 | AMR | CLM | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | CLM | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | CLM | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01258 | hp2 | a0001 | c0001 | t0004 | g0006 | AMR | CLM | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01261 | hp1 | a0001 | c0002 | t0001 | g0227 | AMR | CLM | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0298 | AMR | CLM | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | CLM | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0268 | AMR | CLM | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | CLM | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | CLM | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01433 | hp1 | a0001 | c0001 | t0004 | g0304 | AMR | CLM | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | CLM | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01496 | hp1 | a0001 | c0001 | t0015 | g0317 | AMR | CLM | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01496 | hp2 | a0001 | c0001 | t0010 | g0234 | AMR | CLM | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0208 | EUR | IBS | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01515 | hp2 | a0001 | c0001 | t0008 | g0327 | EUR | IBS | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0249 | AFR | ACB | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01884 | hp2 | a0001 | c0001 | t0009 | g0010 | AFR | ACB | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01891 | hp1 | a0001 | c0001 | t0020 | g0064 | AFR | ACB | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01891 | hp2 | a0001 | c0001 | t0004 | g0162 | AFR | ACB | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0191 | AMR | PEL | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0239 | AMR | PEL | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0061 | AMR | PEL | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PEL | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0302 | AMR | PEL | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01981 | hp2 | a0001 | c0002 | t0001 | g0118 | AMR | PEL | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0194 | AMR | PEL | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PEL | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | KHV | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0284 | EAS | KHV | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | KHV | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0226 | EAS | KHV | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | ACB | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | ACB | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | KHV | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | KHV | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | KHV | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | KHV | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | KHV | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0264 | EAS | KHV | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02129 | hp1 | a0001 | c0001 | t0030 | g0151 | EAS | KHV | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0270 | EAS | KHV | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02132 | hp1 | a0001 | c0001 | t0005 | g0027 | EAS | KHV | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | KHV | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | KHV | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | KHV | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02145 | hp1 | a0001 | c0005 | t0002 | g0176 | AFR | ACB | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | ACB | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | CDX | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | CDX | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0313 | EAS | CDX | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | CDX | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | ACB | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02257 | hp2 | a0001 | c0001 | t0008 | g0326 | AFR | ACB | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02273 | hp1 | a0001 | c0002 | t0001 | g0137 | AMR | PEL | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02273 | hp2 | a0001 | c0002 | t0001 | g0131 | AMR | PEL | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0215 | AFR | ACB | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02280 | hp2 | a0001 | c0001 | t0018 | g0015 | AFR | ACB | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02293 | hp1 | a0001 | c0002 | t0001 | g0135 | AMR | PEL | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0272 | AMR | PEL | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02300 | hp1 | a0001 | c0002 | t0001 | g0091 | AMR | PEL | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PEL | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02451 | hp1 | a0001 | c0001 | t0005 | g0120 | AFR | ACB | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02451 | hp2 | a0001 | c0001 | t0005 | g0287 | AFR | ACB | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0281 | SAS | PJL | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0184 | AFR | GWD | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0072 | AFR | GWD | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | GWD | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0238 | AFR | GWD | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | GWD | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0232 | SAS | PJL | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0247 | AFR | GWD | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02735 | hp1 | a0001 | c0001 | t0016 | g0323 | SAS | PJL | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02738 | hp1 | a0001 | c0001 | t0026 | g0228 | SAS | PJL | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02738 | hp2 | a0001 | c0001 | t0004 | g0285 | SAS | PJL | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02809 | hp2 | a0001 | c0001 | t0006 | g0012 | AFR | GWD | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0182 | AFR | GWD | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02886 | hp1 | a0001 | c0001 | t0014 | g0059 | AFR | GWD | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02895 | hp1 | a0001 | c0001 | t0006 | g0014 | AFR | GWD | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02896 | hp1 | a0001 | c0001 | t0034 | g0319 | AFR | GWD | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | GWD | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02922 | hp1 | a0001 | c0006 | t0004 | g0173 | AFR | ESN | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | ESN | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02965 | hp1 | a0001 | c0001 | t0004 | g0113 | AFR | ESN | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02965 | hp2 | a0001 | c0001 | t0008 | g0325 | AFR | ESN | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0312 | AFR | ESN | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02970 | hp2 | a0001 | c0001 | t0009 | g0011 | AFR | ESN | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0112 | AFR | ESN | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | ESN | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0046 | AFR | GWD | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0183 | AFR | GWD | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | MSL | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | MSL | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG03130 | hp1 | a0001 | c0001 | t0014 | g0058 | AFR | ESN | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | ESN | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG03139 | hp1 | a0001 | c0001 | t0029 | g0021 | AFR | ESN | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG03139 | hp2 | a0001 | c0001 | t0009 | g0009 | AFR | ESN | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0250 | AFR | ESN | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG03195 | hp2 | a0001 | c0001 | t0033 | g0322 | AFR | ESN | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0115 | AFR | MSL | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG03209 | hp2 | a0001 | c0001 | t0006 | g0001 | AFR | MSL | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | MSL | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0243 | AFR | MSL | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG03453 | hp1 | a0001 | c0001 | t0025 | g0056 | AFR | MSL | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG03453 | hp2 | a0001 | c0001 | t0032 | g0055 | AFR | MSL | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG03486 | hp1 | a0001 | c0001 | t0004 | g0071 | AFR | MSL | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0035 | AFR | MSL | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG03516 | hp1 | a0001 | c0001 | t0028 | g0168 | AFR | ESN | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG03516 | hp2 | a0001 | c0001 | t0024 | g0060 | AFR | ESN | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG03540 | hp1 | a0001 | c0001 | t0006 | g0001 | AFR | GWD | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG03540 | hp2 | a0001 | c0001 | t0008 | g0328 | AFR | GWD | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG03579 | hp1 | a0001 | c0001 | t0037 | g0330 | AFR | MSL | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG03579 | hp2 | a0001 | c0001 | t0012 | g0028 | AFR | MSL | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0231 | SAS | PJL | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0233 | SAS | PJL | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0262 | SAS | PJL | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0152 | SAS | STU | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0089 | SAS | STU | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0202 | SAS | PJL | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0230 | SAS | PJL | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0305 | SAS | PJL | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG03710 | hp2 | a0001 | c0001 | t0007 | g0051 | SAS | PJL | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | BEB | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0296 | SAS | BEB | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0198 | SAS | BEB | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG03834 | hp2 | a0003 | c0007 | t0003 | g0034 | SAS | BEB | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | BEB | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0192 | SAS | BEB | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | BEB | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0199 | SAS | BEB | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0081 | SAS | BEB | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0229 | SAS | BEB | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0179 | SAS | STU | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG04228 | hp2 | a0001 | c0001 | t0016 | g0324 | SAS | STU | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18522 | hp1 | a0001 | c0001 | t0027 | g0169 | AFR | YRI | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0069 | AFR | YRI | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18612 | hp1 | a0001 | c0001 | t0038 | g0331 | EAS | CHB | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | CHB | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18747 | hp1 | a0001 | c0001 | t0005 | g0245 | EAS | CHB | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0273 | EAS | CHB | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18906 | hp1 | a0001 | c0001 | t0012 | g0057 | AFR | YRI | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18906 | hp2 | a0001 | c0001 | t0019 | g0289 | AFR | YRI | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18941 | hp2 | a0001 | c0001 | t0007 | g0038 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18947 | hp1 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18948 | hp1 | a0001 | c0001 | t0036 | g0329 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18950 | hp1 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18971 | hp2 | a0001 | c0001 | t0005 | g0263 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0303 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18972 | hp2 | a0001 | c0001 | t0003 | g0297 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0256 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18973 | hp2 | a0001 | c0001 | t0004 | g0092 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18977 | hp2 | a0001 | c0001 | t0035 | g0321 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18980 | hp1 | a0001 | c0001 | t0011 | g0108 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18981 | hp2 | a0001 | c0001 | t0003 | g0039 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18983 | hp2 | a0001 | c0001 | t0004 | g0259 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18988 | hp2 | a0001 | c0001 | t0003 | g0292 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18994 | hp2 | a0001 | c0001 | t0003 | g0314 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19001 | hp2 | a0001 | c0001 | t0007 | g0042 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19002 | hp1 | a0001 | c0002 | t0001 | g0141 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19003 | hp2 | a0001 | c0001 | t0004 | g0301 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19004 | hp1 | a0001 | c0001 | t0039 | g0332 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19006 | hp1 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19006 | hp2 | a0001 | c0001 | t0009 | g0008 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0283 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19012 | hp1 | a0001 | c0001 | t0003 | g0315 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19030 | hp1 | a0001 | c0001 | t0004 | g0054 | AFR | LWK | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19030 | hp2 | a0001 | c0001 | t0004 | g0114 | AFR | LWK | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19043 | hp1 | a0001 | c0001 | t0006 | g0016 | AFR | LWK | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19043 | hp2 | a0001 | c0001 | t0005 | g0288 | AFR | LWK | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0279 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19064 | hp1 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0310 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19079 | hp2 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19081 | hp1 | a0001 | c0001 | t0021 | g0140 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19081 | hp2 | a0001 | c0001 | t0003 | g0316 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19082 | hp1 | a0001 | c0001 | t0005 | g0271 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19084 | hp1 | a0002 | c0004 | t0011 | g0018 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19087 | hp1 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19088 | hp2 | a0001 | c0002 | t0001 | g0132 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0311 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19091 | hp2 | a0001 | c0001 | t0004 | g0240 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0244 | AFR | YRI | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | YRI | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA20129 | hp1 | a0001 | c0001 | t0006 | g0017 | AFR | ASW | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | ASW | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0253 | AFR | ACB | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0070 | AFR | ACB | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | ACB | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | ACB | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0186 | AFR | ACB | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG03471 | hp1 | a0001 | c0001 | t0004 | g0024 | AFR | MSL | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0251 | AFR | MSL | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18955 | hp2 | a0001 | c0001 | t0017 | g0007 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA20300 | hp1 | a0001 | c0001 | t0031 | g0044 | AFR | USA | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA20300 | hp2 | a0001 | c0003 | t0001 | g0154 | AFR | USA | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA21309 | hp1 | a0001 | c0001 | t0022 | g0053 | AFR | LWK | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA21309 | hp2 | a0001 | c0001 | t0005 | g0052 | AFR | LWK | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0015 | g0318 | REF | REF | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0006 | g0013 | REF | REF | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:8923410
|
G | C | 1 | a0003 | 1 | HG03834.hp2 | missense_variant | MODERATE | c.188C>G | p.Thr63Ser | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 3/31 | 809/5831 | 188/3309 | 63/1102 | chr16 | 8923410 | ||
| chr16:8963274
|
C | G | 1 | a0002 | 1 | NA19084.hp1 | missense_variant | MODERATE | c.12G>C | p.Gln4His | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/31 | 633/5831 | 12/3309 | 4/1102 | chr16 | 8963274 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:8894835
|
C | G | 1 | a0001c0003 | 2 | HG01070.hp1 NA20300.hp2 |
synonymous_variant | LOW | c.3060G>C | p.Val1020Val | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 29/31 | 3681/5831 | 3060/3309 | 1020/1102 | chr16 | 8894835 | ||
| chr16:8900559
|
T | C | 1 | a0001c0005 | 1 | HG02145.hp1 | synonymous_variant | LOW | c.2280A>G | p.Leu760Leu | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 21/31 | 2901/5831 | 2280/3309 | 760/1102 | chr16 | 8900559 | ||
| chr16:8905281
|
T | C | 1 | a0001c0002 | 10 | HG01099.hp2 HG01261.hp1 HG01934.hp2 others(7): Show |
synonymous_variant | LOW | c.1479A>G | p.Ala493Ala | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 14/31 | 2100/5831 | 1479/3309 | 493/1102 | chr16 | 8905281 | ||
| chr16:8906447
|
T | C | 1 | a0001c0006 | 1 | HG02922.hp1 | synonymous_variant | LOW | c.1407A>G | p.Leu469Leu | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 13/31 | 2028/5831 | 1407/3309 | 469/1102 | chr16 | 8906447 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:8892248
|
T | C | 1 | a0001c0001t0022 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1750A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 31/31 | 1750 | chr16 | 8892248 | |||||
| chr16:8892253
|
C | T | 1 | a0001c0001t0021 | 1 | NA19081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1745G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 31/31 | 1745 | chr16 | 8892253 | |||||
| chr16:8892498
|
G | A | 1 | a0001c0001t0033 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1500C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 31/31 | 1500 | chr16 | 8892498 | |||||
| chr16:8892598
|
T | C | 1 | a0001c0001t0023 | 1 | HG00140.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1400A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 31/31 | 1400 | chr16 | 8892598 | |||||
| chr16:8892606
|
TA | T | 9 | a0001c0001t0002a0001c0001t0010a0001c0001t0013others(6): Show | 107 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(104): Show |
3_prime_UTR_variant | MODIFIER | c.*1391delT | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 31/31 | 1391 | chr16 | 8892606 | |||||
| chr16:8892606
|
TAA | T | 2 | a0001c0001t0005a0001c0001t0034 | 10 | HG01167.hp1 HG02132.hp1 HG02451.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1390_*1391delTT | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 31/31 | 1390 | chr16 | 8892606 | |||||
| chr16:8892606
|
TAAA | T | 5 | a0001c0001t0007a0001c0001t0012a0001c0001t0014others(2): Show | 13 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1389_*1391delTTT | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 31/31 | 1389 | chr16 | 8892606 | |||||
| chr16:8892606
|
TAAAA | T | 3 | a0001c0001t0003a0001c0001t0016a0003c0007t0003 | 24 | HG00733.hp1 HG01175.hp1 HG02165.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*1388_*1391delTTTT | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 31/31 | 1388 | chr16 | 8892606 | |||||
| chr16:8892606
|
TAAAAA | T | 16 | a0001c0001t0001a0001c0001t0008a0001c0001t0009others(13): Show | 154 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(151): Show |
3_prime_UTR_variant | MODIFIER | c.*1387_*1391delTTTT others(1): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 31/31 | 1387 | chr16 | 8892606 | |||||
| chr16:8892607
|
A | G | 1 | a0001c0001t0025 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1391T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 31/31 | 1391 | chr16 | 8892607 | |||||
| chr16:8892608
|
A | G | 1 | a0001c0001t0024 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1390T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 31/31 | 1390 | chr16 | 8892608 | |||||
| chr16:8892610
|
A | G | 2 | a0001c0001t0012a0001c0001t0014 | 4 | HG02886.hp1 HG03130.hp1 HG03579.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1388T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 31/31 | 1388 | chr16 | 8892610 | |||||
| chr16:8892658
|
G | A | 1 | a0001c0001t0026 | 1 | HG02738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1340C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 31/31 | 1340 | chr16 | 8892658 | |||||
| chr16:8892719
|
C | T | 1 | a0001c0001t0020 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1279G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 31/31 | 1279 | chr16 | 8892719 | |||||
| chr16:8892750
|
C | T | 2 | a0001c0001t0011a0002c0004t0011 | 2 | NA18980.hp1 NA19084.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1248G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 31/31 | 1248 | chr16 | 8892750 | |||||
| chr16:8892853
|
T | C | 2 | a0001c0001t0027a0001c0001t0037 | 2 | HG03579.hp1 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1145A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 31/31 | 1145 | chr16 | 8892853 | |||||
| chr16:8892879
|
T | C | 1 | a0001c0001t0028 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1119A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 31/31 | 1119 | chr16 | 8892879 | |||||
| chr16:8892908
|
T | C | 1 | a0001c0001t0013 | 2 | HG01070.hp2 HG01071.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1090A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 31/31 | 1090 | chr16 | 8892908 | |||||
| chr16:8892975
|
A | T | 1 | a0001c0001t0010 | 3 | HG01099.hp1 HG01106.hp2 HG01496.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1023T>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 31/31 | 1023 | chr16 | 8892975 | |||||
| chr16:8893265
|
T | G | 2 | a0001c0001t0014a0001c0001t0029 | 3 | HG02886.hp1 HG03130.hp1 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*733A>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 31/31 | 733 | chr16 | 8893265 | |||||
| chr16:8893321
|
T | G | 1 | a0001c0001t0030 | 1 | HG02129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*677A>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 31/31 | 677 | chr16 | 8893321 | |||||
| chr16:8893520
|
G | C | 1 | a0001c0001t0031 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*478C>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 31/31 | 478 | chr16 | 8893520 | |||||
| chr16:8893570
|
A | G | 1 | a0001c0001t0019 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*428T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 31/31 | 428 | chr16 | 8893570 | |||||
| chr16:8893733
|
T | C | 1 | a0001c0001t0032 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*265A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 31/31 | 265 | chr16 | 8893733 | |||||
| chr16:8963322
|
C | G | 1 | a0001c0001t0036 | 1 | NA18948.hp1 | 5_prime_UTR_variant | MODIFIER | c.-37G>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/31 | 37 | chr16 | 8963322 | |||||
| chr16:8963422
|
G | A | 1 | a0001c0001t0015 | 2 | HG01496.hp1 homoSapiens_chm13v2.hp1 |
5_prime_UTR_variant | MODIFIER | c.-137C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/31 | 137 | chr16 | 8963422 | |||||
| chr16:8963566
|
G | GGCC | 37 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(34): Show | 316 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(313): Show |
5_prime_UTR_variant | MODIFIER | c.-284_-282dupGGC | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/31 | 282 | chr16 | 8963566 | |||||
| chr16:8963566
|
G | GGCCGCC | 5 | a0001c0001t0008a0001c0001t0016a0001c0001t0033others(2): Show | 10 | HG00140.hp1 HG01515.hp2 HG02257.hp2 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-287_-282dupGGCGGC | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/31 | 282 | chr16 | 8963566 | |||||
| chr16:8963601
|
G | C | 1 | a0001c0001t0036 | 1 | NA18948.hp1 | 5_prime_UTR_variant | MODIFIER | c.-316C>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/31 | 316 | chr16 | 8963601 | |||||
| chr16:8963643
|
C | A | 1 | a0001c0001t0037 | 1 | HG03579.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-358G>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/31 | chr16 | 8963643 | ||||||
| chr16:8963662
|
G | A | 1 | a0001c0001t0038 | 1 | NA18612.hp1 | 5_prime_UTR_variant | MODIFIER | c.-377C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/31 | 377 | chr16 | 8963662 | |||||
| chr16:8963760
|
C | A | 1 | a0001c0001t0039 | 1 | NA19004.hp1 | 5_prime_UTR_variant | MODIFIER | c.-475G>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/31 | 475 | chr16 | 8963760 | |||||
| chr16:8963821
|
G | T | 1 | a0001c0001t0017 | 1 | NA18955.hp2 | 5_prime_UTR_variant | MODIFIER | c.-536C>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/31 | 536 | chr16 | 8963821 | |||||
| chr16:8963822
|
C | T | 1 | a0001c0001t0017 | 1 | NA18955.hp2 | 5_prime_UTR_variant | MODIFIER | c.-537G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/31 | 537 | chr16 | 8963822 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:8894161
|
C | T | 1 | a0001c0001t0031g0044 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.3203-57G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 30/30 | chr16 | 8894161 | ||||||
| chr16:8894239
|
C | G | 1 | a0001c0001t0005g0288 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3203-135G>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 30/30 | chr16 | 8894239 | ||||||
| chr16:8894278
|
C | A | 119 | a0001c0001t0001g0155a0001c0001t0001g0306a0001c0001t0002g0005others(116): Show | 121 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.3203-174G>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 30/30 | chr16 | 8894278 | ||||||
| chr16:8894326
|
C | T | 1 | a0001c0001t0027g0169 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3203-222G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 30/30 | chr16 | 8894326 | ||||||
| chr16:8894331
|
A | G | 128 | a0001c0001t0001g0155a0001c0001t0001g0306a0001c0001t0002g0005others(125): Show | 131 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.3202+219T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 30/30 | chr16 | 8894331 | ||||||
| chr16:8894381
|
C | T | 325 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(322): Show | 330 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.3202+169G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 30/30 | chr16 | 8894381 | ||||||
| chr16:8894382
|
C | A | 1 | a0001c0001t0022g0053 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3202+168G>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 30/30 | chr16 | 8894382 | ||||||
| chr16:8894418
|
C | T | 11 | a0001c0001t0001g0133a0001c0002t0001g0091a0001c0002t0001g0118others(8): Show | 11 | HG01099.hp2 HG01261.hp1 HG01934.hp2 others(8): Show |
intron_variant | MODIFIER | c.3202+132G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 30/30 | chr16 | 8894418 | ||||||
| chr16:8894529
|
C | CG | 145 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(142): Show | 147 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.3202+20dupC | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 30/30 | chr16 | 8894529 | ||||||
| chr16:8894529
|
CG | C | 121 | a0001c0001t0001g0306a0001c0001t0002g0005a0001c0001t0002g0061others(118): Show | 124 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.3202+20delC | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 30/30 | chr16 | 8894529 | ||||||
| chr16:8894721
|
G | A | 8 | a0001c0001t0002g0069a0001c0001t0002g0070a0001c0001t0002g0072others(5): Show | 8 | HG02451.hp1 HG02486.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.3111+63C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 29/30 | chr16 | 8894721 | ||||||
| chr16:8894726
|
G | A | 1 | a0001c0001t0002g0281 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.3111+58C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 29/30 | chr16 | 8894726 | ||||||
| chr16:8894869
|
G | A | 3 | a0001c0001t0025g0056a0001c0001t0027g0169a0001c0001t0037g0330 | 3 | HG03453.hp1 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.3040-14C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 28/30 | chr16 | 8894869 | ||||||
| chr16:8894911
|
G | A | 1 | a0001c0001t0001g0020 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3040-56C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 28/30 | chr16 | 8894911 | ||||||
| chr16:8894920
|
C | G | 102 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(99): Show | 104 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.3040-65G>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 28/30 | chr16 | 8894920 | ||||||
| chr16:8894955
|
C | T | 1 | a0001c0001t0003g0314 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.3039+76G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 28/30 | chr16 | 8894955 | ||||||
| chr16:8895190
|
G | C | 1 | a0001c0001t0002g0266 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.2920-40C>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 27/30 | chr16 | 8895190 | ||||||
| chr16:8895214
|
C | A | 1 | a0001c0001t0001g0063 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2920-64G>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 27/30 | chr16 | 8895214 | ||||||
| chr16:8895261
|
T | TA | 21 | a0001c0001t0001g0041a0001c0001t0001g0096a0001c0001t0001g0204others(18): Show | 21 | HG02132.hp1 HG02165.hp1 HG02970.hp1 others(18): Show |
intron_variant | MODIFIER | c.2920-112dupT | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 27/30 | chr16 | 8895261 | ||||||
| chr16:8895332
|
A | C | 1 | a0001c0001t0001g0290 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.2920-182T>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 27/30 | chr16 | 8895332 | ||||||
| chr16:8895431
|
C | A | 12 | a0001c0001t0001g0041a0001c0001t0003g0029a0001c0001t0003g0030others(9): Show | 12 | HG02132.hp1 NA18941.hp2 NA18947.hp1 others(9): Show |
intron_variant | MODIFIER | c.2919+211G>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 27/30 | chr16 | 8895431 | ||||||
| chr16:8895546
|
A | G | 325 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(322): Show | 330 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.2919+96T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 27/30 | chr16 | 8895546 | ||||||
| chr16:8895763
|
A | T | 1 | a0001c0001t0004g0162 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2820-22T>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 26/30 | chr16 | 8895763 | ||||||
| chr16:8895785
|
T | C | 1 | a0001c0001t0002g0282 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2820-44A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 26/30 | chr16 | 8895785 | ||||||
| chr16:8895839
|
GT | G | 48 | a0001c0001t0001g0041a0001c0001t0001g0068a0001c0001t0001g0074others(45): Show | 49 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.2820-99delA | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 26/30 | chr16 | 8895839 | ||||||
| chr16:8895839
|
GTT | G | 167 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(164): Show | 169 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.2820-100_2820-99de others(3): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 26/30 | chr16 | 8895839 | ||||||
| chr16:8895983
|
C | T | 1 | a0001c0001t0001g0171 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2820-242G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 26/30 | chr16 | 8895983 | ||||||
| chr16:8896091
|
G | A | 2 | a0001c0001t0001g0290a0001c0001t0002g0213 | 2 | NA18990.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.2820-350C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 26/30 | chr16 | 8896091 | ||||||
| chr16:8896137
|
C | CT | 8 | a0001c0001t0001g0004a0001c0001t0001g0073a0001c0001t0001g0090others(5): Show | 9 | HG00741.hp1 HG01361.hp1 HG02040.hp2 others(6): Show |
intron_variant | MODIFIER | c.2820-397dupA | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 26/30 | chr16 | 8896137 | ||||||
| chr16:8896137
|
C | CTT | 8 | a0001c0001t0001g0144a0001c0001t0003g0121a0001c0001t0007g0002others(5): Show | 9 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(6): Show |
intron_variant | MODIFIER | c.2820-398_2820-397d others(4): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 26/30 | chr16 | 8896137 | ||||||
| chr16:8896137
|
CT | C | 106 | a0001c0001t0001g0063a0001c0001t0001g0084a0001c0001t0001g0165others(103): Show | 108 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.2820-397delA | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 26/30 | chr16 | 8896137 | ||||||
| chr16:8896137
|
CTT | C | 16 | a0001c0001t0002g0184a0001c0001t0002g0186a0001c0001t0002g0246others(13): Show | 16 | HG01071.hp2 HG01243.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.2820-398_2820-397d others(4): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 26/30 | chr16 | 8896137 | ||||||
| chr16:8896189
|
A | G | 5 | a0001c0001t0012g0028a0001c0001t0012g0057a0001c0001t0014g0058others(2): Show | 5 | HG02886.hp1 HG03130.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.2820-448T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 26/30 | chr16 | 8896189 | ||||||
| chr16:8896363
|
G | A | 320 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(317): Show | 325 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.2820-622C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 26/30 | chr16 | 8896363 | ||||||
| chr16:8896382
|
T | C | 125 | a0001c0001t0001g0306a0001c0001t0002g0005a0001c0001t0002g0061others(122): Show | 128 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.2819+617A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 26/30 | chr16 | 8896382 | ||||||
| chr16:8896464
|
T | C | 3 | a0001c0001t0025g0056a0001c0001t0027g0169a0001c0001t0037g0330 | 3 | HG03453.hp1 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2819+535A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 26/30 | chr16 | 8896464 | ||||||
| chr16:8896484
|
C | A | 1 | a0001c0001t0001g0150 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.2819+515G>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 26/30 | chr16 | 8896484 | ||||||
| chr16:8896607
|
A | C | 1 | a0001c0001t0001g0309 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2819+392T>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 26/30 | chr16 | 8896607 | ||||||
| chr16:8896648
|
G | A | 325 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(322): Show | 330 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.2819+351C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 26/30 | chr16 | 8896648 | ||||||
| chr16:8896739
|
G | A | 1 | a0001c0001t0001g0156 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.2819+260C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 26/30 | chr16 | 8896739 | ||||||
| chr16:8896812
|
C | G | 2 | a0001c0001t0001g0065a0001c0001t0038g0331 | 2 | NA18612.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.2819+187G>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 26/30 | chr16 | 8896812 | ||||||
| chr16:8896823
|
C | A | 102 | a0001c0001t0001g0306a0001c0001t0002g0005a0001c0001t0002g0061others(99): Show | 104 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.2819+176G>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 26/30 | chr16 | 8896823 | ||||||
| chr16:8896862
|
T | C | 1 | a0001c0001t0009g0010 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2819+137A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 26/30 | chr16 | 8896862 | ||||||
| chr16:8896889
|
A | G | 1 | a0001c0001t0002g0035 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2819+110T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 26/30 | chr16 | 8896889 | ||||||
| chr16:8896928
|
G | A | 1 | a0001c0001t0008g0328 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2819+71C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 26/30 | chr16 | 8896928 | ||||||
| chr16:8896928
|
G | C | 1 | a0001c0001t0001g0155 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2819+71C>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 26/30 | chr16 | 8896928 | ||||||
| chr16:8897307
|
G | C | 1 | a0001c0001t0005g0052 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2719-208C>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897307 | ||||||
| chr16:8897333
|
G | A | 95 | a0001c0001t0001g0306a0001c0001t0002g0005a0001c0001t0002g0061others(92): Show | 97 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.2719-234C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897333 | ||||||
| chr16:8897363
|
C | G | 1 | a0001c0001t0003g0315 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.2719-264G>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897363 | ||||||
| chr16:8897697
|
A | AC | 4 | a0001c0001t0001g0093a0001c0001t0001g0150a0001c0001t0004g0092others(1): Show | 4 | HG00597.hp2 HG01258.hp1 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.2719-599dupG | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897697 | ||||||
| chr16:8897698
|
C | CCA | 27 | a0001c0001t0001g0020a0001c0001t0001g0032a0001c0001t0001g0045others(24): Show | 27 | HG00438.hp1 HG01081.hp2 HG01167.hp2 others(24): Show |
intron_variant | MODIFIER | c.2719-600_2719-599i others(4): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897698 | ||||||
| chr16:8897699
|
A | C | 143 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(140): Show | 145 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.2719-600T>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897699 | ||||||
| chr16:8897714
|
A | ATATATAT others(4): Show |
1 | a0001c0001t0016g0323 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2719-616_2719-615i others(13): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897714 | ||||||
| chr16:8897716
|
A | AATATATA others(3): Show |
2 | a0001c0001t0003g0202a0001c0001t0016g0324 | 2 | HG03704.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2719-618_2719-617i others(12): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897716 | ||||||
| chr16:8897716
|
A | T | 2 | a0001c0001t0008g0328a0001c0001t0016g0323 | 2 | HG02735.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2719-617T>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897716 | ||||||
| chr16:8897718
|
A | AATATATA others(5): Show |
1 | a0001c0001t0008g0325 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2719-620_2719-619i others(14): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897718 | ||||||
| chr16:8897718
|
A | T | 10 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0048others(7): Show | 10 | HG00140.hp1 HG01167.hp2 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.2719-619T>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897718 | ||||||
| chr16:8897720
|
A | AATAT | 14 | a0001c0001t0001g0109a0001c0001t0001g0123a0001c0001t0001g0147others(11): Show | 14 | HG00621.hp2 HG02015.hp1 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.2719-622_2719-621i others(6): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897720 | ||||||
| chr16:8897720
|
A | AATATATA others(3): Show |
1 | a0001c0001t0020g0064 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2719-622_2719-621i others(12): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897720 | ||||||
| chr16:8897720
|
A | ATAT | 5 | a0001c0001t0001g0086a0001c0001t0001g0128a0001c0001t0001g0129others(2): Show | 5 | HG02683.hp1 NA18612.hp1 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.2719-622_2719-621i others(5): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897720 | ||||||
| chr16:8897720
|
A | ATATAT | 4 | a0001c0001t0001g0106a0001c0001t0001g0170a0001c0002t0001g0137others(1): Show | 4 | HG02055.hp1 HG02273.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2719-622_2719-621i others(7): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897720 | ||||||
| chr16:8897720
|
A | T | 35 | a0001c0001t0001g0032a0001c0001t0001g0045a0001c0001t0001g0047others(32): Show | 35 | HG00140.hp1 HG00438.hp1 HG01081.hp2 others(32): Show |
intron_variant | MODIFIER | c.2719-621T>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897720 | ||||||
| chr16:8897722
|
A | AATACATA others(5): Show |
3 | a0001c0001t0007g0049a0001c0001t0007g0051a0001c0001t0023g0050 | 3 | HG00140.hp2 HG00642.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.2719-624_2719-623i others(14): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897722 | ||||||
| chr16:8897722
|
A | AATACATA others(7): Show |
1 | a0001c0001t0003g0121 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2719-624_2719-623i others(16): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897722 | ||||||
| chr16:8897722
|
A | AATAT | 7 | a0001c0001t0001g0080a0001c0001t0001g0088a0001c0001t0001g0097others(4): Show | 7 | HG03139.hp1 NA18947.hp2 NA18956.hp1 others(4): Show |
intron_variant | MODIFIER | c.2719-624_2719-623i others(6): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897722 | ||||||
| chr16:8897722
|
A | ATACATAT others(6): Show |
1 | a0003c0007t0003g0034 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2719-624_2719-623i others(15): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897722 | ||||||
| chr16:8897722
|
A | ATACATAT others(10): Show |
2 | a0001c0001t0007g0002a0001c0001t0007g0033 | 3 | HG00280.hp1 HG01106.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.2719-624_2719-623i others(19): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897722 | ||||||
| chr16:8897722
|
A | ATAT | 38 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(35): Show | 40 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(37): Show |
intron_variant | MODIFIER | c.2719-624_2719-623i others(5): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897722 | ||||||
| chr16:8897722
|
A | ATATAT | 13 | a0001c0001t0001g0101a0001c0001t0001g0117a0001c0001t0001g0300others(10): Show | 13 | HG00738.hp2 HG01099.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.2719-624_2719-623i others(7): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897722 | ||||||
| chr16:8897722
|
A | ATATATAT | 9 | a0001c0001t0001g0095a0001c0001t0001g0107a0001c0001t0001g0111others(6): Show | 9 | HG00733.hp2 HG01934.hp2 HG02165.hp2 others(6): Show |
intron_variant | MODIFIER | c.2719-624_2719-623i others(9): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897722 | ||||||
| chr16:8897722
|
A | ATATATAT others(4): Show |
2 | a0001c0001t0001g0214a0001c0001t0005g0288 | 2 | HG02132.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2719-624_2719-623i others(13): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897722 | ||||||
| chr16:8897722
|
A | T | 64 | a0001c0001t0001g0020a0001c0001t0001g0032a0001c0001t0001g0045others(61): Show | 64 | HG00140.hp1 HG00438.hp1 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.2719-623T>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897722 | ||||||
| chr16:8897723
|
AAAAATAT | A | 8 | a0001c0001t0001g0067a0001c0001t0001g0103a0001c0001t0001g0158others(5): Show | 8 | HG01361.hp2 HG02027.hp2 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.2718+630_2719-625d others(9): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897723 | ||||||
| chr16:8897724
|
A | ATAT | 5 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0298others(2): Show | 5 | HG01070.hp1 HG01257.hp2 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.2719-626_2719-625i others(5): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897724 | ||||||
| chr16:8897724
|
A | ATATATAT | 4 | a0001c0001t0001g0066a0001c0001t0001g0174a0001c0001t0004g0259others(1): Show | 4 | HG02135.hp1 HG03195.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.2719-626_2719-625i others(9): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897724 | ||||||
| chr16:8897724
|
A | T | 146 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(143): Show | 149 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.2719-625T>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897724 | ||||||
| chr16:8897726
|
A | AAAAAAAA others(39): Show |
1 | a0001c0001t0002g0072 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2719-628_2719-627i others(48): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897726 | ||||||
| chr16:8897726
|
A | AAAAAAAA others(34): Show |
1 | a0001c0001t0002g0115 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2719-628_2719-627i others(43): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897726 | ||||||
| chr16:8897726
|
A | AAAAAAAA others(16): Show |
1 | a0001c0001t0002g0182 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2719-628_2719-627i others(25): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897726 | ||||||
| chr16:8897726
|
A | AAAAAAAA others(27): Show |
1 | a0001c0001t0002g0069 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2719-628_2719-627i others(36): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897726 | ||||||
| chr16:8897726
|
A | AAAAAAAA others(19): Show |
1 | a0001c0001t0002g0183 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2719-628_2719-627i others(28): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897726 | ||||||
| chr16:8897726
|
A | AAAAAAAA others(29): Show |
1 | a0001c0001t0005g0120 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2719-628_2719-627i others(38): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897726 | ||||||
| chr16:8897726
|
A | AAAAAAAA others(12): Show |
1 | a0001c0001t0002g0116 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.2719-628_2719-627i others(21): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897726 | ||||||
| chr16:8897726
|
A | AAAAAAAA others(13): Show |
1 | a0001c0001t0002g0213 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.2719-628_2719-627i others(22): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897726 | ||||||
| chr16:8897726
|
A | AAAAAAAA others(13): Show |
1 | a0001c0001t0002g0303 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.2719-628_2719-627i others(22): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897726 | ||||||
| chr16:8897726
|
A | AAAAAAAA others(8): Show |
2 | a0001c0001t0002g0196a0001c0001t0002g0273 | 2 | NA18747.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.2719-628_2719-627i others(17): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897726 | ||||||
| chr16:8897726
|
A | AAAAAAAA others(7): Show |
1 | a0001c0001t0002g0286 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.2719-628_2719-627i others(16): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897726 | ||||||
| chr16:8897726
|
A | AAAAAAAA others(6): Show |
2 | a0001c0001t0002g0311a0001c0001t0010g0236 | 2 | HG01099.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.2719-628_2719-627i others(15): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897726 | ||||||
| chr16:8897726
|
A | AAAAAAAA others(8): Show |
2 | a0001c0001t0002g0272a0001c0001t0002g0283 | 2 | HG02293.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.2719-628_2719-627i others(17): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897726 | ||||||
| chr16:8897726
|
A | AAAAAAAA others(10): Show |
1 | a0001c0001t0002g0195 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.2719-628_2719-627i others(19): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897726 | ||||||
| chr16:8897726
|
A | AAAAAAAA others(5): Show |
4 | a0001c0001t0002g0191a0001c0001t0002g0268a0001c0001t0004g0006others(1): Show | 5 | HG01169.hp2 HG01257.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.2719-628_2719-627i others(14): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897726 | ||||||
| chr16:8897726
|
A | AAAAAAAA others(7): Show |
2 | a0001c0001t0002g0199a0001c0001t0002g0256 | 2 | HG03942.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.2719-628_2719-627i others(16): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897726 | ||||||
| chr16:8897726
|
A | AAAAAAAA others(9): Show |
2 | a0001c0001t0002g0185a0001c0001t0002g0278 | 2 | HG00597.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.2719-628_2719-627i others(18): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897726 | ||||||
| chr16:8897726
|
A | AAAAAAAA others(13): Show |
1 | a0001c0001t0003g0312 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2719-628_2719-627i others(22): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897726 | ||||||
| chr16:8897726
|
A | AAAAAAAA others(15): Show |
1 | a0001c0001t0003g0031 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.2719-628_2719-627i others(24): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897726 | ||||||
| chr16:8897726
|
A | AAAAAAAA others(17): Show |
1 | a0001c0001t0002g0070 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2719-628_2719-627i others(26): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897726 | ||||||
| chr16:8897726
|
A | AAAAAAAT others(4): Show |
6 | a0001c0001t0002g0163a0001c0001t0002g0193a0001c0001t0002g0241others(3): Show | 6 | HG00280.hp2 HG00438.hp2 HG00639.hp2 others(3): Show |
intron_variant | MODIFIER | c.2719-628_2719-627i others(13): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897726 | ||||||
| chr16:8897726
|
A | AAAAAAAT others(6): Show |
5 | a0001c0001t0001g0306a0001c0001t0002g0005a0001c0001t0002g0237others(2): Show | 6 | HG00423.hp1 HG00738.hp1 HG00741.hp2 others(3): Show |
intron_variant | MODIFIER | c.2719-628_2719-627i others(15): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897726 | ||||||
| chr16:8897726
|
A | AAAAAAAT others(8): Show |
4 | a0001c0001t0002g0149a0001c0001t0002g0164a0001c0001t0002g0275others(1): Show | 4 | HG00408.hp1 NA19004.hp2 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.2719-628_2719-627i others(17): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897726 | ||||||
| chr16:8897726
|
A | AAAAAAAT others(14): Show |
1 | a0001c0001t0001g0041 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2719-628_2719-627i others(23): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897726 | ||||||
| chr16:8897726
|
A | AAAAAATA others(3): Show |
3 | a0001c0001t0002g0226a0001c0001t0005g0261a0001c0001t0031g0044 | 3 | HG01167.hp1 HG02040.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2719-628_2719-627i others(12): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897726 | ||||||
| chr16:8897726
|
A | AAAAAATA others(5): Show |
14 | a0001c0001t0002g0100a0001c0001t0002g0189a0001c0001t0002g0190others(11): Show | 14 | HG01109.hp2 HG01993.hp1 HG02027.hp1 others(11): Show |
intron_variant | MODIFIER | c.2719-628_2719-627i others(14): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897726 | ||||||
| chr16:8897726
|
A | AAAAAATA others(7): Show |
3 | a0001c0001t0002g0255a0001c0001t0013g0257a0001c0001t0013g0258 | 3 | HG01070.hp2 HG01071.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.2719-628_2719-627i others(16): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897726 | ||||||
| chr16:8897726
|
A | AAAAAATA others(13): Show |
1 | a0001c0001t0007g0042 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.2719-628_2719-627i others(22): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897726 | ||||||
| chr16:8897726
|
A | AAAAAATA others(15): Show |
1 | a0001c0001t0003g0029 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.2719-628_2719-627i others(24): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897726 | ||||||
| chr16:8897726
|
A | AAAAAATA others(33): Show |
1 | a0001c0001t0002g0035 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2719-628_2719-627i others(42): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897726 | ||||||
| chr16:8897726
|
A | AAAAATAT others(4): Show |
15 | a0001c0001t0002g0098a0001c0001t0002g0152a0001c0001t0002g0179others(12): Show | 15 | HG00609.hp1 HG01106.hp2 HG01433.hp1 others(12): Show |
intron_variant | MODIFIER | c.2719-628_2719-627i others(13): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897726 | ||||||
| chr16:8897726
|
A | AAAAATAT others(6): Show |
4 | a0001c0001t0002g0188a0001c0001t0002g0197a0001c0001t0002g0302others(1): Show | 4 | HG01981.hp1 NA18980.hp2 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.2719-628_2719-627i others(15): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897726 | ||||||
| chr16:8897726
|
A | AAAAATAT others(8): Show |
2 | a0001c0001t0002g0248a0001c0001t0002g0277 | 2 | NA18975.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.2719-628_2719-627i others(17): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897726 | ||||||
| chr16:8897726
|
A | AAAAATAT others(10): Show |
1 | a0001c0001t0003g0316 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.2719-628_2719-627i others(19): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897726 | ||||||
| chr16:8897726
|
A | AAAAATAT others(12): Show |
4 | a0001c0001t0002g0186a0001c0001t0002g0253a0001c0001t0003g0036others(1): Show | 4 | HG02109.hp1 HG02559.hp2 NA18955.hp1 others(1): Show |
intron_variant | MODIFIER | c.2719-628_2719-627i others(21): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897726 | ||||||
| chr16:8897726
|
A | AAAAATAT others(16): Show |
1 | a0001c0001t0005g0027 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2719-628_2719-627i others(25): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897726 | ||||||
| chr16:8897726
|
A | AAAATATA others(3): Show |
1 | a0001c0001t0036g0329 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2719-628_2719-627i others(12): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897726 | ||||||
| chr16:8897726
|
A | AAAATATA others(5): Show |
3 | a0001c0001t0002g0201a0001c0001t0002g0229a0001c0001t0002g0266 | 3 | HG01255.hp1 HG04184.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.2719-628_2719-627i others(14): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897726 | ||||||
| chr16:8897726
|
A | AAAATATA others(7): Show |
1 | a0001c0001t0002g0247 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2719-628_2719-627i others(16): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897726 | ||||||
| chr16:8897726
|
A | AAAATATA others(11): Show |
3 | a0001c0001t0003g0030a0001c0001t0003g0040a0001c0001t0003g0313 | 3 | HG02165.hp1 NA18950.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.2719-628_2719-627i others(20): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897726 | ||||||
| chr16:8897726
|
A | AAAATATA others(13): Show |
1 | a0001c0001t0003g0037 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.2719-628_2719-627i others(22): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897726 | ||||||
| chr16:8897726
|
A | AAAATATA others(17): Show |
1 | a0001c0001t0003g0043 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.2719-628_2719-627i others(26): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897726 | ||||||
| chr16:8897726
|
A | AAAATATA others(21): Show |
1 | a0001c0001t0003g0046 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2719-628_2719-627i others(30): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897726 | ||||||
| chr16:8897726
|
A | AAATATAT others(4): Show |
8 | a0001c0001t0002g0076a0001c0001t0002g0119a0001c0001t0002g0139others(5): Show | 8 | HG01081.hp1 HG02056.hp1 HG02129.hp2 others(5): Show |
intron_variant | MODIFIER | c.2719-628_2719-627i others(13): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897726 | ||||||
| chr16:8897726
|
A | AAATATAT others(6): Show |
3 | a0001c0001t0002g0192a0001c0001t0004g0114a0001c0001t0005g0287 | 3 | HG02451.hp2 HG03927.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2719-628_2719-627i others(15): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897726 | ||||||
| chr16:8897726
|
A | AAATATAT others(8): Show |
2 | a0001c0001t0002g0251a0001c0001t0002g0274 | 2 | HG03471.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.2719-628_2719-627i others(17): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897726 | ||||||
| chr16:8897726
|
A | AAATATAT others(10): Show |
2 | a0001c0001t0003g0315a0001c0001t0007g0038 | 2 | NA18941.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.2719-628_2719-627i others(19): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897726 | ||||||
| chr16:8897726
|
A | AAATATAT others(14): Show |
2 | a0001c0001t0002g0243a0001c0001t0003g0314 | 2 | HG03225.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.2719-628_2719-627i others(23): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897726 | ||||||
| chr16:8897726
|
A | AAATATAT others(22): Show |
1 | a0001c0001t0004g0071 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2719-628_2719-627i others(31): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897726 | ||||||
| chr16:8897726
|
A | AAATATAT others(26): Show |
1 | a0001c0001t0002g0112 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2719-628_2719-627i others(35): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897726 | ||||||
| chr16:8897726
|
A | AATATATA others(3): Show |
2 | a0001c0001t0002g0232a0001c0005t0002g0176 | 2 | HG02145.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.2718+624_2719-628d others(12): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897726 | ||||||
| chr16:8897726
|
A | AATATATA others(5): Show |
1 | a0001c0001t0004g0113 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2718+622_2719-628d others(14): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897726 | ||||||
| chr16:8897726
|
A | AATATATA others(7): Show |
4 | a0001c0001t0002g0246a0001c0001t0002g0249a0001c0001t0002g0250others(1): Show | 4 | HG01243.hp2 HG01884.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2718+620_2719-628d others(16): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897726 | ||||||
| chr16:8897726
|
A | AATATATA others(9): Show |
1 | a0001c0001t0034g0319 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2718+618_2719-628d others(18): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897726 | ||||||
| chr16:8897726
|
A | ATATATAT others(10): Show |
1 | a0001c0001t0002g0184 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2719-628_2719-627i others(19): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897726 | ||||||
| chr16:8897726
|
A | T | 162 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(159): Show | 165 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.2719-627T>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897726 | ||||||
| chr16:8897728
|
T | A | 1 | a0001c0001t0006g0016 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2719-629A>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897728 | ||||||
| chr16:8897730
|
T | A | 1 | a0001c0001t0004g0162 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2718+630A>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897730 | ||||||
| chr16:8897732
|
T | A | 1 | a0001c0001t0004g0162 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2718+628A>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897732 | ||||||
| chr16:8897743
|
A | G | 1 | a0001c0001t0002g0035 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2718+617T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897743 | ||||||
| chr16:8897746
|
T | A | 2 | a0001c0001t0012g0057a0001c0001t0014g0058 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2718+614A>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897746 | ||||||
| chr16:8897746
|
T | TAA | 3 | a0001c0001t0012g0028a0001c0001t0014g0059a0001c0001t0024g0060 | 3 | HG02886.hp1 HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2718+612_2718+613d others(4): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897746 | ||||||
| chr16:8897789
|
C | T | 2 | a0001c0001t0002g0241a0001c0001t0002g0254 | 2 | HG00639.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.2718+571G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897789 | ||||||
| chr16:8897793
|
G | A | 1 | a0001c0001t0002g0191 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2718+567C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897793 | ||||||
| chr16:8897882
|
G | A | 5 | a0001c0001t0012g0028a0001c0001t0012g0057a0001c0001t0014g0058others(2): Show | 5 | HG02886.hp1 HG03130.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.2718+478C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8897882 | ||||||
| chr16:8898051
|
C | T | 1 | a0001c0001t0008g0325 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2718+309G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8898051 | ||||||
| chr16:8898272
|
G | A | 1 | a0001c0001t0002g0286 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.2718+88C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 25/30 | chr16 | 8898272 | ||||||
| chr16:8898485
|
G | A | 132 | a0001c0001t0001g0067a0001c0001t0001g0103a0001c0001t0001g0148others(129): Show | 135 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.2640+46C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 24/30 | chr16 | 8898485 | ||||||
| chr16:8898658
|
T | C | 1 | a0001c0001t0002g0035 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2532-19A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 23/30 | chr16 | 8898658 | ||||||
| chr16:8898682
|
G | A | 1 | a0001c0001t0002g0265 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.2532-43C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 23/30 | chr16 | 8898682 | ||||||
| chr16:8898695
|
T | C | 19 | a0001c0001t0001g0041a0001c0001t0003g0029a0001c0001t0003g0030others(16): Show | 19 | HG02132.hp1 HG02165.hp1 HG02970.hp1 others(16): Show |
intron_variant | MODIFIER | c.2532-56A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 23/30 | chr16 | 8898695 | ||||||
| chr16:8898913
|
C | T | 1 | a0001c0001t0001g0298 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2531+208G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 23/30 | chr16 | 8898913 | ||||||
| chr16:8898971
|
G | T | 130 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(127): Show | 132 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.2531+150C>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 23/30 | chr16 | 8898971 | ||||||
| chr16:8899011
|
A | C | 325 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(322): Show | 330 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.2531+110T>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 23/30 | chr16 | 8899011 | ||||||
| chr16:8899012
|
C | A | 325 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(322): Show | 330 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.2531+109G>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 23/30 | chr16 | 8899012 | ||||||
| chr16:8899081
|
T | G | 1 | a0001c0001t0031g0044 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2531+40A>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 23/30 | chr16 | 8899081 | ||||||
| chr16:8899229
|
T | C | 1 | a0001c0001t0001g0174 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.2464-41A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 22/30 | chr16 | 8899229 | ||||||
| chr16:8899891
|
G | A | 1 | a0001c0001t0001g0067 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2310-134C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 21/30 | chr16 | 8899891 | ||||||
| chr16:8899892
|
G | A | 1 | a0001c0001t0008g0326 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2310-135C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 21/30 | chr16 | 8899892 | ||||||
| chr16:8899929
|
G | A | 5 | a0001c0001t0012g0028a0001c0001t0012g0057a0001c0001t0014g0058others(2): Show | 5 | HG02886.hp1 HG03130.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.2310-172C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 21/30 | chr16 | 8899929 | ||||||
| chr16:8900008
|
C | A | 1 | a0001c0001t0001g0216 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2310-251G>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 21/30 | chr16 | 8900008 | ||||||
| chr16:8900035
|
T | A | 120 | a0001c0001t0001g0067a0001c0001t0001g0103a0001c0001t0001g0148others(117): Show | 122 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.2310-278A>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 21/30 | chr16 | 8900035 | ||||||
| chr16:8900117
|
T | G | 1 | a0001c0006t0004g0173 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2310-360A>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 21/30 | chr16 | 8900117 | ||||||
| chr16:8900335
|
G | C | 135 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(132): Show | 137 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.2309+195C>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 21/30 | chr16 | 8900335 | ||||||
| chr16:8900344
|
T | G | 5 | a0001c0001t0012g0028a0001c0001t0012g0057a0001c0001t0014g0058others(2): Show | 5 | HG02886.hp1 HG03130.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.2309+186A>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 21/30 | chr16 | 8900344 | ||||||
| chr16:8900368
|
C | A | 1 | a0001c0001t0002g0035 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2309+162G>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 21/30 | chr16 | 8900368 | ||||||
| chr16:8900406
|
T | C | 1 | a0001c0001t0002g0035 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2309+124A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 21/30 | chr16 | 8900406 | ||||||
| chr16:8900422
|
A | G | 1 | a0001c0001t0003g0043 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.2309+108T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 21/30 | chr16 | 8900422 | ||||||
| chr16:8900468
|
C | T | 1 | a0001c0001t0001g0073 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2309+62G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 21/30 | chr16 | 8900468 | ||||||
| chr16:8900522
|
G | A | 2 | a0001c0001t0001g0148a0001c0001t0001g0293 | 2 | NA18943.hp1 NA18971.hp1 |
splice_region_variant&intron_variant | LOW | c.2309+8C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 21/30 | chr16 | 8900522 | ||||||
| chr16:8900706
|
C | T | 89 | a0001c0001t0001g0306a0001c0001t0002g0005a0001c0001t0002g0061others(86): Show | 91 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.2209-76G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 20/30 | chr16 | 8900706 | ||||||
| chr16:8900763
|
G | C | 3 | a0001c0001t0025g0056a0001c0001t0027g0169a0001c0001t0037g0330 | 3 | HG03453.hp1 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2209-133C>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 20/30 | chr16 | 8900763 | ||||||
| chr16:8900814
|
A | G | 1 | a0001c0001t0032g0055 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2208+176T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 20/30 | chr16 | 8900814 | ||||||
| chr16:8900822
|
T | TA | 11 | a0001c0001t0001g0080a0001c0001t0001g0295a0001c0001t0004g0071others(8): Show | 11 | HG02886.hp1 HG02965.hp1 HG03130.hp1 others(8): Show |
intron_variant | MODIFIER | c.2208+167dupT | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 20/30 | chr16 | 8900822 | ||||||
| chr16:8900886
|
C | G | 3 | a0001c0001t0002g0242a0001c0001t0004g0235a0001c0001t0005g0261 | 3 | HG00280.hp2 HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2208+104G>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 20/30 | chr16 | 8900886 | ||||||
| chr16:8900898
|
A | T | 1 | a0001c0001t0005g0027 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2208+92T>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 20/30 | chr16 | 8900898 | ||||||
| chr16:8900904
|
T | C | 3 | a0001c0001t0004g0071a0001c0001t0004g0113a0001c0001t0004g0114 | 3 | HG02965.hp1 HG03486.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2208+86A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 20/30 | chr16 | 8900904 | ||||||
| chr16:8901299
|
A | C | 31 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0023others(28): Show | 31 | HG01167.hp2 HG01169.hp1 HG01192.hp1 others(28): Show |
intron_variant | MODIFIER | c.2048-65T>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 18/30 | chr16 | 8901299 | ||||||
| chr16:8901319
|
C | A | 1 | a0001c0001t0017g0007 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.2048-85G>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 18/30 | chr16 | 8901319 | ||||||
| chr16:8901320
|
G | C | 1 | a0001c0001t0017g0007 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.2048-86C>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 18/30 | chr16 | 8901320 | ||||||
| chr16:8901320
|
GA | G | 193 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(190): Show | 195 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(192): Show |
intron_variant | MODIFIER | c.2048-87delT | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 18/30 | chr16 | 8901320 | ||||||
| chr16:8901320
|
GAA | G | 7 | a0001c0001t0001g0129a0001c0001t0002g0181a0001c0001t0012g0028others(4): Show | 7 | HG02886.hp1 HG03130.hp1 HG03516.hp2 others(4): Show |
intron_variant | MODIFIER | c.2048-88_2048-87del others(2): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 18/30 | chr16 | 8901320 | ||||||
| chr16:8901320
|
GAAA | G | 108 | a0001c0001t0001g0306a0001c0001t0002g0005a0001c0001t0002g0061others(105): Show | 110 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.2048-89_2048-87del others(3): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 18/30 | chr16 | 8901320 | ||||||
| chr16:8901320
|
GAAAA | G | 7 | a0001c0001t0003g0121a0001c0001t0007g0002a0001c0001t0007g0033others(4): Show | 8 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(5): Show |
intron_variant | MODIFIER | c.2048-90_2048-87del others(4): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 18/30 | chr16 | 8901320 | ||||||
| chr16:8901321
|
A | G | 1 | a0001c0001t0017g0007 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.2048-87T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 18/30 | chr16 | 8901321 | ||||||
| chr16:8901332
|
A | C | 1 | a0001c0001t0020g0064 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2048-98T>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 18/30 | chr16 | 8901332 | ||||||
| chr16:8901549
|
C | T | 1 | a0001c0001t0002g0265 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.2048-315G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 18/30 | chr16 | 8901549 | ||||||
| chr16:8901557
|
C | T | 100 | a0001c0001t0001g0306a0001c0001t0002g0005a0001c0001t0002g0061others(97): Show | 102 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.2048-323G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 18/30 | chr16 | 8901557 | ||||||
| chr16:8901618
|
C | T | 8 | a0001c0001t0002g0069a0001c0001t0002g0070a0001c0001t0002g0072others(5): Show | 8 | HG02451.hp1 HG02486.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.2048-384G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 18/30 | chr16 | 8901618 | ||||||
| chr16:8901950
|
G | C | 1 | a0001c0001t0002g0035 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2047+132C>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 18/30 | chr16 | 8901950 | ||||||
| chr16:8902070
|
G | A | 141 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(138): Show | 143 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.2047+12C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 18/30 | chr16 | 8902070 | ||||||
| chr16:8902254
|
A | G | 1 | a0001c0001t0002g0035 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1942-67T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 17/30 | chr16 | 8902254 | ||||||
| chr16:8902520
|
C | T | 115 | a0001c0001t0001g0306a0001c0001t0002g0005a0001c0001t0002g0061others(112): Show | 118 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.1840-38G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 16/30 | chr16 | 8902520 | ||||||
| chr16:8902546
|
C | T | 3 | a0001c0001t0025g0056a0001c0001t0027g0169a0001c0001t0037g0330 | 3 | HG03453.hp1 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1840-64G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 16/30 | chr16 | 8902546 | ||||||
| chr16:8902779
|
T | C | 120 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(117): Show | 122 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.1840-297A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 16/30 | chr16 | 8902779 | ||||||
| chr16:8902894
|
G | A | 170 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(167): Show | 172 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.1839+374C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 16/30 | chr16 | 8902894 | ||||||
| chr16:8902931
|
C | T | 76 | a0001c0001t0001g0306a0001c0001t0002g0005a0001c0001t0002g0061others(73): Show | 78 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.1839+337G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 16/30 | chr16 | 8902931 | ||||||
| chr16:8902936
|
G | A | 1 | a0001c0001t0002g0180 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1839+332C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 16/30 | chr16 | 8902936 | ||||||
| chr16:8902937
|
A | T | 1 | a0001c0001t0002g0180 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1839+331T>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 16/30 | chr16 | 8902937 | ||||||
| chr16:8902940
|
T | G | 1 | a0001c0001t0002g0180 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1839+328A>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 16/30 | chr16 | 8902940 | ||||||
| chr16:8902969
|
G | A | 1 | a0001c0001t0002g0035 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1839+299C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 16/30 | chr16 | 8902969 | ||||||
| chr16:8902981
|
A | T | 200 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(197): Show | 203 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.1839+287T>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 16/30 | chr16 | 8902981 | ||||||
| chr16:8903161
|
C | G | 1 | a0001c0001t0029g0021 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1839+107G>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 16/30 | chr16 | 8903161 | ||||||
| chr16:8903211
|
G | A | 1 | a0001c0001t0004g0259 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1839+57C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 16/30 | chr16 | 8903211 | ||||||
| chr16:8903225
|
G | A | 1 | a0001c0001t0009g0010 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1839+43C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 16/30 | chr16 | 8903225 | ||||||
| chr16:8903236
|
C | T | 2 | a0001c0001t0001g0218a0001c0001t0001g0219 | 2 | HG00323.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.1839+32G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 16/30 | chr16 | 8903236 | ||||||
| chr16:8903245
|
A | G | 1 | a0001c0001t0022g0053 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1839+23T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 16/30 | chr16 | 8903245 | ||||||
| chr16:8903412
|
T | C | 1 | a0001c0001t0001g0172 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1705-10A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 15/30 | chr16 | 8903412 | ||||||
| chr16:8903441
|
C | G | 3 | a0001c0001t0004g0071a0001c0001t0004g0113a0001c0001t0004g0114 | 3 | HG02965.hp1 HG03486.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1705-39G>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 15/30 | chr16 | 8903441 | ||||||
| chr16:8903821
|
C | T | 1 | a0001c0001t0005g0052 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1705-419G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 15/30 | chr16 | 8903821 | ||||||
| chr16:8903854
|
T | TGA | 3 | a0001c0001t0004g0071a0001c0001t0004g0113a0001c0001t0004g0114 | 3 | HG02965.hp1 HG03486.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1705-454_1705-453d others(4): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 15/30 | chr16 | 8903854 | ||||||
| chr16:8903867
|
CA | C | 151 | a0001c0001t0001g0041a0001c0001t0001g0205a0001c0001t0001g0306others(148): Show | 154 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.1705-466delT | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 15/30 | chr16 | 8903867 | ||||||
| chr16:8904020
|
G | C | 1 | a0001c0001t0001g0125 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1704+415C>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 15/30 | chr16 | 8904020 | ||||||
| chr16:8904259
|
G | A | 3 | a0001c0001t0004g0071a0001c0001t0004g0113a0001c0001t0004g0114 | 3 | HG02965.hp1 HG03486.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1704+176C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 15/30 | chr16 | 8904259 | ||||||
| chr16:8904283
|
T | C | 1 | a0001c0001t0001g0082 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1704+152A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 15/30 | chr16 | 8904283 | ||||||
| chr16:8904343
|
T | G | 1 | a0001c0001t0001g0079 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1704+92A>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 15/30 | chr16 | 8904343 | ||||||
| chr16:8904344
|
C | T | 1 | a0001c0001t0001g0079 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1704+91G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 15/30 | chr16 | 8904344 | ||||||
| chr16:8904348
|
G | C | 1 | a0001c0001t0002g0195 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1704+87C>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 15/30 | chr16 | 8904348 | ||||||
| chr16:8904590
|
G | C | 2 | a0001c0001t0003g0046a0001c0001t0003g0312 | 2 | HG02970.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1574-25C>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 14/30 | chr16 | 8904590 | ||||||
| chr16:8904608
|
T | G | 1 | a0001c0001t0002g0201 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1574-43A>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 14/30 | chr16 | 8904608 | ||||||
| chr16:8904653
|
A | G | 1 | a0001c0001t0035g0321 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1574-88T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 14/30 | chr16 | 8904653 | ||||||
| chr16:8904666
|
G | A | 3 | a0001c0001t0025g0056a0001c0001t0027g0169a0001c0001t0037g0330 | 3 | HG03453.hp1 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1574-101C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 14/30 | chr16 | 8904666 | ||||||
| chr16:8904696
|
A | C | 7 | a0001c0001t0003g0121a0001c0001t0007g0002a0001c0001t0007g0033others(4): Show | 8 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(5): Show |
intron_variant | MODIFIER | c.1574-131T>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 14/30 | chr16 | 8904696 | ||||||
| chr16:8904697
|
C | A | 7 | a0001c0001t0003g0121a0001c0001t0007g0002a0001c0001t0007g0033others(4): Show | 8 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(5): Show |
intron_variant | MODIFIER | c.1574-132G>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 14/30 | chr16 | 8904697 | ||||||
| chr16:8904708
|
T | G | 1 | a0001c0001t0001g0079 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1574-143A>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 14/30 | chr16 | 8904708 | ||||||
| chr16:8904714
|
G | A | 4 | a0001c0001t0001g0157a0001c0001t0001g0217a0001c0001t0003g0215others(1): Show | 4 | HG02145.hp2 HG02280.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1574-149C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 14/30 | chr16 | 8904714 | ||||||
| chr16:8904714
|
G | C | 104 | a0001c0001t0001g0306a0001c0001t0002g0005a0001c0001t0002g0061others(101): Show | 106 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.1574-149C>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 14/30 | chr16 | 8904714 | ||||||
| chr16:8904725
|
G | A | 1 | a0001c0001t0031g0044 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1574-160C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 14/30 | chr16 | 8904725 | ||||||
| chr16:8904781
|
T | TA | 121 | a0001c0001t0001g0041a0001c0001t0001g0177a0001c0001t0001g0306others(118): Show | 123 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.1574-217dupT | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 14/30 | chr16 | 8904781 | ||||||
| chr16:8904788
|
A | T | 3 | a0001c0001t0004g0071a0001c0001t0004g0113a0001c0001t0004g0114 | 3 | HG02965.hp1 HG03486.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1574-223T>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 14/30 | chr16 | 8904788 | ||||||
| chr16:8904980
|
A | C | 1 | a0001c0001t0017g0007 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1573+207T>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 14/30 | chr16 | 8904980 | ||||||
| chr16:8905029
|
C | T | 2 | a0001c0001t0002g0194a0001c0001t0002g0268 | 2 | HG01346.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.1573+158G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 14/30 | chr16 | 8905029 | ||||||
| chr16:8905081
|
G | A | 3 | a0001c0001t0007g0049a0001c0001t0007g0051a0001c0001t0023g0050 | 3 | HG00140.hp2 HG00642.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.1573+106C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 14/30 | chr16 | 8905081 | ||||||
| chr16:8905098
|
G | A | 2 | a0001c0001t0003g0315a0001c0001t0003g0316 | 2 | NA19012.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.1573+89C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 14/30 | chr16 | 8905098 | ||||||
| chr16:8905124
|
T | C | 1 | a0001c0001t0019g0289 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1573+63A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 14/30 | chr16 | 8905124 | ||||||
| chr16:8905369
|
A | G | 1 | a0001c0001t0002g0035 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1429-38T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 13/30 | chr16 | 8905369 | ||||||
| chr16:8905429
|
T | C | 3 | a0001c0001t0004g0071a0001c0001t0004g0113a0001c0001t0004g0114 | 3 | HG02965.hp1 HG03486.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1429-98A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 13/30 | chr16 | 8905429 | ||||||
| chr16:8905499
|
G | A | 9 | a0001c0001t0003g0121a0001c0001t0007g0002a0001c0001t0007g0033others(6): Show | 10 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(7): Show |
intron_variant | MODIFIER | c.1429-168C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 13/30 | chr16 | 8905499 | ||||||
| chr16:8905514
|
A | G | 1 | a0001c0001t0022g0053 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1429-183T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 13/30 | chr16 | 8905514 | ||||||
| chr16:8905522
|
A | C | 1 | a0001c0001t0005g0052 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1429-191T>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 13/30 | chr16 | 8905522 | ||||||
| chr16:8905605
|
C | A | 2 | a0001c0001t0001g0117a0001c0001t0003g0138 | 2 | HG01175.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.1429-274G>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 13/30 | chr16 | 8905605 | ||||||
| chr16:8905614
|
T | C | 1 | a0001c0001t0001g0171 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1429-283A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 13/30 | chr16 | 8905614 | ||||||
| chr16:8905691
|
C | T | 105 | a0001c0001t0001g0306a0001c0001t0002g0005a0001c0001t0002g0061others(102): Show | 107 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.1429-360G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 13/30 | chr16 | 8905691 | ||||||
| chr16:8905696
|
C | A | 3 | a0001c0001t0004g0071a0001c0001t0004g0113a0001c0001t0004g0114 | 3 | HG02965.hp1 HG03486.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1429-365G>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 13/30 | chr16 | 8905696 | ||||||
| chr16:8905748
|
C | A | 1 | a0001c0001t0001g0159 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1429-417G>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 13/30 | chr16 | 8905748 | ||||||
| chr16:8905853
|
A | C | 2 | a0001c0001t0001g0147a0001c0001t0001g0174 | 2 | HG02015.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.1429-522T>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 13/30 | chr16 | 8905853 | ||||||
| chr16:8905879
|
C | T | 1 | a0001c0001t0002g0035 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1428+547G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 13/30 | chr16 | 8905879 | ||||||
| chr16:8905882
|
A | C | 3 | a0001c0001t0004g0071a0001c0001t0004g0113a0001c0001t0004g0114 | 3 | HG02965.hp1 HG03486.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1428+544T>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 13/30 | chr16 | 8905882 | ||||||
| chr16:8905899
|
C | T | 1 | a0001c0001t0001g0208 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1428+527G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 13/30 | chr16 | 8905899 | ||||||
| chr16:8906146
|
G | A | 135 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(132): Show | 137 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.1428+280C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 13/30 | chr16 | 8906146 | ||||||
| chr16:8906217
|
T | A | 11 | a0001c0001t0002g0069a0001c0001t0002g0070a0001c0001t0002g0072others(8): Show | 11 | HG01891.hp2 HG02451.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.1428+209A>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 13/30 | chr16 | 8906217 | ||||||
| chr16:8906228
|
A | C | 104 | a0001c0001t0001g0306a0001c0001t0002g0005a0001c0001t0002g0061others(101): Show | 106 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.1428+198T>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 13/30 | chr16 | 8906228 | ||||||
| chr16:8906358
|
C | G | 2 | a0001c0001t0004g0054a0001c0001t0032g0055 | 2 | HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1428+68G>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 13/30 | chr16 | 8906358 | ||||||
| chr16:8906364
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1428+62C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 13/30 | chr16 | 8906364 | ||||||
| chr16:8906729
|
G | A | 1 | a0001c0001t0002g0035 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1272-147C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 12/30 | chr16 | 8906729 | ||||||
| chr16:8906799
|
A | G | 320 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(317): Show | 325 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.1272-217T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 12/30 | chr16 | 8906799 | ||||||
| chr16:8906872
|
A | C | 7 | a0001c0001t0003g0121a0001c0001t0007g0002a0001c0001t0007g0033others(4): Show | 8 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(5): Show |
intron_variant | MODIFIER | c.1272-290T>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 12/30 | chr16 | 8906872 | ||||||
| chr16:8906975
|
T | C | 1 | a0001c0001t0002g0243 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1272-393A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 12/30 | chr16 | 8906975 | ||||||
| chr16:8907046
|
G | A | 1 | a0001c0001t0034g0319 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1272-464C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 12/30 | chr16 | 8907046 | ||||||
| chr16:8907061
|
G | T | 1 | a0001c0001t0031g0044 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1272-479C>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 12/30 | chr16 | 8907061 | ||||||
| chr16:8907094
|
C | T | 3 | a0001c0001t0004g0071a0001c0001t0004g0113a0001c0001t0004g0114 | 3 | HG02965.hp1 HG03486.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1272-512G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 12/30 | chr16 | 8907094 | ||||||
| chr16:8907110
|
C | T | 1 | a0001c0001t0001g0208 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1272-528G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 12/30 | chr16 | 8907110 | ||||||
| chr16:8907132
|
G | A | 1 | a0001c0001t0001g0159 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1272-550C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 12/30 | chr16 | 8907132 | ||||||
| chr16:8907409
|
G | C | 1 | a0001c0001t0034g0319 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1272-827C>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 12/30 | chr16 | 8907409 | ||||||
| chr16:8907420
|
C | T | 3 | a0001c0001t0005g0052a0001c0001t0022g0053a0001c0001t0031g0044 | 3 | NA20300.hp1 NA21309.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1272-838G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 12/30 | chr16 | 8907420 | ||||||
| chr16:8907429
|
C | G | 1 | a0001c0001t0002g0035 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1272-847G>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 12/30 | chr16 | 8907429 | ||||||
| chr16:8907430
|
T | C | 1 | a0001c0001t0005g0052 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1272-848A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 12/30 | chr16 | 8907430 | ||||||
| chr16:8907588
|
G | A | 1 | a0001c0001t0002g0112 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1271+753C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 12/30 | chr16 | 8907588 | ||||||
| chr16:8907626
|
C | A | 1 | a0001c0001t0002g0194 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1271+715G>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 12/30 | chr16 | 8907626 | ||||||
| chr16:8907687
|
C | A | 1 | a0001c0001t0004g0162 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1271+654G>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 12/30 | chr16 | 8907687 | ||||||
| chr16:8907957
|
A | G | 10 | a0001c0001t0003g0121a0001c0001t0005g0052a0001c0001t0007g0002others(7): Show | 11 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(8): Show |
intron_variant | MODIFIER | c.1271+384T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 12/30 | chr16 | 8907957 | ||||||
| chr16:8908008
|
C | G | 1 | a0001c0001t0002g0256 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1271+333G>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 12/30 | chr16 | 8908008 | ||||||
| chr16:8908098
|
G | C | 3 | a0001c0001t0001g0063a0001c0001t0001g0096a0001c0001t0001g0175 | 3 | HG00741.hp1 HG01978.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1271+243C>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 12/30 | chr16 | 8908098 | ||||||
| chr16:8908201
|
C | G | 1 | a0001c0001t0031g0044 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1271+140G>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 12/30 | chr16 | 8908201 | ||||||
| chr16:8908513
|
G | C | 5 | a0001c0001t0012g0028a0001c0001t0012g0057a0001c0001t0014g0058others(2): Show | 5 | HG02886.hp1 HG03130.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1162-63C>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 11/30 | chr16 | 8908513 | ||||||
| chr16:8908521
|
G | A | 3 | a0001c0001t0004g0071a0001c0001t0004g0113a0001c0001t0004g0114 | 3 | HG02965.hp1 HG03486.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1162-71C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 11/30 | chr16 | 8908521 | ||||||
| chr16:8908803
|
C | A | 2 | a0001c0001t0004g0054a0001c0001t0032g0055 | 2 | HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1162-353G>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 11/30 | chr16 | 8908803 | ||||||
| chr16:8908815
|
C | A | 183 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(180): Show | 185 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.1162-365G>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 11/30 | chr16 | 8908815 | ||||||
| chr16:8908847
|
A | C | 1 | a0001c0001t0002g0265 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1162-397T>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 11/30 | chr16 | 8908847 | ||||||
| chr16:8908918
|
C | T | 1 | a0001c0001t0001g0296 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1162-468G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 11/30 | chr16 | 8908918 | ||||||
| chr16:8908932
|
G | A | 1 | a0001c0001t0035g0321 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1162-482C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 11/30 | chr16 | 8908932 | ||||||
| chr16:8909111
|
C | T | 1 | a0001c0001t0031g0044 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1162-661G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 11/30 | chr16 | 8909111 | ||||||
| chr16:8909117
|
T | C | 3 | a0001c0001t0004g0071a0001c0001t0004g0113a0001c0001t0004g0114 | 3 | HG02965.hp1 HG03486.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1162-667A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 11/30 | chr16 | 8909117 | ||||||
| chr16:8909164
|
T | C | 1 | a0001c0001t0002g0035 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1162-714A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 11/30 | chr16 | 8909164 | ||||||
| chr16:8909348
|
A | G | 6 | a0001c0001t0004g0054a0001c0001t0025g0056a0001c0001t0027g0169others(3): Show | 6 | HG02922.hp1 HG03453.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.1162-898T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 11/30 | chr16 | 8909348 | ||||||
| chr16:8909393
|
T | G | 123 | a0001c0001t0001g0105a0001c0001t0001g0174a0001c0001t0001g0306others(120): Show | 125 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.1162-943A>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 11/30 | chr16 | 8909393 | ||||||
| chr16:8909523
|
C | T | 1 | a0001c0002t0001g0132 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1162-1073G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 11/30 | chr16 | 8909523 | ||||||
| chr16:8909651
|
G | A | 1 | a0001c0001t0005g0052 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1161+1094C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 11/30 | chr16 | 8909651 | ||||||
| chr16:8909671
|
T | C | 9 | a0001c0001t0003g0202a0001c0001t0005g0288a0001c0001t0008g0320others(6): Show | 9 | HG00140.hp1 HG01515.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1161+1074A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 11/30 | chr16 | 8909671 | ||||||
| chr16:8909693
|
C | T | 1 | a0001c0001t0002g0035 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1161+1052G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 11/30 | chr16 | 8909693 | ||||||
| chr16:8909720
|
G | A | 1 | a0001c0001t0001g0094 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1161+1025C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 11/30 | chr16 | 8909720 | ||||||
| chr16:8909765
|
A | C | 7 | a0001c0001t0001g0020a0001c0001t0012g0028a0001c0001t0012g0057others(4): Show | 7 | HG02647.hp1 HG02886.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.1161+980T>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 11/30 | chr16 | 8909765 | ||||||
| chr16:8909775
|
A | G | 3 | a0001c0001t0004g0071a0001c0001t0004g0113a0001c0001t0004g0114 | 3 | HG02965.hp1 HG03486.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1161+970T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 11/30 | chr16 | 8909775 | ||||||
| chr16:8909831
|
T | G | 2 | a0001c0001t0002g0152a0001c0001t0002g0192 | 2 | HG03688.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.1161+914A>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 11/30 | chr16 | 8909831 | ||||||
| chr16:8909911
|
C | G | 1 | a0001c0001t0002g0035 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1161+834G>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 11/30 | chr16 | 8909911 | ||||||
| chr16:8909913
|
G | A | 3 | a0001c0001t0004g0071a0001c0001t0004g0113a0001c0001t0004g0114 | 3 | HG02965.hp1 HG03486.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1161+832C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 11/30 | chr16 | 8909913 | ||||||
| chr16:8909958
|
A | G | 1 | a0001c0001t0002g0112 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1161+787T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 11/30 | chr16 | 8909958 | ||||||
| chr16:8910043
|
G | T | 1 | a0001c0001t0022g0053 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1161+702C>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 11/30 | chr16 | 8910043 | ||||||
| chr16:8910211
|
AC | A | 18 | a0001c0001t0001g0041a0001c0001t0003g0029a0001c0001t0003g0030others(15): Show | 18 | HG02132.hp1 HG02165.hp1 HG02970.hp1 others(15): Show |
intron_variant | MODIFIER | c.1161+533delG | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 11/30 | chr16 | 8910211 | ||||||
| chr16:8910332
|
A | T | 4 | a0001c0001t0002g0070a0001c0001t0002g0072a0001c0001t0002g0115others(1): Show | 4 | HG02486.hp1 HG02622.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1161+413T>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 11/30 | chr16 | 8910332 | ||||||
| chr16:8910409
|
C | T | 2 | a0001c0001t0004g0006a0001c0001t0004g0304 | 3 | HG01257.hp1 HG01258.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.1161+336G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 11/30 | chr16 | 8910409 | ||||||
| chr16:8910594
|
C | G | 1 | a0001c0001t0002g0035 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1161+151G>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 11/30 | chr16 | 8910594 | ||||||
| chr16:8910707
|
C | A | 325 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(322): Show | 330 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.1161+38G>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 11/30 | chr16 | 8910707 | ||||||
| chr16:8910948
|
A | C | 1 | a0001c0001t0004g0162 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1079-121T>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 10/30 | chr16 | 8910948 | ||||||
| chr16:8910967
|
C | T | 4 | a0001c0001t0006g0001a0001c0001t0006g0016a0001c0001t0006g0017others(1): Show | 5 | HG02280.hp2 HG03209.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1079-140G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 10/30 | chr16 | 8910967 | ||||||
| chr16:8911174
|
A | G | 3 | a0001c0001t0001g0019a0001c0001t0001g0111a0001c0001t0017g0007 | 3 | HG00423.hp2 HG02165.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.1079-347T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 10/30 | chr16 | 8911174 | ||||||
| chr16:8911210
|
T | C | 124 | a0001c0001t0001g0306a0001c0001t0002g0005a0001c0001t0002g0035others(121): Show | 127 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.1079-383A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 10/30 | chr16 | 8911210 | ||||||
| chr16:8911266
|
T | C | 2 | a0001c0001t0002g0243a0001c0001t0005g0287 | 2 | HG02451.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1079-439A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 10/30 | chr16 | 8911266 | ||||||
| chr16:8911492
|
T | C | 11 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0099others(8): Show | 11 | HG00408.hp2 HG00621.hp1 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.1079-665A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 10/30 | chr16 | 8911492 | ||||||
| chr16:8911530
|
C | A | 2 | a0001c0001t0022g0053a0001c0001t0031g0044 | 2 | NA20300.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1079-703G>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 10/30 | chr16 | 8911530 | ||||||
| chr16:8911550
|
C | T | 1 | a0001c0001t0001g0146 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1079-723G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 10/30 | chr16 | 8911550 | ||||||
| chr16:8911739
|
A | G | 1 | a0001c0001t0001g0300 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1079-912T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 10/30 | chr16 | 8911739 | ||||||
| chr16:8911783
|
A | G | 121 | a0001c0001t0001g0306a0001c0001t0002g0005a0001c0001t0002g0035others(118): Show | 123 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.1079-956T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 10/30 | chr16 | 8911783 | ||||||
| chr16:8911887
|
C | G | 1 | a0001c0001t0025g0056 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1079-1060G>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 10/30 | chr16 | 8911887 | ||||||
| chr16:8911923
|
G | A | 1 | a0001c0001t0001g0126 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1079-1096C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 10/30 | chr16 | 8911923 | ||||||
| chr16:8912067
|
T | C | 7 | a0001c0001t0003g0121a0001c0001t0007g0002a0001c0001t0007g0033others(4): Show | 8 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(5): Show |
intron_variant | MODIFIER | c.1079-1240A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 10/30 | chr16 | 8912067 | ||||||
| chr16:8912082
|
G | C | 1 | a0001c0001t0001g0146 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1079-1255C>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 10/30 | chr16 | 8912082 | ||||||
| chr16:8912090
|
T | C | 2 | a0001c0001t0004g0162a0001c0001t0019g0289 | 2 | HG01891.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1079-1263A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 10/30 | chr16 | 8912090 | ||||||
| chr16:8912280
|
C | T | 5 | a0001c0001t0012g0028a0001c0001t0012g0057a0001c0001t0014g0058others(2): Show | 5 | HG02886.hp1 HG03130.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1079-1453G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 10/30 | chr16 | 8912280 | ||||||
| chr16:8912281
|
G | A | 8 | a0001c0001t0002g0229a0001c0001t0002g0230a0001c0001t0002g0231others(5): Show | 8 | HG01070.hp2 HG01071.hp2 HG02698.hp1 others(5): Show |
intron_variant | MODIFIER | c.1079-1454C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 10/30 | chr16 | 8912281 | ||||||
| chr16:8912328
|
T | C | 121 | a0001c0001t0001g0306a0001c0001t0002g0005a0001c0001t0002g0061others(118): Show | 123 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.1079-1501A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 10/30 | chr16 | 8912328 | ||||||
| chr16:8912363
|
T | C | 2 | a0001c0001t0033g0322a0001c0001t0035g0321 | 2 | HG03195.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.1079-1536A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 10/30 | chr16 | 8912363 | ||||||
| chr16:8912423
|
C | T | 1 | a0001c0001t0003g0039 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1079-1596G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 10/30 | chr16 | 8912423 | ||||||
| chr16:8912449
|
C | CA | 105 | a0001c0001t0001g0306a0001c0001t0002g0005a0001c0001t0002g0061others(102): Show | 107 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.1079-1623dupT | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 10/30 | chr16 | 8912449 | ||||||
| chr16:8912460
|
A | C | 18 | a0001c0001t0001g0041a0001c0001t0003g0029a0001c0001t0003g0030others(15): Show | 18 | HG02132.hp1 HG02165.hp1 HG02970.hp1 others(15): Show |
intron_variant | MODIFIER | c.1079-1633T>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 10/30 | chr16 | 8912460 | ||||||
| chr16:8912664
|
A | G | 1 | a0001c0001t0005g0288 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1079-1837T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 10/30 | chr16 | 8912664 | ||||||
| chr16:8912679
|
C | T | 2 | a0001c0001t0004g0054a0001c0001t0032g0055 | 2 | HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1079-1852G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 10/30 | chr16 | 8912679 | ||||||
| chr16:8912692
|
C | A | 2 | a0001c0001t0015g0317a0001c0001t0015g0318 | 2 | HG01496.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1079-1865G>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 10/30 | chr16 | 8912692 | ||||||
| chr16:8912795
|
A | G | 1 | a0001c0001t0007g0042 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1079-1968T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 10/30 | chr16 | 8912795 | ||||||
| chr16:8912819
|
T | A | 1 | a0001c0001t0029g0021 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1079-1992A>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 10/30 | chr16 | 8912819 | ||||||
| chr16:8912854
|
A | G | 5 | a0001c0001t0002g0035a0001c0001t0004g0071a0001c0001t0004g0113others(2): Show | 5 | HG02965.hp1 HG03486.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1079-2027T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 10/30 | chr16 | 8912854 | ||||||
| chr16:8912864
|
A | G | 7 | a0001c0001t0003g0121a0001c0001t0007g0002a0001c0001t0007g0033others(4): Show | 8 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(5): Show |
intron_variant | MODIFIER | c.1079-2037T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 10/30 | chr16 | 8912864 | ||||||
| chr16:8913068
|
A | G | 1 | a0001c0001t0031g0044 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1078+2186T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 10/30 | chr16 | 8913068 | ||||||
| chr16:8913132
|
G | C | 1 | a0001c0003t0001g0154 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1078+2122C>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 10/30 | chr16 | 8913132 | ||||||
| chr16:8913153
|
C | A | 1 | a0001c0001t0001g0086 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1078+2101G>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 10/30 | chr16 | 8913153 | ||||||
| chr16:8913218
|
T | C | 2 | a0001c0001t0004g0054a0001c0001t0032g0055 | 2 | HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1078+2036A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 10/30 | chr16 | 8913218 | ||||||
| chr16:8913314
|
C | G | 4 | a0001c0001t0002g0035a0001c0001t0004g0071a0001c0001t0004g0113others(1): Show | 4 | HG02965.hp1 HG03486.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1078+1940G>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 10/30 | chr16 | 8913314 | ||||||
| chr16:8913325
|
C | T | 1 | a0001c0001t0004g0301 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1078+1929G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 10/30 | chr16 | 8913325 | ||||||
| chr16:8913335
|
A | G | 1 | a0001c0001t0031g0044 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1078+1919T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 10/30 | chr16 | 8913335 | ||||||
| chr16:8913351
|
C | G | 1 | a0001c0001t0031g0044 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1078+1903G>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 10/30 | chr16 | 8913351 | ||||||
| chr16:8913361
|
G | A | 1 | a0001c0001t0031g0044 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1078+1893C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 10/30 | chr16 | 8913361 | ||||||
| chr16:8913363
|
G | A | 1 | a0001c0001t0031g0044 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1078+1891C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 10/30 | chr16 | 8913363 | ||||||
| chr16:8913364
|
G | A | 1 | a0001c0001t0031g0044 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1078+1890C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 10/30 | chr16 | 8913364 | ||||||
| chr16:8913366
|
G | A | 1 | a0001c0001t0031g0044 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1078+1888C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 10/30 | chr16 | 8913366 | ||||||
| chr16:8913368
|
G | A | 1 | a0001c0001t0031g0044 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1078+1886C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 10/30 | chr16 | 8913368 | ||||||
| chr16:8913370
|
AGAGGGAA others(1050): Show |
A | 1 | a0001c0001t0031g0044 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1078+827_1078+1883 others(3): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 10/30 | chr16 | 8913370 | ||||||
| chr16:8913394
|
A | C | 2 | a0001c0001t0002g0229a0001c0001t0026g0228 | 2 | HG02738.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1078+1860T>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 10/30 | chr16 | 8913394 | ||||||
| chr16:8913396
|
T | A | 2 | a0001c0001t0002g0262a0001c0001t0002g0305 | 2 | HG03669.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.1078+1858A>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 10/30 | chr16 | 8913396 | ||||||
| chr16:8913412
|
G | A | 1 | a0001c0001t0030g0151 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1078+1842C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 10/30 | chr16 | 8913412 | ||||||
| chr16:8913513
|
G | A | 1 | a0001c0001t0002g0284 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1078+1741C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 10/30 | chr16 | 8913513 | ||||||
| chr16:8913516
|
T | C | 1 | a0001c0001t0005g0288 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1078+1738A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 10/30 | chr16 | 8913516 | ||||||
| chr16:8913653
|
T | C | 10 | a0001c0001t0002g0035a0001c0001t0003g0121a0001c0001t0005g0052others(7): Show | 11 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(8): Show |
intron_variant | MODIFIER | c.1078+1601A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 10/30 | chr16 | 8913653 | ||||||
| chr16:8913906
|
G | A | 2 | a0001c0001t0004g0054a0001c0001t0032g0055 | 2 | HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1078+1348C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 10/30 | chr16 | 8913906 | ||||||
| chr16:8913917
|
T | C | 3 | a0001c0001t0025g0056a0001c0001t0027g0169a0001c0001t0037g0330 | 3 | HG03453.hp1 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1078+1337A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 10/30 | chr16 | 8913917 | ||||||
| chr16:8913969
|
T | C | 1 | a0001c0001t0001g0300 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1078+1285A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 10/30 | chr16 | 8913969 | ||||||
| chr16:8913975
|
C | G | 1 | a0001c0001t0022g0053 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1078+1279G>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 10/30 | chr16 | 8913975 | ||||||
| chr16:8914157
|
C | T | 1 | a0001c0001t0001g0080 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1078+1097G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 10/30 | chr16 | 8914157 | ||||||
| chr16:8914180
|
A | G | 115 | a0001c0001t0001g0306a0001c0001t0002g0005a0001c0001t0002g0061others(112): Show | 117 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.1078+1074T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 10/30 | chr16 | 8914180 | ||||||
| chr16:8914296
|
G | C | 3 | a0001c0001t0004g0071a0001c0001t0004g0113a0001c0001t0004g0114 | 3 | HG02965.hp1 HG03486.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1078+958C>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 10/30 | chr16 | 8914296 | ||||||
| chr16:8914350
|
T | C | 1 | a0001c0006t0004g0173 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1078+904A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 10/30 | chr16 | 8914350 | ||||||
| chr16:8914378
|
G | A | 1 | a0001c0001t0010g0234 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1078+876C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 10/30 | chr16 | 8914378 | ||||||
| chr16:8914394
|
C | A | 1 | a0001c0001t0002g0180 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1078+860G>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 10/30 | chr16 | 8914394 | ||||||
| chr16:8914398
|
A | ACAGG | 9 | a0001c0001t0001g0208a0001c0001t0005g0288a0001c0001t0008g0320others(6): Show | 9 | HG00140.hp1 HG01515.hp1 HG01515.hp2 others(6): Show |
intron_variant | MODIFIER | c.1078+852_1078+855d others(6): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 10/30 | chr16 | 8914398 | ||||||
| chr16:8914431
|
C | A | 1 | a0001c0001t0031g0044 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1078+823G>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 10/30 | chr16 | 8914431 | ||||||
| chr16:8914433
|
G | A | 1 | a0001c0001t0031g0044 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1078+821C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 10/30 | chr16 | 8914433 | ||||||
| chr16:8914434
|
G | A | 1 | a0001c0001t0031g0044 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1078+820C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 10/30 | chr16 | 8914434 | ||||||
| chr16:8914435
|
C | A | 1 | a0001c0001t0031g0044 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1078+819G>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 10/30 | chr16 | 8914435 | ||||||
| chr16:8914437
|
T | A | 1 | a0001c0001t0031g0044 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1078+817A>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 10/30 | chr16 | 8914437 | ||||||
| chr16:8914438
|
T | A | 1 | a0001c0001t0031g0044 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1078+816A>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 10/30 | chr16 | 8914438 | ||||||
| chr16:8914618
|
G | A | 195 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(192): Show | 198 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.1078+636C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 10/30 | chr16 | 8914618 | ||||||
| chr16:8914920
|
C | G | 1 | a0001c0001t0022g0053 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1078+334G>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 10/30 | chr16 | 8914920 | ||||||
| chr16:8914974
|
C | T | 1 | a0001c0001t0005g0052 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1078+280G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 10/30 | chr16 | 8914974 | ||||||
| chr16:8915221
|
A | C | 1 | a0001c0001t0001g0295 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1078+33T>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 10/30 | chr16 | 8915221 | ||||||
| chr16:8915429
|
A | G | 7 | a0001c0001t0003g0121a0001c0001t0007g0002a0001c0001t0007g0033others(4): Show | 8 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(5): Show |
intron_variant | MODIFIER | c.987+16T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 9/30 | chr16 | 8915429 | ||||||
| chr16:8915612
|
G | A | 1 | a0001c0001t0001g0142 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.907-87C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 8/30 | chr16 | 8915612 | ||||||
| chr16:8915616
|
A | T | 1 | a0001c0001t0001g0062 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.907-91T>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 8/30 | chr16 | 8915616 | ||||||
| chr16:8915617
|
A | ATATAGAA others(8): Show |
1 | a0001c0001t0001g0062 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.907-93_907-92insAG others(13): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 8/30 | chr16 | 8915617 | ||||||
| chr16:8915622
|
G | A | 1 | a0001c0001t0001g0062 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.907-97C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 8/30 | chr16 | 8915622 | ||||||
| chr16:8915641
|
T | G | 7 | a0001c0001t0002g0100a0001c0001t0002g0191a0001c0001t0002g0256others(4): Show | 7 | HG01934.hp1 HG02071.hp2 NA18747.hp1 others(4): Show |
intron_variant | MODIFIER | c.907-116A>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 8/30 | chr16 | 8915641 | ||||||
| chr16:8915733
|
C | A | 1 | a0001c0001t0032g0055 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.907-208G>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 8/30 | chr16 | 8915733 | ||||||
| chr16:8915912
|
T | A | 1 | a0001c0001t0019g0289 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.907-387A>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 8/30 | chr16 | 8915912 | ||||||
| chr16:8916014
|
T | C | 2 | a0001c0001t0003g0121a0003c0007t0003g0034 | 2 | HG00733.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.906+488A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 8/30 | chr16 | 8916014 | ||||||
| chr16:8916072
|
C | T | 6 | a0001c0001t0002g0100a0001c0001t0002g0191a0001c0001t0002g0256others(3): Show | 6 | HG01934.hp1 HG02071.hp2 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.906+430G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 8/30 | chr16 | 8916072 | ||||||
| chr16:8916094
|
C | G | 1 | a0001c0001t0031g0044 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.906+408G>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 8/30 | chr16 | 8916094 | ||||||
| chr16:8916189
|
G | A | 1 | a0001c0001t0003g0030 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.906+313C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 8/30 | chr16 | 8916189 | ||||||
| chr16:8916200
|
C | A | 1 | a0001c0001t0002g0282 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.906+302G>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 8/30 | chr16 | 8916200 | ||||||
| chr16:8916227
|
A | G | 1 | a0001c0001t0002g0181 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.906+275T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 8/30 | chr16 | 8916227 | ||||||
| chr16:8916234
|
C | A | 297 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(294): Show | 302 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.906+268G>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 8/30 | chr16 | 8916234 | ||||||
| chr16:8916356
|
T | G | 183 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(180): Show | 186 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.906+146A>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 8/30 | chr16 | 8916356 | ||||||
| chr16:8916403
|
ATTTTCTG others(9): Show |
A | 118 | a0001c0001t0001g0306a0001c0001t0002g0005a0001c0001t0002g0061others(115): Show | 120 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.906+83_906+98delGA others(14): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 8/30 | chr16 | 8916403 | ||||||
| chr16:8916589
|
A | AC | 317 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(314): Show | 322 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.852-34_852-33insG | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 7/30 | chr16 | 8916589 | ||||||
| chr16:8916625
|
A | C | 2 | a0001c0001t0004g0054a0001c0001t0032g0055 | 2 | HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.852-69T>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 7/30 | chr16 | 8916625 | ||||||
| chr16:8916657
|
T | C | 1 | a0001c0001t0003g0202 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.852-101A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 7/30 | chr16 | 8916657 | ||||||
| chr16:8916854
|
G | T | 7 | a0001c0001t0001g0063a0001c0001t0001g0066a0001c0001t0001g0096others(4): Show | 7 | HG00741.hp1 HG01978.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.851+172C>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 7/30 | chr16 | 8916854 | ||||||
| chr16:8916890
|
C | T | 2 | a0001c0001t0004g0054a0001c0001t0032g0055 | 2 | HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.851+136G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 7/30 | chr16 | 8916890 | ||||||
| chr16:8916949
|
T | C | 1 | a0001c0001t0019g0289 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.851+77A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 7/30 | chr16 | 8916949 | ||||||
| chr16:8916969
|
T | TA | 14 | a0001c0001t0001g0047a0001c0001t0001g0110a0001c0001t0001g0117others(11): Show | 14 | HG01169.hp1 HG02486.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.851+56dupT | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 7/30 | chr16 | 8916969 | ||||||
| chr16:8916969
|
T | TAA | 159 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(156): Show | 161 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(158): Show |
intron_variant | MODIFIER | c.851+55_851+56dupTT | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 7/30 | chr16 | 8916969 | ||||||
| chr16:8916969
|
TA | T | 33 | a0001c0001t0001g0041a0001c0001t0002g0112a0001c0001t0002g0226others(30): Show | 34 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.851+56delT | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 7/30 | chr16 | 8916969 | ||||||
| chr16:8917222
|
G | A | 1 | a0001c0003t0001g0154 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.721-66C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 6/30 | chr16 | 8917222 | ||||||
| chr16:8917232
|
T | C | 1 | a0001c0001t0007g0042 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.721-76A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 6/30 | chr16 | 8917232 | ||||||
| chr16:8917274
|
G | A | 1 | a0001c0001t0003g0312 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.721-118C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 6/30 | chr16 | 8917274 | ||||||
| chr16:8917334
|
G | A | 1 | a0001c0001t0009g0010 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.721-178C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 6/30 | chr16 | 8917334 | ||||||
| chr16:8917366
|
A | G | 4 | a0001c0001t0006g0001a0001c0001t0006g0016a0001c0001t0006g0017others(1): Show | 5 | HG02280.hp2 HG03209.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.721-210T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 6/30 | chr16 | 8917366 | ||||||
| chr16:8917501
|
C | T | 1 | a0001c0001t0002g0252 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.721-345G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 6/30 | chr16 | 8917501 | ||||||
| chr16:8917535
|
C | T | 19 | a0001c0001t0001g0041a0001c0001t0003g0029a0001c0001t0003g0030others(16): Show | 19 | HG02132.hp1 HG02165.hp1 HG02970.hp1 others(16): Show |
intron_variant | MODIFIER | c.721-379G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 6/30 | chr16 | 8917535 | ||||||
| chr16:8917597
|
T | C | 1 | a0001c0001t0001g0126 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.721-441A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 6/30 | chr16 | 8917597 | ||||||
| chr16:8917661
|
G | C | 3 | a0001c0001t0004g0071a0001c0001t0004g0113a0001c0001t0004g0114 | 3 | HG02965.hp1 HG03486.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.721-505C>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 6/30 | chr16 | 8917661 | ||||||
| chr16:8917774
|
A | G | 1 | a0001c0001t0033g0322 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.721-618T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 6/30 | chr16 | 8917774 | ||||||
| chr16:8917829
|
A | G | 5 | a0001c0001t0012g0028a0001c0001t0012g0057a0001c0001t0014g0058others(2): Show | 5 | HG02886.hp1 HG03130.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.721-673T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 6/30 | chr16 | 8917829 | ||||||
| chr16:8917833
|
A | G | 3 | a0001c0001t0025g0056a0001c0001t0027g0169a0001c0001t0037g0330 | 3 | HG03453.hp1 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.721-677T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 6/30 | chr16 | 8917833 | ||||||
| chr16:8917850
|
C | T | 1 | a0001c0001t0038g0331 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.721-694G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 6/30 | chr16 | 8917850 | ||||||
| chr16:8917891
|
G | A | 1 | a0001c0001t0024g0060 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.721-735C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 6/30 | chr16 | 8917891 | ||||||
| chr16:8917926
|
A | G | 172 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(169): Show | 174 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.721-770T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 6/30 | chr16 | 8917926 | ||||||
| chr16:8917942
|
G | A | 1 | a0001c0001t0002g0035 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.721-786C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 6/30 | chr16 | 8917942 | ||||||
| chr16:8918171
|
G | A | 325 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(322): Show | 330 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.720+860C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 6/30 | chr16 | 8918171 | ||||||
| chr16:8918338
|
C | T | 1 | a0001c0001t0002g0262 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.720+693G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 6/30 | chr16 | 8918338 | ||||||
| chr16:8918390
|
A | G | 16 | a0001c0001t0002g0164a0001c0001t0002g0185a0001c0001t0002g0195others(13): Show | 16 | HG00423.hp1 HG00597.hp1 HG02040.hp1 others(13): Show |
intron_variant | MODIFIER | c.720+641T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 6/30 | chr16 | 8918390 | ||||||
| chr16:8918407
|
C | G | 1 | a0001c0001t0002g0199 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.720+624G>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 6/30 | chr16 | 8918407 | ||||||
| chr16:8918426
|
T | C | 1 | a0001c0001t0002g0199 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.720+605A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 6/30 | chr16 | 8918426 | ||||||
| chr16:8918532
|
G | C | 4 | a0001c0001t0006g0001a0001c0001t0006g0016a0001c0001t0006g0017others(1): Show | 5 | HG02280.hp2 HG03209.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.720+499C>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 6/30 | chr16 | 8918532 | ||||||
| chr16:8918603
|
A | G | 1 | a0001c0001t0001g0107 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.720+428T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 6/30 | chr16 | 8918603 | ||||||
| chr16:8918719
|
G | C | 2 | a0001c0001t0015g0317a0001c0001t0015g0318 | 2 | HG01496.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.720+312C>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 6/30 | chr16 | 8918719 | ||||||
| chr16:8918732
|
C | T | 3 | a0001c0001t0004g0071a0001c0001t0004g0113a0001c0001t0004g0114 | 3 | HG02965.hp1 HG03486.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.720+299G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 6/30 | chr16 | 8918732 | ||||||
| chr16:8918740
|
C | A | 11 | a0001c0001t0002g0069a0001c0001t0002g0070a0001c0001t0002g0072others(8): Show | 11 | HG01891.hp2 HG02451.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.720+291G>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 6/30 | chr16 | 8918740 | ||||||
| chr16:8918829
|
G | A | 168 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(165): Show | 170 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.720+202C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 6/30 | chr16 | 8918829 | ||||||
| chr16:8919173
|
C | T | 1 | a0001c0001t0031g0044 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.612-34G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 5/30 | chr16 | 8919173 | ||||||
| chr16:8919178
|
A | G | 10 | a0001c0001t0002g0035a0001c0001t0003g0121a0001c0001t0005g0052others(7): Show | 11 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(8): Show |
intron_variant | MODIFIER | c.612-39T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 5/30 | chr16 | 8919178 | ||||||
| chr16:8919239
|
G | A | 1 | a0001c0001t0022g0053 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.612-100C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 5/30 | chr16 | 8919239 | ||||||
| chr16:8919251
|
A | G | 19 | a0001c0001t0001g0041a0001c0001t0003g0029a0001c0001t0003g0030others(16): Show | 19 | HG02132.hp1 HG02165.hp1 HG02970.hp1 others(16): Show |
intron_variant | MODIFIER | c.612-112T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 5/30 | chr16 | 8919251 | ||||||
| chr16:8919354
|
A | G | 1 | a0001c0001t0005g0052 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.612-215T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 5/30 | chr16 | 8919354 | ||||||
| chr16:8919404
|
C | G | 4 | a0001c0001t0025g0056a0001c0001t0027g0169a0001c0001t0037g0330others(1): Show | 4 | HG02922.hp1 HG03453.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.612-265G>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 5/30 | chr16 | 8919404 | ||||||
| chr16:8919555
|
A | G | 325 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(322): Show | 330 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.612-416T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 5/30 | chr16 | 8919555 | ||||||
| chr16:8919607
|
T | C | 7 | a0001c0001t0003g0121a0001c0001t0007g0002a0001c0001t0007g0033others(4): Show | 8 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(5): Show |
intron_variant | MODIFIER | c.612-468A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 5/30 | chr16 | 8919607 | ||||||
| chr16:8919807
|
G | T | 1 | a0001c0001t0002g0282 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.611+552C>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 5/30 | chr16 | 8919807 | ||||||
| chr16:8919839
|
G | A | 6 | a0001c0001t0003g0121a0001c0001t0007g0002a0001c0001t0007g0033others(3): Show | 7 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(4): Show |
intron_variant | MODIFIER | c.611+520C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 5/30 | chr16 | 8919839 | ||||||
| chr16:8919947
|
T | C | 2 | a0001c0001t0004g0054a0001c0001t0032g0055 | 2 | HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.611+412A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 5/30 | chr16 | 8919947 | ||||||
| chr16:8919953
|
T | C | 1 | a0001c0001t0022g0053 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.611+406A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 5/30 | chr16 | 8919953 | ||||||
| chr16:8919988
|
C | T | 1 | a0001c0001t0022g0053 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.611+371G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 5/30 | chr16 | 8919988 | ||||||
| chr16:8920056
|
G | C | 1 | a0001c0001t0003g0215 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.611+303C>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 5/30 | chr16 | 8920056 | ||||||
| chr16:8920143
|
A | C | 1 | a0001c0001t0005g0245 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.611+216T>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 5/30 | chr16 | 8920143 | ||||||
| chr16:8920293
|
G | A | 1 | a0001c0001t0001g0124 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.611+66C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 5/30 | chr16 | 8920293 | ||||||
| chr16:8920493
|
T | C | 325 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(322): Show | 330 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.523-46A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 4/30 | chr16 | 8920493 | ||||||
| chr16:8920528
|
G | A | 171 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(168): Show | 173 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.523-81C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 4/30 | chr16 | 8920528 | ||||||
| chr16:8920559
|
T | A | 1 | a0001c0001t0002g0035 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.523-112A>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 4/30 | chr16 | 8920559 | ||||||
| chr16:8920577
|
T | G | 325 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(322): Show | 330 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.523-130A>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 4/30 | chr16 | 8920577 | ||||||
| chr16:8920803
|
C | T | 7 | a0001c0001t0003g0121a0001c0001t0007g0002a0001c0001t0007g0033others(4): Show | 8 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(5): Show |
intron_variant | MODIFIER | c.522+354G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 4/30 | chr16 | 8920803 | ||||||
| chr16:8920834
|
A | C | 1 | a0001c0001t0001g0146 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.522+323T>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 4/30 | chr16 | 8920834 | ||||||
| chr16:8920870
|
A | T | 1 | a0001c0001t0002g0035 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.522+287T>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 4/30 | chr16 | 8920870 | ||||||
| chr16:8920948
|
T | A | 183 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(180): Show | 185 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.522+209A>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 4/30 | chr16 | 8920948 | ||||||
| chr16:8921071
|
C | G | 324 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(321): Show | 329 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(326): Show |
intron_variant | MODIFIER | c.522+86G>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 4/30 | chr16 | 8921071 | ||||||
| chr16:8921071
|
C | T | 1 | a0001c0001t0003g0043 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.522+86G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 4/30 | chr16 | 8921071 | ||||||
| chr16:8921124
|
C | T | 18 | a0001c0001t0001g0041a0001c0001t0003g0029a0001c0001t0003g0030others(15): Show | 18 | HG02132.hp1 HG02165.hp1 HG02970.hp1 others(15): Show |
intron_variant | MODIFIER | c.522+33G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 4/30 | chr16 | 8921124 | ||||||
| chr16:8921395
|
A | T | 325 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(322): Show | 330 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.384-100T>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 3/30 | chr16 | 8921395 | ||||||
| chr16:8921401
|
T | C | 187 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(184): Show | 189 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.384-106A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 3/30 | chr16 | 8921401 | ||||||
| chr16:8921429
|
A | G | 1 | a0001c0001t0002g0262 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.384-134T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 3/30 | chr16 | 8921429 | ||||||
| chr16:8921710
|
G | T | 1 | a0001c0001t0005g0288 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.384-415C>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 3/30 | chr16 | 8921710 | ||||||
| chr16:8921744
|
C | A | 1 | a0001c0001t0002g0275 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.384-449G>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 3/30 | chr16 | 8921744 | ||||||
| chr16:8921856
|
A | C | 1 | a0001c0001t0001g0102 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.384-561T>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 3/30 | chr16 | 8921856 | ||||||
| chr16:8921858
|
C | A | 1 | a0001c0001t0001g0102 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.384-563G>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 3/30 | chr16 | 8921858 | ||||||
| chr16:8921859
|
A | T | 1 | a0001c0001t0001g0102 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.384-564T>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 3/30 | chr16 | 8921859 | ||||||
| chr16:8921864
|
T | C | 7 | a0001c0001t0003g0121a0001c0001t0007g0002a0001c0001t0007g0033others(4): Show | 8 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(5): Show |
intron_variant | MODIFIER | c.384-569A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 3/30 | chr16 | 8921864 | ||||||
| chr16:8921902
|
T | A | 301 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(298): Show | 306 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.384-607A>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 3/30 | chr16 | 8921902 | ||||||
| chr16:8921984
|
C | G | 1 | a0001c0001t0002g0164 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.384-689G>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 3/30 | chr16 | 8921984 | ||||||
| chr16:8922017
|
C | T | 1 | a0001c0001t0005g0052 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.384-722G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 3/30 | chr16 | 8922017 | ||||||
| chr16:8922207
|
G | A | 5 | a0001c0001t0002g0197a0001c0001t0002g0248a0001c0001t0002g0274others(2): Show | 5 | NA18975.hp1 NA18990.hp1 NA19004.hp2 others(2): Show |
intron_variant | MODIFIER | c.384-912C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 3/30 | chr16 | 8922207 | ||||||
| chr16:8922217
|
G | C | 1 | a0001c0001t0035g0321 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.384-922C>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 3/30 | chr16 | 8922217 | ||||||
| chr16:8922280
|
G | A | 1 | a0001c0001t0005g0052 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.383+935C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 3/30 | chr16 | 8922280 | ||||||
| chr16:8922359
|
A | T | 301 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(298): Show | 306 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.383+856T>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 3/30 | chr16 | 8922359 | ||||||
| chr16:8922404
|
C | A | 1 | a0001c0002t0001g0136 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.383+811G>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 3/30 | chr16 | 8922404 | ||||||
| chr16:8922517
|
C | A | 3 | a0001c0001t0004g0071a0001c0001t0004g0113a0001c0001t0004g0114 | 3 | HG02965.hp1 HG03486.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.383+698G>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 3/30 | chr16 | 8922517 | ||||||
| chr16:8922642
|
G | A | 1 | a0001c0001t0031g0044 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.383+573C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 3/30 | chr16 | 8922642 | ||||||
| chr16:8922675
|
C | A | 7 | a0001c0001t0003g0121a0001c0001t0007g0002a0001c0001t0007g0033others(4): Show | 8 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(5): Show |
intron_variant | MODIFIER | c.383+540G>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 3/30 | chr16 | 8922675 | ||||||
| chr16:8922692
|
G | C | 1 | a0001c0001t0031g0044 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.383+523C>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 3/30 | chr16 | 8922692 | ||||||
| chr16:8922720
|
T | C | 3 | a0001c0001t0002g0224a0001c0001t0002g0225a0001c0001t0002g0226 | 3 | HG02040.hp1 NA18988.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.383+495A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 3/30 | chr16 | 8922720 | ||||||
| chr16:8922767
|
C | T | 103 | a0001c0001t0002g0005a0001c0001t0002g0061a0001c0001t0002g0069others(100): Show | 105 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.383+448G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 3/30 | chr16 | 8922767 | ||||||
| chr16:8922988
|
T | C | 1 | a0001c0001t0005g0052 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.383+227A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 3/30 | chr16 | 8922988 | ||||||
| chr16:8923204
|
T | TACAACGA others(28): Show |
1 | a0001c0001t0001g0290 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.383+10_383+11insTT others(33): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 3/30 | chr16 | 8923204 | ||||||
| chr16:8923204
|
T | TACAACGA others(28): Show |
319 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(316): Show | 324 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.383+10_383+11insTT others(33): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 3/30 | chr16 | 8923204 | ||||||
| chr16:8923445
|
C | G | 2 | a0001c0001t0004g0054a0001c0001t0032g0055 | 2 | HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.185-32G>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8923445 | ||||||
| chr16:8923492
|
T | C | 1 | a0001c0001t0008g0320 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.185-79A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8923492 | ||||||
| chr16:8923568
|
A | G | 1 | a0001c0001t0001g0211 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.185-155T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8923568 | ||||||
| chr16:8923661
|
C | A | 1 | a0001c0001t0002g0100 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.185-248G>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8923661 | ||||||
| chr16:8923720
|
G | C | 4 | a0001c0001t0003g0313a0001c0001t0003g0314a0001c0001t0003g0315others(1): Show | 4 | HG02165.hp1 NA18994.hp2 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.185-307C>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8923720 | ||||||
| chr16:8923783
|
G | A | 1 | a0001c0001t0031g0044 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.185-370C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8923783 | ||||||
| chr16:8923792
|
G | A | 3 | a0001c0001t0012g0057a0001c0001t0014g0058a0001c0001t0014g0059 | 3 | HG02886.hp1 HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.185-379C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8923792 | ||||||
| chr16:8923819
|
G | A | 2 | a0001c0001t0004g0054a0001c0001t0032g0055 | 2 | HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.185-406C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8923819 | ||||||
| chr16:8923820
|
G | C | 2 | a0001c0001t0004g0054a0001c0001t0032g0055 | 2 | HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.185-407C>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8923820 | ||||||
| chr16:8923952
|
T | C | 1 | a0001c0001t0005g0288 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.185-539A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8923952 | ||||||
| chr16:8923957
|
G | A | 4 | a0001c0001t0002g0188a0001c0001t0002g0189a0001c0001t0002g0279others(1): Show | 4 | NA18948.hp1 NA18956.hp2 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.185-544C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8923957 | ||||||
| chr16:8924027
|
A | AT | 13 | a0001c0001t0002g0035a0001c0001t0005g0052a0001c0001t0007g0002others(10): Show | 14 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.185-615dupA | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8924027 | ||||||
| chr16:8924194
|
T | C | 1 | a0001c0005t0002g0176 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.185-781A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8924194 | ||||||
| chr16:8924808
|
T | G | 119 | a0001c0001t0001g0067a0001c0001t0001g0187a0001c0001t0002g0005others(116): Show | 121 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.185-1395A>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8924808 | ||||||
| chr16:8924916
|
G | A | 1 | a0001c0001t0038g0331 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.185-1503C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8924916 | ||||||
| chr16:8924965
|
C | A | 1 | a0001c0001t0001g0308 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.185-1552G>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8924965 | ||||||
| chr16:8924980
|
G | C | 1 | a0001c0001t0001g0172 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.185-1567C>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8924980 | ||||||
| chr16:8924988
|
G | A | 2 | a0001c0001t0004g0054a0001c0001t0032g0055 | 2 | HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.185-1575C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8924988 | ||||||
| chr16:8925039
|
T | C | 1 | a0001c0001t0008g0327 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.185-1626A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8925039 | ||||||
| chr16:8925166
|
G | A | 1 | a0001c0002t0001g0137 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.185-1753C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8925166 | ||||||
| chr16:8925192
|
T | C | 1 | a0001c0001t0001g0062 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.185-1779A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8925192 | ||||||
| chr16:8925295
|
A | G | 329 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(326): Show | 335 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.185-1882T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8925295 | ||||||
| chr16:8925559
|
C | T | 6 | a0001c0001t0007g0002a0001c0001t0007g0033a0001c0001t0007g0049others(3): Show | 7 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(4): Show |
intron_variant | MODIFIER | c.185-2146G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8925559 | ||||||
| chr16:8925594
|
T | C | 1 | a0001c0001t0017g0007 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.185-2181A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8925594 | ||||||
| chr16:8925650
|
C | T | 1 | a0001c0001t0003g0313 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.185-2237G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8925650 | ||||||
| chr16:8925853
|
A | G | 7 | a0001c0001t0001g0104a0001c0001t0001g0106a0001c0001t0001g0167others(4): Show | 7 | HG01891.hp1 HG02055.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.185-2440T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8925853 | ||||||
| chr16:8925914
|
G | T | 18 | a0001c0001t0001g0041a0001c0001t0003g0029a0001c0001t0003g0030others(15): Show | 18 | HG02132.hp1 HG02165.hp1 HG02970.hp1 others(15): Show |
intron_variant | MODIFIER | c.185-2501C>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8925914 | ||||||
| chr16:8925935
|
A | T | 1 | a0001c0001t0002g0035 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.185-2522T>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8925935 | ||||||
| chr16:8926003
|
A | C | 3 | a0001c0001t0002g0035a0001c0001t0005g0052a0001c0001t0022g0053 | 3 | HG03486.hp2 NA21309.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.185-2590T>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8926003 | ||||||
| chr16:8926061
|
G | C | 1 | a0001c0001t0031g0044 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.185-2648C>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8926061 | ||||||
| chr16:8926112
|
C | G | 1 | a0001c0001t0031g0044 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.185-2699G>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8926112 | ||||||
| chr16:8926131
|
G | C | 1 | a0001c0001t0005g0052 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.185-2718C>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8926131 | ||||||
| chr16:8926153
|
CA | C | 192 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(189): Show | 195 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.185-2741delT | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8926153 | ||||||
| chr16:8926199
|
C | T | 55 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0025others(52): Show | 55 | HG00140.hp1 HG00323.hp1 HG01070.hp1 others(52): Show |
intron_variant | MODIFIER | c.185-2786G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8926199 | ||||||
| chr16:8926206
|
G | A | 1 | a0001c0001t0002g0192 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.185-2793C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8926206 | ||||||
| chr16:8926214
|
G | A | 1 | a0001c0001t0002g0112 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.185-2801C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8926214 | ||||||
| chr16:8926244
|
G | C | 1 | a0001c0001t0012g0028 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.185-2831C>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8926244 | ||||||
| chr16:8926271
|
A | C | 1 | a0001c0001t0001g0171 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.185-2858T>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8926271 | ||||||
| chr16:8926272
|
G | A | 1 | a0001c0001t0031g0044 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.185-2859C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8926272 | ||||||
| chr16:8926295
|
T | C | 2 | a0001c0001t0002g0035a0001c0001t0005g0052 | 2 | HG03486.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.185-2882A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8926295 | ||||||
| chr16:8926311
|
C | T | 8 | a0001c0001t0002g0184a0001c0001t0002g0186a0001c0001t0002g0246others(5): Show | 8 | HG01243.hp2 HG01884.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.185-2898G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8926311 | ||||||
| chr16:8926369
|
C | G | 2 | a0001c0001t0001g0103a0001c0001t0001g0156 | 2 | HG02027.hp2 NA18943.hp2 |
intron_variant | MODIFIER | c.185-2956G>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8926369 | ||||||
| chr16:8926382
|
G | C | 1 | a0001c0001t0001g0146 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.185-2969C>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8926382 | ||||||
| chr16:8926435
|
T | C | 2 | a0001c0001t0001g0020a0001c0001t0029g0021 | 2 | HG02647.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.185-3022A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8926435 | ||||||
| chr16:8926503
|
G | C | 1 | a0001c0001t0002g0266 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.185-3090C>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8926503 | ||||||
| chr16:8926710
|
A | T | 8 | a0001c0002t0001g0091a0001c0002t0001g0118a0001c0002t0001g0131others(5): Show | 8 | HG01099.hp2 HG01261.hp1 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.185-3297T>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8926710 | ||||||
| chr16:8926886
|
A | G | 18 | a0001c0001t0001g0041a0001c0001t0003g0029a0001c0001t0003g0030others(15): Show | 18 | HG02132.hp1 HG02165.hp1 HG02970.hp1 others(15): Show |
intron_variant | MODIFIER | c.184+3407T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8926886 | ||||||
| chr16:8926952
|
T | G | 306 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(303): Show | 310 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(307): Show |
intron_variant | MODIFIER | c.184+3341A>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8926952 | ||||||
| chr16:8927037
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.184+3256C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8927037 | ||||||
| chr16:8927090
|
G | T | 1 | a0001c0001t0002g0035 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.184+3203C>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8927090 | ||||||
| chr16:8927095
|
G | A | 1 | a0001c0001t0022g0053 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.184+3198C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8927095 | ||||||
| chr16:8927245
|
C | A | 1 | a0001c0001t0004g0259 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.184+3048G>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8927245 | ||||||
| chr16:8927320
|
G | GA | 7 | a0001c0001t0002g0035a0001c0001t0002g0252a0001c0001t0005g0052others(4): Show | 7 | HG03195.hp2 HG03486.hp2 NA18977.hp2 others(4): Show |
intron_variant | MODIFIER | c.184+2972dupT | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8927320 | ||||||
| chr16:8927495
|
T | C | 1 | a0001c0001t0002g0035 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.184+2798A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8927495 | ||||||
| chr16:8927511
|
A | C | 1 | a0001c0001t0031g0044 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.184+2782T>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8927511 | ||||||
| chr16:8927530
|
T | G | 2 | a0001c0001t0001g0020a0001c0001t0029g0021 | 2 | HG02647.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.184+2763A>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8927530 | ||||||
| chr16:8927582
|
T | A | 2 | a0001c0001t0001g0003a0001c0001t0001g0124 | 3 | HG00639.hp1 HG02735.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.184+2711A>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8927582 | ||||||
| chr16:8927697
|
G | A | 1 | a0001c0001t0002g0115 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.184+2596C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8927697 | ||||||
| chr16:8927707
|
T | G | 4 | a0001c0001t0008g0320a0001c0001t0008g0327a0001c0001t0016g0323others(1): Show | 4 | HG00140.hp1 HG01515.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.184+2586A>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8927707 | ||||||
| chr16:8927851
|
A | G | 1 | a0001c0001t0001g0088 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.184+2442T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8927851 | ||||||
| chr16:8928003
|
G | A | 2 | a0001c0001t0005g0052a0001c0001t0031g0044 | 2 | NA20300.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.184+2290C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8928003 | ||||||
| chr16:8928077
|
T | C | 1 | a0001c0001t0001g0290 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.184+2216A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8928077 | ||||||
| chr16:8928162
|
T | C | 1 | a0001c0001t0002g0098 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.184+2131A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8928162 | ||||||
| chr16:8928190
|
C | A | 1 | a0001c0001t0005g0052 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.184+2103G>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8928190 | ||||||
| chr16:8928248
|
T | G | 1 | a0001c0001t0002g0035 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.184+2045A>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8928248 | ||||||
| chr16:8928284
|
G | A | 1 | a0001c0001t0022g0053 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.184+2009C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8928284 | ||||||
| chr16:8928293
|
C | A | 1 | a0001c0001t0022g0053 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.184+2000G>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8928293 | ||||||
| chr16:8928307
|
G | A | 5 | a0001c0001t0012g0028a0001c0001t0012g0057a0001c0001t0014g0058others(2): Show | 5 | HG02886.hp1 HG03130.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.184+1986C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8928307 | ||||||
| chr16:8928347
|
G | C | 2 | a0001c0001t0002g0163a0001c0001t0004g0301 | 2 | NA19003.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.184+1946C>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8928347 | ||||||
| chr16:8928368
|
T | C | 1 | a0001c0001t0004g0285 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.184+1925A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8928368 | ||||||
| chr16:8928402
|
T | G | 1 | a0001c0001t0002g0035 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.184+1891A>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8928402 | ||||||
| chr16:8928425
|
T | A | 2 | a0001c0001t0004g0054a0001c0001t0032g0055 | 2 | HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.184+1868A>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8928425 | ||||||
| chr16:8928481
|
C | G | 1 | a0001c0006t0004g0173 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.184+1812G>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8928481 | ||||||
| chr16:8928568
|
G | A | 1 | a0001c0001t0031g0044 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.184+1725C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8928568 | ||||||
| chr16:8928590
|
T | C | 1 | a0001c0001t0005g0052 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.184+1703A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8928590 | ||||||
| chr16:8928746
|
G | C | 1 | a0001c0001t0031g0044 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.184+1547C>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8928746 | ||||||
| chr16:8928883
|
T | C | 3 | a0001c0001t0001g0063a0001c0001t0001g0096a0001c0001t0001g0175 | 3 | HG00741.hp1 HG01978.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.184+1410A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8928883 | ||||||
| chr16:8928910
|
C | T | 12 | a0001c0001t0002g0035a0001c0001t0004g0054a0001c0001t0007g0002others(9): Show | 13 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.184+1383G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8928910 | ||||||
| chr16:8929018
|
CTA | C | 227 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(224): Show | 231 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(228): Show |
intron_variant | MODIFIER | c.184+1273_184+1274d others(4): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8929018 | ||||||
| chr16:8929038
|
T | C | 2 | a0001c0001t0004g0006a0001c0001t0004g0304 | 3 | HG01257.hp1 HG01258.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.184+1255A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8929038 | ||||||
| chr16:8929043
|
C | T | 1 | a0001c0001t0002g0035 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.184+1250G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8929043 | ||||||
| chr16:8929045
|
T | TA | 62 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0023others(59): Show | 62 | HG00140.hp1 HG00323.hp1 HG01070.hp1 others(59): Show |
intron_variant | MODIFIER | c.184+1247dupT | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8929045 | ||||||
| chr16:8929070
|
G | T | 4 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0211others(1): Show | 4 | HG00609.hp2 HG02015.hp2 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.184+1223C>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8929070 | ||||||
| chr16:8929089
|
T | C | 1 | a0001c0001t0022g0053 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.184+1204A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8929089 | ||||||
| chr16:8929122
|
T | C | 1 | a0001c0001t0005g0052 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.184+1171A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8929122 | ||||||
| chr16:8929197
|
C | G | 4 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0211others(1): Show | 4 | HG00609.hp2 HG02015.hp2 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.184+1096G>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8929197 | ||||||
| chr16:8929226
|
G | A | 1 | a0001c0001t0001g0223 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.184+1067C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8929226 | ||||||
| chr16:8929298
|
T | C | 13 | a0001c0001t0001g0067a0001c0001t0001g0103a0001c0001t0001g0155others(10): Show | 13 | HG00323.hp1 HG01070.hp1 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.184+995A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8929298 | ||||||
| chr16:8929305
|
C | T | 1 | a0001c0001t0002g0275 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.184+988G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8929305 | ||||||
| chr16:8929306
|
G | A | 2 | a0001c0001t0006g0001a0001c0001t0018g0015 | 3 | HG02280.hp2 HG03209.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.184+987C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8929306 | ||||||
| chr16:8929683
|
T | C | 2 | a0001c0001t0003g0046a0001c0001t0005g0287 | 2 | HG02451.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.184+610A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8929683 | ||||||
| chr16:8929793
|
G | C | 1 | a0001c0001t0020g0064 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.184+500C>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8929793 | ||||||
| chr16:8929864
|
G | A | 1 | a0001c0001t0002g0282 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.184+429C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8929864 | ||||||
| chr16:8930025
|
C | G | 1 | a0001c0001t0025g0056 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.184+268G>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8930025 | ||||||
| chr16:8930186
|
C | T | 1 | a0001c0001t0039g0332 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.184+107G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 2/30 | chr16 | 8930186 | ||||||
| chr16:8930425
|
G | C | 8 | a0001c0001t0005g0052a0001c0001t0007g0002a0001c0001t0007g0033others(5): Show | 9 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(6): Show |
intron_variant | MODIFIER | c.80-28C>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8930425 | ||||||
| chr16:8930483
|
T | C | 1 | a0001c0001t0002g0119 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.80-86A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8930483 | ||||||
| chr16:8930613
|
C | T | 5 | a0001c0001t0012g0028a0001c0001t0012g0057a0001c0001t0014g0058others(2): Show | 5 | HG02886.hp1 HG03130.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.80-216G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8930613 | ||||||
| chr16:8930630
|
T | C | 1 | a0001c0001t0030g0151 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.80-233A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8930630 | ||||||
| chr16:8930631
|
T | G | 1 | a0001c0001t0005g0052 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.80-234A>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8930631 | ||||||
| chr16:8930633
|
CT | C | 3 | a0001c0001t0004g0071a0001c0001t0004g0113a0001c0001t0004g0114 | 3 | HG02965.hp1 HG03486.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.80-237delA | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8930633 | ||||||
| chr16:8930668
|
A | C | 1 | a0001c0001t0005g0052 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.80-271T>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8930668 | ||||||
| chr16:8930707
|
G | A | 228 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(225): Show | 232 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.80-310C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8930707 | ||||||
| chr16:8930798
|
G | A | 2 | a0001c0001t0001g0003a0001c0001t0001g0124 | 3 | HG00639.hp1 HG02735.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.80-401C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8930798 | ||||||
| chr16:8930900
|
C | T | 63 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0023others(60): Show | 63 | HG00140.hp1 HG00323.hp1 HG00733.hp1 others(60): Show |
intron_variant | MODIFIER | c.80-503G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8930900 | ||||||
| chr16:8930921
|
A | T | 2 | a0001c0001t0002g0077a0001c0001t0003g0121 | 2 | HG00733.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.80-524T>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8930921 | ||||||
| chr16:8930949
|
T | A | 325 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(322): Show | 330 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.80-552A>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8930949 | ||||||
| chr16:8930973
|
T | TA | 226 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(223): Show | 230 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.80-577dupT | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8930973 | ||||||
| chr16:8930973
|
T | TAA | 6 | a0001c0001t0001g0109a0001c0001t0002g0112a0001c0001t0002g0199others(3): Show | 6 | HG01099.hp1 HG02976.hp1 HG03942.hp2 others(3): Show |
intron_variant | MODIFIER | c.80-578_80-577dupTT | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8930973 | ||||||
| chr16:8931062
|
T | A | 1 | a0001c0001t0008g0328 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.80-665A>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8931062 | ||||||
| chr16:8931190
|
C | CT | 12 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0075others(9): Show | 13 | HG00140.hp2 HG00280.hp1 HG00642.hp1 others(10): Show |
intron_variant | MODIFIER | c.80-794dupA | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8931190 | ||||||
| chr16:8931234
|
C | G | 2 | a0001c0001t0001g0307a0001c0001t0001g0308 | 2 | NA18968.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.80-837G>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8931234 | ||||||
| chr16:8931236
|
T | C | 1 | a0001c0001t0001g0148 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.80-839A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8931236 | ||||||
| chr16:8931395
|
T | C | 6 | a0001c0001t0007g0002a0001c0001t0007g0033a0001c0001t0007g0049others(3): Show | 7 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(4): Show |
intron_variant | MODIFIER | c.80-998A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8931395 | ||||||
| chr16:8931396
|
C | G | 1 | a0001c0001t0031g0044 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.80-999G>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8931396 | ||||||
| chr16:8931457
|
G | C | 1 | a0001c0001t0001g0084 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.80-1060C>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8931457 | ||||||
| chr16:8931548
|
G | T | 1 | a0001c0001t0015g0317 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.80-1151C>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8931548 | ||||||
| chr16:8931645
|
C | T | 1 | a0001c0001t0001g0159 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.80-1248G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8931645 | ||||||
| chr16:8931666
|
A | G | 60 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0023others(57): Show | 60 | HG00140.hp1 HG00323.hp1 HG01070.hp1 others(57): Show |
intron_variant | MODIFIER | c.80-1269T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8931666 | ||||||
| chr16:8931698
|
A | C | 2 | a0001c0001t0001g0065a0001c0001t0038g0331 | 2 | NA18612.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.80-1301T>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8931698 | ||||||
| chr16:8931908
|
A | G | 1 | a0001c0001t0002g0035 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.80-1511T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8931908 | ||||||
| chr16:8931960
|
G | T | 1 | a0001c0001t0002g0035 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.80-1563C>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8931960 | ||||||
| chr16:8932115
|
T | A | 2 | a0001c0001t0002g0207a0001c0001t0002g0210 | 2 | HG00621.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.80-1718A>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8932115 | ||||||
| chr16:8932242
|
C | T | 6 | a0001c0001t0007g0002a0001c0001t0007g0033a0001c0001t0007g0049others(3): Show | 7 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(4): Show |
intron_variant | MODIFIER | c.80-1845G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8932242 | ||||||
| chr16:8932288
|
C | T | 3 | a0001c0001t0002g0224a0001c0001t0002g0225a0001c0001t0002g0226 | 3 | HG02040.hp1 NA18988.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.80-1891G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8932288 | ||||||
| chr16:8932322
|
C | T | 325 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(322): Show | 330 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.80-1925G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8932322 | ||||||
| chr16:8932344
|
C | G | 1 | a0001c0001t0001g0075 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.80-1947G>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8932344 | ||||||
| chr16:8932354
|
C | A | 1 | a0001c0001t0003g0046 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.80-1957G>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8932354 | ||||||
| chr16:8932383
|
T | C | 1 | a0001c0001t0003g0138 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.80-1986A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8932383 | ||||||
| chr16:8932395
|
A | C | 1 | a0001c0001t0001g0167 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.80-1998T>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8932395 | ||||||
| chr16:8932467
|
CCAT | C | 5 | a0001c0001t0012g0028a0001c0001t0012g0057a0001c0001t0014g0058others(2): Show | 5 | HG02886.hp1 HG03130.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.80-2073_80-2071del others(3): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8932467 | ||||||
| chr16:8932543
|
G | A | 258 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(255): Show | 263 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(260): Show |
intron_variant | MODIFIER | c.80-2146C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8932543 | ||||||
| chr16:8932587
|
C | T | 2 | a0001c0001t0002g0098a0001c0001t0002g0284 | 2 | HG02027.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.80-2190G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8932587 | ||||||
| chr16:8932619
|
AAGAG | A | 231 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(228): Show | 235 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.80-2226_80-2223del others(4): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8932619 | ||||||
| chr16:8932674
|
T | C | 1 | a0001c0001t0005g0052 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.80-2277A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8932674 | ||||||
| chr16:8932701
|
A | G | 2 | a0001c0001t0002g0035a0001c0001t0002g0072 | 2 | HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.80-2304T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8932701 | ||||||
| chr16:8932723
|
T | A | 1 | a0001c0001t0004g0285 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.80-2326A>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8932723 | ||||||
| chr16:8932799
|
A | C | 6 | a0001c0001t0007g0002a0001c0001t0007g0033a0001c0001t0007g0049others(3): Show | 7 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(4): Show |
intron_variant | MODIFIER | c.80-2402T>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8932799 | ||||||
| chr16:8932803
|
T | C | 1 | a0001c0001t0003g0039 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.80-2406A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8932803 | ||||||
| chr16:8932805
|
G | C | 1 | a0001c0001t0017g0007 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.80-2408C>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8932805 | ||||||
| chr16:8933265
|
C | T | 11 | a0001c0001t0001g0088a0001c0001t0001g0090a0001c0001t0001g0097others(8): Show | 11 | HG00621.hp2 HG02056.hp2 NA18947.hp2 others(8): Show |
intron_variant | MODIFIER | c.80-2868G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8933265 | ||||||
| chr16:8933307
|
G | T | 1 | a0001c0001t0031g0044 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.80-2910C>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8933307 | ||||||
| chr16:8933329
|
A | G | 1 | a0001c0001t0037g0330 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.80-2932T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8933329 | ||||||
| chr16:8933369
|
A | G | 1 | a0001c0001t0002g0035 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.80-2972T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8933369 | ||||||
| chr16:8933494
|
A | G | 61 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0023others(58): Show | 61 | HG00140.hp1 HG00323.hp1 HG01070.hp1 others(58): Show |
intron_variant | MODIFIER | c.80-3097T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8933494 | ||||||
| chr16:8933548
|
T | C | 1 | a0001c0001t0002g0035 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.80-3151A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8933548 | ||||||
| chr16:8933584
|
T | G | 235 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(232): Show | 239 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.80-3187A>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8933584 | ||||||
| chr16:8933613
|
C | T | 8 | a0001c0001t0007g0002a0001c0001t0007g0033a0001c0001t0007g0049others(5): Show | 9 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(6): Show |
intron_variant | MODIFIER | c.80-3216G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8933613 | ||||||
| chr16:8933644
|
G | A | 2 | a0001c0001t0001g0109a0001c0001t0011g0108 | 2 | NA18980.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.80-3247C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8933644 | ||||||
| chr16:8933665
|
T | C | 17 | a0001c0001t0001g0041a0001c0001t0003g0029a0001c0001t0003g0030others(14): Show | 17 | HG02132.hp1 HG02165.hp1 HG02970.hp1 others(14): Show |
intron_variant | MODIFIER | c.80-3268A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8933665 | ||||||
| chr16:8933758
|
CT | C | 16 | a0001c0001t0001g0104a0001c0001t0001g0106a0001c0001t0001g0161others(13): Show | 17 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(14): Show |
intron_variant | MODIFIER | c.80-3362delA | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8933758 | ||||||
| chr16:8933913
|
G | A | 1 | a0001c0001t0002g0193 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.80-3516C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8933913 | ||||||
| chr16:8933969
|
C | G | 1 | a0001c0001t0031g0044 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.80-3572G>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8933969 | ||||||
| chr16:8933970
|
T | G | 1 | a0001c0001t0031g0044 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.80-3573A>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8933970 | ||||||
| chr16:8934124
|
C | T | 325 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(322): Show | 330 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.80-3727G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8934124 | ||||||
| chr16:8934225
|
G | A | 1 | a0001c0001t0031g0044 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.80-3828C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8934225 | ||||||
| chr16:8934282
|
T | C | 1 | a0001c0001t0001g0104 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.80-3885A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8934282 | ||||||
| chr16:8934327
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.80-3930G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8934327 | ||||||
| chr16:8934338
|
G | C | 4 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0211others(1): Show | 4 | HG00609.hp2 HG02015.hp2 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.80-3941C>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8934338 | ||||||
| chr16:8934491
|
C | T | 18 | a0001c0001t0001g0041a0001c0001t0003g0029a0001c0001t0003g0030others(15): Show | 18 | HG02132.hp1 HG02165.hp1 HG02970.hp1 others(15): Show |
intron_variant | MODIFIER | c.80-4094G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8934491 | ||||||
| chr16:8934511
|
G | A | 1 | a0001c0001t0031g0044 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.80-4114C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8934511 | ||||||
| chr16:8934519
|
T | G | 1 | a0001c0001t0031g0044 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.80-4122A>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8934519 | ||||||
| chr16:8934571
|
G | C | 18 | a0001c0001t0001g0041a0001c0001t0003g0029a0001c0001t0003g0030others(15): Show | 18 | HG02132.hp1 HG02165.hp1 HG02970.hp1 others(15): Show |
intron_variant | MODIFIER | c.80-4174C>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8934571 | ||||||
| chr16:8934679
|
T | C | 9 | a0001c0001t0002g0195a0001c0001t0002g0196a0001c0001t0002g0213others(6): Show | 9 | NA18747.hp2 NA18972.hp1 NA18991.hp1 others(6): Show |
intron_variant | MODIFIER | c.80-4282A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8934679 | ||||||
| chr16:8934684
|
G | C | 237 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(234): Show | 241 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(238): Show |
intron_variant | MODIFIER | c.80-4287C>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8934684 | ||||||
| chr16:8934773
|
T | C | 231 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(228): Show | 235 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.80-4376A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8934773 | ||||||
| chr16:8934782
|
G | A | 1 | a0001c0001t0002g0035 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.80-4385C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8934782 | ||||||
| chr16:8934788
|
A | C | 141 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(138): Show | 143 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(140): Show |
intron_variant | MODIFIER | c.80-4391T>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8934788 | ||||||
| chr16:8934936
|
TAAGACAT others(4): Show |
T | 1 | a0001c0001t0022g0053 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.80-4550_80-4540del others(11): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8934936 | ||||||
| chr16:8934951
|
C | A | 1 | a0001c0001t0031g0044 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.80-4554G>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8934951 | ||||||
| chr16:8934955
|
A | G | 325 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(322): Show | 330 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.80-4558T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8934955 | ||||||
| chr16:8935151
|
T | C | 60 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0023others(57): Show | 60 | HG00140.hp1 HG00323.hp1 HG01070.hp1 others(57): Show |
intron_variant | MODIFIER | c.80-4754A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8935151 | ||||||
| chr16:8935201
|
A | AT | 103 | a0001c0001t0001g0062a0001c0001t0001g0066a0001c0001t0001g0142others(100): Show | 105 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.80-4805dupA | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8935201 | ||||||
| chr16:8935201
|
A | ATT | 9 | a0001c0001t0001g0147a0001c0001t0002g0193a0001c0001t0002g0199others(6): Show | 9 | HG00280.hp2 HG00438.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.80-4806_80-4805dup others(2): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8935201 | ||||||
| chr16:8935201
|
AT | A | 22 | a0001c0001t0001g0041a0001c0001t0001g0086a0001c0001t0001g0105others(19): Show | 24 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.80-4805delA | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8935201 | ||||||
| chr16:8935269
|
C | T | 1 | a0001c0001t0022g0053 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.80-4872G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8935269 | ||||||
| chr16:8935315
|
T | G | 1 | a0001c0001t0001g0087 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.80-4918A>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8935315 | ||||||
| chr16:8935352
|
G | A | 1 | a0001c0001t0003g0039 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.80-4955C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8935352 | ||||||
| chr16:8935366
|
T | C | 5 | a0001c0001t0012g0028a0001c0001t0012g0057a0001c0001t0014g0058others(2): Show | 5 | HG02886.hp1 HG03130.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.80-4969A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8935366 | ||||||
| chr16:8935403
|
G | T | 6 | a0001c0001t0007g0002a0001c0001t0007g0033a0001c0001t0007g0049others(3): Show | 7 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(4): Show |
intron_variant | MODIFIER | c.80-5006C>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8935403 | ||||||
| chr16:8935412
|
C | G | 1 | a0001c0001t0001g0079 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.80-5015G>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8935412 | ||||||
| chr16:8935432
|
A | C | 1 | a0001c0001t0001g0150 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.80-5035T>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8935432 | ||||||
| chr16:8935508
|
G | A | 1 | a0001c0001t0022g0053 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.80-5111C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8935508 | ||||||
| chr16:8935563
|
T | C | 4 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(1): Show | 4 | HG01081.hp2 HG01433.hp2 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.80-5166A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8935563 | ||||||
| chr16:8935656
|
G | A | 1 | a0001c0002t0001g0239 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.80-5259C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8935656 | ||||||
| chr16:8935752
|
T | C | 329 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(326): Show | 335 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.80-5355A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8935752 | ||||||
| chr16:8935939
|
G | A | 19 | a0001c0001t0001g0041a0001c0001t0002g0193a0001c0001t0003g0029others(16): Show | 19 | HG00438.hp2 HG02132.hp1 HG02165.hp1 others(16): Show |
intron_variant | MODIFIER | c.80-5542C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8935939 | ||||||
| chr16:8935942
|
A | T | 6 | a0001c0001t0007g0002a0001c0001t0007g0033a0001c0001t0007g0049others(3): Show | 7 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(4): Show |
intron_variant | MODIFIER | c.80-5545T>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8935942 | ||||||
| chr16:8935998
|
C | T | 1 | a0001c0001t0002g0149 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.80-5601G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8935998 | ||||||
| chr16:8936020
|
A | G | 2 | a0001c0001t0002g0186a0001c0001t0002g0253 | 2 | HG02109.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.80-5623T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8936020 | ||||||
| chr16:8936058
|
G | A | 1 | a0001c0001t0001g0171 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.80-5661C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8936058 | ||||||
| chr16:8936064
|
C | T | 1 | a0001c0001t0001g0146 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.80-5667G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8936064 | ||||||
| chr16:8936131
|
G | C | 1 | a0001c0001t0002g0179 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.80-5734C>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8936131 | ||||||
| chr16:8936150
|
G | A | 5 | a0001c0001t0001g0104a0001c0001t0001g0106a0001c0001t0001g0170others(2): Show | 5 | HG01891.hp1 HG02055.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.80-5753C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8936150 | ||||||
| chr16:8936219
|
A | G | 6 | a0001c0001t0001g0068a0001c0001t0001g0123a0001c0001t0001g0293others(3): Show | 6 | HG02015.hp1 HG02155.hp1 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.80-5822T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8936219 | ||||||
| chr16:8936291
|
C | G | 1 | a0001c0001t0002g0035 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.80-5894G>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8936291 | ||||||
| chr16:8936339
|
G | C | 241 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(238): Show | 246 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.80-5942C>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8936339 | ||||||
| chr16:8936384
|
T | A | 1 | a0001c0001t0002g0035 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.80-5987A>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8936384 | ||||||
| chr16:8936479
|
T | C | 1 | a0001c0001t0001g0296 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.80-6082A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8936479 | ||||||
| chr16:8936587
|
C | A | 3 | a0001c0001t0001g0066a0001c0001t0001g0109a0001c0001t0011g0108 | 3 | HG02135.hp1 NA18980.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.80-6190G>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8936587 | ||||||
| chr16:8936587
|
C | G | 317 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(314): Show | 322 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.80-6190G>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8936587 | ||||||
| chr16:8936638
|
C | T | 1 | a0001c0001t0001g0088 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.80-6241G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8936638 | ||||||
| chr16:8936662
|
C | G | 2 | a0001c0001t0004g0054a0001c0001t0032g0055 | 2 | HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.80-6265G>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8936662 | ||||||
| chr16:8936800
|
C | T | 3 | a0001c0001t0025g0056a0001c0001t0027g0169a0001c0001t0037g0330 | 3 | HG03453.hp1 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.80-6403G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8936800 | ||||||
| chr16:8936936
|
T | C | 1 | a0001c0001t0002g0193 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.80-6539A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8936936 | ||||||
| chr16:8937019
|
T | C | 1 | a0001c0001t0002g0311 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.80-6622A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8937019 | ||||||
| chr16:8937059
|
C | G | 242 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(239): Show | 247 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.80-6662G>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8937059 | ||||||
| chr16:8937136
|
G | C | 58 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0023others(55): Show | 58 | HG00140.hp1 HG00323.hp1 HG01070.hp1 others(55): Show |
intron_variant | MODIFIER | c.80-6739C>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8937136 | ||||||
| chr16:8937206
|
CT | C | 284 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(281): Show | 288 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(285): Show |
intron_variant | MODIFIER | c.80-6810delA | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8937206 | ||||||
| chr16:8937213
|
T | A | 10 | a0001c0001t0001g0187a0001c0001t0001g0298a0001c0001t0004g0054others(7): Show | 11 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(8): Show |
intron_variant | MODIFIER | c.80-6816A>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8937213 | ||||||
| chr16:8937213
|
TA | T | 27 | a0001c0001t0001g0041a0001c0001t0002g0164a0001c0001t0002g0185others(24): Show | 27 | HG00438.hp2 HG00597.hp1 HG02132.hp1 others(24): Show |
intron_variant | MODIFIER | c.80-6817delT | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8937213 | ||||||
| chr16:8937247
|
T | C | 294 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(291): Show | 298 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(295): Show |
intron_variant | MODIFIER | c.80-6850A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8937247 | ||||||
| chr16:8937286
|
T | C | 1 | a0001c0001t0002g0035 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.80-6889A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8937286 | ||||||
| chr16:8937316
|
G | A | 11 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0099others(8): Show | 11 | HG00408.hp2 HG00621.hp1 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.80-6919C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8937316 | ||||||
| chr16:8937328
|
T | G | 1 | a0001c0001t0004g0285 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.80-6931A>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8937328 | ||||||
| chr16:8937398
|
C | T | 1 | a0001c0001t0007g0002 | 2 | HG01106.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.80-7001G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8937398 | ||||||
| chr16:8937435
|
A | G | 17 | a0001c0001t0002g0164a0001c0001t0002g0185a0001c0001t0002g0195others(14): Show | 17 | HG00423.hp1 HG00597.hp1 HG02040.hp1 others(14): Show |
intron_variant | MODIFIER | c.80-7038T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8937435 | ||||||
| chr16:8937498
|
C | T | 1 | a0001c0001t0002g0035 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.80-7101G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8937498 | ||||||
| chr16:8937630
|
A | G | 320 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(317): Show | 325 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.80-7233T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8937630 | ||||||
| chr16:8937843
|
G | A | 1 | a0001c0001t0001g0178 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.80-7446C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8937843 | ||||||
| chr16:8937899
|
A | G | 1 | a0001c0001t0031g0044 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.80-7502T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8937899 | ||||||
| chr16:8937936
|
A | G | 1 | a0001c0001t0012g0028 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.80-7539T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8937936 | ||||||
| chr16:8938158
|
G | A | 56 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0025others(53): Show | 56 | HG00140.hp1 HG00323.hp1 HG01070.hp1 others(53): Show |
intron_variant | MODIFIER | c.80-7761C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8938158 | ||||||
| chr16:8938243
|
G | A | 19 | a0001c0001t0001g0041a0001c0001t0002g0193a0001c0001t0003g0029others(16): Show | 19 | HG00438.hp2 HG02132.hp1 HG02165.hp1 others(16): Show |
intron_variant | MODIFIER | c.80-7846C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8938243 | ||||||
| chr16:8938339
|
C | CA | 99 | a0001c0001t0001g0084a0001c0001t0001g0187a0001c0001t0001g0269others(96): Show | 101 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.80-7943dupT | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8938339 | ||||||
| chr16:8938339
|
CA | C | 78 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0023others(75): Show | 79 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.80-7943delT | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8938339 | ||||||
| chr16:8938349
|
A | G | 1 | a0001c0001t0003g0043 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.80-7952T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8938349 | ||||||
| chr16:8938372
|
T | C | 6 | a0001c0001t0007g0002a0001c0001t0007g0033a0001c0001t0007g0049others(3): Show | 7 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(4): Show |
intron_variant | MODIFIER | c.80-7975A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8938372 | ||||||
| chr16:8938466
|
A | G | 9 | a0001c0001t0002g0100a0001c0002t0001g0091a0001c0002t0001g0118others(6): Show | 9 | HG01099.hp2 HG01261.hp1 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.80-8069T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8938466 | ||||||
| chr16:8938535
|
A | G | 1 | a0001c0001t0001g0306 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.80-8138T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8938535 | ||||||
| chr16:8938605
|
C | T | 1 | a0001c0001t0002g0277 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.80-8208G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8938605 | ||||||
| chr16:8938627
|
G | A | 3 | a0001c0001t0025g0056a0001c0001t0027g0169a0001c0001t0037g0330 | 3 | HG03453.hp1 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.80-8230C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8938627 | ||||||
| chr16:8938639
|
G | A | 4 | a0001c0001t0025g0056a0001c0001t0027g0169a0001c0001t0037g0330others(1): Show | 4 | HG02922.hp1 HG03453.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.80-8242C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8938639 | ||||||
| chr16:8938682
|
G | C | 1 | a0001c0001t0001g0178 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.80-8285C>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8938682 | ||||||
| chr16:8938710
|
C | CA | 149 | a0001c0001t0001g0045a0001c0001t0001g0062a0001c0001t0001g0063others(146): Show | 151 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.80-8314dupT | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8938710 | ||||||
| chr16:8938710
|
C | CAA | 58 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0023others(55): Show | 58 | HG00140.hp1 HG00323.hp1 HG01070.hp1 others(55): Show |
intron_variant | MODIFIER | c.80-8315_80-8314dup others(2): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8938710 | ||||||
| chr16:8938845
|
C | A | 1 | a0001c0001t0017g0007 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.80-8448G>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8938845 | ||||||
| chr16:8938888
|
T | C | 19 | a0001c0001t0001g0041a0001c0001t0002g0193a0001c0001t0003g0029others(16): Show | 19 | HG00438.hp2 HG02132.hp1 HG02165.hp1 others(16): Show |
intron_variant | MODIFIER | c.80-8491A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8938888 | ||||||
| chr16:8938983
|
C | T | 1 | a0001c0001t0002g0035 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.80-8586G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8938983 | ||||||
| chr16:8939020
|
T | C | 236 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(233): Show | 240 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.80-8623A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8939020 | ||||||
| chr16:8939107
|
A | G | 61 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0023others(58): Show | 61 | HG00140.hp1 HG00323.hp1 HG01070.hp1 others(58): Show |
intron_variant | MODIFIER | c.80-8710T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8939107 | ||||||
| chr16:8939129
|
T | A | 9 | a0001c0001t0002g0098a0001c0002t0001g0091a0001c0002t0001g0118others(6): Show | 9 | HG01099.hp2 HG01261.hp1 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.80-8732A>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8939129 | ||||||
| chr16:8939164
|
G | A | 1 | a0001c0001t0002g0035 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.80-8767C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8939164 | ||||||
| chr16:8939194
|
G | A | 1 | a0001c0002t0001g0137 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.80-8797C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8939194 | ||||||
| chr16:8939249
|
G | T | 1 | a0001c0001t0002g0035 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.80-8852C>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8939249 | ||||||
| chr16:8939413
|
G | T | 1 | a0001c0001t0002g0112 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.80-9016C>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8939413 | ||||||
| chr16:8939521
|
T | C | 2 | a0001c0001t0013g0257a0001c0001t0013g0258 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.80-9124A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8939521 | ||||||
| chr16:8939657
|
C | A | 19 | a0001c0001t0001g0041a0001c0001t0002g0193a0001c0001t0003g0029others(16): Show | 19 | HG00438.hp2 HG02132.hp1 HG02165.hp1 others(16): Show |
intron_variant | MODIFIER | c.80-9260G>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8939657 | ||||||
| chr16:8939733
|
T | C | 221 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(218): Show | 225 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.80-9336A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8939733 | ||||||
| chr16:8939775
|
T | C | 1 | a0001c0001t0002g0256 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.80-9378A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8939775 | ||||||
| chr16:8939875
|
A | G | 1 | a0001c0006t0004g0173 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.80-9478T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8939875 | ||||||
| chr16:8939898
|
A | G | 12 | a0001c0001t0001g0041a0001c0001t0003g0029a0001c0001t0003g0030others(9): Show | 12 | HG02132.hp1 NA18941.hp2 NA18947.hp1 others(9): Show |
intron_variant | MODIFIER | c.80-9501T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8939898 | ||||||
| chr16:8939939
|
A | T | 6 | a0001c0001t0007g0002a0001c0001t0007g0033a0001c0001t0007g0049others(3): Show | 7 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(4): Show |
intron_variant | MODIFIER | c.80-9542T>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8939939 | ||||||
| chr16:8939955
|
A | G | 325 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(322): Show | 330 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.80-9558T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8939955 | ||||||
| chr16:8939989
|
T | C | 2 | a0001c0001t0004g0054a0001c0001t0032g0055 | 2 | HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.80-9592A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8939989 | ||||||
| chr16:8940001
|
G | A | 1 | a0001c0001t0003g0046 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.80-9604C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8940001 | ||||||
| chr16:8940111
|
C | G | 1 | a0001c0001t0001g0161 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.80-9714G>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8940111 | ||||||
| chr16:8940127
|
T | C | 2 | a0001c0001t0001g0020a0001c0001t0029g0021 | 2 | HG02647.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.80-9730A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8940127 | ||||||
| chr16:8940293
|
G | A | 2 | a0001c0001t0001g0157a0001c0001t0001g0178 | 2 | HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.80-9896C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8940293 | ||||||
| chr16:8940365
|
A | G | 1 | a0001c0005t0002g0176 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.80-9968T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8940365 | ||||||
| chr16:8940403
|
G | T | 2 | a0001c0001t0001g0128a0001c0001t0001g0129 | 2 | NA18966.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.80-10006C>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8940403 | ||||||
| chr16:8940477
|
T | C | 1 | a0001c0001t0022g0053 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.80-10080A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8940477 | ||||||
| chr16:8940528
|
G | A | 1 | a0001c0001t0003g0312 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.80-10131C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8940528 | ||||||
| chr16:8940566
|
A | G | 325 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(322): Show | 330 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.80-10169T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8940566 | ||||||
| chr16:8940673
|
C | T | 3 | a0001c0001t0001g0123a0001c0001t0001g0293a0001c0001t0002g0256 | 3 | HG02015.hp1 NA18971.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.80-10276G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8940673 | ||||||
| chr16:8940733
|
T | A | 8 | a0001c0001t0002g0184a0001c0001t0002g0186a0001c0001t0002g0246others(5): Show | 8 | HG01243.hp2 HG01884.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.80-10336A>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8940733 | ||||||
| chr16:8940742
|
C | T | 1 | a0001c0001t0010g0236 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.80-10345G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8940742 | ||||||
| chr16:8940839
|
G | C | 1 | a0001c0001t0001g0095 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.80-10442C>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8940839 | ||||||
| chr16:8940859
|
A | G | 87 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0023others(84): Show | 87 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.80-10462T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8940859 | ||||||
| chr16:8940872
|
GTCCAGAA others(18): Show |
G | 1 | a0001c0001t0002g0182 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.80-10500_80-10476d others(27): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8940872 | ||||||
| chr16:8940969
|
C | A | 63 | a0001c0001t0001g0020a0001c0001t0001g0041a0001c0001t0001g0103others(60): Show | 65 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(62): Show |
intron_variant | MODIFIER | c.80-10572G>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8940969 | ||||||
| chr16:8941007
|
C | T | 1 | a0001c0001t0001g0150 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.80-10610G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8941007 | ||||||
| chr16:8941074
|
G | A | 16 | a0001c0001t0001g0041a0001c0001t0002g0179a0001c0001t0002g0193others(13): Show | 16 | HG00438.hp2 HG02132.hp1 HG02970.hp1 others(13): Show |
intron_variant | MODIFIER | c.80-10677C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8941074 | ||||||
| chr16:8941091
|
T | A | 1 | a0001c0001t0003g0312 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.80-10694A>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8941091 | ||||||
| chr16:8941127
|
A | G | 1 | a0001c0001t0002g0267 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.80-10730T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8941127 | ||||||
| chr16:8941267
|
T | C | 124 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(121): Show | 126 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.80-10870A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8941267 | ||||||
| chr16:8941355
|
A | G | 1 | a0001c0001t0002g0061 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.80-10958T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8941355 | ||||||
| chr16:8941406
|
C | T | 2 | a0001c0001t0004g0054a0001c0001t0032g0055 | 2 | HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.80-11009G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8941406 | ||||||
| chr16:8941427
|
T | A | 1 | a0001c0001t0002g0179 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.80-11030A>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8941427 | ||||||
| chr16:8941448
|
G | C | 3 | a0001c0001t0001g0208a0001c0001t0001g0300a0001c0001t0003g0138 | 3 | HG00738.hp2 HG01175.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.80-11051C>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8941448 | ||||||
| chr16:8941449
|
G | A | 3 | a0001c0001t0001g0172a0001c0001t0033g0322a0001c0001t0035g0321 | 3 | HG01255.hp2 HG03195.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.80-11052C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8941449 | ||||||
| chr16:8941527
|
T | C | 230 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(227): Show | 234 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.80-11130A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8941527 | ||||||
| chr16:8941558
|
T | C | 1 | a0001c0001t0024g0060 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.80-11161A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8941558 | ||||||
| chr16:8941610
|
C | T | 6 | a0001c0001t0007g0002a0001c0001t0007g0033a0001c0001t0007g0049others(3): Show | 7 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(4): Show |
intron_variant | MODIFIER | c.80-11213G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8941610 | ||||||
| chr16:8941703
|
C | G | 3 | a0001c0001t0025g0056a0001c0001t0027g0169a0001c0001t0037g0330 | 3 | HG03453.hp1 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.80-11306G>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8941703 | ||||||
| chr16:8941791
|
C | A | 1 | a0001c0001t0026g0228 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.80-11394G>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8941791 | ||||||
| chr16:8941821
|
A | G | 1 | a0001c0002t0001g0131 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.80-11424T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8941821 | ||||||
| chr16:8941838
|
T | C | 1 | a0001c0001t0001g0085 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.80-11441A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8941838 | ||||||
| chr16:8941893
|
T | A | 1 | a0001c0001t0030g0151 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.80-11496A>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8941893 | ||||||
| chr16:8941924
|
T | C | 63 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0023others(60): Show | 63 | HG00140.hp1 HG00323.hp1 HG01070.hp1 others(60): Show |
intron_variant | MODIFIER | c.80-11527A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8941924 | ||||||
| chr16:8941986
|
G | A | 1 | a0001c0001t0001g0080 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.80-11589C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8941986 | ||||||
| chr16:8942020
|
G | C | 1 | a0001c0001t0002g0179 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.80-11623C>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8942020 | ||||||
| chr16:8942050
|
G | A | 2 | a0001c0001t0001g0155a0001c0001t0001g0233 | 2 | HG03239.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.80-11653C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8942050 | ||||||
| chr16:8942191
|
A | G | 1 | a0001c0001t0024g0060 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.80-11794T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8942191 | ||||||
| chr16:8942240
|
T | C | 3 | a0001c0001t0025g0056a0001c0001t0031g0044a0001c0006t0004g0173 | 3 | HG02922.hp1 HG03453.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.80-11843A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8942240 | ||||||
| chr16:8942274
|
T | C | 1 | a0001c0001t0001g0127 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.80-11877A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8942274 | ||||||
| chr16:8942301
|
A | G | 1 | a0001c0001t0002g0035 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.80-11904T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8942301 | ||||||
| chr16:8942360
|
G | T | 2 | a0001c0001t0002g0077a0001c0001t0003g0121 | 2 | HG00733.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.80-11963C>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8942360 | ||||||
| chr16:8942424
|
C | G | 264 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(261): Show | 270 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.80-12027G>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8942424 | ||||||
| chr16:8942523
|
C | T | 1 | a0001c0001t0001g0172 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.80-12126G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8942523 | ||||||
| chr16:8942525
|
G | T | 1 | a0001c0001t0001g0172 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.80-12128C>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8942525 | ||||||
| chr16:8942595
|
T | C | 125 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(122): Show | 127 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.80-12198A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8942595 | ||||||
| chr16:8942676
|
C | T | 320 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(317): Show | 325 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.80-12279G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8942676 | ||||||
| chr16:8942840
|
A | G | 325 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(322): Show | 330 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.80-12443T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8942840 | ||||||
| chr16:8942981
|
C | T | 1 | a0001c0001t0008g0325 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.80-12584G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8942981 | ||||||
| chr16:8943031
|
T | C | 1 | a0001c0001t0026g0228 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.80-12634A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8943031 | ||||||
| chr16:8943032
|
G | A | 1 | a0001c0001t0004g0259 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.80-12635C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8943032 | ||||||
| chr16:8943285
|
GGTTTAAT others(114): Show |
G | 1 | a0001c0001t0005g0052 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.80-13009_80-12889d others(2): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8943285 | ||||||
| chr16:8943375
|
C | T | 1 | a0001c0001t0002g0198 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.80-12978G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8943375 | ||||||
| chr16:8943433
|
G | A | 1 | a0001c0001t0001g0062 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.80-13036C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8943433 | ||||||
| chr16:8943537
|
T | C | 2 | a0001c0001t0016g0323a0001c0001t0016g0324 | 2 | HG02735.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.80-13140A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8943537 | ||||||
| chr16:8943550
|
C | A | 1 | a0001c0001t0002g0265 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.80-13153G>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8943550 | ||||||
| chr16:8943550
|
C | T | 6 | a0001c0001t0007g0002a0001c0001t0007g0033a0001c0001t0007g0049others(3): Show | 7 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(4): Show |
intron_variant | MODIFIER | c.80-13153G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8943550 | ||||||
| chr16:8943613
|
A | T | 1 | a0001c0001t0002g0035 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.80-13216T>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8943613 | ||||||
| chr16:8943615
|
C | T | 6 | a0001c0001t0007g0002a0001c0001t0007g0033a0001c0001t0007g0049others(3): Show | 7 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(4): Show |
intron_variant | MODIFIER | c.80-13218G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8943615 | ||||||
| chr16:8943657
|
G | C | 1 | a0001c0001t0031g0044 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.80-13260C>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8943657 | ||||||
| chr16:8943808
|
G | A | 1 | a0001c0001t0002g0232 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.80-13411C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8943808 | ||||||
| chr16:8943857
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.80-13460G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8943857 | ||||||
| chr16:8943978
|
A | T | 64 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0023others(61): Show | 64 | HG00140.hp1 HG00323.hp1 HG01070.hp1 others(61): Show |
intron_variant | MODIFIER | c.80-13581T>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8943978 | ||||||
| chr16:8944018
|
T | G | 8 | a0001c0001t0002g0184a0001c0001t0002g0186a0001c0001t0002g0246others(5): Show | 8 | HG01243.hp2 HG01884.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.80-13621A>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8944018 | ||||||
| chr16:8944047
|
G | A | 75 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0023others(72): Show | 76 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.80-13650C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8944047 | ||||||
| chr16:8944141
|
C | T | 1 | a0001c0001t0004g0113 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.80-13744G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8944141 | ||||||
| chr16:8944232
|
C | CA | 100 | a0001c0001t0001g0097a0001c0001t0001g0187a0001c0001t0001g0269others(97): Show | 102 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.80-13836dupT | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8944232 | ||||||
| chr16:8944232
|
CA | C | 82 | a0001c0001t0001g0020a0001c0001t0001g0032a0001c0001t0001g0041others(79): Show | 83 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.80-13836delT | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8944232 | ||||||
| chr16:8944260
|
T | C | 141 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(138): Show | 143 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(140): Show |
intron_variant | MODIFIER | c.80-13863A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8944260 | ||||||
| chr16:8944345
|
G | C | 1 | a0001c0001t0005g0052 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.80-13948C>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8944345 | ||||||
| chr16:8944407
|
G | C | 320 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(317): Show | 325 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.80-14010C>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8944407 | ||||||
| chr16:8944488
|
G | A | 1 | a0001c0001t0005g0052 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.80-14091C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8944488 | ||||||
| chr16:8944513
|
T | A | 1 | a0001c0001t0035g0321 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.80-14116A>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8944513 | ||||||
| chr16:8944587
|
A | G | 2 | a0001c0001t0001g0097a0001c0001t0002g0190 | 2 | NA19000.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.80-14190T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8944587 | ||||||
| chr16:8944743
|
C | G | 1 | a0001c0001t0002g0035 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.80-14346G>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8944743 | ||||||
| chr16:8944759
|
G | A | 2 | a0001c0001t0004g0054a0001c0001t0032g0055 | 2 | HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.80-14362C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8944759 | ||||||
| chr16:8944824
|
G | A | 1 | a0001c0001t0001g0146 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.80-14427C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8944824 | ||||||
| chr16:8944836
|
T | C | 1 | a0001c0001t0001g0128 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.80-14439A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8944836 | ||||||
| chr16:8944904
|
T | TC | 59 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0025others(56): Show | 59 | HG00140.hp1 HG00323.hp1 HG01070.hp1 others(56): Show |
intron_variant | MODIFIER | c.80-14508dupG | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8944904 | ||||||
| chr16:8944922
|
A | G | 62 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0023others(59): Show | 62 | HG00140.hp1 HG00323.hp1 HG01070.hp1 others(59): Show |
intron_variant | MODIFIER | c.80-14525T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8944922 | ||||||
| chr16:8944937
|
G | A | 1 | a0001c0001t0001g0147 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.80-14540C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8944937 | ||||||
| chr16:8945025
|
A | G | 74 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0023others(71): Show | 75 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(72): Show |
intron_variant | MODIFIER | c.80-14628T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8945025 | ||||||
| chr16:8945111
|
C | T | 6 | a0001c0001t0001g0067a0001c0001t0001g0086a0001c0001t0001g0094others(3): Show | 6 | HG01192.hp2 HG01257.hp2 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.80-14714G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8945111 | ||||||
| chr16:8945211
|
C | T | 2 | a0001c0001t0004g0054a0001c0001t0032g0055 | 2 | HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.80-14814G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8945211 | ||||||
| chr16:8945299
|
G | A | 1 | a0001c0001t0001g0161 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.80-14902C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8945299 | ||||||
| chr16:8945391
|
C | A | 1 | a0001c0001t0002g0199 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.80-14994G>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8945391 | ||||||
| chr16:8945477
|
T | G | 75 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0023others(72): Show | 76 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.80-15080A>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8945477 | ||||||
| chr16:8945565
|
G | A | 3 | a0001c0001t0002g0164a0001c0001t0002g0185a0001c0001t0002g0278 | 3 | HG00597.hp1 NA18966.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.80-15168C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8945565 | ||||||
| chr16:8945622
|
A | T | 1 | a0001c0001t0004g0024 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.80-15225T>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8945622 | ||||||
| chr16:8945646
|
T | C | 3 | a0001c0001t0001g0106a0001c0001t0001g0170a0001c0001t0028g0168 | 3 | HG02055.hp1 HG03130.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.80-15249A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8945646 | ||||||
| chr16:8945733
|
T | C | 1 | a0001c0001t0003g0297 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.80-15336A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8945733 | ||||||
| chr16:8945845
|
G | A | 2 | a0001c0001t0025g0056a0001c0001t0031g0044 | 2 | HG03453.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.80-15448C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8945845 | ||||||
| chr16:8945887
|
A | G | 3 | a0001c0001t0002g0164a0001c0001t0002g0185a0001c0001t0002g0278 | 3 | HG00597.hp1 NA18966.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.80-15490T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8945887 | ||||||
| chr16:8945916
|
A | G | 1 | a0001c0001t0004g0259 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.80-15519T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8945916 | ||||||
| chr16:8946160
|
G | A | 6 | a0001c0001t0007g0002a0001c0001t0007g0033a0001c0001t0007g0049others(3): Show | 7 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(4): Show |
intron_variant | MODIFIER | c.80-15763C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8946160 | ||||||
| chr16:8946226
|
G | C | 1 | a0001c0001t0022g0053 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.80-15829C>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8946226 | ||||||
| chr16:8946264
|
T | G | 1 | a0001c0001t0005g0052 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.80-15867A>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8946264 | ||||||
| chr16:8946319
|
G | C | 3 | a0001c0001t0025g0056a0001c0001t0031g0044a0001c0006t0004g0173 | 3 | HG02922.hp1 HG03453.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.80-15922C>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8946319 | ||||||
| chr16:8946413
|
T | A | 6 | a0001c0001t0007g0002a0001c0001t0007g0033a0001c0001t0007g0049others(3): Show | 7 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(4): Show |
intron_variant | MODIFIER | c.80-16016A>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8946413 | ||||||
| chr16:8946419
|
T | C | 5 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(2): Show | 5 | HG01070.hp1 HG01081.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.80-16022A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8946419 | ||||||
| chr16:8946444
|
T | G | 72 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0023others(69): Show | 73 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.80-16047A>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8946444 | ||||||
| chr16:8946462
|
T | C | 228 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(225): Show | 232 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.80-16065A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8946462 | ||||||
| chr16:8946463
|
G | A | 1 | a0001c0001t0015g0318 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.80-16066C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8946463 | ||||||
| chr16:8946543
|
G | C | 61 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0023others(58): Show | 61 | HG00140.hp1 HG00323.hp1 HG01167.hp2 others(58): Show |
intron_variant | MODIFIER | c.80-16146C>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8946543 | ||||||
| chr16:8946560
|
T | C | 6 | a0001c0001t0007g0002a0001c0001t0007g0033a0001c0001t0007g0049others(3): Show | 7 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(4): Show |
intron_variant | MODIFIER | c.80-16163A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8946560 | ||||||
| chr16:8946567
|
A | G | 1 | a0001c0001t0004g0259 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.80-16170T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8946567 | ||||||
| chr16:8946631
|
A | G | 1 | a0001c0001t0009g0009 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.80-16234T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8946631 | ||||||
| chr16:8946690
|
A | G | 302 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(299): Show | 307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.80-16293T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8946690 | ||||||
| chr16:8946762
|
A | G | 1 | a0001c0001t0005g0052 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.80-16365T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8946762 | ||||||
| chr16:8946781
|
G | C | 1 | a0001c0001t0004g0285 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.80-16384C>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8946781 | ||||||
| chr16:8946913
|
C | T | 3 | a0001c0001t0025g0056a0001c0001t0031g0044a0001c0006t0004g0173 | 3 | HG02922.hp1 HG03453.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.79+16294G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8946913 | ||||||
| chr16:8946928
|
G | A | 1 | a0001c0001t0002g0035 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.79+16279C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8946928 | ||||||
| chr16:8947015
|
T | G | 1 | a0001c0001t0012g0028 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.79+16192A>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8947015 | ||||||
| chr16:8947060
|
A | G | 2 | a0001c0001t0002g0181a0001c0001t0002g0237 | 2 | NA18967.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.79+16147T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8947060 | ||||||
| chr16:8947250
|
T | TTTGGAAA others(25): Show |
8 | a0001c0001t0001g0093a0001c0001t0001g0147a0001c0001t0001g0148others(5): Show | 8 | HG00597.hp2 HG00609.hp2 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.79+15925_79+15956d others(34): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8947250 | ||||||
| chr16:8947294
|
T | G | 2 | a0001c0001t0004g0054a0001c0001t0032g0055 | 2 | HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.79+15913A>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8947294 | ||||||
| chr16:8947337
|
C | G | 2 | a0001c0001t0025g0056a0001c0001t0031g0044 | 2 | HG03453.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.79+15870G>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8947337 | ||||||
| chr16:8947353
|
C | A | 8 | a0001c0001t0007g0002a0001c0001t0007g0033a0001c0001t0007g0049others(5): Show | 9 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(6): Show |
intron_variant | MODIFIER | c.79+15854G>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8947353 | ||||||
| chr16:8947475
|
A | C | 2 | a0001c0001t0001g0079a0001c0001t0001g0122 | 2 | NA18991.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.79+15732T>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8947475 | ||||||
| chr16:8947594
|
C | A | 3 | a0001c0001t0001g0079a0001c0001t0001g0122a0001c0001t0001g0125 | 3 | HG02083.hp2 NA18991.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.79+15613G>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8947594 | ||||||
| chr16:8947636
|
A | ATTG | 64 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0023others(61): Show | 64 | HG00140.hp1 HG00323.hp1 HG01167.hp2 others(61): Show |
intron_variant | MODIFIER | c.79+15570_79+15571i others(5): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8947636 | ||||||
| chr16:8947747
|
C | T | 1 | a0001c0001t0017g0007 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.79+15460G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8947747 | ||||||
| chr16:8947839
|
A | T | 1 | a0001c0001t0002g0035 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.79+15368T>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8947839 | ||||||
| chr16:8947859
|
C | A | 1 | a0001c0001t0002g0035 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.79+15348G>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8947859 | ||||||
| chr16:8947935
|
T | C | 1 | a0001c0001t0001g0172 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.79+15272A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8947935 | ||||||
| chr16:8948048
|
C | A | 1 | a0001c0001t0001g0158 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.79+15159G>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8948048 | ||||||
| chr16:8948070
|
C | T | 1 | a0001c0001t0001g0158 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.79+15137G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8948070 | ||||||
| chr16:8948071
|
G | A | 1 | a0001c0001t0002g0199 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.79+15136C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8948071 | ||||||
| chr16:8948201
|
T | C | 1 | a0001c0001t0002g0035 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.79+15006A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8948201 | ||||||
| chr16:8948480
|
T | C | 1 | a0001c0001t0001g0209 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.79+14727A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8948480 | ||||||
| chr16:8948506
|
A | C | 2 | a0001c0001t0007g0049a0001c0001t0007g0051 | 2 | HG00642.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.79+14701T>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8948506 | ||||||
| chr16:8948554
|
T | G | 7 | a0001c0001t0002g0035a0001c0001t0007g0002a0001c0001t0007g0033others(4): Show | 8 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(5): Show |
intron_variant | MODIFIER | c.79+14653A>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8948554 | ||||||
| chr16:8948587
|
C | G | 2 | a0001c0001t0002g0077a0001c0001t0003g0121 | 2 | HG00733.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.79+14620G>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8948587 | ||||||
| chr16:8948652
|
G | A | 302 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(299): Show | 307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.79+14555C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8948652 | ||||||
| chr16:8948678
|
G | C | 1 | a0001c0001t0020g0064 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.79+14529C>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8948678 | ||||||
| chr16:8948685
|
A | C | 1 | a0001c0001t0020g0064 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.79+14522T>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8948685 | ||||||
| chr16:8948744
|
A | G | 302 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(299): Show | 307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.79+14463T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8948744 | ||||||
| chr16:8948774
|
A | C | 71 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0023others(68): Show | 72 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.79+14433T>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8948774 | ||||||
| chr16:8948796
|
T | C | 1 | a0001c0001t0002g0035 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.79+14411A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8948796 | ||||||
| chr16:8948824
|
C | T | 1 | a0001c0001t0002g0243 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.79+14383G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8948824 | ||||||
| chr16:8948825
|
G | A | 1 | a0001c0001t0001g0126 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.79+14382C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8948825 | ||||||
| chr16:8948967
|
GA | G | 6 | a0001c0001t0004g0071a0001c0001t0004g0113a0001c0001t0004g0114others(3): Show | 6 | HG01891.hp2 HG02965.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.79+14239delT | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8948967 | ||||||
| chr16:8948968
|
A | G | 1 | a0001c0001t0003g0081 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.79+14239T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8948968 | ||||||
| chr16:8949001
|
T | C | 1 | a0001c0001t0031g0044 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.79+14206A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8949001 | ||||||
| chr16:8949039
|
T | C | 1 | a0001c0002t0001g0141 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.79+14168A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8949039 | ||||||
| chr16:8949123
|
C | G | 1 | a0001c0001t0001g0306 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.79+14084G>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8949123 | ||||||
| chr16:8949328
|
A | C | 6 | a0001c0001t0007g0002a0001c0001t0007g0033a0001c0001t0007g0049others(3): Show | 7 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(4): Show |
intron_variant | MODIFIER | c.79+13879T>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8949328 | ||||||
| chr16:8949334
|
A | C | 1 | a0001c0001t0025g0056 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.79+13873T>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8949334 | ||||||
| chr16:8949358
|
T | C | 62 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0023others(59): Show | 62 | HG00140.hp1 HG00323.hp1 HG01070.hp1 others(59): Show |
intron_variant | MODIFIER | c.79+13849A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8949358 | ||||||
| chr16:8949565
|
C | G | 4 | a0001c0001t0001g0102a0001c0001t0001g0128a0001c0001t0001g0129others(1): Show | 4 | NA18956.hp1 NA18966.hp1 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.79+13642G>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8949565 | ||||||
| chr16:8949631
|
T | C | 63 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0023others(60): Show | 63 | HG00140.hp1 HG00323.hp1 HG01070.hp1 others(60): Show |
intron_variant | MODIFIER | c.79+13576A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8949631 | ||||||
| chr16:8949685
|
T | G | 70 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0023others(67): Show | 71 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.79+13522A>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8949685 | ||||||
| chr16:8949722
|
T | C | 4 | a0001c0001t0002g0035a0001c0001t0025g0056a0001c0001t0031g0044others(1): Show | 4 | HG02922.hp1 HG03453.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.79+13485A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8949722 | ||||||
| chr16:8949845
|
C | T | 1 | a0001c0001t0001g0023 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.79+13362G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8949845 | ||||||
| chr16:8949882
|
A | C | 6 | a0001c0001t0007g0002a0001c0001t0007g0033a0001c0001t0007g0049others(3): Show | 7 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(4): Show |
intron_variant | MODIFIER | c.79+13325T>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8949882 | ||||||
| chr16:8950009
|
T | C | 325 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(322): Show | 330 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.79+13198A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8950009 | ||||||
| chr16:8950108
|
A | C | 1 | a0001c0001t0001g0187 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.79+13099T>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8950108 | ||||||
| chr16:8950188
|
C | T | 1 | a0001c0001t0002g0035 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.79+13019G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8950188 | ||||||
| chr16:8950224
|
C | G | 1 | a0001c0001t0001g0080 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.79+12983G>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8950224 | ||||||
| chr16:8950305
|
T | C | 229 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(226): Show | 233 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(230): Show |
intron_variant | MODIFIER | c.79+12902A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8950305 | ||||||
| chr16:8950381
|
C | T | 1 | a0001c0001t0031g0044 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.79+12826G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8950381 | ||||||
| chr16:8950493
|
C | G | 18 | a0001c0001t0001g0041a0001c0001t0003g0029a0001c0001t0003g0030others(15): Show | 18 | HG02132.hp1 HG02165.hp1 HG02970.hp1 others(15): Show |
intron_variant | MODIFIER | c.79+12714G>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8950493 | ||||||
| chr16:8950647
|
C | T | 1 | a0001c0001t0001g0082 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.79+12560G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8950647 | ||||||
| chr16:8950653
|
T | C | 1 | a0001c0001t0001g0161 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.79+12554A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8950653 | ||||||
| chr16:8950819
|
T | C | 6 | a0001c0001t0007g0002a0001c0001t0007g0033a0001c0001t0007g0049others(3): Show | 7 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(4): Show |
intron_variant | MODIFIER | c.79+12388A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8950819 | ||||||
| chr16:8951142
|
G | C | 3 | a0001c0001t0002g0189a0001c0001t0002g0279a0001c0001t0036g0329 | 3 | NA18948.hp1 NA18956.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.79+12065C>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8951142 | ||||||
| chr16:8951266
|
T | TCTGTCAG others(89): Show |
3 | a0001c0001t0001g0095a0001c0001t0001g0142a0001c0001t0001g0143 | 3 | HG01257.hp2 HG01346.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.79+11940_79+11941i others(98): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8951266 | ||||||
| chr16:8951266
|
T | TCTGTCAG others(89): Show |
299 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(296): Show | 304 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(301): Show |
intron_variant | MODIFIER | c.79+11940_79+11941i others(98): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8951266 | ||||||
| chr16:8951367
|
C | A | 1 | a0001c0001t0004g0162 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.79+11840G>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8951367 | ||||||
| chr16:8951381
|
A | G | 1 | a0001c0001t0001g0150 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.79+11826T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8951381 | ||||||
| chr16:8951563
|
G | A | 2 | a0001c0001t0004g0054a0001c0001t0032g0055 | 2 | HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.79+11644C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8951563 | ||||||
| chr16:8951563
|
G | C | 1 | a0001c0001t0002g0199 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.79+11644C>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8951563 | ||||||
| chr16:8951605
|
G | C | 58 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0023others(55): Show | 58 | HG00140.hp1 HG00323.hp1 HG01070.hp1 others(55): Show |
intron_variant | MODIFIER | c.79+11602C>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8951605 | ||||||
| chr16:8951726
|
T | C | 1 | a0001c0001t0002g0284 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.79+11481A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8951726 | ||||||
| chr16:8952076
|
AC | A | 313 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(310): Show | 318 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.79+11130delG | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8952076 | ||||||
| chr16:8952115
|
T | G | 295 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(292): Show | 300 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.79+11092A>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8952115 | ||||||
| chr16:8952230
|
C | T | 1 | a0001c0001t0001g0124 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.79+10977G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8952230 | ||||||
| chr16:8952304
|
T | C | 1 | a0001c0001t0001g0167 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.79+10903A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8952304 | ||||||
| chr16:8952465
|
T | C | 6 | a0001c0001t0007g0002a0001c0001t0007g0033a0001c0001t0007g0049others(3): Show | 7 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(4): Show |
intron_variant | MODIFIER | c.79+10742A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8952465 | ||||||
| chr16:8952492
|
G | T | 8 | a0001c0001t0002g0181a0001c0001t0002g0197a0001c0001t0002g0237others(5): Show | 8 | NA18967.hp2 NA18975.hp1 NA18990.hp1 others(5): Show |
intron_variant | MODIFIER | c.79+10715C>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8952492 | ||||||
| chr16:8952528
|
T | C | 1 | a0001c0001t0002g0195 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.79+10679A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8952528 | ||||||
| chr16:8952539
|
C | T | 4 | a0001c0001t0002g0188a0001c0001t0002g0189a0001c0001t0002g0279others(1): Show | 4 | NA18948.hp1 NA18956.hp2 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.79+10668G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8952539 | ||||||
| chr16:8952540
|
C | G | 2 | a0001c0001t0004g0054a0001c0001t0032g0055 | 2 | HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.79+10667G>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8952540 | ||||||
| chr16:8952597
|
TAGGCCCA others(12): Show |
T | 1 | a0001c0001t0001g0062 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.79+10591_79+10609d others(21): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8952597 | ||||||
| chr16:8952762
|
A | G | 1 | a0001c0001t0005g0287 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.79+10445T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8952762 | ||||||
| chr16:8952815
|
C | T | 1 | a0001c0001t0001g0214 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.79+10392G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8952815 | ||||||
| chr16:8952836
|
C | T | 9 | a0001c0001t0003g0029a0001c0001t0003g0030a0001c0001t0003g0036others(6): Show | 9 | NA18941.hp2 NA18947.hp1 NA18950.hp1 others(6): Show |
intron_variant | MODIFIER | c.79+10371G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8952836 | ||||||
| chr16:8952838
|
C | CT | 9 | a0001c0001t0002g0274a0001c0001t0004g0054a0001c0001t0007g0002others(6): Show | 10 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(7): Show |
intron_variant | MODIFIER | c.79+10368dupA | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8952838 | ||||||
| chr16:8952856
|
G | A | 1 | a0001c0001t0002g0250 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.79+10351C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8952856 | ||||||
| chr16:8952856
|
G | C | 1 | a0001c0001t0002g0035 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.79+10351C>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8952856 | ||||||
| chr16:8952953
|
C | T | 1 | a0001c0001t0002g0035 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.79+10254G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8952953 | ||||||
| chr16:8952995
|
C | T | 2 | a0001c0001t0002g0241a0001c0001t0002g0254 | 2 | HG00639.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.79+10212G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8952995 | ||||||
| chr16:8953087
|
G | T | 2 | a0001c0001t0025g0056a0001c0001t0031g0044 | 2 | HG03453.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.79+10120C>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8953087 | ||||||
| chr16:8953132
|
C | T | 1 | a0001c0001t0002g0035 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.79+10075G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8953132 | ||||||
| chr16:8953190
|
G | A | 17 | a0001c0001t0001g0041a0001c0001t0003g0029a0001c0001t0003g0030others(14): Show | 17 | HG02132.hp1 HG02165.hp1 HG02970.hp1 others(14): Show |
intron_variant | MODIFIER | c.79+10017C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8953190 | ||||||
| chr16:8953203
|
G | A | 1 | a0001c0001t0022g0053 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.79+10004C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8953203 | ||||||
| chr16:8953238
|
T | C | 2 | a0001c0001t0002g0196a0001c0001t0002g0273 | 2 | NA18747.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.79+9969A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8953238 | ||||||
| chr16:8953305
|
G | C | 57 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0023others(54): Show | 57 | HG00140.hp1 HG00323.hp1 HG01070.hp1 others(54): Show |
intron_variant | MODIFIER | c.79+9902C>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8953305 | ||||||
| chr16:8953341
|
C | T | 63 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0023others(60): Show | 64 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(61): Show |
intron_variant | MODIFIER | c.79+9866G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8953341 | ||||||
| chr16:8953342
|
G | A | 1 | a0001c0001t0022g0053 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.79+9865C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8953342 | ||||||
| chr16:8953359
|
G | A | 3 | a0001c0001t0012g0057a0001c0001t0014g0058a0001c0001t0014g0059 | 3 | HG02886.hp1 HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.79+9848C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8953359 | ||||||
| chr16:8953437
|
A | C | 1 | a0001c0006t0004g0173 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.79+9770T>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8953437 | ||||||
| chr16:8953502
|
G | A | 1 | a0001c0001t0002g0226 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.79+9705C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8953502 | ||||||
| chr16:8953512
|
C | A | 1 | a0001c0001t0010g0234 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.79+9695G>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8953512 | ||||||
| chr16:8953513
|
G | C | 6 | a0001c0001t0007g0002a0001c0001t0007g0033a0001c0001t0007g0049others(3): Show | 7 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(4): Show |
intron_variant | MODIFIER | c.79+9694C>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8953513 | ||||||
| chr16:8953515
|
T | C | 2 | a0001c0001t0001g0298a0001c0001t0002g0005 | 3 | HG00738.hp1 HG00741.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.79+9692A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8953515 | ||||||
| chr16:8953521
|
T | C | 80 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0023others(77): Show | 82 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.79+9686A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8953521 | ||||||
| chr16:8953548
|
A | ATGCGGTG others(32): Show |
1 | a0001c0006t0004g0173 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.79+9658_79+9659ins others(39): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8953548 | ||||||
| chr16:8953548
|
A | G | 4 | a0001c0001t0001g0110a0001c0001t0001g0178a0001c0001t0003g0215others(1): Show | 4 | HG02145.hp1 HG02280.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.79+9659T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8953548 | ||||||
| chr16:8953554
|
C | T | 42 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0025others(39): Show | 42 | HG00323.hp1 HG01070.hp1 HG01192.hp1 others(39): Show |
intron_variant | MODIFIER | c.79+9653G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8953554 | ||||||
| chr16:8953564
|
AGCAGAGG others(149): Show |
A | 4 | a0001c0001t0001g0079a0001c0001t0001g0122a0001c0001t0001g0125others(1): Show | 4 | HG02083.hp1 HG02083.hp2 NA18991.hp2 others(1): Show |
intron_variant | MODIFIER | c.79+9487_79+9642del | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8953564 | ||||||
| chr16:8953564
|
AGCAGAGG others(461): Show |
A | 2 | a0001c0001t0002g0119a0001c0001t0002g0198 | 2 | HG01081.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.79+9175_79+9642del | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8953564 | ||||||
| chr16:8953587
|
A | G | 76 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0023others(73): Show | 77 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.79+9620T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8953587 | ||||||
| chr16:8953594
|
G | A | 1 | a0001c0001t0007g0042 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.79+9613C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8953594 | ||||||
| chr16:8953599
|
C | G | 22 | a0001c0001t0001g0032a0001c0001t0001g0041a0001c0001t0001g0045others(19): Show | 22 | HG01167.hp2 HG01169.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.79+9608G>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8953599 | ||||||
| chr16:8953600
|
G | A | 1 | a0001c0001t0002g0035 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.79+9607C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8953600 | ||||||
| chr16:8953603
|
A | AGCAGAGG others(32): Show |
2 | a0001c0001t0025g0056a0001c0001t0031g0044 | 2 | HG03453.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.79+9603_79+9604ins others(39): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8953603 | ||||||
| chr16:8953603
|
A | G | 7 | a0001c0001t0007g0002a0001c0001t0007g0033a0001c0001t0007g0049others(4): Show | 8 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(5): Show |
intron_variant | MODIFIER | c.79+9604T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8953603 | ||||||
| chr16:8953626
|
G | A | 70 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0023others(67): Show | 70 | HG00140.hp1 HG00323.hp1 HG01070.hp1 others(67): Show |
intron_variant | MODIFIER | c.79+9581C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8953626 | ||||||
| chr16:8953626
|
GTGCGGCG others(110): Show |
G | 198 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(195): Show | 202 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.79+9464_79+9580del | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8953626 | ||||||
| chr16:8953642
|
A | G | 42 | a0001c0001t0001g0074a0001c0001t0001g0203a0001c0001t0001g0299others(39): Show | 43 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.79+9565T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8953642 | ||||||
| chr16:8953665
|
GTGCGGCG others(110): Show |
G | 1 | a0001c0001t0002g0255 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.79+9425_79+9541del | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8953665 | ||||||
| chr16:8953677
|
C | T | 1 | a0001c0001t0001g0167 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.79+9530G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8953677 | ||||||
| chr16:8953678
|
G | T | 22 | a0001c0001t0001g0032a0001c0001t0001g0041a0001c0001t0001g0045others(19): Show | 22 | HG01167.hp2 HG01169.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.79+9529C>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8953678 | ||||||
| chr16:8953704
|
G | C | 1 | a0001c0001t0001g0167 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.79+9503C>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8953704 | ||||||
| chr16:8953704
|
G | GTGCGGCG others(149): Show |
1 | a0001c0001t0002g0035 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.79+9502_79+9503ins others(156): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8953704 | ||||||
| chr16:8953704
|
G | GTGCGGCG others(188): Show |
5 | a0001c0001t0007g0002a0001c0001t0007g0033a0001c0001t0007g0049others(2): Show | 6 | HG00280.hp1 HG00642.hp2 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.79+9502_79+9503ins others(195): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8953704 | ||||||
| chr16:8953704
|
G | GTGCGGCG others(227): Show |
1 | a0001c0001t0023g0050 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.79+9502_79+9503ins others(234): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8953704 | ||||||
| chr16:8953704
|
G | GTGCGGCG others(695): Show |
1 | a0001c0001t0022g0053 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.79+9502_79+9503ins others(702): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8953704 | ||||||
| chr16:8953704
|
GTGCGGCG others(110): Show |
G | 18 | a0001c0001t0001g0203a0001c0001t0001g0299a0001c0001t0002g0069others(15): Show | 18 | HG02451.hp1 HG02698.hp1 HG02818.hp2 others(15): Show |
intron_variant | MODIFIER | c.79+9386_79+9502del | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8953704 | ||||||
| chr16:8953704
|
GTGCGGCG others(188): Show |
G | 2 | a0001c0001t0001g0074a0001c0001t0002g0112 | 2 | HG01175.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.79+9308_79+9502del | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8953704 | ||||||
| chr16:8953716
|
C | CGGAGGCA others(32): Show |
1 | a0001c0001t0001g0105 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.79+9490_79+9491ins others(39): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8953716 | ||||||
| chr16:8953716
|
C | CGGAGGCA others(110): Show |
1 | a0001c0001t0001g0165 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.79+9490_79+9491ins others(117): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8953716 | ||||||
| chr16:8953716
|
C | CGGAGGCA others(149): Show |
16 | a0001c0001t0001g0023a0001c0001t0001g0025a0001c0001t0001g0026others(13): Show | 16 | HG01891.hp1 HG02055.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.79+9490_79+9491ins others(156): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8953716 | ||||||
| chr16:8953716
|
C | CGGAGGCA others(7846): Show |
1 | a0001c0001t0001g0220 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.79+9490_79+9491ins others(7853): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8953716 | ||||||
| chr16:8953716
|
C | T | 45 | a0001c0001t0001g0032a0001c0001t0001g0041a0001c0001t0001g0045others(42): Show | 45 | HG00140.hp1 HG00323.hp1 HG01070.hp1 others(42): Show |
intron_variant | MODIFIER | c.79+9491G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8953716 | ||||||
| chr16:8953716
|
CGGAGGCA others(110): Show |
C | 4 | a0001c0001t0002g0070a0001c0001t0002g0072a0001c0001t0002g0115others(1): Show | 4 | HG02486.hp1 HG02622.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.79+9374_79+9490del | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8953716 | ||||||
| chr16:8953743
|
C | G | 63 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0032others(60): Show | 63 | HG00140.hp1 HG00323.hp1 HG01070.hp1 others(60): Show |
intron_variant | MODIFIER | c.79+9464G>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8953743 | ||||||
| chr16:8953755
|
C | CGGAGGCA others(32): Show |
1 | a0001c0001t0005g0052 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.79+9413_79+9451dup others(39): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8953755 | ||||||
| chr16:8953755
|
C | T | 68 | a0001c0001t0001g0023a0001c0001t0001g0025a0001c0001t0001g0026others(65): Show | 68 | HG00140.hp1 HG00323.hp1 HG01070.hp1 others(65): Show |
intron_variant | MODIFIER | c.79+9452G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8953755 | ||||||
| chr16:8953782
|
C | A | 21 | a0001c0001t0001g0023a0001c0001t0001g0025a0001c0001t0001g0026others(18): Show | 21 | HG01891.hp1 HG02055.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.79+9425G>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8953782 | ||||||
| chr16:8953782
|
C | G | 210 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(207): Show | 214 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(211): Show |
intron_variant | MODIFIER | c.79+9425G>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8953782 | ||||||
| chr16:8953794
|
T | C | 20 | a0001c0001t0002g0035a0001c0001t0006g0016a0001c0001t0006g0017others(17): Show | 21 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(18): Show |
intron_variant | MODIFIER | c.79+9413A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8953794 | ||||||
| chr16:8953813
|
C | CGTGCCCC others(71): Show |
1 | a0001c0006t0004g0173 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.79+9393_79+9394ins others(78): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8953813 | ||||||
| chr16:8953813
|
C | CGTGCCCC others(110): Show |
25 | a0001c0001t0001g0103a0001c0001t0001g0155a0001c0001t0001g0156others(22): Show | 25 | HG00140.hp1 HG00323.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.79+9393_79+9394ins others(117): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8953813 | ||||||
| chr16:8953813
|
C | CGTGCCCC others(149): Show |
3 | a0001c0001t0001g0022a0001c0001t0001g0171a0001c0001t0001g0172 | 3 | HG01192.hp1 HG01255.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.79+9393_79+9394ins others(156): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8953813 | ||||||
| chr16:8953813
|
C | CGTGCCCC others(188): Show |
3 | a0001c0001t0001g0110a0001c0001t0001g0178a0001c0005t0002g0176 | 3 | HG02145.hp1 HG02486.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.79+9393_79+9394ins others(195): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8953813 | ||||||
| chr16:8953813
|
C | G | 19 | a0001c0001t0001g0023a0001c0001t0001g0025a0001c0001t0001g0026others(16): Show | 19 | HG01891.hp1 HG02055.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.79+9394G>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8953813 | ||||||
| chr16:8953821
|
C | G | 201 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(198): Show | 205 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.79+9386G>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8953821 | ||||||
| chr16:8953833
|
T | C | 11 | a0001c0001t0002g0035a0001c0001t0007g0002a0001c0001t0007g0033others(8): Show | 12 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.79+9374A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8953833 | ||||||
| chr16:8953852
|
C | CGTGCCCC others(71): Show |
1 | a0001c0001t0002g0179 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.79+9354_79+9355ins others(78): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8953852 | ||||||
| chr16:8953860
|
C | G | 2 | a0001c0001t0001g0065a0001c0001t0038g0331 | 2 | NA18612.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.79+9347G>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8953860 | ||||||
| chr16:8953872
|
T | C | 9 | a0001c0001t0002g0035a0001c0001t0007g0002a0001c0001t0007g0033others(6): Show | 10 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(7): Show |
intron_variant | MODIFIER | c.79+9335A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8953872 | ||||||
| chr16:8953899
|
A | ATGCGGCG others(32): Show |
1 | a0001c0001t0001g0105 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.79+9307_79+9308ins others(39): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8953899 | ||||||
| chr16:8953899
|
A | C | 288 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(285): Show | 293 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.79+9308T>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8953899 | ||||||
| chr16:8953911
|
T | C | 7 | a0001c0001t0002g0035a0001c0001t0007g0002a0001c0001t0007g0033others(4): Show | 8 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(5): Show |
intron_variant | MODIFIER | c.79+9296A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8953911 | ||||||
| chr16:8953915
|
G | A | 1 | a0001c0001t0004g0285 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.79+9292C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8953915 | ||||||
| chr16:8953938
|
C | A | 4 | a0001c0001t0001g0020a0001c0001t0025g0056a0001c0001t0029g0021others(1): Show | 4 | HG02647.hp1 HG03139.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.79+9269G>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8953938 | ||||||
| chr16:8953938
|
CTGCGGCG others(71): Show |
C | 219 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(216): Show | 223 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(220): Show |
intron_variant | MODIFIER | c.79+9191_79+9268del others(78): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8953938 | ||||||
| chr16:8953950
|
T | C | 6 | a0001c0001t0007g0002a0001c0001t0007g0033a0001c0001t0007g0049others(3): Show | 7 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(4): Show |
intron_variant | MODIFIER | c.79+9257A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8953950 | ||||||
| chr16:8953977
|
CTGCGGCG others(32): Show |
C | 2 | a0001c0001t0004g0054a0001c0001t0032g0055 | 2 | HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.79+9191_79+9229del others(39): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8953977 | ||||||
| chr16:8953977
|
CTGCGGCG others(110): Show |
C | 4 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(1): Show | 4 | HG01081.hp2 HG01433.hp2 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.79+9113_79+9229del | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8953977 | ||||||
| chr16:8953983
|
C | CGCCACTG others(32): Show |
1 | a0001c0001t0002g0179 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.79+9223_79+9224ins others(39): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8953983 | ||||||
| chr16:8954016
|
A | C | 11 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0025others(8): Show | 11 | HG01175.hp2 HG02647.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.79+9191T>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8954016 | ||||||
| chr16:8954019
|
C | T | 1 | a0001c0001t0025g0056 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.79+9188G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8954019 | ||||||
| chr16:8954020
|
G | T | 1 | a0001c0001t0001g0128 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.79+9187C>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8954020 | ||||||
| chr16:8954055
|
C | A | 1 | a0001c0001t0022g0053 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.79+9152G>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8954055 | ||||||
| chr16:8954094
|
A | C | 14 | a0001c0001t0001g0020a0001c0001t0001g0074a0001c0001t0002g0112others(11): Show | 15 | HG00140.hp2 HG00280.hp1 HG00621.hp2 others(12): Show |
intron_variant | MODIFIER | c.79+9113T>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8954094 | ||||||
| chr16:8954153
|
G | A | 7 | a0001c0001t0002g0069a0001c0001t0002g0070a0001c0001t0002g0072others(4): Show | 7 | HG02486.hp1 HG02622.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.79+9054C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8954153 | ||||||
| chr16:8954172
|
C | A | 2 | a0001c0001t0001g0020a0001c0001t0029g0021 | 2 | HG02647.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.79+9035G>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8954172 | ||||||
| chr16:8954175
|
C | T | 1 | a0001c0001t0022g0053 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.79+9032G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8954175 | ||||||
| chr16:8954178
|
T | C | 262 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(259): Show | 266 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(263): Show |
intron_variant | MODIFIER | c.79+9029A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8954178 | ||||||
| chr16:8954204
|
G | A | 4 | a0001c0001t0002g0249a0001c0001t0002g0250a0001c0001t0002g0253others(1): Show | 4 | HG01884.hp1 HG02109.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.79+9003C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8954204 | ||||||
| chr16:8954240
|
C | T | 1 | a0001c0001t0001g0067 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.79+8967G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8954240 | ||||||
| chr16:8954243
|
G | T | 22 | a0001c0001t0001g0032a0001c0001t0001g0041a0001c0001t0001g0045others(19): Show | 22 | HG01167.hp2 HG01169.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.79+8964C>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8954243 | ||||||
| chr16:8954278
|
G | C | 1 | a0001c0001t0001g0161 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.79+8929C>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8954278 | ||||||
| chr16:8954381
|
G | C | 1 | a0001c0001t0004g0240 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.79+8826C>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8954381 | ||||||
| chr16:8954442
|
G | A | 2 | a0001c0001t0025g0056a0001c0001t0031g0044 | 2 | HG03453.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.79+8765C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8954442 | ||||||
| chr16:8954472
|
C | G | 59 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0023others(56): Show | 59 | HG00140.hp1 HG00323.hp1 HG01070.hp1 others(56): Show |
intron_variant | MODIFIER | c.79+8735G>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8954472 | ||||||
| chr16:8954495
|
T | C | 102 | a0001c0001t0001g0187a0001c0001t0001g0269a0001c0001t0001g0306others(99): Show | 104 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.79+8712A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8954495 | ||||||
| chr16:8954513
|
C | G | 1 | a0001c0001t0010g0234 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.79+8694G>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8954513 | ||||||
| chr16:8954542
|
A | G | 22 | a0001c0001t0001g0032a0001c0001t0001g0041a0001c0001t0001g0045others(19): Show | 22 | HG01167.hp2 HG01169.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.79+8665T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8954542 | ||||||
| chr16:8954680
|
T | C | 1 | a0001c0001t0005g0027 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.79+8527A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8954680 | ||||||
| chr16:8954704
|
G | A | 7 | a0001c0001t0002g0035a0001c0001t0007g0002a0001c0001t0007g0033others(4): Show | 8 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(5): Show |
intron_variant | MODIFIER | c.79+8503C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8954704 | ||||||
| chr16:8954737
|
G | A | 2 | a0001c0001t0001g0096a0001c0001t0001g0175 | 2 | HG00741.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.79+8470C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8954737 | ||||||
| chr16:8954752
|
G | A | 1 | a0001c0001t0002g0035 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.79+8455C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8954752 | ||||||
| chr16:8954765
|
G | A | 2 | a0001c0001t0008g0320a0001c0001t0008g0327 | 2 | HG00140.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.79+8442C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8954765 | ||||||
| chr16:8954790
|
C | G | 1 | a0001c0001t0002g0243 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.79+8417G>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8954790 | ||||||
| chr16:8954818
|
G | A | 2 | a0001c0001t0025g0056a0001c0001t0031g0044 | 2 | HG03453.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.79+8389C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8954818 | ||||||
| chr16:8954915
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.79+8292C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8954915 | ||||||
| chr16:8955016
|
C | G | 1 | a0001c0001t0002g0237 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.79+8191G>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8955016 | ||||||
| chr16:8955030
|
C | T | 2 | a0001c0001t0001g0105a0001c0001t0002g0199 | 2 | HG03098.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.79+8177G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8955030 | ||||||
| chr16:8955047
|
G | C | 2 | a0001c0001t0001g0097a0001c0001t0001g0309 | 2 | HG02155.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.79+8160C>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8955047 | ||||||
| chr16:8955214
|
C | G | 318 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(315): Show | 323 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.79+7993G>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8955214 | ||||||
| chr16:8955237
|
T | C | 66 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0023others(63): Show | 67 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(64): Show |
intron_variant | MODIFIER | c.79+7970A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8955237 | ||||||
| chr16:8955253
|
C | T | 225 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(222): Show | 229 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.79+7954G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8955253 | ||||||
| chr16:8955320
|
C | A | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0011 | 3 | HG01884.hp2 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.79+7887G>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8955320 | ||||||
| chr16:8955361
|
C | T | 1 | a0001c0001t0035g0321 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.79+7846G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8955361 | ||||||
| chr16:8955362
|
G | A | 3 | a0001c0001t0002g0164a0001c0001t0002g0185a0001c0001t0002g0278 | 3 | HG00597.hp1 NA18966.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.79+7845C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8955362 | ||||||
| chr16:8955435
|
T | C | 22 | a0001c0001t0001g0032a0001c0001t0001g0041a0001c0001t0001g0045others(19): Show | 22 | HG01167.hp2 HG01169.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.79+7772A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8955435 | ||||||
| chr16:8955597
|
T | G | 1 | a0001c0001t0004g0071 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.79+7610A>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8955597 | ||||||
| chr16:8955599
|
G | C | 1 | a0001c0001t0038g0331 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.79+7608C>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8955599 | ||||||
| chr16:8955647
|
A | G | 1 | a0001c0001t0007g0033 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.79+7560T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8955647 | ||||||
| chr16:8955704
|
C | CA | 21 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0099others(18): Show | 21 | HG00280.hp2 HG00408.hp2 HG00621.hp1 others(18): Show |
intron_variant | MODIFIER | c.79+7502dupT | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8955704 | ||||||
| chr16:8955704
|
C | CAA | 162 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0062others(159): Show | 165 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.79+7501_79+7502dup others(2): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8955704 | ||||||
| chr16:8955704
|
C | CAAA | 43 | a0001c0001t0001g0003a0001c0001t0001g0063a0001c0001t0001g0074others(40): Show | 44 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.79+7500_79+7502dup others(3): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8955704 | ||||||
| chr16:8955704
|
CA | C | 62 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0023others(59): Show | 63 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(60): Show |
intron_variant | MODIFIER | c.79+7502delT | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8955704 | ||||||
| chr16:8955717
|
A | C | 1 | a0001c0001t0001g0104 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.79+7490T>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8955717 | ||||||
| chr16:8955719
|
A | C | 1 | a0001c0001t0004g0162 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.79+7488T>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8955719 | ||||||
| chr16:8955720
|
A | AC | 4 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0003g0043others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.79+7486_79+7487ins others(1): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8955720 | ||||||
| chr16:8955720
|
A | C | 83 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0023others(80): Show | 84 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.79+7487T>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8955720 | ||||||
| chr16:8955761
|
A | C | 1 | a0001c0001t0002g0305 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.79+7446T>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8955761 | ||||||
| chr16:8955906
|
C | T | 1 | a0001c0001t0022g0053 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.79+7301G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8955906 | ||||||
| chr16:8956042
|
C | T | 1 | a0001c0001t0003g0313 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.79+7165G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8956042 | ||||||
| chr16:8956135
|
G | A | 1 | a0001c0001t0002g0098 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.79+7072C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8956135 | ||||||
| chr16:8956152
|
T | A | 55 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0023others(52): Show | 55 | HG00140.hp1 HG00323.hp1 HG01070.hp1 others(52): Show |
intron_variant | MODIFIER | c.79+7055A>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8956152 | ||||||
| chr16:8956175
|
A | C | 2 | a0001c0001t0002g0241a0001c0001t0002g0254 | 2 | HG00639.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.79+7032T>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8956175 | ||||||
| chr16:8956242
|
C | A | 1 | a0001c0001t0001g0099 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.79+6965G>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8956242 | ||||||
| chr16:8956474
|
C | A | 106 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(103): Show | 108 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.79+6733G>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8956474 | ||||||
| chr16:8956531
|
G | A | 1 | a0001c0001t0038g0331 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.79+6676C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8956531 | ||||||
| chr16:8956594
|
A | G | 5 | a0001c0001t0001g0032a0001c0001t0001g0045a0001c0001t0001g0047others(2): Show | 5 | HG01167.hp2 HG01169.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.79+6613T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8956594 | ||||||
| chr16:8956656
|
G | C | 92 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0023others(89): Show | 93 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.79+6551C>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8956656 | ||||||
| chr16:8956707
|
G | A | 1 | a0001c0001t0003g0312 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.79+6500C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8956707 | ||||||
| chr16:8956769
|
A | C | 5 | a0001c0001t0012g0028a0001c0001t0012g0057a0001c0001t0014g0058others(2): Show | 5 | HG02886.hp1 HG03130.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.79+6438T>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8956769 | ||||||
| chr16:8956769
|
AC | A | 3 | a0001c0001t0003g0043a0001c0001t0003g0315a0001c0001t0007g0042 | 3 | NA19001.hp2 NA19006.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.79+6437delG | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8956769 | ||||||
| chr16:8956770
|
C | A | 27 | a0001c0001t0001g0032a0001c0001t0001g0041a0001c0001t0001g0045others(24): Show | 27 | HG01167.hp2 HG01169.hp1 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.79+6437G>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8956770 | ||||||
| chr16:8956771
|
A | C | 1 | a0001c0001t0031g0044 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.79+6436T>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8956771 | ||||||
| chr16:8956772
|
A | C | 1 | a0001c0001t0022g0053 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.79+6435T>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8956772 | ||||||
| chr16:8956776
|
C | A | 3 | a0001c0001t0003g0043a0001c0001t0003g0315a0001c0001t0007g0042 | 3 | NA19001.hp2 NA19006.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.79+6431G>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8956776 | ||||||
| chr16:8956776
|
C | CA | 88 | a0001c0001t0001g0187a0001c0001t0001g0269a0001c0001t0001g0306others(85): Show | 90 | HG00423.hp1 HG00438.hp2 HG00609.hp1 others(87): Show |
intron_variant | MODIFIER | c.79+6430dupT | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8956776 | ||||||
| chr16:8956778
|
A | C | 3 | a0001c0001t0003g0043a0001c0001t0003g0315a0001c0001t0007g0042 | 3 | NA19001.hp2 NA19006.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.79+6429T>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8956778 | ||||||
| chr16:8956780
|
A | C | 61 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0023others(58): Show | 61 | HG00140.hp1 HG00323.hp1 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.79+6427T>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8956780 | ||||||
| chr16:8956781
|
A | C | 1 | a0001c0001t0031g0044 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.79+6426T>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8956781 | ||||||
| chr16:8956782
|
A | C | 121 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(118): Show | 123 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.79+6425T>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8956782 | ||||||
| chr16:8956788
|
AAC | A | 19 | a0001c0001t0001g0032a0001c0001t0001g0041a0001c0001t0001g0045others(16): Show | 19 | HG01167.hp2 HG01169.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.79+6417_79+6418del others(2): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8956788 | ||||||
| chr16:8956789
|
A | C | 4 | a0001c0001t0001g0157a0001c0001t0001g0216a0001c0001t0001g0217others(1): Show | 4 | HG02145.hp2 HG02280.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.79+6418T>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8956789 | ||||||
| chr16:8956790
|
C | A | 3 | a0001c0001t0003g0043a0001c0001t0003g0315a0001c0001t0007g0042 | 3 | NA19001.hp2 NA19006.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.79+6417G>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8956790 | ||||||
| chr16:8956794
|
G | C | 22 | a0001c0001t0001g0032a0001c0001t0001g0041a0001c0001t0001g0045others(19): Show | 22 | HG01167.hp2 HG01169.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.79+6413C>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8956794 | ||||||
| chr16:8956842
|
C | T | 1 | a0001c0001t0002g0238 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.79+6365G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8956842 | ||||||
| chr16:8956846
|
G | A | 1 | a0001c0001t0025g0056 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.79+6361C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8956846 | ||||||
| chr16:8956854
|
T | C | 22 | a0001c0001t0001g0032a0001c0001t0001g0041a0001c0001t0001g0045others(19): Show | 22 | HG01167.hp2 HG01169.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.79+6353A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8956854 | ||||||
| chr16:8956877
|
C | A | 1 | a0001c0001t0002g0286 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.79+6330G>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8956877 | ||||||
| chr16:8956881
|
C | T | 1 | a0001c0001t0001g0067 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.79+6326G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8956881 | ||||||
| chr16:8957090
|
T | C | 6 | a0001c0001t0007g0002a0001c0001t0007g0033a0001c0001t0007g0049others(3): Show | 7 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(4): Show |
intron_variant | MODIFIER | c.79+6117A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8957090 | ||||||
| chr16:8957445
|
G | A | 1 | a0001c0001t0001g0150 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.79+5762C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8957445 | ||||||
| chr16:8957470
|
GAGGTGGC others(2): Show |
G | 6 | a0001c0001t0007g0002a0001c0001t0007g0033a0001c0001t0007g0049others(3): Show | 7 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(4): Show |
intron_variant | MODIFIER | c.79+5728_79+5736del others(9): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8957470 | ||||||
| chr16:8957496
|
T | C | 93 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0023others(90): Show | 94 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.79+5711A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8957496 | ||||||
| chr16:8957497
|
G | A | 22 | a0001c0001t0001g0032a0001c0001t0001g0041a0001c0001t0001g0045others(19): Show | 22 | HG01167.hp2 HG01169.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.79+5710C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8957497 | ||||||
| chr16:8957544
|
C | T | 2 | a0001c0001t0002g0181a0001c0001t0002g0237 | 2 | NA18967.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.79+5663G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8957544 | ||||||
| chr16:8957591
|
C | CA | 9 | a0001c0001t0002g0035a0001c0001t0002g0303a0001c0001t0002g0311others(6): Show | 9 | HG02451.hp1 HG02886.hp1 HG03130.hp1 others(6): Show |
intron_variant | MODIFIER | c.79+5615dupT | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8957591 | ||||||
| chr16:8957591
|
CA | C | 23 | a0001c0001t0001g0078a0001c0001t0001g0122a0001c0001t0001g0123others(20): Show | 25 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.79+5615delT | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8957591 | ||||||
| chr16:8957763
|
TA | T | 85 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0023others(82): Show | 86 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.79+5443delT | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8957763 | ||||||
| chr16:8957765
|
A | T | 2 | a0001c0001t0001g0103a0001c0001t0001g0156 | 2 | HG02027.hp2 NA18943.hp2 |
intron_variant | MODIFIER | c.79+5442T>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8957765 | ||||||
| chr16:8957774
|
C | A | 3 | a0001c0001t0004g0054a0001c0001t0009g0008a0001c0001t0032g0055 | 3 | HG03453.hp2 NA19006.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.79+5433G>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8957774 | ||||||
| chr16:8957775
|
A | C | 229 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(226): Show | 233 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(230): Show |
intron_variant | MODIFIER | c.79+5432T>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8957775 | ||||||
| chr16:8957776
|
A | C | 1 | a0001c0001t0009g0008 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.79+5431T>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8957776 | ||||||
| chr16:8957829
|
G | A | 1 | a0001c0001t0001g0150 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.79+5378C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8957829 | ||||||
| chr16:8957861
|
A | G | 2 | a0001c0001t0001g0020a0001c0001t0029g0021 | 2 | HG02647.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.79+5346T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8957861 | ||||||
| chr16:8957973
|
G | A | 4 | a0001c0001t0001g0066a0001c0001t0001g0107a0001c0001t0001g0109others(1): Show | 4 | HG02135.hp1 NA18980.hp1 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.79+5234C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8957973 | ||||||
| chr16:8957988
|
C | T | 1 | a0001c0001t0005g0052 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.79+5219G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8957988 | ||||||
| chr16:8958186
|
A | G | 1 | a0001c0001t0008g0320 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.79+5021T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8958186 | ||||||
| chr16:8958241
|
G | A | 3 | a0001c0001t0001g0101a0001c0001t0001g0214a0001c0001t0030g0151 | 3 | HG02129.hp1 HG02132.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.79+4966C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8958241 | ||||||
| chr16:8958340
|
T | C | 1 | a0001c0001t0005g0287 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.79+4867A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8958340 | ||||||
| chr16:8958406
|
G | A | 1 | a0001c0001t0003g0316 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.79+4801C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8958406 | ||||||
| chr16:8958442
|
G | A | 2 | a0001c0001t0005g0288a0001c0001t0019g0289 | 2 | NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.79+4765C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8958442 | ||||||
| chr16:8958586
|
C | T | 2 | a0001c0001t0002g0077a0001c0001t0003g0121 | 2 | HG00733.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.79+4621G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8958586 | ||||||
| chr16:8958591
|
C | T | 6 | a0001c0001t0007g0002a0001c0001t0007g0033a0001c0001t0007g0049others(3): Show | 7 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(4): Show |
intron_variant | MODIFIER | c.79+4616G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8958591 | ||||||
| chr16:8958616
|
C | A | 57 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0023others(54): Show | 57 | HG00140.hp1 HG00323.hp1 HG01070.hp1 others(54): Show |
intron_variant | MODIFIER | c.79+4591G>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8958616 | ||||||
| chr16:8958636
|
T | G | 1 | a0001c0001t0005g0027 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.79+4571A>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8958636 | ||||||
| chr16:8958705
|
C | T | 10 | a0001c0001t0001g0032a0001c0001t0001g0045a0001c0001t0001g0047others(7): Show | 10 | HG01167.hp2 HG01169.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.79+4502G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8958705 | ||||||
| chr16:8958781
|
C | G | 2 | a0001c0003t0001g0153a0001c0003t0001g0154 | 2 | HG01070.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.79+4426G>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8958781 | ||||||
| chr16:8958916
|
T | C | 2 | a0001c0001t0025g0056a0001c0001t0031g0044 | 2 | HG03453.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.79+4291A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8958916 | ||||||
| chr16:8959132
|
T | A | 58 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0023others(55): Show | 58 | HG00140.hp1 HG00323.hp1 HG01070.hp1 others(55): Show |
intron_variant | MODIFIER | c.79+4075A>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8959132 | ||||||
| chr16:8959192
|
C | T | 2 | a0001c0001t0015g0317a0001c0001t0015g0318 | 2 | HG01496.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.79+4015G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8959192 | ||||||
| chr16:8959356
|
C | CA | 111 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(108): Show | 113 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.79+3850dupT | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8959356 | ||||||
| chr16:8959356
|
CA | C | 57 | a0001c0001t0001g0032a0001c0001t0001g0045a0001c0001t0001g0047others(54): Show | 58 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.79+3850delT | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8959356 | ||||||
| chr16:8959482
|
C | T | 1 | a0001c0002t0001g0227 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.79+3725G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8959482 | ||||||
| chr16:8959662
|
G | C | 26 | a0001c0001t0001g0032a0001c0001t0001g0045a0001c0001t0001g0047others(23): Show | 27 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.79+3545C>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8959662 | ||||||
| chr16:8959871
|
T | G | 2 | a0001c0001t0001g0110a0001c0005t0002g0176 | 2 | HG02145.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.79+3336A>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8959871 | ||||||
| chr16:8960074
|
G | A | 5 | a0001c0001t0001g0177a0001c0001t0001g0220a0001c0001t0001g0221others(2): Show | 5 | HG02257.hp1 HG02647.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.79+3133C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8960074 | ||||||
| chr16:8960390
|
A | G | 26 | a0001c0001t0001g0032a0001c0001t0001g0045a0001c0001t0001g0047others(23): Show | 27 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.79+2817T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8960390 | ||||||
| chr16:8960604
|
G | C | 1 | a0001c0001t0001g0178 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.79+2603C>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8960604 | ||||||
| chr16:8960629
|
A | T | 2 | a0001c0001t0003g0036a0001c0001t0003g0037 | 2 | NA18955.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.79+2578T>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8960629 | ||||||
| chr16:8960631
|
C | G | 1 | a0001c0001t0001g0111 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.79+2576G>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8960631 | ||||||
| chr16:8960663
|
A | C | 2 | a0001c0001t0001g0068a0001c0001t0039g0332 | 2 | NA19004.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.79+2544T>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8960663 | ||||||
| chr16:8960729
|
C | T | 1 | a0001c0001t0001g0067 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.79+2478G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8960729 | ||||||
| chr16:8960869
|
C | T | 3 | a0001c0001t0002g0224a0001c0001t0002g0225a0001c0001t0002g0226 | 3 | HG02040.hp1 NA18988.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.79+2338G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8960869 | ||||||
| chr16:8961010
|
G | A | 1 | a0001c0001t0001g0102 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.79+2197C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8961010 | ||||||
| chr16:8961035
|
T | C | 6 | a0001c0001t0012g0028a0001c0001t0012g0057a0001c0001t0014g0058others(3): Show | 6 | HG02886.hp1 HG03130.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.79+2172A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8961035 | ||||||
| chr16:8961190
|
A | T | 6 | a0001c0001t0012g0028a0001c0001t0012g0057a0001c0001t0014g0058others(3): Show | 6 | HG02886.hp1 HG03130.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.79+2017T>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8961190 | ||||||
| chr16:8961221
|
G | T | 10 | a0001c0001t0001g0032a0001c0001t0001g0045a0001c0001t0001g0047others(7): Show | 10 | HG01167.hp2 HG01169.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.79+1986C>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8961221 | ||||||
| chr16:8961222
|
A | G | 26 | a0001c0001t0001g0032a0001c0001t0001g0045a0001c0001t0001g0047others(23): Show | 27 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.79+1985T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8961222 | ||||||
| chr16:8961224
|
G | A | 1 | a0001c0001t0002g0152 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.79+1983C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8961224 | ||||||
| chr16:8961355
|
G | C | 1 | a0001c0001t0031g0044 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.79+1852C>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8961355 | ||||||
| chr16:8961357
|
TTGCACAT others(24): Show |
T | 1 | a0001c0001t0036g0329 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.79+1819_79+1849del others(31): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8961357 | ||||||
| chr16:8961492
|
CA | C | 13 | a0001c0001t0001g0216a0001c0001t0001g0217a0001c0001t0001g0218others(10): Show | 13 | HG00323.hp1 HG01361.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.79+1714delT | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8961492 | ||||||
| chr16:8961503
|
A | AG | 10 | a0001c0001t0001g0022a0001c0001t0001g0103a0001c0001t0001g0104others(7): Show | 10 | HG01192.hp1 HG02027.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.79+1703_79+1704ins others(1): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8961503 | ||||||
| chr16:8961503
|
A | AGG | 3 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0020g0064 | 3 | HG01891.hp1 HG02135.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.79+1703_79+1704ins others(2): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8961503 | ||||||
| chr16:8961503
|
A | AGGG | 3 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0009g0008 | 3 | HG01978.hp2 NA18948.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.79+1703_79+1704ins others(3): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8961503 | ||||||
| chr16:8961504
|
A | AG | 50 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0187others(47): Show | 52 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.79+1702dupC | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8961504 | ||||||
| chr16:8961504
|
A | AGG | 48 | a0001c0001t0001g0003a0001c0001t0001g0111a0001c0001t0001g0117others(45): Show | 49 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(46): Show |
intron_variant | MODIFIER | c.79+1701_79+1702dup others(2): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8961504 | ||||||
| chr16:8961504
|
A | AGGG | 40 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0073others(37): Show | 40 | HG00597.hp2 HG00621.hp1 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.79+1700_79+1702dup others(3): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8961504 | ||||||
| chr16:8961504
|
A | G | 51 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0025others(48): Show | 51 | HG00741.hp1 HG01070.hp1 HG01192.hp1 others(48): Show |
intron_variant | MODIFIER | c.79+1703T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8961504 | ||||||
| chr16:8961505
|
G | A | 12 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0048others(9): Show | 13 | HG00140.hp2 HG00642.hp2 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.79+1702C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8961505 | ||||||
| chr16:8961507
|
G | C | 2 | a0001c0001t0004g0006a0001c0001t0004g0304 | 3 | HG01257.hp1 HG01258.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.79+1700C>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8961507 | ||||||
| chr16:8961653
|
G | A | 1 | a0001c0001t0002g0305 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.79+1554C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8961653 | ||||||
| chr16:8961927
|
T | C | 2 | a0001c0001t0005g0052a0001c0001t0022g0053 | 2 | NA21309.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.79+1280A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8961927 | ||||||
| chr16:8961973
|
T | C | 2 | a0001c0001t0004g0054a0001c0001t0032g0055 | 2 | HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.79+1234A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8961973 | ||||||
| chr16:8962113
|
G | A | 1 | a0001c0001t0025g0056 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.79+1094C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8962113 | ||||||
| chr16:8962236
|
T | C | 3 | a0001c0001t0012g0057a0001c0001t0014g0058a0001c0001t0014g0059 | 3 | HG02886.hp1 HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.79+971A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8962236 | ||||||
| chr16:8962267
|
G | A | 1 | a0001c0001t0025g0056 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.79+940C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8962267 | ||||||
| chr16:8962374
|
T | C | 9 | a0001c0001t0008g0320a0001c0001t0008g0325a0001c0001t0008g0326others(6): Show | 9 | HG00140.hp1 HG01515.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.79+833A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8962374 | ||||||
| chr16:8962398
|
C | A | 1 | a0001c0001t0001g0306 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.79+809G>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8962398 | ||||||
| chr16:8962500
|
T | C | 2 | a0001c0001t0001g0307a0001c0001t0001g0308 | 2 | NA18968.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.79+707A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8962500 | ||||||
| chr16:8962567
|
C | G | 1 | a0001c0001t0002g0061 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.79+640G>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8962567 | ||||||
| chr16:8962582
|
A | C | 1 | a0001c0001t0024g0060 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.79+625T>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8962582 | ||||||
| chr16:8962582
|
A | G | 39 | a0001c0001t0001g0032a0001c0001t0001g0041a0001c0001t0001g0045others(36): Show | 40 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.79+625T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8962582 | ||||||
| chr16:8962630
|
G | A | 1 | a0001c0001t0001g0309 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.79+577C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8962630 | ||||||
| chr16:8962660
|
G | A | 4 | a0001c0001t0012g0057a0001c0001t0014g0058a0001c0001t0014g0059others(1): Show | 4 | HG02886.hp1 HG03130.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.79+547C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8962660 | ||||||
| chr16:8962683
|
G | C | 285 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(282): Show | 289 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(286): Show |
intron_variant | MODIFIER | c.79+524C>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8962683 | ||||||
| chr16:8962685
|
A | G | 325 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(322): Show | 330 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.79+522T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8962685 | ||||||
| chr16:8962719
|
G | A | 2 | a0001c0001t0002g0310a0001c0001t0002g0311 | 2 | NA19064.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.79+488C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8962719 | ||||||
| chr16:8962726
|
A | C | 5 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0025others(2): Show | 5 | HG01192.hp1 HG02622.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.79+481T>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8962726 | ||||||
| chr16:8962953
|
C | T | 2 | a0001c0001t0001g0020a0001c0001t0029g0021 | 2 | HG02647.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.79+254G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8962953 | ||||||
| chr16:8963033
|
G | A | 5 | a0001c0001t0003g0312a0001c0001t0003g0313a0001c0001t0003g0314others(2): Show | 5 | HG02165.hp1 HG02970.hp1 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.79+174C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8963033 | ||||||
| chr16:8963058
|
G | GC | 324 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0020others(321): Show | 329 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(326): Show |
intron_variant | MODIFIER | c.79+148dupG | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8963058 | ||||||
| chr16:8963060
|
A | G | 325 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(322): Show | 330 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.79+147T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8963060 |