Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 | 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 | MNHQQ others(1097): Show |
chr16 | 8887097 | 8968906 |
| a0002 | 0/0 | 1102 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | USP7_chr16_8887097_8968906 | USP7 | MNHQQ others(1097): Show |
chr16 | 8887097 | 8968906 |
| a0003 | 0/0 | 1102 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | MNHHQ others(1097): Show |
chr16 | 8887097 | 8968906 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 3306 | 322 | 87 | 53 | 137 | 8 | 35 | USP7_chr16_8887097_8968906 | USP7 | ATGAA others(3301): Show |
chr16 | 8887097 | 8968906 | ||
| a0001c0002 | 0/0 | 3306 | 10 | 0 | 8 | 2 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | ATGAA others(3301): Show |
chr16 | 8887097 | 8968906 | ||
| a0001c0003 | 0/0 | 3306 | 2 | 1 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | ATGAA others(3301): Show |
chr16 | 8887097 | 8968906 | ||
| a0001c0005 | 0/0 | 3306 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | ATGAA others(3301): Show |
chr16 | 8887097 | 8968906 | ||
| a0001c0006 | 0/0 | 3306 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | ATGAA others(3301): Show |
chr16 | 8887097 | 8968906 | ||
| a0002c0007 | 0/0 | 3306 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | ATGAA others(3301): Show |
chr16 | 8887097 | 8968906 | ||
| a0003c0004 | 0/0 | 3306 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | ATGAA others(3301): Show |
chr16 | 8887097 | 8968906 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5834 | 269 | 57 | 47 | 128 | 5 | 32 | USP7_chr16_8887097_8968906 | USP7 | GACAT others(5829): Show |
chr16 | 8887097 | 8968906 |
| a0001c0001t0002 | 1/0 | 5831 | 12 | 10 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | GACAT others(5826): Show |
chr16 | 8887097 | 8968906 |
| a0001c0001t0003 | 0/0 | 5837 | 9 | 4 | 0 | 1 | 2 | 2 | USP7_chr16_8887097_8968906 | USP7 | GACAT others(5832): Show |
chr16 | 8887097 | 8968906 |
| a0001c0001t0004 | 0/0 | 5834 | 3 | 0 | 3 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | GACAT others(5829): Show |
chr16 | 8887097 | 8968906 |
| a0001c0001t0005 | 0/0 | 5834 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | GACAT others(5829): Show |
chr16 | 8887097 | 8968906 |
| a0001c0001t0006 | 0/0 | 5834 | 2 | 2 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | GACAT others(5829): Show |
chr16 | 8887097 | 8968906 |
| a0001c0001t0007 | 0/0 | 5834 | 2 | 0 | 2 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | GACAT others(5829): Show |
chr16 | 8887097 | 8968906 |
| a0001c0001t0008 | 0/0 | 5834 | 2 | 2 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | GACAT others(5829): Show |
chr16 | 8887097 | 8968906 |
| a0001c0001t0009 | 0/0 | 5834 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | GACAT others(5829): Show |
chr16 | 8887097 | 8968906 |
| a0001c0001t0010 | 0/0 | 5834 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | GACAT others(5829): Show |
chr16 | 8887097 | 8968906 |
| a0001c0001t0011 | 0/0 | 5834 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | GACAT others(5829): Show |
chr16 | 8887097 | 8968906 |
| a0001c0001t0012 | 0/0 | 5834 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | GACAT others(5829): Show |
chr16 | 8887097 | 8968906 |
| a0001c0001t0013 | 0/0 | 5834 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | GACAT others(5829): Show |
chr16 | 8887097 | 8968906 |
| a0001c0001t0014 | 0/0 | 5834 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | GACAT others(5829): Show |
chr16 | 8887097 | 8968906 |
| a0001c0001t0015 | 0/0 | 5834 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | GACAT others(5829): Show |
chr16 | 8887097 | 8968906 |
| a0001c0001t0016 | 0/0 | 5834 | 1 | 0 | 0 | 0 | 1 | 0 | USP7_chr16_8887097_8968906 | USP7 | GACAT others(5829): Show |
chr16 | 8887097 | 8968906 |
| a0001c0001t0017 | 0/0 | 5834 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | GACAT others(5829): Show |
chr16 | 8887097 | 8968906 |
| a0001c0001t0018 | 0/0 | 5834 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | GACAT others(5829): Show |
chr16 | 8887097 | 8968906 |
| a0001c0001t0019 | 0/0 | 5834 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | GACAT others(5829): Show |
chr16 | 8887097 | 8968906 |
| a0001c0001t0020 | 0/0 | 5834 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | GACAT others(5829): Show |
chr16 | 8887097 | 8968906 |
| a0001c0001t0021 | 0/0 | 5834 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | GACAT others(5829): Show |
chr16 | 8887097 | 8968906 |
| a0001c0001t0022 | 0/0 | 5834 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | GACAT others(5829): Show |
chr16 | 8887097 | 8968906 |
| a0001c0001t0023 | 0/0 | 5834 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | GACAT others(5829): Show |
chr16 | 8887097 | 8968906 |
| a0001c0001t0024 | 0/1 | 5833 | 1 | 0 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | GACAT others(5828): Show |
chr16 | 8887097 | 8968906 |
| a0001c0001t0025 | 0/0 | 5834 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | GACAT others(5829): Show |
chr16 | 8887097 | 8968906 |
| a0001c0001t0026 | 0/0 | 5837 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | GACAT others(5832): Show |
chr16 | 8887097 | 8968906 |
| a0001c0001t0027 | 0/0 | 5834 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | GACAT others(5829): Show |
chr16 | 8887097 | 8968906 |
| a0001c0001t0028 | 0/0 | 5834 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | GACAT others(5829): Show |
chr16 | 8887097 | 8968906 |
| a0001c0001t0029 | 0/0 | 5834 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | GACAT others(5829): Show |
chr16 | 8887097 | 8968906 |
| a0001c0001t0030 | 0/0 | 5834 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | GACAT others(5829): Show |
chr16 | 8887097 | 8968906 |
| a0001c0002t0001 | 0/0 | 5834 | 10 | 0 | 8 | 2 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | GACAT others(5829): Show |
chr16 | 8887097 | 8968906 |
| a0001c0003t0001 | 0/0 | 5834 | 2 | 1 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | GACAT others(5829): Show |
chr16 | 8887097 | 8968906 |
| a0001c0005t0001 | 0/0 | 5834 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | GACAT others(5829): Show |
chr16 | 8887097 | 8968906 |
| a0001c0006t0001 | 0/0 | 5834 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | GACAT others(5829): Show |
chr16 | 8887097 | 8968906 |
| a0002c0007t0001 | 0/0 | 5834 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | GACAT others(5829): Show |
chr16 | 8887097 | 8968906 |
| a0003c0004t0005 | 0/0 | 5834 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | GACAT others(5829): Show |
chr16 | 8887097 | 8968906 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 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 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0077 | 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 | 1 | 0 | 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 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 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 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0100 | 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 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 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 |
| a0001c0001t0001g0149 | 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 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 0 | 1 | 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 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 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 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0207 | 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 |
| a0001c0001t0001g0210 | 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 |
| a0001c0001t0001g0213 | 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 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 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 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0289 | 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 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 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 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0017 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0003g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0003g0314 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0003g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0003g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0003g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0003g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0003g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0004g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0004g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0004g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0005g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0006g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0006g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0007g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0007g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0008g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0008g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0009g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0010g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0011g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0012g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0013g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0014g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0015g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0016g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0017g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0018g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0019g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0020g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0021g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0022g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0023g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0024g0312 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0025g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0026g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0027g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0028g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0029g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0001t0030g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0002t0001g0133 | 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 |
| a0001c0002t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0002t0001g0237 | 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 |
| a0001c0005t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0001c0006t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0002c0007t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| a0003c0004t0005g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | t0003 | g0314 | EUR | GBR | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG00140 | hp2 | a0001 | c0001 | t0016 | g0052 | EUR | GBR | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0035 | EUR | FIN | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0240 | EUR | FIN | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | FIN | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | FIN | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | CHS | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | CHS | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | CHS | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | CHS | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | CHS | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | CHS | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | CHS | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | CHS | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | 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 | g0101 | EAS | CHS | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | CHS | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0295 | 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 | t0001 | g0010 | 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 | t0007 | g0262 | AMR | PUR | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0253 | AMR | PUR | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01071 | hp2 | a0001 | c0001 | t0007 | g0261 | AMR | PUR | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01099 | hp1 | a0001 | c0001 | t0004 | g0234 | 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 | t0001 | g0005 | AMR | PUR | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01106 | hp2 | a0001 | c0001 | t0004 | g0275 | AMR | PUR | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | PUR | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | PUR | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | CLM | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | CLM | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0002 | 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 | t0001 | g0002 | AMR | CLM | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01261 | hp1 | a0001 | c0002 | t0001 | g0225 | AMR | CLM | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0293 | 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 | t0001 | g0265 | AMR | CLM | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | CLM | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | CLM | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01496 | hp1 | a0001 | c0001 | t0025 | g0311 | AMR | CLM | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01496 | hp2 | a0001 | c0001 | t0004 | g0232 | 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 | t0003 | g0321 | EUR | IBS | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | ACB | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | ACB | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01891 | hp1 | a0001 | c0001 | t0011 | g0066 | AFR | ACB | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | ACB | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PEL | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0237 | AMR | PEL | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PEL | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PEL | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0297 | AMR | PEL | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01981 | hp2 | a0001 | c0002 | t0001 | g0120 | AMR | PEL | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PEL | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | PEL | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0125 | 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 | t0001 | g0279 | EAS | KHV | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | KHV | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | ACB | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | KHV | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | KHV | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | KHV | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | KHV | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02129 | hp1 | a0001 | c0001 | t0021 | g0151 | EAS | KHV | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0029 | 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 | g0068 | EAS | KHV | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02145 | hp1 | a0001 | c0005 | t0001 | 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 | g0303 | 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 | t0001 | g0308 | EAS | CDX | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | CDX | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | ACB | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0317 | 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 | g0132 | AMR | PEL | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | ACB | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0019 | 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 | t0001 | g0001 | AMR | PEL | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02300 | hp1 | a0001 | c0002 | t0001 | g0089 | AMR | PEL | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | ACB | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0282 | 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 | t0001 | g0276 | SAS | PJL | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | GWD | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0074 | 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 | t0001 | g0236 | AFR | GWD | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0024 | 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 | g0084 | SAS | PJL | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0230 | SAS | PJL | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | GWD | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0319 | SAS | PJL | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02738 | hp1 | a0001 | c0001 | t0017 | g0226 | SAS | PJL | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0280 | SAS | PJL | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | GWD | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02886 | hp1 | a0001 | c0001 | t0008 | g0061 | AFR | GWD | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | GWD | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | GWD | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0313 | AFR | GWD | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | GWD | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02922 | hp1 | a0001 | c0006 | t0001 | g0168 | AFR | ESN | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | ESN | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | ESN | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0316 | AFR | ESN | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0306 | AFR | ESN | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | ESN | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0114 | 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 | t0001 | g0048 | AFR | GWD | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0107 | 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 | t0008 | g0060 | AFR | ESN | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | ESN | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG03139 | hp1 | a0001 | c0001 | t0020 | g0025 | AFR | ESN | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | ESN | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0248 | AFR | ESN | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG03195 | hp2 | a0001 | c0001 | t0026 | g0318 | AFR | ESN | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | MSL | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | MSL | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | MSL | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0241 | 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 | t0013 | g0058 | AFR | MSL | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG03453 | hp2 | a0001 | c0001 | t0023 | g0057 | AFR | MSL | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | MSL | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | MSL | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0126 | 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 | t0019 | g0172 | AFR | ESN | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG03516 | hp2 | a0001 | c0001 | t0012 | g0062 | AFR | ESN | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | GWD | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0322 | AFR | GWD | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG03579 | hp1 | a0001 | c0001 | t0028 | g0324 | AFR | MSL | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG03579 | hp2 | a0001 | c0001 | t0006 | g0030 | AFR | MSL | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0229 | 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 | g0231 | SAS | PJL | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0258 | SAS | PJL | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0152 | SAS | STU | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | STU | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0299 | SAS | PJL | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | BEB | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0291 | SAS | BEB | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0198 | SAS | BEB | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG03834 | hp2 | a0002 | c0007 | t0001 | g0036 | SAS | BEB | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | BEB | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0192 | SAS | BEB | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | BEB | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0199 | SAS | BEB | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | BEB | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0227 | SAS | BEB | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | STU | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0320 | SAS | STU | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18522 | hp1 | a0001 | c0001 | t0018 | g0169 | AFR | YRI | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | YRI | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18612 | hp1 | a0001 | c0001 | t0029 | g0325 | EAS | CHB | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | CHB | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | CHB | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | CHB | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18906 | hp1 | a0001 | c0001 | t0006 | g0059 | AFR | YRI | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18906 | hp2 | a0001 | c0001 | t0010 | g0284 | AFR | YRI | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0041 | 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 | t0001 | g0031 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18948 | hp1 | a0001 | c0001 | t0027 | g0323 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0032 | 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 | g0267 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18977 | hp2 | a0001 | c0001 | t0003 | g0315 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18980 | hp1 | a0001 | c0001 | t0005 | g0110 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0187 | 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 | t0001 | g0042 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0040 | 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 | t0001 | g0250 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19004 | hp1 | a0001 | c0001 | t0030 | g0326 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19006 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | LWK | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | LWK | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0020 | AFR | LWK | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0283 | AFR | LWK | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0274 | 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 | t0001 | g0043 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0264 | 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 | g0290 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0039 | 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 | t0001 | g0195 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19081 | hp1 | a0001 | c0001 | t0014 | g0140 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0269 | 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 | a0003 | c0004 | t0005 | g0022 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19088 | hp2 | a0001 | c0002 | t0001 | g0133 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | YRI | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | YRI | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0021 | 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 | t0001 | g0251 | AFR | ACB | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0071 | 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 | g0106 | AFR | ACB | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | ACB | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | MSL | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | MSL | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA18955 | hp2 | a0001 | c0001 | t0009 | g0011 | EAS | JPT | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA20300 | hp1 | a0001 | c0001 | t0022 | g0046 | 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 | t0015 | g0055 | AFR | LWK | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | LWK | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0024 | g0312 | REF | REF | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0017 | REF | REF | USP7_chr16_8887097_8968906 | USP7 | chr16 | 8887097 | 8968906 |
| view | 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 | a0002 | 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 | a0003 | 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 |
| view | 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 |
| view | 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 | a0001c0001t0015 | 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 | a0001c0001t0014 | 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 | a0001c0001t0026 | 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 | a0001c0001t0016 | 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 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(6): Show |
106 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(103): 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 | a0001c0001t0001 a0001c0001t0003 |
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 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0008 others(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 | a0001c0001t0001 a0001c0001t0003 a0002c0007t0001 |
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 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(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 | a0001c0001t0013 | 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 | a0001c0001t0012 | 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 | a0001c0001t0006 a0001c0001t0008 |
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 | a0001c0001t0017 | 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 | a0001c0001t0011 | 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 | a0001c0001t0005 a0003c0004t0005 |
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 | a0001c0001t0018 a0001c0001t0028 |
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 | a0001c0001t0019 | 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 | a0001c0001t0007 | 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 | a0001c0001t0004 | 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 | a0001c0001t0008 a0001c0001t0020 |
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 | a0001c0001t0021 | 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 | a0001c0001t0022 | 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 | a0001c0001t0010 | 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 | a0001c0001t0023 | 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 | a0001c0001t0027 | 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 | a0001c0001t0025 | 1 | HG01496.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 | 32 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(29): Show |
315 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(312): 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 | 2 | a0001c0001t0003 a0001c0001t0026 |
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 | a0001c0001t0027 | 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 | a0001c0001t0028 | 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 | a0001c0001t0029 | 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 | a0001c0001t0030 | 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 | a0001c0001t0009 | 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 | a0001c0001t0009 | 1 | NA18955.hp2 | 5_prime_UTR_variant | MODIFIER | c.-537G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/31 | 537 | chr16 | 8963822 |
| view | 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 | a0001c0001t0022g0046 | 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 | a0001c0001t0001g0283 | 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 | 115 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(112): Show |
120 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(117): 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 | a0001c0001t0018g0169 | 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 | 124 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(121): Show |
130 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.3202+219T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 30/30 | chr16 | 8894331 | |||||||
| chr16:8894381 | C | T | 318 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(315): Show |
329 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(326): 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 | a0001c0001t0015g0055 | 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 | a0001c0001t0001g0134 a0001c0002t0001g0089 a0001c0002t0001g0120 others(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 | 143 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(140): 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 | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(114): Show |
123 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.3202+20delC | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 30/30 | chr16 | 8894529 | |||||||
| chr16:8894721 | G | A | 8 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0074 others(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 | a0001c0001t0001g0276 | 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 | a0001c0001t0013g0058 a0001c0001t0018g0169 a0001c0001t0028g0324 |
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 | a0001c0001t0001g0024 | 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 | 101 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(98): 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 | a0001c0001t0001g0309 | 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 | a0001c0001t0001g0264 | 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 | a0001c0001t0001g0065 | 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 | a0001c0001t0001g0029 a0001c0001t0001g0031 a0001c0001t0001g0032 others(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 | a0001c0001t0001g0285 | 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 | a0001c0001t0001g0029 a0001c0001t0001g0031 a0001c0001t0001g0032 others(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 | 318 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(315): Show |
329 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(326): 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 | a0001c0001t0001g0162 | 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 | a0001c0001t0001g0277 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0028 a0001c0001t0001g0029 others(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 | 164 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(161): 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 | a0001c0001t0001g0166 | 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 | a0001c0001t0001g0213 a0001c0001t0001g0285 |
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 | a0001c0001t0001g0008 a0001c0001t0001g0075 a0001c0001t0001g0088 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0051 others(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 | 102 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(99): Show |
107 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.2820-397delA | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 26/30 | chr16 | 8896137 | |||||||
| chr16:8896137 | CTT | C | 16 | a0001c0001t0001g0028 a0001c0001t0001g0056 a0001c0001t0001g0184 others(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 | a0001c0001t0006g0030 a0001c0001t0006g0059 a0001c0001t0008g0060 others(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 | 313 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(310): Show |
324 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.2820-622C>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 26/30 | chr16 | 8896363 | |||||||
| chr16:8896382 | T | C | 121 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(118): Show |
127 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(124): 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 | a0001c0001t0013g0058 a0001c0001t0018g0169 a0001c0001t0028g0324 |
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 | a0001c0001t0001g0303 | 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 | 318 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(315): Show |
329 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(326): 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 | a0001c0001t0001g0067 a0001c0001t0029g0325 |
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 | 100 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0028 others(97): Show |
103 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(100): 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 | a0001c0001t0002g0014 | 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 | a0001c0001t0001g0037 | 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 | a0001c0001t0003g0322 | 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 | a0001c0001t0001g0054 | 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 | 93 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0063 others(90): Show |
96 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(93): 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 | a0001c0001t0001g0307 | 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 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0150 others(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 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0047 others(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 | 141 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(138): 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 | a0001c0001t0003g0319 | 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 | a0001c0001t0001g0202 a0001c0001t0003g0320 |
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 | a0001c0001t0003g0319 a0001c0001t0003g0322 |
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 | a0001c0001t0003g0316 | 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 | a0001c0001t0001g0047 a0001c0001t0001g0049 a0001c0001t0001g0050 others(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 | a0001c0001t0001g0111 a0001c0001t0001g0125 a0001c0001t0001g0147 others(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 | a0001c0001t0011g0066 | 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 | a0001c0001t0001g0084 a0001c0001t0001g0130 a0001c0001t0001g0131 others(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 | a0001c0001t0001g0108 a0001c0001t0001g0171 a0001c0002t0001g0137 others(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 | a0001c0001t0001g0034 a0001c0001t0001g0047 a0001c0001t0001g0049 others(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 | a0001c0001t0001g0051 a0001c0001t0001g0053 a0001c0001t0016g0052 |
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 | a0001c0001t0001g0123 | 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 | a0001c0001t0001g0082 a0001c0001t0001g0086 a0001c0001t0001g0099 others(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 | a0002c0007t0001g0036 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0035 |
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 | 37 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(34): 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 | a0001c0001t0001g0079 a0001c0001t0001g0103 a0001c0001t0001g0119 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0054 a0001c0001t0001g0097 others(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 | a0001c0001t0001g0214 a0001c0001t0001g0283 |
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 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0047 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0069 a0001c0001t0001g0105 others(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 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0293 others(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 | a0001c0001t0001g0068 a0001c0001t0001g0174 a0001c0001t0001g0255 others(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 | 144 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(141): 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 | a0001c0001t0001g0074 | 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 | a0001c0001t0001g0117 | 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 | a0001c0001t0001g0182 | 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 | a0001c0001t0001g0072 | 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 | a0001c0001t0001g0183 | 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 | a0001c0001t0001g0122 | 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 | a0001c0001t0001g0118 | 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 | a0001c0001t0001g0213 | 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 | a0001c0001t0001g0298 | 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 | a0001c0001t0001g0196 a0001c0001t0001g0268 |
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 | a0001c0001t0001g0281 | 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 | a0001c0001t0001g0305 a0001c0001t0004g0234 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0278 |
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 | a0001c0001t0001g0195 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0191 a0001c0001t0001g0233 others(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 | a0001c0001t0001g0199 a0001c0001t0001g0254 |
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 | a0001c0001t0001g0185 a0001c0001t0001g0273 |
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 | a0001c0001t0001g0306 | 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 | a0001c0001t0001g0033 | 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 | a0001c0001t0001g0071 | 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 | a0001c0001t0001g0163 a0001c0001t0001g0193 a0001c0001t0001g0239 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0235 a0001c0001t0001g0276 others(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 | a0001c0001t0001g0149 a0001c0001t0001g0164 a0001c0001t0001g0270 others(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 | a0001c0001t0001g0044 | 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 | a0001c0001t0001g0224 a0001c0001t0001g0257 a0001c0001t0022g0046 |
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 | a0001c0001t0001g0102 a0001c0001t0001g0188 a0001c0001t0001g0190 others(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 | a0001c0001t0001g0253 a0001c0001t0007g0261 a0001c0001t0007g0262 |
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 | a0001c0001t0001g0040 | 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 | a0001c0001t0001g0031 | 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 | a0001c0001t0001g0037 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0100 others(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 |
3 | a0001c0001t0001g0187 a0001c0001t0001g0197 a0001c0001t0001g0297 |
3 | HG01981.hp1 NA18980.hp2 NA19066.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 | AAAAATAT others(8): Show |
2 | a0001c0001t0001g0246 a0001c0001t0001g0272 |
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 | a0001c0001t0001g0310 | 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 | a0001c0001t0001g0038 a0001c0001t0001g0042 a0001c0001t0001g0186 others(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 | a0001c0001t0001g0029 | 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 | a0001c0001t0027g0323 | 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 | a0001c0001t0001g0201 a0001c0001t0001g0227 a0001c0001t0001g0264 |
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 | a0001c0001t0001g0245 | 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 | a0001c0001t0001g0032 a0001c0001t0001g0043 a0001c0001t0001g0308 |
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 | a0001c0001t0001g0039 | 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 | a0001c0001t0001g0045 | 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 | a0001c0001t0001g0048 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0078 a0001c0001t0001g0121 others(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 | a0001c0001t0001g0116 a0001c0001t0001g0192 a0001c0001t0001g0282 |
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 | a0001c0001t0001g0249 a0001c0001t0001g0269 |
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 | a0001c0001t0001g0041 a0001c0001t0001g0307 |
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 | a0001c0001t0001g0241 a0001c0001t0001g0309 |
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 | a0001c0001t0001g0073 | 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 | a0001c0001t0001g0114 | 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 | a0001c0001t0001g0230 a0001c0005t0001g0176 |
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 | a0001c0001t0001g0115 | 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 | a0001c0001t0001g0244 a0001c0001t0001g0247 a0001c0001t0001g0248 others(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 | a0001c0001t0003g0313 | 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 | a0001c0001t0001g0184 | 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 | 160 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(157): 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 | a0001c0001t0002g0020 | 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 | a0001c0001t0001g0162 | 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 | a0001c0001t0001g0162 | 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 | a0001c0001t0001g0037 | 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 | a0001c0001t0006g0059 a0001c0001t0008g0060 |
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 | a0001c0001t0006g0030 a0001c0001t0008g0061 a0001c0001t0012g0062 |
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 | a0001c0001t0001g0239 a0001c0001t0001g0252 |
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 | a0001c0001t0001g0191 | 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 | a0001c0001t0006g0030 a0001c0001t0006g0059 a0001c0001t0008g0060 others(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 | a0001c0001t0003g0316 | 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 | a0001c0001t0001g0281 | 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 | 129 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(126): Show |
134 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(131): 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 | a0001c0001t0001g0037 | 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 | a0001c0001t0001g0263 | 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 | a0001c0001t0001g0029 a0001c0001t0001g0031 a0001c0001t0001g0032 others(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 | a0001c0001t0001g0293 | 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 | 129 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(126): 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 | 318 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(315): Show |
329 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(326): Show |
intron_variant | MODIFIER | c.2531+110T>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 23/30 | chr16 | 8899011 | |||||||
| chr16:8899012 | C | A | 318 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(315): Show |
329 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(326): 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 | a0001c0001t0022g0046 | 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 | a0001c0001t0001g0069 | 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 | a0001c0001t0003g0317 | 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 | a0001c0001t0006g0030 a0001c0001t0006g0059 a0001c0001t0008g0060 others(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 | 117 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(114): Show |
121 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(118): 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 | a0001c0006t0001g0168 | 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 | 132 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(129): 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 | a0001c0001t0006g0030 a0001c0001t0006g0059 a0001c0001t0008g0060 others(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 | a0001c0001t0001g0037 | 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 | a0001c0001t0001g0037 | 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 | a0001c0001t0001g0045 | 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 | a0001c0001t0001g0075 | 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 | a0001c0001t0001g0148 a0001c0001t0001g0288 |
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 | 87 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0063 others(84): Show |
90 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(87): 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 | a0001c0001t0013g0058 a0001c0001t0018g0169 a0001c0001t0028g0324 |
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 | a0001c0001t0023g0057 | 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 | a0001c0001t0001g0054 a0001c0001t0001g0073 a0001c0001t0001g0082 others(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 | a0001c0001t0001g0233 a0001c0001t0001g0240 a0001c0001t0001g0257 |
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 | a0001c0001t0001g0029 | 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 | a0001c0001t0001g0073 a0001c0001t0001g0115 a0001c0001t0001g0116 |
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 | 30 | a0001c0001t0001g0004 a0001c0001t0001g0024 a0001c0001t0001g0026 others(27): 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 | a0001c0001t0009g0011 | 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 | a0001c0001t0009g0011 | 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 | 188 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(185): 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 | a0001c0001t0001g0131 a0001c0001t0001g0181 a0001c0001t0006g0030 others(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 | 106 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0028 others(103): Show |
109 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(106): 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 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0051 others(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 | a0001c0001t0009g0011 | 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 | a0001c0001t0011g0066 | 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 | a0001c0001t0001g0263 | 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 | 98 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0063 others(95): Show |
101 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(98): 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 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0074 others(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 | a0001c0001t0001g0037 | 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 | 138 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(135): 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 | a0001c0001t0001g0037 | 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 | 113 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(110): Show |
117 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(114): 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 | a0001c0001t0013g0058 a0001c0001t0018g0169 a0001c0001t0028g0324 |
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 | 117 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(114): 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 | 167 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(164): 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 | 74 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0063 others(71): Show |
77 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(74): 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 | a0001c0001t0001g0180 | 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 | a0001c0001t0001g0180 | 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 | a0001c0001t0001g0180 | 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 | a0001c0001t0001g0037 | 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 | 197 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(194): 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 | a0001c0001t0020g0025 | 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 | a0001c0001t0001g0255 | 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 | a0001c0001t0002g0014 | 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 | 1 | a0001c0001t0001g0009 | 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 | a0001c0001t0015g0055 | 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 | a0001c0001t0001g0167 | 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 | a0001c0001t0001g0073 a0001c0001t0001g0115 a0001c0001t0001g0116 |
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 | a0001c0001t0001g0054 | 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 | a0001c0001t0001g0073 a0001c0001t0001g0115 a0001c0001t0001g0116 |
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 | 147 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(144): Show |
153 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.1705-466delT | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 15/30 | chr16 | 8903867 | |||||||
| chr16:8904020 | G | C | 1 | a0001c0001t0001g0127 | 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 | a0001c0001t0001g0073 a0001c0001t0001g0115 a0001c0001t0001g0116 |
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 | a0001c0001t0001g0092 | 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 | a0001c0001t0001g0081 | 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 | a0001c0001t0001g0081 | 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 | a0001c0001t0001g0195 | 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 | a0001c0001t0001g0048 a0001c0001t0001g0306 |
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 | a0001c0001t0001g0201 | 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 | a0001c0001t0003g0315 | 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 | a0001c0001t0013g0058 a0001c0001t0018g0169 a0001c0001t0028g0324 |
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 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0051 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0051 others(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 | a0001c0001t0001g0081 | 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 | a0001c0001t0001g0157 a0001c0001t0001g0215 a0001c0001t0001g0217 others(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 | 100 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(97): Show |
105 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(102): 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 | a0001c0001t0022g0046 | 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 | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(114): Show |
122 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.1574-217dupT | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 14/30 | chr16 | 8904781 | |||||||
| chr16:8904788 | A | T | 3 | a0001c0001t0001g0073 a0001c0001t0001g0115 a0001c0001t0001g0116 |
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 | a0001c0001t0009g0011 | 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 | a0001c0001t0001g0194 a0001c0001t0001g0265 |
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 | a0001c0001t0001g0051 a0001c0001t0001g0053 a0001c0001t0016g0052 |
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 | a0001c0001t0001g0307 a0001c0001t0001g0310 |
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 | a0001c0001t0010g0284 | 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 | a0001c0001t0001g0037 | 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 | a0001c0001t0001g0073 a0001c0001t0001g0115 a0001c0001t0001g0116 |
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 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0051 others(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 | a0001c0001t0015g0055 | 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 | a0001c0001t0001g0054 | 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 | a0001c0001t0001g0119 a0001c0001t0001g0138 |
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 | a0001c0001t0001g0166 | 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 | 103 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0056 others(100): Show |
106 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(103): 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 | a0001c0001t0001g0073 a0001c0001t0001g0115 a0001c0001t0001g0116 |
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 | a0001c0001t0001g0147 a0001c0001t0001g0174 |
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 | a0001c0001t0001g0037 | 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 | a0001c0001t0001g0073 a0001c0001t0001g0115 a0001c0001t0001g0116 |
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 | 133 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(130): 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 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0074 others(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 | 100 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(97): Show |
105 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(102): 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 | a0001c0001t0001g0056 a0001c0001t0023g0057 |
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 | a0001c0001t0001g0127 | 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 | a0001c0001t0001g0037 | 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 | 313 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(310): Show |
324 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(321): 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 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0051 others(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 | a0001c0001t0001g0241 | 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 | a0001c0001t0003g0313 | 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 | a0001c0001t0022g0046 | 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 | a0001c0001t0001g0073 a0001c0001t0001g0115 a0001c0001t0001g0116 |
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 | a0001c0001t0003g0313 | 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 | a0001c0001t0001g0054 a0001c0001t0015g0055 a0001c0001t0022g0046 |
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 | a0001c0001t0001g0037 | 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 | a0001c0001t0001g0054 | 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 | a0001c0001t0001g0114 | 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 | a0001c0001t0001g0194 | 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 | a0001c0001t0001g0162 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0051 others(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 | a0001c0001t0001g0254 | 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 | a0001c0001t0001g0065 a0001c0001t0001g0098 a0001c0001t0001g0175 |
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 | a0001c0001t0022g0046 | 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 | a0001c0001t0006g0030 a0001c0001t0006g0059 a0001c0001t0008g0060 others(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 | a0001c0001t0001g0073 a0001c0001t0001g0115 a0001c0001t0001g0116 |
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 | a0001c0001t0001g0056 a0001c0001t0023g0057 |
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 | 180 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(177): 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 | a0001c0001t0001g0263 | 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 | a0001c0001t0001g0291 | 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 | a0001c0001t0003g0315 | 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 | a0001c0001t0022g0046 | 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 | a0001c0001t0001g0073 a0001c0001t0001g0115 a0001c0001t0001g0116 |
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 | a0001c0001t0001g0037 | 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 | a0001c0001t0001g0056 a0001c0001t0013g0058 a0001c0001t0018g0169 others(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 | 119 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(116): Show |
124 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(121): 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 | a0001c0002t0001g0133 | 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 | a0001c0001t0001g0054 | 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 | a0001c0001t0001g0202 a0001c0001t0001g0283 a0001c0001t0003g0314 others(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 | a0001c0001t0001g0037 | 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 | a0001c0001t0001g0096 | 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 | a0001c0001t0001g0024 a0001c0001t0006g0030 a0001c0001t0006g0059 others(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 | a0001c0001t0001g0073 a0001c0001t0001g0115 a0001c0001t0001g0116 |
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 | a0001c0001t0001g0152 a0001c0001t0001g0192 |
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 | a0001c0001t0001g0037 | 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 | a0001c0001t0001g0073 a0001c0001t0001g0115 a0001c0001t0001g0116 |
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 | a0001c0001t0001g0114 | 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 | a0001c0001t0015g0055 | 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 | a0001c0001t0001g0029 a0001c0001t0001g0031 a0001c0001t0001g0032 others(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 | a0001c0001t0001g0071 a0001c0001t0001g0074 a0001c0001t0001g0117 others(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 | 1 | a0001c0001t0001g0002 | 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 | a0001c0001t0001g0037 | 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 | 318 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(315): Show |
329 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(326): 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 | a0001c0001t0001g0162 | 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 | a0001c0001t0002g0003 a0001c0001t0002g0019 a0001c0001t0002g0020 others(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 | a0001c0001t0001g0023 a0001c0001t0001g0113 a0001c0001t0009g0011 |
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 | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(117): Show |
126 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(123): 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 | a0001c0001t0001g0241 a0001c0001t0001g0282 |
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 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0101 others(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 | a0001c0001t0015g0055 a0001c0001t0022g0046 |
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 | a0001c0001t0001g0295 | 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 | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(114): Show |
122 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(119): 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 | a0001c0001t0013g0058 | 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 | a0001c0001t0001g0128 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0051 others(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 | a0001c0001t0001g0162 a0001c0001t0010g0284 |
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 | a0001c0001t0006g0030 a0001c0001t0006g0059 a0001c0001t0008g0060 others(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 | a0001c0001t0001g0227 a0001c0001t0001g0228 a0001c0001t0001g0229 others(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 | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(114): Show |
122 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(119): 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 | a0001c0001t0003g0315 a0001c0001t0026g0318 |
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 | a0001c0001t0001g0042 | 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 | 101 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(98): Show |
106 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.1079-1623dupT | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 10/30 | chr16 | 8912449 | |||||||
| chr16:8912460 | A | C | 18 | a0001c0001t0001g0029 a0001c0001t0001g0031 a0001c0001t0001g0032 others(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 | a0001c0001t0001g0283 | 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 | a0001c0001t0001g0056 a0001c0001t0023g0057 |
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 | 1 | a0001c0001t0025g0311 | 1 | HG01496.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 | a0001c0001t0001g0040 | 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 | a0001c0001t0020g0025 | 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 | a0001c0001t0001g0037 a0001c0001t0001g0054 a0001c0001t0001g0073 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0051 others(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 | a0001c0001t0022g0046 | 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 | a0001c0001t0001g0084 | 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 | a0001c0001t0001g0056 a0001c0001t0023g0057 |
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 | a0001c0001t0001g0037 a0001c0001t0001g0073 a0001c0001t0001g0115 others(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 | a0001c0001t0001g0296 | 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 | a0001c0001t0022g0046 | 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 | a0001c0001t0022g0046 | 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 | a0001c0001t0022g0046 | 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 | a0001c0001t0022g0046 | 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 | a0001c0001t0022g0046 | 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 | a0001c0001t0022g0046 | 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 | a0001c0001t0022g0046 | 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 | a0001c0001t0022g0046 | 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 | a0001c0001t0001g0227 a0001c0001t0017g0226 |
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 | a0001c0001t0001g0258 a0001c0001t0001g0299 |
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 | a0001c0001t0021g0151 | 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 | a0001c0001t0001g0279 | 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 | a0001c0001t0001g0283 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0037 others(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 | a0001c0001t0001g0056 a0001c0001t0023g0057 |
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 | a0001c0001t0013g0058 a0001c0001t0018g0169 a0001c0001t0028g0324 |
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 | a0001c0001t0001g0295 | 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 | a0001c0001t0015g0055 | 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 | a0001c0001t0001g0082 | 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 | 111 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(108): Show |
116 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(113): 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 | a0001c0001t0001g0073 a0001c0001t0001g0115 a0001c0001t0001g0116 |
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 | a0001c0006t0001g0168 | 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 | a0001c0001t0004g0232 | 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 | a0001c0001t0001g0180 | 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 | a0001c0001t0001g0208 a0001c0001t0001g0283 a0001c0001t0003g0314 others(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 | a0001c0001t0022g0046 | 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 | a0001c0001t0022g0046 | 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 | a0001c0001t0022g0046 | 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 | a0001c0001t0022g0046 | 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 | a0001c0001t0022g0046 | 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 | a0001c0001t0022g0046 | 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 | 192 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(189): 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 | a0001c0001t0015g0055 | 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 | a0001c0001t0001g0054 | 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 | a0001c0001t0001g0290 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0051 others(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 | a0001c0001t0001g0064 | 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 | a0001c0001t0001g0064 | 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 | a0001c0001t0001g0064 | 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 | a0001c0001t0001g0102 a0001c0001t0001g0191 a0001c0001t0001g0243 others(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 | a0001c0001t0023g0057 | 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 | a0001c0001t0010g0284 | 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 | a0001c0001t0001g0123 a0002c0007t0001g0036 |
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 | a0001c0001t0001g0102 a0001c0001t0001g0191 a0001c0001t0001g0254 others(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 | a0001c0001t0022g0046 | 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 | a0001c0001t0001g0032 | 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 | a0001c0001t0001g0277 | 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 | a0001c0001t0001g0181 | 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 | 290 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(287): Show |
301 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.906+268G>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 8/30 | chr16 | 8916234 | |||||||
| chr16:8916356 | T | G | 180 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(177): 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 | 114 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(111): Show |
119 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(116): 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 | 310 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(307): Show |
321 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(318): 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 | a0001c0001t0001g0056 a0001c0001t0023g0057 |
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 | a0001c0001t0001g0202 | 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 | a0001c0001t0001g0065 a0001c0001t0001g0068 a0001c0001t0001g0098 others(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 | a0001c0001t0001g0056 a0001c0001t0023g0057 |
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 | a0001c0001t0010g0284 | 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 | a0001c0001t0001g0049 a0001c0001t0001g0112 a0001c0001t0001g0119 others(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 | 156 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(153): 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 | a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0031 others(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 | a0001c0001t0001g0040 | 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 | a0001c0001t0001g0306 | 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 | a0001c0001t0002g0014 | 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 | a0001c0001t0002g0003 a0001c0001t0002g0019 a0001c0001t0002g0020 others(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 | a0001c0001t0001g0250 | 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 | a0001c0001t0001g0029 a0001c0001t0001g0031 a0001c0001t0001g0032 others(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 | a0001c0001t0001g0128 | 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 | a0001c0001t0001g0073 a0001c0001t0001g0115 a0001c0001t0001g0116 |
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 | a0001c0001t0026g0318 | 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 | a0001c0001t0006g0030 a0001c0001t0006g0059 a0001c0001t0008g0060 others(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 | a0001c0001t0013g0058 a0001c0001t0018g0169 a0001c0001t0028g0324 |
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 | a0001c0001t0029g0325 | 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 | a0001c0001t0012g0062 | 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 | 169 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(166): 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 | a0001c0001t0001g0037 | 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 | 318 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(315): Show |
329 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(326): 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 | a0001c0001t0001g0258 | 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 | a0001c0001t0001g0164 a0001c0001t0001g0185 a0001c0001t0001g0195 others(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 | a0001c0001t0001g0199 | 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 | a0001c0001t0001g0199 | 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 | a0001c0001t0002g0003 a0001c0001t0002g0019 a0001c0001t0002g0020 others(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 | a0001c0001t0001g0109 | 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 | 1 | a0001c0001t0025g0311 | 1 | HG01496.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 | a0001c0001t0001g0073 a0001c0001t0001g0115 a0001c0001t0001g0116 |
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 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0074 others(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 | 165 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(162): 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 | a0001c0001t0022g0046 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0037 others(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 | a0001c0001t0015g0055 | 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 | a0001c0001t0001g0029 a0001c0001t0001g0031 a0001c0001t0001g0032 others(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 | a0001c0001t0001g0054 | 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 | a0001c0001t0013g0058 a0001c0001t0018g0169 a0001c0001t0028g0324 others(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 | 318 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(315): Show |
329 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(326): 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 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0051 others(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 | a0001c0001t0001g0277 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0051 others(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 | a0001c0001t0001g0056 a0001c0001t0023g0057 |
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 | a0001c0001t0015g0055 | 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 | a0001c0001t0015g0055 | 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 | a0001c0001t0001g0215 | 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 | a0001c0001t0001g0243 | 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 | a0001c0001t0001g0126 | 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 | 318 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(315): Show |
329 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(326): Show |
intron_variant | MODIFIER | c.523-46A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 4/30 | chr16 | 8920493 | |||||||
| chr16:8920528 | G | A | 168 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(165): 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 | a0001c0001t0001g0037 | 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 | 318 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(315): Show |
329 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(326): 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 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0051 others(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 | a0001c0001t0001g0037 | 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 | 178 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(175): 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 | 317 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(314): Show |
328 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(325): 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 | a0001c0001t0001g0045 | 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 | a0001c0001t0001g0029 a0001c0001t0001g0031 a0001c0001t0001g0032 others(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 | 318 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(315): Show |
329 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(326): Show |
intron_variant | MODIFIER | c.384-100T>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 3/30 | chr16 | 8921395 | |||||||
| chr16:8921401 | T | C | 182 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(179): 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 | a0001c0001t0001g0258 | 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 | a0001c0001t0001g0283 | 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 | a0001c0001t0001g0270 | 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 | a0001c0001t0001g0104 | 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 | a0001c0001t0001g0104 | 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 | a0001c0001t0001g0104 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0051 others(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 | 294 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(291): Show |
305 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(302): 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 | a0001c0001t0001g0164 | 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 | a0001c0001t0001g0054 | 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 | a0001c0001t0001g0197 a0001c0001t0001g0246 a0001c0001t0001g0269 others(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 | a0001c0001t0003g0315 | 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 | a0001c0001t0001g0054 | 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 | 294 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(291): Show |
305 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(302): 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 | a0001c0001t0001g0073 a0001c0001t0001g0115 a0001c0001t0001g0116 |
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 | a0001c0001t0022g0046 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0051 others(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 | a0001c0001t0022g0046 | 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 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0224 |
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 | 101 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0056 others(98): Show |
104 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(101): 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 | a0001c0001t0001g0054 | 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 | a0001c0001t0001g0285 | 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 |
312 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(309): Show |
323 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(320): 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 | a0001c0001t0001g0056 a0001c0001t0023g0057 |
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 | a0001c0001t0003g0314 | 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 | a0001c0001t0001g0102 | 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 | a0001c0001t0001g0307 a0001c0001t0001g0308 a0001c0001t0001g0309 others(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 | a0001c0001t0022g0046 | 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 | a0001c0001t0006g0059 a0001c0001t0008g0060 a0001c0001t0008g0061 |
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 | a0001c0001t0001g0056 a0001c0001t0023g0057 |
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 | a0001c0001t0001g0056 a0001c0001t0023g0057 |
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 | a0001c0001t0001g0283 | 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 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0274 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0037 others(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 | a0001c0005t0001g0176 | 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 | 115 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(112): Show |
120 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(117): 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 | a0001c0001t0029g0325 | 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 | a0001c0001t0001g0302 | 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 | a0001c0001t0001g0167 | 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 | a0001c0001t0001g0056 a0001c0001t0023g0057 |
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 | a0001c0001t0003g0321 | 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 | a0001c0001t0001g0064 | 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 | 322 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(319): Show |
334 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(331): 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 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0051 others(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 | a0001c0001t0009g0011 | 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 | a0001c0001t0001g0308 | 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 | a0001c0001t0001g0106 a0001c0001t0001g0108 a0001c0001t0001g0166 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0031 a0001c0001t0001g0032 others(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 | a0001c0001t0001g0037 | 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 | a0001c0001t0001g0037 a0001c0001t0001g0054 a0001c0001t0015g0055 |
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 | a0001c0001t0022g0046 | 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 | a0001c0001t0022g0046 | 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 | a0001c0001t0001g0054 | 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 | 189 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(186): 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 | 53 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0026 others(50): 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 | a0001c0001t0001g0192 | 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 | a0001c0001t0001g0114 | 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 | a0001c0001t0006g0030 | 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 | a0001c0001t0001g0166 | 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 | a0001c0001t0022g0046 | 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 | a0001c0001t0001g0037 a0001c0001t0001g0054 |
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 | a0001c0001t0001g0184 a0001c0001t0001g0186 a0001c0001t0001g0244 others(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 | a0001c0001t0001g0105 a0001c0001t0001g0156 |
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 | a0001c0001t0001g0024 a0001c0001t0020g0025 |
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 | a0001c0001t0001g0264 | 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 | a0001c0002t0001g0089 a0001c0002t0001g0120 a0001c0002t0001g0132 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0031 a0001c0001t0001g0032 others(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 | 299 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(296): Show |
309 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(306): 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 | a0001c0001t0001g0092 | 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 | a0001c0001t0001g0037 | 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 | a0001c0001t0015g0055 | 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 | a0001c0001t0001g0255 | 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 | a0001c0001t0001g0037 a0001c0001t0001g0054 a0001c0001t0001g0250 others(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 | a0001c0001t0001g0037 | 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 | a0001c0001t0022g0046 | 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 | a0001c0001t0001g0024 a0001c0001t0020g0025 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0126 |
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 | a0001c0001t0001g0117 | 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 | a0001c0001t0003g0314 a0001c0001t0003g0319 a0001c0001t0003g0320 others(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 | a0001c0001t0001g0086 | 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 | a0001c0001t0001g0054 a0001c0001t0022g0046 |
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 | a0001c0001t0001g0285 | 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 | a0001c0001t0001g0100 | 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 | a0001c0001t0001g0054 | 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 | a0001c0001t0001g0037 | 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 | a0001c0001t0015g0055 | 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 | a0001c0001t0015g0055 | 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 | a0001c0001t0006g0030 a0001c0001t0006g0059 a0001c0001t0008g0060 others(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 | a0001c0001t0001g0163 a0001c0001t0001g0296 |
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 | a0001c0001t0001g0280 | 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 | a0001c0001t0001g0037 | 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 | a0001c0001t0001g0056 a0001c0001t0023g0057 |
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 | a0001c0006t0001g0168 | 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 | a0001c0001t0022g0046 | 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 | a0001c0001t0001g0054 | 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 | a0001c0001t0022g0046 | 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 | a0001c0001t0001g0065 a0001c0001t0001g0098 a0001c0001t0001g0175 |
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 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0037 others(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 | 222 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(219): Show |
230 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(227): 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 | 1 | a0001c0001t0001g0002 | 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 | a0001c0001t0001g0037 | 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 | 60 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0024 others(57): 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 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0211 others(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 | a0001c0001t0015g0055 | 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 | a0001c0001t0001g0054 | 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 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0211 others(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 | a0001c0001t0001g0221 | 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 | 12 | a0001c0001t0001g0009 a0001c0001t0001g0069 a0001c0001t0001g0105 others(9): 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 | a0001c0001t0001g0270 | 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 | a0001c0001t0002g0003 a0001c0001t0002g0019 |
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 | a0001c0001t0001g0048 a0001c0001t0001g0282 |
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 | a0001c0001t0011g0066 | 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 | a0001c0001t0001g0277 | 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 | a0001c0001t0013g0058 | 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 | a0001c0001t0030g0326 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0051 others(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 | a0001c0001t0001g0121 | 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 | a0001c0001t0006g0030 a0001c0001t0006g0059 a0001c0001t0008g0060 others(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 | a0001c0001t0021g0151 | 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 | a0001c0001t0001g0054 | 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 | a0001c0001t0001g0073 a0001c0001t0001g0115 a0001c0001t0001g0116 |
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 | a0001c0001t0001g0054 | 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 | 223 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(220): Show |
231 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(228): 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 | a0001c0001t0001g0007 a0001c0001t0001g0126 |
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 | 61 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0024 others(58): 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 | a0001c0001t0001g0079 a0001c0001t0001g0123 |
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 | 318 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(315): Show |
329 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(326): Show |
intron_variant | MODIFIER | c.80-552A>T | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8930949 | |||||||
| chr16:8930973 | T | TA | 221 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(218): Show |
229 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.80-577dupT | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8930973 | |||||||
| chr16:8930973 | T | TAA | 6 | a0001c0001t0001g0111 a0001c0001t0001g0114 a0001c0001t0001g0199 others(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 | a0001c0001t0003g0322 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0051 others(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 | a0001c0001t0001g0301 a0001c0001t0001g0302 |
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 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0051 others(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 | a0001c0001t0022g0046 | 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 | a0001c0001t0001g0094 | 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 | a0001c0001t0025g0311 | 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 | 58 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0024 others(55): 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 | a0001c0001t0001g0067 a0001c0001t0029g0325 |
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 | a0001c0001t0001g0037 | 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 | a0001c0001t0001g0037 | 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 | a0001c0001t0001g0207 a0001c0001t0001g0210 |
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 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0051 others(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 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0224 |
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 | 318 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(315): Show |
329 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(326): 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 | a0001c0001t0001g0077 | 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 | a0001c0001t0001g0048 | 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 | a0001c0001t0001g0138 | 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 | a0001c0001t0001g0173 | 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 | a0001c0001t0006g0030 a0001c0001t0006g0059 a0001c0001t0008g0060 others(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 | 253 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(250): Show |
262 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(259): 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 | a0001c0001t0001g0100 a0001c0001t0001g0279 |
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 | 226 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(223): Show |
234 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(231): 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 | a0001c0001t0001g0054 | 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 | a0001c0001t0001g0037 a0001c0001t0001g0074 |
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 | a0001c0001t0001g0280 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0051 others(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 | a0001c0001t0001g0042 | 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 | a0001c0001t0009g0011 | 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 | a0001c0001t0001g0086 a0001c0001t0001g0088 a0001c0001t0001g0099 others(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 | a0001c0001t0022g0046 | 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 | a0001c0001t0028g0324 | 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 | a0001c0001t0001g0037 | 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 | 59 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0024 others(56): 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 | a0001c0001t0001g0037 | 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 | 230 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(227): Show |
238 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(235): 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 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0051 others(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 | a0001c0001t0001g0111 a0001c0001t0005g0110 |
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 | a0001c0001t0001g0029 a0001c0001t0001g0031 a0001c0001t0001g0032 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0045 others(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 | a0001c0001t0001g0193 | 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 | a0001c0001t0022g0046 | 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 | a0001c0001t0022g0046 | 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 | 318 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(315): Show |
329 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(326): 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 | a0001c0001t0022g0046 | 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 | a0001c0001t0001g0106 | 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 | a0001c0001t0001g0112 | 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 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0211 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0031 a0001c0001t0001g0032 others(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 | a0001c0001t0022g0046 | 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 | a0001c0001t0022g0046 | 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 | a0001c0001t0001g0029 a0001c0001t0001g0031 a0001c0001t0001g0032 others(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 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0213 others(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 | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(229): Show |
240 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.80-4287C>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8934684 | |||||||
| chr16:8934773 | T | C | 226 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(223): Show |
234 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(231): 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 | a0001c0001t0001g0037 | 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 | 138 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(135): 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 | a0001c0001t0015g0055 | 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 | a0001c0001t0022g0046 | 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 | 318 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(315): Show |
329 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(326): Show |
intron_variant | MODIFIER | c.80-4558T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8934955 | |||||||
| chr16:8935151 | T | C | 58 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0024 others(55): 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 | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(96): Show |
104 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(101): Show |
intron_variant | MODIFIER | c.80-4805dupA | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8935201 | |||||||
| chr16:8935201 | A | ATT | 9 | a0001c0001t0001g0147 a0001c0001t0001g0193 a0001c0001t0001g0199 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0033 a0001c0001t0001g0035 others(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 | a0001c0001t0015g0055 | 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 | a0001c0001t0001g0085 | 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 | a0001c0001t0001g0042 | 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 | a0001c0001t0006g0030 a0001c0001t0006g0059 a0001c0001t0008g0060 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0051 others(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 | a0001c0001t0001g0081 | 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 | a0001c0001t0015g0055 | 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 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0094 others(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 | a0001c0002t0001g0237 | 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 | 322 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(319): Show |
334 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(331): 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 | a0001c0001t0001g0029 a0001c0001t0001g0031 a0001c0001t0001g0032 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0051 others(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 | a0001c0001t0001g0149 | 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 | a0001c0001t0001g0186 a0001c0001t0001g0251 |
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 | a0001c0001t0001g0166 | 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 | a0001c0001t0001g0179 | 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 | a0001c0001t0001g0106 a0001c0001t0001g0108 a0001c0001t0001g0171 others(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 | a0001c0001t0001g0070 a0001c0001t0001g0125 a0001c0001t0001g0254 others(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 | a0001c0001t0001g0037 | 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 | 236 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(233): Show |
245 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(242): 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 | a0001c0001t0001g0037 | 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 | a0001c0001t0001g0291 | 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 | a0001c0001t0001g0068 a0001c0001t0001g0111 a0001c0001t0005g0110 |
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 | 310 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(307): Show |
321 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(318): 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 | a0001c0001t0001g0086 | 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 | a0001c0001t0001g0056 a0001c0001t0023g0057 |
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 | a0001c0001t0013g0058 a0001c0001t0018g0169 a0001c0001t0028g0324 |
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 | a0001c0001t0001g0193 | 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 | a0001c0001t0001g0305 | 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 | 237 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(234): Show |
246 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.80-6662G>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8937059 | |||||||
| chr16:8937136 | G | C | 56 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0024 others(53): 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 | 277 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(274): Show |
287 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(284): Show |
intron_variant | MODIFIER | c.80-6810delA | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8937206 | |||||||
| chr16:8937213 | T | A | 10 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0051 others(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 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0031 others(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 | 287 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(284): Show |
297 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(294): 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 | a0001c0001t0001g0037 | 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 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0101 others(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 | a0001c0001t0001g0280 | 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 | a0001c0001t0001g0005 | 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 | a0001c0001t0001g0164 a0001c0001t0001g0185 a0001c0001t0001g0195 others(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 | a0001c0001t0001g0037 | 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 | 313 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(310): Show |
324 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(321): 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 | a0001c0001t0022g0046 | 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 | a0001c0001t0006g0030 | 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 | 54 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0026 others(51): 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 | a0001c0001t0001g0029 a0001c0001t0001g0031 a0001c0001t0001g0032 others(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 | 95 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(92): Show |
100 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.80-7943dupT | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8938339 | |||||||
| chr16:8938339 | CA | C | 77 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0024 others(74): 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 | a0001c0001t0001g0045 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0051 others(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 | a0001c0001t0001g0102 a0001c0002t0001g0089 a0001c0002t0001g0120 others(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 | a0001c0001t0001g0300 | 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 | a0001c0001t0001g0272 | 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 | a0001c0001t0013g0058 a0001c0001t0018g0169 a0001c0001t0028g0324 |
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 | a0001c0001t0013g0058 a0001c0001t0018g0169 a0001c0001t0028g0324 others(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 | 145 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(142): Show |
150 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.80-8314dupT | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8938710 | |||||||
| chr16:8938710 | C | CAA | 56 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0024 others(53): 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 | a0001c0001t0009g0011 | 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 | a0001c0001t0001g0029 a0001c0001t0001g0031 a0001c0001t0001g0032 others(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 | a0001c0001t0001g0037 | 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 | 231 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(228): Show |
239 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.80-8623A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8939020 | |||||||
| chr16:8939107 | A | G | 59 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0024 others(56): 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 | a0001c0001t0001g0100 a0001c0002t0001g0089 a0001c0002t0001g0120 others(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 | a0001c0001t0001g0037 | 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 | a0001c0001t0001g0037 | 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 | a0001c0001t0001g0114 | 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 | a0001c0001t0007g0261 a0001c0001t0007g0262 |
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 | a0001c0001t0001g0029 a0001c0001t0001g0031 a0001c0001t0001g0032 others(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 | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(213): Show |
224 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(221): 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 | a0001c0001t0001g0254 | 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 | a0001c0006t0001g0168 | 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 | a0001c0001t0001g0029 a0001c0001t0001g0031 a0001c0001t0001g0032 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0051 others(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 | 318 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(315): Show |
329 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(326): 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 | a0001c0001t0001g0056 a0001c0001t0023g0057 |
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 | a0001c0001t0001g0048 | 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 | a0001c0001t0001g0024 a0001c0001t0020g0025 |
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 | a0001c0001t0001g0157 a0001c0001t0001g0178 |
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 | a0001c0005t0001g0176 | 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 | a0001c0001t0001g0130 a0001c0001t0001g0131 |
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 | a0001c0001t0015g0055 | 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 | a0001c0001t0001g0306 | 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 | 318 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(315): Show |
329 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(326): 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 | a0001c0001t0001g0125 a0001c0001t0001g0254 a0001c0001t0001g0288 |
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 | a0001c0001t0001g0184 a0001c0001t0001g0186 a0001c0001t0001g0244 others(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 | a0001c0001t0004g0234 | 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 | a0001c0001t0001g0097 | 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 | 85 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0024 others(82): 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 | a0001c0001t0001g0182 | 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 | 62 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0024 others(59): 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 | a0001c0001t0001g0029 a0001c0001t0001g0031 a0001c0001t0001g0032 others(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 | a0001c0001t0001g0306 | 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 | a0001c0001t0001g0266 | 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 | 121 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(118): 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 | a0001c0001t0001g0063 | 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 | a0001c0001t0001g0056 a0001c0001t0023g0057 |
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 | a0001c0001t0001g0179 | 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 | a0001c0001t0001g0138 a0001c0001t0001g0208 a0001c0001t0001g0295 |
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 | a0001c0001t0001g0167 a0001c0001t0003g0315 a0001c0001t0026g0318 |
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 | 225 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(222): Show |
233 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(230): 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 | a0001c0001t0012g0062 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0051 others(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 | a0001c0001t0013g0058 a0001c0001t0018g0169 a0001c0001t0028g0324 |
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 | a0001c0001t0017g0226 | 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 | a0001c0002t0001g0132 | 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 | a0001c0001t0001g0095 | 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 | a0001c0001t0021g0151 | 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 | 61 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0024 others(58): 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 | a0001c0001t0001g0082 | 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 | a0001c0001t0001g0179 | 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 | a0001c0001t0001g0155 a0001c0001t0001g0231 |
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 | a0001c0001t0012g0062 | 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 | a0001c0001t0013g0058 a0001c0001t0022g0046 a0001c0006t0001g0168 |
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 | a0001c0001t0001g0129 | 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 | a0001c0001t0001g0037 | 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 | a0001c0001t0001g0079 a0001c0001t0001g0123 |
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 | 259 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(256): Show |
269 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(266): 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 | a0001c0001t0001g0167 | 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 | a0001c0001t0001g0167 | 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 | 122 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(119): 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 | 313 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(310): Show |
324 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.80-12279G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8942676 | |||||||
| chr16:8942840 | A | G | 318 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(315): Show |
329 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(326): 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 | a0001c0001t0003g0316 | 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 | a0001c0001t0017g0226 | 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 | a0001c0001t0001g0255 | 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 | a0001c0001t0001g0054 | 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 | a0001c0001t0001g0198 | 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 | a0001c0001t0001g0064 | 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 | a0001c0001t0003g0319 a0001c0001t0003g0320 |
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 | a0001c0001t0001g0263 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0051 others(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 | a0001c0001t0001g0037 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0051 others(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 | a0001c0001t0022g0046 | 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 | a0001c0001t0001g0230 | 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 | a0001c0001t0001g0119 | 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 | 62 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0024 others(59): 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 | a0001c0001t0001g0184 a0001c0001t0001g0186 a0001c0001t0001g0244 others(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 | 73 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(70): 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 | a0001c0001t0001g0115 | 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 | 96 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(93): Show |
101 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.80-13836dupT | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8944232 | |||||||
| chr16:8944232 | CA | C | 81 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0024 others(78): 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 | 138 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(135): 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 | a0001c0001t0001g0054 | 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 | 313 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(310): Show |
324 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(321): 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 | a0001c0001t0001g0054 | 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 | a0001c0001t0003g0315 | 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 | a0001c0001t0001g0099 a0001c0001t0001g0190 |
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 | a0001c0001t0001g0037 | 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 | a0001c0001t0001g0056 a0001c0001t0023g0057 |
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 | a0001c0001t0001g0130 | 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 | 57 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0026 others(54): 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 | 60 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0024 others(57): 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 | 72 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(69): 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 | a0001c0001t0001g0069 a0001c0001t0001g0084 a0001c0001t0001g0096 others(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 | a0001c0001t0001g0056 a0001c0001t0023g0057 |
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 | a0001c0001t0001g0199 | 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 | 73 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(70): 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 | a0001c0001t0001g0164 a0001c0001t0001g0185 a0001c0001t0001g0273 |
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 | a0001c0001t0001g0028 | 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 | a0001c0001t0001g0108 a0001c0001t0001g0171 a0001c0001t0019g0172 |
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 | a0001c0001t0001g0292 | 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 | a0001c0001t0013g0058 a0001c0001t0022g0046 |
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 | a0001c0001t0001g0164 a0001c0001t0001g0185 a0001c0001t0001g0273 |
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 | a0001c0001t0001g0255 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0051 others(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 | a0001c0001t0015g0055 | 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 | a0001c0001t0001g0054 | 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 | a0001c0001t0013g0058 a0001c0001t0022g0046 a0001c0006t0001g0168 |
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 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0051 others(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 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0094 others(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 | 70 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(67): 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 | 223 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(220): Show |
231 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(228): Show |
intron_variant | MODIFIER | c.80-16065A>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8946462 | |||||||
| chr16:8946543 | G | C | 59 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0024 others(56): 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 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0051 others(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 | a0001c0001t0001g0255 | 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 | a0001c0001t0002g0013 | 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 | 295 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(292): Show |
306 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(303): 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 | a0001c0001t0001g0054 | 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 | a0001c0001t0001g0280 | 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 | a0001c0001t0013g0058 a0001c0001t0022g0046 a0001c0006t0001g0168 |
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 | a0001c0001t0001g0037 | 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 | a0001c0001t0006g0030 | 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 | a0001c0001t0001g0181 a0001c0001t0001g0235 |
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 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0147 others(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 | a0001c0001t0001g0056 a0001c0001t0023g0057 |
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 | a0001c0001t0013g0058 a0001c0001t0022g0046 |
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 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0051 others(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 | a0001c0001t0001g0081 a0001c0001t0001g0124 |
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 | a0001c0001t0001g0081 a0001c0001t0001g0124 a0001c0001t0001g0127 |
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 | 62 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0024 others(59): 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 | a0001c0001t0009g0011 | 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 | a0001c0001t0001g0037 | 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 | a0001c0001t0001g0037 | 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 | a0001c0001t0001g0167 | 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 | a0001c0001t0001g0199 | 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 | a0001c0001t0001g0037 | 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 | a0001c0001t0001g0051 a0001c0001t0001g0053 |
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 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0037 others(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 | a0001c0001t0001g0079 a0001c0001t0001g0123 |
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 | 295 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(292): Show |
306 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(303): 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 | a0001c0001t0011g0066 | 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 | a0001c0001t0011g0066 | 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 | 295 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(292): Show |
306 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.79+14463T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8948744 | |||||||
| chr16:8948774 | A | C | 69 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(66): 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 | a0001c0001t0001g0037 | 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 | a0001c0001t0001g0241 | 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 | a0001c0001t0001g0128 | 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 | a0001c0001t0001g0073 a0001c0001t0001g0115 a0001c0001t0001g0116 others(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 | a0001c0001t0001g0083 | 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 | a0001c0001t0022g0046 | 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 | a0001c0001t0001g0300 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0051 others(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 | a0001c0001t0013g0058 | 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 | 60 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0024 others(57): 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 | a0001c0001t0001g0104 a0001c0001t0001g0130 a0001c0001t0001g0131 others(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 | 61 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0024 others(58): 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 | 68 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(65): 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 | a0001c0001t0001g0037 a0001c0001t0013g0058 a0001c0001t0022g0046 others(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 | a0001c0001t0001g0027 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0051 others(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 | 318 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(315): Show |
329 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(326): 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 | a0001c0001t0001g0189 | 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 | a0001c0001t0001g0037 | 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 | a0001c0001t0001g0082 | 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 | 224 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(221): Show |
232 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(229): 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 | a0001c0001t0022g0046 | 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 | a0001c0001t0001g0029 a0001c0001t0001g0031 a0001c0001t0001g0032 others(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 | a0001c0001t0001g0092 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0051 others(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 | a0001c0001t0001g0188 a0001c0001t0001g0274 a0001c0001t0027g0323 |
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 | a0001c0001t0001g0097 a0001c0001t0001g0142 a0001c0001t0001g0143 |
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 |
292 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(289): Show |
303 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(300): 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 | a0001c0001t0001g0162 | 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 | a0001c0001t0001g0056 a0001c0001t0023g0057 |
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 | a0001c0001t0001g0199 | 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 | 56 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0024 others(53): 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 | a0001c0001t0001g0279 | 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 | 306 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(303): Show |
317 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(314): Show |
intron_variant | MODIFIER | c.79+11130delG | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8952076 | |||||||
| chr16:8952115 | T | G | 288 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(285): Show |
299 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(296): 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 | a0001c0001t0001g0126 | 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 | a0001c0001t0001g0173 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0051 others(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 | a0001c0001t0001g0181 a0001c0001t0001g0197 a0001c0001t0001g0235 others(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 | a0001c0001t0001g0195 | 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 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0274 others(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 | a0001c0001t0001g0056 a0001c0001t0023g0057 |
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 | a0001c0001t0001g0064 | 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 | a0001c0001t0001g0282 | 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 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0038 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0051 others(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 | a0001c0001t0001g0248 | 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 | a0001c0001t0001g0037 | 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 | a0001c0001t0001g0037 | 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 | a0001c0001t0001g0239 a0001c0001t0001g0252 |
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 | a0001c0001t0013g0058 a0001c0001t0022g0046 |
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 | a0001c0001t0001g0037 | 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 | a0001c0001t0001g0029 a0001c0001t0001g0031 a0001c0001t0001g0032 others(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 | a0001c0001t0015g0055 | 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 | a0001c0001t0001g0196 a0001c0001t0001g0268 |
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 | 55 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0024 others(52): 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 | 61 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(58): 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 | a0001c0001t0015g0055 | 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 | a0001c0001t0006g0059 a0001c0001t0008g0060 a0001c0001t0008g0061 |
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 | a0001c0006t0001g0168 | 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 | a0001c0001t0001g0224 | 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 | a0001c0001t0004g0232 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0051 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0293 |
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 | 78 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(75): 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 | a0001c0006t0001g0168 | 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 | a0001c0001t0001g0112 a0001c0001t0001g0178 a0001c0001t0001g0215 others(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 | 40 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0026 others(37): 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 | a0001c0001t0001g0081 a0001c0001t0001g0124 a0001c0001t0001g0127 others(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 | a0001c0001t0001g0121 a0001c0001t0001g0198 |
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 | 74 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(71): 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 | a0001c0001t0001g0040 | 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 | a0001c0001t0001g0029 a0001c0001t0001g0031 a0001c0001t0001g0032 others(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 | a0001c0001t0001g0037 | 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 | a0001c0001t0013g0058 a0001c0001t0022g0046 |
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 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0051 others(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 | 68 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0024 others(65): 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 | 193 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(190): Show |
201 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(198): 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 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0037 others(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 | a0001c0001t0001g0253 | 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 | a0001c0001t0001g0173 | 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 | a0001c0001t0001g0029 a0001c0001t0001g0031 a0001c0001t0001g0032 others(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 | a0001c0001t0001g0173 | 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 | a0001c0001t0001g0037 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0051 others(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 | a0001c0001t0016g0052 | 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 | a0001c0001t0015g0055 | 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 | a0001c0001t0001g0072 a0001c0001t0001g0122 a0001c0001t0001g0181 others(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 | a0001c0001t0001g0076 a0001c0001t0001g0114 |
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 | a0001c0001t0001g0107 | 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 |
15 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0028 others(12): 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 | a0001c0001t0001g0218 | 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 | a0001c0001t0001g0009 a0001c0001t0001g0029 a0001c0001t0001g0031 others(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 | a0001c0001t0001g0071 a0001c0001t0001g0074 a0001c0001t0001g0117 others(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 | 62 | a0001c0001t0001g0009 a0001c0001t0001g0024 a0001c0001t0001g0026 others(59): 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 | a0001c0001t0001g0054 | 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 | 66 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0027 others(63): 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 | 20 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0028 others(17): 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 | 205 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(202): Show |
213 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(210): 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 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0037 others(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 | a0001c0006t0001g0168 | 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 |
24 | a0001c0001t0001g0009 a0001c0001t0001g0105 a0001c0001t0001g0155 others(21): 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 | a0001c0001t0001g0026 a0001c0001t0001g0166 a0001c0001t0001g0167 |
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 | a0001c0001t0001g0112 a0001c0001t0001g0178 a0001c0005t0001g0176 |
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 | 18 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0028 others(15): 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 | 196 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(193): Show |
204 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(201): 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 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0037 others(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 | a0001c0001t0001g0179 | 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 | a0001c0001t0001g0067 a0001c0001t0029g0325 |
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 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0037 others(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 | a0001c0001t0001g0107 | 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 | 281 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(278): Show |
292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): 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 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0037 others(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 | a0001c0001t0001g0280 | 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 | a0001c0001t0001g0024 a0001c0001t0013g0058 a0001c0001t0020g0025 others(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 | 212 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(209): Show |
220 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(217): Show |
intron_variant | MODIFIER | c.79+9191_79+9268del others(78): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8953938 | |||||||
| chr16:8953938 | CTGCGGCG others(71): Show |
G | 2 | a0001c0001t0001g0099 a0001c0001t0001g0303 |
2 | HG02155.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.79+9191_79+9269del others(83): Show |
USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8953938 | |||||||
| chr16:8953950 | T | C | 6 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0051 others(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 | a0001c0001t0001g0056 a0001c0001t0023g0057 |
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 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0094 others(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 | a0001c0001t0001g0179 | 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 | a0001c0001t0001g0004 a0001c0001t0001g0024 a0001c0001t0001g0027 others(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 | a0001c0001t0013g0058 | 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 | a0001c0001t0001g0130 | 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 | a0001c0001t0015g0055 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0035 others(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 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0074 others(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 | a0001c0001t0001g0024 a0001c0001t0020g0025 |
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 | a0001c0001t0015g0055 | 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 | 257 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(254): Show |
265 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(262): 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 | a0001c0001t0001g0247 a0001c0001t0001g0248 a0001c0001t0001g0251 others(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 | a0001c0001t0001g0069 | 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 | a0001c0001t0001g0029 a0001c0001t0001g0031 a0001c0001t0001g0032 others(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 | a0001c0001t0001g0238 | 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 | a0001c0001t0013g0058 a0001c0001t0022g0046 |
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 | 57 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0024 others(54): 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 | 98 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(95): Show |
103 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(100): 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 | a0001c0001t0004g0232 | 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 | a0001c0001t0001g0029 a0001c0001t0001g0031 a0001c0001t0001g0032 others(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 | a0001c0001t0001g0029 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0037 others(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 | a0001c0001t0001g0098 a0001c0001t0001g0175 |
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 | a0001c0001t0001g0037 | 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 | a0001c0001t0003g0314 a0001c0001t0003g0321 |
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 | a0001c0001t0001g0241 | 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 | a0001c0001t0013g0058 a0001c0001t0022g0046 |
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 | a0001c0001t0001g0068 | 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 | a0001c0001t0001g0235 | 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 | a0001c0001t0001g0107 a0001c0001t0001g0199 |
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 | a0001c0001t0001g0099 a0001c0001t0001g0303 |
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 | 311 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(308): Show |
322 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.79+7993G>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8955214 | |||||||
| chr16:8955237 | T | C | 64 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(61): 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 | 220 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(217): Show |
228 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(225): 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 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0015 |
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 | a0001c0001t0003g0315 | 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 | a0001c0001t0001g0164 a0001c0001t0001g0185 a0001c0001t0001g0273 |
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 | a0001c0001t0001g0029 a0001c0001t0001g0031 a0001c0001t0001g0032 others(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 | a0001c0001t0001g0073 | 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 | a0001c0001t0029g0325 | 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 | a0001c0001t0001g0035 | 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 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 others(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 | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(155): 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 | 42 | a0001c0001t0001g0007 a0001c0001t0001g0065 a0001c0001t0001g0074 others(39): Show |
43 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(40): 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 | 60 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(57): 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 | a0001c0001t0001g0106 | 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 | a0001c0001t0001g0162 | 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 | a0001c0001t0001g0045 a0001c0001t0001g0048 a0001c0001t0001g0049 others(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 | 81 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(78): 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 | a0001c0001t0001g0299 | 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 | a0001c0001t0015g0055 | 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 | a0001c0001t0001g0308 | 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 | a0001c0001t0001g0100 | 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 | 53 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0024 others(50): 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 | a0001c0001t0001g0239 a0001c0001t0001g0252 |
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 | a0001c0001t0001g0101 | 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 | 105 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(102): 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 | a0001c0001t0029g0325 | 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 | a0001c0001t0001g0034 a0001c0001t0001g0047 a0001c0001t0001g0048 others(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 | 90 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(87): 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 | a0001c0001t0001g0306 | 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 | a0001c0001t0006g0030 a0001c0001t0006g0059 a0001c0001t0008g0060 others(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 | a0001c0001t0001g0040 a0001c0001t0001g0045 a0001c0001t0001g0307 |
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 | a0001c0001t0001g0029 a0001c0001t0001g0031 a0001c0001t0001g0032 others(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 | a0001c0001t0022g0046 | 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 | a0001c0001t0015g0055 | 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 | a0001c0001t0001g0040 a0001c0001t0001g0045 a0001c0001t0001g0307 |
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 | 84 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(81): Show |
89 | HG00423.hp1 HG00438.hp2 HG00609.hp1 others(86): Show |
intron_variant | MODIFIER | c.79+6430dupT | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8956776 | |||||||
| chr16:8956778 | A | C | 3 | a0001c0001t0001g0040 a0001c0001t0001g0045 a0001c0001t0001g0307 |
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 | 59 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0024 others(56): 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 | a0001c0001t0022g0046 | 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 | 120 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(117): 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 | a0001c0001t0001g0029 a0001c0001t0001g0031 a0001c0001t0001g0032 others(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 | a0001c0001t0001g0157 a0001c0001t0001g0215 a0001c0001t0001g0216 others(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 | a0001c0001t0001g0040 a0001c0001t0001g0045 a0001c0001t0001g0307 |
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 | a0001c0001t0001g0029 a0001c0001t0001g0031 a0001c0001t0001g0032 others(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 | a0001c0001t0001g0236 | 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 | a0001c0001t0013g0058 | 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 | a0001c0001t0001g0029 a0001c0001t0001g0031 a0001c0001t0001g0032 others(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 | a0001c0001t0001g0281 | 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 | a0001c0001t0001g0069 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0051 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0051 others(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 | 91 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(88): 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 | a0001c0001t0001g0029 a0001c0001t0001g0031 a0001c0001t0001g0032 others(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 | a0001c0001t0001g0181 a0001c0001t0001g0235 |
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 | a0001c0001t0001g0037 a0001c0001t0001g0054 a0001c0001t0001g0122 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0035 others(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 | 83 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(80): 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 | a0001c0001t0001g0105 a0001c0001t0001g0156 |
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 | a0001c0001t0001g0056 a0001c0001t0002g0012 a0001c0001t0023g0057 |
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 | 224 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(221): Show |
232 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(229): 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 | a0001c0001t0002g0012 | 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 | a0001c0001t0001g0024 a0001c0001t0020g0025 |
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 | a0001c0001t0001g0068 a0001c0001t0001g0109 a0001c0001t0001g0111 others(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 | a0001c0001t0001g0054 | 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 | a0001c0001t0003g0314 | 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 | a0001c0001t0001g0103 a0001c0001t0001g0214 a0001c0001t0021g0151 |
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 | a0001c0001t0001g0282 | 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 | a0001c0001t0001g0310 | 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 | a0001c0001t0001g0283 a0001c0001t0010g0284 |
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 | a0001c0001t0001g0079 a0001c0001t0001g0123 |
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 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0051 others(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 | 55 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0024 others(52): 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 | a0001c0001t0001g0029 | 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 | a0001c0001t0001g0034 a0001c0001t0001g0047 a0001c0001t0001g0048 others(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 | a0001c0003t0001g0153 a0001c0003t0001g0154 |
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 | a0001c0001t0013g0058 a0001c0001t0022g0046 |
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 | 56 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0024 others(53): 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 | 1 | a0001c0001t0025g0311 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.79+4015G>A | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8959192 | |||||||
| chr16:8959356 | C | CA | 110 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(107): 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 | 56 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0034 others(53): 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 | a0001c0002t0001g0225 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0034 a0001c0001t0001g0035 others(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 | a0001c0001t0001g0112 a0001c0005t0001g0176 |
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 | a0001c0001t0001g0177 a0001c0001t0001g0218 a0001c0001t0001g0219 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0034 a0001c0001t0001g0035 others(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 | a0001c0001t0001g0038 a0001c0001t0001g0039 |
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 | a0001c0001t0001g0113 | 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 | a0001c0001t0001g0070 a0001c0001t0030g0326 |
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 | a0001c0001t0001g0069 | 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 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0224 |
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 | a0001c0001t0001g0104 | 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 | a0001c0001t0006g0030 a0001c0001t0006g0059 a0001c0001t0008g0060 others(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 | a0001c0001t0006g0030 a0001c0001t0006g0059 a0001c0001t0008g0060 others(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 | a0001c0001t0001g0034 a0001c0001t0001g0047 a0001c0001t0001g0048 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0034 a0001c0001t0001g0035 others(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 | a0001c0001t0001g0152 | 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 | a0001c0001t0022g0046 | 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 | a0001c0001t0027g0323 | 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 | 12 | a0001c0001t0001g0009 a0001c0001t0001g0215 a0001c0001t0001g0216 others(9): 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 | a0001c0001t0001g0026 a0001c0001t0001g0105 a0001c0001t0001g0106 others(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 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0011g0066 |
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 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0002g0012 |
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 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0031 others(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 | 47 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0029 others(44): 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 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0071 others(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 | 50 | a0001c0001t0001g0004 a0001c0001t0001g0026 a0001c0001t0001g0027 others(47): 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 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(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 | 1 | a0001c0001t0001g0002 | 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 | a0001c0001t0001g0299 | 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 | a0001c0001t0001g0054 a0001c0001t0015g0055 |
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 | a0001c0001t0001g0056 a0001c0001t0023g0057 |
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 | a0001c0001t0013g0058 | 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 | a0001c0001t0006g0059 a0001c0001t0008g0060 a0001c0001t0008g0061 |
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 | a0001c0001t0013g0058 | 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 | a0001c0001t0003g0314 a0001c0001t0003g0315 a0001c0001t0003g0316 others(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 | a0001c0001t0001g0300 | 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 | a0001c0001t0001g0301 a0001c0001t0001g0302 |
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 | a0001c0001t0001g0063 | 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 | a0001c0001t0012g0062 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0031 others(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 | a0001c0001t0001g0303 | 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 | a0001c0001t0006g0059 a0001c0001t0008g0060 a0001c0001t0008g0061 others(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 | 278 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(275): Show |
288 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(285): Show |
intron_variant | MODIFIER | c.79+524C>G | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8962683 | |||||||
| chr16:8962685 | A | G | 318 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(315): Show |
329 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(326): 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 | a0001c0001t0001g0304 a0001c0001t0001g0305 |
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 | 4 | a0001c0001t0001g0004 a0001c0001t0001g0026 a0001c0001t0001g0027 others(1): 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 | a0001c0001t0001g0024 a0001c0001t0020g0025 |
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 | a0001c0001t0001g0306 a0001c0001t0001g0307 a0001c0001t0001g0308 others(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 | 317 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(314): Show |
328 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(325): Show |
intron_variant | MODIFIER | c.79+148dupG | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8963058 | |||||||
| chr16:8963060 | A | G | 318 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(315): Show |
329 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(326): Show |
intron_variant | MODIFIER | c.79+147T>C | USP7 | ENSG00000187555.17 | transcript | ENST00000344836.9 | protein_coding | 1/30 | chr16 | 8963060 |