Item | Value |
---|---|
geneid | 84132 |
ensemblid | ENSG00000106346.12 |
hgncid | 20068 |
symbol | USP42 |
name | ubiquitin specific peptidase 42 |
refseq_nuc | NM_032172.3 |
refseq_prot | NP_115548.1 |
ensembl_nuc | ENST00000306177.10 |
ensembl_prot | ENSP00000301962.5 |
mane_status | MANE Select |
chr | chr7 |
start | 6104949 |
end | 6161564 |
strand | + |
ver | v1.2 |
region | chr7:6104949-6161564 |
region5000 | chr7:6099949-6166564 |
regionname0 | USP42_chr7_6104949_6161564 |
regionname5000 | USP42_chr7_6099949_6166564 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 1316 | 123 | 13 | 35 | 44 | 8 | 22 | 32 | USP42_chr7_6099949_6166564 | USP42 | MTIVD others(1311): Show |
chr7 | 6099949 | 6166564 |
a0002 | 0/0 | 1316 | 117 | 34 | 14 | 62 | 2 | 5 | 41 | USP42_chr7_6099949_6166564 | USP42 | MTIVD others(1311): Show |
chr7 | 6099949 | 6166564 |
a0003 | 0/0 | 1316 | 94 | 20 | 10 | 56 | 0 | 8 | 46 | USP42_chr7_6099949_6166564 | USP42 | MTIVD others(1311): Show |
chr7 | 6099949 | 6166564 |
a0004 | 0/0 | 1316 | 23 | 5 | 11 | 1 | 1 | 5 | 0 | USP42_chr7_6099949_6166564 | USP42 | MTIVD others(1311): Show |
chr7 | 6099949 | 6166564 |
a0005 | 0/0 | 1316 | 10 | 9 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | MTIVD others(1311): Show |
chr7 | 6099949 | 6166564 |
a0006 | 0/0 | 1316 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | MTIVD others(1311): Show |
chr7 | 6099949 | 6166564 |
a0007 | 0/0 | 1316 | 2 | 0 | 1 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | MTIVD others(1311): Show |
chr7 | 6099949 | 6166564 |
a0008 | 0/0 | 1316 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | MTIVD others(1311): Show |
chr7 | 6099949 | 6166564 |
a0009 | 0/0 | 1316 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | MTIVD others(1311): Show |
chr7 | 6099949 | 6166564 |
a0010 | 0/0 | 1316 | 2 | 0 | 0 | 1 | 0 | 1 | 1 | USP42_chr7_6099949_6166564 | USP42 | MTIVD others(1311): Show |
chr7 | 6099949 | 6166564 |
a0011 | 0/0 | 1316 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | USP42_chr7_6099949_6166564 | USP42 | MTIVD others(1311): Show |
chr7 | 6099949 | 6166564 |
a0012 | 0/0 | 1316 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | MTIVD others(1311): Show |
chr7 | 6099949 | 6166564 |
a0013 | 0/0 | 1316 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | MTIVD others(1311): Show |
chr7 | 6099949 | 6166564 |
a0014 | 0/0 | 1316 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | MTIVD others(1311): Show |
chr7 | 6099949 | 6166564 |
a0015 | 0/0 | 1316 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | MTIVD others(1311): Show |
chr7 | 6099949 | 6166564 |
a0016 | 0/0 | 1316 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | MTIVD others(1311): Show |
chr7 | 6099949 | 6166564 |
a0017 | 0/0 | 1316 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | MTIVD others(1311): Show |
chr7 | 6099949 | 6166564 |
a0018 | 0/0 | 1316 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | MTIVD others(1311): Show |
chr7 | 6099949 | 6166564 |
a0019 | 0/0 | 1316 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | MTIVD others(1311): Show |
chr7 | 6099949 | 6166564 |
a0020 | 0/0 | 1316 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | MTIVD others(1311): Show |
chr7 | 6099949 | 6166564 |
a0021 | 0/0 | 1316 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | USP42_chr7_6099949_6166564 | USP42 | MTIVD others(1311): Show |
chr7 | 6099949 | 6166564 |
a0022 | 0/0 | 1316 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | USP42_chr7_6099949_6166564 | USP42 | MTIVD others(1311): Show |
chr7 | 6099949 | 6166564 |
a0023 | 0/0 | 1316 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | MTIVD others(1311): Show |
chr7 | 6099949 | 6166564 |
a0024 | 0/0 | 1316 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | MTIVD others(1311): Show |
chr7 | 6099949 | 6166564 |
a0025 | 0/0 | 1316 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | USP42_chr7_6099949_6166564 | USP42 | MTIVD others(1311): Show |
chr7 | 6099949 | 6166564 |
a0026 | 0/1 | 1316 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | MTIVD others(1311): Show |
chr7 | 6099949 | 6166564 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 3948 | 117 | 10 | 35 | 43 | 7 | 21 | USP42_chr7_6099949_6166564 | USP42 | ATGAC others(3943): Show |
chr7 | 6099949 | 6166564 | ||
a0001c0013 | 0/0 | 3948 | 3 | 3 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | ATGAC others(3943): Show |
chr7 | 6099949 | 6166564 | ||
a0001c0031 | 0/0 | 3948 | 1 | 0 | 0 | 0 | 0 | 1 | USP42_chr7_6099949_6166564 | USP42 | ATGAC others(3943): Show |
chr7 | 6099949 | 6166564 | ||
a0001c0046 | 0/0 | 3948 | 1 | 0 | 0 | 0 | 1 | 0 | USP42_chr7_6099949_6166564 | USP42 | ATGAC others(3943): Show |
chr7 | 6099949 | 6166564 | ||
a0001c0048 | 0/0 | 3948 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | ATGAC others(3943): Show |
chr7 | 6099949 | 6166564 | ||
a0002c0003 | 0/0 | 3948 | 60 | 2 | 10 | 47 | 0 | 1 | USP42_chr7_6099949_6166564 | USP42 | ATGAC others(3943): Show |
chr7 | 6099949 | 6166564 | ||
a0002c0004 | 0/0 | 3948 | 14 | 14 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | ATGAC others(3943): Show |
chr7 | 6099949 | 6166564 | ||
a0002c0006 | 0/0 | 3948 | 12 | 4 | 1 | 5 | 0 | 2 | USP42_chr7_6099949_6166564 | USP42 | ATGAC others(3943): Show |
chr7 | 6099949 | 6166564 | ||
a0002c0007 | 0/0 | 3948 | 9 | 2 | 1 | 6 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | ATGAC others(3943): Show |
chr7 | 6099949 | 6166564 | ||
a0002c0010 | 0/0 | 3948 | 7 | 6 | 1 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | ATGAC others(3943): Show |
chr7 | 6099949 | 6166564 | ||
a0002c0014 | 0/0 | 3948 | 3 | 3 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | ATGAC others(3943): Show |
chr7 | 6099949 | 6166564 | ||
a0002c0015 | 0/0 | 3948 | 3 | 0 | 0 | 0 | 2 | 1 | USP42_chr7_6099949_6166564 | USP42 | ATGAC others(3943): Show |
chr7 | 6099949 | 6166564 | ||
a0002c0018 | 0/0 | 3948 | 2 | 0 | 0 | 2 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | ATGAC others(3943): Show |
chr7 | 6099949 | 6166564 | ||
a0002c0027 | 0/0 | 3948 | 2 | 0 | 1 | 0 | 0 | 1 | USP42_chr7_6099949_6166564 | USP42 | ATGAC others(3943): Show |
chr7 | 6099949 | 6166564 | ||
a0002c0028 | 0/0 | 3948 | 2 | 0 | 0 | 2 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | ATGAC others(3943): Show |
chr7 | 6099949 | 6166564 | ||
a0002c0034 | 0/0 | 3948 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | ATGAC others(3943): Show |
chr7 | 6099949 | 6166564 | ||
a0002c0035 | 0/0 | 3948 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | ATGAC others(3943): Show |
chr7 | 6099949 | 6166564 | ||
a0002c0050 | 0/0 | 3948 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | ATGAC others(3943): Show |
chr7 | 6099949 | 6166564 | ||
a0003c0002 | 0/0 | 3948 | 77 | 17 | 8 | 44 | 0 | 8 | USP42_chr7_6099949_6166564 | USP42 | ATGAC others(3943): Show |
chr7 | 6099949 | 6166564 | ||
a0003c0008 | 0/0 | 3948 | 9 | 0 | 0 | 9 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | ATGAC others(3943): Show |
chr7 | 6099949 | 6166564 | ||
a0003c0012 | 0/0 | 3948 | 3 | 2 | 1 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | ATGAC others(3943): Show |
chr7 | 6099949 | 6166564 | ||
a0003c0017 | 0/0 | 3948 | 2 | 1 | 1 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | ATGAC others(3943): Show |
chr7 | 6099949 | 6166564 | ||
a0003c0020 | 0/0 | 3948 | 2 | 0 | 0 | 2 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | ATGAC others(3943): Show |
chr7 | 6099949 | 6166564 | ||
a0003c0029 | 0/0 | 3948 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | ATGAC others(3943): Show |
chr7 | 6099949 | 6166564 | ||
a0004c0005 | 0/0 | 3948 | 13 | 1 | 8 | 0 | 1 | 3 | USP42_chr7_6099949_6166564 | USP42 | ATGAC others(3943): Show |
chr7 | 6099949 | 6166564 | ||
a0004c0009 | 0/0 | 3948 | 9 | 3 | 3 | 1 | 0 | 2 | USP42_chr7_6099949_6166564 | USP42 | ATGAC others(3943): Show |
chr7 | 6099949 | 6166564 | ||
a0004c0038 | 0/0 | 3948 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | ATGAC others(3943): Show |
chr7 | 6099949 | 6166564 | ||
a0005c0011 | 0/0 | 3948 | 6 | 5 | 1 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | ATGAC others(3943): Show |
chr7 | 6099949 | 6166564 | ||
a0005c0019 | 0/0 | 3948 | 2 | 2 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | ATGAC others(3943): Show |
chr7 | 6099949 | 6166564 | ||
a0005c0024 | 0/0 | 3948 | 2 | 2 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | ATGAC others(3943): Show |
chr7 | 6099949 | 6166564 | ||
a0006c0023 | 0/0 | 3948 | 2 | 0 | 2 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | ATGAC others(3943): Show |
chr7 | 6099949 | 6166564 | ||
a0007c0025 | 0/0 | 3948 | 2 | 0 | 1 | 0 | 1 | 0 | USP42_chr7_6099949_6166564 | USP42 | ATGAC others(3943): Show |
chr7 | 6099949 | 6166564 | ||
a0008c0021 | 0/0 | 3948 | 2 | 2 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | ATGAC others(3943): Show |
chr7 | 6099949 | 6166564 | ||
a0009c0026 | 0/0 | 3948 | 2 | 2 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | ATGAC others(3943): Show |
chr7 | 6099949 | 6166564 | ||
a0010c0022 | 0/0 | 3948 | 2 | 0 | 0 | 1 | 0 | 1 | USP42_chr7_6099949_6166564 | USP42 | ATGAC others(3943): Show |
chr7 | 6099949 | 6166564 | ||
a0011c0016 | 0/0 | 3948 | 2 | 0 | 0 | 2 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | ATGAC others(3943): Show |
chr7 | 6099949 | 6166564 | ||
a0012c0045 | 0/0 | 3948 | 1 | 0 | 0 | 0 | 1 | 0 | USP42_chr7_6099949_6166564 | USP42 | ATGAC others(3943): Show |
chr7 | 6099949 | 6166564 | ||
a0013c0037 | 0/0 | 3948 | 1 | 0 | 1 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | ATGAC others(3943): Show |
chr7 | 6099949 | 6166564 | ||
a0014c0049 | 0/0 | 3948 | 1 | 0 | 1 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | ATGAC others(3943): Show |
chr7 | 6099949 | 6166564 | ||
a0015c0051 | 0/0 | 3948 | 1 | 0 | 1 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | ATGAC others(3943): Show |
chr7 | 6099949 | 6166564 | ||
a0016c0043 | 0/0 | 3948 | 1 | 0 | 1 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | ATGAC others(3943): Show |
chr7 | 6099949 | 6166564 | ||
a0017c0040 | 0/0 | 3948 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | ATGAC others(3943): Show |
chr7 | 6099949 | 6166564 | ||
a0018c0036 | 0/0 | 3948 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | ATGAC others(3943): Show |
chr7 | 6099949 | 6166564 | ||
a0019c0030 | 0/0 | 3948 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | ATGAC others(3943): Show |
chr7 | 6099949 | 6166564 | ||
a0020c0033 | 0/0 | 3948 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | ATGAC others(3943): Show |
chr7 | 6099949 | 6166564 | ||
a0021c0039 | 0/0 | 3948 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | ATGAC others(3943): Show |
chr7 | 6099949 | 6166564 | ||
a0022c0042 | 0/0 | 3948 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | ATGAC others(3943): Show |
chr7 | 6099949 | 6166564 | ||
a0023c0041 | 0/0 | 3948 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | ATGAC others(3943): Show |
chr7 | 6099949 | 6166564 | ||
a0024c0047 | 0/0 | 3948 | 1 | 0 | 0 | 0 | 1 | 0 | USP42_chr7_6099949_6166564 | USP42 | ATGAC others(3943): Show |
chr7 | 6099949 | 6166564 | ||
a0025c0044 | 0/0 | 3948 | 1 | 0 | 0 | 0 | 0 | 1 | USP42_chr7_6099949_6166564 | USP42 | ATGAC others(3943): Show |
chr7 | 6099949 | 6166564 | ||
a0026c0032 | 0/1 | 3948 | 1 | 0 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | ATGAC others(3943): Show |
chr7 | 6099949 | 6166564 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 5090 | 116 | 10 | 34 | 43 | 7 | 21 | USP42_chr7_6099949_6166564 | USP42 | ATTGT others(5085): Show |
chr7 | 6099949 | 6166564 |
a0001c0001t0007 | 0/0 | 5090 | 1 | 0 | 1 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | ATTGT others(5085): Show |
chr7 | 6099949 | 6166564 |
a0001c0013t0001 | 0/0 | 5090 | 3 | 3 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | ATTGT others(5085): Show |
chr7 | 6099949 | 6166564 |
a0001c0031t0001 | 0/0 | 5090 | 1 | 0 | 0 | 0 | 0 | 1 | USP42_chr7_6099949_6166564 | USP42 | ATTGT others(5085): Show |
chr7 | 6099949 | 6166564 |
a0001c0046t0001 | 0/0 | 5090 | 1 | 0 | 0 | 0 | 1 | 0 | USP42_chr7_6099949_6166564 | USP42 | ATTGT others(5085): Show |
chr7 | 6099949 | 6166564 |
a0001c0048t0001 | 0/0 | 5090 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | ATTGT others(5085): Show |
chr7 | 6099949 | 6166564 |
a0002c0003t0001 | 0/0 | 5090 | 60 | 2 | 10 | 47 | 0 | 1 | USP42_chr7_6099949_6166564 | USP42 | ATTGT others(5085): Show |
chr7 | 6099949 | 6166564 |
a0002c0004t0001 | 0/0 | 5090 | 14 | 14 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | ATTGT others(5085): Show |
chr7 | 6099949 | 6166564 |
a0002c0006t0001 | 0/0 | 5090 | 6 | 0 | 1 | 3 | 0 | 2 | USP42_chr7_6099949_6166564 | USP42 | ATTGT others(5085): Show |
chr7 | 6099949 | 6166564 |
a0002c0006t0003 | 0/0 | 5090 | 4 | 4 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | ATTGT others(5085): Show |
chr7 | 6099949 | 6166564 |
a0002c0006t0005 | 0/0 | 5090 | 2 | 0 | 0 | 2 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | ATTGT others(5085): Show |
chr7 | 6099949 | 6166564 |
a0002c0007t0001 | 0/0 | 5090 | 6 | 2 | 1 | 3 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | ATTGT others(5085): Show |
chr7 | 6099949 | 6166564 |
a0002c0007t0004 | 0/0 | 5090 | 2 | 0 | 0 | 2 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | ATTGT others(5085): Show |
chr7 | 6099949 | 6166564 |
a0002c0007t0009 | 0/0 | 5090 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | ATTGT others(5085): Show |
chr7 | 6099949 | 6166564 |
a0002c0010t0001 | 0/0 | 5090 | 7 | 6 | 1 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | ATTGT others(5085): Show |
chr7 | 6099949 | 6166564 |
a0002c0014t0001 | 0/0 | 5090 | 3 | 3 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | ATTGT others(5085): Show |
chr7 | 6099949 | 6166564 |
a0002c0015t0001 | 0/0 | 5090 | 3 | 0 | 0 | 0 | 2 | 1 | USP42_chr7_6099949_6166564 | USP42 | ATTGT others(5085): Show |
chr7 | 6099949 | 6166564 |
a0002c0018t0001 | 0/0 | 5090 | 2 | 0 | 0 | 2 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | ATTGT others(5085): Show |
chr7 | 6099949 | 6166564 |
a0002c0027t0001 | 0/0 | 5090 | 2 | 0 | 1 | 0 | 0 | 1 | USP42_chr7_6099949_6166564 | USP42 | ATTGT others(5085): Show |
chr7 | 6099949 | 6166564 |
a0002c0028t0001 | 0/0 | 5090 | 2 | 0 | 0 | 2 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | ATTGT others(5085): Show |
chr7 | 6099949 | 6166564 |
a0002c0034t0001 | 0/0 | 5090 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | ATTGT others(5085): Show |
chr7 | 6099949 | 6166564 |
a0002c0035t0001 | 0/0 | 5090 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | ATTGT others(5085): Show |
chr7 | 6099949 | 6166564 |
a0002c0050t0001 | 0/0 | 5090 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | ATTGT others(5085): Show |
chr7 | 6099949 | 6166564 |
a0003c0002t0001 | 0/0 | 5090 | 72 | 13 | 7 | 44 | 0 | 8 | USP42_chr7_6099949_6166564 | USP42 | ATTGT others(5085): Show |
chr7 | 6099949 | 6166564 |
a0003c0002t0002 | 0/0 | 5090 | 5 | 4 | 1 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | ATTGT others(5085): Show |
chr7 | 6099949 | 6166564 |
a0003c0008t0001 | 0/0 | 5090 | 9 | 0 | 0 | 9 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | ATTGT others(5085): Show |
chr7 | 6099949 | 6166564 |
a0003c0012t0001 | 0/0 | 5090 | 3 | 2 | 1 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | ATTGT others(5085): Show |
chr7 | 6099949 | 6166564 |
a0003c0017t0001 | 0/0 | 5090 | 2 | 1 | 1 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | ATTGT others(5085): Show |
chr7 | 6099949 | 6166564 |
a0003c0020t0001 | 0/0 | 5090 | 2 | 0 | 0 | 2 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | ATTGT others(5085): Show |
chr7 | 6099949 | 6166564 |
a0003c0029t0001 | 0/0 | 5090 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | ATTGT others(5085): Show |
chr7 | 6099949 | 6166564 |
a0004c0005t0001 | 0/0 | 5090 | 12 | 1 | 7 | 0 | 1 | 3 | USP42_chr7_6099949_6166564 | USP42 | ATTGT others(5085): Show |
chr7 | 6099949 | 6166564 |
a0004c0005t0008 | 0/0 | 5090 | 1 | 0 | 1 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | ATTGT others(5085): Show |
chr7 | 6099949 | 6166564 |
a0004c0009t0001 | 0/0 | 5090 | 9 | 3 | 3 | 1 | 0 | 2 | USP42_chr7_6099949_6166564 | USP42 | ATTGT others(5085): Show |
chr7 | 6099949 | 6166564 |
a0004c0038t0001 | 0/0 | 5090 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | ATTGT others(5085): Show |
chr7 | 6099949 | 6166564 |
a0005c0011t0001 | 0/0 | 5090 | 6 | 5 | 1 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | ATTGT others(5085): Show |
chr7 | 6099949 | 6166564 |
a0005c0019t0001 | 0/0 | 5090 | 2 | 2 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | ATTGT others(5085): Show |
chr7 | 6099949 | 6166564 |
a0005c0024t0001 | 0/0 | 5090 | 2 | 2 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | ATTGT others(5085): Show |
chr7 | 6099949 | 6166564 |
a0006c0023t0001 | 0/0 | 5090 | 2 | 0 | 2 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | ATTGT others(5085): Show |
chr7 | 6099949 | 6166564 |
a0007c0025t0001 | 0/0 | 5090 | 2 | 0 | 1 | 0 | 1 | 0 | USP42_chr7_6099949_6166564 | USP42 | ATTGT others(5085): Show |
chr7 | 6099949 | 6166564 |
a0008c0021t0001 | 0/0 | 5090 | 2 | 2 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | ATTGT others(5085): Show |
chr7 | 6099949 | 6166564 |
a0009c0026t0001 | 0/0 | 5090 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | ATTGT others(5085): Show |
chr7 | 6099949 | 6166564 |
a0009c0026t0006 | 0/0 | 5090 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | ATTGT others(5085): Show |
chr7 | 6099949 | 6166564 |
a0010c0022t0001 | 0/0 | 5090 | 2 | 0 | 0 | 1 | 0 | 1 | USP42_chr7_6099949_6166564 | USP42 | ATTGT others(5085): Show |
chr7 | 6099949 | 6166564 |
a0011c0016t0001 | 0/0 | 5090 | 2 | 0 | 0 | 2 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | ATTGT others(5085): Show |
chr7 | 6099949 | 6166564 |
a0012c0045t0001 | 0/0 | 5090 | 1 | 0 | 0 | 0 | 1 | 0 | USP42_chr7_6099949_6166564 | USP42 | ATTGT others(5085): Show |
chr7 | 6099949 | 6166564 |
a0013c0037t0001 | 0/0 | 5090 | 1 | 0 | 1 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | ATTGT others(5085): Show |
chr7 | 6099949 | 6166564 |
a0014c0049t0001 | 0/0 | 5090 | 1 | 0 | 1 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | ATTGT others(5085): Show |
chr7 | 6099949 | 6166564 |
a0015c0051t0001 | 0/0 | 5090 | 1 | 0 | 1 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | ATTGT others(5085): Show |
chr7 | 6099949 | 6166564 |
a0016c0043t0001 | 0/0 | 5090 | 1 | 0 | 1 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | ATTGT others(5085): Show |
chr7 | 6099949 | 6166564 |
a0017c0040t0001 | 0/0 | 5090 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | ATTGT others(5085): Show |
chr7 | 6099949 | 6166564 |
a0018c0036t0001 | 0/0 | 5090 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | ATTGT others(5085): Show |
chr7 | 6099949 | 6166564 |
a0019c0030t0001 | 0/0 | 5090 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | ATTGT others(5085): Show |
chr7 | 6099949 | 6166564 |
a0020c0033t0001 | 0/0 | 5090 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | ATTGT others(5085): Show |
chr7 | 6099949 | 6166564 |
a0021c0039t0001 | 0/0 | 5090 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | ATTGT others(5085): Show |
chr7 | 6099949 | 6166564 |
a0022c0042t0001 | 0/0 | 5090 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | ATTGT others(5085): Show |
chr7 | 6099949 | 6166564 |
a0023c0041t0001 | 0/0 | 5090 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | ATTGT others(5085): Show |
chr7 | 6099949 | 6166564 |
a0024c0047t0001 | 0/0 | 5090 | 1 | 0 | 0 | 0 | 1 | 0 | USP42_chr7_6099949_6166564 | USP42 | ATTGT others(5085): Show |
chr7 | 6099949 | 6166564 |
a0025c0044t0001 | 0/0 | 5090 | 1 | 0 | 0 | 0 | 0 | 1 | USP42_chr7_6099949_6166564 | USP42 | ATTGT others(5085): Show |
chr7 | 6099949 | 6166564 |
a0026c0032t0001 | 0/1 | 5090 | 1 | 0 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | ATTGT others(5085): Show |
chr7 | 6099949 | 6166564 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 9 | 3 | 0 | 4 | 0 | 2 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0003 | 0/0 | 7 | 0 | 2 | 2 | 0 | 3 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0005 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0233 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0001t0007g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0013t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0013t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0013t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0031t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0046t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0001c0048t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0003t0001g0002 | 0/0 | 7 | 0 | 3 | 4 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0003t0001g0004 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0003t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0003t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0003t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0003t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0003t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0003t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0003t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0003t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0003t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0003t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0003t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0003t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0003t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0003t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0003t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0003t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0003t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0003t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0003t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0003t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0003t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0003t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0003t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0003t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0003t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0003t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0003t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0003t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0003t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0003t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0003t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0003t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0003t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0003t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0003t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0003t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0003t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0003t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0003t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0003t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0003t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0003t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0003t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0003t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0003t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0003t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0004t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0004t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0004t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0004t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0004t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0004t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0004t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0004t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0004t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0004t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0004t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0004t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0004t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0004t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0006t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0006t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0006t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0006t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0006t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0006t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0006t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0006t0003g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0006t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0006t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0006t0005g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0006t0005g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0007t0001g0019 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0007t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0007t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0007t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0007t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0007t0004g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0007t0004g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0007t0009g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0010t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0010t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0010t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0010t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0010t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0010t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0010t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0014t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0014t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0015t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0015t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0015t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0018t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0018t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0027t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0027t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0028t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0028t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0034t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0035t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0002c0050t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0003c0002t0001g0007 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0003c0002t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0003c0002t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0003c0002t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0003c0002t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0003c0002t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0003c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0003c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0003c0002t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0003c0002t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0003c0002t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0003c0002t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0003c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0003c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0003c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0003c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0003c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0003c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0003c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0003c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0003c0002t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0003c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0003c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0003c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0003c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0003c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0003c0002t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0003c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0003c0002t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0003c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0003c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0003c0002t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0003c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0003c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0003c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0003c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0003c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0003c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0003c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0003c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0003c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0003c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0003c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0003c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0003c0002t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0003c0002t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0003c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0003c0002t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0003c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0003c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0003c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0003c0002t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0003c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0003c0002t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0003c0002t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0003c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0003c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0003c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0003c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0003c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0003c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0003c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0003c0002t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0003c0002t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0003c0002t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0003c0002t0002g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0003c0002t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0003c0002t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0003c0002t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0003c0008t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0003c0008t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0003c0008t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0003c0008t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0003c0008t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0003c0008t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0003c0008t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0003c0008t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0003c0012t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0003c0012t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0003c0012t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0003c0017t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0003c0017t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0003c0020t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0003c0020t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0003c0029t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0004c0005t0001g0008 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0004c0005t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0004c0005t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0004c0005t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0004c0005t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0004c0005t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0004c0005t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0004c0005t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0004c0005t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0004c0005t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0004c0005t0008g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0004c0009t0001g0013 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0004c0009t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0004c0009t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0004c0009t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0004c0009t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0004c0009t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0004c0009t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0004c0009t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0004c0038t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0005c0011t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0005c0011t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0005c0011t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0005c0011t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0005c0011t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0005c0011t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0005c0019t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0005c0019t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0005c0024t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0005c0024t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0006c0023t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0006c0023t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0007c0025t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0007c0025t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0008c0021t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0008c0021t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0009c0026t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0009c0026t0006g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0010c0022t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0010c0022t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0011c0016t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0011c0016t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0012c0045t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0013c0037t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0014c0049t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0015c0051t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0016c0043t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0017c0040t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0018c0036t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0019c0030t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0020c0033t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0021c0039t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0022c0042t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0023c0041t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0024c0047t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0025c0044t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
a0026c0032t0001g0241 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0046 | t0001 | g0023 | EUR | GBR | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0252 | EUR | GBR | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0246 | EUR | GBR | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0213 | EUR | GBR | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG00280 | hp1 | a0004 | c0005 | t0001 | g0306 | EUR | FIN | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG00280 | hp2 | a0012 | c0045 | t0001 | g0022 | EUR | FIN | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG00408 | hp1 | a0002 | c0003 | t0001 | g0077 | EAS | CHS | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG00408 | hp2 | a0002 | c0003 | t0001 | g0004 | EAS | CHS | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG00423 | hp1 | a0003 | c0008 | t0001 | g0017 | EAS | CHS | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG00423 | hp2 | a0002 | c0003 | t0001 | g0099 | EAS | CHS | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | CHS | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG00438 | hp2 | a0003 | c0002 | t0001 | g0153 | EAS | CHS | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG00544 | hp1 | a0003 | c0002 | t0001 | g0146 | EAS | CHS | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG00544 | hp2 | a0002 | c0003 | t0001 | g0180 | EAS | CHS | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG00558 | hp1 | a0002 | c0003 | t0001 | g0004 | EAS | CHS | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG00558 | hp2 | a0003 | c0002 | t0001 | g0085 | EAS | CHS | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG00597 | hp1 | a0002 | c0018 | t0001 | g0150 | EAS | CHS | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG00597 | hp2 | a0003 | c0002 | t0001 | g0147 | EAS | CHS | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG00621 | hp1 | a0002 | c0007 | t0001 | g0169 | EAS | CHS | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG00621 | hp2 | a0003 | c0008 | t0001 | g0017 | EAS | CHS | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG00639 | hp2 | a0003 | c0002 | t0001 | g0156 | AMR | PUR | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG00642 | hp1 | a0004 | c0009 | t0001 | g0078 | AMR | PUR | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG00642 | hp2 | a0002 | c0003 | t0001 | g0116 | AMR | PUR | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG00673 | hp1 | a0004 | c0009 | t0001 | g0080 | EAS | CHS | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG00673 | hp2 | a0002 | c0003 | t0001 | g0096 | EAS | CHS | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG00733 | hp1 | a0003 | c0002 | t0001 | g0155 | AMR | PUR | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG00735 | hp1 | a0002 | c0003 | t0001 | g0002 | AMR | PUR | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | PUR | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG00738 | hp1 | a0013 | c0037 | t0001 | g0290 | AMR | PUR | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG00741 | hp1 | a0003 | c0002 | t0001 | g0178 | AMR | PUR | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG00741 | hp2 | a0004 | c0005 | t0001 | g0008 | AMR | PUR | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG01069 | hp1 | a0002 | c0003 | t0001 | g0002 | AMR | PUR | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG01070 | hp1 | a0014 | c0049 | t0001 | g0295 | AMR | PUR | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG01070 | hp2 | a0006 | c0023 | t0001 | g0070 | AMR | PUR | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG01071 | hp1 | a0006 | c0023 | t0001 | g0228 | AMR | PUR | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG01081 | hp1 | a0003 | c0012 | t0001 | g0073 | AMR | PUR | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG01081 | hp2 | a0002 | c0007 | t0001 | g0019 | AMR | PUR | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG01099 | hp1 | a0001 | c0001 | t0007 | g0247 | AMR | PUR | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0284 | AMR | PUR | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0277 | AMR | PUR | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG01109 | hp1 | a0003 | c0002 | t0001 | g0323 | AMR | PUR | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG01109 | hp2 | a0004 | c0005 | t0001 | g0303 | AMR | PUR | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG01167 | hp2 | a0002 | c0006 | t0001 | g0324 | AMR | PUR | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG01168 | hp2 | a0003 | c0017 | t0001 | g0065 | AMR | PUR | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG01175 | hp2 | a0003 | c0002 | t0002 | g0047 | AMR | PUR | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG01192 | hp2 | a0002 | c0003 | t0001 | g0106 | AMR | PUR | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG01243 | hp1 | a0002 | c0010 | t0001 | g0196 | AMR | PUR | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0272 | AMR | PUR | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG01255 | hp1 | a0003 | c0002 | t0001 | g0170 | AMR | CLM | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG01255 | hp2 | a0004 | c0005 | t0001 | g0297 | AMR | CLM | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG01256 | hp1 | a0015 | c0051 | t0001 | g0312 | AMR | CLM | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | CLM | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG01261 | hp1 | a0004 | c0005 | t0001 | g0008 | AMR | CLM | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0309 | AMR | CLM | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG01346 | hp1 | a0005 | c0011 | t0001 | g0057 | AMR | CLM | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0276 | AMR | CLM | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG01358 | hp1 | a0003 | c0002 | t0001 | g0135 | AMR | CLM | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | CLM | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG01433 | hp1 | a0016 | c0043 | t0001 | g0300 | AMR | CLM | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0278 | AMR | CLM | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG01496 | hp1 | a0002 | c0027 | t0001 | g0311 | AMR | CLM | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0318 | AMR | CLM | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG01515 | hp1 | a0002 | c0015 | t0001 | g0040 | EUR | IBS | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0226 | EUR | IBS | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG01516 | hp1 | a0007 | c0025 | t0001 | g0212 | EUR | IBS | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0012 | EUR | IBS | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG01517 | hp1 | a0002 | c0015 | t0001 | g0041 | EUR | IBS | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0012 | EUR | IBS | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | ACB | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG01884 | hp2 | a0002 | c0007 | t0001 | g0163 | AFR | ACB | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG01891 | hp1 | a0005 | c0024 | t0001 | g0062 | AFR | ACB | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG01891 | hp2 | a0002 | c0003 | t0001 | g0097 | AFR | ACB | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG01928 | hp2 | a0004 | c0009 | t0001 | g0013 | AMR | PEL | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG01934 | hp1 | a0007 | c0025 | t0001 | g0244 | AMR | PEL | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG01934 | hp2 | a0004 | c0005 | t0008 | g0301 | AMR | PEL | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG01943 | hp1 | a0004 | c0009 | t0001 | g0081 | AMR | PEL | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0288 | AMR | PEL | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0265 | AMR | PEL | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PEL | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0286 | AMR | PEL | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PEL | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG01978 | hp1 | a0004 | c0005 | t0001 | g0305 | AMR | PEL | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG01978 | hp2 | a0002 | c0003 | t0001 | g0114 | AMR | PEL | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG01981 | hp1 | a0004 | c0005 | t0001 | g0008 | AMR | PEL | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG01981 | hp2 | a0002 | c0003 | t0001 | g0004 | AMR | PEL | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0291 | AMR | PEL | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | PEL | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02004 | hp1 | a0002 | c0003 | t0001 | g0002 | AMR | PEL | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | KHV | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02027 | hp1 | a0002 | c0007 | t0004 | g0292 | EAS | KHV | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02027 | hp2 | a0002 | c0003 | t0001 | g0109 | EAS | KHV | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02040 | hp1 | a0003 | c0008 | t0001 | g0089 | EAS | KHV | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02040 | hp2 | a0002 | c0003 | t0001 | g0108 | EAS | KHV | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02055 | hp1 | a0003 | c0002 | t0001 | g0054 | AFR | ACB | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0274 | AFR | ACB | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02056 | hp1 | a0002 | c0028 | t0001 | g0095 | EAS | KHV | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | KHV | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02071 | hp1 | a0003 | c0002 | t0001 | g0127 | EAS | KHV | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | KHV | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | KHV | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02074 | hp2 | a0003 | c0002 | t0001 | g0200 | EAS | KHV | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02080 | hp1 | a0002 | c0003 | t0001 | g0092 | EAS | KHV | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | KHV | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | KHV | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02083 | hp2 | a0002 | c0003 | t0001 | g0002 | EAS | KHV | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | KHV | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02129 | hp2 | a0002 | c0006 | t0005 | g0315 | EAS | KHV | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02135 | hp1 | a0002 | c0003 | t0001 | g0113 | EAS | KHV | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02135 | hp2 | a0003 | c0002 | t0001 | g0007 | EAS | KHV | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02145 | hp1 | a0003 | c0002 | t0001 | g0043 | AFR | ACB | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02145 | hp2 | a0003 | c0002 | t0001 | g0139 | AFR | ACB | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02155 | hp1 | a0002 | c0003 | t0001 | g0102 | EAS | CDX | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | CDX | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | CDX | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02165 | hp2 | a0002 | c0003 | t0001 | g0084 | EAS | CDX | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02257 | hp1 | a0002 | c0006 | t0003 | g0036 | AFR | ACB | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02257 | hp2 | a0002 | c0004 | t0001 | g0332 | AFR | ACB | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02258 | hp1 | a0004 | c0009 | t0001 | g0046 | AFR | ACB | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02258 | hp2 | a0002 | c0004 | t0001 | g0334 | AFR | ACB | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02273 | hp1 | a0003 | c0002 | t0001 | g0132 | AMR | PEL | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02273 | hp2 | a0002 | c0003 | t0001 | g0166 | AMR | PEL | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02280 | hp1 | a0008 | c0021 | t0001 | g0059 | AFR | ACB | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02280 | hp2 | a0002 | c0010 | t0001 | g0195 | AFR | ACB | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02293 | hp1 | a0002 | c0003 | t0001 | g0186 | AMR | PEL | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0275 | AMR | PEL | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02300 | hp2 | a0002 | c0003 | t0001 | g0161 | AMR | PEL | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02451 | hp1 | a0018 | c0036 | t0001 | g0264 | AFR | ACB | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02451 | hp2 | a0002 | c0004 | t0001 | g0335 | AFR | ACB | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02523 | hp1 | a0002 | c0018 | t0001 | g0140 | EAS | KHV | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02523 | hp2 | a0002 | c0007 | t0004 | g0293 | EAS | KHV | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02572 | hp1 | a0003 | c0002 | t0001 | g0011 | AFR | GWD | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0267 | AFR | GWD | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02602 | hp1 | a0003 | c0002 | t0001 | g0138 | SAS | PJL | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02602 | hp2 | a0004 | c0009 | t0001 | g0079 | SAS | PJL | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02622 | hp1 | a0008 | c0021 | t0001 | g0060 | AFR | GWD | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02622 | hp2 | a0001 | c0013 | t0001 | g0281 | AFR | GWD | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02630 | hp1 | a0005 | c0011 | t0001 | g0030 | AFR | GWD | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02630 | hp2 | a0003 | c0017 | t0001 | g0192 | AFR | GWD | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | GWD | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02647 | hp2 | a0019 | c0030 | t0001 | g0173 | AFR | GWD | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02698 | hp1 | a0004 | c0005 | t0001 | g0296 | SAS | PJL | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0245 | SAS | PJL | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02717 | hp1 | a0009 | c0026 | t0001 | g0053 | AFR | GWD | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02717 | hp2 | a0005 | c0019 | t0001 | g0050 | AFR | GWD | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02723 | hp1 | a0003 | c0002 | t0001 | g0055 | AFR | GWD | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02723 | hp2 | a0003 | c0002 | t0002 | g0048 | AFR | GWD | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02735 | hp1 | a0002 | c0027 | t0001 | g0316 | SAS | PJL | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0224 | SAS | PJL | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0289 | SAS | PJL | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02738 | hp2 | a0003 | c0002 | t0001 | g0191 | SAS | PJL | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02809 | hp1 | a0002 | c0004 | t0001 | g0326 | AFR | GWD | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02809 | hp2 | a0002 | c0006 | t0003 | g0034 | AFR | GWD | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02818 | hp1 | a0002 | c0010 | t0001 | g0199 | AFR | GWD | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02818 | hp2 | a0002 | c0004 | t0001 | g0328 | AFR | GWD | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02886 | hp2 | a0002 | c0010 | t0001 | g0198 | AFR | GWD | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02895 | hp1 | a0005 | c0011 | t0001 | g0031 | AFR | GWD | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02895 | hp2 | a0003 | c0012 | t0001 | g0075 | AFR | GWD | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02897 | hp1 | a0002 | c0010 | t0001 | g0194 | AFR | GWD | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02897 | hp2 | a0003 | c0012 | t0001 | g0074 | AFR | GWD | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02922 | hp1 | a0002 | c0014 | t0001 | g0020 | AFR | ESN | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02922 | hp2 | a0020 | c0033 | t0001 | g0162 | AFR | ESN | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02965 | hp1 | a0003 | c0002 | t0001 | g0320 | AFR | ESN | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02965 | hp2 | a0002 | c0004 | t0001 | g0327 | AFR | ESN | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02970 | hp1 | a0003 | c0002 | t0002 | g0009 | AFR | ESN | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02970 | hp2 | a0002 | c0004 | t0001 | g0329 | AFR | ESN | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02976 | hp1 | a0002 | c0004 | t0001 | g0325 | AFR | ESN | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02976 | hp2 | a0009 | c0026 | t0006 | g0052 | AFR | ESN | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG03017 | hp1 | a0002 | c0015 | t0001 | g0310 | SAS | PJL | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG03017 | hp2 | a0004 | c0009 | t0001 | g0082 | SAS | PJL | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG03041 | hp2 | a0002 | c0006 | t0003 | g0035 | AFR | GWD | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG03098 | hp1 | a0002 | c0004 | t0001 | g0336 | AFR | MSL | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG03098 | hp2 | a0004 | c0009 | t0001 | g0045 | AFR | MSL | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG03130 | hp1 | a0002 | c0003 | t0001 | g0098 | AFR | ESN | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG03130 | hp2 | a0003 | c0002 | t0001 | g0010 | AFR | ESN | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG03139 | hp1 | a0004 | c0038 | t0001 | g0044 | AFR | ESN | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG03139 | hp2 | a0001 | c0013 | t0001 | g0242 | AFR | ESN | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG03195 | hp1 | a0002 | c0034 | t0001 | g0331 | AFR | ESN | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG03195 | hp2 | a0002 | c0006 | t0003 | g0033 | AFR | ESN | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG03209 | hp1 | a0005 | c0011 | t0001 | g0038 | AFR | MSL | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG03209 | hp2 | a0003 | c0002 | t0001 | g0058 | AFR | MSL | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG03239 | hp1 | a0003 | c0002 | t0001 | g0007 | SAS | PJL | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG03453 | hp1 | a0002 | c0004 | t0001 | g0340 | AFR | MSL | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG03453 | hp2 | a0002 | c0035 | t0001 | g0072 | AFR | MSL | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG03486 | hp1 | a0003 | c0002 | t0001 | g0011 | AFR | MSL | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG03486 | hp2 | a0005 | c0019 | t0001 | g0051 | AFR | MSL | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG03491 | hp1 | a0002 | c0006 | t0001 | g0314 | SAS | PJL | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG03492 | hp2 | a0003 | c0002 | t0001 | g0037 | SAS | PJL | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG03516 | hp1 | a0005 | c0011 | t0001 | g0063 | AFR | ESN | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG03516 | hp2 | a0003 | c0002 | t0001 | g0010 | AFR | ESN | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG03540 | hp1 | a0002 | c0007 | t0001 | g0019 | AFR | GWD | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG03540 | hp2 | a0002 | c0004 | t0001 | g0338 | AFR | GWD | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0343 | SAS | PJL | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | STU | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG03688 | hp2 | a0003 | c0002 | t0001 | g0258 | SAS | STU | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG03704 | hp2 | a0002 | c0006 | t0001 | g0313 | SAS | PJL | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG03710 | hp1 | a0003 | c0002 | t0001 | g0007 | SAS | PJL | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG03831 | hp1 | a0002 | c0003 | t0001 | g0083 | SAS | BEB | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG03831 | hp2 | a0003 | c0002 | t0001 | g0177 | SAS | BEB | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG03834 | hp1 | a0004 | c0005 | t0001 | g0299 | SAS | BEB | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0211 | SAS | BEB | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG03942 | hp1 | a0001 | c0031 | t0001 | g0216 | SAS | BEB | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0210 | SAS | BEB | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | STU | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG04115 | hp2 | a0004 | c0005 | t0001 | g0298 | SAS | STU | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG04184 | hp1 | a0010 | c0022 | t0001 | g0076 | SAS | BEB | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0255 | SAS | BEB | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0283 | SAS | STU | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0307 | SAS | STU | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0308 | SAS | STU | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0330 | AFR | YRI | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA18747 | hp1 | a0002 | c0003 | t0001 | g0118 | EAS | CHB | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | CHB | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA18906 | hp1 | a0002 | c0004 | t0001 | g0339 | AFR | YRI | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA18906 | hp2 | a0003 | c0002 | t0001 | g0184 | AFR | YRI | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA18941 | hp2 | a0003 | c0002 | t0001 | g0068 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA18945 | hp2 | a0003 | c0002 | t0001 | g0179 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA18947 | hp2 | a0002 | c0003 | t0001 | g0101 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA18949 | hp2 | a0003 | c0002 | t0001 | g0193 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA18951 | hp1 | a0003 | c0002 | t0001 | g0171 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA18951 | hp2 | a0003 | c0002 | t0001 | g0136 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA18952 | hp1 | a0002 | c0003 | t0001 | g0181 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA18952 | hp2 | a0002 | c0006 | t0001 | g0322 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA18953 | hp1 | a0003 | c0002 | t0001 | g0018 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA18953 | hp2 | a0002 | c0003 | t0001 | g0183 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA18954 | hp1 | a0002 | c0006 | t0005 | g0317 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA18954 | hp2 | a0003 | c0002 | t0001 | g0133 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA18957 | hp1 | a0003 | c0002 | t0001 | g0014 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA18959 | hp2 | a0003 | c0008 | t0001 | g0157 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA18960 | hp1 | a0010 | c0022 | t0001 | g0137 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA18961 | hp1 | a0011 | c0016 | t0001 | g0168 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA18961 | hp2 | a0003 | c0020 | t0001 | g0069 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA18962 | hp1 | a0002 | c0003 | t0001 | g0342 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA18962 | hp2 | a0003 | c0008 | t0001 | g0172 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA18963 | hp1 | a0002 | c0003 | t0001 | g0004 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA18964 | hp1 | a0002 | c0003 | t0001 | g0100 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA18964 | hp2 | a0011 | c0016 | t0001 | g0115 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA18965 | hp1 | a0003 | c0002 | t0001 | g0032 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA18966 | hp1 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA18966 | hp2 | a0003 | c0002 | t0001 | g0018 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA18967 | hp1 | a0003 | c0002 | t0001 | g0152 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA18967 | hp2 | a0002 | c0003 | t0001 | g0165 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA18968 | hp2 | a0021 | c0039 | t0001 | g0176 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA18970 | hp1 | a0002 | c0007 | t0009 | g0158 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA18970 | hp2 | a0003 | c0002 | t0001 | g0159 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA18971 | hp1 | a0002 | c0028 | t0001 | g0002 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA18973 | hp2 | a0003 | c0002 | t0001 | g0086 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA18975 | hp2 | a0002 | c0007 | t0001 | g0164 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA18977 | hp2 | a0002 | c0003 | t0001 | g0117 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA18979 | hp1 | a0002 | c0003 | t0001 | g0103 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA18979 | hp2 | a0003 | c0002 | t0001 | g0121 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA18981 | hp1 | a0002 | c0003 | t0001 | g0006 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA18981 | hp2 | a0003 | c0002 | t0001 | g0145 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA18982 | hp1 | a0002 | c0003 | t0001 | g0104 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA18982 | hp2 | a0003 | c0002 | t0001 | g0341 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA18983 | hp1 | a0002 | c0003 | t0001 | g0006 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA18985 | hp1 | a0002 | c0003 | t0001 | g0112 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA18985 | hp2 | a0003 | c0008 | t0001 | g0125 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA18986 | hp1 | a0003 | c0002 | t0001 | g0190 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA18986 | hp2 | a0002 | c0003 | t0001 | g0066 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA18988 | hp1 | a0002 | c0003 | t0001 | g0187 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA18989 | hp2 | a0003 | c0002 | t0001 | g0128 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA18990 | hp1 | a0002 | c0003 | t0001 | g0094 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA18990 | hp2 | a0001 | c0048 | t0001 | g0253 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA18991 | hp1 | a0002 | c0003 | t0001 | g0093 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA18991 | hp2 | a0003 | c0002 | t0001 | g0014 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA18992 | hp2 | a0002 | c0003 | t0001 | g0174 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA18994 | hp1 | a0003 | c0002 | t0001 | g0090 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA18994 | hp2 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA18995 | hp1 | a0003 | c0002 | t0001 | g0148 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA18995 | hp2 | a0002 | c0003 | t0001 | g0091 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA18998 | hp2 | a0002 | c0003 | t0001 | g0182 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA18999 | hp1 | a0003 | c0020 | t0001 | g0123 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA18999 | hp2 | a0003 | c0002 | t0001 | g0124 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA19000 | hp1 | a0003 | c0002 | t0001 | g0130 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA19000 | hp2 | a0003 | c0002 | t0001 | g0131 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA19002 | hp1 | a0003 | c0008 | t0001 | g0067 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA19005 | hp2 | a0003 | c0002 | t0001 | g0141 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA19006 | hp1 | a0003 | c0008 | t0001 | g0134 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA19007 | hp1 | a0022 | c0042 | t0001 | g0143 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA19007 | hp2 | a0002 | c0007 | t0001 | g0160 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA19011 | hp2 | a0002 | c0003 | t0001 | g0107 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA19012 | hp1 | a0002 | c0003 | t0001 | g0028 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA19012 | hp2 | a0003 | c0002 | t0001 | g0154 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA19030 | hp1 | a0005 | c0024 | t0001 | g0061 | AFR | LWK | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA19030 | hp2 | a0002 | c0050 | t0001 | g0294 | AFR | LWK | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0319 | AFR | LWK | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA19043 | hp2 | a0023 | c0041 | t0001 | g0056 | AFR | LWK | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA19054 | hp1 | a0002 | c0003 | t0001 | g0119 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA19054 | hp2 | a0003 | c0002 | t0001 | g0175 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA19056 | hp1 | a0003 | c0002 | t0001 | g0120 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA19056 | hp2 | a0002 | c0003 | t0001 | g0105 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA19062 | hp1 | a0003 | c0008 | t0001 | g0088 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA19062 | hp2 | a0002 | c0003 | t0001 | g0110 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA19065 | hp2 | a0002 | c0003 | t0001 | g0006 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA19067 | hp2 | a0003 | c0002 | t0001 | g0149 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA19074 | hp1 | a0003 | c0002 | t0001 | g0015 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA19074 | hp2 | a0003 | c0002 | t0001 | g0129 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA19075 | hp1 | a0002 | c0006 | t0001 | g0027 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA19075 | hp2 | a0003 | c0002 | t0001 | g0087 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA19080 | hp1 | a0002 | c0003 | t0001 | g0016 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA19080 | hp2 | a0003 | c0002 | t0001 | g0142 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA19084 | hp1 | a0003 | c0002 | t0001 | g0188 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA19084 | hp2 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA19085 | hp1 | a0003 | c0002 | t0001 | g0189 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA19085 | hp2 | a0002 | c0003 | t0001 | g0167 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA19088 | hp1 | a0003 | c0002 | t0001 | g0015 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA19088 | hp2 | a0003 | c0029 | t0001 | g0122 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA19089 | hp1 | a0002 | c0003 | t0001 | g0111 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA19089 | hp2 | a0002 | c0006 | t0001 | g0039 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA19091 | hp1 | a0002 | c0003 | t0001 | g0016 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA19240 | hp1 | a0001 | c0013 | t0001 | g0042 | AFR | YRI | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA19240 | hp2 | a0002 | c0004 | t0001 | g0333 | AFR | YRI | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA20129 | hp1 | a0002 | c0010 | t0001 | g0321 | AFR | ASW | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA20129 | hp2 | a0003 | c0002 | t0001 | g0126 | AFR | ASW | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0209 | EUR | TSI | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA20752 | hp2 | a0024 | c0047 | t0001 | g0273 | EUR | TSI | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA20905 | hp1 | a0025 | c0044 | t0001 | g0243 | SAS | GIH | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA20905 | hp2 | a0003 | c0002 | t0001 | g0151 | SAS | GIH | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG01123 | hp1 | a0004 | c0005 | t0001 | g0302 | AMR | CLM | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02109 | hp1 | a0003 | c0002 | t0002 | g0009 | AFR | ACB | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02109 | hp2 | a0017 | c0040 | t0001 | g0064 | AFR | ACB | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | ACB | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02486 | hp2 | a0003 | c0002 | t0001 | g0185 | AFR | ACB | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02559 | hp1 | a0002 | c0010 | t0001 | g0197 | AFR | ACB | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG02559 | hp2 | a0002 | c0014 | t0001 | g0270 | AFR | ACB | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG03471 | hp1 | a0002 | c0014 | t0001 | g0020 | AFR | MSL | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG03471 | hp2 | a0005 | c0011 | t0001 | g0029 | AFR | MSL | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG06807 | hp1 | a0002 | c0004 | t0001 | g0337 | AFR | USA | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
HG06807 | hp2 | a0004 | c0005 | t0001 | g0304 | AFR | USA | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA18955 | hp1 | a0003 | c0002 | t0001 | g0144 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA20300 | hp1 | a0003 | c0002 | t0002 | g0049 | AFR | USA | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
NA20300 | hp2 | a0004 | c0009 | t0001 | g0013 | AFR | USA | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
homoSapiens | chm13v2 | a0026 | c0032 | t0001 | g0241 | REF | REF | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0233 | REF | REF | USP42_chr7_6099949_6166564 | USP42 | chr7 | 6099949 | 6166564 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:6146202 | A | G | 1 | a0014 | 1 | HG01070.hp1 | missense_variant | MODERATE | c.1186A>G | p.Ile396Val | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 11/18 | 1279/5090 | 1186/3951 | 396/1316 | chr7 | 6146202 | |||
chr7:6147830 | G | A | 1 | a0019 | 1 | HG02647.hp2 | missense_variant | MODERATE | c.1324G>A | p.Val442Ile | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 12/18 | 1417/5090 | 1324/3951 | 442/1316 | chr7 | 6147830 | |||
chr7:6147840 | A | G | 1 | a0009 | 2 | HG02717.hp1 HG02976.hp2 |
missense_variant | MODERATE | c.1334A>G | p.Lys445Arg | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 12/18 | 1427/5090 | 1334/3951 | 445/1316 | chr7 | 6147840 | |||
chr7:6149742 | C | T | 1 | a0007 | 2 | HG01516.hp1 HG01934.hp1 |
missense_variant | MODERATE | c.1546C>T | p.His516Tyr | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 13/18 | 1639/5090 | 1546/3951 | 516/1316 | chr7 | 6149742 | |||
chr7:6150222 | C | T | 1 | a0024 | 1 | NA20752.hp2 | missense_variant | MODERATE | c.2026C>T | p.Pro676Ser | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 13/18 | 2119/5090 | 2026/3951 | 676/1316 | chr7 | 6150222 | |||
chr7:6153826 | G | C | 1 | a0013 | 1 | HG00738.hp1 | missense_variant | MODERATE | c.2272G>C | p.Glu758Gln | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 15/18 | 2365/5090 | 2272/3951 | 758/1316 | chr7 | 6153826 | |||
chr7:6153833 | T | G | 5 | a0002 a0011 a0015 others(2): Show |
122 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(119): Show |
missense_variant | MODERATE | c.2279T>G | p.Leu760Arg | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 15/18 | 2372/5090 | 2279/3951 | 760/1316 | chr7 | 6153833 | |||
chr7:6153889 | C | T | 1 | a0005 | 2 | HG01891.hp1 NA19030.hp1 |
missense_variant | MODERATE | c.2335C>T | p.Arg779Cys | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 15/18 | 2428/5090 | 2335/3951 | 779/1316 | chr7 | 6153889 | |||
chr7:6153890 | G | C | 16 | a0002 a0003 a0004 others(13): Show |
260 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(257): Show |
missense_variant | MODERATE | c.2336G>C | p.Arg779Pro | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 15/18 | 2429/5090 | 2336/3951 | 779/1316 | chr7 | 6153890 | |||
chr7:6153907 | G | T | 1 | a0010 | 2 | HG04184.hp1 NA18960.hp1 |
missense_variant | MODERATE | c.2353G>T | p.Ala785Ser | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 15/18 | 2446/5090 | 2353/3951 | 785/1316 | chr7 | 6153907 | |||
chr7:6153934 | A | G | 1 | a0012 | 1 | HG00280.hp2 | missense_variant | MODERATE | c.2380A>G | p.Met794Val | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 15/18 | 2473/5090 | 2380/3951 | 794/1316 | chr7 | 6153934 | |||
chr7:6154091 | C | T | 1 | a0015 | 1 | HG01256.hp1 | missense_variant | MODERATE | c.2537C>T | p.Ser846Leu | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 15/18 | 2630/5090 | 2537/3951 | 846/1316 | chr7 | 6154091 | |||
chr7:6154108 | C | T | 1 | a0024 | 1 | NA20752.hp2 | missense_variant | MODERATE | c.2554C>T | p.Pro852Ser | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 15/18 | 2647/5090 | 2554/3951 | 852/1316 | chr7 | 6154108 | |||
chr7:6154121 | G | A | 3 | a0004 a0014 a0016 |
25 | HG00280.hp1 HG00642.hp1 HG00673.hp1 others(22): Show |
missense_variant | MODERATE | c.2567G>A | p.Ser856Asn | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 15/18 | 2660/5090 | 2567/3951 | 856/1316 | chr7 | 6154121 | |||
chr7:6154177 | C | T | 1 | a0022 | 1 | NA19007.hp1 | missense_variant | MODERATE | c.2623C>T | p.Pro875Ser | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 15/18 | 2716/5090 | 2623/3951 | 875/1316 | chr7 | 6154177 | |||
chr7:6154240 | G | T | 1 | a0012 | 1 | HG00280.hp2 | missense_variant | MODERATE | c.2686G>T | p.Ala896Ser | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 15/18 | 2779/5090 | 2686/3951 | 896/1316 | chr7 | 6154240 | |||
chr7:6154277 | C | T | 1 | a0008 | 2 | HG02280.hp1 HG02622.hp1 |
missense_variant | MODERATE | c.2723C>T | p.Pro908Leu | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 15/18 | 2816/5090 | 2723/3951 | 908/1316 | chr7 | 6154277 | |||
chr7:6154522 | C | T | 1 | a0025 | 1 | NA20905.hp1 | missense_variant | MODERATE | c.2968C>T | p.Arg990Cys | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 15/18 | 3061/5090 | 2968/3951 | 990/1316 | chr7 | 6154522 | |||
chr7:6154532 | G | A | 1 | a0020 | 1 | HG02922.hp2 | missense_variant | MODERATE | c.2978G>A | p.Arg993His | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 15/18 | 3071/5090 | 2978/3951 | 993/1316 | chr7 | 6154532 | |||
chr7:6154582 | G | A | 1 | a0006 | 2 | HG01070.hp2 HG01071.hp1 |
missense_variant | MODERATE | c.3028G>A | p.Glu1010Lys | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 15/18 | 3121/5090 | 3028/3951 | 1010/1316 | chr7 | 6154582 | |||
chr7:6154640 | A | C | 2 | a0017 a0023 |
2 | HG02109.hp2 NA19043.hp2 |
missense_variant | MODERATE | c.3086A>C | p.Glu1029Ala | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 15/18 | 3179/5090 | 3086/3951 | 1029/1316 | chr7 | 6154640 | |||
chr7:6154643 | T | C | 10 | a0002 a0003 a0009 others(7): Show |
222 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(219): Show |
missense_variant | MODERATE | c.3089T>C | p.Leu1030Pro | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 15/18 | 3182/5090 | 3089/3951 | 1030/1316 | chr7 | 6154643 | |||
chr7:6155012 | A | C | 1 | a0023 | 1 | NA19043.hp2 | missense_variant | MODERATE | c.3458A>C | p.Glu1153Ala | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 15/18 | 3551/5090 | 3458/3951 | 1153/1316 | chr7 | 6155012 | |||
chr7:6155032 | C | T | 1 | a0021 | 1 | NA18968.hp2 | missense_variant | MODERATE | c.3478C>T | p.Arg1160Trp | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 15/18 | 3571/5090 | 3478/3951 | 1160/1316 | chr7 | 6155032 | |||
chr7:6156926 | A | G | 1 | a0018 | 1 | HG02451.hp1 | missense_variant | MODERATE | c.3814A>G | p.Arg1272Gly | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 16/18 | 3907/5090 | 3814/3951 | 1272/1316 | chr7 | 6156926 | |||
chr7:6157007 | C | T | 1 | a0011 | 2 | NA18961.hp1 NA18964.hp2 |
missense_variant | MODERATE | c.3895C>T | p.Arg1299Trp | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 16/18 | 3988/5090 | 3895/3951 | 1299/1316 | chr7 | 6157007 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:6111286 | A | G | 1 | a0002c0028 | 2 | HG02056.hp1 NA18971.hp1 |
synonymous_variant | LOW | c.153A>G | p.Thr51Thr | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/18 | 246/5090 | 153/3951 | 51/1316 | chr7 | 6111286 | |||
chr7:6139162 | T | A | 1 | a0003c0029 | 1 | NA19088.hp2 | synonymous_variant | LOW | c.624T>A | p.Ala208Ala | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 5/18 | 717/5090 | 624/3951 | 208/1316 | chr7 | 6139162 | |||
chr7:6145563 | A | G | 5 | a0002c0006 a0002c0010 a0002c0015 others(2): Show |
25 | HG01167.hp2 HG01243.hp1 HG01256.hp1 others(22): Show |
synonymous_variant | LOW | c.1038A>G | p.Gln346Gln | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 10/18 | 1131/5090 | 1038/3951 | 346/1316 | chr7 | 6145563 | |||
chr7:6145569 | C | T | 1 | a0002c0050 | 1 | NA19030.hp2 | synonymous_variant | LOW | c.1044C>T | p.Asn348Asn | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 10/18 | 1137/5090 | 1044/3951 | 348/1316 | chr7 | 6145569 | |||
chr7:6149789 | T | G | 1 | a0001c0031 | 1 | HG03942.hp1 | synonymous_variant | LOW | c.1593T>G | p.Pro531Pro | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 13/18 | 1686/5090 | 1593/3951 | 531/1316 | chr7 | 6149789 | |||
chr7:6149885 | A | G | 1 | a0001c0048 | 1 | NA18990.hp2 | synonymous_variant | LOW | c.1689A>G | p.Val563Val | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 13/18 | 1782/5090 | 1689/3951 | 563/1316 | chr7 | 6149885 | |||
chr7:6150086 | G | A | 3 | a0002c0006 a0002c0027 a0015c0051 |
15 | HG01167.hp2 HG01256.hp1 HG01496.hp1 others(12): Show |
synonymous_variant | LOW | c.1890G>A | p.Thr630Thr | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 13/18 | 1983/5090 | 1890/3951 | 630/1316 | chr7 | 6150086 | |||
chr7:6150119 | C | T | 5 | a0002c0006 a0002c0010 a0002c0014 others(2): Show |
25 | HG01167.hp2 HG01243.hp1 HG01256.hp1 others(22): Show |
synonymous_variant | LOW | c.1923C>T | p.Ala641Ala | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 13/18 | 2016/5090 | 1923/3951 | 641/1316 | chr7 | 6150119 | |||
chr7:6150149 | T | C | 17 | a0002c0003 a0002c0004 a0002c0006 others(14): Show |
120 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(117): Show |
synonymous_variant | LOW | c.1953T>C | p.Leu651Leu | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 13/18 | 2046/5090 | 1953/3951 | 651/1316 | chr7 | 6150149 | |||
chr7:6150212 | C | T | 1 | a0002c0014 | 3 | HG02559.hp2 HG02922.hp1 HG03471.hp1 |
synonymous_variant | LOW | c.2016C>T | p.Asn672Asn | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 13/18 | 2109/5090 | 2016/3951 | 672/1316 | chr7 | 6150212 | |||
chr7:6150495 | G | A | 1 | a0003c0008 | 9 | HG00423.hp1 HG00621.hp2 HG02040.hp1 others(6): Show |
synonymous_variant | LOW | c.2190G>A | p.Thr730Thr | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 14/18 | 2283/5090 | 2190/3951 | 730/1316 | chr7 | 6150495 | |||
chr7:6150495 | G | T | 1 | a0001c0046 | 1 | HG00099.hp1 | synonymous_variant | LOW | c.2190G>T | p.Thr730Thr | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 14/18 | 2283/5090 | 2190/3951 | 730/1316 | chr7 | 6150495 | |||
chr7:6153855 | C | A | 1 | a0003c0012 | 3 | HG01081.hp1 HG02895.hp2 HG02897.hp2 |
synonymous_variant | LOW | c.2301C>A | p.Ala767Ala | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 15/18 | 2394/5090 | 2301/3951 | 767/1316 | chr7 | 6153855 | |||
chr7:6153981 | C | A | 1 | a0004c0038 | 1 | HG03139.hp1 | synonymous_variant | LOW | c.2427C>A | p.Ile809Ile | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 15/18 | 2520/5090 | 2427/3951 | 809/1316 | chr7 | 6153981 | |||
chr7:6154131 | G | A | 1 | a0005c0019 | 2 | HG02717.hp2 HG03486.hp2 |
synonymous_variant | LOW | c.2577G>A | p.Pro859Pro | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 15/18 | 2670/5090 | 2577/3951 | 859/1316 | chr7 | 6154131 | |||
chr7:6154329 | G | A | 1 | a0011c0016 | 2 | NA18961.hp1 NA18964.hp2 |
synonymous_variant | LOW | c.2775G>A | p.Glu925Glu | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 15/18 | 2868/5090 | 2775/3951 | 925/1316 | chr7 | 6154329 | |||
chr7:6154533 | C | A | 1 | a0001c0013 | 3 | HG02622.hp2 HG03139.hp2 NA19240.hp1 |
synonymous_variant | LOW | c.2979C>A | p.Arg993Arg | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 15/18 | 3072/5090 | 2979/3951 | 993/1316 | chr7 | 6154533 | |||
chr7:6154539 | C | T | 1 | a0002c0035 | 1 | HG03453.hp2 | synonymous_variant | LOW | c.2985C>T | p.Ala995Ala | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 15/18 | 3078/5090 | 2985/3951 | 995/1316 | chr7 | 6154539 | |||
chr7:6154635 | G | C | 6 | a0002c0007 a0002c0018 a0002c0034 others(3): Show |
16 | HG00597.hp1 HG00621.hp1 HG01081.hp2 others(13): Show |
synonymous_variant | LOW | c.3081G>C | p.Gly1027Gly | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 15/18 | 3174/5090 | 3081/3951 | 1027/1316 | chr7 | 6154635 | |||
chr7:6154752 | C | T | 3 | a0004c0005 a0014c0049 a0016c0043 |
15 | HG00280.hp1 HG00741.hp2 HG01070.hp1 others(12): Show |
synonymous_variant | LOW | c.3198C>T | p.Tyr1066Tyr | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 15/18 | 3291/5090 | 3198/3951 | 1066/1316 | chr7 | 6154752 | |||
chr7:6154812 | C | T | 2 | a0002c0004 a0002c0034 |
15 | HG02257.hp2 HG02258.hp2 HG02451.hp2 others(12): Show |
synonymous_variant | LOW | c.3258C>T | p.Ala1086Ala | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 15/18 | 3351/5090 | 3258/3951 | 1086/1316 | chr7 | 6154812 | |||
chr7:6154854 | T | C | 1 | a0002c0027 | 2 | HG01496.hp1 HG02735.hp1 |
synonymous_variant | LOW | c.3300T>C | p.Arg1100Arg | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 15/18 | 3393/5090 | 3300/3951 | 1100/1316 | chr7 | 6154854 | |||
chr7:6155154 | G | A | 2 | a0003c0020 a0022c0042 |
3 | NA18961.hp2 NA18999.hp1 NA19007.hp1 |
synonymous_variant | LOW | c.3600G>A | p.Lys1200Lys | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 15/18 | 3693/5090 | 3600/3951 | 1200/1316 | chr7 | 6155154 | |||
chr7:6156847 | A | G | 1 | a0002c0050 | 1 | NA19030.hp2 | synonymous_variant | LOW | c.3735A>G | p.Arg1245Arg | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 16/18 | 3828/5090 | 3735/3951 | 1245/1316 | chr7 | 6156847 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:6104971 | G | C | 1 | a0009c0026t0006 | 1 | HG02976.hp2 | 5_prime_UTR_variant | MODIFIER | c.-71G>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 1/18 | 6163 | chr7 | 6104971 | ||||||
chr7:6104973 | C | T | 1 | a0002c0007t0009 | 1 | NA18970.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-69C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 1/18 | chr7 | 6104973 | |||||||
chr7:6160719 | G | A | 1 | a0003c0002t0002 | 5 | HG01175.hp2 HG02109.hp1 HG02723.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*201G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 18/18 | 1262 | chr7 | 6160719 | ||||||
chr7:6160768 | A | G | 1 | a0002c0006t0005 | 2 | HG02129.hp2 NA18954.hp1 |
3_prime_UTR_variant | MODIFIER | c.*250A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 18/18 | 1311 | chr7 | 6160768 | ||||||
chr7:6160989 | T | C | 1 | a0002c0007t0004 | 2 | HG02027.hp1 HG02523.hp2 |
3_prime_UTR_variant | MODIFIER | c.*471T>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 18/18 | 1532 | chr7 | 6160989 | ||||||
chr7:6161076 | T | C | 1 | a0001c0001t0007 | 1 | HG01099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*558T>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 18/18 | 1619 | chr7 | 6161076 | ||||||
chr7:6161333 | A | G | 1 | a0004c0005t0008 | 1 | HG01934.hp2 | 3_prime_UTR_variant | MODIFIER | c.*815A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 18/18 | 1876 | chr7 | 6161333 | ||||||
chr7:6161388 | G | A | 1 | a0002c0006t0003 | 4 | HG02257.hp1 HG02809.hp2 HG03041.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*870G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 18/18 | 1931 | chr7 | 6161388 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:6105082 | G | A | 1 | a0002c0006t0001g0027 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-10+50G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 1/17 | chr7 | 6105082 | |||||||
chr7:6105189 | G | A | 1 | a0002c0003t0001g0028 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-10+157G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 1/17 | chr7 | 6105189 | |||||||
chr7:6105257 | G | A | 3 | a0005c0011t0001g0029 a0005c0011t0001g0030 a0005c0011t0001g0031 |
3 | HG02630.hp1 HG02895.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-10+225G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 1/17 | chr7 | 6105257 | |||||||
chr7:6105293 | C | T | 1 | a0001c0001t0001g0343 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-10+261C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 1/17 | chr7 | 6105293 | |||||||
chr7:6105309 | G | T | 2 | a0002c0003t0001g0342 a0003c0002t0001g0341 |
2 | NA18962.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.-10+277G>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 1/17 | chr7 | 6105309 | |||||||
chr7:6105530 | G | T | 16 | a0001c0001t0001g0330 a0002c0004t0001g0325 a0002c0004t0001g0326 others(13): Show |
16 | HG02257.hp2 HG02258.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.-10+498G>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 1/17 | chr7 | 6105530 | |||||||
chr7:6105587 | C | A | 1 | a0003c0002t0001g0032 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-10+555C>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 1/17 | chr7 | 6105587 | |||||||
chr7:6105592 | C | T | 1 | a0002c0006t0001g0324 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-10+560C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 1/17 | chr7 | 6105592 | |||||||
chr7:6105618 | G | C | 4 | a0002c0006t0003g0033 a0002c0006t0003g0034 a0002c0006t0003g0035 others(1): Show |
4 | HG02257.hp1 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10+586G>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 1/17 | chr7 | 6105618 | |||||||
chr7:6105647 | G | C | 1 | a0003c0002t0001g0037 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.-10+615G>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 1/17 | chr7 | 6105647 | |||||||
chr7:6105665 | G | A | 1 | a0005c0011t0001g0038 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-10+633G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 1/17 | chr7 | 6105665 | |||||||
chr7:6105680 | G | C | 1 | a0002c0006t0001g0039 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-10+648G>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 1/17 | chr7 | 6105680 | |||||||
chr7:6105731 | G | A | 3 | a0002c0004t0001g0325 a0002c0004t0001g0326 a0002c0004t0001g0327 |
3 | HG02809.hp1 HG02965.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-10+699G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 1/17 | chr7 | 6105731 | |||||||
chr7:6105901 | G | C | 2 | a0002c0015t0001g0040 a0002c0015t0001g0041 |
2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-10+869G>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 1/17 | chr7 | 6105901 | |||||||
chr7:6105934 | G | C | 1 | a0001c0013t0001g0042 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-10+902G>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 1/17 | chr7 | 6105934 | |||||||
chr7:6106240 | G | A | 1 | a0003c0002t0001g0043 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-10+1208G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 1/17 | chr7 | 6106240 | |||||||
chr7:6106260 | G | T | 1 | a0003c0002t0001g0323 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-10+1228G>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 1/17 | chr7 | 6106260 | |||||||
chr7:6106362 | C | T | 1 | a0002c0006t0001g0322 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-10+1330C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 1/17 | chr7 | 6106362 | |||||||
chr7:6106446 | C | G | 1 | a0002c0010t0001g0321 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-10+1414C>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 1/17 | chr7 | 6106446 | |||||||
chr7:6106500 | A | G | 1 | a0003c0002t0001g0320 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-10+1468A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 1/17 | chr7 | 6106500 | |||||||
chr7:6106702 | C | A | 1 | a0002c0006t0001g0324 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-10+1670C>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 1/17 | chr7 | 6106702 | |||||||
chr7:6106731 | AT | A | 30 | a0002c0004t0001g0328 a0002c0006t0001g0324 a0003c0002t0001g0010 others(27): Show |
33 | HG01167.hp2 HG01175.hp2 HG01346.hp1 others(30): Show |
intron_variant | MODIFIER | c.-10+1713delT | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 6106731 | ||||||
chr7:6106858 | G | A | 7 | a0003c0002t0002g0009 a0003c0002t0002g0047 a0003c0002t0002g0048 others(4): Show |
8 | HG01175.hp2 HG02109.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.-10+1826G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 1/17 | chr7 | 6106858 | |||||||
chr7:6106984 | A | G | 2 | a0001c0001t0001g0318 a0001c0001t0001g0319 |
2 | HG01496.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-10+1952A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 1/17 | chr7 | 6106984 | |||||||
chr7:6107409 | C | CT | 23 | a0001c0001t0001g0026 a0001c0001t0001g0307 a0001c0001t0001g0308 others(20): Show |
26 | HG00280.hp1 HG00741.hp2 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.-10+2394dupT | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 6107409 | ||||||
chr7:6107409 | C | CTT | 14 | a0002c0006t0001g0027 a0002c0006t0001g0039 a0002c0006t0001g0313 others(11): Show |
14 | HG01167.hp2 HG01256.hp1 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.-10+2393_-10+2394d others(4): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 6107409 | ||||||
chr7:6107409 | CT | C | 8 | a0001c0001t0001g0071 a0002c0003t0001g0066 a0002c0035t0001g0072 others(5): Show |
8 | HG01070.hp2 HG01168.hp2 HG03453.hp2 others(5): Show |
intron_variant | MODIFIER | c.-10+2394delT | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 6107409 | ||||||
chr7:6107471 | G | A | 1 | a0001c0001t0001g0012 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.-10+2439G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 1/17 | chr7 | 6107471 | |||||||
chr7:6107524 | C | T | 2 | a0002c0007t0004g0292 a0002c0007t0004g0293 |
2 | HG02027.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.-10+2492C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 1/17 | chr7 | 6107524 | |||||||
chr7:6107660 | C | T | 1 | a0002c0035t0001g0072 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-10+2628C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 1/17 | chr7 | 6107660 | |||||||
chr7:6107689 | G | A | 2 | a0005c0019t0001g0050 a0005c0019t0001g0051 |
2 | HG02717.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-10+2657G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 1/17 | chr7 | 6107689 | |||||||
chr7:6107718 | T | C | 3 | a0003c0012t0001g0073 a0003c0012t0001g0074 a0003c0012t0001g0075 |
3 | HG01081.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-10+2686T>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 1/17 | chr7 | 6107718 | |||||||
chr7:6107865 | T | A | 234 | a0001c0001t0001g0330 a0002c0003t0001g0002 a0002c0003t0001g0004 others(231): Show |
260 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(257): Show |
intron_variant | MODIFIER | c.-10+2833T>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 1/17 | chr7 | 6107865 | |||||||
chr7:6107868 | T | C | 1 | a0010c0022t0001g0076 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-10+2836T>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 1/17 | chr7 | 6107868 | |||||||
chr7:6107930 | A | C | 1 | a0005c0011t0001g0063 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-10+2898A>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 1/17 | chr7 | 6107930 | |||||||
chr7:6107938 | TAA | T | 5 | a0005c0011t0001g0038 a0005c0024t0001g0061 a0005c0024t0001g0062 others(2): Show |
5 | HG01891.hp1 HG02280.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10+2907_-10+2908d others(4): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 1/17 | chr7 | 6107938 | |||||||
chr7:6108025 | A | G | 1 | a0003c0002t0001g0200 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-10+2993A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 1/17 | chr7 | 6108025 | |||||||
chr7:6108138 | G | A | 1 | a0001c0001t0001g0201 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-9-2987G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 1/17 | chr7 | 6108138 | |||||||
chr7:6108317 | C | T | 22 | a0002c0006t0001g0027 a0002c0006t0001g0039 a0002c0006t0001g0313 others(19): Show |
23 | HG01167.hp2 HG01243.hp1 HG01256.hp1 others(20): Show |
intron_variant | MODIFIER | c.-9-2808C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 1/17 | chr7 | 6108317 | |||||||
chr7:6108318 | G | A | 1 | a0003c0017t0001g0065 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-9-2807G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 1/17 | chr7 | 6108318 | |||||||
chr7:6108520 | C | T | 1 | a0001c0001t0001g0309 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-9-2605C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 1/17 | chr7 | 6108520 | |||||||
chr7:6108544 | G | A | 25 | a0002c0006t0001g0027 a0002c0006t0001g0039 a0002c0006t0001g0313 others(22): Show |
26 | HG01167.hp2 HG01243.hp1 HG01256.hp1 others(23): Show |
intron_variant | MODIFIER | c.-9-2581G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 1/17 | chr7 | 6108544 | |||||||
chr7:6108583 | C | A | 1 | a0001c0001t0001g0202 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-9-2542C>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 1/17 | chr7 | 6108583 | |||||||
chr7:6108601 | T | C | 233 | a0001c0001t0001g0330 a0002c0003t0001g0002 a0002c0003t0001g0004 others(230): Show |
259 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(256): Show |
intron_variant | MODIFIER | c.-9-2524T>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 1/17 | chr7 | 6108601 | |||||||
chr7:6108606 | G | A | 1 | a0002c0004t0001g0325 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-9-2519G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 1/17 | chr7 | 6108606 | |||||||
chr7:6108636 | A | G | 3 | a0005c0011t0001g0029 a0005c0011t0001g0030 a0005c0011t0001g0031 |
3 | HG02630.hp1 HG02895.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-9-2489A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 1/17 | chr7 | 6108636 | |||||||
chr7:6108775 | A | T | 26 | a0002c0006t0001g0027 a0002c0006t0001g0039 a0002c0006t0001g0313 others(23): Show |
27 | HG01167.hp2 HG01243.hp1 HG01256.hp1 others(24): Show |
intron_variant | MODIFIER | c.-9-2350A>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 1/17 | chr7 | 6108775 | |||||||
chr7:6108796 | A | T | 6 | a0001c0001t0001g0291 a0001c0001t0001g0308 a0005c0011t0001g0029 others(3): Show |
6 | HG00738.hp1 HG01993.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9-2329A>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 1/17 | chr7 | 6108796 | |||||||
chr7:6108797 | T | A | 1 | a0002c0003t0001g0077 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-9-2328T>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 1/17 | chr7 | 6108797 | |||||||
chr7:6108897 | G | T | 1 | a0003c0017t0001g0065 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-9-2228G>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 1/17 | chr7 | 6108897 | |||||||
chr7:6109079 | G | T | 3 | a0005c0011t0001g0029 a0005c0011t0001g0030 a0005c0011t0001g0031 |
3 | HG02630.hp1 HG02895.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-9-2046G>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 1/17 | chr7 | 6109079 | |||||||
chr7:6109141 | G | T | 234 | a0001c0001t0001g0330 a0002c0003t0001g0002 a0002c0003t0001g0004 others(231): Show |
260 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(257): Show |
intron_variant | MODIFIER | c.-9-1984G>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 1/17 | chr7 | 6109141 | |||||||
chr7:6109166 | A | T | 1 | a0003c0002t0001g0193 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-9-1959A>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 1/17 | chr7 | 6109166 | |||||||
chr7:6109200 | G | A | 2 | a0002c0007t0004g0292 a0002c0007t0004g0293 |
2 | HG02027.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.-9-1925G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 1/17 | chr7 | 6109200 | |||||||
chr7:6109277 | A | T | 1 | a0003c0017t0001g0192 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-9-1848A>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 1/17 | chr7 | 6109277 | |||||||
chr7:6109279 | G | A | 4 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0205 others(1): Show |
4 | HG02083.hp1 NA18945.hp1 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9-1846G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 1/17 | chr7 | 6109279 | |||||||
chr7:6109284 | G | A | 2 | a0001c0001t0001g0207 a0001c0001t0001g0208 |
2 | HG01952.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.-9-1841G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 1/17 | chr7 | 6109284 | |||||||
chr7:6109349 | T | C | 1 | a0005c0011t0001g0029 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-9-1776T>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 1/17 | chr7 | 6109349 | |||||||
chr7:6109354 | G | A | 1 | a0002c0035t0001g0072 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-9-1771G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 1/17 | chr7 | 6109354 | |||||||
chr7:6109453 | C | T | 151 | a0002c0003t0001g0002 a0002c0003t0001g0004 a0002c0003t0001g0006 others(148): Show |
170 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(167): Show |
intron_variant | MODIFIER | c.-9-1672C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 1/17 | chr7 | 6109453 | |||||||
chr7:6109659 | G | T | 1 | a0003c0002t0001g0191 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-9-1466G>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 1/17 | chr7 | 6109659 | |||||||
chr7:6109687 | C | T | 1 | a0001c0001t0001g0289 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-9-1438C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 1/17 | chr7 | 6109687 | |||||||
chr7:6109688 | G | A | 3 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0205 |
3 | HG02083.hp1 NA18945.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.-9-1437G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 1/17 | chr7 | 6109688 | |||||||
chr7:6109700 | C | CT | 17 | a0001c0001t0001g0005 a0001c0001t0001g0280 a0001c0001t0001g0282 others(14): Show |
20 | HG00639.hp1 HG01099.hp2 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.-9-1407dupT | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 6109700 | ||||||
chr7:6109700 | CT | C | 48 | a0002c0006t0001g0027 a0002c0006t0001g0039 a0002c0006t0001g0313 others(45): Show |
51 | HG01167.hp2 HG01243.hp1 HG01256.hp1 others(48): Show |
intron_variant | MODIFIER | c.-9-1407delT | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 6109700 | ||||||
chr7:6109762 | A | G | 1 | a0002c0003t0001g0186 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-9-1363A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 1/17 | chr7 | 6109762 | |||||||
chr7:6109804 | G | A | 1 | a0002c0003t0001g0083 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-9-1321G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 1/17 | chr7 | 6109804 | |||||||
chr7:6109847 | C | T | 150 | a0002c0003t0001g0002 a0002c0003t0001g0004 a0002c0003t0001g0006 others(147): Show |
169 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(166): Show |
intron_variant | MODIFIER | c.-9-1278C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 1/17 | chr7 | 6109847 | |||||||
chr7:6109857 | C | T | 1 | a0003c0002t0001g0323 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-9-1268C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 1/17 | chr7 | 6109857 | |||||||
chr7:6109861 | C | T | 1 | a0002c0035t0001g0072 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-9-1264C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 1/17 | chr7 | 6109861 | |||||||
chr7:6109867 | A | G | 2 | a0003c0002t0001g0184 a0003c0002t0001g0185 |
2 | HG02486.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-9-1258A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 1/17 | chr7 | 6109867 | |||||||
chr7:6109945 | C | T | 23 | a0002c0006t0001g0027 a0002c0006t0001g0039 a0002c0006t0001g0313 others(20): Show |
24 | HG01167.hp2 HG01243.hp1 HG01256.hp1 others(21): Show |
intron_variant | MODIFIER | c.-9-1180C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 1/17 | chr7 | 6109945 | |||||||
chr7:6109967 | C | G | 3 | a0003c0012t0001g0073 a0003c0012t0001g0074 a0003c0012t0001g0075 |
3 | HG01081.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-9-1158C>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 1/17 | chr7 | 6109967 | |||||||
chr7:6109979 | G | A | 1 | a0001c0001t0001g0209 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-9-1146G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 1/17 | chr7 | 6109979 | |||||||
chr7:6110044 | G | C | 1 | a0001c0001t0001g0280 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-9-1081G>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 1/17 | chr7 | 6110044 | |||||||
chr7:6110226 | G | A | 1 | a0001c0001t0001g0210 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-9-899G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 1/17 | chr7 | 6110226 | |||||||
chr7:6110239 | G | A | 1 | a0001c0001t0001g0211 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-9-886G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 1/17 | chr7 | 6110239 | |||||||
chr7:6110326 | T | A | 7 | a0002c0004t0001g0332 a0002c0004t0001g0333 a0002c0004t0001g0334 others(4): Show |
7 | HG02257.hp2 HG02258.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.-9-799T>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 1/17 | chr7 | 6110326 | |||||||
chr7:6110478 | C | G | 1 | a0003c0002t0001g0058 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-9-647C>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 1/17 | chr7 | 6110478 | |||||||
chr7:6110945 | C | T | 9 | a0005c0011t0001g0038 a0005c0011t0001g0057 a0005c0011t0001g0063 others(6): Show |
9 | HG01346.hp1 HG01891.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.-9-180C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 1/17 | chr7 | 6110945 | |||||||
chr7:6110978 | TAGAA | T | 5 | a0002c0003t0001g0083 a0002c0003t0001g0180 a0002c0003t0001g0181 others(2): Show |
5 | HG00544.hp2 HG03831.hp1 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9-144_-9-141delAA others(2): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 6110978 | ||||||
chr7:6111458 | A | G | 1 | a0002c0050t0001g0294 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.241+84A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | chr7 | 6111458 | |||||||
chr7:6111474 | G | A | 1 | a0007c0025t0001g0212 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.241+100G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | chr7 | 6111474 | |||||||
chr7:6111501 | A | G | 1 | a0003c0002t0001g0179 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.241+127A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | chr7 | 6111501 | |||||||
chr7:6111530 | C | A | 3 | a0001c0001t0001g0211 a0001c0001t0001g0213 a0001c0001t0001g0214 |
3 | HG00140.hp2 HG01106.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.241+156C>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | chr7 | 6111530 | |||||||
chr7:6111579 | ATAT | A | 2 | a0003c0002t0001g0014 a0003c0002t0001g0085 |
3 | HG00558.hp2 NA18957.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.241+211_241+213del others(3): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 6111579 | ||||||
chr7:6111603 | A | AT | 33 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0002c0006t0001g0027 others(30): Show |
35 | HG00741.hp1 HG01167.hp2 HG01175.hp2 others(32): Show |
intron_variant | MODIFIER | c.241+246dupT | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 6111603 | ||||||
chr7:6111666 | G | T | 2 | a0002c0004t0001g0338 a0002c0004t0001g0339 |
2 | HG03540.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.241+292G>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | chr7 | 6111666 | |||||||
chr7:6111715 | G | C | 1 | a0003c0017t0001g0065 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.241+341G>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | chr7 | 6111715 | |||||||
chr7:6111739 | A | G | 3 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0001t0001g0278 |
3 | HG01106.hp1 HG01346.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.241+365A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | chr7 | 6111739 | |||||||
chr7:6111769 | A | AT | 48 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0024 others(45): Show |
59 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.241+412dupT | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 6111769 | ||||||
chr7:6111769 | A | ATT | 207 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0330 others(204): Show |
230 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(227): Show |
intron_variant | MODIFIER | c.241+411_241+412dup others(2): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 6111769 | ||||||
chr7:6111769 | A | ATTT | 14 | a0002c0003t0001g0174 a0002c0003t0001g0183 a0002c0004t0001g0328 others(11): Show |
15 | HG01891.hp1 HG02109.hp1 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.241+410_241+412dup others(3): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 6111769 | ||||||
chr7:6111769 | ATTTTT | A | 9 | a0003c0002t0001g0010 a0003c0002t0001g0011 a0003c0002t0001g0043 others(6): Show |
11 | HG02055.hp1 HG02145.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.241+408_241+412del others(5): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 6111769 | ||||||
chr7:6111800 | A | G | 1 | a0003c0002t0001g0185 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.241+426A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | chr7 | 6111800 | |||||||
chr7:6111905 | G | A | 3 | a0001c0001t0001g0211 a0001c0001t0001g0213 a0001c0001t0001g0214 |
3 | HG00140.hp2 HG01106.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.241+531G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | chr7 | 6111905 | |||||||
chr7:6112051 | A | C | 26 | a0002c0006t0001g0027 a0002c0006t0001g0039 a0002c0006t0001g0313 others(23): Show |
27 | HG01167.hp2 HG01243.hp1 HG01256.hp1 others(24): Show |
intron_variant | MODIFIER | c.241+677A>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | chr7 | 6112051 | |||||||
chr7:6112067 | A | G | 3 | a0005c0011t0001g0029 a0005c0011t0001g0030 a0005c0011t0001g0031 |
3 | HG02630.hp1 HG02895.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.241+693A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | chr7 | 6112067 | |||||||
chr7:6112392 | T | A | 1 | a0001c0001t0001g0276 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.241+1018T>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | chr7 | 6112392 | |||||||
chr7:6112404 | C | T | 2 | a0002c0015t0001g0040 a0002c0015t0001g0041 |
2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.241+1030C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | chr7 | 6112404 | |||||||
chr7:6112415 | A | G | 1 | a0002c0004t0001g0337 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.241+1041A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | chr7 | 6112415 | |||||||
chr7:6112466 | A | G | 1 | a0001c0001t0001g0205 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.241+1092A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | chr7 | 6112466 | |||||||
chr7:6112471 | A | G | 206 | a0001c0001t0001g0330 a0002c0003t0001g0002 a0002c0003t0001g0004 others(203): Show |
231 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(228): Show |
intron_variant | MODIFIER | c.241+1097A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | chr7 | 6112471 | |||||||
chr7:6112547 | T | C | 1 | a0003c0002t0001g0323 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.241+1173T>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | chr7 | 6112547 | |||||||
chr7:6112550 | A | G | 1 | a0002c0035t0001g0072 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.241+1176A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | chr7 | 6112550 | |||||||
chr7:6112900 | C | CT | 55 | a0001c0001t0001g0209 a0001c0001t0001g0250 a0001c0001t0001g0251 others(52): Show |
61 | HG00642.hp1 HG00673.hp1 HG00735.hp2 others(58): Show |
intron_variant | MODIFIER | c.241+1547dupT | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 6112900 | ||||||
chr7:6112900 | C | CTT | 7 | a0002c0050t0001g0294 a0003c0002t0001g0055 a0004c0005t0001g0306 others(4): Show |
7 | HG00280.hp1 HG02630.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.241+1546_241+1547d others(4): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 6112900 | ||||||
chr7:6112900 | C | CTTT | 6 | a0001c0001t0001g0330 a0002c0004t0001g0328 a0002c0004t0001g0329 others(3): Show |
6 | HG02258.hp1 HG02818.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.241+1545_241+1547d others(5): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 6112900 | ||||||
chr7:6112900 | CT | C | 75 | a0001c0001t0001g0215 a0002c0003t0001g0002 a0002c0003t0001g0004 others(72): Show |
89 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.241+1547delT | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 6112900 | ||||||
chr7:6112905 | T | C | 1 | a0003c0008t0001g0088 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.241+1531T>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | chr7 | 6112905 | |||||||
chr7:6112934 | C | T | 2 | a0001c0001t0001g0249 a0001c0001t0001g0271 |
2 | NA19005.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.241+1560C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | chr7 | 6112934 | |||||||
chr7:6113141 | C | T | 1 | a0003c0008t0001g0172 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.241+1767C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | chr7 | 6113141 | |||||||
chr7:6113190 | C | T | 3 | a0003c0002t0001g0171 a0003c0002t0001g0189 a0003c0002t0001g0190 |
3 | NA18951.hp1 NA18986.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.241+1816C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | chr7 | 6113190 | |||||||
chr7:6113296 | C | T | 1 | a0003c0002t0002g0009 | 2 | HG02109.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.241+1922C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | chr7 | 6113296 | |||||||
chr7:6113371 | C | T | 1 | a0002c0035t0001g0072 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.242-1952C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | chr7 | 6113371 | |||||||
chr7:6113375 | C | T | 2 | a0002c0003t0001g0118 a0002c0003t0001g0119 |
2 | NA18747.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.242-1948C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | chr7 | 6113375 | |||||||
chr7:6113451 | T | C | 1 | a0005c0011t0001g0063 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.242-1872T>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | chr7 | 6113451 | |||||||
chr7:6113666 | G | A | 3 | a0001c0001t0001g0274 a0001c0001t0001g0318 a0001c0001t0001g0319 |
3 | HG01496.hp2 HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.242-1657G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | chr7 | 6113666 | |||||||
chr7:6113707 | C | T | 1 | a0002c0004t0001g0328 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.242-1616C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | chr7 | 6113707 | |||||||
chr7:6113765 | G | T | 3 | a0003c0002t0001g0184 a0003c0002t0001g0185 a0019c0030t0001g0173 |
3 | HG02486.hp2 HG02647.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.242-1558G>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | chr7 | 6113765 | |||||||
chr7:6113781 | C | T | 1 | a0017c0040t0001g0064 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.242-1542C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | chr7 | 6113781 | |||||||
chr7:6113791 | T | G | 1 | a0001c0001t0001g0272 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.242-1532T>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | chr7 | 6113791 | |||||||
chr7:6113836 | T | C | 1 | a0004c0009t0001g0079 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.242-1487T>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | chr7 | 6113836 | |||||||
chr7:6113897 | AG | A | 26 | a0003c0002t0002g0009 a0003c0002t0002g0047 a0003c0002t0002g0048 others(23): Show |
30 | HG00280.hp1 HG00642.hp1 HG00673.hp1 others(27): Show |
intron_variant | MODIFIER | c.242-1424delG | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 6113897 | ||||||
chr7:6114010 | A | T | 1 | a0001c0001t0001g0215 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.242-1313A>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | chr7 | 6114010 | |||||||
chr7:6114185 | G | A | 2 | a0009c0026t0001g0053 a0009c0026t0006g0052 |
2 | HG02717.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.242-1138G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | chr7 | 6114185 | |||||||
chr7:6114232 | A | T | 19 | a0004c0005t0001g0008 a0004c0005t0001g0296 a0004c0005t0001g0297 others(16): Show |
22 | HG00280.hp1 HG00642.hp1 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.242-1091A>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | chr7 | 6114232 | |||||||
chr7:6114327 | T | C | 50 | a0001c0001t0001g0330 a0002c0004t0001g0328 a0002c0004t0001g0329 others(47): Show |
56 | HG00280.hp1 HG00642.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.242-996T>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | chr7 | 6114327 | |||||||
chr7:6114405 | A | G | 1 | a0001c0001t0001g0274 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.242-918A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | chr7 | 6114405 | |||||||
chr7:6114417 | A | G | 1 | a0003c0002t0001g0170 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.242-906A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | chr7 | 6114417 | |||||||
chr7:6114488 | C | G | 1 | a0002c0014t0001g0270 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.242-835C>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | chr7 | 6114488 | |||||||
chr7:6114627 | C | T | 1 | a0002c0004t0001g0335 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.242-696C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | chr7 | 6114627 | |||||||
chr7:6114646 | A | G | 8 | a0001c0001t0001g0201 a0001c0001t0001g0248 a0002c0004t0001g0332 others(5): Show |
8 | HG02257.hp2 HG02258.hp2 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.242-677A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | chr7 | 6114646 | |||||||
chr7:6114654 | G | A | 6 | a0002c0004t0001g0332 a0002c0004t0001g0333 a0002c0004t0001g0334 others(3): Show |
6 | HG02257.hp2 HG02258.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.242-669G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | chr7 | 6114654 | |||||||
chr7:6114654 | G | GTATATAT others(3): Show |
2 | a0003c0002t0001g0014 a0003c0002t0001g0193 |
3 | NA18949.hp2 NA18957.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.242-668_242-667ins others(10): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 6114654 | ||||||
chr7:6114654 | G | GTATATAT others(5): Show |
2 | a0003c0002t0001g0121 a0003c0029t0001g0122 |
2 | NA18979.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.242-668_242-667ins others(12): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 6114654 | ||||||
chr7:6114654 | G | GTATATAT others(7): Show |
1 | a0003c0002t0001g0124 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.242-668_242-667ins others(14): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 6114654 | ||||||
chr7:6114654 | G | GTATATAT others(9): Show |
1 | a0003c0002t0001g0200 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.242-668_242-667ins others(16): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 6114654 | ||||||
chr7:6114656 | G | A | 117 | a0001c0001t0001g0330 a0002c0004t0001g0328 a0002c0004t0001g0329 others(114): Show |
126 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(123): Show |
intron_variant | MODIFIER | c.242-667G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | chr7 | 6114656 | |||||||
chr7:6114656 | G | GTATATAT others(1): Show |
6 | a0002c0003t0001g0028 a0002c0003t0001g0174 a0002c0003t0001g0180 others(3): Show |
6 | HG00544.hp2 NA18952.hp1 NA18953.hp2 others(3): Show |
intron_variant | MODIFIER | c.242-651_242-644dup others(8): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 6114656 | ||||||
chr7:6114656 | G | GTATATAT others(3): Show |
4 | a0002c0003t0001g0092 a0002c0004t0001g0325 a0002c0007t0001g0019 others(1): Show |
5 | HG01081.hp2 HG01884.hp2 HG02080.hp1 others(2): Show |
intron_variant | MODIFIER | c.242-653_242-644dup others(10): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 6114656 | ||||||
chr7:6114656 | G | GTATATAT others(7): Show |
1 | a0002c0007t0004g0293 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.242-657_242-644dup others(14): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 6114656 | ||||||
chr7:6114656 | G | GTATATAT others(11): Show |
3 | a0002c0003t0001g0161 a0002c0007t0001g0160 a0015c0051t0001g0312 |
3 | HG01256.hp1 HG02300.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.242-661_242-644dup others(18): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 6114656 | ||||||
chr7:6114656 | G | GTATATAT others(15): Show |
1 | a0003c0008t0001g0157 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.242-665_242-644dup others(22): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 6114656 | ||||||
chr7:6114656 | G | GTGTATAT others(7): Show |
2 | a0002c0010t0001g0321 a0005c0011t0001g0031 |
2 | HG02895.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.242-666_242-665ins others(14): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 6114656 | ||||||
chr7:6114656 | G | GTGTATAT others(13): Show |
1 | a0002c0006t0001g0314 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.242-666_242-665ins others(20): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 6114656 | ||||||
chr7:6114656 | G | GTGTGTAT others(7): Show |
2 | a0003c0012t0001g0074 a0003c0012t0001g0075 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.242-666_242-665ins others(14): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 6114656 | ||||||
chr7:6114658 | A | G | 9 | a0002c0003t0001g0117 a0002c0003t0001g0119 a0002c0006t0003g0036 others(6): Show |
9 | HG01081.hp1 HG01109.hp1 HG02129.hp2 others(6): Show |
intron_variant | MODIFIER | c.242-665A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | chr7 | 6114658 | |||||||
chr7:6114670 | A | AT | 6 | a0001c0001t0001g0245 a0001c0013t0001g0042 a0001c0013t0001g0242 others(3): Show |
6 | HG01516.hp1 HG01934.hp1 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.242-652dupT | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 6114670 | ||||||
chr7:6114670 | A | T | 5 | a0001c0001t0001g0023 a0001c0001t0001g0214 a0001c0001t0001g0246 others(2): Show |
5 | HG00099.hp1 HG00140.hp1 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.242-653A>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | chr7 | 6114670 | |||||||
chr7:6114672 | A | AT | 4 | a0001c0001t0001g0001 a0001c0001t0001g0225 a0001c0001t0001g0236 others(1): Show |
8 | HG02015.hp1 HG02622.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.242-650dupT | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 6114672 | ||||||
chr7:6114672 | A | ATT | 5 | a0001c0001t0001g0210 a0001c0001t0001g0227 a0001c0001t0001g0276 others(2): Show |
5 | HG01106.hp1 HG01346.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.242-650_242-649ins others(2): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 6114672 | ||||||
chr7:6114672 | A | T | 16 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(13): Show |
16 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(13): Show |
intron_variant | MODIFIER | c.242-651A>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | chr7 | 6114672 | |||||||
chr7:6114672 | ATATATAT others(9): Show |
A | 13 | a0001c0001t0001g0330 a0002c0004t0001g0328 a0002c0004t0001g0329 others(10): Show |
15 | HG00673.hp1 HG00741.hp2 HG01123.hp1 others(12): Show |
intron_variant | MODIFIER | c.242-649_242-634del others(16): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 6114672 | ||||||
chr7:6114674 | A | AT | 12 | a0001c0001t0001g0003 a0001c0001t0001g0203 a0001c0001t0001g0211 others(9): Show |
14 | HG00140.hp2 HG01069.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.242-648dupT | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 6114674 | ||||||
chr7:6114674 | A | ATT | 6 | a0001c0001t0001g0001 a0001c0001t0001g0206 a0001c0001t0001g0223 others(3): Show |
6 | HG00099.hp2 HG01358.hp2 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.242-648_242-647ins others(2): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 6114674 | ||||||
chr7:6114674 | A | T | 32 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0021 others(29): Show |
38 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(35): Show |
intron_variant | MODIFIER | c.242-649A>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | chr7 | 6114674 | |||||||
chr7:6114674 | ATATATTT others(9): Show |
A | 17 | a0003c0002t0002g0009 a0003c0002t0002g0047 a0003c0002t0002g0048 others(14): Show |
19 | HG00280.hp1 HG00642.hp1 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.242-647_242-632del others(16): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 6114674 | ||||||
chr7:6114676 | A | AT | 26 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0026 others(23): Show |
28 | HG00438.hp1 HG00639.hp1 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.242-646dupT | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 6114676 | ||||||
chr7:6114676 | A | ATT | 14 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0024 others(11): Show |
14 | HG00733.hp2 HG00738.hp1 HG01515.hp1 others(11): Show |
intron_variant | MODIFIER | c.242-646_242-645ins others(2): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 6114676 | ||||||
chr7:6114676 | A | T | 53 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(50): Show |
62 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(59): Show |
intron_variant | MODIFIER | c.242-647A>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | chr7 | 6114676 | |||||||
chr7:6114677 | TA | T | 3 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0275 |
3 | HG02293.hp2 NA18980.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.242-645delA | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | chr7 | 6114677 | |||||||
chr7:6114678 | A | AT | 12 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0024 others(9): Show |
12 | HG01168.hp2 HG01952.hp1 HG01952.hp2 others(9): Show |
intron_variant | MODIFIER | c.242-617dupT | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 6114678 | ||||||
chr7:6114678 | A | ATATAT | 7 | a0002c0003t0001g0066 a0002c0003t0001g0093 a0003c0002t0001g0010 others(4): Show |
7 | HG02055.hp1 HG02717.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.242-644_242-643ins others(5): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 6114678 | ||||||
chr7:6114678 | A | ATATATAT others(4): Show |
5 | a0002c0003t0001g0117 a0002c0004t0001g0326 a0003c0002t0001g0146 others(2): Show |
5 | HG00544.hp1 HG00733.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.242-644_242-643ins others(11): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 6114678 | ||||||
chr7:6114678 | A | ATATATAT others(6): Show |
3 | a0002c0004t0001g0327 a0002c0004t0001g0335 a0003c0002t0001g0178 |
3 | HG00741.hp1 HG02451.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.242-644_242-643ins others(13): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 6114678 | ||||||
chr7:6114678 | A | ATATATAT others(8): Show |
1 | a0002c0007t0001g0169 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.242-644_242-643ins others(15): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 6114678 | ||||||
chr7:6114678 | A | ATATATAT others(10): Show |
1 | a0003c0002t0001g0188 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.242-644_242-643ins others(17): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 6114678 | ||||||
chr7:6114678 | A | ATATATAT others(18): Show |
1 | a0002c0006t0001g0027 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.242-644_242-643ins others(25): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 6114678 | ||||||
chr7:6114678 | A | ATATATAT others(15): Show |
1 | a0002c0006t0001g0039 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.242-644_242-643ins others(22): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 6114678 | ||||||
chr7:6114678 | A | ATATATAT others(10): Show |
3 | a0002c0027t0001g0316 a0003c0002t0001g0175 a0003c0012t0001g0073 |
3 | HG01081.hp1 HG02735.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.242-644_242-643ins others(17): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 6114678 | ||||||
chr7:6114678 | A | ATATATAT others(11): Show |
2 | a0002c0010t0001g0197 a0011c0016t0001g0168 |
2 | HG02559.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.242-644_242-643ins others(18): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 6114678 | ||||||
chr7:6114678 | A | ATATATAT others(13): Show |
1 | a0002c0027t0001g0311 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.242-644_242-643ins others(20): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 6114678 | ||||||
chr7:6114678 | A | ATATATAT others(14): Show |
1 | a0002c0006t0005g0317 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.242-644_242-643ins others(21): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 6114678 | ||||||
chr7:6114678 | A | ATATATAT others(16): Show |
1 | a0002c0006t0005g0315 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.242-644_242-643ins others(23): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 6114678 | ||||||
chr7:6114678 | A | ATATATAT others(7): Show |
1 | a0002c0028t0001g0002 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.242-644_242-643ins others(14): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 6114678 | ||||||
chr7:6114678 | A | ATATATAT others(8): Show |
2 | a0003c0002t0001g0128 a0003c0002t0001g0129 |
2 | NA18989.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.242-644_242-643ins others(15): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 6114678 | ||||||
chr7:6114678 | A | ATATATAT others(9): Show |
2 | a0002c0014t0001g0020 a0003c0002t0001g0127 |
2 | HG02071.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.242-644_242-643ins others(16): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 6114678 | ||||||
chr7:6114678 | A | ATATATAT others(10): Show |
1 | a0002c0010t0001g0198 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.242-644_242-643ins others(17): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 6114678 | ||||||
chr7:6114678 | A | ATATATAT others(12): Show |
1 | a0002c0010t0001g0195 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.242-644_242-643ins others(19): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 6114678 | ||||||
chr7:6114678 | A | ATATATAT others(5): Show |
8 | a0003c0002t0001g0018 a0003c0002t0001g0085 a0003c0002t0001g0133 others(5): Show |
8 | HG00423.hp1 HG00558.hp2 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.242-644_242-643ins others(12): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 6114678 | ||||||
chr7:6114678 | A | ATATATAT others(6): Show |
5 | a0002c0003t0001g0110 a0002c0003t0001g0111 a0002c0028t0001g0095 others(2): Show |
5 | HG02056.hp1 HG02273.hp1 NA19007.hp1 others(2): Show |
intron_variant | MODIFIER | c.242-644_242-643ins others(13): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 6114678 | ||||||
chr7:6114678 | A | ATATATAT others(8): Show |
3 | a0003c0002t0001g0171 a0003c0002t0001g0189 a0003c0002t0001g0190 |
3 | NA18951.hp1 NA18986.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.242-644_242-643ins others(15): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 6114678 | ||||||
chr7:6114678 | A | ATATATAT others(9): Show |
1 | a0002c0014t0001g0020 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.242-644_242-643ins others(16): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 6114678 | ||||||
chr7:6114678 | A | ATATATAT others(10): Show |
2 | a0002c0010t0001g0196 a0003c0002t0001g0138 |
2 | HG01243.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.242-644_242-643ins others(17): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 6114678 | ||||||
chr7:6114678 | A | ATATATAT others(11): Show |
2 | a0002c0006t0001g0324 a0002c0010t0001g0199 |
2 | HG01167.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.242-644_242-643ins others(18): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 6114678 | ||||||
chr7:6114678 | A | ATATATAT others(3): Show |
23 | a0002c0003t0001g0002 a0002c0003t0001g0016 a0002c0003t0001g0083 others(20): Show |
28 | HG00597.hp2 HG00642.hp2 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.242-644_242-643ins others(10): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 6114678 | ||||||
chr7:6114678 | A | ATATATAT others(4): Show |
10 | a0002c0003t0001g0104 a0002c0003t0001g0108 a0003c0002t0001g0007 others(7): Show |
10 | HG01358.hp1 HG02040.hp2 HG03710.hp1 others(7): Show |
intron_variant | MODIFIER | c.242-644_242-643ins others(11): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 6114678 | ||||||
chr7:6114678 | A | ATATATAT others(5): Show |
8 | a0002c0003t0001g0002 a0003c0002t0001g0015 a0003c0002t0001g0043 others(5): Show |
8 | HG00621.hp2 HG02145.hp1 NA18960.hp1 others(5): Show |
intron_variant | MODIFIER | c.242-644_242-643ins others(12): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 6114678 | ||||||
chr7:6114678 | A | ATATATAT others(6): Show |
4 | a0002c0003t0001g0096 a0002c0006t0003g0033 a0002c0006t0003g0034 others(1): Show |
4 | HG00673.hp2 HG02809.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.242-644_242-643ins others(13): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 6114678 | ||||||
chr7:6114678 | A | ATATATAT others(7): Show |
2 | a0002c0003t0001g0112 a0002c0006t0003g0036 |
2 | HG02257.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.242-644_242-643ins others(14): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 6114678 | ||||||
chr7:6114678 | A | ATATATAT others(1): Show |
11 | a0002c0003t0001g0002 a0002c0003t0001g0004 a0002c0003t0001g0099 others(8): Show |
13 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(10): Show |
intron_variant | MODIFIER | c.242-644_242-643ins others(8): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 6114678 | ||||||
chr7:6114678 | A | ATATATAT others(3): Show |
5 | a0002c0018t0001g0140 a0003c0002t0001g0141 a0003c0002t0001g0153 others(2): Show |
5 | HG00438.hp2 HG02523.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.242-644_242-643ins others(10): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 6114678 | ||||||
chr7:6114678 | A | ATATATAT others(4): Show |
1 | a0003c0002t0001g0177 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.242-644_242-643ins others(11): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 6114678 | ||||||
chr7:6114678 | A | ATATATAT others(6): Show |
1 | a0002c0003t0001g0118 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.242-644_242-643ins others(13): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 6114678 | ||||||
chr7:6114678 | A | ATATATTT others(3): Show |
2 | a0002c0003t0001g0119 a0003c0002t0001g0144 |
2 | NA18955.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.242-644_242-643ins others(10): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 6114678 | ||||||
chr7:6114678 | A | ATATATTT others(4): Show |
3 | a0002c0003t0001g0167 a0002c0006t0003g0035 a0003c0002t0001g0007 |
3 | HG03041.hp2 HG03239.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.242-644_242-643ins others(11): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 6114678 | ||||||
chr7:6114678 | A | ATT | 11 | a0001c0001t0001g0001 a0001c0001t0001g0222 a0001c0001t0001g0230 others(8): Show |
12 | HG01167.hp1 HG01168.hp1 HG01256.hp2 others(9): Show |
intron_variant | MODIFIER | c.242-618_242-617dup others(2): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 6114678 | ||||||
chr7:6114678 | A | T | 100 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(97): Show |
117 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(114): Show |
intron_variant | MODIFIER | c.242-645A>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | chr7 | 6114678 | |||||||
chr7:6114679 | T | TATATATA | 3 | a0002c0010t0001g0194 a0003c0008t0001g0088 a0003c0008t0001g0125 |
3 | HG02897.hp1 NA18985.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.242-644_242-643ins others(7): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | chr7 | 6114679 | |||||||
chr7:6114679 | T | TATATATA others(2): Show |
7 | a0002c0003t0001g0091 a0002c0004t0001g0332 a0002c0004t0001g0333 others(4): Show |
7 | HG02257.hp2 HG02922.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.242-644_242-643ins others(9): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | chr7 | 6114679 | |||||||
chr7:6114679 | T | TATATATA others(4): Show |
1 | a0003c0002t0001g0120 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.242-644_242-643ins others(11): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | chr7 | 6114679 | |||||||
chr7:6114679 | T | TATATATA others(6): Show |
2 | a0002c0007t0004g0292 a0003c0020t0001g0123 |
2 | HG02027.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.242-644_242-643ins others(13): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | chr7 | 6114679 | |||||||
chr7:6114679 | T | TATATATA others(10): Show |
1 | a0003c0002t0001g0159 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.242-644_242-643ins others(17): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | chr7 | 6114679 | |||||||
chr7:6114679 | T | TATATATA others(12): Show |
1 | a0002c0007t0009g0158 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.242-644_242-643ins others(19): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | chr7 | 6114679 | |||||||
chr7:6114680 | T | A | 9 | a0002c0003t0001g0174 a0002c0003t0001g0180 a0002c0004t0001g0334 others(6): Show |
9 | HG00544.hp2 HG02258.hp2 HG06807.hp1 others(6): Show |
intron_variant | MODIFIER | c.242-643T>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | chr7 | 6114680 | |||||||
chr7:6114681 | T | A | 8 | a0002c0004t0001g0332 a0002c0004t0001g0333 a0002c0004t0001g0336 others(5): Show |
8 | HG02257.hp2 HG02897.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.242-642T>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | chr7 | 6114681 | |||||||
chr7:6114682 | T | A | 3 | a0002c0004t0001g0334 a0002c0004t0001g0337 a0003c0002t0001g0126 |
3 | HG02258.hp2 HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.242-641T>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | chr7 | 6114682 | |||||||
chr7:6114683 | T | A | 2 | a0003c0008t0001g0088 a0003c0008t0001g0125 |
2 | NA18985.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.242-640T>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | chr7 | 6114683 | |||||||
chr7:6114723 | C | G | 47 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0024 others(44): Show |
58 | HG00438.hp1 HG00639.hp1 HG01069.hp2 others(55): Show |
intron_variant | MODIFIER | c.242-600C>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | chr7 | 6114723 | |||||||
chr7:6114806 | T | A | 1 | a0001c0048t0001g0253 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.242-517T>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | chr7 | 6114806 | |||||||
chr7:6114828 | C | G | 1 | a0004c0005t0001g0305 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.242-495C>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | chr7 | 6114828 | |||||||
chr7:6114970 | G | A | 1 | a0003c0002t0001g0184 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.242-353G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | chr7 | 6114970 | |||||||
chr7:6114976 | C | T | 1 | a0003c0017t0001g0065 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.242-347C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | chr7 | 6114976 | |||||||
chr7:6114992 | A | G | 1 | a0005c0019t0001g0050 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.242-331A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | chr7 | 6114992 | |||||||
chr7:6115000 | A | T | 1 | a0002c0007t0001g0164 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.242-323A>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | chr7 | 6115000 | |||||||
chr7:6115031 | C | A | 12 | a0002c0004t0001g0325 a0002c0004t0001g0326 a0002c0004t0001g0327 others(9): Show |
12 | HG02257.hp2 HG02258.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.242-292C>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | chr7 | 6115031 | |||||||
chr7:6115046 | C | G | 1 | a0003c0002t0001g0185 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.242-277C>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | chr7 | 6115046 | |||||||
chr7:6115160 | C | T | 1 | a0003c0017t0001g0065 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.242-163C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 2/17 | chr7 | 6115160 | |||||||
chr7:6115535 | G | T | 19 | a0001c0001t0001g0012 a0001c0001t0001g0022 a0001c0001t0001g0023 others(16): Show |
20 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(17): Show |
intron_variant | MODIFIER | c.442+12G>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6115535 | |||||||
chr7:6115960 | T | C | 1 | a0001c0031t0001g0216 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.442+437T>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6115960 | |||||||
chr7:6116018 | C | T | 1 | a0002c0035t0001g0072 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.442+495C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6116018 | |||||||
chr7:6116059 | G | A | 1 | a0002c0035t0001g0072 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.442+536G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6116059 | |||||||
chr7:6116077 | C | T | 1 | a0003c0002t0002g0047 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.442+554C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6116077 | |||||||
chr7:6116103 | C | CA | 51 | a0001c0001t0001g0024 a0001c0001t0001g0026 a0001c0001t0001g0201 others(48): Show |
54 | HG00735.hp2 HG01106.hp1 HG01109.hp1 others(51): Show |
intron_variant | MODIFIER | c.442+598dupA | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 6116103 | ||||||
chr7:6116103 | C | CAA | 34 | a0001c0001t0001g0249 a0001c0001t0001g0318 a0002c0010t0001g0194 others(31): Show |
35 | HG00423.hp1 HG00621.hp2 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.442+597_442+598dup others(2): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 6116103 | ||||||
chr7:6116121 | AC | A | 11 | a0003c0002t0001g0010 a0003c0002t0001g0011 a0003c0002t0001g0043 others(8): Show |
13 | HG02055.hp1 HG02145.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.442+599delC | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6116121 | |||||||
chr7:6116122 | C | A | 217 | a0002c0003t0001g0002 a0002c0003t0001g0004 a0002c0003t0001g0006 others(214): Show |
241 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(238): Show |
intron_variant | MODIFIER | c.442+599C>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6116122 | |||||||
chr7:6116140 | T | C | 1 | a0007c0025t0001g0244 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.442+617T>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6116140 | |||||||
chr7:6116242 | C | A | 202 | a0002c0003t0001g0002 a0002c0003t0001g0004 a0002c0003t0001g0006 others(199): Show |
227 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(224): Show |
intron_variant | MODIFIER | c.442+719C>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6116242 | |||||||
chr7:6116254 | C | T | 1 | a0003c0002t0001g0055 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.442+731C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6116254 | |||||||
chr7:6116255 | G | A | 1 | a0002c0050t0001g0294 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.442+732G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6116255 | |||||||
chr7:6116369 | G | T | 2 | a0003c0002t0001g0184 a0003c0002t0001g0185 |
2 | HG02486.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.442+846G>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6116369 | |||||||
chr7:6116372 | A | G | 1 | a0003c0017t0001g0065 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.442+849A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6116372 | |||||||
chr7:6116508 | G | C | 1 | a0003c0012t0001g0073 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.442+985G>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6116508 | |||||||
chr7:6117104 | A | G | 8 | a0003c0002t0001g0010 a0003c0002t0001g0011 a0003c0002t0001g0054 others(5): Show |
10 | HG02055.hp1 HG02572.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.442+1581A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6117104 | |||||||
chr7:6117169 | C | T | 1 | a0003c0002t0001g0037 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.442+1646C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6117169 | |||||||
chr7:6117219 | G | T | 1 | a0001c0001t0001g0215 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.442+1696G>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6117219 | |||||||
chr7:6117240 | C | T | 1 | a0003c0017t0001g0065 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.442+1717C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6117240 | |||||||
chr7:6117481 | G | A | 1 | a0003c0002t0001g0127 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.442+1958G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6117481 | |||||||
chr7:6117513 | A | G | 1 | a0001c0001t0001g0307 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.442+1990A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6117513 | |||||||
chr7:6117709 | G | T | 229 | a0002c0003t0001g0002 a0002c0003t0001g0004 a0002c0003t0001g0006 others(226): Show |
255 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(252): Show |
intron_variant | MODIFIER | c.442+2186G>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6117709 | |||||||
chr7:6117816 | C | T | 1 | a0003c0017t0001g0065 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.442+2293C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6117816 | |||||||
chr7:6117885 | T | C | 203 | a0002c0003t0001g0002 a0002c0003t0001g0004 a0002c0003t0001g0006 others(200): Show |
228 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(225): Show |
intron_variant | MODIFIER | c.442+2362T>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6117885 | |||||||
chr7:6117891 | G | C | 1 | a0002c0004t0001g0338 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.442+2368G>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6117891 | |||||||
chr7:6117968 | C | T | 1 | a0002c0035t0001g0072 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.442+2445C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6117968 | |||||||
chr7:6118144 | A | G | 2 | a0005c0019t0001g0050 a0005c0019t0001g0051 |
2 | HG02717.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.442+2621A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6118144 | |||||||
chr7:6118210 | G | A | 146 | a0002c0003t0001g0002 a0002c0003t0001g0004 a0002c0003t0001g0006 others(143): Show |
165 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(162): Show |
intron_variant | MODIFIER | c.442+2687G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6118210 | |||||||
chr7:6118261 | G | T | 1 | a0003c0002t0001g0155 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.442+2738G>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6118261 | |||||||
chr7:6118439 | A | G | 1 | a0008c0021t0001g0060 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.442+2916A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6118439 | |||||||
chr7:6118543 | A | G | 1 | a0004c0005t0001g0304 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.442+3020A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6118543 | |||||||
chr7:6118553 | C | A | 24 | a0002c0003t0001g0094 a0002c0006t0001g0027 a0002c0006t0001g0039 others(21): Show |
25 | HG01167.hp2 HG01243.hp1 HG01256.hp1 others(22): Show |
intron_variant | MODIFIER | c.442+3030C>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6118553 | |||||||
chr7:6118575 | A | G | 1 | a0003c0017t0001g0065 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.442+3052A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6118575 | |||||||
chr7:6118588 | T | C | 1 | a0002c0006t0001g0039 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.442+3065T>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6118588 | |||||||
chr7:6118708 | C | T | 3 | a0003c0012t0001g0073 a0003c0012t0001g0074 a0003c0012t0001g0075 |
3 | HG01081.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.442+3185C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6118708 | |||||||
chr7:6118724 | A | G | 10 | a0002c0004t0001g0340 a0003c0002t0001g0010 a0003c0002t0001g0011 others(7): Show |
12 | HG02055.hp1 HG02145.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.442+3201A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6118724 | |||||||
chr7:6118837 | C | T | 1 | a0005c0024t0001g0062 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.442+3314C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6118837 | |||||||
chr7:6119046 | C | G | 69 | a0002c0018t0001g0140 a0002c0018t0001g0150 a0003c0002t0001g0007 others(66): Show |
74 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.442+3523C>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6119046 | |||||||
chr7:6119048 | C | G | 1 | a0002c0003t0001g0116 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.442+3525C>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6119048 | |||||||
chr7:6119147 | T | C | 4 | a0003c0002t0002g0009 a0003c0002t0002g0047 a0003c0002t0002g0048 others(1): Show |
5 | HG01175.hp2 HG02109.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.442+3624T>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6119147 | |||||||
chr7:6119290 | T | C | 1 | a0002c0050t0001g0294 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.442+3767T>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6119290 | |||||||
chr7:6119302 | G | A | 24 | a0002c0003t0001g0094 a0002c0006t0001g0027 a0002c0006t0001g0039 others(21): Show |
25 | HG01167.hp2 HG01243.hp1 HG01256.hp1 others(22): Show |
intron_variant | MODIFIER | c.442+3779G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6119302 | |||||||
chr7:6119387 | C | G | 1 | a0001c0001t0001g0288 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.442+3864C>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6119387 | |||||||
chr7:6119436 | G | A | 24 | a0002c0003t0001g0094 a0002c0006t0001g0027 a0002c0006t0001g0039 others(21): Show |
25 | HG01167.hp2 HG01243.hp1 HG01256.hp1 others(22): Show |
intron_variant | MODIFIER | c.442+3913G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6119436 | |||||||
chr7:6119468 | G | A | 1 | a0003c0002t0001g0323 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.442+3945G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6119468 | |||||||
chr7:6119561 | C | T | 1 | a0003c0002t0001g0323 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.442+4038C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6119561 | |||||||
chr7:6119691 | T | G | 2 | a0009c0026t0001g0053 a0009c0026t0006g0052 |
2 | HG02717.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.442+4168T>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6119691 | |||||||
chr7:6119713 | T | G | 1 | a0002c0035t0001g0072 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.442+4190T>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6119713 | |||||||
chr7:6119816 | G | A | 67 | a0002c0018t0001g0140 a0002c0018t0001g0150 a0003c0002t0001g0007 others(64): Show |
72 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.442+4293G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6119816 | |||||||
chr7:6119876 | T | A | 1 | a0015c0051t0001g0312 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.442+4353T>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6119876 | |||||||
chr7:6119925 | C | T | 1 | a0004c0009t0001g0082 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.442+4402C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6119925 | |||||||
chr7:6119927 | C | T | 1 | a0001c0001t0001g0267 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.442+4404C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6119927 | |||||||
chr7:6119931 | C | T | 2 | a0002c0003t0001g0118 a0002c0003t0001g0119 |
2 | NA18747.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.442+4408C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6119931 | |||||||
chr7:6119963 | T | C | 1 | a0001c0001t0001g0213 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.442+4440T>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6119963 | |||||||
chr7:6119989 | G | A | 1 | a0002c0004t0001g0335 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.442+4466G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6119989 | |||||||
chr7:6119996 | C | T | 1 | a0002c0010t0001g0198 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.442+4473C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6119996 | |||||||
chr7:6119998 | C | A | 1 | a0010c0022t0001g0076 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.442+4475C>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6119998 | |||||||
chr7:6120004 | C | T | 9 | a0003c0002t0001g0010 a0003c0002t0001g0011 a0003c0002t0001g0043 others(6): Show |
11 | HG02055.hp1 HG02145.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.442+4481C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6120004 | |||||||
chr7:6120066 | G | A | 2 | a0002c0015t0001g0040 a0002c0015t0001g0041 |
2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.442+4543G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6120066 | |||||||
chr7:6120458 | G | A | 1 | a0003c0017t0001g0065 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.442+4935G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6120458 | |||||||
chr7:6120590 | A | G | 1 | a0001c0001t0001g0266 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.442+5067A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6120590 | |||||||
chr7:6120593 | C | A | 1 | a0001c0001t0001g0246 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.442+5070C>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6120593 | |||||||
chr7:6120653 | G | A | 2 | a0003c0002t0001g0184 a0019c0030t0001g0173 |
2 | HG02647.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.442+5130G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6120653 | |||||||
chr7:6120764 | A | G | 1 | a0003c0017t0001g0065 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.442+5241A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6120764 | |||||||
chr7:6120918 | A | G | 28 | a0002c0004t0001g0328 a0002c0004t0001g0329 a0003c0002t0002g0009 others(25): Show |
32 | HG00280.hp1 HG00642.hp1 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.442+5395A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6120918 | |||||||
chr7:6120965 | T | C | 1 | a0001c0001t0001g0245 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.442+5442T>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6120965 | |||||||
chr7:6121074 | A | G | 1 | a0001c0001t0001g0279 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.442+5551A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6121074 | |||||||
chr7:6121082 | C | T | 1 | a0003c0002t0001g0154 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.442+5559C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6121082 | |||||||
chr7:6121231 | A | C | 1 | a0002c0006t0001g0324 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.442+5708A>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6121231 | |||||||
chr7:6121283 | A | G | 2 | a0001c0001t0001g0026 a0001c0001t0001g0307 |
3 | HG03669.hp2 HG03710.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.442+5760A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6121283 | |||||||
chr7:6121301 | G | C | 1 | a0001c0001t0001g0221 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.442+5778G>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6121301 | |||||||
chr7:6121381 | A | G | 1 | a0003c0002t0001g0323 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.442+5858A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6121381 | |||||||
chr7:6121381 | A | T | 1 | a0001c0001t0001g0265 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.442+5858A>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6121381 | |||||||
chr7:6121430 | G | A | 216 | a0002c0003t0001g0002 a0002c0003t0001g0004 a0002c0003t0001g0006 others(213): Show |
240 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(237): Show |
intron_variant | MODIFIER | c.442+5907G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6121430 | |||||||
chr7:6121478 | G | A | 1 | a0001c0001t0001g0209 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.442+5955G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6121478 | |||||||
chr7:6121626 | C | T | 1 | a0003c0002t0001g0058 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.442+6103C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6121626 | |||||||
chr7:6121920 | A | G | 1 | a0002c0050t0001g0294 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.442+6397A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6121920 | |||||||
chr7:6121978 | A | G | 3 | a0001c0001t0001g0246 a0002c0004t0001g0333 a0002c0004t0001g0336 |
3 | HG00140.hp1 HG03098.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.442+6455A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6121978 | |||||||
chr7:6121984 | C | T | 1 | a0018c0036t0001g0264 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.442+6461C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6121984 | |||||||
chr7:6121999 | T | C | 2 | a0002c0015t0001g0040 a0002c0015t0001g0041 |
2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.442+6476T>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6121999 | |||||||
chr7:6122007 | A | G | 1 | a0003c0017t0001g0065 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.442+6484A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6122007 | |||||||
chr7:6122111 | T | A | 9 | a0005c0011t0001g0038 a0005c0011t0001g0057 a0005c0011t0001g0063 others(6): Show |
9 | HG01346.hp1 HG01891.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.442+6588T>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6122111 | |||||||
chr7:6122184 | C | G | 1 | a0003c0017t0001g0065 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.442+6661C>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6122184 | |||||||
chr7:6122279 | G | GT | 10 | a0001c0001t0001g0220 a0001c0001t0001g0237 a0001c0001t0001g0251 others(7): Show |
10 | HG00438.hp2 HG00544.hp2 HG00735.hp2 others(7): Show |
intron_variant | MODIFIER | c.442+6775dupT | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 6122279 | ||||||
chr7:6122279 | GT | G | 57 | a0001c0001t0001g0222 a0001c0001t0001g0257 a0002c0003t0001g0118 others(54): Show |
62 | HG00280.hp1 HG00642.hp1 HG00673.hp1 others(59): Show |
intron_variant | MODIFIER | c.442+6775delT | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 6122279 | ||||||
chr7:6122286 | T | G | 1 | a0001c0001t0001g0209 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.442+6763T>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6122286 | |||||||
chr7:6122287 | T | G | 2 | a0005c0019t0001g0050 a0005c0019t0001g0051 |
2 | HG02717.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.442+6764T>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6122287 | |||||||
chr7:6122325 | G | C | 2 | a0001c0001t0001g0071 a0001c0001t0001g0257 |
2 | HG02155.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.442+6802G>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6122325 | |||||||
chr7:6122431 | A | G | 1 | a0003c0002t0001g0151 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.442+6908A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6122431 | |||||||
chr7:6122468 | G | A | 2 | a0002c0007t0001g0163 a0020c0033t0001g0162 |
2 | HG01884.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.442+6945G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6122468 | |||||||
chr7:6122484 | G | A | 1 | a0003c0002t0001g0043 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.442+6961G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6122484 | |||||||
chr7:6122540 | G | A | 1 | a0005c0011t0001g0029 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.442+7017G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6122540 | |||||||
chr7:6122556 | C | T | 1 | a0002c0035t0001g0072 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.442+7033C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6122556 | |||||||
chr7:6122669 | A | T | 28 | a0002c0006t0001g0027 a0002c0006t0001g0039 a0002c0006t0001g0313 others(25): Show |
29 | HG01167.hp2 HG01168.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.442+7146A>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6122669 | |||||||
chr7:6122771 | A | G | 1 | a0004c0005t0001g0303 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.442+7248A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6122771 | |||||||
chr7:6122788 | G | T | 15 | a0002c0003t0001g0161 a0002c0007t0001g0019 a0002c0007t0001g0160 others(12): Show |
16 | HG00621.hp1 HG01081.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.442+7265G>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6122788 | |||||||
chr7:6122789 | A | T | 15 | a0002c0003t0001g0161 a0002c0007t0001g0019 a0002c0007t0001g0160 others(12): Show |
16 | HG00621.hp1 HG01081.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.442+7266A>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6122789 | |||||||
chr7:6122800 | C | T | 1 | a0003c0002t0001g0200 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.442+7277C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6122800 | |||||||
chr7:6122801 | A | G | 230 | a0002c0003t0001g0002 a0002c0003t0001g0004 a0002c0003t0001g0006 others(227): Show |
256 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(253): Show |
intron_variant | MODIFIER | c.442+7278A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6122801 | |||||||
chr7:6122818 | C | T | 28 | a0002c0006t0001g0027 a0002c0006t0001g0039 a0002c0006t0001g0313 others(25): Show |
29 | HG01167.hp2 HG01168.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.442+7295C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6122818 | |||||||
chr7:6122833 | G | C | 1 | a0002c0003t0001g0077 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.442+7310G>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6122833 | |||||||
chr7:6122839 | A | G | 1 | a0003c0002t0001g0200 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.442+7316A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6122839 | |||||||
chr7:6122856 | T | C | 1 | a0001c0001t0001g0207 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.442+7333T>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6122856 | |||||||
chr7:6122870 | C | G | 1 | a0003c0002t0002g0047 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.442+7347C>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6122870 | |||||||
chr7:6122934 | A | G | 4 | a0002c0050t0001g0294 a0003c0002t0001g0184 a0003c0002t0001g0185 others(1): Show |
4 | HG02486.hp2 HG02647.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.442+7411A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6122934 | |||||||
chr7:6123021 | C | T | 1 | a0002c0035t0001g0072 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.442+7498C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6123021 | |||||||
chr7:6123026 | G | A | 3 | a0005c0011t0001g0029 a0005c0011t0001g0030 a0005c0011t0001g0031 |
3 | HG02630.hp1 HG02895.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.442+7503G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6123026 | |||||||
chr7:6123125 | C | T | 1 | a0002c0050t0001g0294 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.442+7602C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6123125 | |||||||
chr7:6123183 | C | A | 1 | a0003c0002t0001g0177 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.442+7660C>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6123183 | |||||||
chr7:6123208 | A | G | 26 | a0002c0006t0001g0027 a0002c0006t0001g0039 a0002c0006t0001g0313 others(23): Show |
27 | HG01167.hp2 HG01243.hp1 HG01256.hp1 others(24): Show |
intron_variant | MODIFIER | c.442+7685A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6123208 | |||||||
chr7:6123378 | A | G | 163 | a0002c0003t0001g0002 a0002c0003t0001g0004 a0002c0003t0001g0006 others(160): Show |
184 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(181): Show |
intron_variant | MODIFIER | c.442+7855A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6123378 | |||||||
chr7:6123379 | T | C | 83 | a0002c0003t0001g0002 a0002c0003t0001g0004 a0002c0003t0001g0006 others(80): Show |
97 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.442+7856T>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6123379 | |||||||
chr7:6123419 | T | G | 19 | a0001c0001t0001g0012 a0001c0001t0001g0022 a0001c0001t0001g0023 others(16): Show |
20 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(17): Show |
intron_variant | MODIFIER | c.442+7896T>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6123419 | |||||||
chr7:6123428 | C | T | 162 | a0002c0003t0001g0002 a0002c0003t0001g0004 a0002c0003t0001g0006 others(159): Show |
183 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.442+7905C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6123428 | |||||||
chr7:6123445 | C | T | 1 | a0003c0017t0001g0065 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.442+7922C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6123445 | |||||||
chr7:6123459 | C | T | 2 | a0003c0002t0001g0184 a0003c0002t0001g0185 |
2 | HG02486.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.442+7936C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6123459 | |||||||
chr7:6123460 | G | A | 1 | a0004c0005t0001g0296 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.442+7937G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6123460 | |||||||
chr7:6123522 | C | T | 1 | a0003c0002t0002g0047 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.442+7999C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6123522 | |||||||
chr7:6123523 | G | A | 3 | a0003c0012t0001g0073 a0003c0012t0001g0074 a0003c0012t0001g0075 |
3 | HG01081.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.442+8000G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6123523 | |||||||
chr7:6123533 | G | A | 2 | a0004c0005t0001g0297 a0004c0005t0001g0305 |
2 | HG01255.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.442+8010G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6123533 | |||||||
chr7:6123534 | C | T | 12 | a0002c0004t0001g0325 a0002c0004t0001g0326 a0002c0004t0001g0327 others(9): Show |
12 | HG02257.hp2 HG02258.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.442+8011C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6123534 | |||||||
chr7:6123588 | G | A | 37 | a0003c0002t0002g0009 a0003c0002t0002g0047 a0003c0002t0002g0048 others(34): Show |
41 | HG00280.hp1 HG00642.hp1 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.442+8065G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6123588 | |||||||
chr7:6123589 | G | C | 2 | a0002c0003t0001g0091 a0002c0003t0001g0174 |
2 | NA18992.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.442+8066G>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6123589 | |||||||
chr7:6123602 | G | T | 1 | a0003c0002t0001g0179 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.442+8079G>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6123602 | |||||||
chr7:6123739 | T | A | 1 | a0010c0022t0001g0137 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.442+8216T>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6123739 | |||||||
chr7:6123748 | C | T | 11 | a0005c0011t0001g0038 a0005c0011t0001g0057 a0005c0011t0001g0063 others(8): Show |
11 | HG01346.hp1 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.442+8225C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6123748 | |||||||
chr7:6123814 | C | T | 4 | a0001c0001t0001g0236 a0001c0001t0001g0256 a0001c0001t0001g0262 others(1): Show |
4 | HG02074.hp1 NA18747.hp2 NA18947.hp1 others(1): Show |
intron_variant | MODIFIER | c.442+8291C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6123814 | |||||||
chr7:6123826 | C | T | 1 | a0002c0003t0001g0114 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.442+8303C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6123826 | |||||||
chr7:6123832 | C | CA | 156 | a0001c0001t0001g0223 a0001c0001t0001g0237 a0001c0001t0001g0248 others(153): Show |
177 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(174): Show |
intron_variant | MODIFIER | c.442+8328dupA | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 6123832 | ||||||
chr7:6123832 | C | CAA | 15 | a0002c0003t0001g0083 a0002c0003t0001g0096 a0002c0003t0001g0165 others(12): Show |
15 | HG00544.hp2 HG00673.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.442+8327_442+8328d others(4): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 6123832 | ||||||
chr7:6123832 | CA | C | 25 | a0002c0006t0001g0027 a0002c0006t0001g0039 a0002c0006t0001g0313 others(22): Show |
26 | HG01167.hp2 HG01243.hp1 HG01256.hp1 others(23): Show |
intron_variant | MODIFIER | c.442+8328delA | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 6123832 | ||||||
chr7:6124099 | A | G | 4 | a0002c0006t0003g0033 a0002c0006t0003g0034 a0002c0006t0003g0035 others(1): Show |
4 | HG02257.hp1 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.442+8576A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6124099 | |||||||
chr7:6124102 | T | C | 2 | a0001c0001t0001g0318 a0001c0001t0001g0319 |
2 | HG01496.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.442+8579T>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6124102 | |||||||
chr7:6124200 | G | A | 2 | a0003c0002t0001g0184 a0003c0002t0001g0185 |
2 | HG02486.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.442+8677G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6124200 | |||||||
chr7:6124263 | T | C | 1 | a0003c0029t0001g0122 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.442+8740T>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6124263 | |||||||
chr7:6124296 | C | T | 1 | a0003c0002t0001g0258 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.442+8773C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6124296 | |||||||
chr7:6124408 | C | T | 7 | a0002c0010t0001g0194 a0002c0010t0001g0195 a0002c0010t0001g0196 others(4): Show |
7 | HG01243.hp1 HG02280.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.442+8885C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6124408 | |||||||
chr7:6124462 | C | T | 194 | a0002c0003t0001g0002 a0002c0003t0001g0004 a0002c0003t0001g0006 others(191): Show |
217 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(214): Show |
intron_variant | MODIFIER | c.442+8939C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6124462 | |||||||
chr7:6124497 | C | T | 7 | a0003c0002t0002g0009 a0003c0002t0002g0047 a0003c0002t0002g0048 others(4): Show |
8 | HG01175.hp2 HG02109.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.442+8974C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6124497 | |||||||
chr7:6124581 | T | C | 204 | a0002c0003t0001g0002 a0002c0003t0001g0004 a0002c0003t0001g0006 others(201): Show |
229 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(226): Show |
intron_variant | MODIFIER | c.442+9058T>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6124581 | |||||||
chr7:6124647 | T | A | 1 | a0003c0002t0001g0191 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.442+9124T>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6124647 | |||||||
chr7:6124807 | T | C | 1 | a0003c0002t0001g0058 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.442+9284T>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6124807 | |||||||
chr7:6124816 | T | A | 1 | a0003c0002t0001g0054 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.442+9293T>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6124816 | |||||||
chr7:6124863 | G | A | 1 | a0002c0003t0001g0077 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.442+9340G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6124863 | |||||||
chr7:6124902 | C | T | 37 | a0003c0002t0002g0009 a0003c0002t0002g0047 a0003c0002t0002g0048 others(34): Show |
41 | HG00280.hp1 HG00642.hp1 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.442+9379C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6124902 | |||||||
chr7:6124978 | C | T | 1 | a0002c0035t0001g0072 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.442+9455C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6124978 | |||||||
chr7:6125056 | T | C | 336 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(333): Show |
384 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(381): Show |
intron_variant | MODIFIER | c.442+9533T>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6125056 | |||||||
chr7:6125073 | C | G | 37 | a0003c0002t0002g0009 a0003c0002t0002g0047 a0003c0002t0002g0048 others(34): Show |
41 | HG00280.hp1 HG00642.hp1 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.442+9550C>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6125073 | |||||||
chr7:6125096 | G | A | 1 | a0004c0009t0001g0078 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.442+9573G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6125096 | |||||||
chr7:6125100 | G | A | 1 | a0003c0002t0001g0179 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.442+9577G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6125100 | |||||||
chr7:6125182 | AC | A | 19 | a0002c0006t0001g0027 a0002c0006t0001g0039 a0002c0006t0001g0313 others(16): Show |
19 | HG01243.hp1 HG01256.hp1 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.442+9660delC | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6125182 | |||||||
chr7:6125183 | C | A | 5 | a0002c0006t0001g0324 a0002c0010t0001g0197 a0002c0010t0001g0198 others(2): Show |
6 | HG01167.hp2 HG02559.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.442+9660C>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6125183 | |||||||
chr7:6125183 | C | CA | 93 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(90): Show |
97 | HG00423.hp2 HG00544.hp2 HG00642.hp1 others(94): Show |
intron_variant | MODIFIER | c.442+9681dupA | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 6125183 | ||||||
chr7:6125257 | G | A | 23 | a0002c0006t0001g0027 a0002c0006t0001g0039 a0002c0006t0001g0313 others(20): Show |
24 | HG01167.hp2 HG01243.hp1 HG01256.hp1 others(21): Show |
intron_variant | MODIFIER | c.442+9734G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6125257 | |||||||
chr7:6125286 | T | G | 11 | a0002c0003t0001g0161 a0002c0007t0001g0160 a0002c0007t0001g0164 others(8): Show |
11 | HG00621.hp1 HG02027.hp1 HG02300.hp2 others(8): Show |
intron_variant | MODIFIER | c.442+9763T>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6125286 | |||||||
chr7:6125383 | C | T | 1 | a0003c0002t0001g0058 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.442+9860C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6125383 | |||||||
chr7:6125528 | A | G | 1 | a0001c0001t0001g0205 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.442+10005A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6125528 | |||||||
chr7:6125592 | G | A | 181 | a0002c0003t0001g0002 a0002c0003t0001g0004 a0002c0003t0001g0006 others(178): Show |
201 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.442+10069G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6125592 | |||||||
chr7:6125622 | T | C | 1 | a0003c0017t0001g0065 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.442+10099T>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6125622 | |||||||
chr7:6125698 | C | G | 2 | a0003c0002t0001g0184 a0003c0002t0001g0185 |
2 | HG02486.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.443-10143C>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6125698 | |||||||
chr7:6125747 | C | T | 22 | a0002c0006t0001g0027 a0002c0006t0001g0039 a0002c0006t0001g0313 others(19): Show |
22 | HG01167.hp2 HG01243.hp1 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.443-10094C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6125747 | |||||||
chr7:6125880 | T | G | 1 | a0002c0004t0001g0335 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.443-9961T>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6125880 | |||||||
chr7:6125955 | C | G | 1 | a0001c0031t0001g0216 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.443-9886C>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6125955 | |||||||
chr7:6125964 | C | T | 153 | a0002c0003t0001g0002 a0002c0003t0001g0004 a0002c0003t0001g0006 others(150): Show |
172 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(169): Show |
intron_variant | MODIFIER | c.443-9877C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6125964 | |||||||
chr7:6126062 | A | G | 2 | a0001c0001t0001g0021 a0025c0044t0001g0243 |
3 | HG03491.hp2 HG03492.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.443-9779A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6126062 | |||||||
chr7:6126113 | C | T | 23 | a0003c0002t0001g0032 a0003c0002t0001g0120 a0003c0002t0001g0121 others(20): Show |
24 | HG00423.hp1 HG00621.hp2 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.443-9728C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6126113 | |||||||
chr7:6126206 | C | G | 3 | a0005c0011t0001g0029 a0005c0011t0001g0030 a0005c0011t0001g0031 |
3 | HG02630.hp1 HG02895.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.443-9635C>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6126206 | |||||||
chr7:6126249 | T | C | 74 | a0001c0001t0001g0274 a0001c0001t0001g0318 a0001c0001t0001g0319 others(71): Show |
88 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.443-9592T>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6126249 | |||||||
chr7:6126288 | C | CTT | 25 | a0003c0002t0002g0009 a0003c0002t0002g0047 a0003c0002t0002g0048 others(22): Show |
29 | HG00280.hp1 HG00642.hp1 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.443-9540_443-9539d others(4): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 6126288 | ||||||
chr7:6126385 | C | T | 1 | a0002c0003t0001g0112 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.443-9456C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6126385 | |||||||
chr7:6126509 | T | C | 1 | a0002c0004t0001g0336 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.443-9332T>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6126509 | |||||||
chr7:6126585 | G | C | 1 | a0002c0035t0001g0072 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.443-9256G>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6126585 | |||||||
chr7:6126616 | C | T | 1 | a0003c0002t0002g0009 | 2 | HG02109.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.443-9225C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6126616 | |||||||
chr7:6126637 | T | C | 3 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0205 |
3 | HG02083.hp1 NA18945.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.443-9204T>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6126637 | |||||||
chr7:6126830 | G | A | 231 | a0001c0001t0001g0272 a0001c0001t0001g0330 a0002c0003t0001g0002 others(228): Show |
257 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(254): Show |
intron_variant | MODIFIER | c.443-9011G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6126830 | |||||||
chr7:6126899 | G | A | 1 | a0003c0017t0001g0065 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.443-8942G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6126899 | |||||||
chr7:6126992 | T | C | 2 | a0002c0007t0004g0292 a0002c0007t0004g0293 |
2 | HG02027.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.443-8849T>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6126992 | |||||||
chr7:6127023 | A | G | 1 | a0002c0003t0001g0084 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.443-8818A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6127023 | |||||||
chr7:6127316 | T | C | 26 | a0002c0006t0001g0027 a0002c0006t0001g0039 a0002c0006t0001g0313 others(23): Show |
27 | HG01167.hp2 HG01243.hp1 HG01256.hp1 others(24): Show |
intron_variant | MODIFIER | c.443-8525T>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6127316 | |||||||
chr7:6127482 | C | G | 1 | a0002c0018t0001g0150 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.443-8359C>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6127482 | |||||||
chr7:6127580 | T | C | 1 | a0003c0017t0001g0065 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.443-8261T>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6127580 | |||||||
chr7:6127639 | G | A | 1 | a0001c0001t0001g0284 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.443-8202G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6127639 | |||||||
chr7:6127694 | C | T | 1 | a0002c0027t0001g0311 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.443-8147C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6127694 | |||||||
chr7:6127762 | G | A | 2 | a0002c0004t0001g0333 a0002c0004t0001g0336 |
2 | HG03098.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.443-8079G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6127762 | |||||||
chr7:6127964 | C | T | 7 | a0003c0002t0002g0009 a0003c0002t0002g0047 a0003c0002t0002g0048 others(4): Show |
8 | HG01175.hp2 HG02109.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.443-7877C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6127964 | |||||||
chr7:6128024 | A | G | 29 | a0002c0006t0001g0027 a0002c0006t0001g0039 a0002c0006t0001g0313 others(26): Show |
30 | HG01167.hp2 HG01168.hp2 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.443-7817A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6128024 | |||||||
chr7:6128029 | A | C | 234 | a0002c0003t0001g0002 a0002c0003t0001g0004 a0002c0003t0001g0006 others(231): Show |
260 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(257): Show |
intron_variant | MODIFIER | c.443-7812A>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6128029 | |||||||
chr7:6128150 | G | T | 1 | a0001c0001t0001g0235 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.443-7691G>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6128150 | |||||||
chr7:6128164 | G | T | 1 | a0015c0051t0001g0312 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.443-7677G>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6128164 | |||||||
chr7:6128256 | C | CT | 32 | a0001c0001t0001g0255 a0001c0001t0001g0263 a0001c0001t0001g0289 others(29): Show |
33 | HG00438.hp2 HG00673.hp2 HG01167.hp2 others(30): Show |
intron_variant | MODIFIER | c.443-7568dupT | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 6128256 | ||||||
chr7:6128325 | C | T | 2 | a0003c0012t0001g0074 a0003c0012t0001g0075 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.443-7516C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6128325 | |||||||
chr7:6128432 | T | A | 1 | a0005c0011t0001g0038 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.443-7409T>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6128432 | |||||||
chr7:6128469 | A | G | 29 | a0002c0006t0001g0027 a0002c0006t0001g0039 a0002c0006t0001g0313 others(26): Show |
30 | HG01167.hp2 HG01168.hp2 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.443-7372A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6128469 | |||||||
chr7:6128677 | T | G | 9 | a0003c0002t0001g0018 a0003c0002t0001g0068 a0003c0002t0001g0086 others(6): Show |
10 | NA18941.hp2 NA18953.hp1 NA18966.hp2 others(7): Show |
intron_variant | MODIFIER | c.443-7164T>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6128677 | |||||||
chr7:6128685 | A | G | 1 | a0001c0001t0001g0236 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.443-7156A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6128685 | |||||||
chr7:6128690 | G | A | 1 | a0002c0007t0001g0163 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.443-7151G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6128690 | |||||||
chr7:6128809 | T | G | 1 | a0002c0014t0001g0020 | 2 | HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.443-7032T>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6128809 | |||||||
chr7:6128814 | C | T | 152 | a0002c0003t0001g0002 a0002c0003t0001g0004 a0002c0003t0001g0006 others(149): Show |
171 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(168): Show |
intron_variant | MODIFIER | c.443-7027C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6128814 | |||||||
chr7:6128833 | G | A | 7 | a0002c0010t0001g0194 a0002c0010t0001g0195 a0002c0010t0001g0196 others(4): Show |
7 | HG01243.hp1 HG02280.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.443-7008G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6128833 | |||||||
chr7:6128852 | T | TCA | 233 | a0002c0003t0001g0002 a0002c0003t0001g0004 a0002c0003t0001g0006 others(230): Show |
259 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(256): Show |
intron_variant | MODIFIER | c.443-6988_443-6987i others(4): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 6128852 | ||||||
chr7:6128896 | C | T | 5 | a0001c0001t0001g0005 a0001c0001t0001g0283 a0001c0001t0001g0284 others(2): Show |
8 | HG00639.hp1 HG01099.hp2 HG01928.hp1 others(5): Show |
intron_variant | MODIFIER | c.443-6945C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6128896 | |||||||
chr7:6128906 | A | T | 1 | a0003c0002t0001g0151 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.443-6935A>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6128906 | |||||||
chr7:6129087 | C | A | 2 | a0002c0003t0001g0097 a0002c0003t0001g0098 |
2 | HG01891.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.443-6754C>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6129087 | |||||||
chr7:6129112 | C | A | 1 | a0001c0001t0001g0224 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.443-6729C>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6129112 | |||||||
chr7:6129216 | T | G | 1 | a0003c0002t0002g0048 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.443-6625T>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6129216 | |||||||
chr7:6129273 | A | C | 3 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0279 |
3 | HG00438.hp1 HG02015.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.443-6568A>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6129273 | |||||||
chr7:6129276 | C | A | 2 | a0001c0001t0001g0238 a0001c0001t0001g0291 |
2 | HG01192.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.443-6565C>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6129276 | |||||||
chr7:6129426 | G | A | 10 | a0002c0003t0001g0006 a0002c0003t0001g0028 a0002c0003t0001g0066 others(7): Show |
12 | HG00423.hp2 HG02135.hp1 HG02155.hp1 others(9): Show |
intron_variant | MODIFIER | c.443-6415G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6129426 | |||||||
chr7:6129518 | C | T | 3 | a0005c0011t0001g0029 a0005c0011t0001g0030 a0005c0011t0001g0031 |
3 | HG02630.hp1 HG02895.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.443-6323C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6129518 | |||||||
chr7:6129559 | G | GA | 36 | a0001c0001t0001g0202 a0001c0001t0001g0217 a0001c0001t0001g0255 others(33): Show |
37 | HG00438.hp1 HG01167.hp2 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.443-6264dupA | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 6129559 | ||||||
chr7:6129636 | G | A | 1 | a0001c0001t0001g0272 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.443-6205G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6129636 | |||||||
chr7:6129677 | A | G | 2 | a0003c0008t0001g0088 a0003c0008t0001g0125 |
2 | NA18985.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.443-6164A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6129677 | |||||||
chr7:6129738 | C | T | 1 | a0001c0001t0001g0214 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.443-6103C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6129738 | |||||||
chr7:6129860 | C | CA | 12 | a0001c0001t0001g0208 a0001c0001t0001g0237 a0002c0003t0001g0083 others(9): Show |
12 | HG01109.hp1 HG01978.hp1 HG01993.hp2 others(9): Show |
intron_variant | MODIFIER | c.443-5965dupA | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 6129860 | ||||||
chr7:6129860 | C | CAA | 25 | a0002c0006t0001g0027 a0002c0006t0001g0039 a0002c0006t0001g0313 others(22): Show |
26 | HG01167.hp2 HG01243.hp1 HG01256.hp1 others(23): Show |
intron_variant | MODIFIER | c.443-5966_443-5965d others(4): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 6129860 | ||||||
chr7:6129892 | C | A | 1 | a0003c0002t0001g0200 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.443-5949C>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6129892 | |||||||
chr7:6129958 | A | G | 1 | a0002c0050t0001g0294 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.443-5883A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6129958 | |||||||
chr7:6129959 | G | C | 2 | a0003c0002t0001g0184 a0003c0002t0001g0185 |
2 | HG02486.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.443-5882G>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6129959 | |||||||
chr7:6130081 | G | A | 1 | a0001c0001t0001g0225 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.443-5760G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6130081 | |||||||
chr7:6130110 | G | A | 1 | a0004c0038t0001g0044 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.443-5731G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6130110 | |||||||
chr7:6130110 | G | C | 169 | a0002c0003t0001g0002 a0002c0003t0001g0004 a0002c0003t0001g0006 others(166): Show |
189 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(186): Show |
intron_variant | MODIFIER | c.443-5731G>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6130110 | |||||||
chr7:6130141 | G | A | 1 | a0002c0018t0001g0140 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.443-5700G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6130141 | |||||||
chr7:6130204 | T | A | 2 | a0002c0010t0001g0195 a0002c0010t0001g0197 |
2 | HG02280.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.443-5637T>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6130204 | |||||||
chr7:6130332 | G | A | 2 | a0002c0027t0001g0311 a0002c0027t0001g0316 |
2 | HG01496.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.443-5509G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6130332 | |||||||
chr7:6130458 | T | G | 234 | a0001c0001t0001g0272 a0002c0003t0001g0002 a0002c0003t0001g0004 others(231): Show |
260 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(257): Show |
intron_variant | MODIFIER | c.443-5383T>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6130458 | |||||||
chr7:6130461 | C | G | 28 | a0002c0006t0001g0027 a0002c0006t0001g0039 a0002c0006t0001g0313 others(25): Show |
29 | HG01167.hp2 HG01168.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.443-5380C>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6130461 | |||||||
chr7:6130490 | G | T | 2 | a0002c0003t0001g0006 a0002c0003t0001g0093 |
4 | NA18981.hp1 NA18983.hp1 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.443-5351G>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6130490 | |||||||
chr7:6130599 | G | A | 1 | a0002c0035t0001g0072 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.443-5242G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6130599 | |||||||
chr7:6130630 | A | G | 3 | a0002c0006t0001g0027 a0002c0006t0001g0039 a0002c0006t0001g0322 |
3 | NA18952.hp2 NA19075.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.443-5211A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6130630 | |||||||
chr7:6130681 | G | T | 26 | a0002c0006t0001g0027 a0002c0006t0001g0039 a0002c0006t0001g0313 others(23): Show |
27 | HG01167.hp2 HG01243.hp1 HG01256.hp1 others(24): Show |
intron_variant | MODIFIER | c.443-5160G>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6130681 | |||||||
chr7:6130870 | A | G | 1 | a0003c0002t0001g0151 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.443-4971A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6130870 | |||||||
chr7:6131129 | T | C | 3 | a0005c0011t0001g0029 a0005c0011t0001g0030 a0005c0011t0001g0031 |
3 | HG02630.hp1 HG02895.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.443-4712T>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6131129 | |||||||
chr7:6131352 | G | T | 26 | a0003c0002t0002g0009 a0003c0002t0002g0047 a0003c0002t0002g0048 others(23): Show |
30 | HG00280.hp1 HG00642.hp1 HG00673.hp1 others(27): Show |
intron_variant | MODIFIER | c.443-4489G>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6131352 | |||||||
chr7:6131526 | A | G | 1 | a0003c0002t0001g0142 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.443-4315A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6131526 | |||||||
chr7:6131535 | C | A | 1 | a0002c0003t0001g0099 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.443-4306C>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6131535 | |||||||
chr7:6131647 | T | G | 28 | a0002c0006t0001g0027 a0002c0006t0001g0039 a0002c0006t0001g0313 others(25): Show |
29 | HG01167.hp2 HG01243.hp1 HG01256.hp1 others(26): Show |
intron_variant | MODIFIER | c.443-4194T>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6131647 | |||||||
chr7:6131751 | C | T | 1 | a0004c0005t0001g0302 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.443-4090C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6131751 | |||||||
chr7:6131836 | C | G | 26 | a0002c0006t0001g0027 a0002c0006t0001g0039 a0002c0006t0001g0313 others(23): Show |
27 | HG01167.hp2 HG01243.hp1 HG01256.hp1 others(24): Show |
intron_variant | MODIFIER | c.443-4005C>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6131836 | |||||||
chr7:6131860 | A | C | 3 | a0002c0006t0001g0027 a0002c0006t0001g0039 a0002c0006t0001g0322 |
3 | NA18952.hp2 NA19075.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.443-3981A>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6131860 | |||||||
chr7:6131957 | C | G | 1 | a0002c0035t0001g0072 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.443-3884C>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6131957 | |||||||
chr7:6132163 | C | G | 2 | a0002c0003t0001g0110 a0002c0003t0001g0111 |
2 | NA19062.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.443-3678C>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6132163 | |||||||
chr7:6132243 | C | G | 1 | a0003c0002t0001g0323 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.443-3598C>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6132243 | |||||||
chr7:6132273 | C | T | 23 | a0002c0006t0001g0027 a0002c0006t0001g0039 a0002c0006t0001g0313 others(20): Show |
24 | HG01167.hp2 HG01243.hp1 HG01256.hp1 others(21): Show |
intron_variant | MODIFIER | c.443-3568C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6132273 | |||||||
chr7:6132398 | C | T | 2 | a0002c0006t0005g0315 a0002c0006t0005g0317 |
2 | HG02129.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.443-3443C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6132398 | |||||||
chr7:6132418 | T | TG | 84 | a0002c0003t0001g0161 a0002c0007t0001g0019 a0002c0007t0001g0160 others(81): Show |
90 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.443-3422dupG | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 6132418 | ||||||
chr7:6132474 | C | A | 1 | a0004c0005t0001g0304 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.443-3367C>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6132474 | |||||||
chr7:6132532 | G | T | 28 | a0002c0006t0001g0027 a0002c0006t0001g0039 a0002c0006t0001g0313 others(25): Show |
29 | HG01167.hp2 HG01168.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.443-3309G>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6132532 | |||||||
chr7:6132600 | C | G | 1 | a0003c0002t0001g0323 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.443-3241C>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6132600 | |||||||
chr7:6132636 | G | A | 19 | a0004c0005t0001g0008 a0004c0005t0001g0296 a0004c0005t0001g0297 others(16): Show |
22 | HG00280.hp1 HG00642.hp1 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.443-3205G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6132636 | |||||||
chr7:6132650 | A | G | 2 | a0004c0005t0001g0298 a0004c0005t0008g0301 |
2 | HG01934.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.443-3191A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6132650 | |||||||
chr7:6132694 | C | T | 1 | a0001c0001t0001g0240 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.443-3147C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6132694 | |||||||
chr7:6132738 | C | G | 1 | a0001c0001t0001g0272 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.443-3103C>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6132738 | |||||||
chr7:6132759 | C | A | 1 | a0003c0002t0001g0177 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.443-3082C>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6132759 | |||||||
chr7:6132874 | G | A | 1 | a0002c0035t0001g0072 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.443-2967G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6132874 | |||||||
chr7:6132920 | C | G | 1 | a0001c0001t0001g0224 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.443-2921C>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6132920 | |||||||
chr7:6132967 | G | A | 1 | a0003c0017t0001g0065 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.443-2874G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6132967 | |||||||
chr7:6133023 | T | C | 29 | a0002c0006t0001g0027 a0002c0006t0001g0039 a0002c0006t0001g0313 others(26): Show |
30 | HG01167.hp2 HG01168.hp2 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.443-2818T>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6133023 | |||||||
chr7:6133365 | G | A | 2 | a0001c0001t0001g0025 a0001c0001t0001g0202 |
3 | NA18955.hp2 NA18957.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.443-2476G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6133365 | |||||||
chr7:6133398 | T | C | 9 | a0005c0011t0001g0038 a0005c0011t0001g0057 a0005c0011t0001g0063 others(6): Show |
9 | HG01346.hp1 HG01891.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.443-2443T>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6133398 | |||||||
chr7:6133621 | C | T | 1 | a0001c0001t0001g0274 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.443-2220C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6133621 | |||||||
chr7:6133653 | G | T | 1 | a0002c0050t0001g0294 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.443-2188G>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6133653 | |||||||
chr7:6133662 | A | G | 1 | a0009c0026t0001g0053 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.443-2179A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6133662 | |||||||
chr7:6133763 | G | A | 1 | a0001c0001t0001g0274 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.443-2078G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6133763 | |||||||
chr7:6133802 | A | G | 30 | a0001c0001t0001g0272 a0002c0006t0001g0027 a0002c0006t0001g0039 others(27): Show |
31 | HG01167.hp2 HG01168.hp2 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.443-2039A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6133802 | |||||||
chr7:6133805 | C | G | 1 | a0002c0003t0001g0180 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.443-2036C>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6133805 | |||||||
chr7:6133859 | G | A | 1 | a0002c0003t0001g0103 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.443-1982G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6133859 | |||||||
chr7:6133879 | A | G | 1 | a0004c0038t0001g0044 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.443-1962A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6133879 | |||||||
chr7:6133891 | C | CT | 102 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0223 others(99): Show |
117 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.443-1933dupT | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 6133891 | ||||||
chr7:6133930 | G | C | 1 | a0005c0011t0001g0030 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.443-1911G>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6133930 | |||||||
chr7:6134035 | T | C | 234 | a0002c0003t0001g0002 a0002c0003t0001g0004 a0002c0003t0001g0006 others(231): Show |
260 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(257): Show |
intron_variant | MODIFIER | c.443-1806T>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6134035 | |||||||
chr7:6134308 | G | A | 1 | a0001c0001t0001g0267 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.443-1533G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6134308 | |||||||
chr7:6134407 | A | G | 26 | a0003c0002t0002g0009 a0003c0002t0002g0047 a0003c0002t0002g0048 others(23): Show |
30 | HG00280.hp1 HG00642.hp1 HG00673.hp1 others(27): Show |
intron_variant | MODIFIER | c.443-1434A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6134407 | |||||||
chr7:6134567 | C | G | 1 | a0001c0001t0001g0309 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.443-1274C>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6134567 | |||||||
chr7:6134603 | G | A | 1 | a0001c0001t0001g0226 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.443-1238G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6134603 | |||||||
chr7:6134720 | A | G | 1 | a0002c0004t0001g0332 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.443-1121A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6134720 | |||||||
chr7:6134748 | G | A | 41 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0024 others(38): Show |
52 | HG00438.hp1 HG00639.hp1 HG01069.hp2 others(49): Show |
intron_variant | MODIFIER | c.443-1093G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6134748 | |||||||
chr7:6134842 | G | T | 22 | a0002c0006t0001g0027 a0002c0006t0001g0039 a0002c0006t0001g0313 others(19): Show |
23 | HG01167.hp2 HG01243.hp1 HG01256.hp1 others(20): Show |
intron_variant | MODIFIER | c.443-999G>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6134842 | |||||||
chr7:6134950 | C | G | 2 | a0002c0003t0001g0097 a0002c0003t0001g0098 |
2 | HG01891.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.443-891C>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6134950 | |||||||
chr7:6135034 | C | G | 2 | a0002c0010t0001g0195 a0002c0010t0001g0197 |
2 | HG02280.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.443-807C>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6135034 | |||||||
chr7:6135061 | A | G | 3 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0205 |
3 | HG02083.hp1 NA18945.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.443-780A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6135061 | |||||||
chr7:6135069 | C | T | 1 | a0003c0002t0001g0258 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.443-772C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6135069 | |||||||
chr7:6135262 | C | G | 154 | a0002c0003t0001g0002 a0002c0003t0001g0004 a0002c0003t0001g0006 others(151): Show |
173 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.443-579C>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6135262 | |||||||
chr7:6135363 | A | G | 3 | a0005c0011t0001g0029 a0005c0011t0001g0030 a0005c0011t0001g0031 |
3 | HG02630.hp1 HG02895.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.443-478A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6135363 | |||||||
chr7:6135445 | C | T | 67 | a0002c0003t0001g0002 a0002c0003t0001g0004 a0002c0003t0001g0006 others(64): Show |
79 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.443-396C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6135445 | |||||||
chr7:6135481 | C | G | 27 | a0002c0006t0001g0027 a0002c0006t0001g0039 a0002c0006t0001g0313 others(24): Show |
28 | HG01167.hp2 HG01243.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.443-360C>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6135481 | |||||||
chr7:6135579 | G | A | 1 | a0003c0002t0001g0320 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.443-262G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6135579 | |||||||
chr7:6135618 | C | G | 1 | a0005c0011t0001g0031 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.443-223C>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6135618 | |||||||
chr7:6135650 | TCAAAAAA others(23): Show |
T | 2 | a0003c0002t0001g0126 a0003c0002t0001g0156 |
2 | HG00639.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.443-181_443-152del others(30): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 6135650 | ||||||
chr7:6135651 | C | CA | 132 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(129): Show |
142 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.443-164dupA | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 6135651 | ||||||
chr7:6135651 | C | CAA | 73 | a0001c0001t0001g0001 a0001c0001t0001g0203 a0001c0001t0001g0271 others(70): Show |
82 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.443-165_443-164dup others(2): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 6135651 | ||||||
chr7:6135651 | C | CAAA | 14 | a0002c0003t0001g0002 a0002c0003t0001g0004 a0002c0003t0001g0077 others(11): Show |
14 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(11): Show |
intron_variant | MODIFIER | c.443-166_443-164dup others(3): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 6135651 | ||||||
chr7:6135651 | CAAAAAAA others(3): Show |
C | 3 | a0002c0007t0001g0169 a0002c0007t0004g0292 a0002c0007t0004g0293 |
3 | HG00621.hp1 HG02027.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.443-173_443-164del others(10): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 6135651 | ||||||
chr7:6135651 | CAAAAAAA others(5): Show |
C | 1 | a0003c0002t0001g0138 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.443-175_443-164del others(12): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 6135651 | ||||||
chr7:6135651 | CAAAAAAA others(7): Show |
C | 1 | a0002c0003t0001g0167 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.443-177_443-164del others(14): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 6135651 | ||||||
chr7:6135678 | G | A | 1 | a0002c0003t0001g0103 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.443-163G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6135678 | |||||||
chr7:6135681 | C | G | 1 | a0002c0003t0001g0103 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.443-160C>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6135681 | |||||||
chr7:6135684 | A | C | 1 | a0002c0003t0001g0103 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.443-157A>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 3/17 | chr7 | 6135684 | |||||||
chr7:6135968 | G | A | 1 | a0010c0022t0001g0076 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.553+17G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 4/17 | chr7 | 6135968 | |||||||
chr7:6136002 | CT | C | 102 | a0001c0001t0001g0230 a0002c0003t0001g0066 a0002c0003t0001g0104 others(99): Show |
109 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.553+70delT | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr7 | 6136002 | ||||||
chr7:6136107 | C | T | 2 | a0002c0003t0001g0108 a0002c0003t0001g0109 |
2 | HG02027.hp2 HG02040.hp2 |
intron_variant | MODIFIER | c.553+156C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 4/17 | chr7 | 6136107 | |||||||
chr7:6136132 | G | A | 26 | a0003c0002t0002g0009 a0003c0002t0002g0047 a0003c0002t0002g0048 others(23): Show |
30 | HG00280.hp1 HG00642.hp1 HG00673.hp1 others(27): Show |
intron_variant | MODIFIER | c.553+181G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 4/17 | chr7 | 6136132 | |||||||
chr7:6136185 | G | T | 9 | a0002c0004t0001g0328 a0002c0004t0001g0329 a0002c0004t0001g0332 others(6): Show |
9 | HG02257.hp2 HG02258.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.553+234G>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 4/17 | chr7 | 6136185 | |||||||
chr7:6136224 | A | G | 183 | a0001c0001t0001g0221 a0002c0003t0001g0002 a0002c0003t0001g0004 others(180): Show |
203 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(200): Show |
intron_variant | MODIFIER | c.553+273A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 4/17 | chr7 | 6136224 | |||||||
chr7:6136348 | A | G | 1 | a0002c0006t0003g0033 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.553+397A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 4/17 | chr7 | 6136348 | |||||||
chr7:6136423 | A | G | 2 | a0004c0005t0001g0297 a0004c0005t0001g0305 |
2 | HG01255.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.553+472A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 4/17 | chr7 | 6136423 | |||||||
chr7:6136488 | A | G | 3 | a0003c0012t0001g0073 a0003c0012t0001g0074 a0003c0012t0001g0075 |
3 | HG01081.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.553+537A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 4/17 | chr7 | 6136488 | |||||||
chr7:6136497 | A | T | 1 | a0023c0041t0001g0056 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.553+546A>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 4/17 | chr7 | 6136497 | |||||||
chr7:6136580 | A | C | 1 | a0002c0018t0001g0150 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.553+629A>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 4/17 | chr7 | 6136580 | |||||||
chr7:6136651 | G | T | 1 | a0014c0049t0001g0295 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.553+700G>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 4/17 | chr7 | 6136651 | |||||||
chr7:6136892 | C | T | 1 | a0005c0011t0001g0030 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.553+941C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 4/17 | chr7 | 6136892 | |||||||
chr7:6137083 | C | T | 1 | a0002c0004t0001g0332 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.553+1132C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 4/17 | chr7 | 6137083 | |||||||
chr7:6137156 | G | T | 23 | a0002c0006t0001g0027 a0002c0006t0001g0039 a0002c0006t0001g0313 others(20): Show |
24 | HG01167.hp2 HG01243.hp1 HG01256.hp1 others(21): Show |
intron_variant | MODIFIER | c.553+1205G>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 4/17 | chr7 | 6137156 | |||||||
chr7:6137188 | A | G | 1 | a0002c0010t0001g0321 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.553+1237A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 4/17 | chr7 | 6137188 | |||||||
chr7:6137191 | C | G | 1 | a0003c0012t0001g0073 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.553+1240C>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 4/17 | chr7 | 6137191 | |||||||
chr7:6137367 | C | T | 24 | a0002c0006t0001g0027 a0002c0006t0001g0039 a0002c0006t0001g0313 others(21): Show |
25 | HG01167.hp2 HG01168.hp2 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.553+1416C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 4/17 | chr7 | 6137367 | |||||||
chr7:6137450 | T | A | 4 | a0003c0002t0001g0124 a0003c0020t0001g0069 a0003c0020t0001g0123 others(1): Show |
4 | NA18961.hp2 NA18999.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.553+1499T>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 4/17 | chr7 | 6137450 | |||||||
chr7:6137555 | A | G | 1 | a0002c0035t0001g0072 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.554-1537A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 4/17 | chr7 | 6137555 | |||||||
chr7:6137602 | C | T | 2 | a0003c0002t0001g0126 a0003c0002t0001g0156 |
2 | HG00639.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.554-1490C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 4/17 | chr7 | 6137602 | |||||||
chr7:6137794 | C | T | 1 | a0003c0002t0001g0136 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.554-1298C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 4/17 | chr7 | 6137794 | |||||||
chr7:6137831 | C | A | 1 | a0002c0003t0001g0097 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.554-1261C>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 4/17 | chr7 | 6137831 | |||||||
chr7:6137870 | G | C | 1 | a0001c0031t0001g0216 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.554-1222G>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 4/17 | chr7 | 6137870 | |||||||
chr7:6137893 | A | G | 3 | a0001c0001t0001g0223 a0001c0001t0001g0229 a0001c0001t0001g0309 |
3 | HG01074.hp1 HG01261.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.554-1199A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 4/17 | chr7 | 6137893 | |||||||
chr7:6137948 | G | T | 1 | a0002c0010t0001g0197 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.554-1144G>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 4/17 | chr7 | 6137948 | |||||||
chr7:6138003 | T | G | 1 | a0002c0003t0001g0105 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.554-1089T>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 4/17 | chr7 | 6138003 | |||||||
chr7:6138083 | G | A | 1 | a0002c0050t0001g0294 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.554-1009G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 4/17 | chr7 | 6138083 | |||||||
chr7:6138102 | C | G | 49 | a0002c0003t0001g0002 a0002c0003t0001g0004 a0002c0003t0001g0006 others(46): Show |
61 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.554-990C>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 4/17 | chr7 | 6138102 | |||||||
chr7:6138204 | G | A | 1 | a0002c0014t0001g0020 | 2 | HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.554-888G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 4/17 | chr7 | 6138204 | |||||||
chr7:6138309 | C | G | 1 | a0001c0001t0001g0309 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.554-783C>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 4/17 | chr7 | 6138309 | |||||||
chr7:6138386 | T | C | 3 | a0002c0003t0001g0016 a0002c0003t0001g0117 a0002c0003t0001g0187 |
4 | NA18977.hp2 NA18988.hp1 NA19080.hp1 others(1): Show |
intron_variant | MODIFIER | c.554-706T>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 4/17 | chr7 | 6138386 | |||||||
chr7:6138477 | A | G | 1 | a0004c0009t0001g0081 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.554-615A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 4/17 | chr7 | 6138477 | |||||||
chr7:6138527 | G | A | 1 | a0001c0001t0001g0231 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.554-565G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 4/17 | chr7 | 6138527 | |||||||
chr7:6138536 | C | T | 1 | a0002c0003t0001g0092 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.554-556C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 4/17 | chr7 | 6138536 | |||||||
chr7:6138624 | A | G | 1 | a0001c0001t0001g0246 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.554-468A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 4/17 | chr7 | 6138624 | |||||||
chr7:6138736 | C | T | 1 | a0002c0035t0001g0072 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.554-356C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 4/17 | chr7 | 6138736 | |||||||
chr7:6138765 | T | A | 1 | a0003c0002t0001g0323 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.554-327T>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 4/17 | chr7 | 6138765 | |||||||
chr7:6138841 | C | G | 1 | a0002c0003t0001g0107 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.554-251C>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 4/17 | chr7 | 6138841 | |||||||
chr7:6138868 | TC | T | 25 | a0002c0006t0001g0027 a0002c0006t0001g0039 a0002c0006t0001g0313 others(22): Show |
25 | HG01167.hp2 HG01243.hp1 HG01256.hp1 others(22): Show |
intron_variant | MODIFIER | c.554-222delC | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr7 | 6138868 | ||||||
chr7:6138869 | C | A | 1 | a0001c0001t0001g0214 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.554-223C>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 4/17 | chr7 | 6138869 | |||||||
chr7:6138882 | C | A | 1 | a0002c0027t0001g0316 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.554-210C>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 4/17 | chr7 | 6138882 | |||||||
chr7:6138965 | A | G | 1 | a0001c0001t0001g0255 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.554-127A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 4/17 | chr7 | 6138965 | |||||||
chr7:6139002 | C | T | 1 | a0002c0003t0001g0117 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.554-90C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 4/17 | chr7 | 6139002 | |||||||
chr7:6139008 | A | G | 1 | a0001c0001t0001g0218 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.554-84A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 4/17 | chr7 | 6139008 | |||||||
chr7:6139050 | T | A | 1 | a0023c0041t0001g0056 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.554-42T>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 4/17 | chr7 | 6139050 | |||||||
chr7:6139265 | C | T | 1 | a0004c0009t0001g0078 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.656+71C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 5/17 | chr7 | 6139265 | |||||||
chr7:6139299 | A | G | 1 | a0001c0001t0001g0205 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.656+105A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 5/17 | chr7 | 6139299 | |||||||
chr7:6139300 | G | A | 193 | a0002c0003t0001g0002 a0002c0003t0001g0004 a0002c0003t0001g0006 others(190): Show |
212 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(209): Show |
intron_variant | MODIFIER | c.656+106G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 5/17 | chr7 | 6139300 | |||||||
chr7:6139590 | T | C | 2 | a0003c0002t0001g0184 a0003c0002t0001g0185 |
2 | HG02486.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.656+396T>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 5/17 | chr7 | 6139590 | |||||||
chr7:6139667 | G | A | 26 | a0003c0002t0002g0009 a0003c0002t0002g0047 a0003c0002t0002g0048 others(23): Show |
30 | HG00280.hp1 HG00642.hp1 HG00673.hp1 others(27): Show |
intron_variant | MODIFIER | c.657-461G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 5/17 | chr7 | 6139667 | |||||||
chr7:6139683 | G | GC | 233 | a0002c0003t0001g0002 a0002c0003t0001g0004 a0002c0003t0001g0006 others(230): Show |
258 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(255): Show |
intron_variant | MODIFIER | c.657-445_657-444ins others(1): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 5/17 | chr7 | 6139683 | |||||||
chr7:6139726 | C | T | 1 | a0005c0019t0001g0051 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.657-402C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 5/17 | chr7 | 6139726 | |||||||
chr7:6139826 | G | A | 1 | a0003c0017t0001g0065 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.657-302G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 5/17 | chr7 | 6139826 | |||||||
chr7:6139931 | C | T | 1 | a0003c0002t0001g0323 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.657-197C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 5/17 | chr7 | 6139931 | |||||||
chr7:6139970 | A | G | 2 | a0001c0001t0001g0026 a0001c0001t0001g0307 |
3 | HG03669.hp2 HG03710.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.657-158A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 5/17 | chr7 | 6139970 | |||||||
chr7:6140074 | C | A | 2 | a0002c0004t0001g0333 a0002c0004t0001g0336 |
2 | HG03098.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.657-54C>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 5/17 | chr7 | 6140074 | |||||||
chr7:6140404 | C | G | 65 | a0002c0003t0001g0002 a0002c0003t0001g0004 a0002c0003t0001g0006 others(62): Show |
78 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.724+209C>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 6/17 | chr7 | 6140404 | |||||||
chr7:6140433 | G | A | 25 | a0002c0006t0001g0027 a0002c0006t0001g0039 a0002c0006t0001g0313 others(22): Show |
25 | HG01167.hp2 HG01243.hp1 HG01256.hp1 others(22): Show |
intron_variant | MODIFIER | c.724+238G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 6/17 | chr7 | 6140433 | |||||||
chr7:6140484 | T | TTC | 25 | a0002c0006t0001g0027 a0002c0006t0001g0039 a0002c0006t0001g0313 others(22): Show |
25 | HG01167.hp2 HG01243.hp1 HG01256.hp1 others(22): Show |
intron_variant | MODIFIER | c.724+290_724+291ins others(2): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr7 | 6140484 | ||||||
chr7:6140510 | T | C | 1 | a0001c0001t0001g0286 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.724+315T>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 6/17 | chr7 | 6140510 | |||||||
chr7:6140856 | T | C | 1 | a0002c0003t0001g0077 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.725-58T>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 6/17 | chr7 | 6140856 | |||||||
chr7:6140880 | T | C | 3 | a0005c0011t0001g0029 a0005c0011t0001g0030 a0005c0011t0001g0031 |
3 | HG02630.hp1 HG02895.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.725-34T>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 6/17 | chr7 | 6140880 | |||||||
chr7:6141041 | C | G | 1 | a0002c0003t0001g0161 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.795+57C>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 7/17 | chr7 | 6141041 | |||||||
chr7:6141049 | C | T | 22 | a0002c0006t0001g0027 a0002c0006t0001g0039 a0002c0006t0001g0313 others(19): Show |
22 | HG01167.hp2 HG01243.hp1 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.795+65C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 7/17 | chr7 | 6141049 | |||||||
chr7:6141142 | A | G | 1 | a0003c0002t0001g0151 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.795+158A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 7/17 | chr7 | 6141142 | |||||||
chr7:6141196 | C | CT | 22 | a0002c0006t0001g0027 a0002c0006t0001g0039 a0002c0006t0001g0313 others(19): Show |
22 | HG01243.hp1 HG01256.hp1 HG01496.hp1 others(19): Show |
intron_variant | MODIFIER | c.795+216dupT | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 6141196 | ||||||
chr7:6141201 | C | CT | 12 | a0001c0001t0001g0206 a0001c0001t0001g0214 a0001c0001t0001g0252 others(9): Show |
12 | HG00099.hp2 HG00673.hp1 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.795+236dupT | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 6141201 | ||||||
chr7:6141201 | C | T | 26 | a0002c0006t0001g0027 a0002c0006t0001g0039 a0002c0006t0001g0313 others(23): Show |
26 | HG01167.hp2 HG01168.hp2 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.795+217C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 7/17 | chr7 | 6141201 | |||||||
chr7:6141406 | A | G | 1 | a0001c0001t0001g0254 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.795+422A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 7/17 | chr7 | 6141406 | |||||||
chr7:6141438 | G | A | 37 | a0003c0002t0002g0009 a0003c0002t0002g0047 a0003c0002t0002g0048 others(34): Show |
41 | HG00280.hp1 HG00642.hp1 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.795+454G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 7/17 | chr7 | 6141438 | |||||||
chr7:6141492 | G | A | 1 | a0002c0003t0001g0110 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.795+508G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 7/17 | chr7 | 6141492 | |||||||
chr7:6141521 | A | C | 1 | a0001c0001t0001g0239 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.795+537A>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 7/17 | chr7 | 6141521 | |||||||
chr7:6141538 | T | C | 1 | a0002c0014t0001g0270 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.795+554T>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 7/17 | chr7 | 6141538 | |||||||
chr7:6141564 | A | AT | 67 | a0002c0003t0001g0002 a0002c0003t0001g0004 a0002c0003t0001g0006 others(64): Show |
82 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.795+592dupT | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 6141564 | ||||||
chr7:6141567 | T | A | 2 | a0002c0006t0001g0324 a0022c0042t0001g0143 |
2 | HG01167.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.795+583T>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 7/17 | chr7 | 6141567 | |||||||
chr7:6141596 | T | G | 1 | a0002c0004t0001g0328 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.795+612T>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 7/17 | chr7 | 6141596 | |||||||
chr7:6141603 | G | C | 2 | a0006c0023t0001g0070 a0006c0023t0001g0228 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.795+619G>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 7/17 | chr7 | 6141603 | |||||||
chr7:6141635 | T | C | 37 | a0003c0002t0002g0009 a0003c0002t0002g0047 a0003c0002t0002g0048 others(34): Show |
41 | HG00280.hp1 HG00642.hp1 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.795+651T>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 7/17 | chr7 | 6141635 | |||||||
chr7:6141656 | T | C | 10 | a0002c0004t0001g0328 a0002c0004t0001g0329 a0002c0004t0001g0332 others(7): Show |
10 | HG02257.hp2 HG02258.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.795+672T>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 7/17 | chr7 | 6141656 | |||||||
chr7:6141743 | A | T | 23 | a0002c0006t0001g0027 a0002c0006t0001g0039 a0002c0006t0001g0313 others(20): Show |
24 | HG01167.hp2 HG01243.hp1 HG01256.hp1 others(21): Show |
intron_variant | MODIFIER | c.795+759A>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 7/17 | chr7 | 6141743 | |||||||
chr7:6141890 | T | C | 234 | a0002c0003t0001g0002 a0002c0003t0001g0004 a0002c0003t0001g0006 others(231): Show |
260 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(257): Show |
intron_variant | MODIFIER | c.795+906T>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 7/17 | chr7 | 6141890 | |||||||
chr7:6142102 | C | T | 6 | a0001c0001t0001g0206 a0001c0001t0001g0256 a0001c0001t0001g0257 others(3): Show |
6 | HG02074.hp1 HG02155.hp2 NA18947.hp1 others(3): Show |
intron_variant | MODIFIER | c.796-830C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 7/17 | chr7 | 6142102 | |||||||
chr7:6142221 | C | CT | 99 | a0002c0004t0001g0325 a0002c0004t0001g0326 a0002c0004t0001g0327 others(96): Show |
106 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.796-698dupT | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 6142221 | ||||||
chr7:6142239 | C | CG | 37 | a0003c0002t0002g0009 a0003c0002t0002g0047 a0003c0002t0002g0048 others(34): Show |
41 | HG00280.hp1 HG00642.hp1 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.796-691dupG | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 6142239 | ||||||
chr7:6142266 | G | C | 9 | a0003c0002t0001g0010 a0003c0002t0001g0011 a0003c0002t0001g0043 others(6): Show |
11 | HG02055.hp1 HG02145.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.796-666G>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 7/17 | chr7 | 6142266 | |||||||
chr7:6142297 | A | G | 1 | a0001c0048t0001g0253 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.796-635A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 7/17 | chr7 | 6142297 | |||||||
chr7:6142437 | G | A | 1 | a0001c0001t0001g0245 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.796-495G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 7/17 | chr7 | 6142437 | |||||||
chr7:6142455 | A | G | 1 | a0002c0035t0001g0072 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.796-477A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 7/17 | chr7 | 6142455 | |||||||
chr7:6142512 | G | A | 1 | a0003c0017t0001g0065 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.796-420G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 7/17 | chr7 | 6142512 | |||||||
chr7:6142899 | G | T | 1 | a0001c0001t0001g0309 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.796-33G>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 7/17 | chr7 | 6142899 | |||||||
chr7:6143053 | T | C | 1 | a0001c0001t0001g0206 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.878+39T>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 8/17 | chr7 | 6143053 | |||||||
chr7:6143055 | C | T | 1 | a0001c0001t0001g0206 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.878+41C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 8/17 | chr7 | 6143055 | |||||||
chr7:6143124 | C | G | 6 | a0005c0011t0001g0038 a0005c0011t0001g0057 a0005c0011t0001g0063 others(3): Show |
6 | HG01346.hp1 HG01891.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.878+110C>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 8/17 | chr7 | 6143124 | |||||||
chr7:6143179 | G | C | 3 | a0005c0011t0001g0038 a0005c0024t0001g0061 a0005c0024t0001g0062 |
3 | HG01891.hp1 HG03209.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.878+165G>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 8/17 | chr7 | 6143179 | |||||||
chr7:6143321 | G | A | 1 | a0003c0002t0001g0037 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.878+307G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 8/17 | chr7 | 6143321 | |||||||
chr7:6143373 | C | T | 22 | a0002c0006t0001g0027 a0002c0006t0001g0039 a0002c0006t0001g0313 others(19): Show |
22 | HG01167.hp2 HG01243.hp1 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.878+359C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 8/17 | chr7 | 6143373 | |||||||
chr7:6143480 | A | G | 1 | a0002c0003t0001g0109 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.878+466A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 8/17 | chr7 | 6143480 | |||||||
chr7:6143528 | A | C | 3 | a0004c0009t0001g0013 a0004c0009t0001g0078 a0004c0009t0001g0081 |
4 | HG00642.hp1 HG01928.hp2 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.878+514A>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 8/17 | chr7 | 6143528 | |||||||
chr7:6144043 | A | T | 18 | a0002c0004t0001g0325 a0002c0004t0001g0326 a0002c0004t0001g0327 others(15): Show |
18 | HG01081.hp1 HG02257.hp2 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.879-42A>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 8/17 | chr7 | 6144043 | |||||||
chr7:6144051 | G | A | 25 | a0002c0006t0001g0027 a0002c0006t0001g0039 a0002c0006t0001g0313 others(22): Show |
25 | HG01167.hp2 HG01243.hp1 HG01256.hp1 others(22): Show |
intron_variant | MODIFIER | c.879-34G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 8/17 | chr7 | 6144051 | |||||||
chr7:6144063 | TTTTGTTT others(3): Show |
T | 1 | a0002c0004t0001g0338 | 1 | HG03540.hp2 | splice_region_variant&intron_variant | LOW | c.879-13_879-4delTGT others(7): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 6144063 | ||||||
chr7:6144082 | A | C | 1 | a0004c0009t0001g0046 | 1 | HG02258.hp1 | splice_region_variant&intron_variant | LOW | c.879-3A>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 8/17 | chr7 | 6144082 | |||||||
chr7:6144205 | A | G | 67 | a0002c0003t0001g0002 a0002c0003t0001g0004 a0002c0003t0001g0006 others(64): Show |
81 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.990+9A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 9/17 | chr7 | 6144205 | |||||||
chr7:6144231 | C | T | 1 | a0002c0050t0001g0294 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.990+35C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 9/17 | chr7 | 6144231 | |||||||
chr7:6144329 | T | G | 4 | a0003c0002t0001g0010 a0003c0002t0001g0054 a0003c0002t0001g0058 others(1): Show |
5 | HG02055.hp1 HG02965.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.990+133T>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 9/17 | chr7 | 6144329 | |||||||
chr7:6144449 | G | A | 1 | a0003c0017t0001g0065 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.990+253G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 9/17 | chr7 | 6144449 | |||||||
chr7:6144497 | C | T | 1 | a0004c0009t0001g0081 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.990+301C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 9/17 | chr7 | 6144497 | |||||||
chr7:6144534 | T | C | 25 | a0002c0006t0001g0027 a0002c0006t0001g0039 a0002c0006t0001g0313 others(22): Show |
25 | HG01167.hp2 HG01243.hp1 HG01256.hp1 others(22): Show |
intron_variant | MODIFIER | c.990+338T>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 9/17 | chr7 | 6144534 | |||||||
chr7:6144591 | C | T | 1 | a0001c0001t0001g0221 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.990+395C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 9/17 | chr7 | 6144591 | |||||||
chr7:6144696 | C | T | 2 | a0003c0002t0001g0184 a0003c0002t0001g0185 |
2 | HG02486.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.990+500C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 9/17 | chr7 | 6144696 | |||||||
chr7:6144735 | T | C | 3 | a0001c0001t0001g0023 a0001c0001t0007g0247 a0001c0046t0001g0023 |
3 | HG00099.hp1 HG01074.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.990+539T>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 9/17 | chr7 | 6144735 | |||||||
chr7:6144852 | A | G | 1 | a0003c0002t0001g0179 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.990+656A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 9/17 | chr7 | 6144852 | |||||||
chr7:6144869 | C | CA | 79 | a0002c0018t0001g0140 a0002c0018t0001g0150 a0003c0002t0001g0007 others(76): Show |
86 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.991-634dupA | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 6144869 | ||||||
chr7:6144956 | C | T | 2 | a0003c0002t0001g0184 a0003c0002t0001g0185 |
2 | HG02486.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.991-560C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 9/17 | chr7 | 6144956 | |||||||
chr7:6144992 | C | G | 64 | a0002c0003t0001g0002 a0002c0003t0001g0004 a0002c0003t0001g0006 others(61): Show |
78 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.991-524C>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 9/17 | chr7 | 6144992 | |||||||
chr7:6145021 | C | G | 1 | a0005c0011t0001g0031 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.991-495C>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 9/17 | chr7 | 6145021 | |||||||
chr7:6145023 | G | A | 25 | a0002c0006t0001g0027 a0002c0006t0001g0039 a0002c0006t0001g0313 others(22): Show |
25 | HG01167.hp2 HG01243.hp1 HG01256.hp1 others(22): Show |
intron_variant | MODIFIER | c.991-493G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 9/17 | chr7 | 6145023 | |||||||
chr7:6145079 | A | G | 1 | a0002c0035t0001g0072 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.991-437A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 9/17 | chr7 | 6145079 | |||||||
chr7:6145116 | G | A | 36 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0024 others(33): Show |
47 | HG00438.hp1 HG00597.hp1 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.991-400G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 9/17 | chr7 | 6145116 | |||||||
chr7:6145300 | C | A | 1 | a0003c0002t0001g0037 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.991-216C>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 9/17 | chr7 | 6145300 | |||||||
chr7:6145303 | C | T | 1 | a0003c0002t0001g0190 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.991-213C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 9/17 | chr7 | 6145303 | |||||||
chr7:6145330 | C | CA | 98 | a0001c0001t0001g0217 a0002c0004t0001g0325 a0002c0004t0001g0326 others(95): Show |
105 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.991-172dupA | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 6145330 | ||||||
chr7:6145330 | CA | C | 63 | a0001c0001t0001g0278 a0002c0003t0001g0002 a0002c0003t0001g0004 others(60): Show |
77 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.991-172delA | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 6145330 | ||||||
chr7:6145696 | A | G | 1 | a0015c0051t0001g0312 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1131+40A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 10/17 | chr7 | 6145696 | |||||||
chr7:6145725 | G | A | 25 | a0002c0006t0001g0027 a0002c0006t0001g0039 a0002c0006t0001g0313 others(22): Show |
25 | HG01167.hp2 HG01243.hp1 HG01256.hp1 others(22): Show |
intron_variant | MODIFIER | c.1131+69G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 10/17 | chr7 | 6145725 | |||||||
chr7:6145741 | A | C | 1 | a0002c0010t0001g0321 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1131+85A>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 10/17 | chr7 | 6145741 | |||||||
chr7:6145777 | A | G | 1 | a0003c0002t0001g0188 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1131+121A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 10/17 | chr7 | 6145777 | |||||||
chr7:6145791 | C | T | 1 | a0002c0003t0001g0094 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1131+135C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 10/17 | chr7 | 6145791 | |||||||
chr7:6145795 | C | T | 1 | a0003c0017t0001g0065 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1131+139C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 10/17 | chr7 | 6145795 | |||||||
chr7:6145846 | G | T | 1 | a0002c0007t0009g0158 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1131+190G>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 10/17 | chr7 | 6145846 | |||||||
chr7:6145875 | A | T | 2 | a0003c0002t0001g0184 a0003c0002t0001g0185 |
2 | HG02486.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1131+219A>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 10/17 | chr7 | 6145875 | |||||||
chr7:6145905 | A | G | 25 | a0002c0006t0001g0027 a0002c0006t0001g0039 a0002c0006t0001g0313 others(22): Show |
25 | HG01167.hp2 HG01243.hp1 HG01256.hp1 others(22): Show |
intron_variant | MODIFIER | c.1132-243A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 10/17 | chr7 | 6145905 | |||||||
chr7:6145908 | A | T | 1 | a0001c0001t0001g0234 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1132-240A>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 10/17 | chr7 | 6145908 | |||||||
chr7:6146078 | A | G | 1 | a0003c0002t0001g0184 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1132-70A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 10/17 | chr7 | 6146078 | |||||||
chr7:6146093 | A | G | 1 | a0002c0035t0001g0072 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1132-55A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 10/17 | chr7 | 6146093 | |||||||
chr7:6146268 | T | C | 1 | a0003c0017t0001g0065 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1232+20T>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 11/17 | chr7 | 6146268 | |||||||
chr7:6146337 | T | A | 36 | a0003c0002t0002g0009 a0003c0002t0002g0047 a0003c0002t0002g0048 others(33): Show |
40 | HG00280.hp1 HG00642.hp1 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.1232+89T>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 11/17 | chr7 | 6146337 | |||||||
chr7:6146337 | T | TA | 98 | a0001c0001t0001g0217 a0002c0004t0001g0325 a0002c0004t0001g0326 others(95): Show |
105 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.1232+104dupA | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 6146337 | ||||||
chr7:6146450 | A | G | 2 | a0001c0001t0001g0210 a0001c0001t0001g0214 |
2 | HG01106.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1232+202A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 11/17 | chr7 | 6146450 | |||||||
chr7:6146464 | G | A | 2 | a0002c0003t0001g0097 a0002c0003t0001g0098 |
2 | HG01891.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1232+216G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 11/17 | chr7 | 6146464 | |||||||
chr7:6146493 | A | G | 1 | a0002c0035t0001g0072 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1232+245A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 11/17 | chr7 | 6146493 | |||||||
chr7:6146606 | A | G | 3 | a0005c0011t0001g0029 a0005c0011t0001g0030 a0005c0011t0001g0031 |
3 | HG02630.hp1 HG02895.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1232+358A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 11/17 | chr7 | 6146606 | |||||||
chr7:6146618 | T | C | 1 | a0010c0022t0001g0076 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1232+370T>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 11/17 | chr7 | 6146618 | |||||||
chr7:6146662 | C | CA | 5 | a0002c0050t0001g0294 a0003c0008t0001g0134 a0003c0012t0001g0073 others(2): Show |
5 | HG01081.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1232+423dupA | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 6146662 | ||||||
chr7:6146671 | A | C | 1 | a0001c0001t0001g0265 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1232+423A>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 11/17 | chr7 | 6146671 | |||||||
chr7:6146771 | A | G | 19 | a0001c0001t0001g0330 a0002c0004t0001g0325 a0002c0004t0001g0326 others(16): Show |
19 | HG01081.hp1 HG02257.hp2 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.1232+523A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 11/17 | chr7 | 6146771 | |||||||
chr7:6146950 | C | T | 1 | a0003c0002t0001g0184 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1232+702C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 11/17 | chr7 | 6146950 | |||||||
chr7:6146976 | A | G | 1 | a0002c0035t0001g0072 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1232+728A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 11/17 | chr7 | 6146976 | |||||||
chr7:6147122 | T | C | 14 | a0001c0013t0001g0242 a0002c0004t0001g0340 a0003c0002t0001g0010 others(11): Show |
16 | HG02055.hp1 HG02280.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.1233-617T>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 11/17 | chr7 | 6147122 | |||||||
chr7:6147148 | G | GA | 7 | a0003c0002t0002g0009 a0003c0002t0002g0047 a0003c0002t0002g0048 others(4): Show |
8 | HG01175.hp2 HG02109.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1233-589dupA | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 6147148 | ||||||
chr7:6147430 | C | T | 1 | a0004c0038t0001g0044 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1233-309C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 11/17 | chr7 | 6147430 | |||||||
chr7:6147491 | A | T | 65 | a0002c0003t0001g0002 a0002c0003t0001g0004 a0002c0003t0001g0006 others(62): Show |
79 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.1233-248A>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 11/17 | chr7 | 6147491 | |||||||
chr7:6147633 | T | C | 2 | a0002c0006t0001g0313 a0002c0006t0001g0314 |
2 | HG03491.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.1233-106T>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 11/17 | chr7 | 6147633 | |||||||
chr7:6147928 | A | C | 1 | a0008c0021t0001g0060 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1386+36A>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 12/17 | chr7 | 6147928 | |||||||
chr7:6148030 | C | G | 1 | a0003c0002t0001g0058 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1386+138C>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 12/17 | chr7 | 6148030 | |||||||
chr7:6148144 | C | T | 36 | a0003c0002t0002g0009 a0003c0002t0002g0047 a0003c0002t0002g0048 others(33): Show |
40 | HG00280.hp1 HG00642.hp1 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.1386+252C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 12/17 | chr7 | 6148144 | |||||||
chr7:6148152 | C | A | 336 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(333): Show |
384 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(381): Show |
intron_variant | MODIFIER | c.1386+260C>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 12/17 | chr7 | 6148152 | |||||||
chr7:6148303 | C | T | 63 | a0002c0003t0001g0002 a0002c0003t0001g0004 a0002c0003t0001g0006 others(60): Show |
76 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.1386+411C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 12/17 | chr7 | 6148303 | |||||||
chr7:6148391 | A | T | 3 | a0003c0012t0001g0073 a0003c0012t0001g0074 a0003c0012t0001g0075 |
3 | HG01081.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1386+499A>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 12/17 | chr7 | 6148391 | |||||||
chr7:6148492 | A | C | 1 | a0002c0010t0001g0196 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1386+600A>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 12/17 | chr7 | 6148492 | |||||||
chr7:6148501 | C | T | 1 | a0003c0017t0001g0065 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1386+609C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 12/17 | chr7 | 6148501 | |||||||
chr7:6148691 | C | T | 63 | a0002c0003t0001g0002 a0002c0003t0001g0004 a0002c0003t0001g0006 others(60): Show |
76 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.1386+799C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 12/17 | chr7 | 6148691 | |||||||
chr7:6148708 | C | T | 3 | a0005c0011t0001g0038 a0005c0024t0001g0061 a0005c0024t0001g0062 |
3 | HG01891.hp1 HG03209.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1386+816C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 12/17 | chr7 | 6148708 | |||||||
chr7:6148787 | A | G | 3 | a0005c0011t0001g0029 a0005c0011t0001g0030 a0005c0011t0001g0031 |
3 | HG02630.hp1 HG02895.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1387-796A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 12/17 | chr7 | 6148787 | |||||||
chr7:6148811 | A | T | 3 | a0003c0012t0001g0073 a0003c0012t0001g0074 a0003c0012t0001g0075 |
3 | HG01081.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1387-772A>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 12/17 | chr7 | 6148811 | |||||||
chr7:6148835 | T | A | 230 | a0002c0003t0001g0002 a0002c0003t0001g0004 a0002c0003t0001g0006 others(227): Show |
255 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(252): Show |
intron_variant | MODIFIER | c.1387-748T>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 12/17 | chr7 | 6148835 | |||||||
chr7:6148857 | C | T | 1 | a0001c0048t0001g0253 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1387-726C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 12/17 | chr7 | 6148857 | |||||||
chr7:6149011 | C | T | 3 | a0003c0012t0001g0073 a0003c0012t0001g0074 a0003c0012t0001g0075 |
3 | HG01081.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1387-572C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 12/17 | chr7 | 6149011 | |||||||
chr7:6149039 | G | C | 1 | a0001c0001t0001g0267 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1387-544G>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 12/17 | chr7 | 6149039 | |||||||
chr7:6149093 | G | A | 1 | a0001c0001t0001g0234 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1387-490G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 12/17 | chr7 | 6149093 | |||||||
chr7:6149131 | G | T | 1 | a0003c0002t0001g0323 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1387-452G>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 12/17 | chr7 | 6149131 | |||||||
chr7:6149168 | C | G | 3 | a0001c0001t0001g0023 a0001c0001t0007g0247 a0001c0046t0001g0023 |
3 | HG00099.hp1 HG01074.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1387-415C>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 12/17 | chr7 | 6149168 | |||||||
chr7:6149168 | C | T | 1 | a0004c0038t0001g0044 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1387-415C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 12/17 | chr7 | 6149168 | |||||||
chr7:6149176 | C | T | 1 | a0002c0003t0001g0108 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1387-407C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 12/17 | chr7 | 6149176 | |||||||
chr7:6149216 | C | T | 1 | a0003c0002t0001g0142 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1387-367C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 12/17 | chr7 | 6149216 | |||||||
chr7:6149241 | G | A | 22 | a0002c0006t0001g0027 a0002c0006t0001g0039 a0002c0006t0001g0313 others(19): Show |
22 | HG01167.hp2 HG01243.hp1 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.1387-342G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 12/17 | chr7 | 6149241 | |||||||
chr7:6149305 | C | T | 5 | a0004c0005t0001g0008 a0004c0005t0001g0296 a0004c0005t0001g0297 others(2): Show |
7 | HG00741.hp2 HG01123.hp1 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.1387-278C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 12/17 | chr7 | 6149305 | |||||||
chr7:6149420 | T | A | 3 | a0005c0011t0001g0029 a0005c0011t0001g0030 a0005c0011t0001g0031 |
3 | HG02630.hp1 HG02895.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1387-163T>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 12/17 | chr7 | 6149420 | |||||||
chr7:6149477 | G | GA | 87 | a0001c0001t0007g0247 a0002c0004t0001g0340 a0002c0018t0001g0140 others(84): Show |
95 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.1387-93dupA | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 6149477 | ||||||
chr7:6149477 | GA | G | 13 | a0002c0004t0001g0325 a0002c0004t0001g0326 a0002c0004t0001g0327 others(10): Show |
13 | HG02257.hp2 HG02258.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.1387-93delA | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 6149477 | ||||||
chr7:6149532 | G | C | 3 | a0005c0011t0001g0029 a0005c0011t0001g0030 a0005c0011t0001g0031 |
3 | HG02630.hp1 HG02895.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1387-51G>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 12/17 | chr7 | 6149532 | |||||||
chr7:6150327 | C | A | 1 | a0002c0003t0001g0108 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2106+25C>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 13/17 | chr7 | 6150327 | |||||||
chr7:6150383 | A | T | 1 | a0002c0035t0001g0072 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2107-29A>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 13/17 | chr7 | 6150383 | |||||||
chr7:6150658 | C | T | 1 | a0001c0001t0001g0214 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2201+152C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 14/17 | chr7 | 6150658 | |||||||
chr7:6150735 | A | G | 1 | a0023c0041t0001g0056 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2201+229A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 14/17 | chr7 | 6150735 | |||||||
chr7:6150897 | C | T | 65 | a0002c0003t0001g0002 a0002c0003t0001g0004 a0002c0003t0001g0006 others(62): Show |
78 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.2201+391C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 14/17 | chr7 | 6150897 | |||||||
chr7:6150910 | C | T | 3 | a0003c0002t0001g0147 a0003c0002t0001g0153 a0003c0002t0001g0154 |
3 | HG00438.hp2 HG00597.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.2201+404C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 14/17 | chr7 | 6150910 | |||||||
chr7:6150929 | A | C | 1 | a0005c0011t0001g0057 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2201+423A>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 14/17 | chr7 | 6150929 | |||||||
chr7:6150956 | T | G | 1 | a0003c0017t0001g0065 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.2201+450T>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 14/17 | chr7 | 6150956 | |||||||
chr7:6151046 | C | A | 2 | a0002c0006t0005g0315 a0002c0006t0005g0317 |
2 | HG02129.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.2201+540C>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 14/17 | chr7 | 6151046 | |||||||
chr7:6151074 | T | A | 1 | a0018c0036t0001g0264 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2201+568T>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 14/17 | chr7 | 6151074 | |||||||
chr7:6151229 | G | A | 2 | a0002c0006t0005g0315 a0002c0006t0005g0317 |
2 | HG02129.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.2201+723G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 14/17 | chr7 | 6151229 | |||||||
chr7:6151274 | C | T | 1 | a0002c0035t0001g0072 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2201+768C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 14/17 | chr7 | 6151274 | |||||||
chr7:6151315 | A | T | 101 | a0002c0003t0001g0002 a0002c0003t0001g0004 a0002c0003t0001g0006 others(98): Show |
114 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.2201+809A>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 14/17 | chr7 | 6151315 | |||||||
chr7:6151431 | T | C | 1 | a0002c0035t0001g0072 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2201+925T>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 14/17 | chr7 | 6151431 | |||||||
chr7:6151446 | T | C | 64 | a0002c0003t0001g0002 a0002c0003t0001g0004 a0002c0003t0001g0006 others(61): Show |
77 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.2201+940T>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 14/17 | chr7 | 6151446 | |||||||
chr7:6151575 | C | T | 6 | a0002c0003t0001g0004 a0002c0003t0001g0091 a0002c0003t0001g0105 others(3): Show |
9 | HG00408.hp2 HG00558.hp1 HG01981.hp2 others(6): Show |
intron_variant | MODIFIER | c.2201+1069C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 14/17 | chr7 | 6151575 | |||||||
chr7:6151596 | C | T | 2 | a0003c0002t0001g0184 a0003c0002t0001g0185 |
2 | HG02486.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2201+1090C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 14/17 | chr7 | 6151596 | |||||||
chr7:6151604 | A | AT | 15 | a0002c0004t0001g0325 a0002c0004t0001g0326 a0002c0004t0001g0327 others(12): Show |
15 | HG02257.hp2 HG02258.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.2201+1108dupT | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr7 | 6151604 | ||||||
chr7:6151662 | C | G | 2 | a0003c0002t0001g0136 a0021c0039t0001g0176 |
2 | NA18951.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.2201+1156C>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 14/17 | chr7 | 6151662 | |||||||
chr7:6151690 | G | T | 4 | a0003c0002t0001g0128 a0003c0002t0001g0129 a0003c0002t0001g0133 others(1): Show |
4 | NA18954.hp2 NA18989.hp2 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.2201+1184G>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 14/17 | chr7 | 6151690 | |||||||
chr7:6151798 | C | T | 73 | a0002c0018t0001g0140 a0002c0018t0001g0150 a0003c0002t0001g0007 others(70): Show |
79 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.2201+1292C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 14/17 | chr7 | 6151798 | |||||||
chr7:6151888 | G | A | 2 | a0002c0004t0001g0338 a0002c0004t0001g0339 |
2 | HG03540.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2201+1382G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 14/17 | chr7 | 6151888 | |||||||
chr7:6152165 | G | A | 2 | a0006c0023t0001g0070 a0006c0023t0001g0228 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.2202-1591G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 14/17 | chr7 | 6152165 | |||||||
chr7:6152175 | G | A | 1 | a0003c0002t0001g0323 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2202-1581G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 14/17 | chr7 | 6152175 | |||||||
chr7:6152230 | G | A | 1 | a0002c0010t0001g0321 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2202-1526G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 14/17 | chr7 | 6152230 | |||||||
chr7:6152253 | G | A | 2 | a0002c0003t0001g0066 a0002c0003t0001g0100 |
2 | NA18964.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.2202-1503G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 14/17 | chr7 | 6152253 | |||||||
chr7:6152264 | A | G | 186 | a0001c0001t0001g0330 a0002c0003t0001g0002 a0002c0003t0001g0004 others(183): Show |
206 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(203): Show |
intron_variant | MODIFIER | c.2202-1492A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 14/17 | chr7 | 6152264 | |||||||
chr7:6152275 | G | T | 6 | a0005c0011t0001g0038 a0005c0011t0001g0057 a0005c0011t0001g0063 others(3): Show |
6 | HG01346.hp1 HG01891.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.2202-1481G>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 14/17 | chr7 | 6152275 | |||||||
chr7:6152290 | C | T | 6 | a0005c0011t0001g0038 a0005c0011t0001g0057 a0005c0011t0001g0063 others(3): Show |
6 | HG01346.hp1 HG01891.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.2202-1466C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 14/17 | chr7 | 6152290 | |||||||
chr7:6152359 | T | C | 1 | a0003c0002t0001g0132 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.2202-1397T>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 14/17 | chr7 | 6152359 | |||||||
chr7:6152442 | T | G | 1 | a0003c0017t0001g0065 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.2202-1314T>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 14/17 | chr7 | 6152442 | |||||||
chr7:6152456 | A | G | 236 | a0001c0001t0001g0330 a0002c0003t0001g0002 a0002c0003t0001g0004 others(233): Show |
262 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(259): Show |
intron_variant | MODIFIER | c.2202-1300A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 14/17 | chr7 | 6152456 | |||||||
chr7:6152504 | C | T | 1 | a0003c0002t0001g0068 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2202-1252C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 14/17 | chr7 | 6152504 | |||||||
chr7:6152522 | C | A | 1 | a0001c0001t0001g0201 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2202-1234C>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 14/17 | chr7 | 6152522 | |||||||
chr7:6152527 | G | C | 1 | a0002c0010t0001g0196 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2202-1229G>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 14/17 | chr7 | 6152527 | |||||||
chr7:6152529 | C | T | 1 | a0003c0002t0001g0058 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2202-1227C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 14/17 | chr7 | 6152529 | |||||||
chr7:6152536 | TAGG | T | 13 | a0003c0002t0001g0010 a0003c0002t0001g0011 a0003c0002t0001g0043 others(10): Show |
16 | HG01175.hp2 HG02055.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.2202-1216_2202-121 others(7): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr7 | 6152536 | ||||||
chr7:6152544 | C | T | 1 | a0002c0006t0005g0315 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2202-1212C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 14/17 | chr7 | 6152544 | |||||||
chr7:6152553 | T | G | 40 | a0002c0004t0001g0325 a0002c0004t0001g0326 a0002c0004t0001g0327 others(37): Show |
40 | HG01167.hp2 HG01243.hp1 HG01256.hp1 others(37): Show |
intron_variant | MODIFIER | c.2202-1203T>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 14/17 | chr7 | 6152553 | |||||||
chr7:6152742 | A | G | 1 | a0002c0003t0001g0099 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.2202-1014A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 14/17 | chr7 | 6152742 | |||||||
chr7:6152757 | C | T | 1 | a0014c0049t0001g0295 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.2202-999C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 14/17 | chr7 | 6152757 | |||||||
chr7:6152867 | C | G | 15 | a0002c0004t0001g0325 a0002c0004t0001g0326 a0002c0004t0001g0327 others(12): Show |
15 | HG02257.hp2 HG02258.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.2202-889C>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 14/17 | chr7 | 6152867 | |||||||
chr7:6152942 | AC | A | 8 | a0003c0002t0001g0010 a0003c0002t0001g0011 a0003c0002t0001g0054 others(5): Show |
10 | HG02055.hp1 HG02572.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.2202-813delC | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 14/17 | chr7 | 6152942 | |||||||
chr7:6152966 | T | TTAGGAAG others(17): Show |
1 | a0003c0008t0001g0089 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2202-789_2202-766d others(26): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr7 | 6152966 | ||||||
chr7:6153041 | C | T | 1 | a0003c0002t0001g0136 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.2202-715C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 14/17 | chr7 | 6153041 | |||||||
chr7:6153238 | G | C | 106 | a0002c0003t0001g0002 a0002c0003t0001g0004 a0002c0003t0001g0006 others(103): Show |
120 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.2202-518G>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 14/17 | chr7 | 6153238 | |||||||
chr7:6153274 | C | CA | 71 | a0003c0002t0001g0007 a0003c0002t0001g0014 a0003c0002t0001g0015 others(68): Show |
77 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.2202-475dupA | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr7 | 6153274 | ||||||
chr7:6153282 | C | A | 1 | a0003c0002t0001g0188 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2202-474C>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 14/17 | chr7 | 6153282 | |||||||
chr7:6153302 | C | CA | 112 | a0001c0001t0001g0023 a0001c0001t0001g0227 a0001c0001t0001g0268 others(109): Show |
126 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.2202-442dupA | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr7 | 6153302 | ||||||
chr7:6153302 | C | CAA | 6 | a0002c0006t0003g0035 a0002c0007t0001g0164 a0002c0007t0009g0158 others(3): Show |
6 | HG01256.hp1 HG03041.hp2 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.2202-443_2202-442d others(4): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr7 | 6153302 | ||||||
chr7:6153323 | T | C | 2 | a0003c0002t0001g0127 a0003c0002t0001g0130 |
2 | HG02071.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.2202-433T>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 14/17 | chr7 | 6153323 | |||||||
chr7:6153351 | C | G | 1 | a0002c0003t0001g0099 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.2202-405C>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 14/17 | chr7 | 6153351 | |||||||
chr7:6153468 | A | G | 27 | a0002c0006t0001g0027 a0002c0006t0001g0039 a0002c0006t0001g0313 others(24): Show |
28 | HG01167.hp2 HG01243.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.2202-288A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 14/17 | chr7 | 6153468 | |||||||
chr7:6153472 | A | G | 71 | a0003c0002t0001g0007 a0003c0002t0001g0014 a0003c0002t0001g0015 others(68): Show |
77 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.2202-284A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 14/17 | chr7 | 6153472 | |||||||
chr7:6153473 | G | A | 71 | a0003c0002t0001g0007 a0003c0002t0001g0014 a0003c0002t0001g0015 others(68): Show |
77 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.2202-283G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 14/17 | chr7 | 6153473 | |||||||
chr7:6153558 | C | T | 1 | a0002c0003t0001g0108 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2202-198C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 14/17 | chr7 | 6153558 | |||||||
chr7:6153579 | C | T | 1 | a0003c0002t0001g0085 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2202-177C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 14/17 | chr7 | 6153579 | |||||||
chr7:6155245 | G | A | 87 | a0002c0003t0001g0002 a0002c0003t0001g0004 a0002c0003t0001g0006 others(84): Show |
100 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.3641+50G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 15/17 | chr7 | 6155245 | |||||||
chr7:6155394 | A | G | 49 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0024 others(46): Show |
60 | HG00438.hp1 HG00639.hp1 HG01069.hp2 others(57): Show |
intron_variant | MODIFIER | c.3641+199A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 15/17 | chr7 | 6155394 | |||||||
chr7:6155435 | C | G | 1 | a0003c0002t0001g0146 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.3641+240C>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 15/17 | chr7 | 6155435 | |||||||
chr7:6155482 | T | C | 2 | a0002c0007t0001g0019 a0002c0034t0001g0331 |
3 | HG01081.hp2 HG03195.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.3641+287T>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 15/17 | chr7 | 6155482 | |||||||
chr7:6155511 | A | G | 3 | a0003c0012t0001g0073 a0003c0012t0001g0074 a0003c0012t0001g0075 |
3 | HG01081.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.3641+316A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 15/17 | chr7 | 6155511 | |||||||
chr7:6155556 | T | G | 2 | a0003c0002t0001g0139 a0003c0002t0001g0155 |
2 | HG00733.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.3641+361T>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 15/17 | chr7 | 6155556 | |||||||
chr7:6155796 | G | T | 32 | a0004c0005t0001g0008 a0004c0005t0001g0296 a0004c0005t0001g0297 others(29): Show |
35 | HG00280.hp1 HG00642.hp1 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.3641+601G>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 15/17 | chr7 | 6155796 | |||||||
chr7:6155898 | G | A | 102 | a0002c0003t0001g0002 a0002c0003t0001g0004 a0002c0003t0001g0006 others(99): Show |
115 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.3641+703G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 15/17 | chr7 | 6155898 | |||||||
chr7:6155939 | T | G | 21 | a0004c0005t0001g0008 a0004c0005t0001g0296 a0004c0005t0001g0297 others(18): Show |
24 | HG00280.hp1 HG00642.hp1 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.3641+744T>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 15/17 | chr7 | 6155939 | |||||||
chr7:6155962 | G | A | 1 | a0001c0001t0001g0209 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.3641+767G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 15/17 | chr7 | 6155962 | |||||||
chr7:6156074 | G | T | 3 | a0003c0012t0001g0073 a0003c0012t0001g0074 a0003c0012t0001g0075 |
3 | HG01081.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.3642-680G>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 15/17 | chr7 | 6156074 | |||||||
chr7:6156080 | G | A | 1 | a0001c0001t0001g0343 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.3642-674G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 15/17 | chr7 | 6156080 | |||||||
chr7:6156114 | G | T | 1 | a0004c0038t0001g0044 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3642-640G>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 15/17 | chr7 | 6156114 | |||||||
chr7:6156404 | T | G | 1 | a0003c0002t0001g0185 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3642-350T>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 15/17 | chr7 | 6156404 | |||||||
chr7:6156560 | C | G | 2 | a0002c0006t0005g0315 a0002c0006t0005g0317 |
2 | HG02129.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.3642-194C>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 15/17 | chr7 | 6156560 | |||||||
chr7:6156598 | C | T | 2 | a0002c0006t0005g0315 a0002c0006t0005g0317 |
2 | HG02129.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.3642-156C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 15/17 | chr7 | 6156598 | |||||||
chr7:6156599 | G | A | 13 | a0003c0002t0001g0010 a0003c0002t0001g0011 a0003c0002t0001g0043 others(10): Show |
16 | HG01175.hp2 HG02055.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.3642-155G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 15/17 | chr7 | 6156599 | |||||||
chr7:6156659 | T | C | 1 | a0002c0035t0001g0072 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3642-95T>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 15/17 | chr7 | 6156659 | |||||||
chr7:6156698 | C | T | 1 | a0001c0001t0001g0308 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.3642-56C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 15/17 | chr7 | 6156698 | |||||||
chr7:6156705 | T | C | 1 | a0002c0006t0005g0317 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.3642-49T>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 15/17 | chr7 | 6156705 | |||||||
chr7:6157105 | A | G | 2 | a0002c0007t0001g0163 a0020c0033t0001g0162 |
2 | HG01884.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.3943+50A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 16/17 | chr7 | 6157105 | |||||||
chr7:6157160 | G | A | 1 | a0004c0009t0001g0080 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.3943+105G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 16/17 | chr7 | 6157160 | |||||||
chr7:6157253 | G | A | 1 | a0002c0003t0001g0106 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.3943+198G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 16/17 | chr7 | 6157253 | |||||||
chr7:6157287 | G | C | 1 | a0002c0050t0001g0294 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3943+232G>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 16/17 | chr7 | 6157287 | |||||||
chr7:6157379 | GTTTTA | G | 4 | a0001c0001t0001g0280 a0001c0001t0001g0282 a0001c0001t0001g0285 others(1): Show |
4 | HG02056.hp2 HG02071.hp2 HG02165.hp1 others(1): Show |
intron_variant | MODIFIER | c.3943+343_3943+347d others(7): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr7 | 6157379 | ||||||
chr7:6157383 | T | G | 14 | a0002c0004t0001g0340 a0003c0002t0001g0010 a0003c0002t0001g0011 others(11): Show |
17 | HG01175.hp2 HG02055.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.3943+328T>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 16/17 | chr7 | 6157383 | |||||||
chr7:6157414 | T | C | 27 | a0002c0006t0001g0027 a0002c0006t0001g0039 a0002c0006t0001g0313 others(24): Show |
28 | HG01167.hp2 HG01243.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.3943+359T>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 16/17 | chr7 | 6157414 | |||||||
chr7:6157460 | C | T | 4 | a0002c0003t0001g0016 a0002c0003t0001g0117 a0002c0003t0001g0187 others(1): Show |
5 | HG03209.hp1 NA18977.hp2 NA18988.hp1 others(2): Show |
intron_variant | MODIFIER | c.3943+405C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 16/17 | chr7 | 6157460 | |||||||
chr7:6157541 | G | A | 1 | a0001c0001t0001g0246 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.3943+486G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 16/17 | chr7 | 6157541 | |||||||
chr7:6157572 | G | A | 1 | a0002c0003t0001g0113 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.3943+517G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 16/17 | chr7 | 6157572 | |||||||
chr7:6157711 | C | T | 1 | a0002c0003t0001g0102 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.3943+656C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 16/17 | chr7 | 6157711 | |||||||
chr7:6157714 | C | G | 1 | a0001c0001t0001g0272 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3943+659C>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 16/17 | chr7 | 6157714 | |||||||
chr7:6157723 | C | T | 6 | a0001c0001t0001g0012 a0001c0001t0001g0022 a0001c0001t0001g0239 others(3): Show |
7 | HG00280.hp2 HG01123.hp2 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.3943+668C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 16/17 | chr7 | 6157723 | |||||||
chr7:6157735 | G | A | 5 | a0002c0003t0001g0016 a0002c0003t0001g0117 a0002c0003t0001g0118 others(2): Show |
6 | NA18747.hp1 NA18977.hp2 NA18988.hp1 others(3): Show |
intron_variant | MODIFIER | c.3943+680G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 16/17 | chr7 | 6157735 | |||||||
chr7:6157743 | G | C | 1 | a0003c0017t0001g0065 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.3943+688G>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 16/17 | chr7 | 6157743 | |||||||
chr7:6157745 | T | G | 140 | a0002c0003t0001g0002 a0002c0003t0001g0004 a0002c0003t0001g0006 others(137): Show |
159 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.3943+690T>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 16/17 | chr7 | 6157745 | |||||||
chr7:6157748 | C | A | 124 | a0002c0003t0001g0002 a0002c0003t0001g0004 a0002c0003t0001g0006 others(121): Show |
140 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.3943+693C>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 16/17 | chr7 | 6157748 | |||||||
chr7:6157825 | C | A | 2 | a0003c0002t0001g0184 a0003c0002t0001g0185 |
2 | HG02486.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.3943+770C>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 16/17 | chr7 | 6157825 | |||||||
chr7:6157890 | C | A | 22 | a0004c0005t0001g0008 a0004c0005t0001g0296 a0004c0005t0001g0297 others(19): Show |
25 | HG00280.hp1 HG00642.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.3943+835C>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 16/17 | chr7 | 6157890 | |||||||
chr7:6157929 | G | A | 2 | a0005c0019t0001g0050 a0005c0019t0001g0051 |
2 | HG02717.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.3943+874G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 16/17 | chr7 | 6157929 | |||||||
chr7:6157976 | T | C | 1 | a0001c0001t0001g0232 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.3943+921T>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 16/17 | chr7 | 6157976 | |||||||
chr7:6157999 | A | G | 2 | a0008c0021t0001g0059 a0008c0021t0001g0060 |
2 | HG02280.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.3943+944A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 16/17 | chr7 | 6157999 | |||||||
chr7:6158043 | A | G | 50 | a0002c0006t0001g0027 a0002c0006t0001g0039 a0002c0006t0001g0313 others(47): Show |
54 | HG00280.hp1 HG00642.hp1 HG00673.hp1 others(51): Show |
intron_variant | MODIFIER | c.3943+988A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 16/17 | chr7 | 6158043 | |||||||
chr7:6158097 | C | T | 47 | a0002c0003t0001g0002 a0002c0003t0001g0004 a0002c0003t0001g0006 others(44): Show |
59 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.3943+1042C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 16/17 | chr7 | 6158097 | |||||||
chr7:6158142 | A | G | 1 | a0002c0035t0001g0072 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3943+1087A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 16/17 | chr7 | 6158142 | |||||||
chr7:6158290 | C | T | 1 | a0003c0017t0001g0065 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.3944-1160C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 16/17 | chr7 | 6158290 | |||||||
chr7:6158367 | G | GTGAAGC | 2 | a0002c0014t0001g0020 a0002c0014t0001g0270 |
3 | HG02559.hp2 HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.3944-1082_3944-107 others(10): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr7 | 6158367 | ||||||
chr7:6158386 | C | T | 1 | a0018c0036t0001g0264 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3944-1064C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 16/17 | chr7 | 6158386 | |||||||
chr7:6158461 | G | A | 70 | a0003c0002t0001g0007 a0003c0002t0001g0014 a0003c0002t0001g0015 others(67): Show |
76 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.3944-989G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 16/17 | chr7 | 6158461 | |||||||
chr7:6158472 | T | TG | 65 | a0002c0003t0001g0002 a0002c0003t0001g0004 a0002c0003t0001g0006 others(62): Show |
78 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.3944-974dupG | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr7 | 6158472 | ||||||
chr7:6158487 | C | G | 1 | a0003c0017t0001g0065 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.3944-963C>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 16/17 | chr7 | 6158487 | |||||||
chr7:6158490 | C | A | 1 | a0002c0050t0001g0294 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3944-960C>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 16/17 | chr7 | 6158490 | |||||||
chr7:6158514 | A | G | 1 | a0003c0002t0002g0009 | 2 | HG02109.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.3944-936A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 16/17 | chr7 | 6158514 | |||||||
chr7:6158559 | G | A | 2 | a0002c0014t0001g0020 a0002c0014t0001g0270 |
3 | HG02559.hp2 HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.3944-891G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 16/17 | chr7 | 6158559 | |||||||
chr7:6158571 | G | A | 19 | a0001c0001t0001g0012 a0001c0001t0001g0022 a0001c0001t0001g0023 others(16): Show |
20 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(17): Show |
intron_variant | MODIFIER | c.3944-879G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 16/17 | chr7 | 6158571 | |||||||
chr7:6158612 | G | A | 1 | a0002c0027t0001g0316 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.3944-838G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 16/17 | chr7 | 6158612 | |||||||
chr7:6158630 | G | T | 1 | a0002c0006t0001g0039 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.3944-820G>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 16/17 | chr7 | 6158630 | |||||||
chr7:6158658 | C | T | 1 | a0003c0002t0001g0145 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.3944-792C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 16/17 | chr7 | 6158658 | |||||||
chr7:6158764 | G | A | 1 | a0003c0002t0001g0185 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3944-686G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 16/17 | chr7 | 6158764 | |||||||
chr7:6158940 | GT | G | 68 | a0002c0003t0001g0002 a0002c0003t0001g0004 a0002c0003t0001g0006 others(65): Show |
82 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.3944-508delT | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr7 | 6158940 | ||||||
chr7:6158956 | C | T | 1 | a0003c0017t0001g0065 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.3944-494C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 16/17 | chr7 | 6158956 | |||||||
chr7:6159000 | G | A | 1 | a0003c0017t0001g0065 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.3944-450G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 16/17 | chr7 | 6159000 | |||||||
chr7:6159003 | G | A | 1 | a0003c0017t0001g0065 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.3944-447G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 16/17 | chr7 | 6159003 | |||||||
chr7:6159066 | C | T | 1 | a0002c0050t0001g0294 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3944-384C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 16/17 | chr7 | 6159066 | |||||||
chr7:6159068 | G | GC | 5 | a0002c0006t0003g0034 a0003c0002t0001g0128 a0003c0002t0001g0138 others(2): Show |
5 | HG02602.hp1 HG02809.hp2 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.3944-378dupC | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr7 | 6159068 | ||||||
chr7:6159073 | G | A | 2 | a0005c0019t0001g0050 a0005c0019t0001g0051 |
2 | HG02717.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.3944-377G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 16/17 | chr7 | 6159073 | |||||||
chr7:6159164 | G | A | 64 | a0002c0003t0001g0002 a0002c0003t0001g0004 a0002c0003t0001g0006 others(61): Show |
77 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.3944-286G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 16/17 | chr7 | 6159164 | |||||||
chr7:6159168 | C | T | 2 | a0005c0011t0001g0029 a0005c0011t0001g0031 |
2 | HG02895.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.3944-282C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 16/17 | chr7 | 6159168 | |||||||
chr7:6159246 | C | T | 3 | a0002c0014t0001g0020 a0002c0014t0001g0270 a0002c0035t0001g0072 |
4 | HG02559.hp2 HG02922.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.3944-204C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 16/17 | chr7 | 6159246 | |||||||
chr7:6159286 | C | T | 1 | a0003c0002t0001g0323 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.3944-164C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 16/17 | chr7 | 6159286 | |||||||
chr7:6159366 | A | G | 71 | a0003c0002t0001g0007 a0003c0002t0001g0014 a0003c0002t0001g0015 others(68): Show |
77 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.3944-84A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 16/17 | chr7 | 6159366 | |||||||
chr7:6159397 | C | A | 1 | a0003c0002t0001g0323 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.3944-53C>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 16/17 | chr7 | 6159397 | |||||||
chr7:6159401 | C | T | 2 | a0008c0021t0001g0059 a0008c0021t0001g0060 |
2 | HG02280.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.3944-49C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 16/17 | chr7 | 6159401 | |||||||
chr7:6159409 | C | T | 1 | a0002c0050t0001g0294 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3944-41C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 16/17 | chr7 | 6159409 | |||||||
chr7:6159441 | G | C | 63 | a0002c0003t0001g0002 a0002c0003t0001g0004 a0002c0003t0001g0006 others(60): Show |
76 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.3944-9G>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 16/17 | chr7 | 6159441 | |||||||
chr7:6159535 | C | T | 18 | a0001c0001t0001g0012 a0001c0001t0001g0022 a0001c0001t0001g0023 others(15): Show |
19 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(16): Show |
intron_variant | MODIFIER | c.*36+42C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 17/17 | chr7 | 6159535 | |||||||
chr7:6159547 | G | A | 1 | a0001c0001t0001g0266 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.*36+54G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 17/17 | chr7 | 6159547 | |||||||
chr7:6159556 | G | A | 1 | a0001c0001t0001g0210 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.*36+63G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 17/17 | chr7 | 6159556 | |||||||
chr7:6159557 | G | A | 1 | a0002c0004t0001g0338 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.*36+64G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 17/17 | chr7 | 6159557 | |||||||
chr7:6159565 | A | G | 1 | a0003c0002t0001g0323 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.*36+72A>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 17/17 | chr7 | 6159565 | |||||||
chr7:6159614 | TGGAGAGG others(4): Show |
T | 1 | a0003c0008t0001g0089 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.*36+124_*36+134del others(11): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr7 | 6159614 | ||||||
chr7:6159625 | C | T | 49 | a0002c0004t0001g0325 a0002c0004t0001g0326 a0002c0004t0001g0327 others(46): Show |
52 | HG00280.hp1 HG00642.hp1 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.*36+132C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 17/17 | chr7 | 6159625 | |||||||
chr7:6159634 | C | G | 28 | a0002c0004t0001g0335 a0002c0006t0001g0027 a0002c0006t0001g0039 others(25): Show |
29 | HG01167.hp2 HG01243.hp1 HG01256.hp1 others(26): Show |
intron_variant | MODIFIER | c.*36+141C>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 17/17 | chr7 | 6159634 | |||||||
chr7:6159698 | T | C | 1 | a0003c0008t0001g0089 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.*36+205T>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 17/17 | chr7 | 6159698 | |||||||
chr7:6159699 | T | G | 1 | a0003c0008t0001g0089 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.*36+206T>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 17/17 | chr7 | 6159699 | |||||||
chr7:6159700 | G | C | 1 | a0003c0008t0001g0089 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.*36+207G>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 17/17 | chr7 | 6159700 | |||||||
chr7:6159704 | T | C | 1 | a0003c0008t0001g0089 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.*36+211T>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 17/17 | chr7 | 6159704 | |||||||
chr7:6159705 | A | C | 1 | a0003c0008t0001g0089 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.*36+212A>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 17/17 | chr7 | 6159705 | |||||||
chr7:6159707 | T | C | 1 | a0003c0008t0001g0089 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.*36+214T>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 17/17 | chr7 | 6159707 | |||||||
chr7:6159708 | G | C | 1 | a0003c0008t0001g0089 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.*36+215G>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 17/17 | chr7 | 6159708 | |||||||
chr7:6159709 | G | C | 1 | a0003c0008t0001g0089 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.*36+216G>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 17/17 | chr7 | 6159709 | |||||||
chr7:6159711 | T | C | 1 | a0003c0008t0001g0089 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.*36+218T>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 17/17 | chr7 | 6159711 | |||||||
chr7:6159712 | G | C | 1 | a0003c0008t0001g0089 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.*36+219G>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 17/17 | chr7 | 6159712 | |||||||
chr7:6159713 | G | C | 1 | a0003c0008t0001g0089 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.*36+220G>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 17/17 | chr7 | 6159713 | |||||||
chr7:6159714 | G | C | 1 | a0003c0008t0001g0089 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.*36+221G>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 17/17 | chr7 | 6159714 | |||||||
chr7:6159715 | G | C | 1 | a0003c0008t0001g0089 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.*36+222G>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 17/17 | chr7 | 6159715 | |||||||
chr7:6159716 | A | C | 1 | a0003c0008t0001g0089 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.*36+223A>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 17/17 | chr7 | 6159716 | |||||||
chr7:6159717 | A | C | 1 | a0003c0008t0001g0089 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.*36+224A>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 17/17 | chr7 | 6159717 | |||||||
chr7:6159718 | G | C | 1 | a0003c0008t0001g0089 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.*36+225G>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 17/17 | chr7 | 6159718 | |||||||
chr7:6159719 | A | C | 1 | a0003c0008t0001g0089 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.*36+226A>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 17/17 | chr7 | 6159719 | |||||||
chr7:6159723 | G | C | 1 | a0003c0008t0001g0089 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.*36+230G>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 17/17 | chr7 | 6159723 | |||||||
chr7:6159725 | A | C | 1 | a0003c0008t0001g0089 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.*36+232A>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 17/17 | chr7 | 6159725 | |||||||
chr7:6159726 | T | C | 1 | a0003c0008t0001g0089 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.*36+233T>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 17/17 | chr7 | 6159726 | |||||||
chr7:6159729 | T | C | 1 | a0003c0008t0001g0089 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.*36+236T>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 17/17 | chr7 | 6159729 | |||||||
chr7:6159730 | T | C | 1 | a0003c0008t0001g0089 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.*36+237T>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 17/17 | chr7 | 6159730 | |||||||
chr7:6159732 | A | C | 1 | a0003c0008t0001g0089 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.*36+239A>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 17/17 | chr7 | 6159732 | |||||||
chr7:6159734 | G | C | 1 | a0003c0008t0001g0089 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.*36+241G>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 17/17 | chr7 | 6159734 | |||||||
chr7:6159736 | A | C | 1 | a0003c0008t0001g0089 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.*36+243A>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 17/17 | chr7 | 6159736 | |||||||
chr7:6159737 | G | C | 1 | a0003c0008t0001g0089 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.*36+244G>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 17/17 | chr7 | 6159737 | |||||||
chr7:6159738 | G | C | 1 | a0003c0008t0001g0089 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.*36+245G>C | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 17/17 | chr7 | 6159738 | |||||||
chr7:6159903 | C | T | 1 | a0002c0006t0003g0035 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.*36+410C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 17/17 | chr7 | 6159903 | |||||||
chr7:6159920 | C | T | 1 | a0002c0003t0001g0167 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.*36+427C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 17/17 | chr7 | 6159920 | |||||||
chr7:6159953 | C | T | 1 | a0003c0002t0001g0184 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.*36+460C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 17/17 | chr7 | 6159953 | |||||||
chr7:6159956 | C | G | 1 | a0001c0001t0001g0263 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.*36+463C>G | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 17/17 | chr7 | 6159956 | |||||||
chr7:6159969 | G | A | 1 | a0003c0017t0001g0065 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.*36+476G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 17/17 | chr7 | 6159969 | |||||||
chr7:6160004 | G | A | 217 | a0002c0003t0001g0002 a0002c0003t0001g0004 a0002c0003t0001g0006 others(214): Show |
242 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(239): Show |
intron_variant | MODIFIER | c.*36+511G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 17/17 | chr7 | 6160004 | |||||||
chr7:6160128 | TGAAAG | T | 66 | a0003c0002t0001g0007 a0003c0002t0001g0014 a0003c0002t0001g0015 others(63): Show |
72 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.*37-422_*37-418del others(5): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr7 | 6160128 | ||||||
chr7:6160350 | G | A | 2 | a0005c0011t0001g0029 a0005c0011t0001g0031 |
2 | HG02895.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.*37-205G>A | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 17/17 | chr7 | 6160350 | |||||||
chr7:6160365 | C | T | 1 | a0001c0001t0001g0267 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.*37-190C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 17/17 | chr7 | 6160365 | |||||||
chr7:6160415 | GGAAGGCA others(2): Show |
G | 86 | a0002c0004t0001g0325 a0002c0004t0001g0326 a0002c0004t0001g0327 others(83): Show |
93 | HG00280.hp1 HG00642.hp1 HG00673.hp1 others(90): Show |
intron_variant | MODIFIER | c.*37-129_*37-121del others(9): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr7 | 6160415 | ||||||
chr7:6160438 | TCTC | T | 41 | a0002c0004t0001g0325 a0002c0004t0001g0326 a0002c0004t0001g0327 others(38): Show |
44 | HG00280.hp1 HG00642.hp1 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.*37-113_*37-111del others(3): Show |
USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr7 | 6160438 | ||||||
chr7:6160489 | C | T | 2 | a0003c0002t0001g0184 a0003c0002t0001g0185 |
2 | HG02486.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.*37-66C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 17/17 | chr7 | 6160489 | |||||||
chr7:6160533 | C | T | 2 | a0002c0007t0004g0292 a0002c0007t0004g0293 |
2 | HG02027.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.*37-22C>T | USP42 | ENSG00000106346.12 | transcript | ENST00000306177.10 | protein_coding | 17/17 | chr7 | 6160533 |